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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

162 related articles for article (PubMed ID: 25160823)

  • 1. The Ap3b1 gene regulates the ocular melanosome biogenesis and tyrosinase distribution differently from the Hps1 gene.
    Jing R; Dong X; Li K; Yan J; Chen X; Feng L
    Exp Eye Res; 2014 Nov; 128():57-66. PubMed ID: 25160823
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Two distinct phenotypes in pigmented cells of different embryonic origins in eyes of pale ear mice.
    Jing R; Dong X; Li K; Zhang J; Yan J; Feng L
    Exp Eye Res; 2014 Feb; 119():35-43. PubMed ID: 24361037
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Hermansky-Pudlak HPS1/pale ear gene regulates epidermal and dermal melanocyte development.
    Nguyen T; Wei ML
    J Invest Dermatol; 2007 Feb; 127(2):421-8. PubMed ID: 17068483
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Different functions of biogenesis of lysosomal organelles complex 3 subunit 1 (Hps1) and adaptor-related protein complex 3, beta 1 subunit (Ap3b1) genes on spermatogenesis and male fertility.
    Jing R; Zhang H; Kong Y; Li K; Dong X; Yan J; Han J; Feng L
    Reprod Fertil Dev; 2019 Apr; 31(5):972-982. PubMed ID: 30786955
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The Hermansky-Pudlak syndrome 1 (HPS1) and HPS2 genes independently contribute to the production and function of platelet dense granules, melanosomes, and lysosomes.
    Feng L; Novak EK; Hartnell LM; Bonifacino JS; Collinson LM; Swank RT
    Blood; 2002 Mar; 99(5):1651-8. PubMed ID: 11861280
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Melanocytes derived from patients with Hermansky-Pudlak Syndrome types 1, 2, and 3 have distinct defects in cargo trafficking.
    Richmond B; Huizing M; Knapp J; Koshoffer A; Zhao Y; Gahl WA; Boissy RE
    J Invest Dermatol; 2005 Feb; 124(2):420-7. PubMed ID: 15675963
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Reduced pigmentation (rp), a mouse model of Hermansky-Pudlak syndrome, encodes a novel component of the BLOC-1 complex.
    Gwynn B; Martina JA; Bonifacino JS; Sviderskaya EV; Lamoreux ML; Bennett DC; Moriyama K; Huizing M; Helip-Wooley A; Gahl WA; Webb LS; Lambert AJ; Peters LL
    Blood; 2004 Nov; 104(10):3181-9. PubMed ID: 15265785
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Abnormal translocation of tyrosinase and tyrosinase-related protein 1 in cutaneous melanocytes of Hermansky-Pudlak Syndrome and in melanoma cells transfected with anti-sense HPS1 cDNA.
    Sarangarajan R; Budev A; Zhao Y; Gahl WA; Boissy RE
    J Invest Dermatol; 2001 Sep; 117(3):641-6. PubMed ID: 11564171
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Hermansky-Pudlak syndrome: models for intracellular vesicle formation.
    Shotelersuk V; Gahl WA
    Mol Genet Metab; 1998 Oct; 65(2):85-96. PubMed ID: 9787100
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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. PubMed ID: 11836498
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Analysis of ocular hypopigmentation in Rab38cht/cht mice.
    Brooks BP; Larson DM; Chan CC; Kjellstrom S; Smith RS; Crawford MA; Lamoreux L; Huizing M; Hess R; Jiao X; Hejtmancik JF; Maminishkis A; John SW; Bush R; Pavan WJ
    Invest Ophthalmol Vis Sci; 2007 Sep; 48(9):3905-13. PubMed ID: 17724166
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The Mutation of the Ap3b1 Gene Causes Uterine Hypoplasia in Pearl Mice.
    Jing R; Kong Y; Han G; Zhang J; Li K; Dong X; Yan J; Zhang H; Han J; Feng L
    Reprod Sci; 2020 Jan; 27(1):182-191. PubMed ID: 32016796
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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. PubMed ID: 9931340
    [TBL] [Abstract][Full Text] [Related]  

  • 15. NGS-based 100-gene panel of hypopigmentation identifies mutations in Chinese Hermansky-Pudlak syndrome patients.
    Wei A; Yuan Y; Bai D; Ma J; Hao Z; Zhang Y; Yu J; Zhou Z; Yang L; Yang X; Li L; Li W
    Pigment Cell Melanoma Res; 2016 Nov; 29(6):702-706. PubMed ID: 27593200
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Characterization of melanosomes in murine Hermansky-Pudlak syndrome: mechanisms of hypopigmentation.
    Nguyen T; Wei ML
    J Invest Dermatol; 2004 Feb; 122(2):452-60. PubMed ID: 15009730
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Aberrant lung structure, composition, and function in a murine model of Hermansky-Pudlak syndrome.
    Lyerla TA; Rusiniak ME; Borchers M; Jahreis G; Tan J; Ohtake P; Novak EK; Swank RT
    Am J Physiol Lung Cell Mol Physiol; 2003 Sep; 285(3):L643-53. PubMed ID: 12777251
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Tyrosinase processing and intracellular trafficking is disrupted in mouse primary melanocytes carrying the underwhite (uw) mutation. A model for oculocutaneous albinism (OCA) type 4.
    Costin GE; Valencia JC; Vieira WD; Lamoreux ML; Hearing VJ
    J Cell Sci; 2003 Aug; 116(Pt 15):3203-12. PubMed ID: 12829739
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Characterization of the murine gene corresponding to human Hermansky-Pudlak syndrome type 3: exclusion of the Subtle gray (sut) locus.
    Huizing M; Anikster Y; White JG; Gahl WA
    Mol Genet Metab; 2001; 74(1-2):217-25. PubMed ID: 11592818
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Ru2 and Ru encode mouse orthologs of the genes mutated in human Hermansky-Pudlak syndrome types 5 and 6.
    Zhang Q; Zhao B; Li W; Oiso N; Novak EK; Rusiniak ME; Gautam R; Chintala S; O'Brien EP; Zhang Y; Roe BA; Elliott RW; Eicher EM; Liang P; Kratz C; Legius E; Spritz RA; O'Sullivan TN; Copeland NG; Jenkins NA; Swank RT
    Nat Genet; 2003 Feb; 33(2):145-53. PubMed ID: 12548288
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.