BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

66 related articles for article (PubMed ID: 8988156)

  • 21. A myogenic switch. Muscle development.
    Taylor MV
    Curr Biol; 1996 Aug; 6(8):924-6. PubMed ID: 8805325
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Deletion of the TWIST gene in a large five-generation family.
    De Heer IM; Hoogeboom AJ; Eussen HJ; Vaandrager JM; De Klein A
    Clin Genet; 2004 May; 65(5):396-9. PubMed ID: 15099347
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Saethre-Chotzen syndrome: notable intrafamilial phenotypic variability in a large family with Q28X TWIST mutation.
    Dollfus H; Biswas P; Kumaramanickavel G; Stoetzel C; Quillet R; Biswas J; Lajeunie E; Renier D; Perrin-Schmitt F
    Am J Med Genet; 2002 May; 109(3):218-25. PubMed ID: 11977182
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Interhelical loops within the bHLH domain are determinant in maintaining TWIST1-DNA complexes.
    Bouard C; Terreux R; Hope J; Chemelle JA; Puisieux A; Ansieau S; Payen L
    J Biomol Struct Dyn; 2014; 32(2):226-41. PubMed ID: 23527594
    [TBL] [Abstract][Full Text] [Related]  

  • 25. A novel mutation in the TWIST gene, implicated in Saethre-Chotzen syndrome, is found in the original case of Robinow-Sorauf syndrome.
    Cai J; Shoo BA; Sorauf T; Jabs EW
    Clin Genet; 2003 Jul; 64(1):79-82. PubMed ID: 12791045
    [No Abstract]   [Full Text] [Related]  

  • 26. A TWIST in the fate of human osteoblasts identifies signaling molecules involved in skull development.
    Jabs EW
    J Clin Invest; 2001 May; 107(9):1075-7. PubMed ID: 11342569
    [No Abstract]   [Full Text] [Related]  

  • 27. Characterization of a dominant negative C. elegans Twist mutant protein with implications for human Saethre-Chotzen syndrome.
    Corsi AK; Brodigan TM; Jorgensen EM; Krause M
    Development; 2002 Jun; 129(11):2761-72. PubMed ID: 12015302
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Germline mutation in the FGFR3 gene in a TWIST1-negative family with Saethre-Chotzen syndrome and breast cancer.
    Sahlin P; Tarnow P; Martinsson T; Stenman G
    Genes Chromosomes Cancer; 2009 Mar; 48(3):285-8. PubMed ID: 19025794
    [No Abstract]   [Full Text] [Related]  

  • 29. A novel TWIST1 gene mutation in a patient with Saethre-Chotzen syndrome.
    Altiner Ş; Karabulut HG; Yararbaş K; Tükün A; Collet C; Kocaay P; Berberoğlu M; Ilgin Ruhi H
    Clin Dysmorphol; 2017 Jul; 26(3):175-178. PubMed ID: 27870659
    [No Abstract]   [Full Text] [Related]  

  • 30. Mga, a dual-specificity transcription factor that interacts with Max and contains a T-domain DNA-binding motif.
    Hurlin PJ; Steingrìmsson E; Copeland NG; Jenkins NA; Eisenman RN
    EMBO J; 1999 Dec; 18(24):7019-28. PubMed ID: 10601024
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Expression of a twist-related gene, Bbtwist, during the development of a lancelet species and its relation to cephalochordate anterior structures.
    Yasui K; Zhang SC; Uemura M; Aizawa S; Ueki T
    Dev Biol; 1998 Mar; 195(1):49-59. PubMed ID: 9520323
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Repression of muscle-specific gene activation by the murine Twist protein.
    Hebrok M; Füchtbauer A; Füchtbauer EM
    Exp Cell Res; 1997 May; 232(2):295-303. PubMed ID: 9168805
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Characterization of msim, a murine homologue of the Drosophila sim transcription factor.
    Moffett P; Dayo M; Reece M; McCormick MK; Pelletier J
    Genomics; 1996 Jul; 35(1):144-55. PubMed ID: 8661115
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Fusion of splicing factor genes PSF and NonO (p54nrb) to the TFE3 gene in papillary renal cell carcinoma.
    Clark J; Lu YJ; Sidhar SK; Parker C; Gill S; Smedley D; Hamoudi R; Linehan WM; Shipley J; Cooper CS
    Oncogene; 1997 Oct; 15(18):2233-9. PubMed ID: 9393982
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Dermo-1: a novel twist-related bHLH protein expressed in the developing dermis.
    Li L; Cserjesi P; Olson EN
    Dev Biol; 1995 Nov; 172(1):280-92. PubMed ID: 7589808
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Fusion of the NH2-terminal domain of the basic helix-loop-helix protein TCF12 to TEC in extraskeletal myxoid chondrosarcoma with translocation t(9;15)(q22;q21).
    Sjögren H; Wedell B; Meis-Kindblom JM; Kindblom LG; Stenman G
    Cancer Res; 2000 Dec; 60(24):6832-5. PubMed ID: 11156374
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Identification and characterisation of the gene TWIST NEIGHBOR (TWISTNB) located in the microdeletion syndrome 7p21 region.
    Kosan C; Kunz J
    Cytogenet Genome Res; 2002; 97(3-4):167-70. PubMed ID: 12438708
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Identification of a polymorphism (G83S) in the TWIST gene in Taiwanese.
    Yang CF; Wu JY; Tsai FJ; Lee CC; Lin WD
    Hum Mutat; 2000 Nov; 16(5):448. PubMed ID: 11058914
    [No Abstract]   [Full Text] [Related]  

  • 39. cato encodes a basic helix-loop-helix transcription factor implicated in the correct differentiation of Drosophila sense organs.
    Goulding SE; White NM; Jarman AP
    Dev Biol; 2000 May; 221(1):120-31. PubMed ID: 10772796
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Single-minded and Down syndrome?
    Chen H; Chrast R; Rossier C; Gos A; Antonarakis SE; Kudoh J; Yamaki A; Shindoh N; Maeda H; Minoshima S
    Nat Genet; 1995 May; 10(1):9-10. PubMed ID: 7647800
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 4.