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Joshua D Smith

Showing results (131-140 of 194) with videos related to

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Nature|April 13, 2012
Sporadic autism exomes reveal a highly interconnected protein network of de novo mutationsBrian J O'Roak, Laura Vives, Santhosh Girirajan, et al.
HGG Advances|November 15, 2024
Proteome-wide association studies for blood lipids and comparison with transcriptome-wide association studiesDaiwei Zhang, Boran Gao, Qidi Feng, et al.
Biorxiv : the Preprint Server for Biology|September 4, 2023
Proteome-Wide Association Studies for Blood Lipids and Comparison with Transcriptome-Wide Association StudiesDaiwei Zhang, Boran Gao, Qidi Feng, et al.
Human Genetics|June 12, 2015
Mutation of ATF6 causes autosomal recessive achromatopsiaMuhammad Ansar, Regie Lyn P Santos-Cortez, Muhammad Arif Nadeem Saqib, et al.
Plos Genetics|June 4, 2011
Identification, replication, and functional fine-mapping of expression quantitative trait loci in primary human liver tissueFederico Innocenti, Gregory M Cooper, Ian B Stanaway, et al.
American Journal of Human Genetics|May 8, 2012
A human homeotic transformation resulting from mutations in PLCB4 and GNAI3 causes auriculocondylar syndromeMark J Rieder, Glenn E Green, Sarah S Park, et al.
Cancer Immunology, Immunotherapy : CII|October 27, 2018
Analysis of tumor-infiltrating CD103 resident memory T-cell content in recurrent laryngeal squamous cell carcinomaJacqueline E Mann, Joshua D Smith, Andrew C Birkeland, et al.
American Journal of Human Genetics|January 5, 2024
Interaction molecular QTL mapping discovers cellular and environmental modifiers of genetic regulatory effectsSilva Kasela, François Aguet, Sarah Kim-Hellmuth, et al.
Biorxiv : the Preprint Server for Biology|July 10, 2023
Interaction molecular QTL mapping discovers cellular and environmental modifiers of genetic regulatory effectsSilva Kasela, François Aguet, Sarah Kim-Hellmuth, et al.
Nature Genetics|March 12, 2014
Mutations in TJP2 cause progressive cholestatic liver diseaseMelissa Sambrotta, Sandra Strautnieks, Efterpi Papouli, et al.
Pageof 20

Showing results (131-140 of 194) with videos related to

Sort By:
Pageof 20
Nature|April 13, 2012
Sporadic autism exomes reveal a highly interconnected protein network of de novo mutationsBrian J O'Roak, Laura Vives, Santhosh Girirajan, et al.
HGG Advances|November 15, 2024
Proteome-wide association studies for blood lipids and comparison with transcriptome-wide association studiesDaiwei Zhang, Boran Gao, Qidi Feng, et al.
Biorxiv : the Preprint Server for Biology|September 4, 2023
Proteome-Wide Association Studies for Blood Lipids and Comparison with Transcriptome-Wide Association StudiesDaiwei Zhang, Boran Gao, Qidi Feng, et al.
Human Genetics|June 12, 2015
Mutation of ATF6 causes autosomal recessive achromatopsiaMuhammad Ansar, Regie Lyn P Santos-Cortez, Muhammad Arif Nadeem Saqib, et al.
Plos Genetics|June 4, 2011
Identification, replication, and functional fine-mapping of expression quantitative trait loci in primary human liver tissueFederico Innocenti, Gregory M Cooper, Ian B Stanaway, et al.
American Journal of Human Genetics|May 8, 2012
A human homeotic transformation resulting from mutations in PLCB4 and GNAI3 causes auriculocondylar syndromeMark J Rieder, Glenn E Green, Sarah S Park, et al.
Cancer Immunology, Immunotherapy : CII|October 27, 2018
Analysis of tumor-infiltrating CD103 resident memory T-cell content in recurrent laryngeal squamous cell carcinomaJacqueline E Mann, Joshua D Smith, Andrew C Birkeland, et al.
American Journal of Human Genetics|January 5, 2024
Interaction molecular QTL mapping discovers cellular and environmental modifiers of genetic regulatory effectsSilva Kasela, François Aguet, Sarah Kim-Hellmuth, et al.
Biorxiv : the Preprint Server for Biology|July 10, 2023
Interaction molecular QTL mapping discovers cellular and environmental modifiers of genetic regulatory effectsSilva Kasela, François Aguet, Sarah Kim-Hellmuth, et al.
Nature Genetics|March 12, 2014
Mutations in TJP2 cause progressive cholestatic liver diseaseMelissa Sambrotta, Sandra Strautnieks, Efterpi Papouli, et al.
Pageof 20