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R Hayden

Showing results (861-870 of 910) with videos related to

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Emerging Infectious Diseases|March 22, 2017
Transmission of Hepatitis A Virus through Combined Liver-Small Intestine-Pancreas TransplantationMonique A Foster, Lauren M Weil, Sherry Jin, et al.
Biochemical and Biophysical Research Communications|January 12, 2002
Expression and functional analyses of novel mutations of ATP-binding cassette transporter-1 in Japanese patients with high-density lipoprotein deficiencyYoshiharu Nishida, Kenichi Hirano, Kosuke Tsukamoto, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|December 14, 2020
Mutant Huntingtin Is Cleared from the Brain via Active Mechanisms in Huntington DiseaseNicholas S Caron, Raul Banos, Christopher Yanick, et al.
American Journal of Human Genetics|May 21, 2019
Length of Uninterrupted CAG, Independent of Polyglutamine Size, Results in Increased Somatic Instability, Hastening Onset of Huntington DiseaseGalen E B Wright, Jennifer A Collins, Chris Kay, et al.
Human Molecular Genetics|January 21, 2012
Rescue from excitotoxicity and axonal degeneration accompanied by age-dependent behavioral and neuroanatomical alterations in caspase-6-deficient miceValeria Uribe, Bibiana K Y Wong, Rona K Graham, et al.
Eneurologicalsci|August 11, 2018
Physicochemical, biological, functional and toxicological characterization of the European follow-on glatiramer acetate product as compared with CopaxoneS Melamed-Gal, P Loupe, B Timan, et al.
Nature Genetics|August 4, 2015
A coding variant in RARG confers susceptibility to anthracycline-induced cardiotoxicity in childhood cancerFolefac Aminkeng, Amit P Bhavsar, Henk Visscher, et al.
Nature Genetics|October 5, 2001
A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2S Hadano, C K Hand, H Osuga, et al.
Cell Chemical Biology|July 30, 2019
Activation of Caspase-6 Is Promoted by a Mutant Huntingtin Fragment and Blocked by an Allosteric Inhibitor CompoundDagmar E Ehrnhoefer, Niels H Skotte, Jeanette Reinshagen, et al.
Journal of Lipid Research|October 29, 2002
Truncation mutations in ABCA1 suppress normal upregulation of full-length ABCA1 by 9-cis-retinoic acid and 22-R-hydroxycholesterolCheryl L Wellington, Yu-Zhou Yang, Stephen Zhou, et al.
Pageof 91

Showing results (861-870 of 910) with videos related to

Sort By:
Pageof 91
Emerging Infectious Diseases|March 22, 2017
Transmission of Hepatitis A Virus through Combined Liver-Small Intestine-Pancreas TransplantationMonique A Foster, Lauren M Weil, Sherry Jin, et al.
Biochemical and Biophysical Research Communications|January 12, 2002
Expression and functional analyses of novel mutations of ATP-binding cassette transporter-1 in Japanese patients with high-density lipoprotein deficiencyYoshiharu Nishida, Kenichi Hirano, Kosuke Tsukamoto, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|December 14, 2020
Mutant Huntingtin Is Cleared from the Brain via Active Mechanisms in Huntington DiseaseNicholas S Caron, Raul Banos, Christopher Yanick, et al.
American Journal of Human Genetics|May 21, 2019
Length of Uninterrupted CAG, Independent of Polyglutamine Size, Results in Increased Somatic Instability, Hastening Onset of Huntington DiseaseGalen E B Wright, Jennifer A Collins, Chris Kay, et al.
Human Molecular Genetics|January 21, 2012
Rescue from excitotoxicity and axonal degeneration accompanied by age-dependent behavioral and neuroanatomical alterations in caspase-6-deficient miceValeria Uribe, Bibiana K Y Wong, Rona K Graham, et al.
Eneurologicalsci|August 11, 2018
Physicochemical, biological, functional and toxicological characterization of the European follow-on glatiramer acetate product as compared with CopaxoneS Melamed-Gal, P Loupe, B Timan, et al.
Nature Genetics|August 4, 2015
A coding variant in RARG confers susceptibility to anthracycline-induced cardiotoxicity in childhood cancerFolefac Aminkeng, Amit P Bhavsar, Henk Visscher, et al.
Nature Genetics|October 5, 2001
A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2S Hadano, C K Hand, H Osuga, et al.
Cell Chemical Biology|July 30, 2019
Activation of Caspase-6 Is Promoted by a Mutant Huntingtin Fragment and Blocked by an Allosteric Inhibitor CompoundDagmar E Ehrnhoefer, Niels H Skotte, Jeanette Reinshagen, et al.
Journal of Lipid Research|October 29, 2002
Truncation mutations in ABCA1 suppress normal upregulation of full-length ABCA1 by 9-cis-retinoic acid and 22-R-hydroxycholesterolCheryl L Wellington, Yu-Zhou Yang, Stephen Zhou, et al.
Pageof 91