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Molecular Genetics & Genomic Medicine
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October 23, 2018
Penetrance and expressivity of the R858H CACNA1C variant in a five-generation pedigree segregating an arrhythmogenic channelopathy
R J McKinlay Gardner, Ian G Crozier, Alex L Binfield, et al.
New Zealand Veterinary Journal
|
March 5, 2010
Mapping a quantitative trait locus for the concentration of beta-lactoglobulin in milk, and the effect of beta-lactoglobulin genetic variants on the composition of milk from Holstein-Friesian x Jersey crossbred cows
S D Berry, N Lopez-Villalobos, E M Beattie, et al.
Translational Psychiatry
|
December 18, 2024
Exploring PDE5A upregulation in bipolar disorder: insights from single-nucleus RNA sequencing of human basal ganglia
Zhixin Bai, Peilong Li, Xu Gao, et al.
Scientific Reports
|
January 26, 2017
Potential molecular consequences of transgene integration: The R6/2 mouse example
Jessie C Jacobsen, Serkan Erdin, Colby Chiang, et al.
Genetics, Selection, Evolution : GSE
|
March 17, 2022
Screening for phenotypic outliers identifies an unusually low concentration of a β-lactoglobulin B protein isoform in bovine milk caused by a synonymous SNP
Stephen R Davis, Hamish E Ward, Van Kelly, et al.
Human Molecular Genetics
|
February 16, 2010
An ovine transgenic Huntington's disease model
Jessie C Jacobsen, C Simon Bawden, Skye R Rudiger, et al.
Journal of Huntington'S Disease
|
July 27, 2014
Further molecular characterisation of the OVT73 transgenic sheep model of Huntington's disease identifies cortical aggregates
, Suzanne J Reid, Stefano Patassini, et al.
The Journal of Biological Chemistry
|
April 10, 2003
Isoform heterogeneity of the human gephyrin gene (GPHN), binding domains to the glycine receptor, and mutation analysis in hyperekplexia
Mark I Rees, Kirsten Harvey, Hamish Ward, et al.
Iscience
|
February 9, 2026
Transcriptomics and functional genomics implicate WNT3 in hemispheric lateralization of speech production
Zixian Wang, Yanxi Chen, Yongqi Feng, et al.
Neurobiology of Aging
|
May 2, 2025
Presenilin 1 hemizygosity has no overt deleterious phenotypic outcomes in sheep: Potential implications for therapeutic targets in Alzheimer's disease
Natasha E Mckean, Jun Liu, Skye R Rudiger, et al.
Page
of 18
Search research articles
Search
Showing results (151-160 of 177) with videos related to
Sort By:
Page
of 18
Molecular Genetics & Genomic Medicine
|
October 23, 2018
Penetrance and expressivity of the R858H CACNA1C variant in a five-generation pedigree segregating an arrhythmogenic channelopathy
R J McKinlay Gardner, Ian G Crozier, Alex L Binfield, et al.
New Zealand Veterinary Journal
|
March 5, 2010
Mapping a quantitative trait locus for the concentration of beta-lactoglobulin in milk, and the effect of beta-lactoglobulin genetic variants on the composition of milk from Holstein-Friesian x Jersey crossbred cows
S D Berry, N Lopez-Villalobos, E M Beattie, et al.
Translational Psychiatry
|
December 18, 2024
Exploring PDE5A upregulation in bipolar disorder: insights from single-nucleus RNA sequencing of human basal ganglia
Zhixin Bai, Peilong Li, Xu Gao, et al.
Scientific Reports
|
January 26, 2017
Potential molecular consequences of transgene integration: The R6/2 mouse example
Jessie C Jacobsen, Serkan Erdin, Colby Chiang, et al.
Genetics, Selection, Evolution : GSE
|
March 17, 2022
Screening for phenotypic outliers identifies an unusually low concentration of a β-lactoglobulin B protein isoform in bovine milk caused by a synonymous SNP
Stephen R Davis, Hamish E Ward, Van Kelly, et al.
Human Molecular Genetics
|
February 16, 2010
An ovine transgenic Huntington's disease model
Jessie C Jacobsen, C Simon Bawden, Skye R Rudiger, et al.
Journal of Huntington'S Disease
|
July 27, 2014
Further molecular characterisation of the OVT73 transgenic sheep model of Huntington's disease identifies cortical aggregates
, Suzanne J Reid, Stefano Patassini, et al.
The Journal of Biological Chemistry
|
April 10, 2003
Isoform heterogeneity of the human gephyrin gene (GPHN), binding domains to the glycine receptor, and mutation analysis in hyperekplexia
Mark I Rees, Kirsten Harvey, Hamish Ward, et al.
Iscience
|
February 9, 2026
Transcriptomics and functional genomics implicate WNT3 in hemispheric lateralization of speech production
Zixian Wang, Yanxi Chen, Yongqi Feng, et al.
Neurobiology of Aging
|
May 2, 2025
Presenilin 1 hemizygosity has no overt deleterious phenotypic outcomes in sheep: Potential implications for therapeutic targets in Alzheimer's disease
Natasha E Mckean, Jun Liu, Skye R Rudiger, et al.
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of 18