For: | Amirneni S, Haep N, Gad MA, Soto-Gutierrez A, Squires JE, Florentino RM. Molecular overview of progressive familial intrahepatic cholestasis. World J Gastroenterol 2020; 26(47): 7470-7484 [PMID: 33384548 DOI: 10.3748/wjg.v26.i47.7470] |
---|---|
URL: | https://www.wjgnet.com/1007-9327/full/v26/i47/7470.htm |
Number | Citing Articles |
1 |
Jaladhi V Bhatt, Ambika Akhoury, Vaidehi V Vekaria, Hardik R Parmar, Dhruval N Patel. A Case of Progressive Familial Intrahepatic Cholestasis Type–3. Cureus 2024; doi: 10.7759/cureus.72782
|
2 |
Sara Hassan, Paula Hertel. Overview of Progressive Familial Intrahepatic Cholestasis. Clinics in Liver Disease 2022; 26(3): 371 doi: 10.1016/j.cld.2022.03.003
|
3 |
Anu K. Vasudevan, Naresh Shanmugam, Ashwin Rammohan, Joseph J. Valamparampil, Kshetra Rinaldhy, Jagadeesh Menon, Ravikumar Thambithurai, Saravanapandian Namasivayam, Ilankumaran Kaliamoorthy, Mohamed Rela. Outcomes of pediatric liver transplantation for progressive familial intrahepatic cholestasis. Pediatric Transplantation 2023; 27(8) doi: 10.1111/petr.14600
|
4 |
Fahad I. Alsohaibani, Musthafa C. Peedikayil, Abdulaziz F. Alfadley, Mohamed K. Aboueissa, Faisal A. Abaalkhail, Saleh A. Alqahtani, Dirk Uhlmann. Progressive Familial Intrahepatic Cholestasis: A Descriptive Study in a Tertiary Care Center. International Journal of Hepatology 2023; 2023: 1 doi: 10.1155/2023/1960152
|
5 |
Katherine Cheng, Philip Rosenthal. Diagnosis and management of Alagille and progressive familial intrahepatic cholestasis. Hepatology Communications 2023; 7(12) doi: 10.1097/HC9.0000000000000314
|
6 |
Yuqing Xu, Yeqing Qian, Ying Yu, Xin Zhan, Pengzhen Jin, Jiawei Hong, Minyue Dong. SLC10A5 deficiency causes hypercholanemia. Hepatology 2024; doi: 10.1097/HEP.0000000000000994
|
7 |
Barath Jagadisan, Anil Dhawan. Emergencies in paediatric hepatology. Journal of Hepatology 2022; 76(5): 1199 doi: 10.1016/j.jhep.2021.12.027
|
8 |
Amanda Caroline Mahle, Bernard David Morris, Zane Frazer, Christopher Novak. Severe vitamin deficiencies in pregnancy complicated by progressive familial intrahepatic cholestasis. BMJ Case Reports 2021; 14(3): e240248 doi: 10.1136/bcr-2020-240248
|
9 |
Rishi Bolia, Akhil Dhanesh Goel, Vishakha Sharma, Anshu Srivastava. Biliary diversion in progressive familial intrahepatic cholestasis: a systematic review and meta-analysis. Expert Review of Gastroenterology & Hepatology 2022; 16(2): 163 doi: 10.1080/17474124.2022.2032660
|
10 |
Li Zeng, Jianxiang Huang, Yi Wang, Yan Hu, Shaoyu Zhou, Yuanfu Lu. Oleanolic acid induces hepatic injury by disrupting hepatocyte tight junction and dysregulation of farnesoid X receptor‐mediated bile acid efflux transporters. Journal of Applied Toxicology 2024; 44(11): 1725 doi: 10.1002/jat.4667
