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 *

197 related articles for article (PubMed ID: 23082118)

  • 1. Functional significance of SRJ domain mutations in CITED2.
    Chen CM; Bentham J; Cosgrove C; Braganca J; Cuenda A; Bamforth SD; Schneider JE; Watkins H; Keavney B; Davies B; Bhattacharya S
    PLoS One; 2012; 7(10):e46256. PubMed ID: 23082118
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Identification and functional analysis of CITED2 mutations in patients with congenital heart defects.
    Sperling S; Grimm CH; Dunkel I; Mebus S; Sperling HP; Ebner A; Galli R; Lehrach H; Fusch C; Berger F; Hammer S
    Hum Mutat; 2005 Dec; 26(6):575-82. PubMed ID: 16287139
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Cardiac malformations, adrenal agenesis, neural crest defects and exencephaly in mice lacking Cited2, a new Tfap2 co-activator.
    Bamforth SD; Bragança J; Eloranta JJ; Murdoch JN; Marques FI; Kranc KR; Farza H; Henderson DJ; Hurst HC; Bhattacharya S
    Nat Genet; 2001 Dec; 29(4):469-74. PubMed ID: 11694877
    [TBL] [Abstract][Full Text] [Related]  

  • 4. CITED2 Mutations in Conserved Regions Contribute to Conotruncal Heart Defects in Chinese Children.
    Li B; Pu T; Liu Y; Xu Y; Xu R
    DNA Cell Biol; 2017 Jul; 36(7):589-595. PubMed ID: 28436679
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A gain-of-function mutation in CITED2 is associated with congenital heart disease.
    Yadav ML; Jain D; Neelabh ; Agrawal D; Kumar A; Mohapatra B
    Mutat Res; 2021; 822():111741. PubMed ID: 33706167
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Cited2 is required both for heart morphogenesis and establishment of the left-right axis in mouse development.
    Weninger WJ; Lopes Floro K; Bennett MB; Withington SL; Preis JI; Barbera JP; Mohun TJ; Dunwoodie SL
    Development; 2005 Mar; 132(6):1337-48. PubMed ID: 15750185
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Epiblastic Cited2 deficiency results in cardiac phenotypic heterogeneity and provides a mechanism for haploinsufficiency.
    MacDonald ST; Bamforth SD; Chen CM; Farthing CR; Franklyn A; Broadbent C; Schneider JE; Saga Y; Lewandoski M; Bhattacharya S
    Cardiovasc Res; 2008 Aug; 79(3):448-57. PubMed ID: 18440989
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Variations of CITED2 are associated with congenital heart disease (CHD) in Chinese population.
    Liu Y; Wang F; Wu Y; Tan S; Wen Q; Wang J; Zhu X; Wang X; Li C; Ma X; Pan H
    PLoS One; 2014; 9(5):e98157. PubMed ID: 24848765
    [TBL] [Abstract][Full Text] [Related]  

  • 9. CITED2 mutation links congenital heart defects to dysregulation of the cardiac gene VEGF and PITX2C expression.
    Li Q; Pan H; Guan L; Su D; Ma X
    Biochem Biophys Res Commun; 2012 Jul; 423(4):895-9. PubMed ID: 22735262
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Novel Point Mutations of CITED2 Gene Are Associated with Non-familial Congenital Heart Disease (CHD) in Sporadic Pediatric Patients.
    Dianatpour S; Khatami M; Heidari MM; Hadadzadeh M
    Appl Biochem Biotechnol; 2020 Mar; 190(3):896-906. PubMed ID: 31515672
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Human CREB-binding protein/p300-interacting transactivator with ED-rich tail (CITED) 4, a new member of the CITED family, functions as a co-activator for transcription factor AP-2.
    Bragança J; Swingler T; Marques FI; Jones T; Eloranta JJ; Hurst HC; Shioda T; Bhattacharya S
    J Biol Chem; 2002 Mar; 277(10):8559-65. PubMed ID: 11744733
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Loss of Cited2 causes congenital heart disease by perturbing left-right patterning of the body axis.
    Lopes Floro K; Artap ST; Preis JI; Fatkin D; Chapman G; Furtado MB; Harvey RP; Hamada H; Sparrow DB; Dunwoodie SL
    Hum Mol Genet; 2011 Mar; 20(6):1097-110. PubMed ID: 21224256
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Physical and functional interactions among AP-2 transcription factors, p300/CREB-binding protein, and CITED2.
    Bragança J; Eloranta JJ; Bamforth SD; Ibbitt JC; Hurst HC; Bhattacharya S
    J Biol Chem; 2003 May; 278(18):16021-9. PubMed ID: 12586840
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Maternal high-fat diet interacts with embryonic Cited2 genotype to reduce Pitx2c expression and enhance penetrance of left-right patterning defects.
    Bentham J; Michell AC; Lockstone H; Andrew D; Schneider JE; Brown NA; Bhattacharya S
    Hum Mol Genet; 2010 Sep; 19(17):3394-401. PubMed ID: 20566713
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Mutation analysis of Cited2 in patients with congenital heart disease].
    Yang XF; Wu XY; Li M; Li YG; Dai JT; Bai YH; Tian J
    Zhonghua Er Ke Za Zhi; 2010 Apr; 48(4):293-6. PubMed ID: 20654020
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A novel role for transcription factor Lmo4 in thymus development through genetic interaction with Cited2.
    Michell AC; Bragança J; Broadbent C; Joyce B; Franklyn A; Schneider JE; Bhattacharya S; Bamforth SD
    Dev Dyn; 2010 Jul; 239(7):1988-94. PubMed ID: 20549734
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Cited2 controls left-right patterning and heart development through a Nodal-Pitx2c pathway.
    Bamforth SD; Bragança J; Farthing CR; Schneider JE; Broadbent C; Michell AC; Clarke K; Neubauer S; Norris D; Brown NA; Anderson RH; Bhattacharya S
    Nat Genet; 2004 Nov; 36(11):1189-96. PubMed ID: 15475956
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Functional Analyses of a Novel CITED2 Nonsynonymous Mutation in Chinese Tibetan Patients with Congenital Heart Disease.
    Liu S; Su Z; Tan S; Ni B; Pan H; Liu B; Wang J; Xiao J; Chen Q
    Pediatr Cardiol; 2017 Aug; 38(6):1226-1231. PubMed ID: 28687891
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Exogenous WNT5A and WNT11 proteins rescue CITED2 dysfunction in mouse embryonic stem cells and zebrafish morphants.
    Santos JMA; Mendes-Silva L; Afonso V; Martins G; Machado RSR; Lopes JA; Cancela L; Futschik ME; Sachinidis A; Gavaia P; Bragança J
    Cell Death Dis; 2019 Aug; 10(8):582. PubMed ID: 31378782
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genetic analysis of the CITED2 gene promoter in isolated and sporadic congenital ventricular septal defects.
    Zheng SQ; Chen HX; Liu XC; Yang Q; He GW
    J Cell Mol Med; 2021 Feb; 25(4):2254-2261. PubMed ID: 33439552
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.