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Cited by in CrossRef
For: Wongkittichote P, Sukasem C, Kikuchi A, Aekplakorn W, Jensen LT, Kure S, Wattanasirichaigoon D. Screening of SLC25A13 mutation in the Thai population. World J Gastroenterol 2013; 19(43): 7735-7742 [PMID: 24282362 DOI: 10.3748/wjg.v19.i43.7735]
URL: https://www.wjgnet.com/1007-9327/full/v19/i43/7735.htm
Number Citing Articles
1
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
2
Mai-Huong Thi Nguyen, Anh-Hoa Pham Nguyen, Diem-Ngoc Ngo, Phuong-Mai Thi Nguyen, Hung-Sang Tang, Hoa Giang, Y-Thanh Lu, Hoai-Nghia Nguyen, Minh-Dien Tran. The mutation spectrum of SLC25A13 gene in citrin deficiency: identification of novel mutations in Vietnamese pediatric cohort with neonatal intrahepatic cholestasisJournal of Human Genetics 2023; 68(5): 305 doi: 10.1038/s10038-022-01112-2
3
Chalongchai Chalermwat, Thitipa Thosapornvichai, Parith Wongkittichote, John D Phillips, James E Cox, Amornrat N Jensen, Duangrurdee Wattanasirichaigoon, Laran T Jensen. Overexpression of the peroxin Pex34p suppresses impaired acetate utilization in yeast lacking the mitochondrial aspartate/glutamate carrier Agc1pFEMS Yeast Research 2019; 19(8) doi: 10.1093/femsyr/foz078
4
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
5
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
6
Chalongchai Chalermwat, Thitipa Thosapornvichai, Laran T. Jensen, Duangrurdee Wattanasirichaigoon. Genetic Analysis of Peroxisomal Genes Required for Longevity in a Yeast Model of Citrin DeficiencyDiseases 2020; 8(1): 2 doi: 10.3390/diseases8010002
7
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
8
Sirilak Chuenwattana, Kanokwan Imtawil, Kanda Sornkayasit, Aree Rattanathongkom, Busara Charoenwat, Khunton Wichajarn. Neonatal intrahepatic cholestasis caused by citrin deficiency (NICCD) in Thai infants: Case reports on clinical presentation, genotype analysis, and considerations for negative newborn screeningMedical Reports 2024; 4: 100051 doi: 10.1016/j.hmedic.2024.100051
9
Jun Kido, Georgios Makris, Saikat Santra, Johannes Häberle. Clinical landscape of citrin deficiency: A global perspective on a multifaceted conditionJournal of Inherited Metabolic Disease 2024;  doi: 10.1002/jimd.12722
10
Yumi Yamaguchi-Kabata, Jun Yasuda, Akira Uruno, Kazuro Shimokawa, Seizo Koshiba, Yoichi Suzuki, Nobuo Fuse, Hiroshi Kawame, Shu Tadaka, Masao Nagasaki, Kaname Kojima, Fumiki Katsuoka, Kazuki Kumada, Osamu Tanabe, Gen Tamiya, Nobuo Yaegashi, Kengo Kinoshita, Masayuki Yamamoto, Shigeo Kure. Estimating carrier frequencies of newborn screening disorders using a whole-genome reference panel of 3552 Japanese individualsHuman Genetics 2019; 138(4): 389 doi: 10.1007/s00439-019-01998-7
11
Zhan-Hui Zhang, Zhi-Gang Yang, Feng-Ping Chen, Atsuo Kikuchi, Zhen-Huan Liu, Li-Zhen Kuang, Wei-Ming Li, Yuan-Zong Song, Shigeo Kure, Takeyori Saheki. Screening for Five Prevalent Mutations of <i>SLC25A13</i> Gene in Guangdong, China: A Molecular Epidemiologic Survey of Citrin DeficiencyThe Tohoku Journal of Experimental Medicine 2014; 233(4): 275 doi: 10.1620/tjem.233.275
12
Song-Chang Chen, Xuan-You Zhou, Shu-Yuan Li, Ming-Min Zhao, He-Feng Huang, Jia Jia, Chen-Ming Xu. Carrier burden of over 300 diseases in Han Chinese identified by expanded carrier testing of 300 couples using assisted reproductive technologyJournal of Assisted Reproduction and Genetics 2023; 40(9): 2157 doi: 10.1007/s10815-023-02876-y
13
Chalitpon Na nakorn, Jariya Waisayarat, Charungthai Dejthevaporn, Pornpen Srisawasdi, Sansanee Wongwaisayawan, Chonlaphat Sukasem. Genetic Variations and Frequencies of the Two Functional Single Nucleotide Polymorphisms of SLCO1B1 in the Thai PopulationFrontiers in Pharmacology 2020; 11 doi: 10.3389/fphar.2020.00728
14
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