BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

387 related articles for article (PubMed ID: 26657204)

  • 21. Holt-Oram syndrome because of the novel TBX5 mutation c.481A>C.
    Koçak Eker H; Altunoglu U; Toksoy G; Kayserili H
    Clin Dysmorphol; 2016 Oct; 25(4):192-4. PubMed ID: 27552067
    [No Abstract]   [Full Text] [Related]  

  • 22. A novel missense mutation in the TBX5 gene in a Saudi infant with Holt-Oram syndrome.
    Al-Qattan MM; Abou Al-Shaar H
    Saudi Med J; 2015 Aug; 36(8):980-2. PubMed ID: 26219450
    [TBL] [Abstract][Full Text] [Related]  

  • 23. HDAC4 and 5 repression of TBX5 is relieved by protein kinase D1.
    Ghosh TK; Aparicio-Sánchez JJ; Buxton S; Brook JD
    Sci Rep; 2019 Nov; 9(1):17992. PubMed ID: 31784580
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Novel compound heterozygous TBX5 variants may induce hypoplastic left heart syndrome.
    Miyao N; Hirono K; Hata Y; Yoshimura N; Ichida F
    Pediatr Int; 2019 Jun; 61(6):607-609. PubMed ID: 31215120
    [No Abstract]   [Full Text] [Related]  

  • 25. Functional analysis of novel TBX5 T-box mutations associated with Holt-Oram syndrome.
    Boogerd CJ; Dooijes D; Ilgun A; Mathijssen IB; Hordijk R; van de Laar IM; Rump P; Veenstra-Knol HE; Moorman AF; Barnett P; Postma AV
    Cardiovasc Res; 2010 Oct; 88(1):130-9. PubMed ID: 20519243
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Genetic Analyses Identified a SALL4 Gene Mutation Associated with Holt-Oram Syndrome.
    Li B; Chen S; Sun K; Xu R; Wu Y
    DNA Cell Biol; 2018 Apr; 37(4):398-404. PubMed ID: 29461882
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Clinical expression of Holt-Oram syndrome on the basis of own clinical experience considering prenatal diagnosis.
    Walencka Z; Jamsheer A; Surmiak P; Baumert M; Jezela-Stanek A; Witek A; Materna-Kiryluk A; Latos-Bieleńska A; Socha M; Sowińska-Seidler A
    Ginekol Pol; 2016; 87(10):706-710. PubMed ID: 27958623
    [TBL] [Abstract][Full Text] [Related]  

  • 28. TBX5: A Key Regulator of Heart Development.
    Steimle JD; Moskowitz IP
    Curr Top Dev Biol; 2017; 122():195-221. PubMed ID: 28057264
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Patient-Specific TBX5-G125R Variant Induces Profound Transcriptional Deregulation and Atrial Dysfunction.
    van Ouwerkerk AF; Bosada FM; van Duijvenboden K; Houweling AC; Scholman KT; Wakker V; Allaart CP; Uhm JS; Mathijssen IB; Baartscheer T; Postma AV; Barnett P; Verkerk AO; Boukens BJ; Christoffels VM
    Circulation; 2022 Feb; 145(8):606-619. PubMed ID: 35113653
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Contiguous gene deletion of TBX5 and TBX3 leads to a varible phenotype with combined features of Holt-Oram and ulnar-mammary syndromes.
    Alby C; Bessieres B; Bieth E; Attie-Bitach T; Fermont L; Citony I; Razavi F; Vekemans M; Escande F; Manouvrier S; Malan V; Amiel J
    Am J Med Genet A; 2013 Jul; 161A(7):1797-802. PubMed ID: 23713051
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Atrial septal defect type II and upper limb malformation in 40-year-old male as a manifestation of Holt-Oram syndrome.
    Szymczyk E; Wejner-Mik P; Lipiec P; Michalski B; Kasprzak JD
    Cardiol J; 2019; 26(3):302-303. PubMed ID: 31246270
    [No Abstract]   [Full Text] [Related]  

  • 32. The paracrine effect of exogenous growth hormone alleviates dysmorphogenesis caused by tbx5 deficiency in zebrafish (Danio rerio) embryos.
    Tsai TC; Lu JK; Choo SL; Yeh SY; Tang RB; Lee HY; Lu JH
    J Biomed Sci; 2012 Jul; 19(1):63. PubMed ID: 22776023
    [TBL] [Abstract][Full Text] [Related]  

  • 33. TBX5 variants and cardiac phenotype: A systematic review of the literature and a novel variant.
    Møller Nielsen AK; Dehn AM; Hjortdal V; Larsen LA
    Eur J Med Genet; 2024 Apr; 68():104920. PubMed ID: 38336121
    [TBL] [Abstract][Full Text] [Related]  

  • 34. T-box genes and retinoic acid signaling regulate the segregation of arterial and venous pole progenitor cells in the murine second heart field.
    De Bono C; Thellier C; Bertrand N; Sturny R; Jullian E; Cortes C; Stefanovic S; Zaffran S; Théveniau-Ruissy M; Kelly RG
    Hum Mol Genet; 2018 Nov; 27(21):3747-3760. PubMed ID: 30016433
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Identification of a novel TBX5 c.755 + 1 G > A variant and related pathogenesis in a family with Holt-Oram syndrome.
    Wang DG; Dong XS; Xiong Y; Li ZM; Xie YJ; Liang SH; Huang TH
    Am J Med Genet A; 2022 Jan; 188(1):58-70. PubMed ID: 34490705
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Holt-Oram syndrome: study of 7 cases].
    Martínez-García M; Lorda-Sanchez I; García-Hoyos M; Ramos C; Ayuso C; Trujillo-Tiebas MJ
    Med Clin (Barc); 2010 Nov; 135(14):653-7. PubMed ID: 21070912
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Zebrafish tbx5 paralogs demonstrate independent essential requirements in cardiac and pectoral fin development.
    Parrie LE; Renfrew EM; Wal AV; Mueller RL; Garrity DM
    Dev Dyn; 2013 May; 242(5):485-502. PubMed ID: 23441045
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Holt-Oram syndrome.
    Goldfarb CA; Wall LB
    J Hand Surg Am; 2014 Aug; 39(8):1646-8. PubMed ID: 24656395
    [No Abstract]   [Full Text] [Related]  

  • 39. TBX5 mutations in non-Holt-Oram syndrome (HOS) malformed hearts.
    Reamon-Buettner SM; Borlak J
    Hum Mutat; 2004 Jul; 24(1):104. PubMed ID: 15221798
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Holt-Oram syndrome associated with anomalies of the feet.
    Garavelli L; De Brasi D; Verri R; Guareschi E; Cariola F; Melis D; Calcagno G; Salvatore F; Unger S; Sebastio G; Albertini G; Rivieri F; Soli F; Superti-Furga A; Gentile M
    Am J Med Genet A; 2008 May; 146A(9):1185-9. PubMed ID: 18351627
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 20.