Found: 19
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Involvement of Vps33a in the Fusion of Uroplakin-Degrading Multivesicular Bodies with Lysosomes.
- Published in:
- Traffic, 2009, v. 10, n. 9, p. 1350, doi. 10.1111/j.1600-0854.2009.00950.x
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- Article
Murine Leukemia Virus Spreading in Mice Impaired in the Biogenesis of Secretory Lysosomes and Ca<sup>2+</sup>- Regulated Exocytosis.
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- PLoS ONE, 2008, v. 3, n. 7, p. 1, doi. 10.1371/journal.pone.0002713
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- Article
Interaction of Hermansky-Pudlak Syndrome Genes in the Regulation of Lysosome-Related Organelles.
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- Traffic, 2006, v. 7, n. 7, p. 779, doi. 10.1111/j.1600-0854.2006.00431.x
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- Article
Defective Surfactant Secretion in a Mouse Model of Hermansky-Pudlak Syndrome.
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- American Journal of Respiratory Cell & Molecular Biology, 2005, v. 33, n. 1, p. 14, doi. 10.1165/rcmb.2004-0293OC
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- Article
Murine Hermansky-Pudlak syndrome genes: regulators of lysosome-related organelles.
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- BioEssays, 2004, v. 26, n. 6, p. 616, doi. 10.1002/bies.20042
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- Article
Hermansky-Pudlak syndrome type 7 (HPS-7) results from mutant dysbindin, a member of the biogenesis of lysosome-related organelles complex 1 (BLOC-1).
- Published in:
- Nature Genetics, 2003, v. 35, n. 1, p. 84, doi. 10.1038/ng1229
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- Article
Melanosome Morphologies in Murine Models of Hermansky–Pudlak Syndrome Reflect Blocks in Organelle Development.
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- Journal of Investigative Dermatology, 2002, v. 119, n. 5, p. 1156, doi. 10.1046/j.1523-1747.2002.19535.x
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- Article
Cell-specific abnormal prenylation of Rab proteins in platelets and melanocytes of the gunmetal mouse.
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- British Journal of Haematology, 2002, v. 117, n. 2, p. 414, doi. 10.1046/j.1365-2141.2002.03444.x
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- Article
Hermansky-Pudlak syndrome is caused by mutations in HPS4, the human homolog of the mouse light-ear gene.
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- Nature Genetics, 2002, v. 30, n. 3, p. 321, doi. 10.1038/ng835
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- Article
Mutation of a new gene causes a unique form of Hermansky?Pudlak syndrome in a genetic isolate of central Puerto Rico.
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- Nature Genetics, 2001, v. 28, n. 4, p. 376, doi. 10.1038/ng576
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- Article
Survival and Lung Pathology of Mouse Models of Hermansky- Pudlak Syndrome and Chediak-Higashi Syndrome.
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- Proceedings of the Society for Experimental Biology & Medicine, 1999, p. 162, doi. 10.3181/00379727-220-44359
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- Article
The β3A 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 blindness.
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- Human Molecular Genetics, 1999, v. 8, n. 2, p. 323, doi. 10.1093/hmg/8.2.323
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- Article
Mutations in orthologous genes in human spondyloepimetaphyseal dysplasia and the brachymorphic mouse.
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- Nature Genetics, 1998, v. 20, n. 2, p. 157, doi. 10.1038/2458
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- Article
The murine misty mutation: Phenotypic effects of melanocytes, platelets and brown fat.
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- Genetics, 1998, v. 148, n. 1, p. 381, doi. 10.1093/genetics/148.1.381
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- Article
Sandy: a new mouse model for platelet storage pool deficiency.
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- Genetics Research, 1991, v. 58, n. 1, p. 51, doi. 10.1017/S0016672300029608
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- Article
Cocoa: a new mouse model for platelet storage pool deficiency.
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- British Journal of Haematology, 1988, v. 69, n. 3, p. 371, doi. 10.1111/j.1365-2141.1988.tb02376.x
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- Article
Pigmentation and lysosome function in mice homozygous for both pale ear and Beige-J pigment genes.
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- Genetics Research, 1980, v. 35, n. 2, p. 195, doi. 10.1017/S001667230001404X
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- Article
LYSOSOMAL DYSFUNCTIONS ASSOCIATED WITH MUTATIONS AT MOUSE PIGMENT GENES.
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- Genetics, 1979, v. 92, n. 1, p. 189
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- Article
The molecular genetics of mammalian glucuronidase.
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- Journal of Cellular Physiology, 1975, v. 85, p. 379, doi. 10.1002/jcp.1040850406
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- Article