These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
249 related articles for article (PubMed ID: 9158155)
21. Identification of a novel transcript produced by the gene responsible for the Hermansky-Pudlak syndrome in Puerto Rico. Wildenberg SC; Fryer JP; Gardner JM; Oetting WS; Brilliant MH; King RA J Invest Dermatol; 1998 May; 110(5):777-81. PubMed ID: 9579545 [TBL] [Abstract][Full Text] [Related]
22. 5'-UTR structural organization, transcript expression, and mutational analysis of the human Rab geranylgeranyl transferase alpha-subunit (RABGGTA) gene. Li W; Detter JC; Weiss HJ; Cramer EM; Zhang Q; Novak EK; Favier R; Kingsmore SF; Swank RT Mol Genet Metab; 2000 Dec; 71(4):599-608. PubMed ID: 11136552 [TBL] [Abstract][Full Text] [Related]
23. Hermansky-Pudlak syndrome type 3 in Ashkenazi Jews and other non-Puerto Rican patients with hypopigmentation and platelet storage-pool deficiency. Huizing M; Anikster Y; Fitzpatrick DL; Jeong AB; D'Souza M; Rausche M; Toro JR; Kaiser-Kupfer MI; White JG; Gahl WA Am J Hum Genet; 2001 Nov; 69(5):1022-32. PubMed ID: 11590544 [TBL] [Abstract][Full Text] [Related]
24. Analyses of proteins involved in vesicular trafficking in platelets of mouse models of Hermansky Pudlak syndrome. Richards-Smith B; Novak EK; Jang EK; He P; Haslam RJ; Castle D; Whiteheart SW; Swank RT Mol Genet Metab; 1999 Sep; 68(1):14-23. PubMed ID: 10479478 [TBL] [Abstract][Full Text] [Related]
26. Molecular genetics of the Hermansky-Pudlak and Chediak-Higashi syndromes. Spritz RA Platelets; 1998; 9(1):21-9. PubMed ID: 16793741 [TBL] [Abstract][Full Text] [Related]
27. The mouse organellar biogenesis mutant buff results from a mutation in Vps33a, a homologue of yeast vps33 and Drosophila carnation. Suzuki T; Oiso N; Gautam R; Novak EK; Panthier JJ; Suprabha PG; Vida T; Swank RT; Spritz RA Proc Natl Acad Sci U S A; 2003 Feb; 100(3):1146-50. PubMed ID: 12538872 [TBL] [Abstract][Full Text] [Related]
28. A new genetic isolate with a unique phenotype of syndromic oculocutaneous albinism: clinical, molecular, and cellular characteristics. Schreyer-Shafir N; Huizing M; Anikster Y; Nusinker Z; Bejarano-Achache I; Maftzir G; Resnik L; Helip-Wooley A; Westbroek W; Gradstein L; Rosenmann A; Blumenfeld A Hum Mutat; 2006 Nov; 27(11):1158. PubMed ID: 17041891 [TBL] [Abstract][Full Text] [Related]
29. A gene causing Hermansky-Pudlak syndrome in a Puerto Rican population maps to chromosome 10q2. Wildenberg SC; Oetting WS; Almodóvar C; Krumwiede M; White JG; King RA Am J Hum Genet; 1995 Oct; 57(4):755-65. PubMed ID: 7573033 [TBL] [Abstract][Full Text] [Related]
30. Mutational data integration in gene-oriented files of the Hermansky-Pudlak Syndrome database. Li W; He M; Zhou H; Bourne JW; Liang P Hum Mutat; 2006 May; 27(5):402-7. PubMed ID: 16550546 [TBL] [Abstract][Full Text] [Related]
31. Hermansky-Pudlak syndrome type 4 (HPS-4): clinical and molecular characteristics. Anderson PD; Huizing M; Claassen DA; White J; Gahl WA Hum Genet; 2003 Jul; 113(1):10-7. PubMed ID: 12664304 [TBL] [Abstract][Full Text] [Related]
32. 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. PubMed ID: 12923531 [TBL] [Abstract][Full Text] [Related]
33. Hermansky-Pudlak syndrome and Chediak-Higashi syndrome: disorders of vesicle formation and trafficking. Huizing M; Anikster Y; Gahl WA Thromb Haemost; 2001 Jul; 86(1):233-45. PubMed ID: 11487012 [TBL] [Abstract][Full Text] [Related]
34. Lung pathology of pale ear mouse (model of Hermansky-Pudlak syndrome 1) and beige mouse (model of Chediak-Higashi syndrome): severity of giant lamellar body degeneration of type II pneumocytes correlates with interstitial inflammation. Tang X; Yamanaka S; Miyagi Y; Nagashima Y; Nakatani Y Pathol Int; 2005 Mar; 55(3):137-43. PubMed ID: 15743322 [TBL] [Abstract][Full Text] [Related]
35. The Hermansky-Pudlak syndrome (HPS) protein is part of a high molecular weight complex involved in biogenesis of early melanosomes. Oh J; Liu ZX; Feng GH; Raposo G; Spritz RA Hum Mol Genet; 2000 Feb; 9(3):375-85. PubMed ID: 10655547 [TBL] [Abstract][Full Text] [Related]
37. The gene for lysosomal protein CD63 is normal in patients with Hermansky-Pudlak syndrome. Armstrong LW; Rom WN; Martiniuk FT Lung; 1998; 176(4):249-56. PubMed ID: 9617741 [TBL] [Abstract][Full Text] [Related]
38. 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. PubMed ID: 9434937 [TBL] [Abstract][Full Text] [Related]
39. Genomic structure of the mouse Ap3b1 gene in normal and pearl mice. Feng L; Rigatti BW; Novak EK; Gorin MB; Swank RT Genomics; 2000 Nov; 69(3):370-9. PubMed ID: 11056055 [TBL] [Abstract][Full Text] [Related]
40. Hermansky-Pudlak syndrome type 1: gene organization, novel mutations, and clinical-molecular review of non-Puerto Rican cases. Hermos CR; Huizing M; Kaiser-Kupfer MI; Gahl WA Hum Mutat; 2002 Dec; 20(6):482. PubMed ID: 12442288 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]