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E K Novak

Showing results (41-50 of 48) with videos related to

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Genome Research|June 1, 1996
An integrated genetic map of the pearl locus of mouse chromosome 13A B Seymour, B L Yanak, E P O'Brien, et al.
Genomics|November 15, 2001
The gene mutated in cocoa mice, carrying a defect of organelle biogenesis, is a homologue of the human Hermansky-Pudlak syndrome-3 geneT Suzuki, W Li, Q Zhang, et al.
Blood|June 1, 1994
von Willebrand disease in the RIIIS/J mouse is caused by a defect outside of the von Willebrand factor geneW C Nichols, K A Cooney, K L Mohlke, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 22, 2000
A mutation in Rab27a causes the vesicle transport defects observed in ashen miceS M Wilson, R Yip, D A Swing, 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.
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.
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 5

Showing results (41-50 of 48) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 48 results.
Genome Research|June 1, 1996
An integrated genetic map of the pearl locus of mouse chromosome 13A B Seymour, B L Yanak, E P O'Brien, et al.
Genomics|November 15, 2001
The gene mutated in cocoa mice, carrying a defect of organelle biogenesis, is a homologue of the human Hermansky-Pudlak syndrome-3 geneT Suzuki, W Li, Q Zhang, et al.
Blood|June 1, 1994
von Willebrand disease in the RIIIS/J mouse is caused by a defect outside of the von Willebrand factor geneW C Nichols, K A Cooney, K L Mohlke, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 22, 2000
A mutation in Rab27a causes the vesicle transport defects observed in ashen miceS M Wilson, R Yip, D A Swing, 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.
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.
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 5