CURRICULUM VITAE
Cheryl A. Hillery MD
Cheryl A. Hillery MD
Professor
Department of Pediatrics
Division of Hematology/Oncology
Department of Pediatrics
Division of Hematology/Oncology
OFFICE ADDRESS: |
The Blood Center |
P O Box 2178 |
Milwaukee, WI 53201 |
EDUCATION: |
8/1976 - 5/1980 BS, Biochemistry, University of Wisconsin, Madison, WI |
8/1980 - 5/1984 MD, Duke University School of Medicine, Durham, NC |
POSTGRADUATE TRAINING AND FELLOWSHIP APPOINTMENTS: |
7/1984 - 6/1988 Resident, Internal Medicine and Pediatrics, University of North Carolina Hospitals, Chapel Hill, NC |
7/1988 - 6/1991 Fellow, Pediatrics and Medicine, Hematology/Oncology (NIH Training grant 7/1989 – 6/1991), University of North Carolina, Chapel Hill, NC |
9/1991 - 6/1993 Postdoctoral Fellow, (NIH Training grant 7/1991 – 6/1992), BloodCenter of Wisconsin, Milwaukee, WI |
FACULTY APPOINTMENTS: |
9/1991 - 6/1993 Instructor, Pediatrics, Medical College of Wisconsin, Milwaukee, WI |
7/1993 - 6/2001 Assistant Professor, Pediatrics, Hematology/Oncology/BMT, Medical College of Wisconsin, Milwaukee, WI |
7/1993 - 6/2003 Associate Investigator, Blood Research Institute, BloodCenter of Wisconsin, Milwaukee, WI |
7/2001 - 6/2006 Associate Professor, Pediatrics, Hematology/Oncology/BMT, Medical College of Wisconsin, Milwaukee, WI |
7/2002 - 6/2006 Associate Investigator, Medicine, Hematology, Medical College of Wisconsin, Milwaukee, WI |
7/2003 - Present Investigator, Blood Research Institute, BloodCenter of Wisconsin, Milwaukee, WI |
7/2006 - Present Professor, Pediatrics, Hematology/Oncology/BMT, Medical College of Wisconsin, Milwaukee, WI |
7/2006 - Present Professor, Medicine, Hematology, Medical College of Wisconsin, Milwaukee, WI |
3/2011 - Present Vice-Chair, Pediatrics, Medical College of Wisconsin, Milwaukee, WI |
ADMINISTRATIVE APPOINTMENTS: |
3/2009 - Present Hematology/Oncology/BMT Leadership Team, Medical College of Wisconsin, Milwaukee, WI |
3/2011 - Present Pediatrics, Executive Committee Member, Medical College of Wisconsin, Milwaukee, WI |
EDUCATIONAL ADMINISTRATIVE APPOINTMENTS: |
7/2010 - Present Co-Director, Basic and Translational Sciences, PhD Program, Medical College of Wisconsin, Milwaukee, WI |
RESEARCH ADMINISTRATIVE APPOINTMENTS: |
7/2000 - Present Scientific Director, Wisconsin Sickle Cell Center, Milwaukee, WI |
HOSPITAL STAFF PRIVILEGES: |
10/1991 - Present Attending Physician, Hematology, Children's Hospital of Wisconsin, Milwaukee, WI |
3/1994 - Present Hematology, Froedtert Hospital, Milwaukee, WI |
SPECIALTY BOARDS AND CERTIFICATION: |
Board Certified | Issue Date | Expiration |
American Board of Internal Medicine | 1988 | None |
American Board of Pediatrics | 1989 | 2007 |
American Board of Pediatrics Hematology-Oncology | 1992 | None |
Licensure | Number | Issue Date | Expiration |
North Carolina | 32732 | 1988 | 1993 |
Wisconsin | 32582 | 1992 | None |
AWARDS AND HONORS: |
1979 Phi Beta Kappa |
1980 Phi Kappa Phi |
1980 - 1984 Rush C. Godfrey Medical Scholarship |
1988 Ciba Geigy Chief Residents Award in Internal Medicine |
1990 - 1991 Research Merit Award, Pediatric Evening of Scholarship |
1993 - 1998 NIH Career Development Award (K08/CIDA) |
1996 Elected to Society of Pediatric Research |
2009 - Present Gerry and Heidi Connolly endowed Sickle Cell Professorship, Children's Hospital of Wisconsin |
2010 Clinical Physician Award – Clinical Scholarship (Pediatrics) |
MEMBERSHIPS IN HONORARY AND PROFESSIONAL SOCIETIES: |
1984 - 1992 American Medical Association (AMA) |
1987 - 1989 American College of Physicians (ACP) |
1993 - 2002 American Heart Association: Council on Arteriosclerosis, Thrombosis, and Vascular Biology |
1994 - 2006 Hemophilia Research Society (HRS) |
1994 - Present American Society of Hematology (ASH) |
1995 - 2000 Milwaukee Blood Club |
1996 - Present Society for Pediatric Research (SPR) |
2004 - 2006 Microcirculatory Society (MCS) |
2006 - Present American Society of Pediatric Hematology/Oncology (ASPHO) |
EDITORSHIPS/EDITORIAL BOARDS/JOURNAL REVIEWS: |
Editorial Board |
2005 - 2010 Blood, journal of the American Society of Hematology (impact factor 10.56) |
Journal Review |
1995 - Present Ad hoc referee for Blood, The Journal of Clinical Investigation, The Journal of Biological Chemistry, European Journal of Haematology, Thrombosis Research, Thrombosis and Haemostasis, Journal of Pedia |
LOCAL/REGIONAL APPOINTED LEADERSHIP AND COMMITTEE POSITIONS: |
1988 - 1991 Selection Committee for Combined Internal Medicine/Pediatric Residency Program, University of North Carolina, Chapel Hill |
1998 - 2000 Search Committee for Vascular, Cell & Molecular Biology Initiative, Blood Research Institute, BloodCenter of Wisconsin |
1999 - Present Appointments and Promotions Committee, Blood Research Institute, BloodCenter of Wisconsin |
2003 - 2011 Search Committee for Vascular Biology Investigators, Blood Research Institute, BloodCenter of Wisconsin |
2003 - 2004 Search Committee for Executive Vice President for Research and Director of the Blood Reserach Institute, BloodCenter of Wisconsin |
NATIONAL ELECTED/APPOINTED LEADERSHIP AND COMMITTEE POSITIONS: |
2000 Ad Hoc Reviewer, Program Project Special Review Committee, National Heart, Lung, and Blood Institute (NHLBI) |
2001 - 2005 Member, Program Project Grant Parent Review Committee, National Heart, Lung, and Blood Institute (NHLBI) |
2002 Ad Hoc Grant Reviewer, March of Dimes |
2004 - 2005 Ad Hoc Reviewer, Study Section (R01s) for ELB, National Institute of Health (NIH) |
2004 - 2009 Member, Hemoglobin/Red Cell Scientific Committee, American Society of Hematology (ASH) |
2005 - 2007 Member, Education and Liaison Committees, World Congress for Microcirculation |
2005 Ad Hoc Reviewer, Program Project Special Review Committee, National Heart, Lung, and Blood Institute (NHLBI) |
2005 Reviewer, Request for Applications Committee (RFA) "Sickle Cell Disease Clinical Research Network”, National Heart, Lung, and Blood Institute (NHLBI) |
2006 Ad Hoc Chair, Program Project Special Review Committee, National Heart, Lung, and Blood Institute (NHLBI) |
2006 - 2010 Member, Erythrocyte and Leukocyte Biology Study Section, National Institute of Health (NIH) |
2007 Panel to advocate for research in genomic studies for risk factors in sickle cell disease, Wellcome Trust, London, England |
