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Experimental Eye Research
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March 19, 2013
Exon-level expression profiling of ocular tissues
Alex H Wagner, V Nikhil Anand, Wan-Heng Wang, et al.
Bioinformatics (Oxford, England)
|
August 16, 2014
Cordova: web-based management of genetic variation data
Sean S Ephraim, Nikhil Anand, Adam P DeLuca, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 4, 2011
Carcinoembryonic antigen-related cell adhesion molecule 16 interacts with alpha-tectorin and is mutated in autosomal dominant hearing loss (DFNA4)
Jing Zheng, Katharine K Miller, Tao Yang, et al.
Human Mutation
|
January 13, 2015
Heterozygous triplication of upstream regulatory sequences leads to dysregulation of matrix metalloproteinase 19 in patients with cavitary optic disc anomaly
Ralph J Hazlewood, Benjamin R Roos, Frances Solivan-Timpe, et al.
Journal of Bioinformatics and Computational Biology
|
January 4, 2008
Transcript annotation prioritization and screening system (TrAPSS) for mutation screening
Brian M O'Leary, Steven G Davis, Michael F Smith, et al.
Human Mutation
|
January 3, 2013
AudioGene: predicting hearing loss genotypes from phenotypes to guide genetic screening
Kyle R Taylor, Adam P Deluca, A Eliot Shearer, et al.
Hearing Research
|
September 15, 2012
Prediction of cochlear implant performance by genetic mutation: the spiral ganglion hypothesis
Robert W Eppsteiner, A Eliot Shearer, Michael S Hildebrand, et al.
Plos One
|
March 29, 2013
A genome-wide association study for primary open angle glaucoma and macular degeneration reveals novel Loci
Todd E Scheetz, John H Fingert, Kai Wang, et al.
JAMA Ophthalmology
|
March 1, 2019
Myocilin Mutations in Patients With Normal-Tension Glaucoma
Wallace L M Alward, Carly van der Heide, Cheryl L Khanna, et al.
Genome Research
|
April 3, 2004
High-density rat radiation hybrid maps containing over 24,000 SSLPs, genes, and ESTs provide a direct link to the rat genome sequence
Anne E Kwitek, Jo Gullings-Handley, Jiaming Yu, et al.
Page
of 13
Search research articles
Search
Showing results (101-110 of 129) with videos related to
Sort By:
Page
of 13
Experimental Eye Research
|
March 19, 2013
Exon-level expression profiling of ocular tissues
Alex H Wagner, V Nikhil Anand, Wan-Heng Wang, et al.
Bioinformatics (Oxford, England)
|
August 16, 2014
Cordova: web-based management of genetic variation data
Sean S Ephraim, Nikhil Anand, Adam P DeLuca, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 4, 2011
Carcinoembryonic antigen-related cell adhesion molecule 16 interacts with alpha-tectorin and is mutated in autosomal dominant hearing loss (DFNA4)
Jing Zheng, Katharine K Miller, Tao Yang, et al.
Human Mutation
|
January 13, 2015
Heterozygous triplication of upstream regulatory sequences leads to dysregulation of matrix metalloproteinase 19 in patients with cavitary optic disc anomaly
Ralph J Hazlewood, Benjamin R Roos, Frances Solivan-Timpe, et al.
Journal of Bioinformatics and Computational Biology
|
January 4, 2008
Transcript annotation prioritization and screening system (TrAPSS) for mutation screening
Brian M O'Leary, Steven G Davis, Michael F Smith, et al.
Human Mutation
|
January 3, 2013
AudioGene: predicting hearing loss genotypes from phenotypes to guide genetic screening
Kyle R Taylor, Adam P Deluca, A Eliot Shearer, et al.
Hearing Research
|
September 15, 2012
Prediction of cochlear implant performance by genetic mutation: the spiral ganglion hypothesis
Robert W Eppsteiner, A Eliot Shearer, Michael S Hildebrand, et al.
Plos One
|
March 29, 2013
A genome-wide association study for primary open angle glaucoma and macular degeneration reveals novel Loci
Todd E Scheetz, John H Fingert, Kai Wang, et al.
JAMA Ophthalmology
|
March 1, 2019
Myocilin Mutations in Patients With Normal-Tension Glaucoma
Wallace L M Alward, Carly van der Heide, Cheryl L Khanna, et al.
Genome Research
|
April 3, 2004
High-density rat radiation hybrid maps containing over 24,000 SSLPs, genes, and ESTs provide a direct link to the rat genome sequence
Anne E Kwitek, Jo Gullings-Handley, Jiaming Yu, et al.
Page
of 13