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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

147 related items for PubMed ID: 7956361

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4. Mutations in xanthine dehydrogenase gene in subjects with hereditary xanthinuria.
    Ichida K, Kamatani N, Nishino T, Saji M, Okabe H, Hosoya T.
    Adv Exp Med Biol; 1998; 431():327-30. PubMed ID: 9598085
    [No Abstract] [Full Text] [Related]

  • 5. Identification of two mutations in human xanthine dehydrogenase gene responsible for classical type I xanthinuria.
    Ichida K, Amaya Y, Kamatani N, Nishino T, Hosoya T, Sakai O.
    J Clin Invest; 1997 May 15; 99(10):2391-7. PubMed ID: 9153281
    [Abstract] [Full Text] [Related]

  • 6. [Unmeasurable uric acid in blood and urine; xanthine dehydrogenase deficiency (or hereditary xanthinuria)].
    Mayaudon H, Bauduceau B, Dupuy O, Ceppa F, Roul G, Burnat P.
    Rev Med Interne; 1999 May 15; 20(5):445. PubMed ID: 10365419
    [No Abstract] [Full Text] [Related]

  • 7. XDH gene mutation is the underlying cause of classical xanthinuria: a second report.
    Levartovsky D, Lagziel A, Sperling O, Liberman U, Yaron M, Hosoya T, Ichida K, Peretz H.
    Kidney Int; 2000 Jun 15; 57(6):2215-20. PubMed ID: 10844591
    [Abstract] [Full Text] [Related]

  • 8. Analysis of aldehyde oxidase and xanthine dehydrogenase/oxidase as possible candidate genes for autosomal recessive familial amyotrophic lateral sclerosis.
    Berger R, Mezey E, Clancy KP, Harta G, Wright RM, Repine JE, Brown RH, Brownstein M, Patterson D.
    Somat Cell Mol Genet; 1995 Mar 15; 21(2):121-31. PubMed ID: 7570184
    [Abstract] [Full Text] [Related]

  • 9. Chromosomal localization of the human ciliary neurotrophic factor gene (CNTF) to 11q12 by fluorescence in situ hybridization.
    Giovannini M, Romo AJ, Evans GA.
    Cytogenet Cell Genet; 1993 Mar 15; 63(1):62-3. PubMed ID: 8449041
    [Abstract] [Full Text] [Related]

  • 10. Human xanthine dehydrogenase cDNA sequence and protein in an atypical case of type I xanthinuria in comparison with normal subjects.
    Yamamoto T, Moriwaki Y, Shibutani Y, Matsui K, Ueo T, Takahashi S, Tsutsumi Z, Hada T.
    Clin Chim Acta; 2001 Feb 15; 304(1-2):153-8. PubMed ID: 11165212
    [Abstract] [Full Text] [Related]

  • 11. Mapping of the breast basic conserved gene (D16S444E) to human chromosome band 16q24.3.
    Cleton-Jansen AM, Moerland HW, Callen DF, Doggett NA, Devilee P, Cornelisse CJ.
    Cytogenet Cell Genet; 1995 Feb 15; 68(1-2):49-51. PubMed ID: 7956357
    [Abstract] [Full Text] [Related]

  • 12. Mapping of the 70 kDa, 34 kDa, and 11 kDa subunit genes of the human multimeric single-stranded DNA binding protein (hSSB/RPA) to chromosome bands 17p13, 1p35-p36.1, and 7p21-p22.
    Ozawa K, Dean FB, Chen M, Lee SH, Shiratori A, Murakami Y, Sakakura T, Hurwitz J, Eki T.
    Cell Struct Funct; 1993 Aug 15; 18(4):221-30. PubMed ID: 8293499
    [Abstract] [Full Text] [Related]

  • 13. Generation and mapping of human chromosome 2 microdissection clone-derived STSs.
    Gingrich JC, Garnes JA, Lee DA, Boehrer DM.
    Cytogenet Cell Genet; 1996 Aug 15; 74(4):272-6. PubMed ID: 8976383
    [Abstract] [Full Text] [Related]

  • 14. Mutation of human molybdenum cofactor sulfurase gene is responsible for classical xanthinuria type II.
    Ichida K, Matsumura T, Sakuma R, Hosoya T, Nishino T.
    Biochem Biophys Res Commun; 2001 Apr 20; 282(5):1194-200. PubMed ID: 11302742
    [Abstract] [Full Text] [Related]

  • 15. Cloning of the cDNA encoding human xanthine dehydrogenase (oxidase): structural analysis of the protein and chromosomal location of the gene.
    Ichida K, Amaya Y, Noda K, Minoshima S, Hosoya T, Sakai O, Shimizu N, Nishino T.
    Gene; 1993 Nov 15; 133(2):279-84. PubMed ID: 8224915
    [Abstract] [Full Text] [Related]

  • 16. Multi-exon deletion in the XDH gene as a cause of classical xanthinuria.
    Eggermann T, Spengler S, Denecke B, Zerres K, Mache CJ.
    Clin Nephrol; 2013 Jan 15; 79(1):78-80. PubMed ID: 23249873
    [Abstract] [Full Text] [Related]

  • 17. Thiopurine-induced toxicity is associated with dysfunction variant of the human molybdenum cofactor sulfurase gene (xanthinuria type II).
    Stiburkova B, Pavelcova K, Petru L, Krijt J.
    Toxicol Appl Pharmacol; 2018 Aug 15; 353():102-108. PubMed ID: 29935280
    [Abstract] [Full Text] [Related]

  • 18. Assignment of the human type I IMP dehydrogenase gene (IMPDH1) to chromosome 7q31.3-q32).
    Gu JJ, Kaiser-Rogers K, Rao K, Mitchell BS.
    Genomics; 1994 Nov 01; 24(1):179-81. PubMed ID: 7896275
    [Abstract] [Full Text] [Related]

  • 19. Mutational analysis of the xanthine dehydrogenase gene in a Turkish family with autosomal recessive classical xanthinuria.
    Gok F, Ichida K, Topaloglu R.
    Nephrol Dial Transplant; 2003 Nov 01; 18(11):2278-83. PubMed ID: 14551354
    [Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 8.