...CRELD1, which is associated with atrioventricular septal defect in people with or without DS, and HEY2, whose mouse orth...
...CRELD1 was performed. The analysis revealed the occurrence of the SNP c.985 C>T of CRELD1 in two of CHD patients and not...
...CRELD1 mutations were identified in the calcium-binding EGF domain in patients with AVSD. CRELD1 is likely to be an AVSD...
...CRELD1, GRK5, SLC25A27 and STC2, and 22 of 22 normal endometriums (100%) were negative. Our newly developed autoscan-vir...
...CRELD1 could interact with ectopic or endogenous RTN3. CRELD1 bound with RTN3 so as to increase the localization of RTN3...
...CRELD1, GATA4 and NKX2.5 genes.,Mutation analysis allowed the identification of three sequence variations in two out of ...
...CRELD1, is also known as the AVSD2 gene as mutations in CRELD1 are associated with cardiac atrioventricular septal defec...
...CRELD1 increases susceptibility to AVSD but is not alone sufficient to cause the defect, indicating that AVSD is multige...
...CRELD1 (previously known as "cirrin") as a candidate gene for the AVSD2 locus mapping to chromosome 3p25. Analysis of th...
...CRELD1 (Cysteine-Rich with EGF-Like Domains 1) gene (previously known as cirrin) was cloned from a human chromosome 3 BA...
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