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J Keats

Showing results (81-90 of 149) with videos related to

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Genomics|November 1, 1992
Linkage studies of Usher syndrome type 1: exclusion results from the Usher syndrome consortiumB J Keats, A A Todorov, L D Atwood, et al.
American Journal of Medical Genetics|March 1, 1994
Clinical diagnosis of the Usher syndromes. Usher Syndrome ConsortiumR J Smith, C I Berlin, J F Hejtmancik, et al.
Nature Genetics|September 6, 2000
A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1CE Verpy, M Leibovici, I Zwaenepoel, et al.
American Journal of Human Genetics|October 1, 1987
Linkage studies of Friedreich ataxia by means of blood-group and protein markersB J Keats, L J Ward, M Lu, et al.
Genomics|December 1, 1992
Localization of two genes for Usher syndrome type I to chromosome 11R J Smith, E C Lee, W J Kimberling, et al.
Genomics|March 1, 1991
Guidelines for human linkage maps: an international system for human linkage maps (ISLM, 1990)B J Keats, S L Sherman, N E Morton, et al.
Annals of Human Genetics|January 1, 1991
Guidelines for human linkage maps. An International System for Human Linkage Maps (ISLM, 1990)B J Keats, S L Sherman, N E Morton, et al.
Nature Genetics|June 1, 1994
A gene for Crouzon craniofacial dysostosis maps to the long arm of chromosome 10R A Preston, J C Post, B J Keats, et al.
Leukemia|February 13, 2014
Promiscuous MYC locus rearrangements hijack enhancers but mostly super-enhancers to dysregulate MYC expression in multiple myelomaMaurizio Affer, Marta Chesi, Wei-Dong G Chen, et al.
Blood|February 4, 2011
RNAi screen of the druggable genome identifies modulators of proteasome inhibitor sensitivity in myeloma including CDK5Yuan Xiao Zhu, Rodger Tiedemann, Chang-Xin Shi, et al.
Pageof 15

Showing results (81-90 of 149) with videos related to

Sort By:
Pageof 15
Genomics|November 1, 1992
Linkage studies of Usher syndrome type 1: exclusion results from the Usher syndrome consortiumB J Keats, A A Todorov, L D Atwood, et al.
American Journal of Medical Genetics|March 1, 1994
Clinical diagnosis of the Usher syndromes. Usher Syndrome ConsortiumR J Smith, C I Berlin, J F Hejtmancik, et al.
Nature Genetics|September 6, 2000
A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1CE Verpy, M Leibovici, I Zwaenepoel, et al.
American Journal of Human Genetics|October 1, 1987
Linkage studies of Friedreich ataxia by means of blood-group and protein markersB J Keats, L J Ward, M Lu, et al.
Genomics|December 1, 1992
Localization of two genes for Usher syndrome type I to chromosome 11R J Smith, E C Lee, W J Kimberling, et al.
Genomics|March 1, 1991
Guidelines for human linkage maps: an international system for human linkage maps (ISLM, 1990)B J Keats, S L Sherman, N E Morton, et al.
Annals of Human Genetics|January 1, 1991
Guidelines for human linkage maps. An International System for Human Linkage Maps (ISLM, 1990)B J Keats, S L Sherman, N E Morton, et al.
Nature Genetics|June 1, 1994
A gene for Crouzon craniofacial dysostosis maps to the long arm of chromosome 10R A Preston, J C Post, B J Keats, et al.
Leukemia|February 13, 2014
Promiscuous MYC locus rearrangements hijack enhancers but mostly super-enhancers to dysregulate MYC expression in multiple myelomaMaurizio Affer, Marta Chesi, Wei-Dong G Chen, et al.
Blood|February 4, 2011
RNAi screen of the druggable genome identifies modulators of proteasome inhibitor sensitivity in myeloma including CDK5Yuan Xiao Zhu, Rodger Tiedemann, Chang-Xin Shi, et al.
Pageof 15