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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

67 related articles for article (PubMed ID: 9184001)

  • 1. Assignment of the human connexin43 gene, GJA1, to chromosome 6q22.3.
    Kato R; Matsumoto N; Niikawa N
    Jpn J Hum Genet; 1997 Mar; 42(1):213-6. PubMed ID: 9184001
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Intercellular communication via connexin43 gap junctions is required for ovarian folliculogenesis in the mouse.
    Ackert CL; Gittens JE; O'Brien MJ; Eppig JJ; Kidder GM
    Dev Biol; 2001 May; 233(2):258-70. PubMed ID: 11336494
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Doubly mutant mice, deficient in connexin32 and -43, show normal prenatal development of organs where the two gap junction proteins are expressed in the same cells.
    Houghton FD; Thönnissen E; Kidder GM; Naus CC; Willecke K; Winterhager E
    Dev Genet; 1999; 24(1-2):5-12. PubMed ID: 10079506
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Regional mapping of the human MP70 (Cx50; connexin 50) gene by fluorescence in situ hybridization to 1q21.1.
    Geyer DD; Church RL; Steele EC; Heinzmann C; Kojis TL; Klisak I; Sparkes RS; Bateman JB
    Mol Vis; 1997 Dec; 3():13. PubMed ID: 9479004
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Analysis of balanced rearrangements of chromosome 6 in acute leukemia: clustered breakpoints in q22-q23 and possible involvement of c-MYB in a new recurrent translocation, t(6;7)(q23;q32 through 36).
    Sinclair P; Harrison CJ; Jarosová M; Foroni L
    Haematologica; 2005 May; 90(5):602-11. PubMed ID: 15921375
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Physical mapping of connexin 32 (GJB1) and 43 (GJA1) genes to bovine chromosomes Xq22 and 9q15/16 by fluorescence in situ hybridization.
    Castiglioni B; Ferretti L; Tenchini ML; Mezzelani A; Simonic T; Duga S
    Mamm Genome; 1996 Aug; 7(8):634-5. PubMed ID: 8678997
    [No Abstract]   [Full Text] [Related]  

  • 7. A novel GJA 1 mutation in oculo-dento-digital dysplasia with curly hair and hyperkeratosis.
    Kelly SC; Ratajczak P; Keller M; Purcell SM; Griffin T; Richard G
    Eur J Dermatol; 2006; 16(3):241-5. PubMed ID: 16709485
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Human connexin43 gene locus, GJA1, sublocalized to band 6q21-->q23.2.
    Corcos IA; Meese EU; Loch-Caruso R
    Cytogenet Cell Genet; 1993; 64(1):31-2. PubMed ID: 8389684
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Fate of connexin43 in cardiac tissue harbouring a disease-linked connexin43 mutant.
    Manias JL; Plante I; Gong XQ; Shao Q; Churko J; Bai D; Laird DW
    Cardiovasc Res; 2008 Dec; 80(3):385-95. PubMed ID: 18678643
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mutations in connexin43 (GJA1) perturb bone growth in zebrafish fins.
    Iovine MK; Higgins EP; Hindes A; Coblitz B; Johnson SL
    Dev Biol; 2005 Feb; 278(1):208-19. PubMed ID: 15649473
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Screening of mouse connexin 31 genomic clone and mapping by fluorescence in situ hybridization].
    Li WZ; Xue ZG; Wang G
    Hunan Yi Ke Da Xue Xue Bao; 2001 Dec; 26(6):499-501. PubMed ID: 12536520
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Functional characterization of connexin43 mutations found in patients with oculodentodigital dysplasia.
    Shibayama J; Paznekas W; Seki A; Taffet S; Jabs EW; Delmar M; Musa H
    Circ Res; 2005 May; 96(10):e83-91. PubMed ID: 15879313
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Assignment of the human UDP-GalNAc:polypeptide, N-acetylgalactosaminyltransferase-type-2 gene to chromosomal region 1q42 by fluorescence in situ hybridization.
    Takai S; Hinoda Y; Adachi T; Oshima M; Imai K
    Jpn J Hum Genet; 1997 Mar; 42(1):237-40. PubMed ID: 9184005
    [No Abstract]   [Full Text] [Related]  

  • 14. Six genes of the human connexin gene family coding for gap junctional proteins are assigned to four different human chromosomes.
    Willecke K; Jungbluth S; Dahl E; Hennemann H; Heynkes R; Grzeschik KH
    Eur J Cell Biol; 1990 Dec; 53(2):275-80. PubMed ID: 1964417
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Lack of evidence for connexin 43 gene mutations in human autosomal recessive lateralization defects.
    Debrus S; Tuffery S; Matsuoka R; Galal O; Sarda P; Sauer U; Bozio A; Tanman B; Toutain A; Claustres M; Le Paslier D; Bouvagnet P
    J Mol Cell Cardiol; 1997 May; 29(5):1423-31. PubMed ID: 9201627
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Assignment of xeroderma pigmentosum group C (XPC) gene to chromosome 3p25.
    Legerski RJ; Liu P; Li L; Peterson CA; Zhao Y; Leach RJ; Naylor SL; Siciliano MJ
    Genomics; 1994 May; 21(1):266-9. PubMed ID: 8088800
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Cloning of GJA1 (connexin43) and its expression in canine ovarian follicles throughout the estrous cycle.
    Willingham-Rocky LA; Golding MC; Wright JM; Kraemer DC; Westhusin ME; Burghardt RC
    Gene Expr Patterns; 2007 Jan; 7(1-2):66-71. PubMed ID: 16829210
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Assignment of the human cytosolic acetoacetyl-coenzyme A thiolase (ACAT2) gene to chromosome 6q25.3-q26.
    Masuno M; Fukao T; Song XQ; Yamaguchi S; Orii T; Kondo N; Imaizumi K; Kuroki Y
    Genomics; 1996 Aug; 36(1):217-8. PubMed ID: 8812443
    [No Abstract]   [Full Text] [Related]  

  • 19. Mapping of low-frequency chimeric yeast artificial chromosome libraries from human chromosomes 16 and 21 by fluorescence in situ hybridization and quantitative image analysis.
    Marrone BL; Campbell EW; Anzick SL; Shera K; Campbell M; Yoshida TM; McCormick MK; Deaven L
    Genomics; 1994 May; 21(1):202-7. PubMed ID: 8088788
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Molecular characterization and chromosomal assignment of the bovine glycinamide ribonucleotide formyltransferase (GART) gene on cattle chromosome 1q12.1-q12.2.
    Wöhlke A; Drögemüller C; Kuiper H; Leeb T; Distl O
    Gene; 2005 Mar; 348():73-81. PubMed ID: 15777723
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.