2007 Summit on Sickle Cell Disease – From Health and Research Disparity to Action, American Society of Pediatric Hematology/Oncology (ASPHO) |
2008 - 2009 Research Working Group on Sickle Cell Disease, American Society of Pediatric Hematology/Oncology (ASPHO) |
2008 Reviewer, Abstract Review for 2008 Meeting, American Society of Hematology (ASH) |
2008 Ad Hoc Reviewer, Program Project Special Emphasis Panel , National Heart, Lung, and Blood Institute (NHLBI) |
2008 Workshop on Sickle Cell Disease - Sub-Committee on Vascular Biology/Pathophysiology, National Heart, Lung, and Blood Institute (NHLBI) |
2009 Coordinating Reviewer, Sickle Cell Abstract Review for 2009 Meeting, American Society of Hematology (ASH) |
2009 Sickle Cell Disease Workshop—Inflammation, Thrombosis, and Vascular Injury Working Group , National Heart, Lung, and Blood Institute (NHLBI) |
2009 Co-Chair, State-of-the-Art Thalassemia Workshop, National Heart, Lung, and Blood Institute (NHLBI) |
2009 Ad Hoc Reviewer, ARRA P30 and R13 Grant Review Committees, National Institute of Health (NIH) |
2009 Ad Hoc Reviewer, Grant Review Committee, Wellcome Trust, London England |
2009 Ad Hoc Reviewer, Program Project Special Emphasis Panel, National Heart, Lung, and Blood Institute (NHLBI) |
2011 Ad Hoc Reviewer, SBIR Grant Review, National Institute of Health (NIH) |
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INVITED LECTURES/WORKSHOPS/PRESENTATIONS: |
Local |
1. Mechanisms of vaso-occlusion in sickle cell disease, Emory School of Medicine, Atlanta, GA, 8/2003 |
2. Sickle cell disease: insights into the pathophysiology of vaso-occlusion, New York Blood Center, New York, NY, 10/2003 |
3. Sickle cell disease: insights into the pathophysiology of vaso-occlusion, Purdue, LaFayette, IN, 7/2004 |
4. Sickle cell disease: insights into the pathophysiology of vaso-occlusion, Children’s Hospital of Philadelphia, University of Pennsylvania, Philadelphia, PA, 1/2005 |
5. Sickle Cell Disease: insights into the pathophysiology of vaso-occlusion, University of North Carolina – Chapel Hill, Chapel Hill, NC, 6/2006 |
6. Pain and vascular dysfunction in sickle cell disease: insights from sickle mice, Visiting Professorship, Emory University School of Medicine, Atlanta, GA, 9/2011 |
National |
1. Phosphorylation of platelet adhesion receptors: Glycoprotein IIb-IIIa and platelet-endothelial cell adhesion molecule-1 (PECAM-1), University of Wisconsin, Madison, WI, 1/1993 |
2. Adhesion of sickle cells to the vascular endothelium, Red Cells Gordon Research Conference, Tilton, NH, 7/1997 |
3. Moderator of Simultaneous Session on Sickle Cell Disease, American Society of Hematology (ASH) Annual Meeting, New Orleans, LA, 12/1999 |
4. Adhesion of erythrocytes to extracellular matrix, American Heart Association Scientific Conference on Interactions of Blood and the Pulmonary Circulation, Sedalia, CO, 9/2000 |
5. Role of coagulation and inflammatory pathways in sickle cell vascular disease, Hemostasis Gordon Research Conference, Waterville, ME, 7/2004 |
6. Coagulation and Vaso-Occlusion: Which is the Chicken and Which is the Egg” – A Look in to the Crystal Ball: What's in the Future for Sickle Cell Disease, National Sickle Cell Disease Meeting, Cincinnati, OH, 4/2005 |
7. Moderator for Basic Science Simultaneous Session, National Sickle Cell Disease Meeting, Memphis, TN, 4/2006 |
8. Coagulation and inflammation in sickle cell disease, Scientific Committee on Thrombosis & Vascular Biology of the American Society of Hematology, Orlando, FL, 12/2006 |
9. Sickle Cell Disease: insights into the pathophysiology of vaso-occlusion, 2nd Annual Sickle Cell Disease Research and Educational Symposium, Fort Lauderdale, FL, 2/2008 |
10. Sickle cell disease is an inflammatory disorder, Hemostasis Gordon Research Conference, Waterville Valley, NH, 7/2008 |
11. Endothelial dysfunction in the sickle cell mouse, Workshop on Vasculopathy in Sickle Cell Disease, National Institutes of Health, Bethesda, MD, 10/2008 |
12. Sickle Cell Disease is an Inflammatory Disorder: Lessons Learned from Sickle Cell Mice, Cardiopulmonary Symposium on Sickle Cell Disease, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, 10/2008 |
13. Sickle Cell Disease: Inflammation and Thrombosis, Moderator of Simultaneous Session, American Society of Hematology, San Francisco, CA, 12/2008 |
14. Sickle Cell Disease: Hydroxyurea, Hemoglobin F and Pain, Moderator of Simultaneous Session, American Society of Hematology, New Orleans, LA, 12/2009 |
15. John I. Hercules, PhD Named Lecture, 5th Annual Sickle Cell Disease Research and Educational Symposium and Annual National Sickle Cell Disease Scientific Meeting, Hollywood, FL, 2/2011 |
16. Cell Free Hemoglobin, Lipid Oxidation and Nitric Oxide in Sickle Cell Disease, Annual Sickle Cell Disease Clinical Research Meetings: Basic Science & Translational Research Program, NIH Campus, Bethesda, MD, 8/2011 |
17. Novel mechanisms of vaso-occlusion in SCD: insights from mouse models, Hematology Oncology Grand Rounds, St Jude Children’s Research Hospital, Memphis, TN, 9/2011 |
International |
1. Red blood cell adhesion in sickle cell disease, Cambridge University, Cambridge, England, 9/1997 |
2. Vascular Biology of thrombospondin: Mechanisms of vaso-occlusion in sickle cell disease: adhesion of sickle red cells to thrombospondin, International Conference on the Biology of Thrombospondins, Madison, WI, 6/2000 |
3. Sickle Cell Disease: insights into the pathophysiology of vaso-occlusion using murine models of sickle cell disease, UK Forum on Haemoglobin Disorders - Plenary Talk, London, England, 10/2006 |
4. Mouse models in the study of sickle cell disease, Genetics Modifiers of Sickle Cell Disease Explorative Meeting, Wellcome Trust, London, England, 3/2007 |
5. Potential Novel therapies in Sickle Cell Disease, Bayer Hematology Innovation Summit, Budapest, Hungary, 10/2011 |
PEER REVIEWED WORKSHOPS/PRESENTATIONS: |
National |
1. Smyth SS, Hillery CA, Parise LV, Phosphatidic and lysophosphatidic acid modulate the fibrinogen binding activity of purified platelet glycoprotein IIb-IIIa, American Society of Hematology (ASH) 32nd Annual Meeting - Poster Presentation, Boston, MA, 12/1990 |
2. Hillery CA, Smyth SS, Parise LV, Stoichiometry of glycoprotein IIIa phosphorylation in whole platelets and in vitro, American Society of Hematology (ASH) 32nd Annual Meeting - Poster Presentation, Boston, MA, 12/1990 |
