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Journal of Neurochemistry
|
October 13, 2005
Carboxypeptidase E is required for normal synaptic transmission from photoreceptors to the inner retina
Xuemei Zhu, Kebin Wu, Lawrence Rife, et al.
The Journal of Biological Chemistry
|
July 27, 2005
RPGR-ORF15, which is mutated in retinitis pigmentosa, associates with SMC1, SMC3, and microtubule transport proteins
Hemant Khanna, Toby W Hurd, Concepcion Lillo, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
February 17, 2006
Physical and functional interaction between protocadherin 15 and myosin VIIa in mechanosensory hair cells
Mathias Senften, Martin Schwander, Piotr Kazmierczak, et al.
Neuron
|
May 19, 2009
Harmonin mutations cause mechanotransduction defects in cochlear hair cells
Nicolas Grillet, Wei Xiong, Anna Reynolds, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
February 28, 2014
UV irradiation accelerates amyloid precursor protein (APP) processing and disrupts APP axonal transport
Angels Almenar-Queralt, Tomas L Falzone, Zhouxin Shen, et al.
Biochemistry
|
January 31, 2007
The tetraspanin protein peripherin-2 forms a complex with melanoregulin, a putative membrane fusion regulator
Kathleen Boesze-Battaglia, Hongman Song, Maxim Sokolov, et al.
Human Molecular Genetics
|
April 25, 2006
In-frame deletion in a novel centrosomal/ciliary protein CEP290/NPHP6 perturbs its interaction with RPGR and results in early-onset retinal degeneration in the rd16 mouse
Bo Chang, Hemant Khanna, Norman Hawes, et al.
Nature Genetics
|
February 22, 2005
Nephrocystin-5, a ciliary IQ domain protein, is mutated in Senior-Loken syndrome and interacts with RPGR and calmodulin
Edgar A Otto, Bart Loeys, Hemant Khanna, et al.
The Journal of Clinical Investigation
|
July 26, 2008
Mutant prominin 1 found in patients with macular degeneration disrupts photoreceptor disk morphogenesis in mice
Zhenglin Yang, Yali Chen, Concepcion Lillo, et al.
Nature Genetics
|
May 10, 2006
The centrosomal protein nephrocystin-6 is mutated in Joubert syndrome and activates transcription factor ATF4
John A Sayer, Edgar A Otto, John F O'Toole, et al.
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Showing results (11-20 of 20) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 20 results.
Journal of Neurochemistry
|
October 13, 2005
Carboxypeptidase E is required for normal synaptic transmission from photoreceptors to the inner retina
Xuemei Zhu, Kebin Wu, Lawrence Rife, et al.
The Journal of Biological Chemistry
|
July 27, 2005
RPGR-ORF15, which is mutated in retinitis pigmentosa, associates with SMC1, SMC3, and microtubule transport proteins
Hemant Khanna, Toby W Hurd, Concepcion Lillo, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
February 17, 2006
Physical and functional interaction between protocadherin 15 and myosin VIIa in mechanosensory hair cells
Mathias Senften, Martin Schwander, Piotr Kazmierczak, et al.
Neuron
|
May 19, 2009
Harmonin mutations cause mechanotransduction defects in cochlear hair cells
Nicolas Grillet, Wei Xiong, Anna Reynolds, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
February 28, 2014
UV irradiation accelerates amyloid precursor protein (APP) processing and disrupts APP axonal transport
Angels Almenar-Queralt, Tomas L Falzone, Zhouxin Shen, et al.
Biochemistry
|
January 31, 2007
The tetraspanin protein peripherin-2 forms a complex with melanoregulin, a putative membrane fusion regulator
Kathleen Boesze-Battaglia, Hongman Song, Maxim Sokolov, et al.
Human Molecular Genetics
|
April 25, 2006
In-frame deletion in a novel centrosomal/ciliary protein CEP290/NPHP6 perturbs its interaction with RPGR and results in early-onset retinal degeneration in the rd16 mouse
Bo Chang, Hemant Khanna, Norman Hawes, et al.
Nature Genetics
|
February 22, 2005
Nephrocystin-5, a ciliary IQ domain protein, is mutated in Senior-Loken syndrome and interacts with RPGR and calmodulin
Edgar A Otto, Bart Loeys, Hemant Khanna, et al.
The Journal of Clinical Investigation
|
July 26, 2008
Mutant prominin 1 found in patients with macular degeneration disrupts photoreceptor disk morphogenesis in mice
Zhenglin Yang, Yali Chen, Concepcion Lillo, et al.
Nature Genetics
|
May 10, 2006
The centrosomal protein nephrocystin-6 is mutated in Joubert syndrome and activates transcription factor ATF4
John A Sayer, Edgar A Otto, John F O'Toole, et al.
Page
of 2