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Cited by in CrossRef
For: Chen R, Wang XH, Fu HY, Zhang SR, Abudouxikuer K, Saheki T, Wang JS. Different regional distribution of SLC25A13 mutations in Chinese patients with neonatal intrahepatic cholestasis. World J Gastroenterol 2013; 19(28): 4545-4551 [PMID: 23901231 DOI: 10.3748/wjg.v19.i28.4545]
URL: https://www.wjgnet.com/1007-9327/full/v19/i28/4545.htm
Number Citing Articles
1
Mohammad Gharavifard, Alireza Sabzevari, Reza Eslami. Anesthetic Management in a Child With Citrullinemia: A Case ReportAnesthesiology and Pain Medicine 2014; 4(3) doi: 10.5812/aapm.21791
2
Meiqing Ren, Qian Xu, Jie Luan, Yan Ni, Bo Xie. Mir-509-3p targets SLC25A13 to regulate ferroptosis and protect retinal endothelial cells in diabetic retinopathyActa Diabetologica 2024;  doi: 10.1007/s00592-024-02400-3
3
Wenjun Sun, Xiaoxi Zhang, Hang Su, Xiaoxia Wang, Fang Qin, Xiangling Gong, Bo Wang, Fei Yu. Genetic and clinical features of patients with intrahepatic cholestasis caused by citrin deficiencyJournal of Pediatric Endocrinology and Metabolism 2023; 0(0) doi: 10.1515/jpem-2022-0616
4
Kena Wang, Biao Zou, Fan Chen, Jianling Zhang, Zhihua Huang, Sainan Shu. Case report: Three novel variants on SLC25A13 in four infants with neonatal intrahepatic cholestasis caused by citrin deficiencyFrontiers in Pediatrics 2023; 11 doi: 10.3389/fped.2023.1103877
5
Zi-Gang Zhao, Li-Min Zhang, Yong-Zhuang Lv, Yong-Hua Si, Chun-Yu Niu, Ji-Cheng Li. Changes in Renal Tissue Proteome Induced by Mesenteric Lymph Drainage in Rats After Hemorrhagic Shock With ResuscitationShock 2014; 42(4): 350 doi: 10.1097/SHK.0000000000000214
6
Liver Dysfunction in Children Cause by Metabolic Diseases: Review of 9 CasesJournal of Clinical Review & Case Reports 2018; 3(6) doi: 10.33140/JCRC/03/06/00004
7
Ayano Inui, Jae Sung Ko, Voranush Chongsrisawat, Anupam Sibal, Winita Hardikar, Mei‐Hwei Chang, Suporn Treepongkaruna, Katsuhiro Arai, Kyung Mo Kim, Huey‐Ling Chen. Update on the diagnosis and management of neonatal intrahepatic cholestasis caused by citrin deficiency: Expert review on behalf of the Asian Pan‐Pacific Society for Pediatric Gastroenterology, Hepatology, and NutritionJournal of Pediatric Gastroenterology and Nutrition 2024; 78(2): 178 doi: 10.1002/jpn3.12042
8
Yiming Lin, Yaru Liu, Lin Zhu, Kaixing Le, Yuyan Shen, Chiju Yang, Xigui Chen, Haili Hu, Qingqing Ma, Xueqin Shi, Zhenzhen Hu, Jianbin Yang, Yaping Shen, Chien‐Hsing Lin, Chenggang Huang, Xinwen Huang. Combining newborn metabolic and genetic screening for neonatal intrahepatic cholestasis caused by citrin deficiencyJournal of Inherited Metabolic Disease 2020; 43(3): 467 doi: 10.1002/jimd.12206
9
Simona De Michele, Jennifer M. Vittorio, Tiffany Thomas, George A. Diaz, Jay H. Lefkowitch, Stephen M. Lagana. A Rare Case of Neonatal Intrahepatic Cholestasis Caused by Citrin Deficiency in the United StatesAJSP: Reviews and Reports 2018; 23(5): 214 doi: 10.1097/PCR.0000000000000266
10
Wei-Xia Lin, Li-Jing Deng, Rui Liu, Jian-Wu Qiu, Yin Cheng, Zhan-Hui Zhang, Feng-Ping Chen, Yuan-Zong Song. 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 SLC25A13European Journal of Medical Genetics 2021; 64(3): 104145 doi: 10.1016/j.ejmg.2021.104145
11
Nike Kwai Cheung Lau, Hencher Han Chih Lee, Sammy Pak Lam Chen, Candy Wai Yan Ng, Chloe Miu Mak, Yeow Kuan Chong, Tammy Tsz Yan Tong, Mei Tik Leung, Chi Chung Shek, Yuet Ping Yuen, Chor Kwan Ching. In-house multiplex ligation-dependent probe amplification assay for citrin deficiency: analytical validation and novel exonic deletions in SLC25A13Pathology 2021; 53(7): 867 doi: 10.1016/j.pathol.2021.02.010
12