|
11 |
Ana Sánchez-Monteagudo, Edna Ripollés, Marina Berenguer, Carmen Espinós. Wilson’s Disease: Facing the Challenge of Diagnosing a Rare Disease. Biomedicines 2021; 9(9): 1100 doi: 10.3390/biomedicines9091100
|
12 |
Alper Gezdirici, Özlem Kalaycik Şengül, Mustafa Doğan, Banu Y. Özgüven, Ekrem Akbulut. Biallelic Novel USP53 Splicing Variant Disrupting the Gene Function that Causes Cholestasis Phenotype and Review of the Literature. Molecular Syndromology 2022; 13(6): 471 doi: 10.1159/000523937
|
13 |
Ya-Xin Xu, Xiao-Xuan Niu, Bei-Li Xu, Yuan Ji, Qun-Yan Yao. Diagnosis and management of benign recurrent intrahepatic cholestasis and psychosocial stressors in an adolescent: A case report. World Journal of Clinical Cases 2024; 12(20): 4427-4433 doi: 10.12998/wjcc.v12.i20.4427
|
14 |
Luca Szabó, Adam R. Pollio, Georg Friedrich Vogel. Intracellular Trafficking Defects in Congenital Intestinal and Hepatic Diseases. Traffic 2024; 25(8) doi: 10.1111/tra.12954
|
15 |
Javier Martínez-García, Angie Molina, Gloria González-Aseguinolaza, Nicholas D. Weber, Cristian Smerdou. Gene Therapy for Acquired and Genetic Cholestasis. Biomedicines 2022; 10(6): 1238 doi: 10.3390/biomedicines10061238
|
16 |
Tasnia Sharin, Lucas J. Leinen, David Schreiber, Vaille A. Swenson, Sarah A. Emsley, E. Jamie Trammell, Patrick Videau, Doug Crump, Michael O. Gaylor. Description of Solvent-Extractable Chemicals in Thermal Receipts and Toxicological Assessment of Bisphenol S and Diphenyl Sulfone. Bulletin of Environmental Contamination and Toxicology 2024; 112(4) doi: 10.1007/s00128-024-03871-4
|
17 |
Jinlin Cheng, Ling Gong, Xiaoxiao Mi, Xiangyan Wu, Jun Zheng, Wenjun Yang. Case series of progressive familial intrahepatic cholestasis type 3: Characterization of variants in ABCB4 in China. Frontiers in Medicine 2022; 9 doi: 10.3389/fmed.2022.962408
|
18 |
T. N. Belkova, E. B. Pavlinova, K. B. Kurieva, Yu. E. Golovanova, A. Yu. Konstantinova, A. Kh. Begjanova. A case report of progressive familial intrahepatic cholestasis in neonatal practice. Meditsinskiy sovet = Medical Council 2024; (11): 306 doi: 10.21518/ms2024-216
|
19 |
Chenyue Hang, Yijie Jin, Yi Luo, Mingxuan Feng, Tao Zhou, Jianjun Zhu, Jianjun Zhang, Yuan Liu, Qiang Xia. Long-Term Results of Pediatric Liver Transplantation for Progressive Familial Intrahepatic Cholestasis. Journal of Clinical Medicine 2022; 11(16): 4684 doi: 10.3390/jcm11164684
|
20 |
Darwin Jhoan Ariza Rodriguez, Valentina Davila Ruales, Carmen Yanette Suarez Quintero, Sandra Amado Garzón. Reporte de caso de colestasis intrahepática asociada a mutación del gen ATP8B1 en un paciente con infección por virus de la inmunodeficiencia humana (VIH): un reto diagnóstico. Revista colombiana de Gastroenterología 2024; 39(3): 323 doi: 10.22516/25007440.1120