3. Hillery CA, Newman PJ, Stoichiometry and kinetics of PECAM-1 phosphorylation and incorporation into the cytoskeleton of intact platelets, American Society of Hematology (ASH) 34th Annual Meeting - Oral Presentation by Cheryl Hillery, Anaheim, CA, 12/1992 |
4. Hillery CA, Wood JD, Scott JP, Kampine JP, Hudetz AG, Sickle red blood cells have enhanced adhesion to rat brain microvasculature in vivo, American Society of Hematology (ASH) 36th Annual Meeting - Poster Presentation, Nashville, TN, 12/1994 |
5. Hillery CA, Du MC, Barbour TJ, Montgomery RR, Scott JP, An acidic lipid purified from sickle red blood cells specifically binds to thrombospondin, American Society of Hematology (ASH) 36th Annual Meeting - Poster Presentation, Nashville, TN, 12/1994 |
6. Hillery CA, Du MC, Scott JP, Montgomery RR, Sickle red blood cells (SS-RBC) demonstrate increased adhesion to thrombospondin and laminin that is inhibited by high molecular weight dextran sulfate, American Heart Association - Oral Presentation by Cheryl Hillery, Dallas, TX, 1994 |
7. Hillery CA, Wood JD, Scott JP, Kampine JP, Hudetz AG, Enhanced adhesion of sickle red blood cells to rat brain microvasculature: an in vivo model, 20th Annual Meeting of the National Sickle Cell Disease Program - Oral Presentation by Cheryl Hillery, Boston, MA, 3/1995 |
8. Hillery CA, Du MC, Barbour TJ, Montgomery RR, Scott JP, Potential role for sulfated glycolipids in the adhesion of sickle red blood cells to thrombospondin, 20th Annual Meeting of the National Sickle Cell Disease Program - Oral Presentation by Cheryl Hillery, Boston, MA, 3/1995 |
9. 12.9. French JA II, Hudetz AG, Kenny D, Du MC, Kampine JP, Scott JP, Hillery CA, Sickle erythrocytes decrease cerebral blood flow in rats when nitric oxide synthesis is inhibited, American Society of Hematology (ASH) 37th Annual Meeting - Poster Presentation, Seattle, WA, 12/1995 |
10. Du MC, Scott JP, Hillery CA, Red blood cells treated with phenylhydrazine or calcium ionophore have increased adhesion to thrombospondin, similar to sickle erythrocytes, American Society of Hematology (ASH) 37th Annual Meeting - Poster Presentation, Seattle, WA, 12/1995 |
11. Hillery CA, Walls EN, Du MC, Scott JP, Hydroxyurea therapy decreases red blood cell adhesion to thrombospondin and laminin in hemoglobin SS disease, American Society of Hematology (ASH) 37th Annual Meeting - Oral Presentation by Cheryl Hillery, Seattle, WA, 12/1995 |
12. French JA II, Hudetz AG, Kenny D, Du MC, Kampine JP, Scott JP, Hillery CA, Sickle erythrocytes decrease cerebral blood flow in rats when nitric oxide synthesis is inhibited, American Society of Hematology (ASH) 37th Annual Meeting - Poster Presentation, Seattle, WA, 12/1995 |
13. Hillery CA, Walls EN, Du MC, Scott JP, Erythrocytes from patients with sickle cell disease on hydroxyurea therapy have decreased adhesion to thrombospondin and laminin, 20th Annual Meeting of the National Sickle Cell Disease Program - Oral Presentation by Cheryl Hillery, Mobile, AL, 3/1996 |
14. French JA II, Hudetz AG, Kenny D, Du MC, Kampine JP, Scott JP, Hillery CA, Nitric oxide synthase inhibition decreases cerebral blood flow in rats infused with sickle erythrocytes, 21st Annual Meeting of the National Sickle Cell Disease Program - Oral Presentation by Jim French, Mobile, AL, 3/1996 |
15. French JA II, Hudetz AG, Kenny D, Du MC, Kampine JP, Scott JP, Hillery CA, Nitric oxide synthase inhibition decreases cerebral blood flow in rats infused with sickle erythrocytes, Pediatric Academic Society - Poster Presentation, Washington, DC, 5/1996 |
16. Hillery CA, Du MC, French JA II, Scott JP, Sickle red blood cells bind to the 140 kDa C-terminal domain of thrombospondin, Pediatric Academic Society - Oral Presentation by Cheryl Hillery, Washington, DC, 5/1996 |
17. Hillery CA, Scott JP, French JA II, Frazier WA, Du MC, Sickle red blood cells bind to the 20 kDa C-terminal domain of thrombospondin, American Society of Hematology (ASH) 38th Annual Meeting - Oral Presentation by Cheryl Hillery, Orlando, FL, 12/1996 |
18. Hillery CA, Du MC, Scott JP, Sickle RBCs bind to the C-terminal cell binding domain of thrombospondin in a conformational-dependent manner, 22nd Annual Meeting of the National Sickle Cell Disease Program - Poster Presentation, Washington, DC, 9/1997 |
19. Osbourne SE, Johnson ST, Scott JP, Hillery CA, Gottschall JG, A simple and effective protocol to reduce red cell alloimmunization among patients with sickle cell disease, American Association of Blood Banks (AABB) 50th Annual Meeting, Denver, CO, 10/1997 |
20. Punzalan RC, Hillery CA, Montgomery RR, Scott JP, Gill JC, Safety and efficacy of low molecular weight heparin (Enoxaparin): a pediatric experience, American Society of Hematology (ASH) 39th Annual Meeting - Poster Presentation, San Diego, CA, 12/1997 |
21. Punzalan RC, Du MC, Low PS, Scott JP, Hillery CA, Role of hydration status in erythrocyte adhesion to thrombospondin, American Society of Hematology (ASH) 39th Annual Meeting - Oral Presentation by Rowena Punzalan, San Diego, CA, 12/1997 |
22. Punzalan RC, Trost BA, Scott JP, Hudetz AG, Hillery CA, Chondroitin sulfate-A limits cerebral ischemia induced by nitric oxide inhibition in sickle erythrocyte-infused rats, American Society of Hematology (ASH) 40th Annual Meeting - Poster Presentation, Miami, FL, 12/1998 |
23. Du MC, Watkins NA, Scott JP, Ouwehand WH, Hillery CA, Single chain antibody fragments derived from a human synthetic phage display library bind the cell binding domain of thrombospondin and inhibit sickle cell adhesion, American Society of Hematology (ASH) 40th Annual Meeting - Poster Presentation, Miami, FL, 12/1998 |
24. Hillery CA, Punzalan RC, Trost BA, Scott JP, Hudetz AG, Chondroitin sulfate-A limits cerebral ischemia in sickle erythrocyte-infused rats, 24th Annual Meeting of the National Sickle Cell Disease Program - Oral Presentation by Cheryl Hillery, San Francisco, CA, 3/1999 |
25. Maloney KW, Hillery CA, Nelson T, Gill JC, The use of aliquoted and frozen tPA in central venous line occlusions, American Society of Hematology (ASH) 41st Annual Meeting - Poster Presentation, New Orleans, LA, 12/1999 |
26. Punzalan RC, Holzman S, Trost BA, Paszty C, Mohandas N, Scott JP, Hillery CA, Spontaneous stroke and increased erythrocyte adhesion in transgenic knockout sickle cell mice, American Society of Hematology (ASH) 41st Annual Meeting - Poster Presentation, New Orleans, LA, 12/1999 |
