Mutations in the nuclear bile acid receptor FXR cause progressive familial intrahepatic cholestasis

Gomez-Ospina, Natalia, Potter, Carol J., Xiao, Rui, Manickam, Kandamurugu, Kim, Mi-Sun, Kim, Kang Ho, Shneider, Benjamin L., Picarsic, Jennifer L. +21 more·2016·Nature Communications
DOI 10.1038/ncomms10713

Cited by (302)

Items 201–300 of 302

  1. Ursodeoxycholic acid and COVID-19 outcomes: a cohort study and data synthesis of state-of-art evidence
    Yang Yu, Guo‐Fu Li, Jian Li, Luyao Han, Zhilong Zhang, Tian-Shuo Liu, S. Jiao, Yu-Wei Qiao, Na Zhang, De-Chuan Zhan et al. · 2024 · Expert Review of Anti-infective Therapy
  2. Sex differences in bile acid homeostasis and excretion underlie the disparity in liver cancer incidence between males and females
    Megan E Patton, Sherwin Kelekar, Lauren J Taylor, Angela Elizabeth Dean, Qianying Zuo, Rhishikesh N. Thakare, Sung-Hwan Lee, Emily C. Gentry, Morgan W. Panitchpakdi, Pieter C. Dorrestein et al. · 2024 · eLife
  3. Progressive familial intrahepatic cholestasis type 5 due to a novel mutation in the NR1H4 gene
    Rim Belhadj, Ines Maaloul, Wissem Besghaier, Roeya Kolsi, Naoual Sabaouni, Frank Broly, Thouraya Kamoun · 2025 · BMC Pediatrics
  4. Loss of the DNA-binding domain of the farnesoid X receptor gene causes severe liver and kidney injuries
    Ikuo Tomioka, Chihiro Ota, Yuka Tanahashi, Kayoko Ikegami, Ayaka Ishihara, Nanami Kohri, Hiroshi Fujii, Kanako Morohaku · 2024 · Biochemical and Biophysical Research Communications
  5. Intrahepatic cholestasis of pregnancy in conjunction with a frameshift deletion in FGFR4
    Syeda Saima Batool, Marc Dauer, Susanne Nicole Weber, Roman Liebe, Frank Lammert, Matthias Reichert · 2021 · Clinics and Research in Hepatology and Gastroenterology
  6. FAMILIAL INTRAHEPATIC CHOLESTASIS IN CHILDREN: PROBLEMS AND PROSPECTS
    Волынец Галина Васильевна · 2019 · Russian Pediatric Journal
  7. Bile Acid Physiology and Alterations in the Enterohepatic Circulation
    James E. Heubi · 2021 · Elsevier eBooks
  8. Gallengangatresie und angeborene Cholestasesyndrome
    Norman Junge, Jens Dingemann, Claus Petersen, M.P. Manns, Nicolas Richter, J. Klempnauer, Ulrich Baumann, Armin Schneider · 2018 · Der Internist
  9. Fxr-alpha Skips Alternatively in Liver Metabolism
    Sayeepriyadarshini Anakk, Angela Elizabeth Dean · 2020 · Gastroenterology
  10. Advances in genetic, epigenetic and environmental aspects of rare liver diseases
    Emma Rachel Andersson, Ansgar Wilhelm Lohse · 2021 · European Journal of Medical Genetics
  11. Alternative splicing is an FXRα loss-of-function mechanism and impacts energy metabolism in hepatocarcinoma cells
    Manon Garcia, Hélène Holota, Angélique De Haze, Jean‐Paul Saru, Phelipe Sanchez, Edwige Battistelli, Laura Thirouard, Mélusine Monrose, Gérard Benoit, David H. Volle et al. · 2024 · Journal of Biological Chemistry
  12. Unfolding the genetic map of monogenic liver diseases in Egypt
    Hanaa Mostafa El-Karaksy, Engy Adel Mogahed, Sherif Baroudy, Haytham Ghita, Afaf Enayet, Marwa Elsharkawy, Noha A. Radwan, Heba Hosny, Mohamed A. Elmonem · 2025 · Human Genetics
  13. The Role of a NICU Hepatology Consult Service in Assessing Liver Dysfunction in the Premature Infant
    Carol Potter · 2020 · JPGN Reports
  14. Clinical symptoms, biochemistry, and liver histology during the native liver period of progressive familial intrahepatic cholestasis type 2
