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Emerging Infectious Diseases
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March 22, 2017
Transmission of Hepatitis A Virus through Combined Liver-Small Intestine-Pancreas Transplantation
Monique 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 deficiency
Yoshiharu 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 Disease
Nicholas 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 Disease
Galen 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 mice
Valeria 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 Copaxone
S 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 cancer
Folefac 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 2
S 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 Compound
Dagmar 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-hydroxycholesterol
Cheryl L Wellington, Yu-Zhou Yang, Stephen Zhou, et al.
Page
of 91
Search research articles
Search
Showing results (861-870 of 910) with videos related to
Sort By:
Page
of 91
Emerging Infectious Diseases
|
March 22, 2017
Transmission of Hepatitis A Virus through Combined Liver-Small Intestine-Pancreas Transplantation
Monique 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 deficiency
Yoshiharu 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 Disease
Nicholas 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 Disease
Galen 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 mice
Valeria 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 Copaxone
S 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 cancer
Folefac 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 2
S 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 Compound
Dagmar 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-hydroxycholesterol
Cheryl L Wellington, Yu-Zhou Yang, Stephen Zhou, et al.
Page
of 91