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Journal Abstract Search

153 related items for PubMed ID: 15794757

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  • 3. Intracellular retention and degradation of tissue-nonspecific alkaline phosphatase with a Gly317-->Asp substitution associated with lethal hypophosphatasia.
    Fukushi M, Amizuka N, Hoshi K, Ozawa H, Kumagai H, Omura S, Misumi Y, Ikehara Y, Oda K.
    Biochem Biophys Res Commun; 1998 May 29; 246(3):613-8. PubMed ID: 9618260
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  • 4. Molecular basis of perinatal hypophosphatasia with tissue-nonspecific alkaline phosphatase bearing a conservative replacement of valine by alanine at position 406. Structural importance of the crown domain.
    Numa N, Ishida Y, Nasu M, Sohda M, Misumi Y, Noda T, Oda K.
    FEBS J; 2008 Jun 29; 275(11):2727-37. PubMed ID: 18422967
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  • 6. Characterization of the mutant (A115V) tissue-nonspecific alkaline phosphatase gene from adult-type hypophosphatasia.
    Watanabe H, Takinami H, Goseki-Sone M, Orimo H, Hamatani R, Ishikawa I.
    Biochem Biophys Res Commun; 2005 Feb 04; 327(1):124-9. PubMed ID: 15629439
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  • 8. Functional analysis of the single nucleotide polymorphism (787T>C) in the tissue-nonspecific alkaline phosphatase gene associated with BMD.
    Goseki-Sone M, Sogabe N, Fukushi-Irie M, Mizoi L, Orimo H, Suzuki T, Nakamura H, Orimo H, Hosoi T.
    J Bone Miner Res; 2005 May 04; 20(5):773-82. PubMed ID: 15824850
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  • 11. Denaturing gradient gel electrophoresis analysis of the tissue nonspecific alkaline phosphatase isoenzyme gene in hypophosphatasia.
    Mumm S, Jones J, Finnegan P, Henthorn PS, Podgornik MN, Whyte MP.
    Mol Genet Metab; 2002 Feb 04; 75(2):143-53. PubMed ID: 11855933
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  • 13. Molecular characterization of tissue-nonspecific alkaline phosphatase with an Ala to Thr substitution at position 116 associated with dominantly inherited hypophosphatasia.
    Ishida Y, Komaru K, Oda K.
    Biochim Biophys Acta; 2011 Mar 04; 1812(3):326-32. PubMed ID: 21168482
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  • 17. Analysis of localization of mutated tissue-nonspecific alkaline phosphatase proteins associated with neonatal hypophosphatasia using green fluorescent protein chimeras.
    Cai G, Michigami T, Yamamoto T, Yasui N, Satomura K, Yamagata M, Shima M, Nakajima S, Mushiake S, Okada S, Ozono K.
    J Clin Endocrinol Metab; 1998 Nov 04; 83(11):3936-42. PubMed ID: 9814472
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  • 18. Molecular phenotype of tissue-nonspecific alkaline phosphatase with a proline (108) to leucine substitution associated with dominant odontohypophosphatasia.
    Numa-Kinjoh N, Komaru K, Ishida Y, Sohda M, Oda K.
    Mol Genet Metab; 2015 Aug 04; 115(4):180-5. PubMed ID: 25982064
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  • 20. Retention at the cis-Golgi and delayed degradation of tissue-non-specific alkaline phosphatase with an Asn153-->Asp substitution, a cause of perinatal hypophosphatasia.
    Ito M, Amizuka N, Ozawa H, Oda K.
    Biochem J; 2002 Feb 01; 361(Pt 3):473-80. PubMed ID: 11802776
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