BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

260 related articles for article (PubMed ID: 10780788)

  • 21. The elastin gene is disrupted in a family with a balanced translocation t(7;16)(q11.23;q13) associated with a variable expression of the Williams-Beuren syndrome.
    Duba HC; Doll A; Neyer M; Erdel M; Mann C; Hammerer I; Utermann G; Grzeschik KH
    Eur J Hum Genet; 2002 Jun; 10(6):351-61. PubMed ID: 12080386
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Genomic organization, chromosomal localization, and the complete 22 kb DNA sequence of the human GCMa/GCM1, a placenta-specific transcription factor gene.
    Yamada K; Ogawa H; Tamiya G; Ikeno M; Morita M; Asakawa S; Shimizu N; Okazaki T
    Biochem Biophys Res Commun; 2000 Nov; 278(1):134-9. PubMed ID: 11071865
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Cloning, expression, and chromosomal mapping of the human 14-3-3gamma gene (YWHAG) to 7q11.23.
    Horie M; Suzuki M; Takahashi E; Tanigami A
    Genomics; 1999 Sep; 60(2):241-3. PubMed ID: 10486217
    [TBL] [Abstract][Full Text] [Related]  

  • 24. A complete physical contig and partial transcript map of the Williams syndrome critical region.
    Hockenhull EL; Carette MJ; Metcalfe K; Donnai D; Read AP; Tassabehji M
    Genomics; 1999 Jun; 58(2):138-45. PubMed ID: 10366445
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Autism and Williams syndrome: a case report.
    Herguner S; Mukaddes NM
    World J Biol Psychiatry; 2006; 7(3):186-8. PubMed ID: 16861145
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Cloning and characterization of the murine genes for bHLH-ZIP transcription factors TFEC and TFEB reveal a common gene organization for all MiT subfamily members.
    Rehli M; Den Elzen N; Cassady AI; Ostrowski MC; Hume DA
    Genomics; 1999 Feb; 56(1):111-20. PubMed ID: 10036191
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Identification of the WBSCR9 gene, encoding a novel transcriptional regulator, in the Williams-Beuren syndrome deletion at 7q11.23.
    Peoples RJ; Cisco MJ; Kaplan P; Francke U
    Cytogenet Cell Genet; 1998; 82(3-4):238-46. PubMed ID: 9858827
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Williams-Beuren syndrome: determination of deletion size using quantitative real-time PCR.
    Schubert C; Laccone F
    Int J Mol Med; 2006 Nov; 18(5):799-806. PubMed ID: 17016608
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Isolation and characterization of a novel gene from the DiGeorge chromosomal region that encodes for a mediator subunit.
    Berti L; Mittler G; Przemeck GK; Stelzer G; Günzler B; Amati F; Conti E; Dallapiccola B; Hrabé de Angelis M; Novelli G; Meisterernst M
    Genomics; 2001 Jun; 74(3):320-32. PubMed ID: 11414760
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Williams-Beuren syndrome: a challenge for genotype-phenotype correlations.
    Tassabehji M
    Hum Mol Genet; 2003 Oct; 12 Spec No 2():R229-37. PubMed ID: 12952863
    [TBL] [Abstract][Full Text] [Related]  

  • 31. KIAA1735 gene on human chromosome 11q23.1 encodes a novel protein with myosine-tail homologous domain and C-terminal DIX domain.
    Katoh M; Katoh M
    Int J Oncol; 2003 Jul; 23(1):145-50. PubMed ID: 12792787
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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; 69(3):380-90. PubMed ID: 11056056
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Characterization and gene structure of a novel retinoblastoma-protein-associated protein similar to the transcription regulator TFII-I.
    Yan X; Zhao X; Qian M; Guo N; Gong X; Zhu X
    Biochem J; 2000 Feb; 345 Pt 3(Pt 3):749-57. PubMed ID: 10642537
    [TBL] [Abstract][Full Text] [Related]  

  • 34. The der(17)t(X;17)(p11;q25) of human alveolar soft part sarcoma fuses the TFE3 transcription factor gene to ASPL, a novel gene at 17q25.
    Ladanyi M; Lui MY; Antonescu CR; Krause-Boehm A; Meindl A; Argani P; Healey JH; Ueda T; Yoshikawa H; Meloni-Ehrig A; Sorensen PH; Mertens F; Mandahl N; van den Berghe H; Sciot R; Dal Cin P; Bridge J
    Oncogene; 2001 Jan; 20(1):48-57. PubMed ID: 11244503
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Williams syndrome without cardiovascular abnormalities].
    Cincinnati P; Genuardi M; Rutiloni C
    Minerva Pediatr; 1998 Nov; 50(11):467-71. PubMed ID: 10207296
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Identification and characterization of human KIAA1391 and mouse Kiaa1391 genes encoding novel RhoGAP family proteins with RA domain and ANXL repeats.
    Katoh M; Katoh M
    Int J Oncol; 2003 Nov; 23(5):1471-6. PubMed ID: 14532992
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Genes for the CPE receptor (CPETR1) and the human homolog of RVP1 (CPETR2) are localized within the Williams-Beuren syndrome deletion.
    Paperna T; Peoples R; Wang YK; Kaplan P; Francke U
    Genomics; 1998 Dec; 54(3):453-9. PubMed ID: 9878248
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [Clinical characterization, molecular and FISH studies in 80 patients with clinical suspicion of Williams-Beuren syndrome].
    Milà M; Carrió A; Sánchez A; Gómez D; Jiménez D; Estivill X; Ballesta F
    Med Clin (Barc); 1999 Jun; 113(2):46-9. PubMed ID: 10425618
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Structure and chromosomal locus of the mouse gene encoding a cerebellar Purkinje cell-specific helix-loop-helix factor Hes-3.
    Sakagami T; Sakurada K; Sakai Y; Watanabe T; Nakanishi S; Kageyama R
    Biochem Biophys Res Commun; 1994 Aug; 203(1):594-601. PubMed ID: 8074710
    [TBL] [Abstract][Full Text] [Related]  

  • 40. cDNA cloning and characterization of the human THRAP2 gene which maps to chromosome 12q24, and its mouse ortholog Thrap2.
    Musante L; Bartsch O; Ropers HH; Kalscheuer VM
    Gene; 2004 May; 332():119-27. PubMed ID: 15145061
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 13.