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Results: 1 to 20 of 87

Similar articles for PubMed (Select 9697856)

1.

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

Kantheti P, Qiao X, Diaz ME, Peden AA, Meyer GE, Carskadon SL, Kapfhamer D, Sufalko D, Robinson MS, Noebels JL, Burmeister M.

Neuron. 1998 Jul;21(1):111-22.

2.

Genetic and phenotypic analysis of the mouse mutant mh2J, an Ap3d allele caused by IAP element insertion.

Kantheti P, Diaz ME, Peden AE, Seong EE, Dolan DF, Robinson MS, Noebels JL, Burmeister ML.

Mamm Genome. 2003 Mar;14(3):157-67.

PMID:
12647238
3.
4.

Abnormal expression and subcellular distribution of subunit proteins of the AP-3 adaptor complex lead to platelet storage pool deficiency in the pearl mouse.

Zhen L, Jiang S, Feng L, Bright NA, Peden AA, Seymour AB, Novak EK, Elliott R, Gorin MB, Robinson MS, Swank RT.

Blood. 1999 Jul 1;94(1):146-55.

5.

SLC35D3 delivery from megakaryocyte early endosomes is required for platelet dense granule biogenesis and is differentially defective in Hermansky-Pudlak syndrome models.

Meng R, Wang Y, Yao Y, Zhang Z, Harper DC, Heijnen HF, Sitaram A, Li W, Raposo G, Weiss MJ, Poncz M, Marks MS.

Blood. 2012 Jul 12;120(2):404-14. doi: 10.1182/blood-2011-11-389551. Epub 2012 May 18.

7.

Cell-specific abnormal prenylation of Rab proteins in platelets and melanocytes of the gunmetal mouse.

Zhang Q, Zhen L, Li W, Novak EK, Collinson LM, Jang EK, Haslam RJ, Elliott RW, Swank RT.

Br J Haematol. 2002 May;117(2):414-23.

PMID:
11972527
8.
9.

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.

Feng L, Seymour AB, Jiang S, To A, Peden AA, Novak EK, Zhen L, Rusiniak ME, Eicher EM, Robinson MS, Gorin MB, Swank RT.

Hum Mol Genet. 1999 Feb;8(2):323-30.

10.

Roles of BLOC-1 and adaptor protein-3 complexes in cargo sorting to synaptic vesicles.

Newell-Litwa K, Salazar G, Smith Y, Faundez V.

Mol Biol Cell. 2009 Mar;20(5):1441-53. doi: 10.1091/mbc.E08-05-0456. Epub 2009 Jan 14.

11.

Sandy: a new mouse model for platelet storage pool deficiency.

Swank RT, Sweet HO, Davisson MT, Reddington M, Novak EK.

Genet Res. 1991 Aug;58(1):51-62.

PMID:
1936982
12.

AP-3 adaptor functions in targeting P-selectin to secretory granules in endothelial cells.

Daugherty BL, Straley KS, Sanders JM, Phillips JW, Disdier M, McEver RP, Green SA.

Traffic. 2001 Jun;2(6):406-13.

PMID:
11389768
13.

rim2 (recombination-induced mutation 2) is a new allele of pearl and a mouse model of human Hermansky-Pudlak syndrome (HPS): genetic and physical mapping.

Sagai T, Koide T, Endo M, Tanoue K, Kikkawa Y, Yonekawa H, Ishiguro S, Tamai M, Matsuda Y, Wakana S, Shiroishi T.

Mamm Genome. 1998 Jan;9(1):2-7. Erratum in: Mamm Genome 1998 Apr;9(4):344.

PMID:
9434937
14.
15.
16.

Cocoa: a new mouse model for platelet storage pool deficiency.

Novak EK, Sweet HO, Prochazka M, Parentis M, Soble R, Reddington M, Cairo A, Swank RT.

Br J Haematol. 1988 Jul;69(3):371-8.

PMID:
3408670
17.

The regulation of platelet-dense granules by Rab27a in the ashen mouse, a model of Hermansky-Pudlak and Griscelli syndromes, is granule-specific and dependent on genetic background.

Novak EK, Gautam R, Reddington M, Collinson LM, Copeland NG, Jenkins NA, McGarry MP, Swank RT.

Blood. 2002 Jul 1;100(1):128-35.

18.

Sorting and targeting of melanosomal membrane proteins: signals, pathways, and mechanisms.

Setaluri V.

Pigment Cell Res. 2000 Jun;13(3):128-34. Review.

PMID:
10885669
19.
20.

Defective pigment granule biogenesis and aberrant behavior caused by mutations in the Drosophila AP-3beta adaptin gene ruby.

Kretzschmar D, Poeck B, Roth H, Ernst R, Keller A, Porsch M, Strauss R, Pflugfelder GO.

Genetics. 2000 May;155(1):213-23.

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