Y. 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.

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 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.

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.

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.

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.

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.

Novel Mutations of ABCB6 Associated with Autosomal Dominant Dyschromatosis Universalis Hereditaria

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

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 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.

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.

[Protective effect of L-carnitine combined with sildenafil on the reproductive endocrine function of diabetic male rats].

Yu-feng Huang, X. Shang, X. Zhan, 2012, Zhonghua nan ke xue = National journal of andrology.

Gonosomal mosaicism from deleted Y chromosomal nondisjunction.

Yun-hua Wang, Yu-feng Huang, B. Yao, 2006, Journal of andrology.

The susceptibility of FSHB -211G > T and FSHR G-29A, 919A > G, 2039A > G polymorphisms to men infertility: an association study and meta-analysis

X. Xia, Shuai-mei Liu, Ming-chao Zhang, 2017, BMC Medical Genetics.

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 .

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.

A parthenogenetic maternal and double paternal contribution to an ovotesticular disorder of sex development

Hongliu Gao, Xiao-jun Li, Wei-ping Wang, 2014, Molecular Cytogenetics.

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.

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.

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

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

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.

A case of agonadism associated with y-chromosome rearrangement: cytogenetic and molecular studies.

Li Jia, Hong-yong Lu, Hai-feng Shao, 2009, Journal of andrology.

[Genetic causes of male infertility].

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

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 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.

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.

[The paternal origin of an extra chromosome 13 from the patient with patau syndrome.].

Yu-feng Huang, Y. Cui, Yongmei Wang, 2005, Yi chuan = Hereditas.

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

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

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

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

Rapid molecular prenatal diagnosis of spondyloepiphyseal dysplasia congenita by PCR-SSP assay.

Hong-yong Lu, Yu-feng Huang, G. Zhou, 2008, Genetic testing.

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.

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.

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.

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.

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.

Partial trisomy 4q: a case report.

Yun-hua Wang, Yun-feng Huang, Y. Cui, 2006, Chinese medical journal.

An infertile male with apparent 45,X turned out to have 45,X,der(Y)t(Y;13)(q11.2;q12),-13: clinicopathologic and cytogenomic studies.

Yun-hua Wang, Yu-feng Huang, B. Yao, 2007, Fertility and sterility.

[A girl with partial monosomy 18q21: cytogenetic and molecular genetics studies].

Hong-yong Lu, Yu-feng Huang, B. Yao, 2008, Yi chuan = Hereditas.

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.