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Jennifer Winter

Showing results (31-40 of 43) with videos related to

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Journal of Clinical Medicine|January 11, 2022
First Results from the Prospective German Registry for Childhood Glaucoma: Phenotype-Genotype AssociationJulia V Stingl, Stefan Diederich, Heidi Diel, et al.
Human Genetics|January 4, 2008
The Opitz syndrome gene product MID1 assembles a microtubule-associated ribonucleoprotein complexBeatriz Aranda-Orgillés, Alexander Trockenbacher, Jennifer Winter, et al.
European Journal of Medical Genetics|January 25, 2019
Heterotopic ossifications and Charcot joints: Congenital insensitivity to pain with anhidrosis (CIPA) and a novel NTRK1 gene mutationZoran Gucev, Velibor Tasic, Ivona Bogevska, et al.
Nature Communications|January 26, 2020
Inhibition of histone deacetylation rescues phenotype in a mouse model of Birk-Barel intellectual disability syndromeAlexis Cooper, Tamer Butto, Niklas Hammer, et al.
BMC Genomics|January 20, 2021
Reliability of genomic variants across different next-generation sequencing platforms and bioinformatic processing pipelinesStephan Weißbach, Stanislav Sys, Charlotte Hewel, et al.
The Journal of Investigative Dermatology|January 19, 2005
Haplotype sharing analysis identifies a retroviral dUTPase as candidate susceptibility gene for psoriasisJohn Foerster, Ilja Nolte, Judith Junge, et al.
Frontiers in Aging Neuroscience|September 11, 2025
Cognitive training gain transfer in cognitively healthy aging: per protocol results of the German AgeGain studyFlorian U Fischer, Bianca Kollmann, Dominik Wolf, et al.
Medrxiv : the Preprint Server for Health Sciences|June 22, 2026
TACR3 variant confers resilience to aging and Alzheimer's diseaseNicolas Ruffini, Florian Udo Fischer, Robert Subirana Slotos, et al.
EMBO Reports|June 29, 2023
DOT1L activity affects neural stem cell division mode and reduces differentiation and ASNS expressionBismark Appiah, Camila L Fullio, Chiara Ossola, et al.
American Journal of Medical Genetics. Part A|November 24, 2004
Mild phenotypes in a series of patients with Opitz GBBB syndrome with MID1 mutationsJoyce So, Vanessa Suckow, Zofia Kijas, et al.
Pageof 5

Showing results (31-40 of 43) with videos related to

Sort By:
Pageof 5
Journal of Clinical Medicine|January 11, 2022
First Results from the Prospective German Registry for Childhood Glaucoma: Phenotype-Genotype AssociationJulia V Stingl, Stefan Diederich, Heidi Diel, et al.
Human Genetics|January 4, 2008
The Opitz syndrome gene product MID1 assembles a microtubule-associated ribonucleoprotein complexBeatriz Aranda-Orgillés, Alexander Trockenbacher, Jennifer Winter, et al.
European Journal of Medical Genetics|January 25, 2019
Heterotopic ossifications and Charcot joints: Congenital insensitivity to pain with anhidrosis (CIPA) and a novel NTRK1 gene mutationZoran Gucev, Velibor Tasic, Ivona Bogevska, et al.
Nature Communications|January 26, 2020
Inhibition of histone deacetylation rescues phenotype in a mouse model of Birk-Barel intellectual disability syndromeAlexis Cooper, Tamer Butto, Niklas Hammer, et al.
BMC Genomics|January 20, 2021
Reliability of genomic variants across different next-generation sequencing platforms and bioinformatic processing pipelinesStephan Weißbach, Stanislav Sys, Charlotte Hewel, et al.
The Journal of Investigative Dermatology|January 19, 2005
Haplotype sharing analysis identifies a retroviral dUTPase as candidate susceptibility gene for psoriasisJohn Foerster, Ilja Nolte, Judith Junge, et al.
Frontiers in Aging Neuroscience|September 11, 2025
Cognitive training gain transfer in cognitively healthy aging: per protocol results of the German AgeGain studyFlorian U Fischer, Bianca Kollmann, Dominik Wolf, et al.
Medrxiv : the Preprint Server for Health Sciences|June 22, 2026
TACR3 variant confers resilience to aging and Alzheimer's diseaseNicolas Ruffini, Florian Udo Fischer, Robert Subirana Slotos, et al.
EMBO Reports|June 29, 2023
DOT1L activity affects neural stem cell division mode and reduces differentiation and ASNS expressionBismark Appiah, Camila L Fullio, Chiara Ossola, et al.
American Journal of Medical Genetics. Part A|November 24, 2004
Mild phenotypes in a series of patients with Opitz GBBB syndrome with MID1 mutationsJoyce So, Vanessa Suckow, Zofia Kijas, et al.
Pageof 5