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Michael E Cheetham

Showing results (81-90 of 161) with videos related to

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Brain : a Journal of Neurology|March 4, 2016
The heat shock response plays an important role in TDP-43 clearance: evidence for dysfunction in amyotrophic lateral sclerosisHan-Jou Chen, Jacqueline C Mitchell, Sergey Novoselov, et al.
Human Molecular Genetics|December 30, 2016
Protein kinase CK2 modulates HSJ1 function through phosphorylation of the UIM2 domainDaniele Ottaviani, Oriano Marin, Giorgio Arrigoni, et al.
Molecular Therapy. Nucleic Acids|September 30, 2021
CRISPR-Cas9 correction of <i>OPA1</i> c.1334G>A: p.R445H restores mitochondrial homeostasis in dominant optic atrophy patient-derived iPSCsPaul E Sladen, Pedro R L Perdigão, Grace Salsbury, et al.
Investigative Ophthalmology & Visual Science|January 8, 2015
Brittle cornea syndrome ZNF469 mutation carrier phenotype and segregation analysis of rare ZNF469 variants in familial keratoconusAlice E Davidson, Edmondo Borasio, Petra Liskova, et al.
JAMA Ophthalmology|June 10, 2016
Recessive Retinopathy Consequent on Mutant G-Protein β Subunit 3 (GNB3)Gavin Arno, Graham E Holder, Christina Chakarova, et al.
Cells|June 28, 2023
Eupatilin Improves Cilia Defects in Human CEP290 Ciliopathy ModelsJulio C Corral-Serrano, Paul E Sladen, Daniele Ottaviani, et al.
Acta Neuropathologica Communications|February 13, 2025
Disruption of mitochondrial homeostasis and permeability transition pore opening in OPA1 iPSC-derived retinal ganglion cellsMichael Whitehead, Joshua P Harvey, Paul E Sladen, et al.
Human Molecular Genetics|November 6, 2002
Localization in the human retina of the X-linked retinitis pigmentosa protein RP2, its homologue cofactor C and the RP2 interacting protein Arl3Celene Grayson, Francesca Bartolini, J Paul Chapple, et al.
Human Molecular Genetics|March 21, 2020
AAV-mediated ERdj5 overexpression protects against P23H rhodopsin toxicityMonica Aguilà, James Bellingham, Dimitra Athanasiou, et al.
Endocrinology|December 29, 2007
The melanocortin 2 receptor accessory protein exists as a homodimer and is essential for the function of the melanocortin 2 receptor in the mouse y1 cell lineSadani N Cooray, Isabel Almiro Do Vale, Kit-Yi Leung, et al.
Pageof 17

Showing results (81-90 of 161) with videos related to

Sort By:
Pageof 17
Brain : a Journal of Neurology|March 4, 2016
The heat shock response plays an important role in TDP-43 clearance: evidence for dysfunction in amyotrophic lateral sclerosisHan-Jou Chen, Jacqueline C Mitchell, Sergey Novoselov, et al.
Human Molecular Genetics|December 30, 2016
Protein kinase CK2 modulates HSJ1 function through phosphorylation of the UIM2 domainDaniele Ottaviani, Oriano Marin, Giorgio Arrigoni, et al.
Molecular Therapy. Nucleic Acids|September 30, 2021
CRISPR-Cas9 correction of <i>OPA1</i> c.1334G>A: p.R445H restores mitochondrial homeostasis in dominant optic atrophy patient-derived iPSCsPaul E Sladen, Pedro R L Perdigão, Grace Salsbury, et al.
Investigative Ophthalmology & Visual Science|January 8, 2015
Brittle cornea syndrome ZNF469 mutation carrier phenotype and segregation analysis of rare ZNF469 variants in familial keratoconusAlice E Davidson, Edmondo Borasio, Petra Liskova, et al.
JAMA Ophthalmology|June 10, 2016
Recessive Retinopathy Consequent on Mutant G-Protein β Subunit 3 (GNB3)Gavin Arno, Graham E Holder, Christina Chakarova, et al.
Cells|June 28, 2023
Eupatilin Improves Cilia Defects in Human CEP290 Ciliopathy ModelsJulio C Corral-Serrano, Paul E Sladen, Daniele Ottaviani, et al.
Acta Neuropathologica Communications|February 13, 2025
Disruption of mitochondrial homeostasis and permeability transition pore opening in OPA1 iPSC-derived retinal ganglion cellsMichael Whitehead, Joshua P Harvey, Paul E Sladen, et al.
Human Molecular Genetics|November 6, 2002
Localization in the human retina of the X-linked retinitis pigmentosa protein RP2, its homologue cofactor C and the RP2 interacting protein Arl3Celene Grayson, Francesca Bartolini, J Paul Chapple, et al.
Human Molecular Genetics|March 21, 2020
AAV-mediated ERdj5 overexpression protects against P23H rhodopsin toxicityMonica Aguilà, James Bellingham, Dimitra Athanasiou, et al.
Endocrinology|December 29, 2007
The melanocortin 2 receptor accessory protein exists as a homodimer and is essential for the function of the melanocortin 2 receptor in the mouse y1 cell lineSadani N Cooray, Isabel Almiro Do Vale, Kit-Yi Leung, et al.
Pageof 17