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Cell
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October 11, 2016
Chemical Hybridization of Glucagon and Thyroid Hormone Optimizes Therapeutic Impact for Metabolic Disease
Brian Finan, Christoffer Clemmensen, Zhimeng Zhu, et al.
American Journal of Ophthalmology
|
June 17, 2026
SEARCHING FOR NEW GENES THAT CAUSE USHER SYNDROME
Ala 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 Clinic
Helmut 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 gene
Lars 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 system
John 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 phenotypes
Silvia Vidali, Raffaele Gerlini, Kyle Thompson, et al.
Nature Communications
|
June 27, 2017
Prevalence of sexual dimorphism in mammalian phenotypic traits
Natasha 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 adulthood
Stephanie 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 discovery
Pilar 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.
Page
of 28
Search research articles
Search
Showing results (241-250 of 272) with videos related to
Sort By:
Page
of 28
Cell
|
October 11, 2016
Chemical Hybridization of Glucagon and Thyroid Hormone Optimizes Therapeutic Impact for Metabolic Disease
Brian Finan, Christoffer Clemmensen, Zhimeng Zhu, et al.
American Journal of Ophthalmology
|
June 17, 2026
SEARCHING FOR NEW GENES THAT CAUSE USHER SYNDROME
Ala 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 Clinic
Helmut 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 gene
Lars 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 system
John 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 phenotypes
Silvia Vidali, Raffaele Gerlini, Kyle Thompson, et al.
Nature Communications
|
June 27, 2017
Prevalence of sexual dimorphism in mammalian phenotypic traits
Natasha 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 adulthood
Stephanie 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 discovery
Pilar 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.
Page
of 28