Xiongwu Fu - Search Results

Year	Number of Results
2006	3
2007	5
2008	7
2009	4
2010	8
2011	4
2012	5
2013	5
2014	4
2015	6
2016	5
2017	6
2018	8
2019	11
2020	11
2021	17
2022	15
2023	15
2024	9

1

Urinary Microbial and Metabolomic Profiles in Kidney Stone Disease.

Gao H, Lin J, Xiong F, Yu Z, Pan S, Huang Y. Gao H, et al. Among authors: xiong f. Front Cell Infect Microbiol. 2022 Sep 5;12:953392. doi: 10.3389/fcimb.2022.953392. eCollection 2022. Front Cell Infect Microbiol. 2022. PMID: 36132987 Free PMC article.

2

Double heterozygous pathogenic mutations in KIF3C and ZNF513 cause hereditary gingival fibromatosis.

Chen J, Xu X, Chen S, Lu T, Zheng Y, Gan Z, Shen Z, Ma S, Wang D, Su L, He F, Shang X, Xu H, Chen D, Zhang L, Xiong F. Chen J, et al. Among authors: xiong f. Int J Oral Sci. 2023 Sep 26;15(1):46. doi: 10.1038/s41368-023-00244-1. Int J Oral Sci. 2023. PMID: 37752101 Free PMC article.

3

Simultaneous T1, T2, and T2* Mapping of Carotid Plaque: The SIMPLE* Technique.

Wang Y, Liu X, Wang J, Wang Y, Qi H, Kong X, Liu D, Liu J, Zheng H, Xiong F, Zhang L, Fu X, Zhang X, Guo R, Qiao H, Chen Z, Si D, Chen H. Wang Y, et al. Among authors: xiong f. Radiology. 2023 May;307(3):e222061. doi: 10.1148/radiol.222061. Epub 2023 Feb 28. Radiology. 2023. PMID: 36853181

4

Plasma-derived exosomal miRNA profiles reveal potential epigenetic pathogenesis of premature ovarian failure.

Lin J, Wu Z, Zheng Y, Shen Z, Gan Z, Ma S, Liu Y, Xiong F. Lin J, et al. Among authors: xiong f. Hum Genet. 2023 Dec 6. doi: 10.1007/s00439-023-02618-1. Online ahead of print. Hum Genet. 2023. PMID: 38054996

5

Intravenous Administration of an AAV9 Vector Ubiquitously Expressing C1orf194 Gene Improved CMT-Like Neuropathy in C1orf194^-/- Mice.

Shen Z, Li M, He F, Huang C, Zheng Y, Wang Z, Ma S, Chen L, Liu Z, Zheng H, Xiong F. Shen Z, et al. Among authors: xiong f. Neurotherapeutics. 2023 Oct;20(6):1835-1846. doi: 10.1007/s13311-023-01429-6. Epub 2023 Oct 16. Neurotherapeutics. 2023. PMID: 37843769 Free article.

6

Identification of a novel missense heterozygous mutation in the KDF1 gene for non-syndromic congenital anodontia.

Pan Y, Yi S, Chen D, Du X, Yao X, He F, Xiong F. Pan Y, et al. Among authors: xiong f. Clin Oral Investig. 2022 Aug;26(8):5171-5179. doi: 10.1007/s00784-022-04485-y. Epub 2022 May 31. Clin Oral Investig. 2022. PMID: 35641834 Review.

7

Renal-hepatic-pancreatic dysplasia-1 with a novel NPHP3 genotype: a case report and review of the literature.

Zhu H, Zhao ZH, Zhu SY, Xiong F, He LH, Zhang Y, Wang J. Zhu H, et al. Among authors: xiong f. BMC Pediatr. 2022 Oct 18;22(1):603. doi: 10.1186/s12887-022-03659-7. BMC Pediatr. 2022. PMID: 36253741 Free PMC article. Review.

8

Transarterial chemoembolization combined with camrelizumab for recurrent hepatocellular carcinoma.

Guo Y, Ren Y, Chen L, Sun T, Zhang W, Sun B, Zhu L, Xiong F, Zheng C. Guo Y, et al. Among authors: xiong f. BMC Cancer. 2022 Mar 14;22(1):270. doi: 10.1186/s12885-022-09325-6. BMC Cancer. 2022. PMID: 35287627 Free PMC article.

9

The molecular mechanism of Gaucher disease caused by compound heterozygous mutations in GBA1 gene.

Liu Q, Shen Z, Pan H, Ma S, Xiong F, He F. Liu Q, et al. Among authors: xiong f. Front Pediatr. 2023 Jan 26;11:1092645. doi: 10.3389/fped.2023.1092645. eCollection 2023. Front Pediatr. 2023. PMID: 36776904 Free PMC article.

10

The loss of function GBA1 c.231C > G mutation associated with Parkinson disease.

Chen D, Zheng Y, Zhang G, Huang Y, Zheng B, Zhang J, Xiong F, Su Q. Chen D, et al. Among authors: xiong f. J Neural Transm (Vienna). 2023 Jul;130(7):905-913. doi: 10.1007/s00702-023-02651-4. Epub 2023 Jun 6. J Neural Transm (Vienna). 2023. PMID: 37280314

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