|
21 |
NR1H4 disease: rapidly progressing neonatal intrahepatic cholestasis and early death. Orphanet Journal of Rare Diseases 2024; 19(1) doi: 10.1186/s13023-024-03166-1
|
22 |
Jinping Gan, Kan He, W. Griffith Humphreys. Overcoming Obstacles in Drug Discovery and Development. 2023; : 107 doi: 10.1016/B978-0-12-817134-9.00010-6
|
23 |
Anushree Sahni, Sangita D Jogdand. Effects of Intrahepatic Cholestasis on the Foetus During Pregnancy. Cureus 2022; doi: 10.7759/cureus.30657
|
24 |
|
25 |
Mukul Vij, Vaibhav Shah. Compound Heterozygous Myosin 5B (Myo5b) Mutation with Early Onset Progressive Cholestasis and No Intestinal Failure. Fetal and Pediatric Pathology 2022; 41(5): 811 doi: 10.1080/15513815.2021.1959690
|
26 |
Mohammad Hossein Anbardar, Seyed Mohsen Dehghani, Maryam Poostkar, Seyed Ali Malek-Hosseini. Liver Transplantation in Progressive Familial Intrahepatic Cholestasis with Normal Gamma-Glutamyl Transferase: Evaluation of Post-transplant Steatosis and Steatohepatitis. Iranian Journal of Pediatrics 2021; 31(5) doi: 10.5812/ijp.117380
|
27 |
Bente Utoft Andreassen, Lise Aunsholt, Elsebet Østergaard, Jakob Ek, Lisa Leth Maroun, Marianne Hørby Jørgensen. Microvillus Inclusion Disease Caused by MYO5B: Different Presentation and Phenotypes Despite Same Mutation. JPGN Reports 2023; 4(2): e309 doi: 10.1097/PG9.0000000000000309
|
28 |
Tian-Fu Liu, Jing-Jing He, Liang Wang, Ling-Yi Zhang. Novel <i>ABCB4</i> mutations in an infertile female with progressive familial intrahepatic cholestasis type 3: A case report. World Journal of Clinical Cases 2022; 10(6): 1998-2006 doi: 10.12998/wjcc.v10.i6.1998
|
29 |
Binbin Liu, Jie Zhang, Lu Shao, Jiaming Yao, Gianfranco D. Alpini. Network pharmacology analysis and molecular docking to unveil the potential mechanisms of San-Huang-Chai-Zhu formula treating cholestasis. PLOS ONE 2022; 17(2): e0264398 doi: 10.1371/journal.pone.0264398
|
30 |
Laura Guerrero, Lorena Carmona‐Rodríguez, Fátima Milhano Santos, Sergio Ciordia, Luiz Stark, Loreto Hierro, Pablo Pérez‐Montero, David Vicent, Fernando J. Corrales. Molecular basis of progressive familial intrahepatic cholestasis 3. A proteomics study. BioFactors 2024; 50(4): 794 doi: 10.1002/biof.2041
|
31 |
Xiping Li, Yue Zu, Guodong Li, Dong Xiang, Chengliang Zhang, Dong Liu. Molecular mechanisms of transporter regulation and their impairment in intrahepatic cholestasis. Acta Materia Medica 2022; 1(3) doi: 10.15212/AMM-2022-0029
|
32 |