27. Hillery CA, Du MC, Scott JP, Ware RE, Rogers ZR, Wynn LW, Wang WC, Red blood cell adhesion remains low in very young children with sickle cell disease receiving hydroxyurea therapy, American Society of Hematology (ASH) 41st Annual Meeting - Poster Presentation, New Orleans, LA, 12/1999 |
28. Hillery CA, Holzman SL, Mohandas N, Scott JP, Trost BA, Organ-specific fibrin deposition is increased in transgenic sickle mice, 25th Annual Meeting of the National Sickle Cell Disease Program - Poster Presentation, Philadelphia, PA, 3/2000 |
29. Bevan JA, Maloney KW, Hillery CA, Gill JC, Montgomery RR, Scott JP, Bleeding disorders are a common cause of adolescent menorrhagia, American Society of Pediatric Hematology/Oncology (ASPHO) 13th Annual Meeting - Poster Presentation, Minneapolis, MN, 9/2000 |
30. Talano JM, Gottschall JL, Pugh TM, Hillery CA, Scott JP, Partial phenotype matching (Rh, Kell) reduces alloimmuniztion in children with sickle cell disease, American Society of Pediatric Hematology/Oncology (ASPHO) 13th Annual Meeting - Poster Presentation, Minneapolis, MN, 9/2000 |
31. Wandersee NJ, Olson SC, Holzman SL, Barker JE, Hillery CA, Increased erythrocyte adhesion in mice with hereditary spherocytosis and hereditary elliptocytosis, American Society of Hematology (ASH) 42nd Annual Meeting - Poster Presentation, San Francisco, CA, 12/2000 |
32. Holzman SL, Shen H, Du LM, Mohandas N, Scott JP, Hudetz A, Hillery CA, Inhibition of nitric oxide synthase induces acute vaso-occlusion in transgenic sickle mice, American Society of Hematology (ASH) 42nd Annual Meeting - Oral Presentation by Cheryl Hillery, San Francisco, CA, 12/2000 |
33. Bayliff SL, Pickens CV, Hillery CA, Ware RE, Changes in surface expression of erythrocyte adhesion molecules in association with hydroxyurea therapy, Pediatric Academic Society Annual Meeting - Oral Presentation by Russell Ware, Baltimore, MD, 5/2001 |
34. Talano JM, Hillery CA, Gottschall JL, Baylerian DM, Scott JP, Delayed hemolytic transfusion reactions in sickle cell disease, Pediatric Academic Societies Annual Meeting - Poster Presentation, Baltimore, MD, 5/2001 |
35. Vice JL, Le L, Fahs SA, Jozwiak MA, Gill JC, Scott JP, Hillery CA, Montgomery RR, von Willebrand factor gene mutation causing 2A and 2B variants of von Willebrand disease, Pediatric Academic Societies Annual Meeting - Poster Presentation, Baltimore, MD, 5/2001 |
36. Wandersee NJ, Sillah NM, Watkins NA, Scott JP, Ouwehand WH, Hillery CA, Single chain antibody fragments derived from a human phage display library preferentially bind sickle red blood cells and inhibit sickle cell adhesion, American Society of Hematology (ASH) 43rd Annual Meeting - Poster Presentation, Orlando, FL, 12/2001 |
37. Hillery CA, Franciosi JP, Ou J, Shi Y, Burglund C, Witte K, Guice K, Oldham KT, Pritchard KA Jr, Increased susceptibility to hypoxic injury in a murine model of sickle cell disease, 27th Annual Meeting of the National Sickle Cell Disease Program - Oral Presentation by Cheryl Hillery, Washington, DC, 3/2002 |
38. Saunthararajah Y, Molokie R, Lavelle D, HILLERY C, Dorn L, DeSimone J, Subcutaneous 5-aza-2’-deoxycytidine is well tolerated and produces robust increases in fetal hemoglobin, 27th Annual Meeting of the National Sickle Cell Disease Program - Oral Presentation by Yogen Saunthararajah, Washington, DC, 3/2002 |
39. 40.32. Franciosi JP, Pritchard KA Jr, Ou J, Shi Y, Ou Z, Ackland-Berglund C, Witte K, Guice K, Oldham KT, Hillery CA, Increased susceptibility to hypoxic injury in a murine model of sickle cell disease, 9th Annual Meeting of the Oxygen Society - Oral Presentation by Kirkwood Pritchard, San Antonio, TX, 11/2002 |
40. Hillery CA, Holzman SA, Franciosi JP, Ou J, Ou Z, Mohandas N, Guice K, Oldham KT, Pritchard, KA Jr, Changes in hsp90 - eNOS interactions following hypoxia-induced acute lung injury in a murine model of sickle cell disease, American Society of Hematology (ASH) 44th Annual Meeting - Oral Presenation by Cheryl Hillery, Philadelphia, PA, 12/2002 |
41. Hillery CA, Sillah NM, Wandersee NJ, Holzman SL, Gavazova S, Foster TD, Scott JP, Montgomery RR, Saunthararajah Y, DeSimone J, Effect of fetal hemoglobin induction by decitabine on erythrocyte adhesion, coagulation parameters and markers of inflammation in patients with sickle cell disease, American Society of Hematology (ASH) 44th Annual Meeting - Oral Presentation by Cheryl Hillery, Philadelphia, PA, 12/2002 |
42. Gavazova S, Gill JC, Scott JP, Hillery CA, Friedman KD, Wetzel N, Jozwiak M, Haberichter SL, Christopherson P, Montgomery RR, A mutation in the D4 domain of von Willebrand factor results in a variant of type 1 von Willebrand disease with accelerated in vivo clearance, American Society of Hematology (ASH) 44th Annual Meeting - Oral Presenation by S. Gavazova, Philadelphia, PA, 12/2002 |
43. Panepinto JA, Hillery CA, Scott JP, Seasonal variation in hospital length of stay in children with sickle cell disease, American Society of Hematology (ASH) 44th Annual Meeting - Oral Presenation by Julie Panepinto, Philadelphia, PA, 12/2002 |
44. Saunthararajah Y, HILLERY C, Lavelle D, Molokie R, Chen A, Dorn L, Hoffman R, DeSimone J, Safety, efficacy and mechanism of action of sub-cutaneous 5-aza-2’-deoxycytidine for elevating fetal hemoglobin levels in patients with sickle cell disease, American Society of Hematology (ASH) 44th Annual Meeting - Poster Presentation, Philadelphia, PA, 12/2002 |
45. Hillery CA, Foster TD, Holzhauer SL, Scott JP, Panepinto JA, Trost BA, Mohandas N, Degen JL, Wandersee NJ, Fibrinogen deficiency decreases hepatic infarction in a stem cell transplant model of murine sickle cell disease, American Society of Hematology (ASH) 45th Annual Meeting - Oral Presentation by Cheryl Hillery, San Diego, CA, 12/2003 |
46. Manci E, Hillery CA, Coller BS, A Systematic Assessment of Organ Pathology in “Berkeley” Sickle Cell Mice: Similarities and differences from human sickle cell disease, American Society of Hematology (ASH) 45th Annual Meeting - Poster Presentation, San Diego, CA, 12/2003 |
47. Brousseau DC, Panepinto JA, Hillery CA, Scott JP, The effect of intravenous magnesium sulfate on length of stay for children hospitalized with sickle cell pain crises, American Society of Hematology (ASH) 45th Annual Meeting - Poster Presentation, San Diego, CA, 12/2003 |
