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 *

122 related articles for article (PubMed ID: 15163635)

  • 1. The subcellular localization of the ChoRE-binding protein, encoded by the Williams-Beuren syndrome critical region gene 14, is regulated by 14-3-3.
    Merla G; Howald C; Antonarakis SE; Reymond A
    Hum Mol Genet; 2004 Jul; 13(14):1505-14. PubMed ID: 15163635
    [TBL] [Abstract][Full Text] [Related]  

  • 2. WBSCR14, a gene mapping to the Williams--Beuren syndrome deleted region, is a new member of the Mlx transcription factor network.
    Cairo S; Merla G; Urbinati F; Ballabio A; Reymond A
    Hum Mol Genet; 2001 Mar; 10(6):617-27. PubMed ID: 11230181
    [TBL] [Abstract][Full Text] [Related]  

  • 3. WBSCR14, a putative transcription factor gene deleted in Williams-Beuren syndrome: complete characterisation of the human gene and the mouse ortholog.
    de Luis O; Valero MC; Jurado LA
    Eur J Hum Genet; 2000 Mar; 8(3):215-22. PubMed ID: 10780788
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mlx is the functional heteromeric partner of the carbohydrate response element-binding protein in glucose regulation of lipogenic enzyme genes.
    Stoeckman AK; Ma L; Towle HC
    J Biol Chem; 2004 Apr; 279(15):15662-9. PubMed ID: 14742444
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A critical role for the loop region of the basic helix-loop-helix/leucine zipper protein Mlx in DNA binding and glucose-regulated transcription.
    Ma L; Sham YY; Walters KJ; Towle HC
    Nucleic Acids Res; 2007; 35(1):35-44. PubMed ID: 17148476
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Isolation and characterisation of GTF2IRD2, a novel fusion gene and member of the TFII-I family of transcription factors, deleted in Williams-Beuren syndrome.
    Tipney HJ; Hinsley TA; Brass A; Metcalfe K; Donnai D; Tassabehji M
    Eur J Hum Genet; 2004 Jul; 12(7):551-60. PubMed ID: 15100712
    [TBL] [Abstract][Full Text] [Related]  

  • 7. GTF2IRD2 is located in the Williams-Beuren syndrome critical region 7q11.23 and encodes a protein with two TFII-I-like helix-loop-helix repeats.
    Makeyev AV; Erdenechimeg L; Mungunsukh O; Roth JJ; Enkhmandakh B; Ruddle FH; Bayarsaihan D
    Proc Natl Acad Sci U S A; 2004 Jul; 101(30):11052-7. PubMed ID: 15243160
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Direct role of ChREBP.Mlx in regulating hepatic glucose-responsive genes.
    Ma L; Tsatsos NG; Towle HC
    J Biol Chem; 2005 Mar; 280(12):12019-27. PubMed ID: 15664996
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Flightless I homolog negatively regulates ChREBP activity in cancer cells.
    Wu L; Chen H; Zhu Y; Meng J; Li Y; Li M; Yang D; Zhang P; Feng M; Tong X
    Int J Biochem Cell Biol; 2013 Nov; 45(11):2688-97. PubMed ID: 24055811
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Identification of GTF2IRD1, a putative transcription factor within the Williams-Beuren syndrome deletion at 7q11.23.
    Franke Y; Peoples RJ; Francke U
    Cytogenet Cell Genet; 1999; 86(3-4):296-304. PubMed ID: 10575229
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Integration of a c-myc transgene results in disruption of the mouse Gtf2ird1 gene, the homologue of the human GTF2IRD1 gene hemizygously deleted in Williams-Beuren syndrome.
    Durkin ME; Keck-Waggoner CL; Popescu NC; Thorgeirsson SS
    Genomics; 2001 Apr; 73(1):20-7. PubMed ID: 11352562
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Complete physical map of the common deletion region in Williams syndrome and identification and characterization of three novel genes.
    Meng X; Lu X; Li Z; Green ED; Massa H; Trask BJ; Morris CA; Keating MT
    Hum Genet; 1998 Nov; 103(5):590-9. PubMed ID: 9860302
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A duplicated gene in the breakpoint regions of the 7q11.23 Williams-Beuren syndrome deletion encodes the initiator binding protein TFII-I and BAP-135, a phosphorylation target of BTK.
    Pérez Jurado LA; Wang YK; Peoples R; Coloma A; Cruces J; Francke U
    Hum Mol Genet; 1998 Mar; 7(3):325-34. PubMed ID: 9466987
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mmip1: a novel leucine zipper protein that reverses the suppressive effects of Mad family members on c-myc.
    Gupta K; Anand G; Yin X; Grove L; Prochownik EV
    Oncogene; 1998 Mar; 16(9):1149-59. PubMed ID: 9528857
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Fine-scale comparative mapping of the human 7q11.23 region and the orthologous region on mouse chromosome 5G: the low-copy repeats that flank the Williams-Beuren syndrome deletion arose at breakpoint sites of an evolutionary inversion(s).
    Valero MC; de Luis O; Cruces J; Pérez Jurado LA
    Genomics; 2000 Oct; 69(1):1-13. PubMed ID: 11013070
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Hepatocyte nuclear factor-4alpha contributes to carbohydrate-induced transcriptional activation of hepatic fatty acid synthase.
    Adamson AW; Suchankova G; Rufo C; Nakamura MT; Teran-Garcia M; Clarke SD; Gettys TW
    Biochem J; 2006 Oct; 399(2):285-95. PubMed ID: 16800817
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genetic factors contributing to autism spectrum disorder in Williams-Beuren syndrome.
    Codina-Sola M; Costa-Roger M; Pérez-García D; Flores R; Palacios-Verdú MG; Cusco I; Pérez-Jurado LA
    J Med Genet; 2019 Dec; 56(12):801-808. PubMed ID: 31413120
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Williams-Beuren syndrome TRIM50 encodes an E3 ubiquitin ligase.
    Micale L; Fusco C; Augello B; Napolitano LM; Dermitzakis ET; Meroni G; Merla G; Reymond A
    Eur J Hum Genet; 2008 Sep; 16(9):1038-49. PubMed ID: 18398435
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. STAG3, a novel gene encoding a protein involved in meiotic chromosome pairing and location of STAG3-related genes flanking the Williams-Beuren syndrome deletion.
    Pezzi N; Prieto I; Kremer L; Pérez Jurado LA; Valero C; Del Mazo J; Martínez-A C; Barbero JL
    FASEB J; 2000 Mar; 14(3):581-92. PubMed ID: 10698974
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.