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R Hayden

Showing results (801-810 of 910) with videos related to

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Neurobiology of Disease|January 14, 2015
Partial rescue of some features of Huntington Disease in the genetic absence of caspase-6 in YAC128 miceBibiana K Y Wong, Dagmar E Ehrnhoefer, Rona K Graham, et al.
Human Molecular Genetics|June 19, 2003
Selective striatal neuronal loss in a YAC128 mouse model of Huntington diseaseElizabeth J Slow, Jeremy van Raamsdonk, Daniel Rogers, et al.
Nature Genetics|November 10, 2009
Genetic variants in TPMT and COMT are associated with hearing loss in children receiving cisplatin chemotherapyColin J D Ross, Hagit Katzov-Eckert, Marie-Pierre Dubé, et al.
BMC Plant Biology|October 8, 2016
Root morphology and seed and leaf ionomic traits in a Brassica napus L. diversity panel show wide phenotypic variation and are characteristic of crop habitC L Thomas, T D Alcock, N S Graham, et al.
Circulation|March 10, 2001
Common genetic variation in ABCA1 is associated with altered lipoprotein levels and a modified risk for coronary artery diseaseS M Clee, A H Zwinderman, J C Engert, et al.
Human Molecular Genetics|April 30, 2016
Structural and molecular myelination deficits occur prior to neuronal loss in the YAC128 and BACHD models of Huntington diseaseRoy Tang Yi Teo, Xin Hong, Libo Yu-Taeger, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|March 5, 2021
Regulation of OATP1B1 Function by Tyrosine Kinase-mediated PhosphorylationElizabeth R Hayden, Mingqing Chen, Kyle Z Pasquariello, et al.
Neurobiology of Disease|February 3, 2005
Cross-species characterization of the ALS2 gene and analysis of its pattern of expression in development and adulthoodRebecca S Devon, Claudia Schwab, Justin D Topp, et al.
Nature Neuroscience|May 16, 2006
Palmitoylation of huntingtin by HIP14 is essential for its trafficking and functionAnat Yanai, Kun Huang, Rujun Kang, et al.
Journal of Lipid Research|August 10, 2015
Targeted next-generation sequencing to diagnose disorders of HDL cholesterolSingh N Sadananda, Jia Nee Foo, Meng Tiak Toh, et al.
Pageof 91

Showing results (801-810 of 910) with videos related to

Sort By:
Pageof 91
Neurobiology of Disease|January 14, 2015
Partial rescue of some features of Huntington Disease in the genetic absence of caspase-6 in YAC128 miceBibiana K Y Wong, Dagmar E Ehrnhoefer, Rona K Graham, et al.
Human Molecular Genetics|June 19, 2003
Selective striatal neuronal loss in a YAC128 mouse model of Huntington diseaseElizabeth J Slow, Jeremy van Raamsdonk, Daniel Rogers, et al.
Nature Genetics|November 10, 2009
Genetic variants in TPMT and COMT are associated with hearing loss in children receiving cisplatin chemotherapyColin J D Ross, Hagit Katzov-Eckert, Marie-Pierre Dubé, et al.
BMC Plant Biology|October 8, 2016
Root morphology and seed and leaf ionomic traits in a Brassica napus L. diversity panel show wide phenotypic variation and are characteristic of crop habitC L Thomas, T D Alcock, N S Graham, et al.
Circulation|March 10, 2001
Common genetic variation in ABCA1 is associated with altered lipoprotein levels and a modified risk for coronary artery diseaseS M Clee, A H Zwinderman, J C Engert, et al.
Human Molecular Genetics|April 30, 2016
Structural and molecular myelination deficits occur prior to neuronal loss in the YAC128 and BACHD models of Huntington diseaseRoy Tang Yi Teo, Xin Hong, Libo Yu-Taeger, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|March 5, 2021
Regulation of OATP1B1 Function by Tyrosine Kinase-mediated PhosphorylationElizabeth R Hayden, Mingqing Chen, Kyle Z Pasquariello, et al.
Neurobiology of Disease|February 3, 2005
Cross-species characterization of the ALS2 gene and analysis of its pattern of expression in development and adulthoodRebecca S Devon, Claudia Schwab, Justin D Topp, et al.
Nature Neuroscience|May 16, 2006
Palmitoylation of huntingtin by HIP14 is essential for its trafficking and functionAnat Yanai, Kun Huang, Rujun Kang, et al.
Journal of Lipid Research|August 10, 2015
Targeted next-generation sequencing to diagnose disorders of HDL cholesterolSingh N Sadananda, Jia Nee Foo, Meng Tiak Toh, et al.
Pageof 91