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Showing results (91-100 of 98) with videos related to

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Genomics|September 15, 1994
Kidney and retinal defects (Krd), a transgene-induced mutation with a deletion of mouse chromosome 19 that includes the Pax2 locusS A Keller, J M Jones, A Boyle, et al.
Blood|June 25, 1999
Abnormal expression and subcellular distribution of subunit proteins of the AP-3 adaptor complex lead to platelet storage pool deficiency in the pearl mouseL Zhen, S Jiang, L Feng, et al.
Nature Genetics|July 17, 2001
Mutation of a new gene causes a unique form of Hermansky-Pudlak syndrome in a genetic isolate of central Puerto RicoY Anikster, M Huizing, J White, et al.
Human Molecular Genetics|February 5, 1999
The beta3A subunit gene (Ap3b1) of the AP-3 adaptor complex is altered in the mouse hypopigmentation mutant pearl, a model for Hermansky-Pudlak syndrome and night blindnessL Feng, A B Seymour, S Jiang, et al.
Nature Genetics|October 15, 1998
Mutations in orthologous genes in human spondyloepimetaphyseal dysplasia and the brachymorphic mouseM Faiyaz ul Haque, L M King, D Krakow, et al.
Blood|December 9, 2000
Defects in the cappuccino (cno) gene on mouse chromosome 5 and human 4p cause Hermansky-Pudlak syndrome by an AP-3-independent mechanismB Gwynn, S L Ciciotte, S J Hunter, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 29, 2000
Rab geranylgeranyl transferase alpha mutation in the gunmetal mouse reduces Rab prenylation and platelet synthesisJ C Detter, Q Zhang, E H Mules, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 19, 1997
The mouse pale ear (ep) mutation is the homologue of human Hermansky-Pudlak syndromeJ M Gardner, S C Wildenberg, N M Keiper, et al.
Pageof 10

Showing results (91-100 of 98) with videos related to

Sort By:
Pageof 10
You have reached the last page of results.This site can display upto 98 results.
Genomics|September 15, 1994
Kidney and retinal defects (Krd), a transgene-induced mutation with a deletion of mouse chromosome 19 that includes the Pax2 locusS A Keller, J M Jones, A Boyle, et al.
Blood|June 25, 1999
Abnormal expression and subcellular distribution of subunit proteins of the AP-3 adaptor complex lead to platelet storage pool deficiency in the pearl mouseL Zhen, S Jiang, L Feng, et al.
Nature Genetics|July 17, 2001
Mutation of a new gene causes a unique form of Hermansky-Pudlak syndrome in a genetic isolate of central Puerto RicoY Anikster, M Huizing, J White, et al.
Human Molecular Genetics|February 5, 1999
The beta3A subunit gene (Ap3b1) of the AP-3 adaptor complex is altered in the mouse hypopigmentation mutant pearl, a model for Hermansky-Pudlak syndrome and night blindnessL Feng, A B Seymour, S Jiang, et al.
Nature Genetics|October 15, 1998
Mutations in orthologous genes in human spondyloepimetaphyseal dysplasia and the brachymorphic mouseM Faiyaz ul Haque, L M King, D Krakow, et al.
Blood|December 9, 2000
Defects in the cappuccino (cno) gene on mouse chromosome 5 and human 4p cause Hermansky-Pudlak syndrome by an AP-3-independent mechanismB Gwynn, S L Ciciotte, S J Hunter, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 29, 2000
Rab geranylgeranyl transferase alpha mutation in the gunmetal mouse reduces Rab prenylation and platelet synthesisJ C Detter, Q Zhang, E H Mules, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 19, 1997
The mouse pale ear (ep) mutation is the homologue of human Hermansky-Pudlak syndromeJ M Gardner, S C Wildenberg, N M Keiper, et al.
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