48. Campanella ME, Anong WA, Wandersee NJ, Hillary CA, Chishti A, Low PS, Characterization of glycolytic enzyme complexes on murine erythrocyte membranes, American Society of Hematology (ASH) 46th Annual Meeting - Poster Presentation, San Diego, CA, 12/2004 |
49. Wandersee NJ, Punzalan RC, Sillah NM, Rettig MP, Kennedy MD, Scott JP, Low PS, Hillery CA, Modulation of erythrocyte adhesion by changes in cellular tonicity and volume, American Society of Hematology (ASH) 46th Annual Meeting - Poster Presentation, San Diego, CA, 12/2004 |
50. Gill JC, Rowe R, Conley S, HILLERY C, Panepinto J, Scott JP, Montgomery RR, Desmopressin and Epsilon Amino-Caproic Acid (EACA) in Adenotonsillectomy (T&A): Are we under-treating patients with mild type 1 von Willebrand disease (VWD) and mild platelet function defects (PFD)? , American Society of Hematology (ASH) 46th Annual Meeting - Poster Presentation, San Diego, CA, 12/2004 |
51. Hillery CA, Foster TD, Holzhauer SL, Scott JP, Panepinto JA, Mohandas N, Mackman N, Wandersee NJ, Tissue factor deficiency decreases sickle cell-induced vascular stasis in a hematopoietic stem cell transplant model of murine sickle cell disease, American Society of Hematology (ASH) 46th Annual Meeting - Oral Presentation by Cheryl Hillery, San Diego, CA, 12/2004 |
52. Hebbel RP, Jiang A, Hillery CA, Scott JP, Nelson SC, Enenstein J, Milbauer L, Bodempudi V, Pan W, Topper JN, Yang RB, Genetic influence on the systems biology of sickle stroke risk detected by endothelial gene expression, American Society of Hematology (ASH) 47th Annual Meeting - Oral Presentation by R. Hebbel, Atlanta, GA, 12/2005 |
International |
1. Wandersee NJ, Punzalan RC, Watkins NA, Ouwehand WH, Low PS, Hillery CA, Role of erythrocyte hydration in adhesion of RBCs to thrombospondin-1, Red Cell Gordon Research Conference - Poster Presentation, Lucca (Barga), Italy, 5/2003 |
BIBLIOGRAPHY |
Refereed Journal Publications/Original Papers |
1. Hillery CA, Smyth SS, Parise LV Phosphorylation of human platelet glycoprotein IIIa (GPIIIa). Dissociation from fibrinogen receptor activation and phosphorylation of GPIIIa in vitro. J Biol Chem. 1991 Aug 5;266(22):14663-9 |
2. Smyth SS, Hillery CA, Parise LV Fibrinogen binding to purified platelet glycoprotein IIb-IIIa (integrin alpha IIb beta 3) is modulated by lipids. J Biol Chem. 1992 Aug 5;267(22):15568-77 |
3. Newman PJ, Hillery CA, Albrecht R, Parise LV, Berndt MC, Mazurov AV, Dunlop LC, Zhang J, Rittenhouse SE Activation-dependent changes in human platelet PECAM-1: phosphorylation, cytoskeletal association, and surface membrane redistribution. J Cell Biol. 1992 Oct;119(1):239-46 |
4. Chusid MJ, Russler SK, Mohr BA, Margolis DA, Hillery CA, Kehl KC Unsuspected brucellosis diagnosed in a child as a result of an outbreak of laboratory-acquired brucellosis. Pediatr Infect Dis J. 1993 Dec;12(12):1031-3 |
5. Hillery CA, Du MC, Montgomery RR, Scott JP Increased adhesion of erythrocytes to components of the extracellular matrix: isolation and characterization of a red blood cell lipid that binds thrombospondin and laminin. Blood. 1996 Jun 1;87(11):4879-86 |
6. Scott JP, Hillery CA, Brown ER, Misiewicz V, Labotka RJ Hydroxyurea therapy in children severely affected with sickle cell disease. J Pediatr. 1996 Jun;128(6):820-8 |
7. French JA 2nd, Kenny D, Scott JP, Hoffmann RG, Wood JD, Hudetz AG, Hillery CA Mechanisms of stroke in sickle cell disease: sickle erythrocytes decrease cerebral blood flow in rats after nitric oxide synthase inhibition. Blood. 1997 Jun 15;89(12):4591-9 |
8. Hillery CA, Mancuso DJ, Evan Sadler J, Ponder JW, Jozwiak MA, Christopherson PA, Cox Gill J, Paul Scott J, Montgomery RR Type 2M von Willebrand disease: F606I and I662F mutations in the glycoprotein Ib binding domain selectively impair ristocetin- but not botrocetin-mediated binding of von Willebrand factor to platelets. Blood. 1998 Mar 1;91(5):1572-81 |
9. Hillery CA, Scott JP, Du MC The carboxy-terminal cell-binding domain of thrombospondin is essential for sickle red blood cell adhesion. Blood. 1999 Jul 1;94(1):302-9 |
10. Punzalan RC, Hillery CA, Montgomery RR, Scott CA, Gill JC Low-molecular-weight heparin in thrombotic disease in children and adolescents. J Pediatr Hematol Oncol. 2000 Mar-Apr;22(2):137-42 |
11. Hillery CA, Du MC, Wang WC, Scott JP Hydroxyurea therapy decreases the in vitro adhesion of sickle erythrocytes to thrombospondin and laminin. Br J Haematol. 2000 May;109(2):322-7 |
12. Bevan JA, Maloney KW, Hillery CA, Gill JC, Montgomery RR, Scott JP Bleeding disorders: A common cause of menorrhagia in adolescents. J Pediatr. 2001 Jun;138(6):856-61 |
13. Gallagher PG, Chang SH, Rettig MP, Neely JE, Hillery CA, Smith BD, Low PS Altered erythrocyte endothelial adherence and membrane phospholipid asymmetry in hereditary hydrocytosis. Blood. 2003 Jun 1;101(11):4625-7 |
14. Rice HE, Oldham KT, Hillery CA, Skinner MA, O'Hara SM, Ware RE Clinical and hematologic benefits of partial splenectomy for congenital hemolytic anemias in children. Ann Surg. 2003 Feb;237(2):281-8 |
15. Watkins NA, Du LM, Scott JP, Ouwehand WH, Hillery CA Single-chain antibody fragments derived from a human synthetic phage-display library bind thrombospondin and inhibit sickle cell adhesion. Blood. 2003 Jul 15;102(2):718-24 |
16. Ou J, Ou Z, Jones DW, Holzhauer S, Hatoum OA, Ackerman AW, Weihrauch DW, Gutterman DD, Guice K, Oldham KT, Hillery CA, Pritchard KA Jr L-4F, an apolipoprotein A-1 mimetic, dramatically improves vasodilation in hypercholesterolemia and sickle cell disease. Circulation. 2003 May 13;107(18):2337-41 |
17. Talano JA, Hillery CA, Gottschall JL, Baylerian DM, Scott JP Delayed hemolytic transfusion reaction/hyperhemolysis syndrome in children with sickle cell disease. Pediatrics. 2003 Jun;111(6 Pt 1):e661-5 |
18. Rathore V, Stapleton MA, Hillery CA, Montgomery RR, Nichols TC, Merricks EP, Newman DK, Newman PJ PECAM-1 negatively regulates GPIb/V/IX signaling in murine platelets. Blood. 2003 Nov 15;102(10):3658-64 |
19. Saunthararajah Y, Hillery CA, Lavelle D, Molokie R, Dorn L, Bressler L, Gavazova S, Chen YH, Hoffman R, DeSimone J Effects of 5-aza-2'-deoxycytidine on fetal hemoglobin levels, red cell adhesion, and hematopoietic differentiation in patients with sickle cell disease. Blood. 2003 Dec 1;102(12):3865-70 |