Juliane Nees, Franziska J Ammon, Johannes Mueller, Herbert Fluhr, Sebastian Mueller. Liver stiffness in pregnant women with intrahepatic cholestasis of pregnancy: A case control study. World Journal of Hepatology 2023; 15(7): 904-913 doi: 10.4254/wjh.v15.i7.904
Abstract(387) |
Core Tip(386) |
Full Article(HTML)(1304)
|
Full Article with Cover (PDF)-3754K(80)
|
Full Article (Word)-219K(29)
|
Audio-822K(9)
|
Peer-Review Report-228K(53)
|
Answering Reviewers-171K(53)
|
Supplementary Material-70K(55)
|
Full Article (PDF)-555K(109)
|
Full Article (XML)-105K(51)
|
Times Cited (1)
|
Total Visits (5366)
|
Open
|
33 |
Sarah M. Bedoyan, Olya T. Lovell, Simon P. Horslen, James E. Squires. Odevixibat: a promising new treatment for progressive familial intrahepatic cholestasis. Expert Opinion on Pharmacotherapy 2022; 23(16): 1771 doi: 10.1080/14656566.2022.2140040
|
34 |
Jia Tang, Meihua Tan, Yihui Deng, Hui Tang, Haihong Shi, Mingzhen Li, Wei Ma, Jia Li, Hongzheng Dai, Jianli Li, Shengmei Zhou, Xu Li, Fengxiang Wei, Xiaofen Ma, Liangping Luo. Two Novel Pathogenic Variants of TJP2 Gene and the Underlying Molecular Mechanisms in Progressive Familial Intrahepatic Cholestasis Type 4 Patients. Frontiers in Cell and Developmental Biology 2021; 9 doi: 10.3389/fcell.2021.661599
|
35 |
Coşkun Fırat Özkeçeci, Melike Arslan, Edibe Gözde Başaran, Yasin Maruf Ergen, Önder Bozdoğan, Necati Balamtekin. Non-syndromic perspective on a unique progressive familial intrahepatic cholestasis variant: <i>ZFYVE19 </i>mutation. The Turkish Journal of Pediatrics 2024; 66(4): 505 doi: 10.24953/turkjpediatr.2024.4655
|
36 |
Laura Guerrero, Jorge Vindel-Alfageme, Loreto Hierro, Luiz Stark, David Vicent, Carlos Óscar S. Sorzano, Fernando J. Corrales. Discrimination of Etiologically Different Cholestasis by Modeling Proteomics Datasets. International Journal of Molecular Sciences 2024; 25(7): 3684 doi: 10.3390/ijms25073684
|
37 |
Nina Komaniecka, Sonia Maroszek, Maria Drozdzik, Stefan Oswald, Marek Drozdzik. Transporter Proteins as Therapeutic Drug Targets—With a Focus on SGLT2 Inhibitors. International Journal of Molecular Sciences 2024; 25(13): 6926 doi: 10.3390/ijms25136926
|
38 |
Shuting Wang, Jie Bao, Jie Li, Wanfang Li, Mengyin Tian, Caixia Qiu, Fei Pang, Xin Li, Jianbo Yang, Yuchi Hu, Sujuan Wang, Hongtao Jin. Fraxinellone Induces Hepatotoxicity in Zebrafish through Oxidative Stress and the Transporters Pathway. Molecules 2022; 27(9): 2647 doi: 10.3390/molecules27092647
|
39 |
Qiong Pan, Gang Luo, Jiaquan Qu, Sheng Chen, Xiaoxun Zhang, Nan Zhao, Jingjing Ding, Hong Yang, Mingqiao Li, Ling Li, Ying Cheng, Xuan Li, Qiaoling Xie, Qiao Li, Xueqian Zhou, Huiling Zou, Shijun Fan, Lingyun Zou, Wei Liu, Guohong Deng, Shi‐Ying Cai, James L Boyer, Jin Chai.
