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Journal Abstract Search

308 related items for PubMed ID: 7959736

  • 21.
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  • 22. Genomic organization of the JEM-1 (BLZF1) gene on human chromosome 1q24: molecular cloning and analysis of its promoter region.
    Tong JH, Fant X, Benoit G, Chen SJ, Chen Z, Lanotte M.
    Genomics; 2000 Nov 01; 69(3):380-90. PubMed ID: 11056056
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  • 23. Dramatically different phenotypes in mouse models of human Tay-Sachs and Sandhoff diseases.
    Phaneuf D, Wakamatsu N, Huang JQ, Borowski A, Peterson AC, Fortunato SR, Ritter G, Igdoura SA, Morales CR, Benoit G, Akerman BR, Leclerc D, Hanai N, Marth JD, Trasler JM, Gravel RA.
    Hum Mol Genet; 1996 Jan 01; 5(1):1-14. PubMed ID: 8789434
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  • 24. The mouse lens fiber-cell intrinsic membrane protein MP19 gene (Lim2) and granule membrane protein GMP-17 gene (Nkg7): Isolation and sequence analysis of two neighboring genes.
    Zhou L, Li X, Church RL.
    Mol Vis; 2001 Apr 02; 7():79-88. PubMed ID: 11290961
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  • 25. The HNF-3 gene family of transcription factors in mice: gene structure, cDNA sequence, and mRNA distribution.
    Kaestner KH, Hiemisch H, Luckow B, Schütz G.
    Genomics; 1994 Apr 02; 20(3):377-85. PubMed ID: 8034310
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  • 26. Mouse testin: complementary DNA cloning, genomic organization, and characterization of its proximal promoter region.
    Cheng CK, Cheung CH, Lee WM.
    Biol Reprod; 2003 Apr 02; 68(4):1376-86. PubMed ID: 12606342
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  • 27. Human N-benzoyl-L-tyrosyl-p-aminobenzoic acid hydrolase (human meprin): genomic structure of the alpha and beta subunits.
    Hahn D, Illisson R, Metspalu A, Sterchi EE.
    Biochem J; 2000 Feb 15; 346 Pt 1(Pt 1):83-91. PubMed ID: 10657243
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  • 28. Mouse homologue of C33 antigen (CD82), a member of the transmembrane 4 superfamily: complementary DNA, genomic structure, and expression.
    Nagira M, Imai T, Ishikawa I, Uwabe KI, Yoshie O.
    Cell Immunol; 1994 Aug 15; 157(1):144-57. PubMed ID: 8039242
    [Abstract] [Full Text] [Related]

  • 29. Isolation of cDNA clones coding for the alpha-subunit of human beta-hexosaminidase. Extensive homology between the alpha- and beta-subunits and studies on Tay-Sachs disease.
    Korneluk RG, Mahuran DJ, Neote K, Klavins MH, O'Dowd BF, Tropak M, Willard HF, Anderson MJ, Lowden JA, Gravel RA.
    J Biol Chem; 1986 Jun 25; 261(18):8407-13. PubMed ID: 3013851
    [Abstract] [Full Text] [Related]

  • 30. The divergent 5' termini of the alpha human folate receptor (hFR) mRNAs originate from two tissue-specific promoters and alternative splicing: characterization of the alpha hFR gene structure.
    Elwood PC, Nachmanoff K, Saikawa Y, Page ST, Pacheco P, Roberts S, Chung KN.
    Biochemistry; 1997 Feb 11; 36(6):1467-78. PubMed ID: 9063895
    [Abstract] [Full Text] [Related]

  • 31. Inefficiency in GM2 ganglioside elimination by human lysosomal beta-hexosaminidase beta-subunit gene transfer to fibroblastic cell line derived from Sandhoff disease model mice.
    Itakura T, Kuroki A, Ishibashi Y, Tsuji D, Kawashita E, Higashine Y, Sakuraba H, Yamanaka S, Itoh K.
    Biol Pharm Bull; 2006 Aug 11; 29(8):1564-9. PubMed ID: 16880605
    [Abstract] [Full Text] [Related]

  • 32. Characterization of the murine beta-hexosaminidase (HEXB) gene.
    Triggs-Raine BL, Benoit G, Salo TJ, Trasler JM, Gravel RA.
    Biochim Biophys Acta; 1994 Oct 21; 1227(1-2):79-86. PubMed ID: 7918686
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  • 36. Production of recombinant beta-hexosaminidase A, a potential enzyme for replacement therapy for Tay-Sachs and Sandhoff diseases, in the methylotrophic yeast Ogataea minuta.
    Akeboshi H, Chiba Y, Kasahara Y, Takashiba M, Takaoka Y, Ohsawa M, Tajima Y, Kawashima I, Tsuji D, Itoh K, Sakuraba H, Jigami Y.
    Appl Environ Microbiol; 2007 Aug 21; 73(15):4805-12. PubMed ID: 17557860
    [Abstract] [Full Text] [Related]

  • 37. Active arginine residues in beta-hexosaminidase. Identification through studies of the B1 variant of Tay-Sachs disease.
    Brown CA, Mahuran DJ.
    J Biol Chem; 1991 Aug 25; 266(24):15855-62. PubMed ID: 1831451
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  • 38. Characterization of the testis and epididymis in mouse models of human Tay Sachs and Sandhoff diseases and partial determination of accumulated gangliosides.
    Trasler J, Saberi F, Somani IH, Adamali HI, Huang JQ, Fortunato SR, Ritter G, Gu M, Aebersold R, Gravel RA, Hermo L.
    Endocrinology; 1998 Jul 25; 139(7):3280-8. PubMed ID: 9645704
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  • 39. Isolation and characterization of the HC8 subunit gene of the human proteasome.
    Akioka H, Forsberg NE, Ishida N, Okumura K, Nogami M, Taguchi H, Noda C, Tanaka K.
    Biochem Biophys Res Commun; 1995 Feb 06; 207(1):318-23. PubMed ID: 7857283
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  • 40.
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