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Molecular Vision
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March 2, 2019
Association of age-related macular degeneration with complement activation products, smoking, and single nucleotide polymorphisms in South Carolinians of European and African descent
Bärbel Rohrer, Ashley Frazer-Abel, Anthony Leonard, et al.
The Journal of Biological Chemistry
|
August 26, 2004
The minimal transactivation domain of the basic motif-leucine zipper transcription factor NRL interacts with TATA-binding protein
James S Friedman, Hemant Khanna, Prabodh K Swain, et al.
Stem Cell Reports
|
December 14, 2017
Accelerated and Improved Differentiation of Retinal Organoids from Pluripotent Stem Cells in Rotating-Wall Vessel Bioreactors
Tyler DiStefano, Holly Yu Chen, Christopher Panebianco, et al.
Investigative Ophthalmology & Visual Science
|
October 8, 2010
XIAP therapy increases survival of transplanted rod precursors in a degenerating host retina
Jingyu Yao, Kecia L Feathers, Hemant Khanna, et al.
Plos One
|
April 6, 2012
Knockdown of Bardet-Biedl syndrome gene BBS9/PTHB1 leads to cilia defects
Shobi Veleri, Kevin Bishop, Damian E Dalle Nogare, et al.
Experimental Eye Research
|
October 22, 2002
Retinal histopathology of an XLRP carrier with a mutation in the RPGR exon ORF15
Gustavo D Aguirre, Beverly M Yashar, Sinoj K John, et al.
Investigative Ophthalmology & Visual Science
|
March 11, 2008
Nrl-knockout mice deficient in Rpe65 fail to synthesize 11-cis retinal and cone outer segments
Kecia L Feathers, Arkady L Lyubarsky, Naheed W Khan, et al.
Human Molecular Genetics
|
December 5, 2013
The transcription-splicing protein NonO/p54nrb and three NonO-interacting proteins bind to distal enhancer region and augment rhodopsin expression
Sharda P Yadav, Hong Hao, Hyun-Jin Yang, et al.
American Journal of Human Genetics
|
May 17, 2005
Strong association of the Y402H variant in complement factor H at 1q32 with susceptibility to age-related macular degeneration
Sepideh Zareparsi, Kari E H Branham, Mingyao Li, et al.
The Journal of Clinical Investigation
|
January 3, 2014
OTX2 loss causes rod differentiation defect in CRX-associated congenital blindness
Jerome E Roger, Avinash Hiriyanna, Norimoto Gotoh, et al.
Page
of 34
Search research articles
Search
Showing results (181-190 of 338) with videos related to
Sort By:
Page
of 34
Molecular Vision
|
March 2, 2019
Association of age-related macular degeneration with complement activation products, smoking, and single nucleotide polymorphisms in South Carolinians of European and African descent
Bärbel Rohrer, Ashley Frazer-Abel, Anthony Leonard, et al.
The Journal of Biological Chemistry
|
August 26, 2004
The minimal transactivation domain of the basic motif-leucine zipper transcription factor NRL interacts with TATA-binding protein
James S Friedman, Hemant Khanna, Prabodh K Swain, et al.
Stem Cell Reports
|
December 14, 2017
Accelerated and Improved Differentiation of Retinal Organoids from Pluripotent Stem Cells in Rotating-Wall Vessel Bioreactors
Tyler DiStefano, Holly Yu Chen, Christopher Panebianco, et al.
Investigative Ophthalmology & Visual Science
|
October 8, 2010
XIAP therapy increases survival of transplanted rod precursors in a degenerating host retina
Jingyu Yao, Kecia L Feathers, Hemant Khanna, et al.
Plos One
|
April 6, 2012
Knockdown of Bardet-Biedl syndrome gene BBS9/PTHB1 leads to cilia defects
Shobi Veleri, Kevin Bishop, Damian E Dalle Nogare, et al.
Experimental Eye Research
|
October 22, 2002
Retinal histopathology of an XLRP carrier with a mutation in the RPGR exon ORF15
Gustavo D Aguirre, Beverly M Yashar, Sinoj K John, et al.
Investigative Ophthalmology & Visual Science
|
March 11, 2008
Nrl-knockout mice deficient in Rpe65 fail to synthesize 11-cis retinal and cone outer segments
Kecia L Feathers, Arkady L Lyubarsky, Naheed W Khan, et al.
Human Molecular Genetics
|
December 5, 2013
The transcription-splicing protein NonO/p54nrb and three NonO-interacting proteins bind to distal enhancer region and augment rhodopsin expression
Sharda P Yadav, Hong Hao, Hyun-Jin Yang, et al.
American Journal of Human Genetics
|
May 17, 2005
Strong association of the Y402H variant in complement factor H at 1q32 with susceptibility to age-related macular degeneration
Sepideh Zareparsi, Kari E H Branham, Mingyao Li, et al.
The Journal of Clinical Investigation
|
January 3, 2014
OTX2 loss causes rod differentiation defect in CRX-associated congenital blindness
Jerome E Roger, Avinash Hiriyanna, Norimoto Gotoh, et al.
Page
of 34