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B Gorin

Showing results (131-140 of 175) with videos related to

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Blood|June 25, 1999
Abnormal expression and subcellular distribution of subunit proteins of the AP-3 adaptor complex lead to platelet storage pool deficiency in the pearl mouseL Zhen, S Jiang, L Feng, et al.
Genetic Epidemiology|February 16, 2017
Genetic risk models: Influence of model size on risk estimates and precisionYing Shan, Gerard Tromp, Helena Kuivaniemi, et al.
American Journal of Human Genetics|March 7, 1998
Linkage analysis of X-linked cone-rod dystrophy: localization to Xp11.4 and definition of a locus distinct from RP2 and RP3A B Seymour, A Dash-Modi, J R O'Connell, et al.
Ocular Immunology and Inflammation|September 16, 2017
Human Embryonic Stem Cell-Derived Mesenchymal Stromal Cells Decrease the Development of Severe Experimental Autoimmune Uveitis in B10.RIII MiceYu Qin, Ann M Chan, Yu-Ling Chang, et al.
American Journal of Human Genetics|March 23, 2000
A juvenile-onset, progressive cataract locus on chromosome 3q21-q22 is associated with a missense mutation in the beaded filament structural protein-2Y P Conley, D Erturk, A Keverline, et al.
Human Molecular Genetics|February 5, 1999
The beta3A subunit gene (Ap3b1) of the AP-3 adaptor complex is altered in the mouse hypopigmentation mutant pearl, a model for Hermansky-Pudlak syndrome and night blindnessL Feng, A B Seymour, S Jiang, et al.
American Journal of Ophthalmology|November 13, 2001
Age-related maculopathy: an expanded genome-wide scan with evidence of susceptibility loci within the 1q31 and 17q25 regionsD E Weeks, Y P Conley, H J Tsai, et al.
BMC Genetics|July 9, 2004
Ordered subset linkage analysis supports a susceptibility locus for age-related macular degeneration on chromosome 16p12Silke Schmidt, William K Scott, Eric A Postel, et al.
Cornea|July 4, 2009
Exclusion of positional candidate gene coding region mutations in the common posterior polymorphous corneal dystrophy 1 candidate gene intervalAnthony J Aldave, Vivek S Yellore, Rosalind C Vo, et al.
Investigative Ophthalmology & Visual Science|April 2, 2010
Linkage of posterior amorphous corneal dystrophy to chromosome 12q21.33 and exclusion of coding region mutations in KERA, LUM, DCN, and EPYCAnthony J Aldave, George O D Rosenwasser, Vivek S Yellore, et al.
Pageof 18

Showing results (131-140 of 175) with videos related to

Sort By:
Pageof 18
Blood|June 25, 1999
Abnormal expression and subcellular distribution of subunit proteins of the AP-3 adaptor complex lead to platelet storage pool deficiency in the pearl mouseL Zhen, S Jiang, L Feng, et al.
Genetic Epidemiology|February 16, 2017
Genetic risk models: Influence of model size on risk estimates and precisionYing Shan, Gerard Tromp, Helena Kuivaniemi, et al.
American Journal of Human Genetics|March 7, 1998
Linkage analysis of X-linked cone-rod dystrophy: localization to Xp11.4 and definition of a locus distinct from RP2 and RP3A B Seymour, A Dash-Modi, J R O'Connell, et al.
Ocular Immunology and Inflammation|September 16, 2017
Human Embryonic Stem Cell-Derived Mesenchymal Stromal Cells Decrease the Development of Severe Experimental Autoimmune Uveitis in B10.RIII MiceYu Qin, Ann M Chan, Yu-Ling Chang, et al.
American Journal of Human Genetics|March 23, 2000
A juvenile-onset, progressive cataract locus on chromosome 3q21-q22 is associated with a missense mutation in the beaded filament structural protein-2Y P Conley, D Erturk, A Keverline, et al.
Human Molecular Genetics|February 5, 1999
The beta3A subunit gene (Ap3b1) of the AP-3 adaptor complex is altered in the mouse hypopigmentation mutant pearl, a model for Hermansky-Pudlak syndrome and night blindnessL Feng, A B Seymour, S Jiang, et al.
American Journal of Ophthalmology|November 13, 2001
Age-related maculopathy: an expanded genome-wide scan with evidence of susceptibility loci within the 1q31 and 17q25 regionsD E Weeks, Y P Conley, H J Tsai, et al.
BMC Genetics|July 9, 2004
Ordered subset linkage analysis supports a susceptibility locus for age-related macular degeneration on chromosome 16p12Silke Schmidt, William K Scott, Eric A Postel, et al.
Cornea|July 4, 2009
Exclusion of positional candidate gene coding region mutations in the common posterior polymorphous corneal dystrophy 1 candidate gene intervalAnthony J Aldave, Vivek S Yellore, Rosalind C Vo, et al.
Investigative Ophthalmology & Visual Science|April 2, 2010
Linkage of posterior amorphous corneal dystrophy to chromosome 12q21.33 and exclusion of coding region mutations in KERA, LUM, DCN, and EPYCAnthony J Aldave, George O D Rosenwasser, Vivek S Yellore, et al.
Pageof 18