Aguayo-Gómez(Adolfo),Arteaga-Vázquez(Jazmí... Pediatr Cardiol 2016-09-09

...CRELD1). The MLPA assay detected a de novo CNV deletion of the probes located in exons 2 and 7 of the TBX1 gene in one o...

Alcántara-Ortigoza(Miguel A),De Rubens-Fig... Pediatr Cardiol 2015-12-17

...CRELD1 mutations, but no previous study has examined the candidate genes, NKX2-5 and GATA4, in DS patients with secundum...

Saji(Tsutomu) Pediatr Int 2015-10-14

...CRELD1 and GATA4 in cardiac abnormalities or their association with pulmonary artery histopathology. Children with DS ha...

Dong(Kunzhe),Yao(Na),Pu(Yabin),He(Xiaohong... PLoS One 2015-12-22

...CRELD1 and RHOG) for DHP. In addition, six selective genes (VPS13A, GNA14, GDAP1, PARP8, FGF10 and ADAMTS16) were shared...

Mass(Elvira),Wachten(Dagmar),Aschenbrenner... Dev Cell 2014-05-21

...Creld1KO mice, we demonstrate that Creld1 is essential for heart development. Creld1 function is required for the VEGF-d...

Guo(Ying),Shen(Jie),Li(Fen),Wang(Jian),Wan... Zhonghua Yi Xue Yi Chuan Xu... 2014-07-29

...CRELD1 gene may increase the risk for AVSD rather than being directly causative. The P286R mutation of CRELD1 can downre...

Peltekova(Iskra T),Macdonald(Athen),Armour... Am J Med Genet A 2013-02-19

...CRELD1, SRGAP3, CAMK1, TADA3, and MTMR14 are discussed with respect to their potential involvement in the 3p deletion sy...

Ghosh(Priyanka),Bhaumik(Pranami),Ghosh(Suj... Am J Med Genet A 2013-06-21

...CRELD1 variants on congenital heart defects, we sequenced the entire reading frame of CRELD1 in the samples from Kolkata...

Ackerman(Christine),Locke(Adam E),Feingold... Am J Hum Genet 2013-03-17

...CRELD1, FBLN2, FRZB, and GATA5. Several of the case-specific variants were recurrent in unrelated individuals, occurring...

Hansen(Henning Gram),Schmidt(Jonas Damgård... J Biol Chem 2013-02-19

...CRELD1 and c18orf45. Interestingly, a broad antioxidant response was not induced. Our findings suggest that the hyperoxi...