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Items: 1 to 20 of 33

1.

Rab38 and Rab32 control post-Golgi trafficking of melanogenic enzymes.

Wasmeier C, Romao M, Plowright L, Bennett DC, Raposo G, Seabra MC.

J Cell Biol. 2006 Oct 23;175(2):271-81. Epub 2006 Oct 16.

2.

Hermansky-Pudlak syndrome: a disease of protein trafficking and organelle function.

Wei ML.

Pigment Cell Res. 2006 Feb;19(1):19-42. Review.

PMID:
16420244
3.

Murine Hermansky-Pudlak syndrome genes: regulators of lysosome-related organelles.

Li W, Rusiniak ME, Chintala S, Gautam R, Novak EK, Swank RT.

Bioessays. 2004 Jun;26(6):616-28. Review.

PMID:
15170859
4.
5.

EFFECTS OF THE LIGHT MUTATION OF MOUSE COAT COLOR ON EYE PIGMENTATION.

PIERRO LJ.

J Exp Zool. 1963 Jun;153:81-7. No abstract available.

PMID:
14047421
6.

The electroretinogram in albinos and carriers of the ocular albino trait.

KRILL AE, LEE GB.

Arch Ophthalmol. 1963 Jan;69:32-8. No abstract available.

PMID:
14035804
7.

Hermansky-Pudlak syndrome type 7 (HPS-7) results from mutant dysbindin, a member of the biogenesis of lysosome-related organelles complex 1 (BLOC-1).

Li W, Zhang Q, Oiso N, Novak EK, Gautam R, O'Brien EP, Tinsley CL, Blake DJ, Spritz RA, Copeland NG, Jenkins NA, Amato D, Roe BA, Starcevic M, Dell'Angelica EC, Elliott RW, Mishra V, Kingsmore SF, Paylor RE, Swank RT.

Nat Genet. 2003 Sep;35(1):84-9. Epub 2003 Aug 17.

8.

The color loci of mice--a genetic century.

Bennett DC, Lamoreux ML.

Pigment Cell Res. 2003 Aug;16(4):333-44. Review.

PMID:
12859616
9.

Characterization of the human RAB38 and RAB7 genes: exclusion of new major pathological loci for Japanese OCA.

Suzuki T, Miyamura Y, Inagaki K, Tomita Y.

J Dermatol Sci. 2003 Aug;32(2):131-6.

PMID:
12850305
10.

Genetic mapping and characterization of the bleeding disorder in the fawn-hooded hypertensive rat.

Datta YH, Wu FC, Dumas PC, Rangel-Filho A, Datta MW, Ning G, Cooley BC, Majewski RR, Provoost AP, Jacob HJ.

Thromb Haemost. 2003 Jun;89(6):1031-42.

PMID:
12783116
11.

Hermansky-Pudlak syndrome: vesicle formation from yeast to man.

Huizing M, Boissy RE, Gahl WA.

Pigment Cell Res. 2002 Dec;15(6):405-19. Review.

PMID:
12453182
12.

Disorders of vesicles of lysosomal lineage: the Hermansky-Pudlak syndromes.

Huizing M, Gahl WA.

Curr Mol Med. 2002 Aug;2(5):451-67. Review.

PMID:
12125811
13.

Mutation of melanosome protein RAB38 in chocolate mice.

Loftus SK, Larson DM, Baxter LL, Antonellis A, Chen Y, Wu X, Jiang Y, Bittner M, Hammer JA 3rd, Pavan WJ.

Proc Natl Acad Sci U S A. 2002 Apr 2;99(7):4471-6. Epub 2002 Mar 26.

14.

Hermansky-Pudlak syndrome is caused by mutations in HPS4, the human homolog of the mouse light-ear gene.

Suzuki T, Li W, Zhang Q, Karim A, Novak EK, Sviderskaya EV, Hill SP, Bennett DC, Levin AV, Nieuwenhuis HK, Fong CT, Castellan C, Miterski B, Swank RT, Spritz RA.

Nat Genet. 2002 Mar;30(3):321-4. Epub 2002 Feb 11.

PMID:
11836498
15.

Rab GTPases, intracellular traffic and disease.

Seabra MC, Mules EH, Hume AN.

Trends Mol Med. 2002 Jan;8(1):23-30. Review.

PMID:
11796263
16.

Tyrp1 and oculocutaneous albinism type 3.

Sarangarajan R, Boissy RE.

Pigment Cell Res. 2001 Dec;14(6):437-44. Review.

PMID:
11775055
17.

Mutations in genes encoding melanosomal proteins cause pigmentary glaucoma in DBA/2J mice.

Anderson MG, Smith RS, Hawes NL, Zabaleta A, Chang B, Wiggs JL, John SW.

Nat Genet. 2002 Jan;30(1):81-5. Epub 2001 Dec 17.

PMID:
11743578
18.

Mutations in the human orthologue of the mouse underwhite gene (uw) underlie a new form of oculocutaneous albinism, OCA4.

Newton JM, Cohen-Barak O, Hagiwara N, Gardner JM, Davisson MT, King RA, Brilliant MH.

Am J Hum Genet. 2001 Nov;69(5):981-8. Epub 2001 Sep 26.

19.
20.

Rab proteins as membrane organizers.

Zerial M, McBride H.

Nat Rev Mol Cell Biol. 2001 Feb;2(2):107-17. Review. Erratum in: Nat Rev Mol Cell Biol 2001 Mar;2(3):216.

PMID:
11252952

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