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Chen R, Wang XH, Fu HY, Zhang SR, Abudouxikuer K, Saheki T, Wang JS. Different regional distribution of |
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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 Report. Anesthesiology and Pain Medicine 2014; 4(3) doi: 10.5812/aapm.21791
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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 retinopathy. Acta Diabetologica 2024; doi: 10.1007/s00592-024-02400-3
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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 deficiency. Journal of Pediatric Endocrinology and Metabolism 2023; 0(0) doi: 10.1515/jpem-2022-0616
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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 deficiency. Frontiers in Pediatrics 2023; 11 doi: 10.3389/fped.2023.1103877
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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 Resuscitation. Shock 2014; 42(4): 350 doi: 10.1097/SHK.0000000000000214
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6 |
Liver Dysfunction in Children Cause by Metabolic Diseases: Review of 9 Cases. Journal of Clinical Review & Case Reports 2018; 3(6) doi: 10.33140/JCRC/03/06/00004
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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 Nutrition. Journal of Pediatric Gastroenterology and Nutrition 2024; 78(2): 178 doi: 10.1002/jpn3.12042
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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 deficiency. Journal of Inherited Metabolic Disease 2020; 43(3): 467 doi: 10.1002/jimd.12206
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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 States. AJSP: Reviews and Reports 2018; 23(5): 214 doi: 10.1097/PCR.0000000000000266
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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 SLC25A13. European Journal of Medical Genetics 2021; 64(3): 104145 doi: 10.1016/j.ejmg.2021.104145
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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 SLC25A13. Pathology 2021; 53(7): 867 doi: 10.1016/j.pathol.2021.02.010
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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 distribution. Scientific Reports 2016; 6(1) doi: 10.1038/srep29732
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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 allele. Oncotarget 2017; 8(50): 87182 doi: 10.18632/oncotarget.19901
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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 Kong. Molecular Genetics and Metabolism Reports 2018; 17: 3 doi: 10.1016/j.ymgmr.2018.08.002
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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 implications. BMC Pediatrics 2019; 19(1) doi: 10.1186/s12887-018-1383-5
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16 |
Sotiria Tavoulari, Denis Lacabanne, Chancievan Thangaratnarajah, Edmund R.S. Kunji. Pathogenic variants of the mitochondrial aspartate/glutamate carrier causing citrin deficiency. Trends in Endocrinology & Metabolism 2022; 33(8): 539 doi: 10.1016/j.tem.2022.05.002
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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 deficiency. Clinica Chimica Acta 2024; 552: 117617 doi: 10.1016/j.cca.2023.117617
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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 patients. Experimental Biology and Medicine 2017; 242(12): 1271 doi: 10.1177/1535370217710918
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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 gene. Gene 2019; 693: 69 doi: 10.1016/j.gene.2019.01.023
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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 penetrance. International Journal of Molecular Medicine 2014; 34(5): 1241 doi: 10.3892/ijmm.2014.1929
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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 Cases. Frontiers in Genetics 2019; 10 doi: 10.3389/fgene.2019.01108
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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
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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 cholestasis. Pediatric Research 2020; 87(1): 112 doi: 10.1038/s41390-019-0548-8
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24 |
Anshu Srivastava, Rishi Bolia. Pediatric Hepatology and Liver Transplantation. 2019; : 743 doi: 10.1007/978-3-319-96400-3_41
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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 Analysis. Frontiers in Pediatrics 2021; 9 doi: 10.3389/fped.2021.654527
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