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Helen Stewart

Showing results (51-60 of 93) with videos related to

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ISME Communications|May 6, 2026
Host plant selects bacterial rhizosphere microbiome function whereas community structure is determined by soil legacyRodrigo G Taketani, Ian M Clark, Payton T O Yau, et al.
European Journal of Human Genetics : EJHG|June 16, 2018
Phenotypic spectrum of Au-Kline syndrome: a report of six new cases and review of the literatureP Y Billie Au, Caitlin Goedhart, Marcia Ferguson, et al.
Human Mutation|October 31, 2009
OBSL1 mutations in 3-M syndrome are associated with a modulation of IGFBP2 and IGFBP5 expression levelsCeline Huber, Mélanie Fradin, Thomas Edouard, et al.
Cell Metabolism|January 14, 2014
Analysis of transcription factors key for mouse pancreatic development establishes NKX2-2 and MNX1 mutations as causes of neonatal diabetes in manSarah E Flanagan, Elisa De Franco, Hana Lango Allen, et al.
HGG Advances|April 3, 2023
Clinical, genetic, epidemiologic, evolutionary, and functional delineation of <i>TSPEAR</i>-related autosomal recessive ectodermal dysplasia 14Adam Jackson, Sheng-Jia Lin, Elizabeth A Jones, et al.
Cell Reports|May 31, 2016
De Novo Mutations in DENR Disrupt Neuronal Development and Link Congenital Neurological Disorders to Faulty mRNA Translation Re-initiationMatilda A Haas, Linh Ngo, Shan Shan Li, et al.
Nature Genetics|March 8, 2011
Mutations in NOTCH2 cause Hajdu-Cheney syndrome, a disorder of severe and progressive bone lossMichael A Simpson, Melita D Irving, Esra Asilmaz, et al.
Nature Genetics|August 15, 2006
Discovery of previously unidentified genomic disorders from the duplication architecture of the human genomeAndrew J Sharp, Sierra Hansen, Rebecca R Selzer, et al.
Journal of Medicinal Chemistry|April 17, 2025
Structure-Guided Design of ISOX-DUAL-Based Degraders Targeting BRD4 and CBP/EP300: A Case of Degrader CollapseAnthony K Edmonds, Dimitrios-Ilias Balourdas, Graham P Marsh, et al.
Clinical Genetics|April 27, 2020
HNRNPH1-related syndromic intellectual disability: Seven additional cases suggestive of a distinct syndromic neurodevelopmental syndromeSara C Reichert, Rachel Li, Scott A Turner, et al.
Pageof 10

Showing results (51-60 of 93) with videos related to

Sort By:
Pageof 10
ISME Communications|May 6, 2026
Host plant selects bacterial rhizosphere microbiome function whereas community structure is determined by soil legacyRodrigo G Taketani, Ian M Clark, Payton T O Yau, et al.
European Journal of Human Genetics : EJHG|June 16, 2018
Phenotypic spectrum of Au-Kline syndrome: a report of six new cases and review of the literatureP Y Billie Au, Caitlin Goedhart, Marcia Ferguson, et al.
Human Mutation|October 31, 2009
OBSL1 mutations in 3-M syndrome are associated with a modulation of IGFBP2 and IGFBP5 expression levelsCeline Huber, Mélanie Fradin, Thomas Edouard, et al.
Cell Metabolism|January 14, 2014
Analysis of transcription factors key for mouse pancreatic development establishes NKX2-2 and MNX1 mutations as causes of neonatal diabetes in manSarah E Flanagan, Elisa De Franco, Hana Lango Allen, et al.
HGG Advances|April 3, 2023
Clinical, genetic, epidemiologic, evolutionary, and functional delineation of <i>TSPEAR</i>-related autosomal recessive ectodermal dysplasia 14Adam Jackson, Sheng-Jia Lin, Elizabeth A Jones, et al.
Cell Reports|May 31, 2016
De Novo Mutations in DENR Disrupt Neuronal Development and Link Congenital Neurological Disorders to Faulty mRNA Translation Re-initiationMatilda A Haas, Linh Ngo, Shan Shan Li, et al.
Nature Genetics|March 8, 2011
Mutations in NOTCH2 cause Hajdu-Cheney syndrome, a disorder of severe and progressive bone lossMichael A Simpson, Melita D Irving, Esra Asilmaz, et al.
Nature Genetics|August 15, 2006
Discovery of previously unidentified genomic disorders from the duplication architecture of the human genomeAndrew J Sharp, Sierra Hansen, Rebecca R Selzer, et al.
Journal of Medicinal Chemistry|April 17, 2025
Structure-Guided Design of ISOX-DUAL-Based Degraders Targeting BRD4 and CBP/EP300: A Case of Degrader CollapseAnthony K Edmonds, Dimitrios-Ilias Balourdas, Graham P Marsh, et al.
Clinical Genetics|April 27, 2020
HNRNPH1-related syndromic intellectual disability: Seven additional cases suggestive of a distinct syndromic neurodevelopmental syndromeSara C Reichert, Rachel Li, Scott A Turner, et al.
Pageof 10