Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Songchang Chen"'
Publikováno v:
BMC Cancer
BMC Cancer, Vol 21, Iss 1, Pp 1-12 (2021)
BMC Cancer, Vol 21, Iss 1, Pp 1-12 (2021)
Background Little data is available on prognostic biomarkers and effective treatment options for Kidney Renal Papillary Cell Carcinoma (KIRP) patients, to find potential prognostic biomarkers and new targets was an urgent mission for KIRP therapy. Me
Publikováno v:
Journal of Ovarian Research, Vol 14, Iss 1, Pp 1-12 (2021)
Journal of Ovarian Research
Journal of Ovarian Research
Background Existing clinical methods for prognosis evaluating for Epithelial Ovarian Cancer (EOC) patients had defects of invasive, unsystematic and subjective and little data are available for individualizing treatment, therefore, to identify potent
Autor:
Hefeng Huang, Chunxin Chang, Chenming Xu, Yiyao Chen, Hongjun Fei, Weihui Shi, Lanlan Zhang, Jun-Yu Zhang, Shuyuan Li, Songchang Chen
Publikováno v:
Journal of Bio-X Research, Vol 1, Iss 3, Pp 140-146 (2018)
Kabuki syndrome (KS) is a rare congenital mental retardation condition characterized by facial dysmorphia, visceral and skeletal malformations, and developmental delay. The integrated phenotype and genotype-based prioritization is critical for diagno
Autor:
Bing Wei, Songchang Chen, Li Jin, Luting Chen, Xiaojin Wang, Hefeng Huang, Bingshun Wang, Huixi Chen, Zhengmu Wu
Publikováno v:
Reproductive biomedicine online. 43(1)
Research question What is the association between homocysteine (Hcy) and IVF/intracytoplasmic sperm injection (ICSI) outcomes, stratified by methylenetetrahydrofolate reductase (MTHFR) C677T polymorphisms? Design This prospective cohort study recruit
Autor:
Songchang Chen, Jianmei Niu, Yanlin Wang, Mujin Ye, Yinghua Shen, Shuyuan Li, Xu Han, Chenming Xu
Publikováno v:
Prenatal diagnosisREFERENCES. 40(12)
Objective To evaluate whether chromosomal microarray (CMA) should be offered to fetuses with ultrasonographic soft markers (USMs) in the second trimester. Methods A prospective cohort study and meta-analysis were conducted. In the prospective cohort
Autor:
Qiong Luo, Chenming Xu, Hua Wang, Songchang Chen, Yanting Wu, Hui Xi, He-Feng Huang, Dan Zhang, Jinglan Zhang, Xiaoqiang Cai
Publikováno v:
BMJ Open, Vol 11, Iss 8 (2021)
BMJ Open
BMJ Open
IntroductionChromosomal abnormalities and monogenic disorders account for ~15%–25% of recognisable birth defects. With limited treatment options, preconception and prenatal screening were developed to reduce the incidence of such disorders. Current
Autor:
Shuyuan Li, Xu Han, Mujin Ye, Songchang Chen, Yinghua Shen, Jianmei Niu, Yanlin Wang, Chenming Xu
Publikováno v:
Frontiers in Genetics, Vol 10 (2019)
Frontiers in Genetics
Frontiers in Genetics
Several recurrent microdeletions and microduplications in the proximal, central, and distal regions of chromosomal 22q11.2 have been identified. However, due to a limited number of patients reported in the literature, highly variable clinical phenoty
Autor:
Xiaoxia Bai, Ning-Ning Hou, Bo Zhu, Yanmei Yang, Minmin Jiang, Songchang Chen, Jun-Yu Zhang, Yuting Hu, He-Feng Huang, Feng Chen, Chenming Xu
Publikováno v:
Reproductive BioMedicine Online. 32:407-413
This study investigated the association between premature ovarian failure (POF), MTHFR C677T/A1298C and MTRR A66G genotypes and serum homocysteine (Hcy) concentration. A prospective study was conducted in Chinese women, which included POF patients (n
Autor:
Xu Han, Li Jin, Songchang Chen, Yanlin Wang, Jianmei Niu, Shuyuan Li, Zhaoxia Qian, Chenming Xu, Pin Li
Publikováno v:
Prenatal diagnosis. 39(3)
Objective To evaluate the usefulness and incremental diagnostic yield of chromosomal microarray analysis (CMA) compared with standard karyotyping in fetuses with congenital anomalies of the kidney and urinary tract (CAKUT). Methods A prospective coho
Autor:
Yuting Hu, He-Feng Huang, Songchang Chen, Yiyao Chen, Jun-Yu Zhang, Shuyuan Li, Xiao-Ping Qi, Li Jin, Chenming Xu, Lanlan Zhang, Li Wang
Publikováno v:
Thyroid : official journal of the American Thyroid Association. 28(3)
The revised guidelines for the management of medullary thyroid carcinoma recommend that genetic counseling regarding reproductive options, including preimplantation genetic diagnosis (PGD), be considered for all RET mutation carriers of reproductive