Wu Y - Search Results

1

Neuropathy-associated Fars2 deficiency affects neuronal development and potentiates neuronal apoptosis by impairing mitochondrial function.

Chen X, Liu F, Li B, Wang Y, Yuan L, Yin A, Chen Q, Hu W, Yao Y, Zhang M, Wu Y, Chen K. Chen X, et al. Among authors: wu y. Cell Biosci. 2022 Jul 6;12(1):103. doi: 10.1186/s13578-022-00838-y. Cell Biosci. 2022. PMID: 35794642 Free PMC article.

2

Two novel CPS1 mutations in a case of carbamoyl phosphate synthetase 1 deficiency causing hyperammonemia and leukodystrophy.

Chen X, Yuan L, Sun M, Liu Q, Wu Y. Chen X, et al. Among authors: wu y. J Clin Lab Anal. 2018 Jun;32(5):e22375. doi: 10.1002/jcla.22375. Epub 2018 Jan 4. J Clin Lab Anal. 2018. PMID: 29314318 Free PMC article.

3

Novel SLCO2A1 mutations cause gender differentiated pachydermoperiostosis.

Yuan L, Chen X, Liu Z, Wu D, Lu J, Bao G, Zhang S, Wang L, Wu Y. Yuan L, et al. Among authors: wu y, wu d. Endocr Connect. 2018 Aug 1;7(11):1116-28. doi: 10.1530/EC-18-0326. Online ahead of print. Endocr Connect. 2018. PMID: 30352415 Free PMC article.

4

Immunohistochemical Evaluation of Histological Change in a Chinese Milroy Disease Family With Venous and Skin Abnormities.

Zhang S, Chen X, Yuan L, Wang S, Moli D, Liu S, Wu Y. Zhang S, et al. Among authors: wu y. Front Genet. 2019 Mar 19;10:206. doi: 10.3389/fgene.2019.00206. eCollection 2019. Front Genet. 2019. PMID: 30941160 Free PMC article.

5

Mutational Analysis of TYR, OCA2, and SLC45A2 Genes in Chinese Families with Oculocutaneous Albinism.

Lin Y, Chen X, Yang Y, Che F, Zhang S, Yuan L, Wu Y. Lin Y, et al. Among authors: wu y. Mol Genet Genomic Med. 2019 Jul;7(7):e00687. doi: 10.1002/mgg3.687. Epub 2019 Jun 14. Mol Genet Genomic Med. 2019. PMID: 31199599 Free PMC article.

6

[Detection and analysis of an ATP2A2 mutation in a family with Darier-White disease].

Chen X, Liu Q, Sun M, Yuan L, Wu Y. Chen X, et al. Among authors: wu y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Aug 10;36(8):794-797. doi: 10.3760/cma.j.issn.1003-9406.2019.08.010. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 31400130 Chinese.

7

Identification of the perpetrator among identical twins using next-generation sequencing technology: A case report.

Yuan L, Chen X, Liu Z, Liu Q, Song A, Bao G, Wei G, Zhang S, Lu J, Wu Y. Yuan L, et al. Among authors: wu y. Forensic Sci Int Genet. 2020 Jan;44:102167. doi: 10.1016/j.fsigen.2019.102167. Epub 2019 Sep 27. Forensic Sci Int Genet. 2020. PMID: 31605960

8

Novel mutations in hyper-IgM syndrome type 2 and X-linked agammaglobulinemia detected in three patients with primary immunodeficiency disease.

Chen X, Liu F, Yuan L, Zhang M, Chen K, Wu Y. Chen X, et al. Among authors: wu y. Mol Genet Genomic Med. 2021 Jan;9(1):e1552. doi: 10.1002/mgg3.1552. Epub 2020 Dec 30. Mol Genet Genomic Med. 2021. PMID: 33377626 Free PMC article.

9

Developmental Angiogenesis Requires the Mitochondrial Phenylalanyl-tRNA Synthetase.

Li B, Chen K, Liu F, Zhang J, Chen X, Chen T, Chen Q, Yao Y, Hu W, Wang L, Wu Y. Li B, et al. Among authors: wu y. Front Cardiovasc Med. 2021 Sep 1;8:724846. doi: 10.3389/fcvm.2021.724846. eCollection 2021. Front Cardiovasc Med. 2021. PMID: 34540921 Free PMC article.

10

A Novel Idiopathic Atrial Calcification: Pathologic Manifestations and Potential Mechanism.

Li B, Liu Q, Chen X, Chen T, Dang W, Zhao J, Cui G, Chen K, Wu Y. Li B, et al. Among authors: wu y. Front Cardiovasc Med. 2022 Mar 21;9:788958. doi: 10.3389/fcvm.2022.788958. eCollection 2022. Front Cardiovasc Med. 2022. PMID: 35387434 Free PMC article.

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