73 related articles for article (PubMed ID: 25230848)
1. Disruption of the SEMA3D gene in a patient with congenital heart defects.
Sanchez-Castro M; Pichon O; Briand A; Poulain D; Gournay V; David A; Le Caignec C
Hum Mutat; 2015 Jan; 36(1):30-3. PubMed ID: 25230848
[TBL] [Abstract][Full Text] [Related]
2. Semaphorin3D regulates invasion of cardiac neural crest cells into the primary heart field.
Sato M; Tsai HJ; Yost HJ
Dev Biol; 2006 Oct; 298(1):12-21. PubMed ID: 16860789
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Semaphorin3d mediates Cx43-dependent phenotypes during fin regeneration.
Ton QV; Kathryn Iovine M
Dev Biol; 2012 Jun; 366(2):195-203. PubMed ID: 22542598
[TBL] [Abstract][Full Text] [Related]
5. Semaphorin 3d promotes cell proliferation and neural crest cell development downstream of TCF in the zebrafish hindbrain.
Berndt JD; Halloran MC
Development; 2006 Oct; 133(20):3983-92. PubMed ID: 16971468
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Characteristic defects in neural crest cell-specific Galphaq/Galpha11- and Galpha12/Galpha13-deficient mice.
Dettlaff-Swiercz DA; Wettschureck N; Moers A; Huber K; Offermanns S
Dev Biol; 2005 Jun; 282(1):174-82. PubMed ID: 15936338
[TBL] [Abstract][Full Text] [Related]
8. Misregulation of SDF1-CXCR4 signaling impairs early cardiac neural crest cell migration leading to conotruncal defects.
Escot S; Blavet C; Härtle S; Duband JL; Fournier-Thibault C
Circ Res; 2013 Aug; 113(5):505-16. PubMed ID: 23838132
[TBL] [Abstract][Full Text] [Related]
9. High frequency of submicroscopic genomic aberrations detected by tiling path array comparative genome hybridisation in patients with isolated congenital heart disease.
Erdogan F; Larsen LA; Zhang L; Tümer Z; Tommerup N; Chen W; Jacobsen JR; Schubert M; Jurkatis J; Tzschach A; Ropers HH; Ullmann R
J Med Genet; 2008 Nov; 45(11):704-9. PubMed ID: 18713793
[TBL] [Abstract][Full Text] [Related]
10. Sema3D, Sema3F, and Sema5A are expressed in overlapping and distinct patterns in chick embryonic heart.
Jin Z; Chau MD; Bao ZZ
Dev Dyn; 2006 Jan; 235(1):163-9. PubMed ID: 16261621
[TBL] [Abstract][Full Text] [Related]
11. Repulsion and attraction of axons by semaphorin3D are mediated by different neuropilins in vivo.
Wolman MA; Liu Y; Tawarayama H; Shoji W; Halloran MC
J Neurosci; 2004 Sep; 24(39):8428-35. PubMed ID: 15456815
[TBL] [Abstract][Full Text] [Related]
12. Congenital heart disease reminiscent of partial trisomy 2p syndrome in mice transgenic for the transcription factor Lbh.
Briegel KJ; Baldwin HS; Epstein JA; Joyner AL
Development; 2005 Jul; 132(14):3305-16. PubMed ID: 15958514
[TBL] [Abstract][Full Text] [Related]
13. [Detection of cryptic copy number variations in a fetus with congenital heart disease by array-based comparative genomic hybridization].
HU P; WANG Y; JI XQ; LIN Y; Li L; ZHOU XY; CHEN J; MA DY; CAO L; Xu Z
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Apr; 28(2):133-6. PubMed ID: 21462121
[TBL] [Abstract][Full Text] [Related]
14. Cryptic chromosomal abnormalities identified in children with congenital heart disease.
Richards AA; Santos LJ; Nichols HA; Crider BP; Elder FF; Hauser NS; Zinn AR; Garg V
Pediatr Res; 2008 Oct; 64(4):358-63. PubMed ID: 18535492
[TBL] [Abstract][Full Text] [Related]
15. Detection of submicroscopic chromosomal aberrations by array-based comparative genomic hybridization in fetuses with congenital heart disease.
Yan Y; Wu Q; Zhang L; Wang X; Dan S; Deng D; Sun L; Yao L; Ma Y; Wang L
Ultrasound Obstet Gynecol; 2014 Apr; 43(4):404-12. PubMed ID: 24323407
[TBL] [Abstract][Full Text] [Related]
16. Cardiac neural crest and outflow tract defects in Lrp6 mutant mice.
Song L; Li Y; Wang K; Zhou CJ
Dev Dyn; 2010 Jan; 239(1):200-10. PubMed ID: 19705442
[TBL] [Abstract][Full Text] [Related]
17. Differential duplication of an intronic region in the NFATC1 gene in patients with congenital heart disease.
Yehya A; Souki R; Bitar F; Nemer G
Genome; 2006 Sep; 49(9):1092-8. PubMed ID: 17110989
[TBL] [Abstract][Full Text] [Related]
18. Semaphorin 3d guides laterality of retinal ganglion cell projections in zebrafish.
Sakai JA; Halloran MC
Development; 2006 Mar; 133(6):1035-44. PubMed ID: 16467361
[TBL] [Abstract][Full Text] [Related]
19. TBX2 gene duplication associated with complex heart defect and skeletal malformations.
Radio FC; Bernardini L; Loddo S; Bottillo I; Novelli A; Mingarelli R; Dallapiccola B
Am J Med Genet A; 2010 Aug; 152A(8):2061-6. PubMed ID: 20635360
[TBL] [Abstract][Full Text] [Related]
20. Novel PITX2c loss-of-function mutations associated with complex congenital heart disease.
Wei D; Gong XH; Qiu G; Wang J; Yang YQ
Int J Mol Med; 2014 May; 33(5):1201-8. PubMed ID: 24604414
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
