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Helmut Fuchs

Showing results (241-250 of 272) with videos related to

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Cell|October 11, 2016
Chemical Hybridization of Glucagon and Thyroid Hormone Optimizes Therapeutic Impact for Metabolic DiseaseBrian Finan, Christoffer Clemmensen, Zhimeng Zhu, et al.
American Journal of Ophthalmology|June 17, 2026
SEARCHING FOR NEW GENES THAT CAUSE USHER SYNDROMEAla Moshiri, Niusha Kasiri, Michael Shea, et al.
Behavioural Brain Research|October 3, 2017
Understanding gene functions and disease mechanisms: Phenotyping pipelines in the German Mouse ClinicHelmut Fuchs, Juan Antonio Aguilar-Pimentel, Oana V Amarie, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|December 18, 2018
A mouse model for intellectual disability caused by mutations in the X-linked 2'‑O‑methyltransferase Ftsj1 geneLars R Jensen, Lillian Garrett, Sabine M Hölter, et al.
Plos One|June 16, 2012
Large-scale phenotyping of an accurate genetic mouse model of JNCL identifies novel early pathology outside the central nervous systemJohn F Staropoli, Larissa Haliw, Sunita Biswas, et al.
EMBO Molecular Medicine|November 9, 2021
Characterising a homozygous two-exon deletion in UQCRH: comparing human and mouse phenotypesSilvia Vidali, Raffaele Gerlini, Kyle Thompson, et al.
Nature Communications|June 27, 2017
Prevalence of sexual dimorphism in mammalian phenotypic traitsNatasha A Karp, Jeremy Mason, Arthur L Beaudet, et al.
Nature Microbiology|September 12, 2018
Male offspring born to mildly ZIKV-infected mice are at risk of developing neurocognitive disorders in adulthoodStephanie Stanelle-Bertram, Kerstin Walendy-Gnirß, Thomas Speiseder, et al.
Nature Communications|February 2, 2020
Human and mouse essentiality screens as a resource for disease gene discoveryPilar Cacheiro, Violeta Muñoz-Fuentes, Stephen A Murray, et al.
Medrxiv : the Preprint Server for Health Sciences|March 30, 2023
Implication of <i>FOXD2</i> dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT)Korbinian M Riedhammer, Thanh-Minh T Nguyen, Can Koşukcu, et al.
Pageof 28

Showing results (241-250 of 272) with videos related to

Sort By:
Pageof 28
Cell|October 11, 2016
Chemical Hybridization of Glucagon and Thyroid Hormone Optimizes Therapeutic Impact for Metabolic DiseaseBrian Finan, Christoffer Clemmensen, Zhimeng Zhu, et al.
American Journal of Ophthalmology|June 17, 2026
SEARCHING FOR NEW GENES THAT CAUSE USHER SYNDROMEAla Moshiri, Niusha Kasiri, Michael Shea, et al.
Behavioural Brain Research|October 3, 2017
Understanding gene functions and disease mechanisms: Phenotyping pipelines in the German Mouse ClinicHelmut Fuchs, Juan Antonio Aguilar-Pimentel, Oana V Amarie, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|December 18, 2018
A mouse model for intellectual disability caused by mutations in the X-linked 2'‑O‑methyltransferase Ftsj1 geneLars R Jensen, Lillian Garrett, Sabine M Hölter, et al.
Plos One|June 16, 2012
Large-scale phenotyping of an accurate genetic mouse model of JNCL identifies novel early pathology outside the central nervous systemJohn F Staropoli, Larissa Haliw, Sunita Biswas, et al.
EMBO Molecular Medicine|November 9, 2021
Characterising a homozygous two-exon deletion in UQCRH: comparing human and mouse phenotypesSilvia Vidali, Raffaele Gerlini, Kyle Thompson, et al.
Nature Communications|June 27, 2017
Prevalence of sexual dimorphism in mammalian phenotypic traitsNatasha A Karp, Jeremy Mason, Arthur L Beaudet, et al.
Nature Microbiology|September 12, 2018
Male offspring born to mildly ZIKV-infected mice are at risk of developing neurocognitive disorders in adulthoodStephanie Stanelle-Bertram, Kerstin Walendy-Gnirß, Thomas Speiseder, et al.
Nature Communications|February 2, 2020
Human and mouse essentiality screens as a resource for disease gene discoveryPilar Cacheiro, Violeta Muñoz-Fuentes, Stephen A Murray, et al.
Medrxiv : the Preprint Server for Health Sciences|March 30, 2023
Implication of <i>FOXD2</i> dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT)Korbinian M Riedhammer, Thanh-Minh T Nguyen, Can Koşukcu, et al.
Pageof 28