290 related articles for article (PubMed ID: 35182466)
1. Transcription factor protein interactomes reveal genetic determinants in heart disease.
Gonzalez-Teran B; Pittman M; Felix F; Thomas R; Richmond-Buccola D; Hüttenhain R; Choudhary K; Moroni E; Costa MW; Huang Y; Padmanabhan A; Alexanian M; Lee CY; Maven BEJ; Samse-Knapp K; Morton SU; McGregor M; Gifford CA; Seidman JG; Seidman CE; Gelb BD; Colombo G; Conklin BR; Black BL; Bruneau BG; Krogan NJ; Pollard KS; Srivastava D
Cell; 2022 Mar; 185(5):794-814.e30. PubMed ID: 35182466
[TBL] [Abstract][Full Text] [Related]
2. GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5.
Garg V; Kathiriya IS; Barnes R; Schluterman MK; King IN; Butler CA; Rothrock CR; Eapen RS; Hirayama-Yamada K; Joo K; Matsuoka R; Cohen JC; Srivastava D
Nature; 2003 Jul; 424(6947):443-7. PubMed ID: 12845333
[TBL] [Abstract][Full Text] [Related]
3. Combined mutation screening of NKX2-5, GATA4, and TBX5 in congenital heart disease: multiple heterozygosity and novel mutations.
Granados-Riveron JT; Pope M; Bu'lock FA; Thornborough C; Eason J; Setchfield K; Ketley A; Kirk EP; Fatkin D; Feneley MP; Harvey RP; Brook JD
Congenit Heart Dis; 2012; 7(2):151-9. PubMed ID: 22011241
[TBL] [Abstract][Full Text] [Related]
4. Association of NKX2-5, GATA4, and TBX5 polymorphisms with congenital heart disease in Egyptian children.
Behiry EG; Al-Azzouny MA; Sabry D; Behairy OG; Salem NE
Mol Genet Genomic Med; 2019 May; 7(5):e612. PubMed ID: 30834692
[TBL] [Abstract][Full Text] [Related]
5. Interaction of Gata4 and Gata6 with Tbx5 is critical for normal cardiac development.
Maitra M; Schluterman MK; Nichols HA; Richardson JA; Lo CW; Srivastava D; Garg V
Dev Biol; 2009 Feb; 326(2):368-77. PubMed ID: 19084512
[TBL] [Abstract][Full Text] [Related]
6. Disease Model of GATA4 Mutation Reveals Transcription Factor Cooperativity in Human Cardiogenesis.
Ang YS; Rivas RN; Ribeiro AJS; Srivas R; Rivera J; Stone NR; Pratt K; Mohamed TMA; Fu JD; Spencer CI; Tippens ND; Li M; Narasimha A; Radzinsky E; Moon-Grady AJ; Yu H; Pruitt BL; Snyder MP; Srivastava D
Cell; 2016 Dec; 167(7):1734-1749.e22. PubMed ID: 27984724
[TBL] [Abstract][Full Text] [Related]
7. Congenital heart diseases and their association with the variant distribution features on susceptibility genes.
Su W; Zhu P; Wang R; Wu Q; Wang M; Zhang X; Mei L; Tang J; Kumar M; Wang X; Su L; Dong N
Clin Genet; 2017 Mar; 91(3):349-354. PubMed ID: 27426723
[TBL] [Abstract][Full Text] [Related]
8. Cardiac gene activation analysis in mammalian non-myoblasic cells by Nkx2-5, Tbx5, Gata4 and Myocd.
Zhou L; Liu Y; Lu L; Lu X; Dixon RA
PLoS One; 2012; 7(10):e48028. PubMed ID: 23144723
[TBL] [Abstract][Full Text] [Related]
9. A New TBX5 Loss-of-Function Mutation Contributes to Congenital Heart Defect and Atrioventricular Block.
Zhang Y; Sun YM; Xu YJ; Zhao CM; Yuan F; Guo XJ; Guo YH; Yang CX; Gu JN; Qiao Q; Wang J; Yang YQ
Int Heart J; 2020 Jul; 61(4):761-768. PubMed ID: 32641638
[TBL] [Abstract][Full Text] [Related]
10. GATA4 screening in Iranian patients of various ethnicities affected with congenital heart disease: Co-occurrence of a novel de novo translocation (5;7) and a likely pathogenic heterozygous GATA4 mutation in a family with autosomal dominant congenital heart disease.
