Ying-xia Cui

发表

Clinical and cytogenetic characterization of a boy with a de novo pure partial trisomy 16q24.1q24.3 and complex chromosome rearrangement

Q. Yao, B. Yao, Xiao-jun Li, 2013, American journal of medical genetics. Part A.

Meiotic pairing error in an infertile male bearing reciprocal deletion of chromosome 13.

Yu-feng Huang, B. Yao, Xiao-jun Li, 2011, Journal of andrology.

Three Novel Heterozygous COL4A4 Mutations Result in Three Different Collagen Type IV Kidney Disease Phenotypes

Asan, Zhi-Hong Liu, Z. Xia, 2018, Cytogenetic and Genome Research.

Clinical, molecular and cytogenetic analysis of 46, XX testicular disorder of sex development with SRY-positive

Y. Cui, X. Xia, Tianfu Li, 2014, BMC Urology.

A novel COL4A1 gene mutation results in autosomal dominant non-syndromic congenital cataract in a Chinese family

Xiao-jun Li, Y. Cui, X. Xia, 2014, BMC Medical Genetics.

The effect of induced anti-follicle-stimulating hormone autoantibody on serum hormone level and apoptosis in rat testis.

W. Ouyang, Shui-gen Zhou, N. Yi, 2012, Life sciences.

Follicle-stimulating hormone autoantibody is involved in idiopathic spermatogenic dysfunction.

W. Liang, Y. Cui, Y. Ge, 2008, Asian journal of andrology.

[Detection and potential function of anti-FSH antibodies in patients with spermatogenesis dysfunction].

Yufeng Huang, B. Yao, Leilei Zhang, 2004, Zhonghua nan ke xue = National journal of andrology.

A novel splice site mutation in the dentin sialophosphoprotein gene in a Chinese family with dentinogenesis imperfecta type II.

Xiaojun Li, Hao-yang Wang, Yanning Hou, 2009, Mutation research.

A G560S mutation in alpha1 (I) collagen causes familial osteogenesis imperfecta type IV.

Yu-feng Huang, B. Yao, Xiao-jun Li, 2009, Clinica chimica acta; international journal of clinical chemistry.

Identification of novel mutations and risk assessment of Han Chinese patients with autosomal dominant polycystic kidney disease

Xiaojun Li, X. Xia, Shuai-mei Liu, 2019, Nephrology.

The P20R mutation of αB-crystallin diminishes its anti-apoptotic activity in human lens epithelial cells.

Xiaojun Li, X. Xia, Shuai-mei Liu, 2017, Biochemical and biophysical research communications.

Polymorphisms in estrogen receptors predict the risk of male infertility: a meta-analysis

Xiao-jun Li, Y. Cui, X. Xia, 2014, Reproductive Biology and Endocrinology.

[Detection of DPY19L2 gene mutation in a globozoospermia patient].

X. Xia, Y. Shao, Tianfu Li, 2013, Zhonghua nan ke xue = National journal of andrology.

Polymorphisms of protamine genes contribute to male infertility susceptibility in the Chinese Han population

X. Xia, Shuai-mei Liu, P. Zhu, 2017, Oncotarget.

A novel P20R mutation in the alpha-B crystallin gene causes autosomal dominant congenital posterior polar cataracts in a Chinese family

Xiao-jun Li, Y. Cui, X. Xia, 2014, BMC Ophthalmology.

Long-term effects of phytoestrogen daidzein on penile cavernosal structures in adult rats.

Yufeng Huang, X. Xia, Y. Cui, 2008, Urology.

Novel Mutations of ABCB6 Associated with Autosomal Dominant Dyschromatosis Universalis Hereditaria

G. Wang, X. Shang, B. Yao, 2013, PloS one.

Meiotic prophase I defects in an oligospermic man with Wolf-Hirschhorn syndrome with ring chromosome 4

Liu Wang, Qinghua Shi, X. Xia, 2014, Molecular Cytogenetics.

Meiotic chromosome behavior in a human male t(8;15) carrier.

Liu Wang, Qinghua Shi, Ying-xia Cui, 2014, Journal of genetics and genomics = Yi chuan xue bao.

The COL4A3 and COL4A4 Digenic Mutations in cis Result in Benign Familial Hematuria in a Large Chinese Family

Asan, Zhi-Hong Liu, Z. Xia, 2018, Cytogenetic and Genome Research.

Gonadotropin-releasing hormone positively regulates steroidogenesis via extracellular signal-regulated kinase in rat Leydig cells.

Hai-yan Liu, Yu-chun Gu, Xiao-qian Tao, 2011, Asian journal of andrology.

