Výsledky vyhledávání - Douglas Vollrath
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An electrophoretic karyotype of Neurospora crassa. Autor Marc J. Orbach, Douglas Vollrath, Ronald W. Davis, Charles Yanofsky
Vydáno 1988Artigo -
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Retinal Dystrophy Due to Paternal Isodisomy for Chromosome 1 or Chromosome 2, with Homoallelism for Mutations in RPE65 or MERTK, Respectively Autor Debra A. Thompson, Christina L. McHenry, Yun Li, Julia E. Richards, Mohammad Othman, E. Schwinger, Douglas Vollrath, Samuel G. Jacobson, Andreas Gal
Vydáno 2002Artigo -
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Detection of Numerous Y Chromosome Biallelic Polymorphisms by Denaturing High-Performance Liquid Chromatography Autor Peter A. Underhill, Jin Li, Alice Lin, S. Qasim Mehdi, Trefor Jenkins, Douglas Vollrath, Ronald W. Davis, L. Luca Cavalli-Sforza, Peter J. Oefner
Vydáno 1997Carta -
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mTOR-mediated dedifferentiation of the retinal pigment epithelium initiates photoreceptor degeneration in mice Autor Chen Zhao, Douglas Yasumura, Xiyan Li, Michael T. Matthes, Marcia Lloyd, Gregory Nielsen, Kelly Ahern, M Snyder, Dean Bok, Joshua L. Dunaief, Matthew M. LaVail, Douglas Vollrath
Vydáno 2010Artigo -
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Autosomal Dominant Nanophthalmos (NNO1) with High Hyperopia and Angle-Closure Glaucoma Maps to Chromosome 11 Autor Mohammad Othman, Scot A. Sullivan, Gregory L. Skuta, David Cockrell, Heather M. Stringham, Catherine A. Downs, Alison Fornés, Andrew B. Mick, Michael Boehnke, Douglas Vollrath, Julia E. Richards
Vydáno 1998Artigo -
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Generation of<i>Cre</i>Transgenic Mice with Postnatal RPE-Specific Ocular Expression Autor Jared Iacovelli, Chen Zhao, Natalie Wolkow, Peter B. Veldman, Kandace Gollomp, P. Ojha, Nina Lukinova, Ayala King, Leonard Feiner, Noriko Esumi, Donald J. Zack, Eric A. Pierce, Douglas Vollrath, Joshua L. Dunaief
Vydáno 2011Artigo -
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Population genetic implications from sequence variation in four Y chromosome genes Autor Peidong Shen, Frank Wang, Peter A. Underhill, Claudia Franco, Wei-Hsien Yang, Adriane Roxas, Raphael Sung, Alice Lin, Richard W. Hyman, Douglas Vollrath, Ronald W. Davis, L. Luca Cavalli-Sforza, Peter J. Oefner
Vydáno 2000Artigo -
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PRPF4 mutations cause autosomal dominant retinitis pigmentosa Autor Xue Chen, Yuan Liu, Xunlun Sheng, Pancy O. S. Tam, Kanxing Zhao, Xuejuan Chen, Weining Rong, Yani Liu, Xiaoxing Liu, Xinyuan Pan, Li Jia Chen, Qingshun Zhao, Douglas Vollrath, Chi Pui Pang, Chen Zhao
Vydáno 2014Artigo -
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Prevalence of Mutations in TIGR/Myocilin in Patients with Adult and Juvenile Primary Open-Angle Glaucoma Autor Janey L. Wiggs, R. Rand Allingham, Douglas Vollrath, Katherine H. Jones, M DE LA PAZ, Jeremy Kern, Kara Patterson, Virna L. Babb, Elizabeth A. Del Bono, Bob Broomer, Margaret A. Pericak‐Vance, Jonathan L. Haines
Vydáno 1998Carta -
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Tyrosine-Mutant AAV8 Delivery of Human<i>MERTK</i>Provides Long-Term Retinal Preservation in RCS Rats Autor Wen‐Tao Deng, Astra Dinculescu, Qiuhong Li, Sanford L. Boye, Jie Li, Marina S. Gorbatyuk, Jijing Pang, Vince A. Chiodo, Michael T. Matthes, Douglas Yasumura, Li Liu, Fowzan S. Alkuraya, Kang Zhang, Douglas Vollrath, Matthew M. LaVail, William W. Hauswirth
Vydáno 2012Artigo -
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Therapeutic blood-brain barrier modulation and stroke treatment by a bioengineered FZD4-selective WNT surrogate in mice Autor Jie Ding, Sung‐Jin Lee, Lukas Vlahos, Kanako Yuki, Cara C. Rada, Vincent van Unen, Meghah Vuppalapaty, Hui Chen, Asmiti Sura, Aaron K. McCormick, Madeline Tomaske, Samira Alwahabi, Huy Nguyen, William Nowatzke, Lily Kim, Lisa D. Kelly, Douglas Vollrath, Andrea Califano, Wen‐Chen Yeh, Yang Li, Calvin J. Kuo
Vydáno 2023Artigo
Vyhledávací nástroje:
Související témata
Biology
Gene
Genetics
Medicine
Glaucoma
Neuroscience
Ophthalmology
Open angle glaucoma
Genotype
Single-nucleotide polymorphism
Cell biology
Biochemistry
Genome-wide association study
Allele
Retina
Genetic association
Retinal
Retinal degeneration
Retinal pigment epithelium
Signal transduction
Bioinformatics
MERTK
Molecular biology
Mutant
Myocilin
Pathology
Receptor tyrosine kinase
Intraocular pressure
Retinitis pigmentosa
Candidate gene