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Journal Abstract Search

291 related items for PubMed ID: 15743322

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  • 2. Histochemical and cellular changes accompanying the appearance of lung fibrosis in an experimental mouse model for Hermansky Pudlak syndrome.
    Wang L, Lyerla T.
    Histochem Cell Biol; 2010 Aug; 134(2):205-13. PubMed ID: 20603711
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  • 4. 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
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  • 6. Interstitial pneumonia in Hermansky-Pudlak syndrome: significance of florid foamy swelling/degeneration (giant lamellar body degeneration) of type-2 pneumocytes.
    Nakatani Y, Nakamura N, Sano J, Inayama Y, Kawano N, Yamanaka S, Miyagi Y, Nagashima Y, Ohbayashi C, Mizushima M, Manabe T, Kuroda M, Yokoi T, Matsubara O.
    Virchows Arch; 2000 Sep; 437(3):304-13. PubMed ID: 11037352
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  • 8. Syndromic albinism: a review of genetics and phenotypes.
    Scheinfeld NS.
    Dermatol Online J; 2003 Dec; 9(5):5. PubMed ID: 14996378
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  • 10. 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 Dec; 74(1-2):217-25. PubMed ID: 11592818
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  • 11. 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
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  • 12. Modeling of lung phenotype of Hermansky-Pudlak syndrome type I using patient-specific iPSCs.
    Suezawa T, Kanagaki S, Korogi Y, Nakao K, Hirai T, Murakami K, Hagiwara M, Gotoh S.
    Respir Res; 2021 Nov 04; 22(1):284. PubMed ID: 34736469
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  • 14. Survival and lung pathology of mouse models of Hermansky-Pudlak syndrome and Chediak-Higashi syndrome.
    McGarry MP, Reddington M, Novak EK, Swank RT.
    Proc Soc Exp Biol Med; 1999 Mar 04; 220(3):162-8. PubMed ID: 10193444
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  • 15. The Chediak-Higashi (beige) mutation in two mouse strains. Allelism and similarity in lysosomal dysfunction.
    Brandt EJ, Swank RT.
    Am J Pathol; 1976 Mar 04; 82(3):573-88. PubMed ID: 1258977
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  • 20. Defective surfactant secretion in a mouse model of Hermansky-Pudlak syndrome.
    Guttentag SH, Akhtar A, Tao JQ, Atochina E, Rusiniak ME, Swank RT, Bates SR.
    Am J Respir Cell Mol Biol; 2005 Jul 04; 33(1):14-21. PubMed ID: 15790974
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