Wei-Xia Lin, Han-Shi Zeng, Zhan-Hui Zhang, Man Mao, Qi-Qi Zheng, Shu-Tao Zhao, Ying Cheng, Feng-Ping Chen, Wang-Rong Wen, Yuan-Zong Song. Molecular diagnosis of pediatric patients with citrin deficiency in China: SLC25A13 mutation spectrum and the geographic distributionScientific Reports 2016; 6(1) doi: 10.1038/srep29732
13
Zhan-Hui Zhang, Wei-Xia Lin, Qi-Qi Zheng, Li Guo, Yuan-Zong Song. Molecular diagnosis of citrin deficiency in an infant with intrahepatic cholestasis: identification of a 21.7kb gross deletion that completely silences the transcriptional and translational expression of the affected SLC25A13 alleleOncotarget 2017; 8(50): 87182 doi: 10.18632/oncotarget.19901
14
S.C. Chong, P. Lo, C.W. Chow, L. Yuen, W.C.W. Chu, T.Y. Leung, J. Hui, F. Scaglia. Molecular and clinical characterization of citrin deficiency in a cohort of Chinese patients in Hong KongMolecular Genetics and Metabolism Reports 2018; 17: 3 doi: 10.1016/j.ymgmr.2018.08.002
15
Kuerbanjiang Abuduxikuer, Rui Chen, Zhong-Lin Wang, Jian-She Wang. Risk factors associated with mortality in neonatal intrahepatic cholestasis caused by citrin deficiency (NICCD) and clinical implicationsBMC Pediatrics 2019; 19(1) doi: 10.1186/s12887-018-1383-5
16
Sotiria Tavoulari, Denis Lacabanne, Chancievan Thangaratnarajah, Edmund R.S. Kunji. Pathogenic variants of the mitochondrial aspartate/glutamate carrier causing citrin deficiencyTrends in Endocrinology & Metabolism 2022; 33(8): 539 doi: 10.1016/j.tem.2022.05.002
17
Jiansheng Lin, Weihua Lin, Yiming Lin, Weilin Peng, Zhenzhu Zheng. Clinical and genetic analysis of 26 Chinese patients with neonatal intrahepatic cholestasis due to citrin deficiencyClinica Chimica Acta 2024; 552: 117617 doi: 10.1016/j.cca.2023.117617
18
Chun-Ting Lu, Qi-Ping Shi, Ze-Jian Li, Jiong Li, Lie Feng. Blood glucose and insulin and correlation of SLC25A13 mutations with biochemical changes in NICCD patientsExperimental Biology and Medicine 2017; 242(12): 1271 doi: 10.1177/1535370217710918
19
Jun-Lin Chen, Zhan-Hui Zhang, Bing-Xiao Li, Zhen Cai, Qing-Hua Zhou. Bioinformatic and functional analysis of promoter region of human SLC25A13 geneGene 2019; 693: 69 doi: 10.1016/j.gene.2019.01.023
20
HAN-SHI ZENG, SHU-TAO ZHAO, MEI DENG, ZHAN-HUI ZHANG, XIANG-RAN CAI, FENG-PING CHEN, YUAN-ZONG SONG. 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 penetranceInternational Journal of Molecular Medicine 2014; 34(5): 1241 doi: 10.3892/ijmm.2014.1929
21
Hui Lin, Jian-Wu Qiu, Yaqub-Muhammad Rauf, Gui-Zhi Lin, Rui Liu, Li-Jing Deng, Mei Deng, Yuan-Zong Song. Sodium Taurocholate Cotransporting Polypeptide (NTCP) Deficiency Hidden Behind Citrin Deficiency in Early Infancy: A Report of Three CasesFrontiers in Genetics 2019; 10 doi: 10.3389/fgene.2019.01108
22
Zhan-Hui Zhang, Wei-Xia Lin, Mei Deng, Shu-Tao Zhao, Han-Shi Zeng, Feng-Ping Chen, Yuan-Zong Song, Andreas R. Janecke. Clinical, Molecular and Functional Investigation on an Infant with Neonatal Intrahepatic Cholestasis Caused by Citrin Deficiency (NICCD)PLoS ONE 2014; 9(2): e89267 doi: 10.1371/journal.pone.0089267
23
Neng-Li Wang, Yi Lu, Jing-Yu Gong, Xin-Bao Xie, Jing Lin, Kuerbanjiang Abuduxikuer, Mei-Hong Zhang, Jian-She Wang. Molecular findings in children with inherited intrahepatic cholestasisPediatric Research 2020; 87(1): 112 doi: 10.1038/s41390-019-0548-8
24
Anshu Srivastava, Rishi Bolia. Pediatric Hepatology and Liver Transplantation2019; : 743 doi: 10.1007/978-3-319-96400-3_41
25
Qinlong Zeng, Yingsong Yang, Jiahong Luo, Jinmei Xu, Choufen Deng, Yuanjuan Yang, Shuming Tan, Shuxiang Sun, Yuping Li, Tong Ou. Rapid Genetic Diagnosis of Citrin Deficiency by Multicolor Melting Curve AnalysisFrontiers in Pediatrics 2021; 9 doi: 10.3389/fped.2021.654527