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M Vance

Showing results (171-180 of 466) with videos related to

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Nature Genetics|August 1, 1994
The Haw River syndrome: dentatorubropallidoluysian atrophy (DRPLA) in an African-American familyJ R Burke, M S Wingfield, K E Lewis, et al.
Pediatric Neurology|May 29, 2003
Identification of MeCP2 mutations in a series of females with autistic disorderRegina M Carney, Chantelle M Wolpert, Sarah A Ravan, et al.
Clinical Immunology (Orlando, Fla.)|October 21, 1999
Peptide T blocks GP120/CCR5 chemokine receptor-mediated chemotaxisL S Redwine, C B Pert, J D Rone, et al.
Nature Medicine|March 1, 1996
Huntingtin and DRPLA proteins selectively interact with the enzyme GAPDHJ R Burke, J J Enghild, M E Martin, et al.
Genes and Immunity|June 10, 2016
GWAS analysis implicates NF-κB-mediated induction of inflammatory T cells in multiple sclerosisJ P Hussman, A H Beecham, M Schmidt, et al.
Journal of Medicinal Chemistry|May 9, 1997
Synthesis, antiviral activity, and biological properties of vinylacetylene analogs of enviroximeF Victor, T J Brown, K Campanale, et al.
American Journal of Medical Genetics|June 22, 2000
Heterogeneity in Paget disease of the boneM A Nance, F Q Nuttall, M J Econs, et al.
Genomics|April 1, 1991
Localization of Charcot-Marie-Tooth disease type 1a (CMT1A) to chromosome 17p11.2J M Vance, D Barker, L H Yamaoka, et al.
Journal of Synchrotron Radiation|February 9, 2026
The design of a low-cost 3D printed flow cell for synchrotron computed microtomographyLiam Perera, Peter Garland, Caroline Kirk, et al.
American Journal of Human Genetics|July 11, 2006
Mutations in the novel mitochondrial protein REEP1 cause hereditary spastic paraplegia type 31Stephan Züchner, Gaofeng Wang, Khanh-Nhat Tran-Viet, et al.
Pageof 47

Showing results (171-180 of 466) with videos related to

Sort By:
Pageof 47
Nature Genetics|August 1, 1994
The Haw River syndrome: dentatorubropallidoluysian atrophy (DRPLA) in an African-American familyJ R Burke, M S Wingfield, K E Lewis, et al.
Pediatric Neurology|May 29, 2003
Identification of MeCP2 mutations in a series of females with autistic disorderRegina M Carney, Chantelle M Wolpert, Sarah A Ravan, et al.
Clinical Immunology (Orlando, Fla.)|October 21, 1999
Peptide T blocks GP120/CCR5 chemokine receptor-mediated chemotaxisL S Redwine, C B Pert, J D Rone, et al.
Nature Medicine|March 1, 1996
Huntingtin and DRPLA proteins selectively interact with the enzyme GAPDHJ R Burke, J J Enghild, M E Martin, et al.
Genes and Immunity|June 10, 2016
GWAS analysis implicates NF-κB-mediated induction of inflammatory T cells in multiple sclerosisJ P Hussman, A H Beecham, M Schmidt, et al.
Journal of Medicinal Chemistry|May 9, 1997
Synthesis, antiviral activity, and biological properties of vinylacetylene analogs of enviroximeF Victor, T J Brown, K Campanale, et al.
American Journal of Medical Genetics|June 22, 2000
Heterogeneity in Paget disease of the boneM A Nance, F Q Nuttall, M J Econs, et al.
Genomics|April 1, 1991
Localization of Charcot-Marie-Tooth disease type 1a (CMT1A) to chromosome 17p11.2J M Vance, D Barker, L H Yamaoka, et al.
Journal of Synchrotron Radiation|February 9, 2026
The design of a low-cost 3D printed flow cell for synchrotron computed microtomographyLiam Perera, Peter Garland, Caroline Kirk, et al.
American Journal of Human Genetics|July 11, 2006
Mutations in the novel mitochondrial protein REEP1 cause hereditary spastic paraplegia type 31Stephan Züchner, Gaofeng Wang, Khanh-Nhat Tran-Viet, et al.
Pageof 47