Xie Y - Search Results

1

Paternal Uniparental Disomy of Chromosome 14 with Hypospadias.

Yuan H, Xie Y, Li Q, Hu X, Li X, Sun X, Zhao W. Yuan H, et al. Among authors: xie y. Cytogenet Genome Res. 2016;148(4):256-61. doi: 10.1159/000446783. Epub 2016 Jun 15. Cytogenet Genome Res. 2016. PMID: 27300571

2

Clinical outcome: a monosomy 18p is better than a tetrasomy 18p.

Wei J, Xie Y, He W, Liu W, Jian W, Chen M, Wang D, Wang X, Sun X. Wei J, et al. Among authors: xie y. Cytogenet Genome Res. 2014;144(4):294-8. doi: 10.1159/000371461. Epub 2015 Jan 28. Cytogenet Genome Res. 2014. PMID: 25634515

3

Single nucleotide polymorphism-based microarray analysis for the diagnosis of hydatidiform moles.

Xie Y, Pei X, Dong Y, Wu H, Wu J, Shi H, Zhuang X, Sun X, He J. Xie Y, et al. Mol Med Rep. 2016 Jul;14(1):137-44. doi: 10.3892/mmr.2016.5211. Epub 2016 May 5. Mol Med Rep. 2016. PMID: 27151252 Free PMC article.

4

FGFR3 gene mutation plus GRB10 gene duplication in a patient with achondroplasia plus growth delay with prenatal onset.

Yuan H, Huang L, Hu X, Li Q, Sun X, Xie Y, Kong S, Wang X. Yuan H, et al. Among authors: xie y. Orphanet J Rare Dis. 2016 Jul 2;11(1):89. doi: 10.1186/s13023-016-0465-4. Orphanet J Rare Dis. 2016. PMID: 27370225 Free PMC article.

5

Autophagy Promoted the Degradation of Mutant ATXN3 in Neurally Differentiated Spinocerebellar Ataxia-3 Human Induced Pluripotent Stem Cells.

Ou Z, Luo M, Niu X, Chen Y, Xie Y, He W, Song B, Xian Y, Fan D, OuYang S, Sun X. Ou Z, et al. Among authors: xie y. Biomed Res Int. 2016;2016:6701793. doi: 10.1155/2016/6701793. Epub 2016 Oct 25. Biomed Res Int. 2016. PMID: 27847820 Free PMC article.

6

A Rare de novo Interstitial Duplication at 4p15.2 in a Boy with Severe Congenital Heart Defects, Limb Anomalies, Hypogonadism, and Global Developmental Delay.

Liang L, Xie Y, Shen Y, Yin Q, Yuan H. Liang L, et al. Among authors: xie y. Cytogenet Genome Res. 2016;150(2):112-117. doi: 10.1159/000454698. Epub 2016 Dec 29. Cytogenet Genome Res. 2016. PMID: 28030855

7

Psychomotor retardation with a 1q42.11-q42.12 deletion.

He J, Xie Y, Kong S, Qiu W, Wang X, Wang D, Sun X, Sun D. He J, et al. Among authors: xie y. Hereditas. 2017 Mar 6;154:6. doi: 10.1186/s41065-016-0022-0. eCollection 2017. Hereditas. 2017. PMID: 28286461 Free PMC article.

8

Chromosomal microarray analysis in prenatal diagnosis.

Xie Y, Sun X. Xie Y, et al. Clin Exp Obstet Gynecol. 2017;44(2):177-179. Clin Exp Obstet Gynecol. 2017. PMID: 29746015 Review.

9

Antioxidants retard the ageing of mouse oocytes.

Xian Y, Liang L, Qi S, Xie Y, Song B, Ouyang S, Xie Y, Sun X, Wang W. Xian Y, et al. Among authors: xie y. Mol Med Rep. 2018 Aug;18(2):1981-1986. doi: 10.3892/mmr.2018.9167. Epub 2018 Jun 14. Mol Med Rep. 2018. PMID: 29901147 Free PMC article.

10

Establishment of an ectodermal dysplasia related gene EDA Knockout human embryonic stem cell line (WAe001-A-22) by CRISPR-Cas9 technology.

Xue Y, Liao B, Xie Y, Li S, Ma X, Sun X. Xue Y, et al. Among authors: xie y. Stem Cell Res. 2019 Jan;34:101379. doi: 10.1016/j.scr.2018.101379. Epub 2018 Dec 21. Stem Cell Res. 2019. PMID: 30605838 Free article.

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