Wu X - Search Results

1

Novel CACNA1S mutation causes autosomal dominant hypokalemic periodic paralysis in a Chinese family.

Wang Q, Liu M, Xu C, Tang Z, Liao Y, Du R, Li W, Wu X, Wang X, Liu P, Zhang X, Zhu J, Ren X, Ke T, Wang Q, Yang J. Wang Q, et al. Among authors: wu x. J Mol Med (Berl). 2005 Mar;83(3):203-8. doi: 10.1007/s00109-005-0638-4. Epub 2005 Feb 22. J Mol Med (Berl). 2005. PMID: 15726306 Free PMC article.

2

Identification of a new lamin A/C mutation in a Chinese family affected with atrioventricular block as the prominent phenotype.

Wu X, Wang QK, Gui L, Liu M, Zhang X, Jin R, Li W, Yan L, Du R, Wang Q, Zhu J, Yang J. Wu X, et al. J Huazhong Univ Sci Technolog Med Sci. 2010 Feb;30(1):103-7. doi: 10.1007/s11596-010-0119-z. Epub 2010 Feb 14. J Huazhong Univ Sci Technolog Med Sci. 2010. PMID: 20155465

3

A novel PAX6 mutation in a large Chinese family with aniridia and congenital cataract.

Cai F, Zhu J, Chen W, Ke T, Wang F, Tu X, Zhang Y, Jin R, Wu X. Cai F, et al. Among authors: wu x. Mol Vis. 2010 Jun 22;16:1141-5. Mol Vis. 2010. PMID: 20664694 Free PMC article.

4

Identification of a p.Trp403* nonsense variant in PHEX causing X-linked hypophosphatemia by inhibiting p38 MAPK signaling.

Li W, Tan L, Li X, Zhang X, Wu X, Chen H, Hu L, Wang X, Luo X, Wang F, Xu C, Chen Q, Jin R, Wang QK. Li W, et al. Among authors: wu x. Hum Mutat. 2019 Jul;40(7):879-885. doi: 10.1002/humu.23743. Epub 2019 Mar 28. Hum Mutat. 2019. PMID: 30920082

5

A De Novo Mutation in MYH9 in a Child With Severe and Prolonged Macrothrombocytopenia.

Li K, Jin R, Xu W, Shen Y, Lu K, Wu X. Li K, et al. Among authors: wu x. J Pediatr Hematol Oncol. 2021 Jan;43(1):e7-e10. doi: 10.1097/MPH.0000000000001846. J Pediatr Hematol Oncol. 2021. PMID: 32520844

6

Severe Hemorrhage in Chinese Children With Immune Thrombocytopenia.

Zhou F, Xu Y, Zhang Z, Wu X, Jin R. Zhou F, et al. Among authors: wu x. J Pediatr Hematol Oncol. 2015 Apr;37(3):e158-61. doi: 10.1097/MPH.0000000000000292. J Pediatr Hematol Oncol. 2015. PMID: 25493457

7

CSF-1R inhibition disrupts the dialog between leukaemia cells and macrophages and delays leukaemia progression.

Li K, Xu W, Lu K, Wen Y, Xin T, Shen Y, Lv X, Hu S, Jin R, Wu X. Li K, et al. Among authors: wu x. J Cell Mol Med. 2020 Nov;24(22):13115-13128. doi: 10.1111/jcmm.15916. Epub 2020 Oct 10. J Cell Mol Med. 2020. PMID: 33037771 Free PMC article.

8

Validity and reliability of the Chinese language version of the eating disorder examination (CEDE) in mainland China: Implications for the identity and nosology of the eating disorders.

Tong J, Shi J, Wang J, Zhang H, Zhang SF, Wu XY, Hsu LK. Tong J, et al. Int J Eat Disord. 2011 Jan;44(1):76-80. doi: 10.1002/eat.20742. Int J Eat Disord. 2011. PMID: 20069567

9

Clinical utility of plasma Epstein-Barr virus DNA monitoring in pediatric Epstein-Barr virus-associated hemophagocytic lymphohistiocytosis: a Chinese retrospective observational study.

Zhang W, Yin Y, Li Y, Cheng L, Zhao L, Peng Y, Wu X. Zhang W, et al. Among authors: wu x. Ital J Pediatr. 2024 Jul 30;50(1):139. doi: 10.1186/s13052-024-01689-8. Ital J Pediatr. 2024. PMID: 39080799 Free PMC article.

10

Distinct FLT3 Pathways Gene Expression Profiles in Pediatric De Novo Acute Lymphoblastic and Myeloid Leukemia with FLT3 Mutations: Implications for Targeted Therapy.

Zhao L, Chen H, Lan F, Hao J, Zhang W, Li Y, Yin Y, Huang M, Wu X. Zhao L, et al. Among authors: wu x. Int J Mol Sci. 2024 Sep 4;25(17):9581. doi: 10.3390/ijms25179581. Int J Mol Sci. 2024. PMID: 39273530 Free PMC article.

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