    Hiroki Kondou, Satoshi Nakano, Tadahaya Mizuno, Kazuhiko Bessho, Yasuhiro Hasegawa, Atsuko Nakazawa, Ken Tanikawa, Yoshihiro Azuma, Tatsuya Okamoto, Ayano Inui et al. · 2024 · Orphanet Journal of Rare Diseases
  15. Progressive familial intrahepatic cholestasis type 4: a case report
    Mohamed Abdelmalak, Saber Waheeb, Wessam Zaghloul, Manal Abdelgawad, Mona Abdel‐Hady, Mohamed Mansy, Mostafa Kotb · 2024 · Journal of Medical Case Reports
  16. A novel mechanism involving USP53-regulated BSEP trafficking underlies low-GGT intrahepatic cholestasis
    Jian Ping Ding, Hui-Yu She, Ye Cheng, Hong-Yuan Sun, Jia‐Yan Feng, Teng Liu, Yi‐Ling Qiu, Bing-Xuan Wei, Jin Zhang, Yu Su et al. · 2025 · Hepatology
  17. Leberbiopsie bei Kindern und Jugendlichen
    C. Lackner, Alex S. Knisely · 2017 · Der Pathologe
  18. Next-Generation Sequencing in Paediatric Hepatology
    Lorenzo D’Antiga · 2019 · Springer eBooks
  19. Proposal of a liver histology‐based scoring system for bile salt export pump deficiency
    Yoh Zen, Hiroki Kondou, Atsuko Nakazawa, Ken Tanikawa, Yasuhiro Hasegawa, Kazuhiko Bessho, Kazuo Imagawa, Takashi Ishige, Ayano Inui, Mitsuyoshi Suzuki et al. · 2020 · Hepatology Research
  20. Pediatric Cholestatic Liver Disease
    Kathleen M. Loomes, Karan McBride Emerick · 2021 · Elsevier eBooks
  21. A New Variant of an Old Itch: Novel Missense Variant in ABCB4 Presenting with Intractable Pruritus
    Sahana Shankar, Apurva Pande, Thenral S. Geetha, Karthik K. Raichurkar, Malikarjun Sakpal, Rajiv Lochan, Sonal Asthana · 2021 · Journal of Clinical and Experimental Hepatology
  22. Progressive Familial Intrahepatic Cholestasis
    Rajeev Khanna, Vipul Gautam · 2022 · Annals of Pediatric Gastroenterology & Hepatology
  23. Inherited Disorders of Bilirubin Metabolism
    Namita Roy‐Chowdhury, Chandan Guha, Jayanta Roy‐Chowdhury · 2022 · Springer eBooks
  24. Familial Hepatocellular Cholestasis
    Frederick J. Suchy, Shikha S. Sundaram, Benjamin L. Shneider · 2021 · Cambridge University Press eBooks
  25. Childhood Liver Disease and Metabolic Disorders
    Jay H. Lefkowitch · 2020 · Elsevier eBooks
  26. Pathophysiologic Basis for Alternative Therapies for Cholestasis
    Claudia Daniela Fuchs, Emina Halilbasic, Michael A Trauner · 2020 · Wiley eBooks
  27. Sex differences in bile acid homeostasis and excretion underlie the disparity in liver cancer incidence between males and females
    Megan E Patton, Sherwin Kelekar, Lauren J Taylor, Angela Elizabeth Dean, Qianying Zuo, Rhishikesh N. Thakare, Sung Hwan Lee, Emily C. Gentry, Morgan W. Panitchpakdi, Pieter C. Dorrestein et al. · 2024 · eLife
  28. Hepatobiliary Transport of Bile Acids
    Tatehiro Kagawa · 2017 · Springer eBooks
  29. Liver Transplantation in Progressive Familial Intrahepatic Cholestasis with Normal Gamma-Glutamyl Transferase: Evaluation of Post-transplant Steatosis and Steatohepatitis
    Mohammad Hossein Anbardar, Seyed Mohsen Dehghani, Maryam Poostkar, Seyed Ali Malek‐Hosseini · 2021 · Iranian Journal of Pediatrics
  30. Hepatocellular and Intrahepatic Cholestasis
    Benjamin J. Wilkins, Kathleen M. Loomes · 2024 · Springer eBooks
  31. Inherited and metabolic disorders of the liver
    Aabha S. Nagral, Snehal Mallakmir · 2024 · Elsevier eBooks
  32. Bile Acid-Mediated Interactions with Various Cell Types in the Cholestatic Liver
    Guanyi He, Jie Qing · 2025 · DNA and Cell Biology
