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American Journal of Human Genetics
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January 28, 2021
Allele-specific editing ameliorates dominant retinitis pigmentosa in a transgenic mouse model
Clarissa Patrizi, Manel Llado, Daniela Benati, et al.
Journal of Neurochemistry
|
July 5, 2005
Treatment with extracellular HSP70/HSC70 protein can reduce polyglutamine toxicity and aggregation
Tatiana V Novoselova, Boris A Margulis, Sergey S Novoselov, et al.
International Journal of Molecular Sciences
|
July 12, 2025
CRISPRa-Mediated Increase of OPA1 Expression in Dominant Optic Atrophy
Giada Becchi, Michael Whitehead, Joshua P Harvey, et al.
Ophthalmic Genetics
|
October 18, 2017
A recurrent splice-site mutation in EPHA2 causing congenital posterior nuclear cataract
Vanita Berry, Nikolas Pontikos, Monica Albarca-Aguilera, et al.
Human Molecular Genetics
|
June 2, 2022
Modelling autosomal dominant optic atrophy associated with OPA1 variants in iPSC-derived retinal ganglion cells
Paul E Sladen, Katarina Jovanovic, Rosellina Guarascio, et al.
Gene
|
July 19, 2005
Isolation and characterization of murine Cds (CDP-diacylglycerol synthase) 1 and 2
Suzanne L Inglis-Broadgate, Louise Ocaka, Ruby Banerjee, et al.
Cell Stress & Chaperones
|
July 30, 2008
Guidelines for the nomenclature of the human heat shock proteins
Harm H Kampinga, Jurre Hageman, Michel J Vos, et al.
Human Molecular Genetics
|
September 12, 2012
NUB1 modulation of GSK3β reduces tau aggregation
Emma Richet, Amy M Pooler, Teresa Rodriguez, et al.
The Biochemical Journal
|
March 22, 2003
Organization on the plasma membrane of the retinitis pigmentosa protein RP2: investigation of association with detergent-resistant membranes and polarized sorting
J Paul Chapple, Celene Grayson, Alison J Hardcastle, et al.
Molecular Vision
|
March 16, 2012
Functional characterization of a novel c.614-622del rhodopsin mutation in a French pedigree with retinitis pigmentosa
Cécilia Maubaret, Maria Kosmaoglou, Sancy Low, et al.
Page
of 17
Search research articles
Search
Showing results (71-80 of 161) with videos related to
Sort By:
Page
of 17
American Journal of Human Genetics
|
January 28, 2021
Allele-specific editing ameliorates dominant retinitis pigmentosa in a transgenic mouse model
Clarissa Patrizi, Manel Llado, Daniela Benati, et al.
Journal of Neurochemistry
|
July 5, 2005
Treatment with extracellular HSP70/HSC70 protein can reduce polyglutamine toxicity and aggregation
Tatiana V Novoselova, Boris A Margulis, Sergey S Novoselov, et al.
International Journal of Molecular Sciences
|
July 12, 2025
CRISPRa-Mediated Increase of OPA1 Expression in Dominant Optic Atrophy
Giada Becchi, Michael Whitehead, Joshua P Harvey, et al.
Ophthalmic Genetics
|
October 18, 2017
A recurrent splice-site mutation in EPHA2 causing congenital posterior nuclear cataract
Vanita Berry, Nikolas Pontikos, Monica Albarca-Aguilera, et al.
Human Molecular Genetics
|
June 2, 2022
Modelling autosomal dominant optic atrophy associated with OPA1 variants in iPSC-derived retinal ganglion cells
Paul E Sladen, Katarina Jovanovic, Rosellina Guarascio, et al.
Gene
|
July 19, 2005
Isolation and characterization of murine Cds (CDP-diacylglycerol synthase) 1 and 2
Suzanne L Inglis-Broadgate, Louise Ocaka, Ruby Banerjee, et al.
Cell Stress & Chaperones
|
July 30, 2008
Guidelines for the nomenclature of the human heat shock proteins
Harm H Kampinga, Jurre Hageman, Michel J Vos, et al.
Human Molecular Genetics
|
September 12, 2012
NUB1 modulation of GSK3β reduces tau aggregation
Emma Richet, Amy M Pooler, Teresa Rodriguez, et al.
The Biochemical Journal
|
March 22, 2003
Organization on the plasma membrane of the retinitis pigmentosa protein RP2: investigation of association with detergent-resistant membranes and polarized sorting
J Paul Chapple, Celene Grayson, Alison J Hardcastle, et al.
Molecular Vision
|
March 16, 2012
Functional characterization of a novel c.614-622del rhodopsin mutation in a French pedigree with retinitis pigmentosa
Cécilia Maubaret, Maria Kosmaoglou, Sancy Low, et al.
Page
of 17