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K Nichol

Showing results (41-50 of 50) with videos related to

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Mammalian Genome : Official Journal of the International Mammalian Genome Society|July 10, 1998
Gene structure and map location of the murine homolog of the Huntington-associated protein, Hap1J Nasir, K Duan, K Nichol, et al.
Journal of Inorganic Biochemistry|February 8, 2014
The solution structure of the copper clioquinol complexM Jake Pushie, Kurt H Nienaber, Kelly L Summers, et al.
Journal of Neurochemistry|February 26, 1999
Life without huntingtin: normal differentiation into functional neuronsM Metzler, N Chen, C D Helgason, et al.
Genomics|January 16, 1999
A yeast artificial chromosome-based physical map of the juvenile amyotrophic lateral sclerosis (ALS2) critical region on human chromosome 2q33-q34S Hadano, K Nichol, R R Brinkman, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|June 29, 1999
Genomic organization of the human caspase-9 gene on Chromosome 1p36. 1-p36.3S Hadano, J Nasir, K Nichol, et al.
Antimicrobial Agents and Chemotherapy|April 22, 2015
Epidemiology of vancomycin-resistant enterococci in Canadian hospitals (CANWARD study, 2007 to 2013)P J Simner, H Adam, M Baxter, et al.
Metallomics : Integrated Biometal Science|November 10, 2020
PBT2 acts through a different mechanism of action than other 8-hydroxyquinolines: an X-ray fluorescence imaging studyKelly L Summers, Natalia V Dolgova, Kenneth B Gagnon, et al.
Human Molecular Genetics|December 20, 2002
Genomic context drives SCA7 CAG repeat instability, while expressed SCA7 cDNAs are intergenerationally and somatically stable in transgenic miceRandell T Libby, Darren G Monckton, Ying-Hui Fu, et al.
Nature Genetics|May 1, 1997
HIP1, a human homologue of S. cerevisiae Sla2p, interacts with membrane-associated huntingtin in the brainM A Kalchman, H B Koide, K McCutcheon, et al.
Human Molecular Genetics|February 1, 1997
Contribution of DNA sequence and CAG size to mutation frequencies of intermediate alleles for Huntington disease: evidence from single sperm analysesS S Chong, E Almqvist, H Telenius, et al.
Pageof 5

Showing results (41-50 of 50) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 50 results.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|July 10, 1998
Gene structure and map location of the murine homolog of the Huntington-associated protein, Hap1J Nasir, K Duan, K Nichol, et al.
Journal of Inorganic Biochemistry|February 8, 2014
The solution structure of the copper clioquinol complexM Jake Pushie, Kurt H Nienaber, Kelly L Summers, et al.
Journal of Neurochemistry|February 26, 1999
Life without huntingtin: normal differentiation into functional neuronsM Metzler, N Chen, C D Helgason, et al.
Genomics|January 16, 1999
A yeast artificial chromosome-based physical map of the juvenile amyotrophic lateral sclerosis (ALS2) critical region on human chromosome 2q33-q34S Hadano, K Nichol, R R Brinkman, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|June 29, 1999
Genomic organization of the human caspase-9 gene on Chromosome 1p36. 1-p36.3S Hadano, J Nasir, K Nichol, et al.
Antimicrobial Agents and Chemotherapy|April 22, 2015
Epidemiology of vancomycin-resistant enterococci in Canadian hospitals (CANWARD study, 2007 to 2013)P J Simner, H Adam, M Baxter, et al.
Metallomics : Integrated Biometal Science|November 10, 2020
PBT2 acts through a different mechanism of action than other 8-hydroxyquinolines: an X-ray fluorescence imaging studyKelly L Summers, Natalia V Dolgova, Kenneth B Gagnon, et al.
Human Molecular Genetics|December 20, 2002
Genomic context drives SCA7 CAG repeat instability, while expressed SCA7 cDNAs are intergenerationally and somatically stable in transgenic miceRandell T Libby, Darren G Monckton, Ying-Hui Fu, et al.
Nature Genetics|May 1, 1997
HIP1, a human homologue of S. cerevisiae Sla2p, interacts with membrane-associated huntingtin in the brainM A Kalchman, H B Koide, K McCutcheon, et al.
Human Molecular Genetics|February 1, 1997
Contribution of DNA sequence and CAG size to mutation frequencies of intermediate alleles for Huntington disease: evidence from single sperm analysesS S Chong, E Almqvist, H Telenius, et al.
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