Jonathan G. Seidman

Jonathan G. Seidman, Ph.D.

Henrietta B. and Frederick H. Bugher Foundation Professor of Genetics, Harvard Medical School

617-432-7830

Publications

T cell receptor (TCR) usage determines disease susceptibility in experimental autoimmune encephalomyelitis: studies with TCR V beta 8.2 transgenic mice.

Authors: Authors: Kuchroo VK, Collins M, al-Sabbagh A, Sobel RA, Whitters MJ, Zamvil SS, Dorf ME, Hafler DA, Seidman JG, Weiner HL, et al.
J Exp Med 1994-05-01
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The clinical and genetic spectrum of the Holt-Oram syndrome (heart-hand syndrome)

Authors: Authors: Basson CT, Cowley GS, Solomon SD, Weissman B, Poznanski AK, Traill TA, Seidman JG, Seidman CE.
N Engl J Med 1994-03-31
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A gene for hereditary haemorrhagic telangiectasia maps to chromosome 9q3.

Authors: Authors: Shovlin CL, Hughes JM, Tuddenham EG, Temperley I, Perembelon YF, Scott J, Seidman CE, Seidman JG.
Nat Genet 1994-02-01
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Cold compressive dressing after total knee arthroplasty.

Authors: Authors: Healy WL, Seidman J, Pfeifer BA, Brown DG.
Clin Orthop Relat Res 1994-02-01
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Functional analysis of myosin missense mutations in familial hypertrophic cardiomyopathy.

Authors: Authors: Straceski AJ, Geisterfer-Lowrance A, Seidman CE, Seidman JG, Leinwand LA.
Proc Natl Acad Sci U S A 1994-01-18
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Inactivation of G-protein genes: double knockout in cell lines.

Authors: Authors: Mortensen RM, Seidman JG.
Methods Enzymol 1994-01-01
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An evaluation of ribonuclease protection assays for the detection of beta-cardiac myosin heavy chain gene mutations.

Authors: Authors: MacRae CA, Watkins HC, Jarcho JA, Thierfelder L, McKenna WJ, Seidman JG, Seidman CE.
Circulation 1994-01-01
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Mutations in the human Ca(2+)-sensing receptor gene cause familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism.

Authors: Authors: Pollak MR, Brown EM, Chou YH, Hebert SC, Marx SJ, Steinmann B, Levi T, Seidman CE, Seidman JG.
Cell 1993-12-31
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Response.

Authors: Authors: Lipes MA, Rosenzweig A, Tan KN, Tanigawa G, Seidman JG, Eisenbarth GS.
Science 1993-12-03
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Independent origin of identical beta cardiac myosin heavy-chain mutations in hypertrophic cardiomyopathy.

Authors: Authors: Watkins H, Thierfelder L, Anan R, Jarcho J, Matsumori A, McKenna W, Seidman JG, Seidman CE.
Am J Hum Genet 1993-12-01
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