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36篇 您的检索式:作者名="Oetting WS"
    题名 作者 年代 出处 被引量
1Identification and characterization of a DNase hypersensitive region of the human tyrosinase gene显示文摘Fryer JP Oetting WS King RA 2003Pigment Cell Res2003,16,6:1
2Molecular basis of albinism mutations and polymorphisms of pigmentation genes associated with albinism 显示文摘Oetting WS King RA 1999Hum Mutat1999,13,:1
3Donor polymorphisms of toll-like receptor 4 associated with graft failure in liver transplant recipients 显示文摘Oetting WS Guan W Schladt DP 2012Liver Transpl2012,18,12:1
4Molecular basis of albinism:mutations and polymorphisms of pigmentation genes associated with albinism显示文摘Oetting WS King RA 1999Hum Mutat1999,13,2:1
5Erratum: Mutations of the human tyrosinase gene associated with tyrosinase related oculocutaneous albinism( OCAI)显示文摘Oetting WS FryerJP King RA 1999Human Mutation1999,13,:1
6Oculocutaneous albinism type Ⅰ : the last 100 years显示文摘Oetting WS Fryer JP Shriram S 2003Pigment Cell Res2003,16,3:1
7Molecular Basis of Albinism: Mutations and Polymorphisms of Pigmentation Genes Associated With Albinism显示文摘Oetting WS King RA 1999Hum Murat1999,13,2:1
8Oculocutaneous albinism type 1: the last 100 years 显示文摘Oetting WS Fryer JP Shriram S 2003Pigment cell res2003,16,:1
9Evidence that a locus for familial high myopia maps to chromosome 18p显示文摘Young TL Ronan SM Drahozal LA Wildenberg SC Alvear AB Oetting WS 1998Am J Hum Genet1998,63,1:1
10Geneticdeterminants of mycophenolate-related anemia and leukopenia after transplantation显示文摘Jacobson PA Schladt D Oetting WS 2011Transplantation2011,91,3:1
11Urinary beta2-microglobulin is associated with acute renal allograft rejection显示文摘Oetting WS Rogers TB Krick TP 2006Am J Kidney Dis2006,47,5:1
12A second locus for familial high myopia maps to chromosome 12q显示文摘Young TL Ronan SM Alvear AB Wildenberg SC Oetting WS Atwood LD eta/ 1998Am J Hum Genet1998,63,5:1
13Evidence that a locus for familial high myopia maps to chromosome 18p 显示文摘Young TL Ronan SM Drahozal LA Wildenberg SC Alvear AB Oetting WS 1998Am J Hum Genet1998,63,1:1
14Exome and genome analysis as a tool for disease identification and treatment: the 2011 Human Genome Variation Society scientific meeting显示文摘Oetting WS 2012Hum Mutat2012,33,3:1
15The tyrosinase gene and oculocutaneous albinismtype 1(OCA1):a model for understanding the molecular biologyof melanin formation显示文摘Oetting WS 2000Pigment Cell Res2000,13,:1
16Urirary beta2 micruglobolin is associated with acute Renal allograft rejection显示文摘Oetting WS Regers TB Kriek TP 2006Am J Kidney Dis2006,47,5:1
17Donor polymorphisms of toll-like receptor 4 associated with graft failure in liver transplant recipients显示文摘Oetting WS Guan W Schladt DP 2012Liver Transpl2012,18,12:1
18A second locus for familial high myopia maps to chromosome 12q显示文摘Young TL Ronan SM Alvear AB Wildenberg SC Oetting WS Atwood LD 1998Am J Hum Genet1998,63,5:1
19Mutation in and lack of expression of tyrosinase-related protein-1 (TRP-1) in melanocytes from an individual with brown oculocuteous albinism:a new subtype of albinism classified as 'OCA3'显示文摘Boissy RE Zhao H Oetting WS 1996Am J Hum Genet1996,58,:1
20Differential geno- type dependent inhibition of CYP2C9 in humans 显示文摘Kumar V Brundage RC Oetting WS 2008Drug Metab Dispos2008,36,7:1
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