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Concepcion Lillo

Showing results (11-20 of 20) with videos related to

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Journal of Neurochemistry|October 13, 2005
Carboxypeptidase E is required for normal synaptic transmission from photoreceptors to the inner retinaXuemei 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 proteinsHemant 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 cellsMathias Senften, Martin Schwander, Piotr Kazmierczak, et al.
Neuron|May 19, 2009
Harmonin mutations cause mechanotransduction defects in cochlear hair cellsNicolas 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 transportAngels 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 regulatorKathleen 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 mouseBo 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 calmodulinEdgar 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 miceZhenglin 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 ATF4John A Sayer, Edgar A Otto, John F O'Toole, et al.
Pageof 2

Showing results (11-20 of 20) with videos related to

Sort By:
Pageof 2
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 retinaXuemei 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 proteinsHemant 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 cellsMathias Senften, Martin Schwander, Piotr Kazmierczak, et al.
Neuron|May 19, 2009
Harmonin mutations cause mechanotransduction defects in cochlear hair cellsNicolas 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 transportAngels 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 regulatorKathleen 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 mouseBo 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 calmodulinEdgar 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 miceZhenglin 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 ATF4John A Sayer, Edgar A Otto, John F O'Toole, et al.
Pageof 2