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Peter L Oliver

Showing results (31-40 of 82) with videos related to

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Human Molecular Genetics|April 25, 2015
The mutant Moonwalker TRPC3 channel links calcium signaling to lipid metabolism in the developing cerebellumAnna Dulneva, Sheena Lee, Peter L Oliver, et al.
Molecular and Cellular Neurosciences|October 3, 2002
Identification of a new Pmp22 mouse mutant and trafficking analysis of a Pmp22 allelic series suggesting that protein aggregates may be protective in Pmp22-associated peripheral neuropathyAdrian M Isaacs, Alexander Jeans, Peter L Oliver, et al.
The Journal of Biological Chemistry|August 10, 2014
A novel mouse model of a patient mucolipidosis II mutation recapitulates disease pathologyLeigh Paton, Emmanuelle Bitoun, Janet Kenyon, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|November 26, 2021
SNAP25 mutation disrupts metabolic homeostasis, steroid hormone production and central neurobehaviorXiao Hao, Bing Zhu, Pinglin Yang, et al.
Journal of Neurochemistry|October 12, 2011
HspB8 mutation causing hereditary distal motor neuropathy impairs lysosomal delivery of autophagosomesAlice S Kwok, Kanchan Phadwal, Bradley J Turner, et al.
Molecular Neurobiology|June 16, 2018
Oxidation Resistance 1 Modulates Glycolytic Pathways in the Cerebellum via an Interaction with Glucose-6-Phosphate IsomeraseMattéa J Finelli, Teresa Paramo, Elisabete Pires, et al.
The EMBO Journal|February 4, 2014
The long non-coding RNA Paupar regulates the expression of both local and distal genesKeith W Vance, Stephen N Sansom, Sheena Lee, et al.
Human Molecular Genetics|September 27, 2013
Chondrolectin affects cell survival and neuronal outgrowth in in vitro and in vivo models of spinal muscular atrophyJames N Sleigh, Antón Barreiro-Iglesias, Peter L Oliver, et al.
Human Molecular Genetics|October 24, 2019
Neuronal over-expression of Oxr1 is protective against ALS-associated mutant TDP-43 mislocalisation in motor neurons and neuromuscular defects in vivoMatthew G Williamson, Mattéa J Finelli, James N Sleigh, et al.
Neuroreport|October 16, 2009
Behavioural characterization of neuregulin 1 type I overexpressing transgenic miceInga H Deakin, Amanda J Law, Peter L Oliver, et al.
Pageof 9

Showing results (31-40 of 82) with videos related to

Sort By:
Pageof 9
Human Molecular Genetics|April 25, 2015
The mutant Moonwalker TRPC3 channel links calcium signaling to lipid metabolism in the developing cerebellumAnna Dulneva, Sheena Lee, Peter L Oliver, et al.
Molecular and Cellular Neurosciences|October 3, 2002
Identification of a new Pmp22 mouse mutant and trafficking analysis of a Pmp22 allelic series suggesting that protein aggregates may be protective in Pmp22-associated peripheral neuropathyAdrian M Isaacs, Alexander Jeans, Peter L Oliver, et al.
The Journal of Biological Chemistry|August 10, 2014
A novel mouse model of a patient mucolipidosis II mutation recapitulates disease pathologyLeigh Paton, Emmanuelle Bitoun, Janet Kenyon, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|November 26, 2021
SNAP25 mutation disrupts metabolic homeostasis, steroid hormone production and central neurobehaviorXiao Hao, Bing Zhu, Pinglin Yang, et al.
Journal of Neurochemistry|October 12, 2011
HspB8 mutation causing hereditary distal motor neuropathy impairs lysosomal delivery of autophagosomesAlice S Kwok, Kanchan Phadwal, Bradley J Turner, et al.
Molecular Neurobiology|June 16, 2018
Oxidation Resistance 1 Modulates Glycolytic Pathways in the Cerebellum via an Interaction with Glucose-6-Phosphate IsomeraseMattéa J Finelli, Teresa Paramo, Elisabete Pires, et al.
The EMBO Journal|February 4, 2014
The long non-coding RNA Paupar regulates the expression of both local and distal genesKeith W Vance, Stephen N Sansom, Sheena Lee, et al.
Human Molecular Genetics|September 27, 2013
Chondrolectin affects cell survival and neuronal outgrowth in in vitro and in vivo models of spinal muscular atrophyJames N Sleigh, Antón Barreiro-Iglesias, Peter L Oliver, et al.
Human Molecular Genetics|October 24, 2019
Neuronal over-expression of Oxr1 is protective against ALS-associated mutant TDP-43 mislocalisation in motor neurons and neuromuscular defects in vivoMatthew G Williamson, Mattéa J Finelli, James N Sleigh, et al.
Neuroreport|October 16, 2009
Behavioural characterization of neuregulin 1 type I overexpressing transgenic miceInga H Deakin, Amanda J Law, Peter L Oliver, et al.
Pageof 9