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Molecular Pharmacology
|
February 10, 2012
mRNA transcript diversity creates new opportunities for pharmacological intervention
Elizabeth S Barrie, Ryan M Smith, Jonathan C Sanford, et al.
The Journal of Molecular Diagnostics : JMD
|
March 29, 2026
Performance evaluation of a PCR/Nanopore assay for carrier screening for cystic fibrosis, spinal muscular atrophy, and fragile X syndrome
Kendall E Martin, Fernanda Sábato, Jesse Lynch, et al.
Molecular Genetics & Genomic Medicine
|
May 7, 2018
Alpha-synuclein mRNA isoform formation and translation affected by polymorphism in the human SNCA 3'UTR
Elizabeth S Barrie, Sung-Ha Lee, John T Frater, et al.
Experimental and Clinical Transplantation : Official Journal of the Middle East Society for Organ Transplantation
|
March 17, 2022
Severe Graft-Versus-Host Disease Following Solid-Organ Transplant Confirmed by Chimerism Studies and Cytogenetic Analyses
Kelly A Rafferty, Elizabeth S Barrie, Scott A Turner, et al.
Pharmacogenetics and Genomics
|
February 13, 2016
Regulatory effects of genomic translocations at the human carboxylesterase-1 (CES1) gene locus
Jonathan C Sanford, Xinwen Wang, Jian Shi, et al.
Human Mutation
|
October 21, 2016
The CHRNA5/CHRNA3/CHRNB4 Nicotinic Receptor Regulome: Genomic Architecture, Regulatory Variants, and Clinical Associations
Elizabeth S Barrie, Katherine Hartmann, Sung-Ha Lee, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 24, 2022
Systematic evidence-based review: The application of noninvasive prenatal screening using cell-free DNA in general-risk pregnancies
Nancy C Rose, Elizabeth S Barrie, Jennifer Malinowski, et al.
The Journal of Endocrinology
|
December 20, 2014
Role of ITGAE in the development of autoimmune diabetes in non-obese diabetic mice
Elizabeth S Barrie, Mels Lodder, Paul H Weinreb, et al.
Cold Spring Harbor Molecular Case Studies
|
June 8, 2019
De novo loss-of-function variants in <i>NSD2</i> (<i>WHSC1</i>) associate with a subset of Wolf-Hirschhorn syndrome
Elizabeth S Barrie, Maria P Alfaro, Ruthann B Pfau, et al.
European Journal of Medical Genetics
|
August 16, 2019
Genotype-phenotype correlation: Inheritance and variant-type infer pathogenicity in IQSEC2 gene
Elizabeth S Barrie, Catherine E Cottrell, Julie Gastier-Foster, et al.
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Search research articles
Search
Showing results (1-10 of 16) with videos related to
Sort By:
Page
of 2
Molecular Pharmacology
|
February 10, 2012
mRNA transcript diversity creates new opportunities for pharmacological intervention
Elizabeth S Barrie, Ryan M Smith, Jonathan C Sanford, et al.
The Journal of Molecular Diagnostics : JMD
|
March 29, 2026
Performance evaluation of a PCR/Nanopore assay for carrier screening for cystic fibrosis, spinal muscular atrophy, and fragile X syndrome
Kendall E Martin, Fernanda Sábato, Jesse Lynch, et al.
Molecular Genetics & Genomic Medicine
|
May 7, 2018
Alpha-synuclein mRNA isoform formation and translation affected by polymorphism in the human SNCA 3'UTR
Elizabeth S Barrie, Sung-Ha Lee, John T Frater, et al.
Experimental and Clinical Transplantation : Official Journal of the Middle East Society for Organ Transplantation
|
March 17, 2022
Severe Graft-Versus-Host Disease Following Solid-Organ Transplant Confirmed by Chimerism Studies and Cytogenetic Analyses
Kelly A Rafferty, Elizabeth S Barrie, Scott A Turner, et al.
Pharmacogenetics and Genomics
|
February 13, 2016
Regulatory effects of genomic translocations at the human carboxylesterase-1 (CES1) gene locus
Jonathan C Sanford, Xinwen Wang, Jian Shi, et al.
Human Mutation
|
October 21, 2016
The CHRNA5/CHRNA3/CHRNB4 Nicotinic Receptor Regulome: Genomic Architecture, Regulatory Variants, and Clinical Associations
Elizabeth S Barrie, Katherine Hartmann, Sung-Ha Lee, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 24, 2022
Systematic evidence-based review: The application of noninvasive prenatal screening using cell-free DNA in general-risk pregnancies
Nancy C Rose, Elizabeth S Barrie, Jennifer Malinowski, et al.
The Journal of Endocrinology
|
December 20, 2014
Role of ITGAE in the development of autoimmune diabetes in non-obese diabetic mice
Elizabeth S Barrie, Mels Lodder, Paul H Weinreb, et al.
Cold Spring Harbor Molecular Case Studies
|
June 8, 2019
De novo loss-of-function variants in <i>NSD2</i> (<i>WHSC1</i>) associate with a subset of Wolf-Hirschhorn syndrome
Elizabeth S Barrie, Maria P Alfaro, Ruthann B Pfau, et al.
European Journal of Medical Genetics
|
August 16, 2019
Genotype-phenotype correlation: Inheritance and variant-type infer pathogenicity in IQSEC2 gene
Elizabeth S Barrie, Catherine E Cottrell, Julie Gastier-Foster, et al.
Page
of 2