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Plos Genetics
|
January 16, 2015
Altered Ca2+ kinetics associated with α-actinin-3 deficiency may explain positive selection for ACTN3 null allele in human evolution
Stewart I Head, Stephen Chan, Peter J Houweling, et al.
Human Mutation
|
October 4, 2018
Is evolutionary loss our gain? The role of ACTN3 p.Arg577Ter (R577X) genotype in athletic performance, ageing, and disease
Peter J Houweling, Ioannis D Papadimitriou, Jane T Seto, et al.
Human Mutation
|
April 14, 2025
An Update on Reported Variants in the Skeletal Muscle <i>α</i>-Actin (<i>ACTA1</i>) Gene
Joshua S Clayton, Mridul Johari, Rhonda L Taylor, et al.
Calcified Tissue International
|
September 6, 2015
Vitamin D Receptor Ablation and Vitamin D Deficiency Result in Reduced Grip Strength, Altered Muscle Fibers, and Increased Myostatin in Mice
Christian M Girgis, Kuan Minn Cha, Peter J Houweling, et al.
Skeletal Muscle
|
June 22, 2022
Absence of the Z-disc protein α-actinin-3 impairs the mechanical stability of Actn3KO mouse fast-twitch muscle fibres without altering their contractile properties or twitch kinetics
Michael Haug, Barbara Reischl, Stefanie Nübler, et al.
Biochimica Et Biophysica Acta
|
August 29, 2006
Neuronal ceroid lipofuscinosis in Devon cattle is caused by a single base duplication (c.662dupG) in the bovine CLN5 gene
Peter J Houweling, Julie A L Cavanagh, David N Palmer, et al.
Bone
|
March 4, 2017
The influence of α-actinin-3 deficiency on bone remodelling markers in young men
Itamar Levinger, Xu Yan, David Bishop, et al.
Plos One
|
February 14, 2014
Evidence based selection of commonly used RT-qPCR reference genes for the analysis of mouse skeletal muscle
Kristen C Thomas, Xi Fiona Zheng, Francia Garces Suarez, et al.
Nature Communications
|
February 1, 2017
Evidence for ACTN3 as a genetic modifier of Duchenne muscular dystrophy
Marshall W Hogarth, Peter J Houweling, Kristen C Thomas, et al.
Biochimica Et Biophysica Acta
|
October 19, 2006
A missense mutation (c.184C>T) in ovine CLN6 causes neuronal ceroid lipofuscinosis in Merino sheep whereas affected South Hampshire sheep have reduced levels of CLN6 mRNA
Imke Tammen, Peter J Houweling, Tony Frugier, et al.
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Search research articles
Search
Showing results (11-20 of 45) with videos related to
Sort By:
Page
of 5
Plos Genetics
|
January 16, 2015
Altered Ca2+ kinetics associated with α-actinin-3 deficiency may explain positive selection for ACTN3 null allele in human evolution
Stewart I Head, Stephen Chan, Peter J Houweling, et al.
Human Mutation
|
October 4, 2018
Is evolutionary loss our gain? The role of ACTN3 p.Arg577Ter (R577X) genotype in athletic performance, ageing, and disease
Peter J Houweling, Ioannis D Papadimitriou, Jane T Seto, et al.
Human Mutation
|
April 14, 2025
An Update on Reported Variants in the Skeletal Muscle <i>α</i>-Actin (<i>ACTA1</i>) Gene
Joshua S Clayton, Mridul Johari, Rhonda L Taylor, et al.
Calcified Tissue International
|
September 6, 2015
Vitamin D Receptor Ablation and Vitamin D Deficiency Result in Reduced Grip Strength, Altered Muscle Fibers, and Increased Myostatin in Mice
Christian M Girgis, Kuan Minn Cha, Peter J Houweling, et al.
Skeletal Muscle
|
June 22, 2022
Absence of the Z-disc protein α-actinin-3 impairs the mechanical stability of Actn3KO mouse fast-twitch muscle fibres without altering their contractile properties or twitch kinetics
Michael Haug, Barbara Reischl, Stefanie Nübler, et al.
Biochimica Et Biophysica Acta
|
August 29, 2006
Neuronal ceroid lipofuscinosis in Devon cattle is caused by a single base duplication (c.662dupG) in the bovine CLN5 gene
Peter J Houweling, Julie A L Cavanagh, David N Palmer, et al.
Bone
|
March 4, 2017
The influence of α-actinin-3 deficiency on bone remodelling markers in young men
Itamar Levinger, Xu Yan, David Bishop, et al.
Plos One
|
February 14, 2014
Evidence based selection of commonly used RT-qPCR reference genes for the analysis of mouse skeletal muscle
Kristen C Thomas, Xi Fiona Zheng, Francia Garces Suarez, et al.
Nature Communications
|
February 1, 2017
Evidence for ACTN3 as a genetic modifier of Duchenne muscular dystrophy
Marshall W Hogarth, Peter J Houweling, Kristen C Thomas, et al.
Biochimica Et Biophysica Acta
|
October 19, 2006
A missense mutation (c.184C>T) in ovine CLN6 causes neuronal ceroid lipofuscinosis in Merino sheep whereas affected South Hampshire sheep have reduced levels of CLN6 mRNA
Imke Tammen, Peter J Houweling, Tony Frugier, et al.
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of 5