Wang X - Search Results

1

VHL Ser65 mutations enhance HIF2α signaling and promote epithelial-mesenchymal transition of renal cancer cells.

Ma X, Tan Z, Zhang Q, Ma K, Xiao J, Wang X, Wang Y, Zhong M, Wang Y, Li J, Zeng X, Guan W, Wang S, Gong K, Wei GH, Wang Z. Ma X, et al. Among authors: wang x, wang z, wang y, wang s. Cell Biosci. 2022 May 3;12(1):52. doi: 10.1186/s13578-022-00790-x. Cell Biosci. 2022. PMID: 35505422 Free PMC article.

2

APOE rs405509 polymorphism and Parkinson's disease risk in the Chinese population.

Huang M, Wang Y, Wang L, Chen B, Wang X, Hu Y. Huang M, et al. Among authors: wang x, wang l, wang y. Neurosci Lett. 2020 Sep 25;736:135256. doi: 10.1016/j.neulet.2020.135256. Epub 2020 Jul 16. Neurosci Lett. 2020. PMID: 32682842 Free article.

3

Risk Factors for Mortality of COVID-19 Patient Based on Clinical Course: A Single Center Retrospective Case-Control Study.

Zhang J, Wang Z, Wang X, Hu Z, Yang C, Lei P. Zhang J, et al. Among authors: wang x, wang z. Front Immunol. 2021 Feb 16;12:581469. doi: 10.3389/fimmu.2021.581469. eCollection 2021. Front Immunol. 2021. PMID: 33664741 Free PMC article.

4

Effective Diagnosis of Prostate Cancer Based on mRNAs From Urinary Exosomes.

Gan J, Zeng X, Wang X, Wu Y, Lei P, Wang Z, Yang C, Hu Z. Gan J, et al. Among authors: wang x, wang z. Front Med (Lausanne). 2022 Mar 23;9:736110. doi: 10.3389/fmed.2022.736110. eCollection 2022. Front Med (Lausanne). 2022. PMID: 35402423 Free PMC article.

5

Congenital fibrinogen disorder caused by digenic mutations of the FGA and FGB genes.

Wang X, Tang N, Shen N, Lu Y, Li D. Wang X, et al. Hematology. 2020 Dec;25(1):145-148. doi: 10.1080/16078454.2020.1746109. Hematology. 2020. PMID: 32228225 Free article.

6

Compound heterozygosity for novel von Willebrand factor genetic variants associated with von Willebrand disease in two Chinese patients.

Wang Y, Wang X, Lu Y, Zhang A, Yu W, Hu Q, Liu A, Huang JF. Wang Y, et al. Among authors: wang x. Blood Coagul Fibrinolysis. 2023 Jan 1;34(1):33-39. doi: 10.1097/MBC.0000000000001174. Epub 2022 Oct 18. Blood Coagul Fibrinolysis. 2023. PMID: 36598376

7

Single-Cell RNA Sequencing Analysis Reveals Metabolic Changes in Epithelial Glycosphingolipids and Establishes a Prognostic Risk Model for Pancreatic Cancer.

Ba Q, Wang X, Hu H, Lu Y. Ba Q, et al. Among authors: wang x. Diagnostics (Basel). 2024 May 24;14(11):1094. doi: 10.3390/diagnostics14111094. Diagnostics (Basel). 2024. PMID: 38893622 Free PMC article.

8

Mutation analysis of a Chinese family with oculocutaneous albinism.

Wang X, Zhu Y, Shen N, Peng J, Wang C, Liu H, Lu Y. Wang X, et al. Among authors: wang c. Oncotarget. 2016 Dec 20;7(51):84981-84988. doi: 10.18632/oncotarget.13109. Oncotarget. 2016. PMID: 27829221 Free PMC article.

9

Mutational analysis of a Chinese family with oculocutaneous albinism type 2.

Wang X, Zhu Y, Shen N, Peng J, Wang C, Liu H, Lu Y. Wang X, et al. Among authors: wang c. Oncotarget. 2017 Jul 31;8(41):70345-70355. doi: 10.18632/oncotarget.19697. eCollection 2017 Sep 19. Oncotarget. 2017. PMID: 29050284 Free PMC article.

10

Two cases of von Willebrand disease type 3 in consanguineous Chinese families.

Wang X, Tang N, Lu Y, Hu Q, Li D. Wang X, et al. Mol Genet Genomic Med. 2020 Feb;8(2):e1075. doi: 10.1002/mgg3.1075. Epub 2019 Dec 2. Mol Genet Genomic Med. 2020. PMID: 31793247 Free PMC article.

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