A homozygous R148W mutation in
Semaphorin 7A
causes progressive familial intrahepatic cholestasis
. EMBO Molecular Medicine 2021; 13(11) doi: 10.15252/emmm.202114563
|
40 |
Serena Pelusi, Luisa Ronzoni, Francesco Malvestiti, Cristiana Bianco, Ilaria Marini, Roberta D'Ambrosio, Juri Alessandro Giannotta, Giorgio Soardo, Marco Maggioni, Daniele Prati, Luca Valenti. Clinical exome sequencing for diagnosing severe cryptogenic liver disease in adults: A case series. Liver International 2022; 42(4): 864 doi: 10.1111/liv.15185
|
41 |
Martina Ferrandino, Giovanna Cardiero, Fabiola Di Dato, Ylenia Cerrato, Luigi Vitagliano, Claudia Mandato, Filomena Morisco, Maria Immacolata Spagnuolo, Raffaele Iorio, Maria Donata Di Taranto, Giuliana Fortunato. Association of Very Rare NOTCH2 Variants with Clinical Features of Alagille Syndrome. Genes 2024; 15(8): 1034 doi: 10.3390/genes15081034
|
42 |
Xiaoyan Guo, Xinhua Li, Ying Yan, Huijuan Cao, Yufeng Zhang, Jing Lai. Efficacy and safety of low-dose rifampicin in patients with benign intrahepatic cholestasis. Liver Research 2022; 6(3): 181 doi: 10.1016/j.livres.2022.08.006
|
43 |
Ana Plaza Fernández, Marta Fernández Carrasco, Olga Sánchez García. FAMILIAL INTRAHEPATIC CHOLESTASIS: AN UNCOMMON CAUSE OF JAUNDICE IN YOUNG PATIENTS. . Revista Española de Enfermedades Digestivas 2024; doi: 10.17235/reed.2024.10628/2024
|
44 |
Shuying Xie, Shizhang Wei, Xiao Ma, Ruilin Wang, Tingting He, Zhao Zhang, Ju Yang, Jiawei Wang, Lei Chang, Manyi Jing, Haotian Li, Xuelin Zhou, Yanling Zhao. Genetic alterations and molecular mechanisms underlying hereditary intrahepatic cholestasis. Frontiers in Pharmacology 2023; 14 doi: 10.3389/fphar.2023.1173542
|
45 |
Willemien F.J. Hof, Jan Freark de Boer, Henkjan J. Verkade. Emerging drugs for the treatment of progressive familial intrahepatic cholestasis: a focus on phase II and III trials. Expert Opinion on Emerging Drugs 2024; 29(3): 305 doi: 10.1080/14728214.2024.2336986
|
46 |
Hana Halabi, Khawla Kalantan, Warif Abdulhaq, Habeib Alshaibi, Mohammed A Almatrafi. A Rare Case of Progressive Familial Intrahepatic Cholestasis Type 4: A Case Report and Literature Review. Cureus 2023; doi: 10.7759/cureus.47276
|
47 |
Alix Bruneau, Adrien Guillot, Frank Tacke. Macrophages in cholangiopathies. Current Opinion in Gastroenterology 2022; 38(2): 114 doi: 10.1097/MOG.0000000000000814
|
48 |
Safa Moussaoui, Mehdi Abdelwahed, Nabil Ben Chaaben, Ahlem Bellalah, Najah Ben Fadhel, Arwa Guediche, Mejda Zakhama, Ramzi Tababi, Karim Aouam, Zakhama Abdelfattah, Hichem Loghmari, Leila Safer. Norethisterone‐induced cholestasis: A case report. Clinical Case Reports 2022; 10(3) doi: 10.1002/ccr3.5522
|
49 |
Abdulla Sahloul, Elke Lainka, Simone Kathemann, Sandra Swoboda, Carola Dröge, Verena Keitel, Yahya Saleh Al-Matary, Michael Berger, Maren Schulze. Progressive familial intrahepatic cholestasis—outcome and time to transplant after biliary diversion according to genetic subtypes. Frontiers in Surgery 2023; 10 doi: 10.3389/fsurg.2023.1074229
|
50 |
Rodrigo M. Florentino, Qin Li, Michael C. Coard, Nils Haep, Takashi Motomura, Ricardo Diaz‐Aragon, Lanuza A. P. Faccioli, Sriram Amirneni, Zehra N. Kocas‐Kilicarslan, Alina Ostrowska, James E. Squires, Andrew P. Feranchak, Alejandro Soto‐Gutierrez. Transmembrane channel activity in human hepatocytes and cholangiocytes derived from induced pluripotent stem cells. Hepatology Communications 2022; 6(7): 1561 doi: 10.1002/hep4.1920
|
51 |
Masahiko Itoh, Kenji Watanabe, Yoichi Mizukami, Hiroyuki Sugimoto. Molecular alterations associated with pathophysiology in liver-specific ZO-1 and ZO-2 knockout mice. Cell Structure and Function 2024; 49(2): 83 doi: 10.1247/csf.24046
|