Resultados da busca - Michael B. Gorin
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Tamoxifen-associated eye disease. A review. por Susan Nayfield, Michael B. Gorin
Publicado em 1996Revisão -
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Candidate gene analysis suggests a role for fatty acid biosynthesis and regulation of the complement system in the etiology of age-related maculopathy por Yvette P. Conley, Anbupalam Thalamuthu, Jóhanna Jakobsdóttir, Daniel E. Weeks, Tammy S. Mah, Robert E. Ferrell, Michael B. Gorin
Publicado em 2005Artigo -
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CFH, ELOVL4, PLEKHA1 and LOC387715 genes and susceptibility to age-related maculopathy: AREDS and CHS cohorts and meta-analyses por Yvette P. Conley, Jóhanna Jakobsdóttir, Tammy S. Mah, Daniel E. Weeks, Ronald Klein, Lewis H. Kuller, Robert E. Ferrell, Michael B. Gorin
Publicado em 2006Revisão -
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Three patients with injection of intravitreal vascular endothelial growth factor inhibitors and subsequent exacerbation of chronic proteinuria and hypertension por Ramy M. Hanna, Eduardo Lopez, Huma Hasnain, Umut Selamet, James M. Wilson, Peter N Youssef, Nermeen Akladeous, Suphamai Bunnapradist, Michael B. Gorin
Publicado em 2018Artigo -
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A systems biology approach towards understanding and treating non-neovascular age-related macular degeneration por James T. Handa, Catherine Bowes Rickman, Andrew D. Dick, Michael B. Gorin, Joan W. Miller, Cynthia A. Toth, Marius Ueffing, Marco A. Zarbin, Lindsay A. Farrer
Publicado em 2019Revisão -
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X-Linked Cone-Rod Dystrophy (Locus COD1): Identification of Mutations in RPGR Exon ORF15 por F. Yesim Demirci, Brian W. Rigatti, Gaiping Wen, Amy L. Radak, Tammy S. Mah, Corrine L. Baic, Elias I. Traboulsi, Tiina Alitalo, Juliane Ramser, Michael B. Gorin
Publicado em 2002Artigo -
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Abnormal Expression and Subcellular Distribution of Subunit Proteins of the AP-3 Adaptor Complex Lead to Platelet Storage Pool Deficiency in the Pearl Mouse por Lijie Zhen, Shelley Jiang, Lijun Feng, Nicholas A. Bright, Andrew A. Peden, Albert Seymour, Edward K. Novak, Rosemary W. Elliott, Michael B. Gorin, Margaret S. Robinson, Richard T. Swank
Publicado em 1999Artigo -
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De Novo Occurrence of a Variant in ARL3 and Apparent Autosomal Dominant Transmission of Retinitis Pigmentosa por Samuel P. Strom, Michael J. Clark, Ariadna Martinez, Sarah Garcia, Amira A. Abelazeem, Anna Matynia, Sachin Parikh, Lori S. Sullivan, Sara J. Bowne, Stephen P. Daiger, Michael B. Gorin
Publicado em 2016Artigo -
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A Juvenile-Onset, Progressive Cataract Locus on Chromosome 3q21-q22 Is Associated with a Missense Mutation in the Beaded Filament Structural Protein–2 por Yvette P. Conley, Deniz Erturk, Andrew Keverline, Tammy S. Mah, Annahita Keravala, Laura R. Barnes, Anna Bruchis, John F. Hess, Paul G. Fitzgerald, Daniel E. Weeks, R E Ferrell, Michael B. Gorin
Publicado em 2000Artigo
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Biology
Genetics
Gene
Medicine
Internal medicine
Ophthalmology
Phenotype
Disease
Genotype
Locus (genetics)
Pathology
Computational biology
Macular degeneration
Allele
Genome
Single-nucleotide polymorphism
Candidate gene
Mutation
Retinitis pigmentosa
ABCA4
Biochemistry
Exome sequencing
Odds ratio
Retinal
Complement system
Exome
Exon
Genome-wide association study
Neuroscience
Sanger sequencing