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A Maw

Showing results (31-40 of 43) with videos related to

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American Journal of Medical Genetics|February 5, 1998
Mitochondrial A7445G mutation in two pedigrees with palmoplantar keratoderma and deafnessK B Sevior, A Hatamochi, I A Stewart, et al.
Molecules (Basel, Switzerland)|November 26, 2022
Discovery of Levesquamide B through Global Natural Product Social Molecular NetworkingMary M LeClair, Zacharie A Maw, Alyssa L Grunwald, et al.
Molecular and Cellular Biology|September 19, 1998
The deafness-associated mitochondrial DNA mutation at position 7445, which affects tRNASer(UCN) precursor processing, has long-range effects on NADH dehydrogenase subunit ND6 gene expressionM X Guan, J A Enriquez, N Fischel-Ghodsian, et al.
Nature|April 22, 1993
Relaxation of insulin-like growth factor II gene imprinting implicated in Wilms' tumourO Ogawa, M R Eccles, J Szeto, et al.
American Journal of Human Genetics|September 1, 1995
The contribution of the DFNB1 locus to neurosensory deafness in a Caucasian populationM A Maw, D R Allen-Powell, R J Goodey, et al.
Clinical & Experimental Ophthalmology|April 6, 2005
Clinical manifestations of a unique X-linked retinal disorder in a large New Zealand family with a novel mutation in CACNA1F, the gene responsible for CSNB2Carolyn I Hope, Dianne M Sharp, Ariana Hemara-Wahanui, et al.
Journal of Medicinal Chemistry|January 8, 1993
Inhibitors of protein kinase C. 3. Potent and highly selective bisindolylmaleimides by conformational restrictionR A Bit, P D Davis, L H Elliott, et al.
Nature Genetics|November 5, 1997
Mutation of the gene encoding cellular retinaldehyde-binding protein in autosomal recessive retinitis pigmentosaM A Maw, B Kennedy, A Knight, et al.
Cancer Research|June 1, 1992
A third Wilms' tumor locus on chromosome 16qM A Maw, P E Grundy, L J Millow, et al.
Human Molecular Genetics|December 10, 1999
A frameshift mutation in prominin (mouse)-like 1 causes human retinal degenerationM A Maw, D Corbeil, J Koch, et al.
Pageof 5

Showing results (31-40 of 43) with videos related to

Sort By:
Pageof 5
American Journal of Medical Genetics|February 5, 1998
Mitochondrial A7445G mutation in two pedigrees with palmoplantar keratoderma and deafnessK B Sevior, A Hatamochi, I A Stewart, et al.
Molecules (Basel, Switzerland)|November 26, 2022
Discovery of Levesquamide B through Global Natural Product Social Molecular NetworkingMary M LeClair, Zacharie A Maw, Alyssa L Grunwald, et al.
Molecular and Cellular Biology|September 19, 1998
The deafness-associated mitochondrial DNA mutation at position 7445, which affects tRNASer(UCN) precursor processing, has long-range effects on NADH dehydrogenase subunit ND6 gene expressionM X Guan, J A Enriquez, N Fischel-Ghodsian, et al.
Nature|April 22, 1993
Relaxation of insulin-like growth factor II gene imprinting implicated in Wilms' tumourO Ogawa, M R Eccles, J Szeto, et al.
American Journal of Human Genetics|September 1, 1995
The contribution of the DFNB1 locus to neurosensory deafness in a Caucasian populationM A Maw, D R Allen-Powell, R J Goodey, et al.
Clinical & Experimental Ophthalmology|April 6, 2005
Clinical manifestations of a unique X-linked retinal disorder in a large New Zealand family with a novel mutation in CACNA1F, the gene responsible for CSNB2Carolyn I Hope, Dianne M Sharp, Ariana Hemara-Wahanui, et al.
Journal of Medicinal Chemistry|January 8, 1993
Inhibitors of protein kinase C. 3. Potent and highly selective bisindolylmaleimides by conformational restrictionR A Bit, P D Davis, L H Elliott, et al.
Nature Genetics|November 5, 1997
Mutation of the gene encoding cellular retinaldehyde-binding protein in autosomal recessive retinitis pigmentosaM A Maw, B Kennedy, A Knight, et al.
Cancer Research|June 1, 1992
A third Wilms' tumor locus on chromosome 16qM A Maw, P E Grundy, L J Millow, et al.
Human Molecular Genetics|December 10, 1999
A frameshift mutation in prominin (mouse)-like 1 causes human retinal degenerationM A Maw, D Corbeil, J Koch, et al.
Pageof 5