Kalayinia S; Maleki M; Rokni-Zadeh H; Changi-Ashtiani M; Ahangar H; Biglari A; Shahani T; Mahdieh N
J Clin Lab Anal; 2019 Sep; 33(7):e22923. PubMed ID: 31115957
[TBL] [Abstract][Full Text] [Related]
11. Congenital heart disease-causing Gata4 mutation displays functional deficits in vivo.
Misra C; Sachan N; McNally CR; Koenig SN; Nichols HA; Guggilam A; Lucchesi PA; Pu WT; Srivastava D; Garg V
PLoS Genet; 2012; 8(5):e1002690. PubMed ID: 22589735
[TBL] [Abstract][Full Text] [Related]
12. Nuclear Receptor-Like Structure and Interaction of Congenital Heart Disease-Associated Factors GATA4 and NKX2-5.
Kinnunen S; Välimäki M; Tölli M; Wohlfahrt G; Darwich R; Komati H; Nemer M; Ruskoaho H
PLoS One; 2015; 10(12):e0144145. PubMed ID: 26642209
[TBL] [Abstract][Full Text] [Related]
13. [Association of single nucleotide polymorphisms of transcription factors with congenital heart diseases in the Chinese population: a Meta analysis].
Chen LT; Yang TB; Wang TT; Zheng Z; Zhao LJ; Ye ZW; Zhang SM; Qin JB
Zhongguo Dang Dai Er Ke Za Zhi; 2018 Jun; 20(6):490-496. PubMed ID: 29972125
[TBL] [Abstract][Full Text] [Related]
14. Clinical and molecular characterisation of Holt-Oram syndrome focusing on cardiac manifestations.
Jhang WK; Lee BH; Kim GH; Lee JO; Yoo HW
Cardiol Young; 2015 Aug; 25(6):1093-8. PubMed ID: 25216260
[TBL] [Abstract][Full Text] [Related]
15. Functional analysis of rare variants of GATA4 identified in Chinese patients with congenital heart defect.
Zhao Z; Zhan Y; Chen W; Ma X; Sheng W; Huang G
Genesis; 2019 Nov; 57(11-12):e23333. PubMed ID: 31513339
[TBL] [Abstract][Full Text] [Related]
16. Identification of functional mutations in GATA4 in patients with congenital heart disease.
Wang E; Sun S; Qiao B; Duan W; Huang G; An Y; Xu S; Zheng Y; Su Z; Gu X; Jin L; Wang H
PLoS One; 2013; 8(4):e62138. PubMed ID: 23626780
[TBL] [Abstract][Full Text] [Related]
17. Insights into the genetic structure of congenital heart disease from human and murine studies on monogenic disorders.
Prendiville T; Jay PY; Pu WT
Cold Spring Harb Perspect Med; 2014 Oct; 4(10):. PubMed ID: 25274754
[TBL] [Abstract][Full Text] [Related]
18. A systematic variant screening in familial cases of congenital heart defects demonstrates the usefulness of molecular genetics in this field.
El Malti R; Liu H; Doray B; Thauvin C; Maltret A; Dauphin C; Gonçalves-Rocha M; Teboul M; Blanchet P; Roume J; Gronier C; Ducreux C; Veyrier M; Marçon F; Acar P; Lusson JR; Levy M; Beyler C; Vigneron J; Cordier-Alex MP; Heitz F; Sanlaville D; Bonnet D; Bouvagnet P
Eur J Hum Genet; 2016 Feb; 24(2):228-36. PubMed ID: 26014430
[TBL] [Abstract][Full Text] [Related]
19. [Genetic screening of Gata4 and Nkx2.5 mutations in hereditary congenital heart defects: 5 familial cases].
Pulignani S; Foffa I; Cresci M; Vittorini S; Ait-Ali L; Andreassi MG
Recenti Prog Med; 2011 Mar; 102(3):120-5. PubMed ID: 21572484
[TBL] [Abstract][Full Text] [Related]
20. GATA4 mutations in 357 unrelated patients with congenital heart malformation.
Butler TL; Esposito G; Blue GM; Cole AD; Costa MW; Waddell LB; Walizada G; Sholler GF; Kirk EP; Feneley M; Harvey RP; Winlaw DS
Genet Test Mol Biomarkers; 2010 Dec; 14(6):797-802. PubMed ID: 20874241
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
