(Q55951827)

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The pallid gene encodes a novel, syntaxin 13-interacting protein involved in platelet storage pool deficiency

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scholarly article

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The pallid gene encodes a novel, syntaxin 13-interacting protein involved in platelet storage pool deficiency (English)

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platelet storage pool deficiency

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author name string

Liping Huang

1

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Yien-Ming Kuo

2

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Jane Gitschier

3

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language of work or name

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publication date

November 1999

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Nature Genetics

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23

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329-332

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3

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https://scigraph.springernature.com/pub.10.1038/15507

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A NEW MUTATION IN THE HOUSE MOUSE (MUS MUSCULUS)

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https://api.crossref.org/works/10.1038%2F15507

7 January 2021

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Ultrastructure of developing melanosomes in C57 Black and pallid mice

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https://api.crossref.org/works/10.1038%2F15507

7 January 2021

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Seven novel mammalian SNARE proteins localize to distinct membrane compartments

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https://api.crossref.org/works/10.1038%2F15507

7 January 2021

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Syntaxin 13 mediates cycling of plasma membrane proteins via tubulovesicular recycling endosomes

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https://api.crossref.org/works/10.1038%2F15507

7 January 2021

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Mutation in AP-3 delta in the mocha mouse links endosomal transport to storage deficiency in platelets, melanosomes, and synaptic vesicles

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https://api.crossref.org/works/10.1038%2F15507

7 January 2021

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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 blindness

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https://api.crossref.org/works/10.1038%2F15507

7 January 2021

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The murine pallid mutation is a platelet storage pool disease associated with the protein 4.2 (pallidin) gene

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https://api.crossref.org/works/10.1038%2F15507

7 January 2021

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Location of the mouse ? 2-microglobulin gene B2m determined by linkage analysis

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https://api.crossref.org/works/10.1038%2F15507

7 January 2021

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The gene encoding protein 4.2 is distinct from the mouse platelet storage pool deficiency mutation pallid

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https://api.crossref.org/works/10.1038%2F15507

7 January 2021

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A genetic linkage map of mouse chromosome 2 extending from thrombospondin to paired box gene 1, including the H3 minor histocompatibility complex

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https://api.crossref.org/works/10.1038%2F15507

7 January 2021

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The skipping of constitutive exons in vivo induced by nonsense mutations

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https://api.crossref.org/works/10.1038%2F15507

7 January 2021

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Association of the AP-3 adaptor complex with clathrin

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https://api.crossref.org/works/10.1038%2F15507

7 January 2021

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Altered expression of a novel adaptin leads to defective pigment granule biogenesis in the Drosophila eye color mutant garnet

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https://api.crossref.org/works/10.1038%2F15507

7 January 2021

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Characterization of the adaptor-related protein complex, AP-3

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https://api.crossref.org/works/10.1038%2F15507

7 January 2021

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AP-3: an adaptor-like protein complex with ubiquitous expression

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https://api.crossref.org/works/10.1038%2F15507

7 January 2021

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Identification of the homologous beige and Chediak-Higashi syndrome genes

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https://api.crossref.org/works/10.1038%2F15507

7 January 2021

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Identification and mutation analysis of the complete gene for Chediak-Higashi syndrome

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https://api.crossref.org/works/10.1038%2F15507

7 January 2021

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Mouse pale ear (ep) is homologous to human Hermansky-Pudlak syndrome and contains a rare 'AT-AC' intron.

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https://api.crossref.org/works/10.1038%2F15507

7 January 2021

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The mouse pale ear (ep) mutation is the homologue of human Hermansky-Pudlak syndrome

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https://api.crossref.org/works/10.1038%2F15507

7 January 2021

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Mutation analysis of patients with Hermansky-Pudlak syndrome: a frameshift hot spot in the HPS gene and apparent locus heterogeneity

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https://api.crossref.org/works/10.1038%2F15507

7 January 2021

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A novel gene involved in zinc transport is deficient in the lethal milk mouse

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https://api.crossref.org/works/10.1038%2F15507

7 January 2021

based on heuristic

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