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Showing results (861-870 of 934) with videos related to

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Science (New York, N.Y.)|January 13, 2022
Measuring the melting curve of iron at super-Earth core conditionsRichard G Kraus, Russell J Hemley, Suzanne J Ali, et al.
Immunity|June 18, 2015
Dominant Mutations in the Autoimmune Regulator AIRE Are Associated with Common Organ-Specific Autoimmune DiseasesBergithe E Oftedal, Alexander Hellesen, Martina M Erichsen, et al.
Medrxiv : the Preprint Server for Health Sciences|February 6, 2026
Systematic analysis of homozygous autosomal copy number losses in exomes improves diagnostic yield and uncovers ultra-rare recessive disordersAnkur Chaurasia, Anju Shukla, Shruti Pande, et al.
European Journal of Human Genetics : EJHG|June 26, 2026
Systematic analysis of homozygous autosomal copy number losses in exomes improves diagnostic yield and uncovers ultra-rare recessive disordersAnkur Chaurasia, Anju Shukla, Shruti Pande, et al.
The Journal of Clinical Investigation|September 13, 2019
Loss-of-function variants in myocardin cause congenital megabladder in humans and miceArjan C Houweling, Glenda M Beaman, Alex V Postma, et al.
Science Advances|May 13, 2026
IgLON5 autoimmune antibodies activate Tau via neuronal hyperactivityBilge Askin, Cagla Kilic, César Cordero Gómez, et al.
American Journal of Human Genetics|May 15, 2021
Bi-allelic premature truncating variants in LTBP1 cause cutis laxa syndromeLore Pottie, Christin S Adamo, Aude Beyens, et al.
Genome Medicine|July 19, 2022
Recommendations for clinical interpretation of variants found in non-coding regions of the genomeJamie M Ellingford, Joo Wook Ahn, Richard D Bagnall, et al.
European Journal of Heart Failure|March 5, 2026
Characterising the heterogeneity of heart failure with preserved ejection fraction: moving beyond subgroups and distinguishing disease from riskFardad Soltani, Nicholas Black, Joshua Bradley, et al.
Nature Genetics|January 10, 2017
Exploring the genetic architecture of inflammatory bowel disease by whole-genome sequencing identifies association at ADCY7Yang Luo, Katrina M de Lange, Luke Jostins, et al.
Pageof 94

Showing results (861-870 of 934) with videos related to

Sort By:
Pageof 94
Science (New York, N.Y.)|January 13, 2022
Measuring the melting curve of iron at super-Earth core conditionsRichard G Kraus, Russell J Hemley, Suzanne J Ali, et al.
Immunity|June 18, 2015
Dominant Mutations in the Autoimmune Regulator AIRE Are Associated with Common Organ-Specific Autoimmune DiseasesBergithe E Oftedal, Alexander Hellesen, Martina M Erichsen, et al.
Medrxiv : the Preprint Server for Health Sciences|February 6, 2026
Systematic analysis of homozygous autosomal copy number losses in exomes improves diagnostic yield and uncovers ultra-rare recessive disordersAnkur Chaurasia, Anju Shukla, Shruti Pande, et al.
European Journal of Human Genetics : EJHG|June 26, 2026
Systematic analysis of homozygous autosomal copy number losses in exomes improves diagnostic yield and uncovers ultra-rare recessive disordersAnkur Chaurasia, Anju Shukla, Shruti Pande, et al.
The Journal of Clinical Investigation|September 13, 2019
Loss-of-function variants in myocardin cause congenital megabladder in humans and miceArjan C Houweling, Glenda M Beaman, Alex V Postma, et al.
Science Advances|May 13, 2026
IgLON5 autoimmune antibodies activate Tau via neuronal hyperactivityBilge Askin, Cagla Kilic, César Cordero Gómez, et al.
American Journal of Human Genetics|May 15, 2021
Bi-allelic premature truncating variants in LTBP1 cause cutis laxa syndromeLore Pottie, Christin S Adamo, Aude Beyens, et al.
Genome Medicine|July 19, 2022
Recommendations for clinical interpretation of variants found in non-coding regions of the genomeJamie M Ellingford, Joo Wook Ahn, Richard D Bagnall, et al.
European Journal of Heart Failure|March 5, 2026
Characterising the heterogeneity of heart failure with preserved ejection fraction: moving beyond subgroups and distinguishing disease from riskFardad Soltani, Nicholas Black, Joshua Bradley, et al.
Nature Genetics|January 10, 2017
Exploring the genetic architecture of inflammatory bowel disease by whole-genome sequencing identifies association at ADCY7Yang Luo, Katrina M de Lange, Luke Jostins, et al.
Pageof 94