20. Melzer-Lange MD, Walsh-Kelly CM, Lea G, Hillery CA, Scott JP Patient-controlled analgesia for sickle cell pain crisis in a pediatric emergency department. Pediatr Emerg Care. 2004 Jan;20(1):2-4 |
21. Wandersee NJ, Olson SC, Holzhauer SL, Hoffmann RG, Barker JE, Hillery CA Increased erythrocyte adhesion in mice and humans with hereditary spherocytosis and hereditary elliptocytosis. Blood. 2004 Jan 15;103(2):710-6 |
22. Pritchard KA Jr, Ou J, Ou Z, Shi Y, Franciosi JP, Signorino P, Kaul S, Ackland-Berglund C, Witte K, Holzhauer S, Mohandas N, Guice KS, Oldham KT, Hillery CA Hypoxia-induced acute lung injury in murine models of sickle cell disease. Am J Physiol Lung Cell Mol Physiol. 2004 Apr;286(4):L705-14 |
23. Brousseau DC, Scott JP, Hillery CA, Panepinto JA The effect of magnesium on length of stay for pediatric sickle cell pain crisis. Acad Emerg Med. 2004 Sep;11(9):968-72 |
24. Panepinto JA, Brousseau DC, Hillery CA, Scott JP Variation in hospitalizations and hospital length of stay in children with vaso-occlusive crises in sickle cell disease. Pediatr Blood Cancer. 2005 Feb;44(2):182-6 |
25. Wandersee NJ, Punzalan RC, Rettig MP, Kennedy MD, Pajewski NM, Sabina RL, Paul Scott J, Low PS, Hillery CA Erythrocyte adhesion is modified by alterations in cellular tonicity and volume. Br J Haematol. 2005 Nov;131(3):366-77 |
26. Manci EA, Hillery CA, Bodian CA, Zhang ZG, Lutty GA, Coller BS Pathology of Berkeley sickle cell mice: similarities and differences with human sickle cell disease. Blood. 2006 Feb 15;107(4):1651-8 |
27. Ataga KI, Moore CG, Hillery CA, Jones S, Whinna HC, Strayhorn D, Sohier C, Hinderliter A, Parise LV, Orringer EP Coagulation activation and inflammation in sickle cell disease-associated pulmonary hypertension. Haematologica. 2008 Jan;93(1):20-6 |
28. Hankins JS, Wynn LW, Brugnara C, Hillery CA, Li CS, Wang WC Phase I study of magnesium pidolate in combination with hydroxycarbamide for children with sickle cell anaemia. Br J Haematol. 2008 Jan;140(1):80-5 |
29. Chang Milbauer L, Wei P, Enenstein J, Jiang A, Hillery CA, Scott JP, Nelson SC, Bodempudi V, Topper JN, Yang RB, Hirsch B, Pan W, Hebbel RP Genetic endothelial systems biology of sickle stroke risk. Blood. 2008 Apr 1;111(7):3872-9 |
30. Nandedkar SD, Feroah TR, Hutchins W, Weihrauch D, Konduri KS, Wang J, Strunk RC, DeBaun MR, Hillery CA, Pritchard KA Histopathology of experimentally induced asthma in a murine model of sickle cell disease. Blood. 2008 Sep 15;112(6):2529-38 |
31. Sabina RL, Wandersee NJ, Hillery CA Ca2+-CaM activation of AMP deaminase contributes to adenine nucleotide dysregulation and phosphatidylserine externalization in human sickle erythrocytes. Br J Haematol. 2009 Feb;144(3):434-45 |
32. Gladwin MT, Barst RJ, Castro OL, Gordeuk VR, Hillery CA, Kato GJ, Kim-Shapiro DB, Machado R, Morris CR, Steinberg MH, Vichinsky EP Pulmonary hypertension and NO in sickle cell. Blood. 2010 Aug 5;116(5):852-4 |
33. Nandedkar SD, Weihrauch D, Xu H, Shi Y, Feroah T, Hutchins W, Rickaby DA, Duzgunes N, Hillery CA, Konduri KS, Pritchard KA Jr D-4F, an apoA-1 mimetic, decreases airway hyperresponsiveness, inflammation, and oxidative stress in a murine model of asthma. J Lipid Res. 2011 Mar;52(3):499-508 |
34. Hanson MS, Piknova B, Keszler A, Diers AR, Wang X, Gladwin MT, Hillery CA, Hogg N Methaemalbumin formation in sickle cell disease: effect on oxidative protein modification and HO-1 induction. Br J Haematol. 2011 Aug;154(4):502-11 |
35. Hillery CA, Kerstein PC, Vilceanu D, Barabas ME, Retherford D, Brandow AM, Wandersee NJ, Stucky CL Transient receptor potential vanilloid 1 mediates pain in mice with severe sickle cell disease. Blood. 2011 Sep 22;118(12):3376-83 |
36. Pritchard KA Jr, Feroah TR, Nandedkar SD, Holzhauer SL, Hutchins W, Schulte ML, Strunk RC, Debaun MR, Hillery CA Effects of experimental asthma on inflammation and lung mechanics in sickle cell mice. Am J Respir Cell Mol Biol. 2012 Mar;46(3):389-96 |
Books, Chapters, and Reviews |
1. Hillery CA Potential therapeutic approaches for the treatment of vaso-occlusion in sickle cell disease. Curr Opin Hematol. 1998 Mar;5(2):151-5 |
2. Hillery CA Adhesion of sickle erythrocytes to extracellular matrix. In: EK Weir, HL Reeve, JT Reeves, ed. Interactions of blood and the pulmonary circulations. Armonk, NY: Futura Publishing Company; 2002:68-92 |
3. Hillery CA, Panepinto JA Pathophysiology of stroke in sickle cell disease. Microcirculation. 2004 Mar;11(2):195-208 |
4. Hillery CA The chicken or the egg? tissue factor and inflammation in sickle cell disease. “Inside Blood” invited editorial comment. Blood. 2004;104(3):595-596 |
5. Pritchard KA, Rivera A, Hillery C, Brugnara C. Novel approaches to treatment. In: MH Steinberg, BG Forget, DR Higgs, DJ Weatherall, ed. Disorders of hemoglobin. 2nd ed. New York NY: Cambridge University Press; 2009 |
6. Larson MC, Woodliff JE, Hillery CA, Kearl TJ, Zhao M Phosphatidylethanolamine is externalized at the surface of microparticles. Biochim Biophys Acta. 2012 Aug 30: |
7. Garrison SR, Kramer AA, Gerges NZ, Hillery CA, Stucky CL Sickle cell mice exhibit mechanical allodynia and enhanced responsiveness in light touch cutaneous mechanoreceptors. Mol Pain. 2012 Sep 10;8(1):62 |
8. Hanson MS, Xu H, Flewelen TC, Holzhauer SL, Retherford D, Jones DW, Frei AC, Pritchard KA Jr, Hillery CA, Hogg N, Wandersee NJ A novel hemoglobin-binding peptide reduces cell-free hemoglobin in murine hemolytic anemia. Am J Physiol Heart Circ Physiol. 2013 Jan;304(2):H328-36 |
9. Larson MC, Luthi MR, Hogg N, Hillery CA Calcium-phosphate microprecipitates mimic microparticles when examined with flow cytometry. Cytometry A. 2012 Nov 2: |
10. Brandow AM, Stucky CL, Hillery CA, Hoffmann RG, Panepinto JA Patients with sickle cell disease have increased sensitivity to cold and heat. Am J Hematol. 2013 Jan;88(1):37-43 |
Abstracts |
1. Hillery CA, Smyth SS, Parise LV. Stoichiometry of glycoprotein IIIa phosphorylation in whole platelets and in vitro. Blood. 1990; 76:459a |
2. Smyth SS, Hillery CA, Parise LV. Phosphatidic and lysophosphatidic acid modulate the fibrinogen binding activity of purified platelet glycoprotein IIb-IIIa. Blood 1991; 78:278a |
3. Hillery CA, Newman PJ. Stoichiometry and kinetics of PECAM-1 phosphorylation and incorporation into the cytoskeleton of intact platelets. Blood 1992; 80:265a |
