Sheng Y - Search Results

1

Novel IKZF1 rearrangement identified in a patient with blastic plasmacytoid dendritic cell neoplasm decreased haematopoietic stem cell function and promoted plasmacytoid dendritic cell abnormality.

Yin L, Yu Q, Zhang H, Zhu H, Deng Z, Xing C, Wang P, Zeng X, Cheng Z, Sheng Y, Peng H. Yin L, et al. Among authors: sheng y. Br J Haematol. 2024 Jun;204(6):2496-2500. doi: 10.1111/bjh.19429. Epub 2024 Apr 15. Br J Haematol. 2024. PMID: 38616623 No abstract available.

2

Proteomic profiling of plasma exosomes from patients with B-cell acute lymphoblastic leukemia.

Zhu S, Xing C, Li R, Cheng Z, Deng M, Luo Y, Li H, Zhang G, Sheng Y, Peng H, Wang Z. Zhu S, et al. Among authors: sheng y. Sci Rep. 2022 Jul 13;12(1):11975. doi: 10.1038/s41598-022-16282-4. Sci Rep. 2022. PMID: 35831551 Free PMC article.

3

Clonal architecture and single-cell transcriptome landscape in Richter's syndrome.

Li H, Yuan L, Wang P, Sheng Y, Fu Z, Peng H. Li H, et al. Among authors: sheng y. Br J Haematol. 2023 Sep;202(5):1055-1060. doi: 10.1111/bjh.18952. Epub 2023 Jul 3. Br J Haematol. 2023. PMID: 37401149 No abstract available.

4

Function of serine/arginine-rich splicing factors in hematopoiesis and hematopoietic malignancies.

Zhang H, Zhu H, Peng H, Sheng Y. Zhang H, et al. Among authors: sheng y. Cancer Cell Int. 2024 Jul 21;24(1):257. doi: 10.1186/s12935-024-03438-7. Cancer Cell Int. 2024. PMID: 39034387 Free PMC article. Review.

5

A novel prognostic model based on pyroptosis signature in AML.

Zhang H, Zhu H, Sheng Y, Cheng Z, Peng H. Zhang H, et al. Among authors: sheng y. Heliyon. 2024 Aug 22;10(17):e36624. doi: 10.1016/j.heliyon.2024.e36624. eCollection 2024 Sep 15. Heliyon. 2024. PMID: 39263179 Free PMC article.

6

Lysine succinylation precisely controls normal erythropoiesis.

Hu B, Gong H, Nie L, Zhang J, Li Y, Liu D, Zhang H, Zhang H, Han L, Yang C, Li M, Xu W, Nakamura Y, Shi L, Ye M, Hillyer CD, Mohandas N, Liang L, Sheng Y, Liu J. Hu B, et al. Among authors: sheng y. Haematologica. 2024 Oct 17. doi: 10.3324/haematol.2024.285752. Online ahead of print. Haematologica. 2024. PMID: 39415677 Free article.

7

Case Report: Exome Sequencing Identified a Novel Frameshift Mutation of α-Actin 1 in a Chinese Family With Macrothrombocytopenia and Mild Bleeding.

Luo FM, Fan LL, Sheng Y, Dong Y, Liu L. Luo FM, et al. Among authors: sheng y. Front Pediatr. 2021 Jun 18;9:679279. doi: 10.3389/fped.2021.679279. eCollection 2021. Front Pediatr. 2021. PMID: 34222148 Free PMC article.

8

A novel POF1B variant in a Chinese patient is associated with premature ovarian failure.

Yuan ZZ, Wang CY, Jin JY, Sheng Y, Zhao MF, Fan LL, Zhang AQ. Yuan ZZ, et al. Among authors: sheng y. Clin Genet. 2021 Dec;100(6):773-774. doi: 10.1111/cge.14048. Epub 2021 Aug 23. Clin Genet. 2021. PMID: 34423420

9

Novel heterozygous mutation of MCTP2 gene in a patient with coarctation of the aorta.

Liu YX, Liu L, Dong Y, Zhao M, Sheng Y, Fan LL. Liu YX, et al. Among authors: sheng y. QJM. 2022 Mar 22;115(3):157-159. doi: 10.1093/qjmed/hcab310. QJM. 2022. PMID: 34878133 No abstract available.

10

Case report: Whole-exome sequencing identifies a novel DES mutation (p. E434K) in a Chinese family with cardiomyopathy and sudden cardiac death.

Liu YX, Yu R, Sheng Y, Fan LL, Deng Y. Liu YX, et al. Among authors: sheng y. Front Cardiovasc Med. 2022 Oct 4;9:971501. doi: 10.3389/fcvm.2022.971501. eCollection 2022. Front Cardiovasc Med. 2022. PMID: 36277747 Free PMC article.

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