相关期刊:《World Journal of Cardiology》《American Journal of Molecular Biology》《Open Journal of Pediatrics》《Journal of Zhejiang University-Science B(Biomedicine & Biotechnology)》更多>>
Dear Editor, Recently, Ren et al. reported an extensive analysis of the incidence of whole genome duplications (WGDs) throughout the evolutionary history of extant angiosperms (Ren et al., 2018). Examining a wealth of...
Genetic analyses of patients with transposition of the great arteries have identified rare copy number variations,suggesting that they may be significant to the aetiology of the disease.This paper reports the identifi...
supported by grants to Q.W.from the National Natural Science Foundation of China(31171015 and 31470820);the Science and Technology Commission of Shanghai Municipality(13XD1402000 and 14JC1403600).
The human genome contains millions of DNA regulatory elements and a large number of gene clusters,most of which have not been tested experimentally.The clustered regularly interspaced short palindromic repeats(CRISPR)...
Alimentary tract duplications are rare congenital lesions normally diagnosed in newborns and children that can occur anywhere from the mouth to the anus and have a reported incidence of approximately 1 in 4500 life bi...
Tuberous sclerosis complex (TSC) is an autosomal dominant disorder characterized by formation of benign tumors called hamartomas. Although the TSC is diagnosed based on clinical findings but approximately 85% of indiv...
Background: Alimentary tract duplications (ATDs) are rare congenital anomalies of the gut tube, seen mainly in neonates and infants. Their presentations are often mimicking other conditions, thus posing a diagnostic c...
Project(No.GREKF09-08)supported by the State Key Laboratory of Genetic Resources and Evolution,Kunming Institute of Zoology,Chinese Academy of Sciences,China
Objective:There are many reports on associations between spermatogenesis and partial azoospermia factor c(AZFc) deletions as well as duplications;however,results are conflicting,possibly due to differences in methodol...
The proteins, which bind albuminspecific dye Evans blue, are revealed in the low-molecular protein fraction of the blood serum from Scorpaena porcus L. and identified as serum albumin. They were represented by three b...
Objective:Duchenne muscular dystrophy (DMD) and Becker muscular dystrophy (BMD) are X-linked disorders caused by mutations in the dystrophin gene. The majority of recognized mutations are copy number changes of i...
the National NaturalSciencc Foundation of China (90208022,30471067) ; IBM Shared University Research (LifeScience).
Genes are continually being created by the processes of genome duplication (ohnolog) and gene duplication (paralog). Whole-genome duplications have been found to be widespread in plant species and play an importan...