BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

274 related articles for article (PubMed ID: 33866394)

  • 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. TBX5 loss-of-function mutation contributes to atrial fibrillation and atypical Holt-Oram syndrome.
    Guo DF; Li RG; Yuan F; Shi HY; Hou XM; Qu XK; Xu YJ; Zhang M; Liu X; Jiang JQ; Yang YQ; Qiu XB
    Mol Med Rep; 2016 May; 13(5):4349-56. PubMed ID: 27035640
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Tbx5 Buffers Inherent Left/Right Asymmetry Ensuring Symmetric Forelimb Formation.
    Sulaiman FA; Nishimoto S; Murphy GR; Kucharska A; Butterfield NC; Newbury-Ecob R; Logan MP
    PLoS Genet; 2016 Dec; 12(12):e1006521. PubMed ID: 27992425
    [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. 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]  

  • 26. 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]  

  • 27. Regulatory variation in a TBX5 enhancer leads to isolated congenital heart disease.
    Smemo S; Campos LC; Moskowitz IP; Krieger JE; Pereira AC; Nobrega MA
    Hum Mol Genet; 2012 Jul; 21(14):3255-63. PubMed ID: 22543974
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. 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]  

  • 30. 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]  

  • 31. 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]  

  • 32. Novel exons in the tbx5 gene locus generate protein isoforms with distinct expression domains and function.
    Yamak A; Georges RO; Sheikh-Hassani M; Morin M; Komati H; Nemer M
    J Biol Chem; 2015 Mar; 290(11):6844-56. PubMed ID: 25623069
    [TBL] [Abstract][Full Text] [Related]  

  • 33.
    Azab B; Aburizeg D; Ji W; Jeffries L; Isbeih NJ; Al-Akily AS; Mohammad H; Osba YA; Shahin MA; Dardas Z; Hatmal MM; Al-Ammouri I; Lakhani S
    Mol Med Rep; 2022 Jun; 25(6):. PubMed ID: 35514310
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [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]  

  • 35. Holt-Oram syndrome: a new mutation in the TBX5 gene in two unrelated families.
    Gruenauer-Kloevekorn C; Froster UG
    Ann Genet; 2003; 46(1):19-23. PubMed ID: 12818525
    [TBL] [Abstract][Full Text] [Related]  

  • 36. 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]  

  • 37. 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]  

  • 38. TBX5 mutations and congenital heart disease: Holt-Oram syndrome revealed.
    Mori AD; Bruneau BG
    Curr Opin Cardiol; 2004 May; 19(3):211-5. PubMed ID: 15096952
    [TBL] [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. Congenital extremity anomalies with a TBX5 pathogenic variant in consecutive IVF assisted pregnancies: a case report of Holt-Oram Syndrome.
    Sobh O; O'Sullivan R; Mahoney MJ; Kleinman G
    J Obstet Gynaecol; 2022 Apr; 42(3):524-526. PubMed ID: 34159885
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 14.