Search research articles
Contact Us
Filters
Showing results (81-90 of 107) with videos related to
Page
of 11
Sort By:
Nature Structural & Molecular Biology
|
July 17, 2023
Sperm chromatin structure and reproductive fitness are altered by substitution of a single amino acid in mouse protamine 1
Lindsay Moritz, Samantha B Schon, Mashiat Rabbani, et al.
Annals of Neurology
|
January 3, 2013
Mutations in KCND3 cause spinocerebellar ataxia type 22
Yi-Chung Lee, Alexandra Durr, Karen Majczenko, et al.
Genome Medicine
|
July 30, 2017
Post-mortem molecular profiling of three psychiatric disorders
Ryne C Ramaker, Kevin M Bowling, Brittany N Lasseigne, et al.
European Journal of Endocrinology
|
May 5, 2021
The phenotypic spectrum associated with OTX2 mutations in humans
Louise C Gregory, Peter Gergics, Marilena Nakaguma, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
December 26, 2012
Linkage analysis identifies a locus for plasma von Willebrand factor undetected by genome-wide association
Karl C Desch, Ayse B Ozel, David Siemieniak, et al.
Genes
|
August 27, 2021
Allelic Variants in Established Hypopituitarism Genes Expand Our Knowledge of the Phenotypic Spectrum
Marilena Nakaguma, Nathalia Garcia Bianchi Pereira Ferreira, Anna Flavia Figueredo Benedetti, et al.
Nature Communications
|
September 5, 2020
Chromosome 1q21.2 and additional loci influence risk of spontaneous coronary artery dissection and myocardial infarction
Jacqueline Saw, Min-Lee Yang, Mark Trinder, et al.
Circulation. Genomic and Precision Medicine
|
November 14, 2022
Fibromuscular Dysplasia and Abdominal Aortic Aneurysms Are Dimorphic Sex-Specific Diseases With Shared Complex Genetic Architecture
Alexander E Katz, Min-Lee Yang, Michael G Levin, et al.
Brain : a Journal of Neurology
|
February 16, 2013
Novel deletion of lysine 7 expands the clinical, histopathological and genetic spectrum of TPM2-related myopathies
Ann E Davidson, Fazeel M Siddiqui, Michael A Lopez, et al.
Molecular Cell
|
August 10, 2019
Landscape of Intercellular Crosstalk in Healthy and NASH Liver Revealed by Single-Cell Secretome Gene Analysis
Xuelian Xiong, Henry Kuang, Sahar Ansari, et al.
Page
of 11
Search research articles
Search
Showing results (81-90 of 107) with videos related to
Sort By:
Page
of 11
Nature Structural & Molecular Biology
|
July 17, 2023
Sperm chromatin structure and reproductive fitness are altered by substitution of a single amino acid in mouse protamine 1
Lindsay Moritz, Samantha B Schon, Mashiat Rabbani, et al.
Annals of Neurology
|
January 3, 2013
Mutations in KCND3 cause spinocerebellar ataxia type 22
Yi-Chung Lee, Alexandra Durr, Karen Majczenko, et al.
Genome Medicine
|
July 30, 2017
Post-mortem molecular profiling of three psychiatric disorders
Ryne C Ramaker, Kevin M Bowling, Brittany N Lasseigne, et al.
European Journal of Endocrinology
|
May 5, 2021
The phenotypic spectrum associated with OTX2 mutations in humans
Louise C Gregory, Peter Gergics, Marilena Nakaguma, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
December 26, 2012
Linkage analysis identifies a locus for plasma von Willebrand factor undetected by genome-wide association
Karl C Desch, Ayse B Ozel, David Siemieniak, et al.
Genes
|
August 27, 2021
Allelic Variants in Established Hypopituitarism Genes Expand Our Knowledge of the Phenotypic Spectrum
Marilena Nakaguma, Nathalia Garcia Bianchi Pereira Ferreira, Anna Flavia Figueredo Benedetti, et al.
Nature Communications
|
September 5, 2020
Chromosome 1q21.2 and additional loci influence risk of spontaneous coronary artery dissection and myocardial infarction
Jacqueline Saw, Min-Lee Yang, Mark Trinder, et al.
Circulation. Genomic and Precision Medicine
|
November 14, 2022
Fibromuscular Dysplasia and Abdominal Aortic Aneurysms Are Dimorphic Sex-Specific Diseases With Shared Complex Genetic Architecture
Alexander E Katz, Min-Lee Yang, Michael G Levin, et al.
Brain : a Journal of Neurology
|
February 16, 2013
Novel deletion of lysine 7 expands the clinical, histopathological and genetic spectrum of TPM2-related myopathies
Ann E Davidson, Fazeel M Siddiqui, Michael A Lopez, et al.
Molecular Cell
|
August 10, 2019
Landscape of Intercellular Crosstalk in Healthy and NASH Liver Revealed by Single-Cell Secretome Gene Analysis
Xuelian Xiong, Henry Kuang, Sahar Ansari, et al.
Page
of 11