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Showing results (421-430 of 439) with videos related to

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Neurobiology of Aging|October 25, 2016
Aβ vaccination in combination with behavioral enrichment in aged beagles: effects on cognition, Aβ, and microhemorrhagesPaulina R Davis, Ginevra Giannini, Karin Rudolph, et al.
Lancet (London, England)|October 19, 2004
Association between mutations in a thyroid hormone transporter and severe X-linked psychomotor retardationEdith C H Friesema, Annette Grueters, Heike Biebermann, et al.
The Journal of Clinical Endocrinology and Metabolism|March 16, 2007
Functional analysis of monocarboxylate transporter 8 mutations identified in patients with X-linked psychomotor retardation and elevated serum triiodothyronineJurgen Jansen, Edith C H Friesema, Monique H A Kester, et al.
Pharmacology Research & Perspectives|December 16, 2014
The in vivo efficacy and side effect pharmacology of GS-5759, a novel bifunctional phosphodiesterase 4 inhibitor and long-acting β 2-adrenoceptor agonist in preclinical animal speciesMichael Salmon, Stacey L Tannheimer, Terry T Gentzler, et al.
BMC Medicine|April 2, 2024
A practical evidence-based approach to management of type 2 diabetes in children and young people (CYP): UK consensusBilly White, S M Ng, J C Agwu, et al.
Biorxiv : the Preprint Server for Biology|December 17, 2020
Thiol drugs decrease SARS-CoV-2 lung injury <i>in vivo</i> and disrupt SARS-CoV-2 spike complex binding to ACE2 <i>in vitro</i>Kritika Khanna, Wilfred Raymond, Jing Jin, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|August 11, 2012
TSHR is the main causative locus in autosomal recessively inherited thyroid dysgenesisHakan Cangul, Zehra Aycan, Halil Saglam, et al.
Journal of Evolutionary Biology|September 24, 2020
Resistance to natural and synthetic gene drive systemsTom A R Price, Nikolai Windbichler, Robert L Unckless, et al.
Diabetes|June 29, 2004
Wolcott-Rallison Syndrome: clinical, genetic, and functional study of EIF2AK3 mutations and suggestion of genetic heterogeneityValérie Senée, Krishna M Vattem, Marc Delépine, et al.
Clinical Endocrinology|August 20, 2010
Novel TSHR mutations in consanguineous families with congenital nongoitrous hypothyroidismHakan Cangul, Neil V Morgan, Julia R Forman, et al.
Pageof 44

Showing results (421-430 of 439) with videos related to

Sort By:
Pageof 44
Neurobiology of Aging|October 25, 2016
Aβ vaccination in combination with behavioral enrichment in aged beagles: effects on cognition, Aβ, and microhemorrhagesPaulina R Davis, Ginevra Giannini, Karin Rudolph, et al.
Lancet (London, England)|October 19, 2004
Association between mutations in a thyroid hormone transporter and severe X-linked psychomotor retardationEdith C H Friesema, Annette Grueters, Heike Biebermann, et al.
The Journal of Clinical Endocrinology and Metabolism|March 16, 2007
Functional analysis of monocarboxylate transporter 8 mutations identified in patients with X-linked psychomotor retardation and elevated serum triiodothyronineJurgen Jansen, Edith C H Friesema, Monique H A Kester, et al.
Pharmacology Research & Perspectives|December 16, 2014
The in vivo efficacy and side effect pharmacology of GS-5759, a novel bifunctional phosphodiesterase 4 inhibitor and long-acting β 2-adrenoceptor agonist in preclinical animal speciesMichael Salmon, Stacey L Tannheimer, Terry T Gentzler, et al.
BMC Medicine|April 2, 2024
A practical evidence-based approach to management of type 2 diabetes in children and young people (CYP): UK consensusBilly White, S M Ng, J C Agwu, et al.
Biorxiv : the Preprint Server for Biology|December 17, 2020
Thiol drugs decrease SARS-CoV-2 lung injury <i>in vivo</i> and disrupt SARS-CoV-2 spike complex binding to ACE2 <i>in vitro</i>Kritika Khanna, Wilfred Raymond, Jing Jin, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|August 11, 2012
TSHR is the main causative locus in autosomal recessively inherited thyroid dysgenesisHakan Cangul, Zehra Aycan, Halil Saglam, et al.
Journal of Evolutionary Biology|September 24, 2020
Resistance to natural and synthetic gene drive systemsTom A R Price, Nikolai Windbichler, Robert L Unckless, et al.
Diabetes|June 29, 2004
Wolcott-Rallison Syndrome: clinical, genetic, and functional study of EIF2AK3 mutations and suggestion of genetic heterogeneityValérie Senée, Krishna M Vattem, Marc Delépine, et al.
Clinical Endocrinology|August 20, 2010
Novel TSHR mutations in consanguineous families with congenital nongoitrous hypothyroidismHakan Cangul, Neil V Morgan, Julia R Forman, et al.
Pageof 44