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| - artículu científicu espublizáu en 2001 (ast)
- vědecký článek publikovaný v roce 2001 (cs)
- 2001 թվականի նոյեմբերին հրատարակված գիտական հոդված (hy)
- наукова стаття, опублікована в листопаді 2001 (uk)
- 2001 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած (hyw)
- مقالة علمية (نشرت في نوفمبر 2001) (ar)
- vedecký článok (publikovaný 2001/11/01) (sk)
- wetenschappelijk artikel (gepubliceerd op 2001/11/01) (nl)
- im November 2001 veröffentlichter wissenschaftlicher Artikel (de)
- scientific journal article (en)
- article scientifique publié en novembre 2001 (fr)
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| - W. Li
- B. A. Roe
- T. Suzuki
- Q. Zhang
- A. Wilson
- E. K. Novak
- R. T. Swank
- D. C. Bennett
- E. V. Sviderskaya
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| rdfs:label
| - The gene mutated in cocoa mice, carrying a defect of organelle biogenesis, is a homologue of the human Hermansky-Pudlak syndrome-3 gene (en)
- The gene mutated in cocoa mice, carrying a defect of organelle biogenesis, is a homologue of the human Hermansky-Pudlak syndrome-3 gene (nl)
- The gene mutated in cocoa mice, carrying a defect of organelle biogenesis, is a homologue of the human Hermansky-Pudlak syndrome-3 gene (ast)
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| skos:prefLabel
| - The gene mutated in cocoa mice, carrying a defect of organelle biogenesis, is a homologue of the human Hermansky-Pudlak syndrome-3 gene (en)
- The gene mutated in cocoa mice, carrying a defect of organelle biogenesis, is a homologue of the human Hermansky-Pudlak syndrome-3 gene (nl)
- The gene mutated in cocoa mice, carrying a defect of organelle biogenesis, is a homologue of the human Hermansky-Pudlak syndrome-3 gene (ast)
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| name
| - The gene mutated in cocoa mice, carrying a defect of organelle biogenesis, is a homologue of the human Hermansky-Pudlak syndrome-3 gene (en)
- The gene mutated in cocoa mice, carrying a defect of organelle biogenesis, is a homologue of the human Hermansky-Pudlak syndrome-3 gene (nl)
- The gene mutated in cocoa mice, carrying a defect of organelle biogenesis, is a homologue of the human Hermansky-Pudlak syndrome-3 gene (ast)
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| title
| - The gene mutated in cocoa mice, carrying a defect of organelle biogenesis, is a homologue of the human Hermansky-Pudlak syndrome-3 gene (en)
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of | - Association of the Hermansky-Pudlak syndrome type-3 protein with clathrin
- BLOC-1 is required for cargo-specific sorting from vacuolar early endosomes toward lysosome-related organelles
- Hermansky-Pudlak syndrome: a disease of protein trafficking and organelle function
- Human and mouse disorders of pigmentation
- The Hermansky-Pudlak syndrome 3 (cocoa) protein is a component of the biogenesis of lysosome-related organelles complex-2 (BLOC-2).
- BLOC-1, a novel complex containing the pallidin and muted proteins involved in the biogenesis of melanosomes and platelet-dense granules
- Pallidin is a component of a multi-protein complex involved in the biogenesis of lysosome-related organelles
- The gene for the muted (mu) mouse, a model for Hermansky-Pudlak syndrome, defines a novel protein which regulates vesicle trafficking
- Hermansky-Pudlak syndrome type 7 (HPS-7) results from mutant dysbindin, a member of the biogenesis of lysosome-related organelles complex 1 (BLOC-1)
- The dark side of lysosome-related organelles: specialization of the endocytic pathway for melanosome biogenesis
- Slc7a11 gene controls production of pheomelanin pigment and proliferation of cultured cells
- The Slc35d3 gene, encoding an orphan nucleotide sugar transporter, regulates platelet-dense granules
- BLOC-3, a protein complex containing the Hermansky-Pudlak syndrome gene products HPS1 and HPS4
- The Hermansky-Pudlak syndrome 1 (HPS1) and HPS4 proteins are components of two complexes, BLOC-3 and BLOC-4, involved in the biogenesis of lysosome-related organelles
- The mouse organellar biogenesis mutant buff results from a mutation in Vps33a, a homologue of yeast vps33 and Drosophila carnation
- Hermansky-Pudlak syndrome is caused by mutations in HPS4, the human homolog of the mouse light-ear gene
- Ru2 and Ru encode mouse orthologs of the genes mutated in human Hermansky-Pudlak syndrome types 5 and 6
- The color loci of mice--a genetic century
- The construction of transgenic and gene knockout/knockin mouse models of human disease
- Genetic determinants of hair and eye colours in the Scottish and Danish populations.
- Aberrant lung structure, composition, and function in a murine model of Hermansky-Pudlak syndrome
- Development of platelet secretory granules
- Hermansky-Pudlak syndrome: vesicle formation from yeast to man.
- Melanocytes derived from patients with Hermansky-Pudlak Syndrome types 1, 2, and 3 have distinct defects in cargo trafficking
- Genetic interstitial lung disease
- BLOC-2 targets recycling endosomal tubules to melanosomes for cargo delivery
- The molecular machinery for the biogenesis of lysosome-related organelles: lessons from Hermansky-Pudlak syndrome
- Melanocyte-specific proteins are aberrantly trafficked in melanocytes of Hermansky-Pudlak syndrome-type 3
- Melanoregulin, product of the dsu locus, links the BLOC-pathway and OA1 in organelle biogenesis
- Platelet dense-granule secretion plays a critical role in thrombosis and subsequent vascular remodeling in atherosclerotic mice.
- Hermansky-Pudlak syndrome: Report of two patients with updated genetic classification and management recommendations.
- Hermansky-Pudlak syndrome type 4 in a patient from Sri Lanka with pulmonary fibrosis.
- A strategy to study tyrosinase transgenes in mouse melanocytes.
- Mouse germ line mutations due to retrotransposon insertions
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