Chen FP - Search Results

1

Genotypic and phenotypic features of citrin deficiency: five-year experience in a Chinese pediatric center.

Song YZ, Deng M, Chen FP, Wen F, Guo L, Cao SL, Gong J, Xu H, Jiang GY, Zhong L, Kobayashi K, Saheki T, Wang ZN. Song YZ, et al. Among authors: chen fp. Int J Mol Med. 2011 Jul;28(1):33-40. doi: 10.3892/ijmm.2011.653. Epub 2011 Mar 21. Int J Mol Med. 2011. PMID: 21424115

2

SLC25A13 gene analysis in citrin deficiency: sixteen novel mutations in East Asian patients, and the mutation distribution in a large pediatric cohort in China.

Song YZ, Zhang ZH, Lin WX, Zhao XJ, Deng M, Ma YL, Guo L, Chen FP, Long XL, He XL, Sunada Y, Soneda S, Nakatomi A, Dateki S, Ngu LH, Kobayashi K, Saheki T. Song YZ, et al. Among authors: chen fp. PLoS One. 2013 Sep 19;8(9):e74544. doi: 10.1371/journal.pone.0074544. eCollection 2013. PLoS One. 2013. PMID: 24069319 Free PMC article.

3

Clinical, molecular and functional investigation on an infant with neonatal intrahepatic cholestasis caused by citrin deficiency (NICCD).

Zhang ZH, Lin WX, Deng M, Zhao ST, Zeng HS, Chen FP, Song YZ. Zhang ZH, et al. Among authors: chen fp. PLoS One. 2014 Feb 21;9(2):e89267. doi: 10.1371/journal.pone.0089267. eCollection 2014. PLoS One. 2014. PMID: 24586645 Free PMC article.

4

Screening for five prevalent mutations of SLC25A13 gene in Guangdong, China: a molecular epidemiologic survey of citrin deficiency.

Zhang ZH, Yang ZG, Chen FP, Kikuchi A, Liu ZH, Kuang LZ, Li WM, Song YZ, Kure S, Saheki T. Zhang ZH, et al. Among authors: chen fp. Tohoku J Exp Med. 2014 Aug;233(4):275-81. doi: 10.1620/tjem.233.275. Tohoku J Exp Med. 2014. PMID: 25110155 Free article.

5

Inspissated bile syndrome in an infant with citrin deficiency and congenital anomalies of the biliary tract and esophagus: identification and pathogenicity analysis of a novel SLC25A13 mutation with incomplete penetrance.

Zeng HS, Zhao ST, Deng M, Zhang ZH, Cai XR, Chen FP, Song YZ. Zeng HS, et al. Among authors: chen fp. Int J Mol Med. 2014 Nov;34(5):1241-8. doi: 10.3892/ijmm.2014.1929. Epub 2014 Sep 10. Int J Mol Med. 2014. PMID: 25216257 Free PMC article.

6

Molecular diagnosis of pediatric patients with citrin deficiency in China: SLC25A13 mutation spectrum and the geographic distribution.

Lin WX, Zeng HS, Zhang ZH, Mao M, Zheng QQ, Zhao ST, Cheng Y, Chen FP, Wen WR, Song YZ. Lin WX, et al. Among authors: chen fp. Sci Rep. 2016 Jul 11;6:29732. doi: 10.1038/srep29732. Sci Rep. 2016. PMID: 27405544 Free PMC article. Clinical Trial.

7

SLC25A13 cDNA cloning analysis using peripheral blood lymphocytes facilitates the identification of a large deletion mutation: Molecular diagnosis of an infant with neonatal intrahepatic cholestasis caused by citrin deficiency.

Zeng HS, Lin WX, Zhao ST, Zhang ZH, Yang HW, Chen FP, Song YZ, Yin ZN. Zeng HS, et al. Among authors: chen fp. Mol Med Rep. 2016 Dec;14(6):5189-5194. doi: 10.3892/mmr.2016.5873. Epub 2016 Oct 21. Mol Med Rep. 2016. PMID: 27779681

8

Clinical and molecular study of a pediatric patient with sodium taurocholate cotransporting polypeptide deficiency.

Deng M, Mao M, Guo L, Chen FP, Wen WR, Song YZ. Deng M, et al. Among authors: chen fp. Exp Ther Med. 2016 Nov;12(5):3294-3300. doi: 10.3892/etm.2016.3752. Epub 2016 Sep 27. Exp Ther Med. 2016. PMID: 27882152 Free PMC article.

9

[Phenotypic and genetic analysis of a family affected with microvillus inclusion disease].

Mao M, Guo L, Zhang Z, Wang B, Huang S, Song Y, Chen F, Wen W. Mao M, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016 Dec 10;33(6):792-796. doi: 10.3760/cma.j.issn.1003-9406.2016.06.010. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016. PMID: 27984607 Chinese.

10

Neonatal Intrahepatic Cholestasis caused by Citrin Deficiency: In vivo and in vitro studies of the aberrant transcription arising from two novel splice-site variants in SLC25A13.

Lin WX, Deng LJ, Liu R, Qiu JW, Cheng Y, Zhang ZH, Chen FP, Song YZ. Lin WX, et al. Among authors: chen fp. Eur J Med Genet. 2021 Mar;64(3):104145. doi: 10.1016/j.ejmg.2021.104145. Epub 2021 Jan 23. Eur J Med Genet. 2021. PMID: 33497767 Free article.

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