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Human Mutation
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June 3, 2021
Integrated in silico and experimental assessment of disease relevance of PCDH19 missense variants
Duyen H Pham, Melissa R Pitman, Raman Kumar, et al.
Biorxiv : the Preprint Server for Biology
|
January 9, 2026
Anatomical White Matter Tracts Span the Cortical Hierarchy to Support Cognitive Diversity
Joëlle Bagautdinova, Golia Shafiei, Audrey C Luo, et al.
Genes
|
August 26, 2023
Aicardi Syndrome Is a Genetically Heterogeneous Disorder
Thuong T Ha, Rosemary Burgess, Morgan Newman, et al.
American Journal of Human Genetics
|
January 17, 2012
PRRT2 mutations cause benign familial infantile epilepsy and infantile convulsions with choreoathetosis syndrome
Sarah E Heron, Bronwyn E Grinton, Sara Kivity, et al.
Frontiers in Molecular Neuroscience
|
March 3, 2020
Expanding Clinical Presentations Due to Variations in THOC2 mRNA Nuclear Export Factor
Raman Kumar, Elizabeth Palmer, Alison E Gardner, et al.
Cancer Research
|
September 16, 2022
Transposon Mutagenesis Reveals RBMS3 Silencing as a Promoter of Malignant Progression of BRAFV600E-Driven Lung Tumorigenesis
Aria Vaishnavi, Joseph Juan, Maebh Jacob, et al.
Journal of Human Nutrition and Dietetics : the Official Journal of the British Dietetic Association
|
July 15, 2004
Dietetic guidelines: diet in secondary prevention of cardiovascular disease (first update, June 2003)
L Hooper, E Griffiths, B Abrahams, et al.
Nature Communications
|
February 8, 2024
Compromised transcription-mRNA export factor THOC2 causes R-loop accumulation, DNA damage and adverse neurodevelopment
Rudrarup Bhattacharjee, Lachlan A Jolly, Mark A Corbett, et al.
Biodata Mining
|
December 19, 2024
Comparing new tools of artificial intelligence to the authentic intelligence of our global health students
Shilpa R Thandla, Grace Q Armstrong, Adil Menon, et al.
NPJ Genomic Medicine
|
December 10, 2020
Missense variant contribution to USP9X-female syndrome
Lachlan A Jolly, Euan Parnell, Alison E Gardner, et al.
Page
of 51
Search research articles
Search
Showing results (491-500 of 504) with videos related to
Sort By:
Page
of 51
Human Mutation
|
June 3, 2021
Integrated in silico and experimental assessment of disease relevance of PCDH19 missense variants
Duyen H Pham, Melissa R Pitman, Raman Kumar, et al.
Biorxiv : the Preprint Server for Biology
|
January 9, 2026
Anatomical White Matter Tracts Span the Cortical Hierarchy to Support Cognitive Diversity
Joëlle Bagautdinova, Golia Shafiei, Audrey C Luo, et al.
Genes
|
August 26, 2023
Aicardi Syndrome Is a Genetically Heterogeneous Disorder
Thuong T Ha, Rosemary Burgess, Morgan Newman, et al.
American Journal of Human Genetics
|
January 17, 2012
PRRT2 mutations cause benign familial infantile epilepsy and infantile convulsions with choreoathetosis syndrome
Sarah E Heron, Bronwyn E Grinton, Sara Kivity, et al.
Frontiers in Molecular Neuroscience
|
March 3, 2020
Expanding Clinical Presentations Due to Variations in THOC2 mRNA Nuclear Export Factor
Raman Kumar, Elizabeth Palmer, Alison E Gardner, et al.
Cancer Research
|
September 16, 2022
Transposon Mutagenesis Reveals RBMS3 Silencing as a Promoter of Malignant Progression of BRAFV600E-Driven Lung Tumorigenesis
Aria Vaishnavi, Joseph Juan, Maebh Jacob, et al.
Journal of Human Nutrition and Dietetics : the Official Journal of the British Dietetic Association
|
July 15, 2004
Dietetic guidelines: diet in secondary prevention of cardiovascular disease (first update, June 2003)
L Hooper, E Griffiths, B Abrahams, et al.
Nature Communications
|
February 8, 2024
Compromised transcription-mRNA export factor THOC2 causes R-loop accumulation, DNA damage and adverse neurodevelopment
Rudrarup Bhattacharjee, Lachlan A Jolly, Mark A Corbett, et al.
Biodata Mining
|
December 19, 2024
Comparing new tools of artificial intelligence to the authentic intelligence of our global health students
Shilpa R Thandla, Grace Q Armstrong, Adil Menon, et al.
NPJ Genomic Medicine
|
December 10, 2020
Missense variant contribution to USP9X-female syndrome
Lachlan A Jolly, Euan Parnell, Alison E Gardner, et al.
Page
of 51