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Journal Abstract Search

167 related items for PubMed ID: 8619797

  • 1. Human CFTR gene sequences in regions flanking exon 10: a simple repeat sequence polymorphism in intron 9.
    Xu Z, Gruenert DC.
    Biochem Biophys Res Commun; 1996 Feb 06; 219(1):140-5. PubMed ID: 8619797
    [Abstract] [Full Text] [Related]

  • 2. Sequence of human tryptophan 2,3-dioxygenase (TDO2): presence of a glucocorticoid response-like element composed of a GTT repeat and an intronic CCCCT repeat.
    Comings DE, Muhleman D, Dietz G, Sherman M, Forest GL.
    Genomics; 1995 Sep 20; 29(2):390-6. PubMed ID: 8666386
    [Abstract] [Full Text] [Related]

  • 3. Insertion of natural intron 6a-6b into a human cDNA-derived gene therapy vector for cystic fibrosis improves plasmid stability and permits facile RNA/DNA discrimination.
    Boyd AC, Popp F, Michaelis U, Davidson H, Davidson-Smith H, Doherty A, McLachlan G, Porteous DJ, Seeber S.
    J Gene Med; 1999 Sep 20; 1(5):312-21. PubMed ID: 10738548
    [Abstract] [Full Text] [Related]

  • 4. Amplification of CFTR exon 9 sequences to multiple locations in the human genome.
    Rozmahel R, Heng HH, Duncan AM, Shi XM, Rommens JM, Tsui LC.
    Genomics; 1997 Nov 01; 45(3):554-61. PubMed ID: 9367680
    [Abstract] [Full Text] [Related]

  • 5. R117H and IVS8-5T cystic fibrosis mutation detection by restriction enzyme digestion.
    Shrimpton AE.
    Mol Diagn; 2000 Sep 01; 5(3):235-8. PubMed ID: 11070158
    [Abstract] [Full Text] [Related]

  • 6. Novel cftr gene sequence variation in Serbian patient with idiopathic disseminated bronchiectasis.
    Nikolic A, Milosevic K, Divac A, Ljujic M, Grkovic S, Nestorovic B.
    Fetal Pediatr Pathol; 2010 Jan 01; 29(2):95-8. PubMed ID: 20334484
    [Abstract] [Full Text] [Related]

  • 7. DNA polymorphisms in potential regulatory elements of the CFTR gene alter transcription factor binding.
    Rowntree R, Harris A.
    Hum Genet; 2002 Jul 01; 111(1):66-74. PubMed ID: 12136238
    [Abstract] [Full Text] [Related]

  • 8. The human Nramp2 gene: characterization of the gene structure, alternative splicing, promoter region and polymorphisms.
    Lee PL, Gelbart T, West C, Halloran C, Beutler E.
    Blood Cells Mol Dis; 1998 Jun 01; 24(2):199-215. PubMed ID: 9642100
    [Abstract] [Full Text] [Related]

  • 9. Isolation and molecular characterization of the porcine stearoyl-CoA desaturase gene.
    Ren J, Knorr C, Huang L, Brenig B.
    Gene; 2004 Sep 29; 340(1):19-30. PubMed ID: 15556291
    [Abstract] [Full Text] [Related]

  • 10. A 96-well formatted method for exon and exon/intron boundary full sequencing of the CFTR gene.
    Lucarelli M, Narzi L, Piergentili R, Ferraguti G, Grandoni F, Quattrucci S, Strom R.
    Anal Biochem; 2006 Jun 15; 353(2):226-35. PubMed ID: 16635477
    [Abstract] [Full Text] [Related]

  • 11. Isolation of CF cell lines corrected at DeltaF508-CFTR locus by SFHR-mediated targeting.
    Bruscia E, Sangiuolo F, Sinibaldi P, Goncz KK, Novelli G, Gruenert DC.
    Gene Ther; 2002 Jun 15; 9(11):683-5. PubMed ID: 12032687
    [Abstract] [Full Text] [Related]

  • 12. Genomic structure of the human bradykinin B1 receptor gene and preliminary characterization of its regulatory regions.
    Yang X, Polgar P.
    Biochem Biophys Res Commun; 1996 May 24; 222(3):718-25. PubMed ID: 8651911
    [Abstract] [Full Text] [Related]

  • 13. Large genomic rearrangements in the CFTR gene contribute to CBAVD.
    Taulan M, Girardet A, Guittard C, Altieri JP, Templin C, Beroud C, des Georges M, Claustres M.
    BMC Med Genet; 2007 Apr 20; 8():22. PubMed ID: 17448246
    [Abstract] [Full Text] [Related]

  • 14. Polymerase chain reaction-single-strand conformation polymorphism analysis for the VHL gene in chemically induced kidney tumors of rats using intron-derived primers.
    Shiao YH, Diwan BA, Perantoni AO, Calvert RJ, Zbar B, Lerman MI, Rice JM.
    Mol Carcinog; 1997 Aug 20; 19(4):230-5. PubMed ID: 9290699
    [Abstract] [Full Text] [Related]

  • 15. Genomic DNA sequence of the cystic fibrosis transmembrane conductance regulator (CFTR) gene.
    Zielenski J, Rozmahel R, Bozon D, Kerem B, Grzelczak Z, Riordan JR, Rommens J, Tsui LC.
    Genomics; 1991 May 20; 10(1):214-28. PubMed ID: 1710598
    [Abstract] [Full Text] [Related]

  • 16. [Comparison and analysis of the molecular character of breakpoints in introns of deletion hotspots of dystrophin gene].
    Sheng WL, Chen JY, Pan SY, Zhang C, Liu ZL.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Oct 20; 20(5):376-80. PubMed ID: 14556187
    [Abstract] [Full Text] [Related]

  • 17. Cystic fibrosis mutation frequencies in upstate New York.
    Shrimpton AE, Borowitz D, Swender P.
    Hum Mutat; 1997 Oct 20; 10(6):436-42. PubMed ID: 9401006
    [Abstract] [Full Text] [Related]

  • 18. Examination of a CYP2E1 repeat polymorphism in a monkey model of alcohol abuse.
    Walker SJ, Grant KA, Vrana KE.
    Alcohol Clin Exp Res; 2001 Aug 20; 25(8):1114-8. PubMed ID: 11505041
    [Abstract] [Full Text] [Related]

  • 19. Identification of ABCC6 pseudogenes on human chromosome 16p: implications for mutation detection in pseudoxanthoma elasticum.
    Pulkkinen L, Nakano A, Ringpfeil F, Uitto J.
    Hum Genet; 2001 Sep 20; 109(3):356-65. PubMed ID: 11702217
    [Abstract] [Full Text] [Related]

  • 20. Improved detection of CFTR mutations in Southern California Hispanic CF patients.
    Wong LJ, Wang J, Zhang YH, Hsu E, Heim RA, Bowman CM, Woo MS.
    Hum Mutat; 2001 Oct 20; 18(4):296-307. PubMed ID: 11668613
    [Abstract] [Full Text] [Related]

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