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Michelle Simon

Showing results (51-60 of 77) with videos related to

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Briefings in Bioinformatics|October 1, 2015
The digital revolution in phenotypingAnika Oellrich, Nigel Collier, Tudor Groza, et al.
Environmental Modelling & Software : with Environment Data News|December 4, 2018
Embedding co-production and addressing uncertainty in watershed modeling decision-support tools: successes and challengesBradley L Barnhart, Heather E Golden, Joseph R Kasprzyk, et al.
Cell Reports|December 20, 2018
A Wars2 Mutant Mouse Model Displays OXPHOS Deficiencies and Activation of Tissue-Specific Stress Response PathwaysThomas Agnew, Michelle Goldsworthy, Carlos Aguilar, et al.
Nature Communications|March 16, 2019
Dissecting features of epigenetic variants underlying cardiometabolic risk using full-resolution epigenome profiling in regulatory elementsFiona Allum, Åsa K Hedman, Xiaojian Shao, et al.
Molecular Metabolism|November 7, 2017
Disruption of the homeodomain transcription factor orthopedia homeobox (Otp) is associated with obesity and anxietyLee Moir, Elena G Bochukova, Rebecca Dumbell, et al.
Nature Genetics|February 29, 2024
Epigenetic variation impacts individual differences in the transcriptional response to influenza infectionKatherine A Aracena, Yen-Lung Lin, Kaixuan Luo, et al.
Nature Metabolism|February 19, 2020
Single-cell analysis of human adipose tissue identifies depot and disease specific cell typesJinchu Vijay, Marie-Frédérique Gauthier, Rebecca L Biswell, et al.
European Journal of Endocrinology|October 29, 2021
Broad-spectrum XX and XY gonadal dysgenesis in patients with a homozygous L193S variant in PPP2R3CDilek Cicek, Nick Warr, Gozde Yesil, et al.
Science Advances|May 25, 2022
Origin, specification and differentiation of a rare supporting-like lineage in the developing mouse gonadChloé Mayère, Violaine Regard, Aitana Perea-Gomez, et al.
Nature Communications|July 30, 2015
Erratum: Characterization of functional methylomes by next-generation capture sequencing identifies novel disease-associated variantsFiona Allum, Xiaojian Shao, Frédéric Guénard, et al.
Pageof 8

Showing results (51-60 of 77) with videos related to

Sort By:
Pageof 8
Briefings in Bioinformatics|October 1, 2015
The digital revolution in phenotypingAnika Oellrich, Nigel Collier, Tudor Groza, et al.
Environmental Modelling & Software : with Environment Data News|December 4, 2018
Embedding co-production and addressing uncertainty in watershed modeling decision-support tools: successes and challengesBradley L Barnhart, Heather E Golden, Joseph R Kasprzyk, et al.
Cell Reports|December 20, 2018
A Wars2 Mutant Mouse Model Displays OXPHOS Deficiencies and Activation of Tissue-Specific Stress Response PathwaysThomas Agnew, Michelle Goldsworthy, Carlos Aguilar, et al.
Nature Communications|March 16, 2019
Dissecting features of epigenetic variants underlying cardiometabolic risk using full-resolution epigenome profiling in regulatory elementsFiona Allum, Åsa K Hedman, Xiaojian Shao, et al.
Molecular Metabolism|November 7, 2017
Disruption of the homeodomain transcription factor orthopedia homeobox (Otp) is associated with obesity and anxietyLee Moir, Elena G Bochukova, Rebecca Dumbell, et al.
Nature Genetics|February 29, 2024
Epigenetic variation impacts individual differences in the transcriptional response to influenza infectionKatherine A Aracena, Yen-Lung Lin, Kaixuan Luo, et al.
Nature Metabolism|February 19, 2020
Single-cell analysis of human adipose tissue identifies depot and disease specific cell typesJinchu Vijay, Marie-Frédérique Gauthier, Rebecca L Biswell, et al.
European Journal of Endocrinology|October 29, 2021
Broad-spectrum XX and XY gonadal dysgenesis in patients with a homozygous L193S variant in PPP2R3CDilek Cicek, Nick Warr, Gozde Yesil, et al.
Science Advances|May 25, 2022
Origin, specification and differentiation of a rare supporting-like lineage in the developing mouse gonadChloé Mayère, Violaine Regard, Aitana Perea-Gomez, et al.
Nature Communications|July 30, 2015
Erratum: Characterization of functional methylomes by next-generation capture sequencing identifies novel disease-associated variantsFiona Allum, Xiaojian Shao, Frédéric Guénard, et al.
Pageof 8