4. Hillery CA, Du MC, Scott JP, Montgomery RR. Sickle red blood cells (SS-RBC) demonstrate increased adhesion to thrombospondin and laminin that is inhibited by high molecular weight dextran sulfate. Circulation. 1994; 90:I-347 |
5. Labotka RJ, Misiewicz VM, Robinson E, Hillery CA, Scott JP. Hydroxyurea (HDU) therapy in severely affected children with sickle cell disease (SCD). Pediatric Research 1994; 35:163a |
6. Hillery CA, Du MC, Barbour TJ, Montgomery RR, Scott JP. An acidic lipid purified from sickle red blood cells specifically binds to thrombospondin. Blood. 1994; 84:406a |
7. Hillery CA, Wood JD, Scott JP, Kampine JP, Hudetz AG. Sickle red blood cells have enhanced adhesion to rat brain microvasculature in vivo. Blood. 1994; 84:413a |
8. Hillery CA, Walls EN, Du MC, Scott JP. Hydroxyurea therapy decreases red blood cell adhesion to thrombospondin and laminin in hemoglobin SS disease. Blood. 1995; 86:986a |
9. Du MC, Scott JP, Hillery CA. Red blood cells treated with phenylhydrazine or calcium ionophore have increased adhesion to thrombospondin, similar to sickle erythrocytes. Blood. 1995; 86:137a |
10. French JA II, Hudetz AG, Kenny D, Du MC, Kampine JP, Scott JP, Hillery CA. Sickle erythrocytes decrease cerebral blood flow in rats when nitric oxide synthesis is inhibited. Blood. 1995; 86:142a |
11. Hillery CA, Du MC, French JA II, Scott JP. Sickle red blood cells bind to the 140 kDa C-terminal domain of thrombospondin. Pediatric Research. 1996; 39:156a |
12. French JA II, Hudetz AG, Kenny D, Du MC, Kampine JP, Scott JP, Hillery CA. Nitric oxide synthase inhibition decreases cerebral blood flow in rats infused with sickle erythrocytes. Pediatric Research. 1996; 39:155a |
13. Hillery CA, Scott JP, French JA II, Frazier WA, Du MC. Sickle red blood cells bind to the 20 kDa C-terminal domain of thrombospondin. Blood. 1996; 88:649a |
14. Punzalan RC, Du MC, Low PS, Scott JP, Hillery CA. Role of hydration status in erythrocyte adhesion to thrombospondin. Blood. 1997; 90:604a |
15. Punzalan RC, Hillery CA, Montgomery RR, Scott JP, Gill JC. Safety and efficacy of low molecular weight heparin (Enoxaparin): a pediatric experience. Blood. 1997; 90:296a |
16. Punzalan RC, Trost BA, Scott JP, Hudetz AG, Hillery CA. Chondroitin sulfate-A limits cerebral ischemia induced by nitric oxide inhibition in sickle erythrocyte-infused rats. Blood. 1998; 92:329a |
17. Du MC, Watkins NA, Scott JP, Ouwehand WH, Hillery CA. Single chain antibody fragments derived from a human synthetic phage display library bind the cell binding domain of thrombospondin and inhibit sickle cell adhesion. Blood. 1998; 92:330a |
18. Osbourne SE, Johnson ST, Scott JP, Hillery CA, Gottschall JG. A simple and effective protocol to reduce red cell alloimmunization among patients with sickle cell disease. Transfusion. 1998 Oct;38(10 Suppl) |
19. Hillery CA, Du MC, Scott JP, Ware RE, Rogers ZR, Wynn LW, Wang WC. Red blood cell adhesion remains low in very young children with sickle cell disease receiving hydroxyurea therapy. Blood. 1999; 94: 416a |
20. Punzalan RC, Holzman S, Trost BA, Paszty C, Mohandas N, Scott JP, Hillery CA. Spontaneous stroke and increased erythrocyte adhesion in transgenic knockout sickle cell mice. Blood. 1999; 94: 419a |
21. Maloney KW, Hillery CA, Nelson T, Gill JC. The use of aliquoted and frozen tPA in central venous line occlusions. Blood. 1999; 94: 29a |
22. Holzman SL, Shen H, Du LM, Mohandas N, Scott JP, Hudetz A, Hillery CA. Inhibition of nitric oxide synthase induces acute vaso-occlusion in transgenic sickle mice. Blood. 2000; 96:528a |
23. Wandersee NJ, Olson SC, Holzman SL, Barker JE, Hillery CA. Increased erythrocyte adhesion in mice with hereditary spherocytosis and hereditary elliptocytosis. Blood. 2000; 96:594a |
24. Bevan JA, Maloney KW, Hillery CA, Gill JC, Montgomery RR, Scott JP. Bleeding disorders are a common cause of adolescent menorrhagia. Pedatric Academic Societies' Abstract Archive 2000. http://www.abstracts2view.com/pasall/view.php?nu=PAS0L_4 |
25. Talano JM, Hillery CA, Gottschall JL, Baylerian DM, Scott JP. Delayed hemolytic transfusion reactions in sickle cell. Pediatric Academic Societies' Abstract Archive 2001. http://www.abstracts2view.com/pasall/view.php?nu=PAS1L_2255 |
26. Bayliff SL, Pickens CV, Hillery CA, Ware RE. Changes in surface expression of erythrocyte adhesion molecules in association with hydroxyurea therapy. Pediatric Academic Societies' Abstract Acrchive 2001. http://www.abstracts2view.com/pasall/view.php?nu=PAS1L_467 |
27. Vice JL, Le L, Fahs SA, Jozwiak MA, Gill JC, Scott JP, Hillery CA, Montgomery RR. von Willebrand factor gene mutation causing 2A and 2B variants of von Willebrand disease. Pediatric Academic Societies' Abstract Archive 2001. http://www.abstracts2view.com/pasall/view.php?nu=PAS1L_311 |
28. Wandersee NJ, Sillah NM, Watkins NA, Scott JP, Ouwehand WH, Hillery CA. Single chain antibody fragments derived from a human phage display library preferentially bind sickle red blood cells and inhibit sickle cell adhesion. Blood. 2001; 98:484a |
29. Chang SH, Gallagher PG, Rettig MP, Neely JE, Hillery CA, Smith BD, Low PS. Altered erythrocyte endothelial adherence and membrane phospholipid asymmetry in hereditary hydrocytosis. Blood. 2001; 98:12a |
30. Hillery CA, Holzman SA, Franciosi JP, Ou J, Ou Z, Mohandas N, Guice K, Oldham KT, Pritchard, KA Jr. Changes in hsp90 - eNOS interactions following hypoxia-induced acute lung injury in a murine model of sickle cell disease. Blood. 2002; 100:29a |
31. Hillery CA, Sillah NM, Wandersee NJ, Holzman SL, Gavazova S, Foster TD, Scott JP, Montgomery RR, Saunthararajah Y, DeSimone J. Effect of fetal hemoglobin induction by decitabine on erythrocyte adhesion, coagulation parameters and markers of inflammation in patients with sickle cell disease. Blood. 2002; 100:25a |
32. Panepinto JA, Hillery CA, Scott JP. Seasonal variation in hospital length of stay in children with sickle cell disease. Blood; 2002; 100:695a |
33. Rathore V, HILLERY C, Montgomery RR, Newman PJ. PECAM-1 negatively regulates GPIb/V/IX-induced aggregation of murine platelets. Blood. 2002; 100:1835a |
34. Saunthararajah Y, HILLERY C, Lavelle D, Molokie R, Chen A, Dorn L, Hoffman R, DeSimone J. Safety, efficacy and mechanism of action of sub-cutaneous 5-aza-2’-deoxycytidine for elevating fetal hemoglobin levels in patients with sickle cell disease. Blood. 2002; 100:2620a |
