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NAR Genomics and Bioinformatics
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December 20, 2024
Mining single-cell data for cell type-disease associations
Kevin G Chen, Kathryn O Farley, Timo Lassmann
Molecular Autism
|
October 1, 2024
Identifying SETBP1 haploinsufficiency molecular pathways to improve patient diagnosis using induced pluripotent stem cells and neural disease modelling
Nicole C Shaw, Kevin Chen, Kathryn O Farley, et al.
HGG Advances
|
November 26, 2023
CRISPR-Cas9-generated PTCHD1 2489T>G stem cells recapitulate patient phenotype when undergoing neural induction
Kathryn O Farley, Catherine A Forbes, Nicole C Shaw, et al.
Molecular Medicine (Cambridge, Mass.)
|
September 30, 2025
Functional characterization of the MED12 p.Arg1138Trp variant in females: implications for neural development and disease mechanism
Nicole C Shaw, Saraya Harrison, Kevin Chen, et al.
Stem Cell Research & Therapy
|
December 4, 2023
Gene editing and cardiac disease modelling for the interpretation of genetic variants of uncertain significance in congenital heart disease
Vanessa S Fear, Catherine A Forbes, Nicole C Shaw, et al.
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of 1
Search research articles
Search
Showing results (1-10 of 5) with videos related to
Sort By:
Page
of 1
NAR Genomics and Bioinformatics
|
December 20, 2024
Mining single-cell data for cell type-disease associations
Kevin G Chen, Kathryn O Farley, Timo Lassmann
Molecular Autism
|
October 1, 2024
Identifying SETBP1 haploinsufficiency molecular pathways to improve patient diagnosis using induced pluripotent stem cells and neural disease modelling
Nicole C Shaw, Kevin Chen, Kathryn O Farley, et al.
HGG Advances
|
November 26, 2023
CRISPR-Cas9-generated PTCHD1 2489T>G stem cells recapitulate patient phenotype when undergoing neural induction
Kathryn O Farley, Catherine A Forbes, Nicole C Shaw, et al.
Molecular Medicine (Cambridge, Mass.)
|
September 30, 2025
Functional characterization of the MED12 p.Arg1138Trp variant in females: implications for neural development and disease mechanism
Nicole C Shaw, Saraya Harrison, Kevin Chen, et al.
Stem Cell Research & Therapy
|
December 4, 2023
Gene editing and cardiac disease modelling for the interpretation of genetic variants of uncertain significance in congenital heart disease
Vanessa S Fear, Catherine A Forbes, Nicole C Shaw, et al.
Page
of 1