检索结果 - Douglas Vollrath
- Showing 1 - 20 results of 36
- Go to Next Page
-
1
-
2
-
3
-
4
-
5
-
6
-
7
-
8
-
9
Retinal Dystrophy Due to Paternal Isodisomy for Chromosome 1 or Chromosome 2, with Homoallelism for Mutations in RPE65 or MERTK, Respectively 由 Debra A. Thompson, Christina L. McHenry, Yun Li, Julia E. Richards, Mohammad Othman, E. Schwinger, Douglas Vollrath, Samuel G. Jacobson, Andreas Gal
出版 2002Artigo -
10
-
11
-
12
mTOR-mediated dedifferentiation of the retinal pigment epithelium initiates photoreceptor degeneration in mice 由 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
出版 2010Artigo -
13
Autosomal Dominant Nanophthalmos (NNO1) with High Hyperopia and Angle-Closure Glaucoma Maps to Chromosome 11 由 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
出版 1998Artigo -
14
-
15
Generation of<i>Cre</i>Transgenic Mice with Postnatal RPE-Specific Ocular Expression 由 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
出版 2011Artigo -
16
Population genetic implications from sequence variation in four Y chromosome genes 由 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
出版 2000Artigo -
17
-
18
Prevalence of Mutations in TIGR/Myocilin in Patients with Adult and Juvenile Primary Open-Angle Glaucoma 由 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
出版 1998Carta -
19
Tyrosine-Mutant AAV8 Delivery of Human<i>MERTK</i>Provides Long-Term Retinal Preservation in RCS Rats 由 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
出版 2012Artigo -
20
Therapeutic blood-brain barrier modulation and stroke treatment by a bioengineered FZD4-selective WNT surrogate in mice 由 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
出版 2023Artigo
相关主题
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