A patient with unusual features and a 69.5 Mb duplication from a de novo extra der (9): A case report

Yu-feng Huang, Xiao-jun Li, Y. Cui, 2015, Molecular medicine reports.

The patient spoke at the age of 3-years and walked without assistance at the age of 2-years

Yu-feng Huang, Y. Cui, X. Xia, 2015 .

ORIGINAL ARTICLE: A rare Y chromosome constitutional rearrangement: a partial AZFb deletion and duplication within chromosome Yp in an infertile man with severe oligoasthenoteratozoospermia: Partial AZFb deletion and duplication within Yp

Hao-yang Wang, Hong-yong Lu, Yu-feng Huang, 2010 .

Novel mutations in COL4A3, COL4A4, and COL4A5 in Chinese patients with Alport Syndrome

Asan, Xiao-Jun Li, Zhi-Hong Liu, 2017, PloS one.

A Novel p. Gly630Ser Mutation of COL2A1 in a Chinese Family with Presentations of Legg–Calvé–Perthes Disease or Avascular Necrosis of the Femoral Head

Xiao-jun Li, X. Xia, Tianfu Li, 2014, PLoS ONE.

A first familial G504S mutation of COL2A1 gene results in distinctive spondyloepiphyseal dysplasia congenita.

Yufeng Huang, X. Xia, B. Jin, 2007, Clinica chimica acta; international journal of clinical chemistry.

A novel mild variant of osteogenesis imperfecta type I caused by a Gly1088Glu mutation in COL1A1.

Xiao-jun Li, X. Xia, Wei-wei Li, 2014, Molecular medicine reports.

A novel RNA-splicing mutation in COL1A1 gene causing osteogenesis imperfecta type I in a Chinese family.

Yi Shi, Bin-Cheng Yang, Hao-yang Wang, 2008, Clinica chimica acta; international journal of clinical chemistry.

[Genetic causes of male infertility].

Yu-feng Huang, Y. Cui, X. Xia, 2008, Zhonghua nan ke xue = National journal of andrology.

A novel insertion mutation in the SEDL gene results in X-linked spondyloepiphyseal dysplasia tarda in a large Chinese pedigree.

Yi Shi, Ting-Ting Huang, Yu-feng Huang, 2009, Clinica chimica acta; international journal of clinical chemistry.

A mouse model for X-linked Alport syndrome induced by Del-ATGG in the Col4a5 gene

C. Zeng, Weiqin Wu, Shan Duan, 2023, Frontiers in Medicine.

A girl with distinctive features of borderline high blood pressure, short stature, characteristic brachydactyly, and 11.47 Mb deletion in 12p11.21–12p12.2 by oligonucleotide array CGH

Hong-yong Lu, Yu-feng Huang, B. Yao, 2009, American journal of medical genetics. Part A.

A duplication upstream of SOX9 was not positively correlated with the SRY-negative 46,XX testicular disorder of sex development: A case report and literature review

Xiao-jun Li, Y. Cui, X. Xia, 2015, Molecular medicine reports.

46,XX testicular disorder of sexual development with SRY-negative caused by some unidentified mechanisms: a case report and review of the literature

Y. Cui, X. Xia, Qing Zhou, 2014, BMC Urology.

[Advances in gonadal differentiation regulated by SRY].

Yufeng Huang, Ying-xia Cui, 2004, Zhonghua nan ke xue = National journal of andrology.

Exposure of juvenile rats to the phytoestrogen daidzein impairs erectile function in a dose-related manner in adulthood.

Yufeng Huang, X. Xia, Y. Cui, 2008, Journal of andrology.

Association between ubiquitin-specific protease USP26 polymorphism and male infertility in Chinese men.

Hao-yang Wang, Hong Li, Yu-feng Huang, 2011, Clinica chimica acta; international journal of clinical chemistry.

A rare Y chromosome constitutional rearrangement: a partial AZFb deletion and duplication within chromosome Yp in an infertile man with severe oligoasthenoteratozoospermia.

H. Y. Wang, Hao-yang Wang, Hong-yong Lu, 2011, International journal of andrology.

Prenatal diagnosis and genetic counseling in a fetus associated with risk of Angelman syndrome with a small supernumerary marker chromosome derived from chromosome 22

Xiaobo Fan, Weiping Wang, Weiwei Li, 2016, Molecular Cytogenetics.

[Effects of semen analysis on human sperm movement parameters at different times after semen collection].

Jin-Chun Lu, Yu-feng Huang, X. Shang, 2010, Zhonghua nan ke xue = National journal of andrology.