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M B Davis

Showing results (61-70 of 106) with videos related to

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Somatic Cell and Molecular Genetics|March 1, 1987
Regional localization of carbonic anhydrase genes CA1 and CA3 on human chromosome 8M B Davis, L F West, J H Barlow, et al.
Neurology|November 19, 2011
Acetazolamide efficacy in hypokalemic periodic paralysis and the predictive role of genotypeE Matthews, S Portaro, Q Ke, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 29, 2000
A Yorkshire family with adult-onset cranio-cervical primary torsion dystoniaA Münchau, E M Valente, M B Davis, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 1, 1993
Transthyretin gene mutations in British and French patients with amyloid neuropathyK Bhatia, M Reilly, D Adams, et al.
Annals of Human Genetics|October 1, 1985
A cytochrome P-450 gene family mapped to human chromosome 19I R Phillips, E A Shephard, S Povey, et al.
The Journal of Investigative Dermatology. Symposium Proceedings|October 28, 1999
Participation of the melanocortin-1 receptor in the UV control of pigmentationI Suzuki, S Im, A Tada, et al.
Annals of the New York Academy of Sciences|November 1, 2017
A Family with Friedreich Ataxia and Onion-Bulb Formations at Sural Nerve BiopsyA A Barreira, W Marques, M G Sweeney, et al.
Cell Growth & Differentiation : the Molecular Biology Journal of the American Association for Cancer Research|August 5, 1998
Endothelin-1 is a paracrine growth factor that modulates melanogenesis of human melanocytes and participates in their responses to ultraviolet radiationA Tada, I Suzuki, S Im, et al.
American Journal of Human Genetics|October 23, 1997
Hereditary geniospasm: linkage to chromosome 9q13-q21 and evidence for genetic heterogeneityP R Jarman, N W Wood, M T Davis, et al.
The British Journal of Ophthalmology|April 29, 2008
Characterisation of the macular dystrophy in patients with the A3243G mitochondrial DNA point mutation with fundus autofluorescenceP P Rath, S Jenkins, M Michaelides, et al.
Pageof 11

Showing results (61-70 of 106) with videos related to

Sort By:
Pageof 11
Somatic Cell and Molecular Genetics|March 1, 1987
Regional localization of carbonic anhydrase genes CA1 and CA3 on human chromosome 8M B Davis, L F West, J H Barlow, et al.
Neurology|November 19, 2011
Acetazolamide efficacy in hypokalemic periodic paralysis and the predictive role of genotypeE Matthews, S Portaro, Q Ke, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 29, 2000
A Yorkshire family with adult-onset cranio-cervical primary torsion dystoniaA Münchau, E M Valente, M B Davis, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 1, 1993
Transthyretin gene mutations in British and French patients with amyloid neuropathyK Bhatia, M Reilly, D Adams, et al.
Annals of Human Genetics|October 1, 1985
A cytochrome P-450 gene family mapped to human chromosome 19I R Phillips, E A Shephard, S Povey, et al.
The Journal of Investigative Dermatology. Symposium Proceedings|October 28, 1999
Participation of the melanocortin-1 receptor in the UV control of pigmentationI Suzuki, S Im, A Tada, et al.
Annals of the New York Academy of Sciences|November 1, 2017
A Family with Friedreich Ataxia and Onion-Bulb Formations at Sural Nerve BiopsyA A Barreira, W Marques, M G Sweeney, et al.
Cell Growth & Differentiation : the Molecular Biology Journal of the American Association for Cancer Research|August 5, 1998
Endothelin-1 is a paracrine growth factor that modulates melanogenesis of human melanocytes and participates in their responses to ultraviolet radiationA Tada, I Suzuki, S Im, et al.
American Journal of Human Genetics|October 23, 1997
Hereditary geniospasm: linkage to chromosome 9q13-q21 and evidence for genetic heterogeneityP R Jarman, N W Wood, M T Davis, et al.
The British Journal of Ophthalmology|April 29, 2008
Characterisation of the macular dystrophy in patients with the A3243G mitochondrial DNA point mutation with fundus autofluorescenceP P Rath, S Jenkins, M Michaelides, et al.
Pageof 11