BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

206 related articles for article (PubMed ID: 15710732)

  • 1. Identification of new mutations in the TBX5 gene in patients with Holt-Oram syndrome.
    Heinritz W; Moschik A; Kujat A; Spranger S; Heilbronner H; Demuth S; Bier A; Tihanyi M; Mundlos S; Gruenauer-Kloevekorn C; Froster UG
    Heart; 2005 Mar; 91(3):383-4. PubMed ID: 15710732
    [No Abstract]   [Full Text] [Related]  

  • 2. Mutations in human TBX5 [corrected] cause limb and cardiac malformation in Holt-Oram syndrome.
    Basson CT; Bachinsky DR; Lin RC; Levi T; Elkins JA; Soults J; Grayzel D; Kroumpouzou E; Traill TA; Leblanc-Straceski J; Renault B; Kucherlapati R; Seidman JG; Seidman CE
    Nat Genet; 1997 Jan; 15(1):30-5. PubMed ID: 8988165
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Holt-Oram syndrome presenting as agenesis of the left pericardium.
    Dias RR; Albuquerque JM; Pereira AC; Stolf NA; Krieger JE; Mady C; Oliveira SA
    Int J Cardiol; 2007 Jan; 114(1):98-100. PubMed ID: 16376438
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene family.
    Li QY; Newbury-Ecob RA; Terrett JA; Wilson DI; Curtis AR; Yi CH; Gebuhr T; Bullen PJ; Robson SC; Strachan T; Bonnet D; Lyonnet S; Young ID; Raeburn JA; Buckler AJ; Law DJ; Brook JD
    Nat Genet; 1997 Jan; 15(1):21-9. PubMed ID: 8988164
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Novel TBX5 mutations in patients with Holt-Oram syndrome.
    Debeer P; Race V; Gewillig M; Devriendt K; Frijns JP
    Clin Orthop Relat Res; 2007 Sep; 462():20-6. PubMed ID: 17534187
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Expanding the spectrum of TBX5 mutations in Holt-Oram syndrome: detection of two intragenic deletions by quantitative real time PCR, and report of eight novel point mutations.
    Borozdin W; Bravo Ferrer Acosta AM; Bamshad MJ; Botzenhart EM; Froster UG; Lemke J; Schinzel A; Spranger S; McGaughran J; Wand D; Chrzanowska KH; Kohlhase J
    Hum Mutat; 2006 Sep; 27(9):975-6. PubMed ID: 16917909
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Molecular genetic and ocular findings in patients with holt-oram syndrome.
    Gruenauer-Kloevekorn C; Reichel MB; Duncker GI; Froster UG
    Ophthalmic Genet; 2005 Mar; 26(1):1-8. PubMed ID: 15823919
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [TBX5 mutation in Chinese patients with Holt-Oram syndrome].
    Yang J; Hu D; Xia J; Yang Y; Yin B; Hu J; Zhou X
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2000 Aug; 17(4):233-5. PubMed ID: 10932003
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The clinical and genetic spectrum of the Holt-Oram syndrome (heart-hand syndrome).
    Basson CT; Cowley GS; Solomon SD; Weissman B; Poznanski AK; Traill TA; Seidman JG; Seidman CE
    N Engl J Med; 1994 Mar; 330(13):885-91. PubMed ID: 8114858
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Structural basis of TBX5-DNA recognition: the T-box domain in its DNA-bound and -unbound form.
    Stirnimann CU; Ptchelkine D; Grimm C; Müller CW
    J Mol Biol; 2010 Jul; 400(1):71-81. PubMed ID: 20450920
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Holt-Oram syndrome.
    Lichiardopol C; Militaru C; Popescu B; Hila G; Mixich F
    Rom J Morphol Embryol; 2007; 48(1):67-70. PubMed ID: 17502954
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Chamber-specific cardiac expression of Tbx5 and heart defects in Holt-Oram syndrome.
    Bruneau BG; Logan M; Davis N; Levi T; Tabin CJ; Seidman JG; Seidman CE
    Dev Biol; 1999 Jul; 211(1):100-8. PubMed ID: 10373308
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Holt-Oram syndrome: family affected without TBX5 mutation and without phenotype manifestations in a probable mutation carrier].
    Murga-Eizagaechevarria N; Garcia-Barcina M; Sarasola Diez E
    Rev Esp Cardiol; 2011 Dec; 64(12):1225-6. PubMed ID: 21752519
    [No Abstract]   [Full Text] [Related]  

  • 15. 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]  

  • 16. TBX5 genetic testing validates strict clinical criteria for Holt-Oram syndrome.
    McDermott DA; Bressan MC; He J; Lee JS; Aftimos S; Brueckner M; Gilbert F; Graham GE; Hannibal MC; Innis JW; Pierpont ME; Raas-Rothschild A; Shanske AL; Smith WE; Spencer RH; St John-Sutton MG; van Maldergem L; Waggoner DJ; Weber M; Basson CT
    Pediatr Res; 2005 Nov; 58(5):981-6. PubMed ID: 16183809
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mutations in human TBX3 alter limb, apocrine and genital development in ulnar-mammary syndrome.
    Bamshad M; Lin RC; Law DJ; Watkins WC; Krakowiak PA; Moore ME; Franceschini P; Lala R; Holmes LB; Gebuhr TC; Bruneau BG; Schinzel A; Seidman JG; Seidman CE; Jorde LB
    Nat Genet; 1997 Jul; 16(3):311-5. PubMed ID: 9207801
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The human TBX5 gene mutation database.
    Heinritz W; Shou L; Moschik A; Froster UG
    Hum Mutat; 2005 Oct; 26(4):397. PubMed ID: 16134140
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Identification and localization of TBX5 transcription factor during human cardiac morphogenesis.
    Hatcher CJ; Goldstein MM; Mah CS; Delia CS; Basson CT
    Dev Dyn; 2000 Sep; 219(1):90-5. PubMed ID: 10974675
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Genetical basis of Holt-Oram syndrome].
    Rokicka A; Rokicki W
    Wiad Lek; 1999; 52(11-12):606-9. PubMed ID: 10745699
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.