Zhang YL - Search Results

1

Ndufa4 Regulates the Proliferation and Apoptosis of Neurons via miR-145a-5p/Homer1/Ccnd2.

Fu F, Chen C, Du K, Li LS, Li R, Lei TY, Deng Q, Wang D, Yu QX, Yang X, Han J, Pan M, Zhen L, Zhang LN, Li J, Li FT, Zhang YL, Jing XY, Li FC, Li DZ, Liao C. Fu F, et al. Among authors: zhang ln, zhang yl. Mol Neurobiol. 2023 Jun;60(6):2986-3003. doi: 10.1007/s12035-023-03239-5. Epub 2023 Feb 10. Mol Neurobiol. 2023. PMID: 36763283 Free PMC article.

2

A new hemoglobin variant: Hb Henan [β90(F6)Glu → Gln; HBB: c.271G < C].

Cai WJ, Xie XM, Zhang YL, Li R, Liao C, Li DZ. Cai WJ, et al. Among authors: zhang yl. Hemoglobin. 2014;38(2):127-9. doi: 10.3109/03630269.2014.880062. Epub 2014 Jan 29. Hemoglobin. 2014. PMID: 24471793

3

Prenatal diagnosis of congenital heart defect by genome-wide high-resolution SNP array.

Liao C, Li R, Fu F, Xie G, Zhang Y, Pan M, Li J, Li D. Liao C, et al. Prenat Diagn. 2014 Sep;34(9):858-63. doi: 10.1002/pd.4383. Epub 2014 May 10. Prenat Diagn. 2014. PMID: 24718970

4

Noninvasive prenatal diagnosis of common aneuploidies by semiconductor sequencing.

Liao C, Yin AH, Peng CF, Fu F, Yang JX, Li R, Chen YY, Luo DH, Zhang YL, Ou YM, Li J, Wu J, Mai MQ, Hou R, Wu F, Luo H, Li DZ, Liu HL, Zhang XZ, Zhang K. Liao C, et al. Among authors: zhang xz, zhang yl, zhang k. Proc Natl Acad Sci U S A. 2014 May 20;111(20):7415-20. doi: 10.1073/pnas.1321997111. Epub 2014 May 5. Proc Natl Acad Sci U S A. 2014. PMID: 24799683 Free PMC article.

5

Prenatal diagnosis of foetuses with congenital abnormalities and duplication of the MECP2 region.

Fu F, Liu HL, Li R, Han J, Yang X, Min P, Zhen L, Zhang YL, Xie GE, Lei TY, Li Y, Li J, Li DZ, Liao C. Fu F, et al. Among authors: zhang yl. Gene. 2014 Aug 10;546(2):222-5. doi: 10.1016/j.gene.2014.06.012. Epub 2014 Jun 7. Gene. 2014. PMID: 24914495 Clinical Trial.

6

[Analysis of 22 patients with congenital cleft lip and palate using high-resolution chromosome microarray].

Lei T, Zhang Y, Wang H, Li F, Cui Y, Fu F, Li R, Xie G, Zhang Y, Liao C. Lei T, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014 Aug;31(4):433-7. doi: 10.3760/cma.j.issn.1003-9406.2014.04.005. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014. PMID: 25119905 Chinese.

7

Prenatal diagnosis of 17q12 duplication and deletion syndrome in two fetuses with congenital anomalies.

Li R, Fu F, Zhang YL, Li DZ, Liao C. Li R, et al. Among authors: zhang yl. Taiwan J Obstet Gynecol. 2014 Dec;53(4):579-82. doi: 10.1016/j.tjog.2014.05.004. Taiwan J Obstet Gynecol. 2014. PMID: 25510704 Free article.

8

[Clinical value of genome-wide high resolution chromosomal microarray analysis in etiological study of fetuses with congenital heart defects].

Wu X, Fu F, Li R, Pan M, Han J, Zhen L, Yang X, Zhang Y, Li F, Liao C. Wu X, et al. Zhonghua Fu Chan Ke Za Zhi. 2014 Dec;49(12):893-8. Zhonghua Fu Chan Ke Za Zhi. 2014. PMID: 25608988 Chinese.

9

Association of an α-globin gene cluster duplication and heterozygous β-thalassemia in a patient with a severe thalassemia syndrome.

Jiang H, Liu S, Zhang YL, Wan JH, Li R, Li DZ. Jiang H, et al. Among authors: zhang yl. Hemoglobin. 2015;39(2):102-6. doi: 10.3109/03630269.2015.1012678. Epub 2015 Feb 18. Hemoglobin. 2015. PMID: 25690803

10

Characterization of 26 deletion CNVs reveals the frequent occurrence of micro-mutations within the breakpoint-flanking regions and frequent repair of double-strand breaks by templated insertions derived from remote genomic regions.

Wang Y, Su P, Hu B, Zhu W, Li Q, Yuan P, Li J, Guan X, Li F, Jing X, Li R, Zhang Y, Férec C, Cooper DN, Wang J, Huang D, Chen JM, Wang Y. Wang Y, et al. Hum Genet. 2015 Jun;134(6):589-603. doi: 10.1007/s00439-015-1539-4. Epub 2015 Mar 20. Hum Genet. 2015. PMID: 25792359

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