Search research articles
Contact Us
Filters
Showing results (41-50 of 184) with videos related to
Page
of 19
Sort By:
American Journal of Human Genetics
|
October 21, 2021
Dystonia-specific mutations in THAP1 alter transcription of genes associated with neurodevelopment and myelin
Aloysius Domingo, Rachita Yadav, Shivangi Shah, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao
|
December 13, 2021
Developmental regulation of neuronal gene expression by Elongator complex protein 1 dosage
Elisabetta Morini, Dadi Gao, Emily M Logan, et al.
Molecular Neuropsychiatry
|
September 8, 2017
WNT/β-Catenin Pathway and Epigenetic Mechanisms Regulate the Pitt-Hopkins Syndrome and Schizophrenia Risk Gene <b></b>
Krista M Hennig, Daniel M Fass, Wen-Ning Zhao, et al.
Cell
|
December 17, 2016
An Ancient, Unified Mechanism for Metformin Growth Inhibition in C. elegans and Cancer
Lianfeng Wu, Ben Zhou, Noriko Oshiro-Rapley, et al.
Plos Genetics
|
March 22, 2019
Hypomorphic mutation of the mouse Huntington's disease gene orthologue
Vidya Murthy, Toma Tebaldi, Toshimi Yoshida, et al.
Cell Genomics
|
February 13, 2025
Activation of the imprinted Prader-Willi syndrome locus by CRISPR-based epigenome editing
Dahlia Rohm, Joshua B Black, Sean R McCutcheon, et al.
Genome Research
|
December 5, 2024
An integrative TAD catalog in lymphoblastoid cell lines discloses the functional impact of deletions and insertions in human genomes
Chong Li, Marc Jan Bonder, Sabriya Syed, et al.
American Journal of Medical Genetics. Part A
|
October 22, 2019
Biallelic mutation of FBXL7 suggests a novel form of Hennekam syndrome
Philip M Boone, Scott Paterson, Kiana Mohajeri, et al.
American Journal of Human Genetics
|
April 9, 2011
Next-generation sequencing strategies enable routine detection of balanced chromosome rearrangements for clinical diagnostics and genetic research
Michael E Talkowski, Carl Ernst, Adrian Heilbut, et al.
Nature Biomedical Engineering
|
April 25, 2019
Ectopic expression of RAD52 and dn53BP1 improves homology-directed repair during CRISPR-Cas9 genome editing
Bruna S Paulsen, Pankaj K Mandal, Richard L Frock, et al.
Page
of 19
Search research articles
Search
Showing results (41-50 of 184) with videos related to
Sort By:
Page
of 19
American Journal of Human Genetics
|
October 21, 2021
Dystonia-specific mutations in THAP1 alter transcription of genes associated with neurodevelopment and myelin
Aloysius Domingo, Rachita Yadav, Shivangi Shah, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao
|
December 13, 2021
Developmental regulation of neuronal gene expression by Elongator complex protein 1 dosage
Elisabetta Morini, Dadi Gao, Emily M Logan, et al.
Molecular Neuropsychiatry
|
September 8, 2017
WNT/β-Catenin Pathway and Epigenetic Mechanisms Regulate the Pitt-Hopkins Syndrome and Schizophrenia Risk Gene <b></b>
Krista M Hennig, Daniel M Fass, Wen-Ning Zhao, et al.
Cell
|
December 17, 2016
An Ancient, Unified Mechanism for Metformin Growth Inhibition in C. elegans and Cancer
Lianfeng Wu, Ben Zhou, Noriko Oshiro-Rapley, et al.
Plos Genetics
|
March 22, 2019
Hypomorphic mutation of the mouse Huntington's disease gene orthologue
Vidya Murthy, Toma Tebaldi, Toshimi Yoshida, et al.
Cell Genomics
|
February 13, 2025
Activation of the imprinted Prader-Willi syndrome locus by CRISPR-based epigenome editing
Dahlia Rohm, Joshua B Black, Sean R McCutcheon, et al.
Genome Research
|
December 5, 2024
An integrative TAD catalog in lymphoblastoid cell lines discloses the functional impact of deletions and insertions in human genomes
Chong Li, Marc Jan Bonder, Sabriya Syed, et al.
American Journal of Medical Genetics. Part A
|
October 22, 2019
Biallelic mutation of FBXL7 suggests a novel form of Hennekam syndrome
Philip M Boone, Scott Paterson, Kiana Mohajeri, et al.
American Journal of Human Genetics
|
April 9, 2011
Next-generation sequencing strategies enable routine detection of balanced chromosome rearrangements for clinical diagnostics and genetic research
Michael E Talkowski, Carl Ernst, Adrian Heilbut, et al.
Nature Biomedical Engineering
|
April 25, 2019
Ectopic expression of RAD52 and dn53BP1 improves homology-directed repair during CRISPR-Cas9 genome editing
Bruna S Paulsen, Pankaj K Mandal, Richard L Frock, et al.
Page
of 19