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Proceedings of the National Academy of Sciences of the United States of America
|
October 27, 2004
Facile isolation and the characterization of human retinal stem cells
Brenda L K Coles, Brigitte Angénieux, Tomoyuki Inoue, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
December 17, 2014
STAT3 promotes survival of mutant photoreceptors in inherited photoreceptor degeneration models
Ke Jiang, Katherine L Wright, Ping Zhu, et al.
Developmental Biology
|
February 24, 2007
The proliferation and expansion of retinal stem cells require functional Pax6
Shunbin Xu, Mary E Sunderland, Brenda L K Coles, et al.
Frontiers in Cellular Neuroscience
|
October 7, 2015
Neto2-null mice have impaired GABAergic inhibition and are susceptible to seizures
Vivek Mahadevan, Zahra Dargaei, Evgueni A Ivakine, et al.
The Journal of Clinical Investigation
|
May 17, 2013
Endothelin-2 deficiency causes growth retardation, hypothermia, and emphysema in mice
Inik Chang, Alexa N Bramall, Amy Greenstein Baynash, et al.
Human Molecular Genetics
|
November 6, 2010
Evidence of severe mitochondrial oxidative stress and a protective effect of low oxygen in mouse models of inherited photoreceptor degeneration
Dafni Vlachantoni, Alexa N Bramall, Michael P Murphy, et al.
Plos One
|
March 8, 2013
Endothelin-2-mediated protection of mutant photoreceptors in inherited photoreceptor degeneration
Alexa N Bramall, Michael J Szego, Laura R Pacione, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 13, 2013
Neto2 is a KCC2 interacting protein required for neuronal Cl- regulation in hippocampal neurons
Evgueni A Ivakine, Brooke A Acton, Vivek Mahadevan, et al.
Human Molecular Genetics
|
July 2, 2004
Nuclear receptor NR2E3 gene mutations distort human retinal laminar architecture and cause an unusual degeneration
Samuel G Jacobson, Alexander Sumaroka, Tomas S Aleman, et al.
Developmental Biology
|
September 27, 2005
The Iroquois homeobox gene, Irx5, is required for retinal cone bipolar cell development
Chi Wa Cheng, Robert L Chow, Mélanie Lebel, et al.
Page
of 4
Search research articles
Search
Showing results (21-30 of 39) with videos related to
Sort By:
Page
of 4
Proceedings of the National Academy of Sciences of the United States of America
|
October 27, 2004
Facile isolation and the characterization of human retinal stem cells
Brenda L K Coles, Brigitte Angénieux, Tomoyuki Inoue, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
December 17, 2014
STAT3 promotes survival of mutant photoreceptors in inherited photoreceptor degeneration models
Ke Jiang, Katherine L Wright, Ping Zhu, et al.
Developmental Biology
|
February 24, 2007
The proliferation and expansion of retinal stem cells require functional Pax6
Shunbin Xu, Mary E Sunderland, Brenda L K Coles, et al.
Frontiers in Cellular Neuroscience
|
October 7, 2015
Neto2-null mice have impaired GABAergic inhibition and are susceptible to seizures
Vivek Mahadevan, Zahra Dargaei, Evgueni A Ivakine, et al.
The Journal of Clinical Investigation
|
May 17, 2013
Endothelin-2 deficiency causes growth retardation, hypothermia, and emphysema in mice
Inik Chang, Alexa N Bramall, Amy Greenstein Baynash, et al.
Human Molecular Genetics
|
November 6, 2010
Evidence of severe mitochondrial oxidative stress and a protective effect of low oxygen in mouse models of inherited photoreceptor degeneration
Dafni Vlachantoni, Alexa N Bramall, Michael P Murphy, et al.
Plos One
|
March 8, 2013
Endothelin-2-mediated protection of mutant photoreceptors in inherited photoreceptor degeneration
Alexa N Bramall, Michael J Szego, Laura R Pacione, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 13, 2013
Neto2 is a KCC2 interacting protein required for neuronal Cl- regulation in hippocampal neurons
Evgueni A Ivakine, Brooke A Acton, Vivek Mahadevan, et al.
Human Molecular Genetics
|
July 2, 2004
Nuclear receptor NR2E3 gene mutations distort human retinal laminar architecture and cause an unusual degeneration
Samuel G Jacobson, Alexander Sumaroka, Tomas S Aleman, et al.
Developmental Biology
|
September 27, 2005
The Iroquois homeobox gene, Irx5, is required for retinal cone bipolar cell development
Chi Wa Cheng, Robert L Chow, Mélanie Lebel, et al.
Page
of 4