35. Gavazova S, Gill JC, Scott JP, Hillery CA, Friedman KD, Wetzel N, Jozwiak M, Haberichter SL, Christopherson P, Montgomery RR. A mutation in the D4 domain of von Willebrand factor results in a variant of type 1 von Willebrand disease with accelerated in vivo clearance. Blood. 2002; 100:476a |
36. Hillery CA, Foster TD, Holzhauer SL, Scott JP, Panepinto JA, Trost BA, Mohandas N, Degen JL, Wandersee NJ. Fibrinogen deficiency decreases hepatic infarction in a stem cell transplant model of murine sickle cell disease. Blood. 2003; 102:274a |
37. Manci E, HILLERY C, Coller BS. A Systematic Assessment of Organ Pathology in “Berkeley” Sickle Cell Mice: Similarities and differences from human sickle cell disease. Blood. 2003; 102:918a |
38. Brousseau DC, Panepinto JA, Hillery CA, Scott JP. The effect of intravenous magnesium sulfate on length of stay for children hospitalized with sickle cell pain crises. Blood. 2003; 102:2815a |
39. Hillery CA, Foster TD, Holzhauer SL, Scott JP, Panepinto JA, Mohandas N, Mackman N, Wandersee NJ. Tissue factor deficiency decreases sickle cell-induced vascular stasis in a hematopoietic stem cell transplant model of murine sickle cell disease Blood. 2004; 104:236a |
40. Wandersee NJ, Punzalan RC, Sillah NM, Rettig MP, Kennedy MD, Scott JP, Low PS, Hillery CA. Modulation of erythrocyte adhesion by changes in cellular tonicity and volume Blood. 2004; 104:1577a |
41. Campanella ME, Anong WA, Wandersee NJ, HILLARY CA, Chishti A, Low PS. Characterization of glycolytic enzyme complexes on murine erythrocyte membranes Blood. 2004; 104:1571a |
42. Gill JC, Rowe R, Conley S, HILLERY C, Panepinto J, Scott JP, Montgomery RR. Desmopressin and Epsilon Amino-Caproic Acid (EACA) in Adenotonsillectomy (T&A): Are we under-treating patients with mild type 1 von Willebrand disease (VWD) and mild platelet function defects (PFD)? Blood. 2004; 104:1024a |
43. Hebbel RP, Jiang A, Hillery CA, Scott JP, Nelson SC, Enenstein J, Milbauer L, Bodempudi V, Pan W, Topper JN, Yang RB. Genetic influence on the systems biology of sickle stroke risk detected by endothelial gene expression. Blood. 2005; 106:73a |
44. Pritchard KA Jr, Besch TL, Wang J, Xu H, Jones DW, Foster TD, Holzhauer SL, Oldham KT, Wandersee NJ, Hillery CA. Differential effects of lovastatin and allopurinol therapy in a murine model of sickle cell disease. Blood. 2005; 106:2325a |
45. Piknova B, Gladwin M, Hillery CA, Hogg N. Electron Paramagnetic Resonance study of cell-free hemoglobin in sickle cell disease: Potential antioxidant role of haptoglobin. Blood. 2005; 106:549a |
46. Sabina RL, Wandersee NJ, Hillery CA. AMP Deaminase activation contributes to accelerated adenine nucleotide pool depletion during periods of energy imbalance in sickle cell erythrocytes. Blood. 2005; 106:1671a |
47. Rennie KM, Scott JP, Panepinto JA, Hillery CA. Increased Red Cell Adhesion is Associated with Overt Stroke in Sickle Cell Disease. Blood. 2005; 106:2320a |
48. Pritchard KA Jr, Wang J, Xu H, Jones DW, Holzhauer S, Foster TD, Oldham KT, Hillery CA. D-4F restores eNOS-dependent vasodilation by decreasing proinflammatory HDL. Blood. 2005; 106:2324a |
49. Hillery CA. Coagulation and Inflammation in Sickle Cell Disease. Blood. 2006; 108a |
50. Uy T, Wandersee NJ, Hillery CA. Modifications of the coagulation system alter inflammation in murine sickle cell disease. Blood. 2006; 108: 1242a |
51. Brandow AM, Rennie KM, Scott JP, Hillery CA, Panepinto JA. Increased red blood cell adhesion is associated with priapism in sickle cell disease. Blood. 2006; 108: 1235a |
52. Hankins J, Wynn L, Brugnara C, HILLERY C, Li CS, Wang W. Phase I study of combination treatment with hydroxyurea and magnesium pidolate in children with sickle cell anemia. Blood. 2006; 108: 686a |
53. Wandersee NJ, Frei AC, Holzhauer SL, Scott JP, Pritchard KA Jr, Fagan KA, Hogg N, Hillery CA. Vascular Dysfunction in Murine Models of Hemolytic Anemia. Blood. 2007; 110: 846a |
54. Hebbel RP, Wei P, Jiang A, HILLERY C, Scott JP, Nelson SC, Enenstein J, Milbauer L, Bodempudi V, Pan W, Hirsch B, Topper JN, Yang RB. Genetic Influence on the Systems Biology of Sickle Stroke Risk Detected by Endothelial Gene Expression. Blood. 2007; 110: 427a |
55. Ataga KI, Hillery CA, Park HA, Moore CG, Jones S, Wang J, Hinderliter A, Pritchard KA Jr. Vascular Dysfunction in Murine Models of Hemolytic Anemia. Proinflammatory Lipids in Sickle Cell Disease-Associated Pulmonary Hypertension. Blood. 2007; 110: 3801a |
56. Wandersee NJ, Uy T, Retherford D, Noon-Abdullah A, Frei AC, Brandow AM, Stucky CL, Hillery CA. Mechanical Hypersensitivity in a Mouse Model of Sickle Cell Disease Blood. 2008; 112: 2479a |
57. Guo Y, Uy T, Wandersee NJ, Scott JP, Weiler H, Holzhauer S, Retherford D, Foster T, Hillery CA. The Protein C Pathway in Human and Murine Sickle Cell Disease: Alterations in Protein C, Thrombomodulin (TM), and Endothelial Protein C Receptor (EPCR) at Baseline and during Acute Vaso-occlusion Blood. 2008; 112: 538a |
58. Guo YH, Field JJ, Foster TD, Scott JP, Wandersee NJ, Hillery CA. Low Molecular Weight Heparin Reduces sVCAM 1 and Lung Congestion in a Murine Model of Sickle Cell Disease. Blood. 2010; 116:1635a |
59. Wandersee NJ, Flewelen TC, Frei AC, Jones DW, Retherford DM, Holzhauer SL, Gokuli S, Hanson MS, Hillery CA, Hogg N, Pritchard KA Jr, Xu H. A novel hemoglobin-binding agent reduces plasma free hemoglobin and partially improves vascular function in murine hemolytic anemia. Blood. 2010; 116:267a |
60. Flewelen TC, Xu H, Jones DW, Pritchard KA Jr, Hillery CA, Wandersee NJ, Hogg N. Characterizing hE-Hb-B10: A Dual Functioning Hemoglobin Binding Peptide. Free Redical Bio Med. 2011 Nov; 51(Suppl):S86 |
61. Hanson MS, Flewelen T, Hao Xu, Johnes DW, PA Kirkwood, Hillery CA, Wandersee NJ, Hoagg N. A Novel Hemoglobin Binding Peptide Increases Intracellular Heme and Potentiates Hemoglobin-Induced Heme Oxygenase-1 (HO-1) Levels in Endothelial Cells. Free Redical Bio Med. 2011 Nov; 51(Suppl):S40 |
62. Brandow AM, Kattappuram R, Hillery CA, Stucky CL, Panepinto JA. Patients with Sickle Cell Disease Have Increased Sensitivity to Cold and Heat Stimuli. Blood 2011; 118: :2116 |
63. Hanson MS, Flewelen TC, Xu H, Pritchard KA Jr, Wandersee NJ, Hogg N, Hillery CA. A Novel Hemoglobin Binding Peptide Increases Intracellular Heme and Potentiates Hemoglobin-Induced Heme Oxygenase-1 (HO-1) Levels in Endothelial Cells. Blood. 2011; 118:1065 |







