188 related articles for article (PubMed ID: 32134193)
1. Haploinsufficiency of the basic helix-loop-helix transcription factor HAND2 causes congenital heart defects.
Cohen ASA; Simotas C; Webb BD; Shi H; Khan WA; Edelmann L; Scott SA; Singh R
Am J Med Genet A; 2020 May; 182(5):1263-1267. PubMed ID: 32134193
[TBL] [Abstract][Full Text] [Related]
2. A HAND2 Loss-of-Function Mutation Causes Familial Ventricular Septal Defect and Pulmonary Stenosis.
Sun YM; Wang J; Qiu XB; Yuan F; Li RG; Xu YJ; Qu XK; Shi HY; Hou XM; Huang RT; Xue S; Yang YQ
G3 (Bethesda); 2016 Apr; 6(4):987-92. PubMed ID: 26865696
[TBL] [Abstract][Full Text] [Related]
3. A novel HAND2 loss-of-function mutation responsible for tetralogy of Fallot.
Lu CX; Gong HR; Liu XY; Wang J; Zhao CM; Huang RT; Xue S; Yang YQ
Int J Mol Med; 2016 Feb; 37(2):445-51. PubMed ID: 26676105
[TBL] [Abstract][Full Text] [Related]
4. Cardiac neural crest expression of Hand2 regulates outflow and second heart field development.
Morikawa Y; Cserjesi P
Circ Res; 2008 Dec; 103(12):1422-9. PubMed ID: 19008477
[TBL] [Abstract][Full Text] [Related]
5. HAND transcription factors cooperatively specify the aorta and pulmonary trunk.
Vincentz JW; Firulli BA; Toolan KP; Osterwalder M; Pennacchio LA; Firulli AB
Dev Biol; 2021 Aug; 476():1-10. PubMed ID: 33757801
[TBL] [Abstract][Full Text] [Related]
6. Transcription factor HAND2 mutations in sporadic Chinese patients with congenital heart disease.
Shen L; Li XF; Shen AD; Wang Q; Liu CX; Guo YJ; Song ZJ; Li ZZ
Chin Med J (Engl); 2010 Jul; 123(13):1623-7. PubMed ID: 20819618
[TBL] [Abstract][Full Text] [Related]
7. Overdosage of Hand2 causes limb and heart defects in the human chromosomal disorder partial trisomy distal 4q.
Tamura M; Hosoya M; Fujita M; Iida T; Amano T; Maeno A; Kataoka T; Otsuka T; Tanaka S; Tomizawa S; Shiroishi T
Hum Mol Genet; 2013 Jun; 22(12):2471-81. PubMed ID: 23449628
[TBL] [Abstract][Full Text] [Related]
8. Chromosome 5q33 deletions associated with congenital heart defects.
Starkovich M; Lalani SR; Mercer CL; Scott DA
Am J Med Genet A; 2016 Dec; 170(12):3338-3342. PubMed ID: 27589475
[TBL] [Abstract][Full Text] [Related]
9. Long non-coding RNA SAP30-2:1 is downregulated in congenital heart disease and regulates cell proliferation by targeting HAND2.
Ma J; Chen S; Hao L; Sheng W; Chen W; Ma X; Zhang B; Ma D; Huang G
Front Med; 2021 Feb; 15(1):91-100. PubMed ID: 32820380
[TBL] [Abstract][Full Text] [Related]
10. Cardiac phenotypes in chromosome 4q- syndrome with and without a deletion of the dHAND gene.
Huang T; Lin AE; Cox GF; Golden WL; Feldman GL; Ute M; Schrander-Stumpel C; Kamisago M; Vermeulen SJ
Genet Med; 2002; 4(6):464-7. PubMed ID: 12509719
[TBL] [Abstract][Full Text] [Related]
11. The lncRNA
Han X; Zhang J; Liu Y; Fan X; Ai S; Luo Y; Li X; Jin H; Luo S; Zheng H; Yue Y; Chang Z; Yang Z; Tang F; He A; Shen X
Development; 2019 Jul; 146(13):. PubMed ID: 31273086
[TBL] [Abstract][Full Text] [Related]
12. Transcription of the non-coding RNA upperhand controls Hand2 expression and heart development.
Anderson KM; Anderson DM; McAnally JR; Shelton JM; Bassel-Duby R; Olson EN
Nature; 2016 Nov; 539(7629):433-436. PubMed ID: 27783597
[TBL] [Abstract][Full Text] [Related]
13. Targeted deletion of Hand2 in cardiac neural crest-derived cells influences cardiac gene expression and outflow tract development.
Holler KL; Hendershot TJ; Troy SE; Vincentz JW; Firulli AB; Howard MJ
Dev Biol; 2010 May; 341(1):291-304. PubMed ID: 20144608
[TBL] [Abstract][Full Text] [Related]
14. Gene replacement strategies to test the functional redundancy of basic helix-loop-helix transcription factor.
Firulli AB; Firulli BA; Wang J; Rogers RH; Conway SJ
Pediatr Cardiol; 2010 Apr; 31(3):438-48. PubMed ID: 20155416
[TBL] [Abstract][Full Text] [Related]
15. Conditional deletion of Hand2 reveals critical functions in neurogenesis and cell type-specific gene expression for development of neural crest-derived noradrenergic sympathetic ganglion neurons.
Hendershot TJ; Liu H; Clouthier DE; Shepherd IT; Coppola E; Studer M; Firulli AB; Pittman DL; Howard MJ
Dev Biol; 2008 Jul; 319(2):179-91. PubMed ID: 18501887
[TBL] [Abstract][Full Text] [Related]
16. A HAND to TBX5 Explains the Link Between Thalidomide and Cardiac Diseases.
Khalil A; Tanos R; El-Hachem N; Kurban M; Bouvagnet P; Bitar F; Nemer G
Sci Rep; 2017 May; 7(1):1416. PubMed ID: 28469241
[TBL] [Abstract][Full Text] [Related]
17. MESP2 variants contribute to conotruncal heart defects by inhibiting cardiac neural crest cell proliferation.
Zhang E; Yang J; Liu Y; Hong N; Xie H; Fu Q; Li F; Chen S; Yu Y; Sun K
J Mol Med (Berl); 2020 Jul; 98(7):1035-1048. PubMed ID: 32572506
[TBL] [Abstract][Full Text] [Related]
18. The basic-helix-loop-helix transcription factor HAND2 directly regulates transcription of the atrial naturetic peptide gene.
Thattaliyath BD; Firulli BA; Firulli AB
J Mol Cell Cardiol; 2002 Oct; 34(10):1335-44. PubMed ID: 12392994
[TBL] [Abstract][Full Text] [Related]
19. The Hand2 gene dosage effect in developmental defects and human congenital disorders.
Tamura M; Amano T; Shiroishi T
Curr Top Dev Biol; 2014; 110():129-52. PubMed ID: 25248475
[TBL] [Abstract][Full Text] [Related]
20. Specification of jaw identity by the Hand2 transcription factor.
Funato N; Kokubo H; Nakamura M; Yanagisawa H; Saga Y
Sci Rep; 2016 Jun; 6():28405. PubMed ID: 27329940
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
