Wang Y - Search Results

1

Spectrum and clinical features of gene mutations in Chinese pediatric acute lymphoblastic leukemia.

Shen D, Liu L, Xu X, Song H, Zhang J, Xu W, Zhao F, Liang J, Liao C, Wang Y, Xia T, Wang C, Lou F, Cao S, Qin J, Tang Y. Shen D, et al. Among authors: wang y, wang c. BMC Pediatr. 2023 Feb 4;23(1):62. doi: 10.1186/s12887-023-03856-y. BMC Pediatr. 2023. PMID: 36739388 Free PMC article.

2

Treatment of Relapsed and Refractory ALK-Positive Anaplastic Large Cell Lymphoma With ALK-Specific Tyrosine Kinase Inhibitor in Children: A Case Series.

Shen D, Song H, Zhang J, Liao C, Wang Y, Fang M, Tang Y. Shen D, et al. Among authors: wang y. J Pediatr Hematol Oncol. 2022 Jan 1;44(1):e1-e4. doi: 10.1097/MPH.0000000000002137. J Pediatr Hematol Oncol. 2022. PMID: 33661174

3

A Novel NUP98/RARG Gene Fusion in Pediatric Acute Myeloid Leukemia Resembling Acute Promyelocytic Leukemia.

Zhang J, Shen H, Song H, Shen D, Liao C, Fang M, Wang Y, Tang Y, Zhu H. Zhang J, et al. Among authors: wang y. J Pediatr Hematol Oncol. 2022 Apr 1;44(3):e665-e671. doi: 10.1097/MPH.0000000000002331. J Pediatr Hematol Oncol. 2022. PMID: 35319505

4

Clinical and Genetic Characteristics of IKZF1 Mutation in Chinese Children With B-Cell Acute Lymphoblastic Leukemia.

Zhang J, Xu XJ, Liu L, Song H, Shen H, Xu W, Zhao F, Liang J, Liao C, Wang Y, Xia T, Cao S, Tang Y, Qin J, Shen D. Zhang J, et al. Among authors: wang y. Front Genet. 2022 Mar 28;13:822832. doi: 10.3389/fgene.2022.822832. eCollection 2022. Front Genet. 2022. PMID: 35419036 Free PMC article.

5

Effect of pausing on the cotranscriptional folding kinetics of RNAs.

Wang K, He Y, Shen Y, Wang Y, Xu X, Song X, Sun T. Wang K, et al. Among authors: wang y. Int J Biol Macromol. 2022 Nov 30;221:1345-1355. doi: 10.1016/j.ijbiomac.2022.09.115. Epub 2022 Sep 15. Int J Biol Macromol. 2022. PMID: 36115451

6

Low skeletal muscle mass as an early sign in children with fabry disease.

Lu Z, Huang G, Yu L, Wang Y, Gao L, Lin L, Hu L, Mao J. Lu Z, et al. Among authors: wang y. Orphanet J Rare Dis. 2023 Jul 21;18(1):199. doi: 10.1186/s13023-023-02806-2. Orphanet J Rare Dis. 2023. PMID: 37480128 Free PMC article.

7

Early onset of nephrogenic diabetes insipidus due to fabry disease in a child with GLA N215S mutation: Case report and literature review.

Lu Z, Wang Y, Gao L, Lin L, Hu L, Mao J. Lu Z, et al. Among authors: wang y. Heliyon. 2023 May 6;9(5):e15993. doi: 10.1016/j.heliyon.2023.e15993. eCollection 2023 May. Heliyon. 2023. PMID: 37205992 Free PMC article.

8

A Review of Inactivated COVID-19 Vaccine Development in China: Focusing on Safety and Efficacy in Special Populations.

Hu L, Sun J, Wang Y, Tan D, Cao Z, Gao L, Guan Y, Jia X, Mao J. Hu L, et al. Among authors: wang y. Vaccines (Basel). 2023 May 31;11(6):1045. doi: 10.3390/vaccines11061045. Vaccines (Basel). 2023. PMID: 37376434 Free PMC article. Review.

9

Dent disease 1-linked novel CLCN5 mutations result in aberrant location and reduced ion currents.

Wang Y, Xu L, Zhang Y, Fu H, Gao L, Guan Y, Gu W, Sun J, Chen X, Yang F, Lai E, Wang J, Jin Y, Kou Z, Qiu X, Mao J, Hu L. Wang Y, et al. Among authors: wang j. Int J Biol Macromol. 2024 Feb;257(Pt 2):128564. doi: 10.1016/j.ijbiomac.2023.128564. Epub 2023 Dec 5. Int J Biol Macromol. 2024. PMID: 38061527

10

Predicting microbial adaptability to climate change in the Anthropocene.

Qian H, Wang Y. Qian H, et al. Among authors: wang y. Glob Chang Biol. 2024 Jan;30(1):e17122. doi: 10.1111/gcb.17122. Glob Chang Biol. 2024. PMID: 38273491 No abstract available.

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