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Annals of Clinical and Translational Neurology
|
July 8, 2016
Deep sequencing of mitochondrial genomes reveals increased mutation load in Friedreich's ataxia
Angela D Bhalla, Alireza Khodadadi-Jamayran, Yanjie Li, et al.
Plos One
|
May 8, 2014
Genome-wide association study of maternal and inherited loci for conotruncal heart defects
A J Agopian, Laura E Mitchell, Joseph Glessner, et al.
Cell Reports
|
July 19, 2016
Stalled DNA Replication Forks at the Endogenous GAA Repeats Drive Repeat Expansion in Friedreich's Ataxia Cells
Jeannine Gerhardt, Angela D Bhalla, Jill Sergesketter Butler, et al.
Nature Structural & Molecular Biology
|
June 9, 2009
A UPF3-mediated regulatory switch that maintains RNA surveillance
Wai-Kin Chan, Angela D Bhalla, Hervé Le Hir, et al.
The Journal of Biological Chemistry
|
December 19, 2008
Nonsense codons trigger an RNA partitioning shift
Angela D Bhalla, Jayanthi P Gudikote, Jun Wang, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
March 12, 2015
Excision of Expanded GAA Repeats Alleviates the Molecular Phenotype of Friedreich's Ataxia
Yanjie Li, Urszula Polak, Angela D Bhalla, et al.
Journal of Cancer Science and Clinical Therapeutics
|
December 7, 2020
AXL Inhibition Enhances MEK Inhibitor Sensitivity in Malignant Peripheral Nerve Sheath Tumors
Sharon M Landers, Angela D Bhalla, XiaoYan Ma, et al.
Biopreservation and Biobanking
|
March 23, 2016
Establishment and Maintenance of Primary Fibroblast Repositories for Rare Diseases-Friedreich's Ataxia Example
Yanjie Li, Urszula Polak, Amanda D Clark, et al.
Human Molecular Genetics
|
September 25, 2015
Expanded GAA repeats impede transcription elongation through the FXN gene and induce transcriptional silencing that is restricted to the FXN locus
Yanjie Li, Yue Lu, Urszula Polak, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology
|
August 6, 2013
Exon sequencing of PAX3 and T (brachyury) in cases with spina bifida
A J Agopian, Angela D Bhalla, Eric Boerwinkle, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 17) with videos related to
Sort By:
Page
of 2
Annals of Clinical and Translational Neurology
|
July 8, 2016
Deep sequencing of mitochondrial genomes reveals increased mutation load in Friedreich's ataxia
Angela D Bhalla, Alireza Khodadadi-Jamayran, Yanjie Li, et al.
Plos One
|
May 8, 2014
Genome-wide association study of maternal and inherited loci for conotruncal heart defects
A J Agopian, Laura E Mitchell, Joseph Glessner, et al.
Cell Reports
|
July 19, 2016
Stalled DNA Replication Forks at the Endogenous GAA Repeats Drive Repeat Expansion in Friedreich's Ataxia Cells
Jeannine Gerhardt, Angela D Bhalla, Jill Sergesketter Butler, et al.
Nature Structural & Molecular Biology
|
June 9, 2009
A UPF3-mediated regulatory switch that maintains RNA surveillance
Wai-Kin Chan, Angela D Bhalla, Hervé Le Hir, et al.
The Journal of Biological Chemistry
|
December 19, 2008
Nonsense codons trigger an RNA partitioning shift
Angela D Bhalla, Jayanthi P Gudikote, Jun Wang, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
March 12, 2015
Excision of Expanded GAA Repeats Alleviates the Molecular Phenotype of Friedreich's Ataxia
Yanjie Li, Urszula Polak, Angela D Bhalla, et al.
Journal of Cancer Science and Clinical Therapeutics
|
December 7, 2020
AXL Inhibition Enhances MEK Inhibitor Sensitivity in Malignant Peripheral Nerve Sheath Tumors
Sharon M Landers, Angela D Bhalla, XiaoYan Ma, et al.
Biopreservation and Biobanking
|
March 23, 2016
Establishment and Maintenance of Primary Fibroblast Repositories for Rare Diseases-Friedreich's Ataxia Example
Yanjie Li, Urszula Polak, Amanda D Clark, et al.
Human Molecular Genetics
|
September 25, 2015
Expanded GAA repeats impede transcription elongation through the FXN gene and induce transcriptional silencing that is restricted to the FXN locus
Yanjie Li, Yue Lu, Urszula Polak, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology
|
August 6, 2013
Exon sequencing of PAX3 and T (brachyury) in cases with spina bifida
A J Agopian, Angela D Bhalla, Eric Boerwinkle, et al.
Page
of 2