Medical College of Wisconsin
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Craig C. Porter MD

Professor

Institution: Medical College of Wisconsin
Department: Pediatrics
Division: Nephrology


I am willing to mentor a junior faculty member.


Research Experience

  • Congenital Abnormalities
  • Congenital, Hereditary, and Neonatal Diseases and Abnormalities
  • Genetic Diseases, Inborn
  • Leadership Positions

  • Vice Chair for Faculty, Department of Pediatrics, Medical College of Wisconsin
  • Publications

  • Mutations in kelch-like 3 and cullin 3 cause hypertension and electrolyte abnormalities. (Boyden LM, Choi M, Choate KA, Nelson-Williams CJ, Farhi A, Toka HR, Tikhonova IR, Bjornson R, Mane SM, Colussi G, Lebel M, Gordon RD, Semmekrot BA, Poujol A, Välimäki MJ, De Ferrari ME, Sanjad SA, Gutkin M, Karet FE, Tucci JR, Stockigt JR, Keppler-Noreuil KM, Porter CC, Anand SK, Whiteford ML, Davis ID, Dewar SB, Bettinelli A, Fadrowski JJ, Belsha CW, Hunley TE, Nelson RD, Trachtman H, Cole TR, Pinsk M, Bockenhauer D, Shenoy M, Vaidyanathan P, Foreman JW, Rasoulpour M, Thameem F, Al-Shahrouri HZ, Radhakrishnan J, Gharavi AG, Goilav B, Lifton RP) Nature 2012 Feb 2;482(7383):98-102 PMID: 22266938 PMCID: PMC3278668
  • E380D: a novel point mutation of CYP21 in an HLA-homozygous patient with salt-losing congenital adrenal hyperplasia due to 21-hydroxylase deficiency. (Kirby-Keyser L, Porter CC, Donohoue PA) Hum Mutat 1997;9(2):181-2 PMID: 9067760
  • Alpha 1B-adrenergic receptors in rat renal microvessels. (Canessa LM, Piccio MM, Vachvanichsanong P, Sidhu A, Porter CC, Robillard JE, Felder RA, Jose PA) Kidney Int 1995 Nov;48(5):1412-9 PMID: 8544397
  • Ontogenic changes and regulation of renal angiotensin II type 1 receptor gene expression during fetal and newborn life. (Robillard JE, Schutte BC, Page WV, Fedderson JA, Porter CC, Segar JL) Pediatr Res 1994 Dec;36(6):755-62 PMID: 7898984
  • A new way to seal glass plates for denaturing gradient gel electrophoresis. (Kyllo JH, Kirby-Keyser L, Donohoue PA, Porter CC) Biotechniques 1994 May;16(5):792 PMID: 8068325
  • Developmental regulation of the alpha 1B-adrenoceptor in the sheep kidney. (Guillery EN, Porter CC, Page WV, Jose PA, Felder R, Robillard JE) Pediatr Res 1993 Aug;34(2):124-8 PMID: 8233711
  • Molecular studies of the fourth component of complement (C4) in glomerulonephritis. (McLean RH, Porter CC, Wyatt RJ) Semin Nephrol 1989 Mar;9(1):102-6 PMID: 2662294
  • Hemolytic-uremic syndrome: a population-based study in Washington, DC and Baltimore, Maryland. (Kinney JS, Gross TP, Porter CC, Rogers MF, Schonberger LB, Hurwitz ES) Am J Public Health 1988 Jan;78(1):64-5 PMID: 3276232 PMCID: PMC1349211
  • Pancreatic endocrine insufficiency in posttransplant cystinosis. (Fivush B, Green OC, Porter CC, Balfe JW, O'Regan S, Gahl WA) Am J Dis Child 1987 Oct;141(10):1087-9 PMID: 3307383
  • Accelerated recovery from immune-mediated thrombocytopenia with plasmapheresis. (Porter CC, Ruley EJ, Luban NL, Phillips TM, Bock GH, Salcedo JR, Fivush BA) Am J Med 1985 Dec;79(6):765-8 PMID: 4073112
  • Last update: 04/21/2015