  33. First Report of Living Donor Liver Transplantation for NR1H4 Disease
    Lakshmi Suresh, Jagadeesh Menon, Naresh Shanmugam, Mukul Vij, Ashwin Rammohan, Mohamed Rela · 2025 · Pediatric Transplantation
  34. Beyond the Very Important Pharmacogenes (VIPs): Uncovering Shadow Pharmacogenes in the Human Drug Response Network
    Nicolly Clemente de Melo, Guilherme Silva Accioli, Karen Sánchez-Luquez, Mateus Freitas de Farias Gomes, Aline Cristina Felicio, Lucas Miguel de Carvalho · 2026 · ACS Omega
  35. Sex-specific KDM6A-HNF4A-CREBH network controls lipoprotein cholesterol metabolism and atherosclerosis via epigenetic reprograming of hepatocytes
    Lin Chen, Zhanfang Kang, Jennifer Härdfeldt, Ziyi Li, Matteo Pedrelli, Qi Li, Ruining Lyu, Philipp Valina Allo, Taras Sych, Xiangru Zheng et al. · 2026 · Nature Communications
  36. FXR–YAP signalling maintains biliary epithelial cell identity and preserves liver homeostasis
    Paula Sánchez-Sánchez, Zhaoshuo Wang, Sladjana Zagorac, María Domínguez, Jasminka Boskovic, Ajay Nair, Andrea Macías‐Camero, Alma Villaseñor, Robert F. Schwabe, Nabil Djouder · 2026 · Nature Metabolism
  37. Frühzeitige Diagnostik ist entscheidend für die Prognose
    Jan Vermehren, Patrick Kwiatkowski, Birgit Knoppke, Dirk Grothues, Michael Melter · 2016 · Pädiatrie
  38. Infantile cholestasis related to ABCB4 gene mutation and cytomegalovirus (CMV) infection: a case report
    Guanming Li, Hanni Lin, Airun Zhang, Jiahong Li, Min Wang, Xiaoyi Fang · 2021 · Digestive Medicine Research
  39. Familial Intrahepatic Cholestasis
    Tassos Grammatikopoulos · 2021 · Springer eBooks
  40. Children with Chronic Liver Disease
    Giuseppe Maggiore, Claudia Della Corte, Daniela Liccardo, Antonella Mosca, Andrea Pietrobattista · 2023 · Springer eBooks
  41. Angeborene Cholestasesyndrome im Erwachsenenalter: Relevantes für Diagnostik und Therapie
    Carola Dröge, Verena Keitel · 2023 · Die Gastroenterologie
  42. Bilirubin metabolism and its disorders
    Namita Roy‐Chowdhury, Patrik Asp, Chandan Guha, Jayanta Roy‐Chowdhury · 2024 · Elsevier eBooks
  43. Familial Intrahepatic Cholestasis
    Tassos Grammatikopoulos, Richard J. Thompson · 2015 · Springer eBooks
  44. Co nowego w cholestazie – część 1. Cholestaza z prawidłową aktywnością gamma-glutamylotranspeptydazy
    Patryk Lipiński, Irena Jankowska · 2017 · Pediatria Polska
  45. Paediatric cholestatic liver disorders for the adult gastroenterologist: a practical guide
    Claire Kelly, Jeremy Shanika Nayagam, Stamatina Vogli, Marianne Samyn, Deepak Joshi · 2020 · Frontline Gastroenterology
  46. Mechanisms of Bile Formation and the Pathogenesis of Cholestasis
    Saul J. Karpen · 2021 · Cambridge University Press eBooks
  47. Behandlung progressiv-familiärer intrahepatischer Cholestasen (PFIC)
    Verena Keitel · 2021 · Elsevier eBooks
  48. Intrahepatic Cholestasis, Refractory Epilepsy, Skeletal Dysplasia, Endocrine Failure, and Dysmorphic Features in a Child With a Monoallelic 2q24-32.2 Deletion Encompassing ABCB11
    Rodrigo Tzovenos Starosta, Jorge Luis Granadillo, Kalyani R. Patel, Milton J. Finegold, Janis M. Stoll, Sakil Kulkarni · 2021 · Pediatric and Developmental Pathology
  49. Progressive Familial Intrahepatic Cholestasis
    Rajeev Khanna, Vipul Gautam · 2022 · GI surgery annual
  50. Hepatic Adenosine Triphosphate‐Binding Cassette Transport Proteins and Their Role in Physiology
    Peter L. M. Jansen · 2020
  51. Fine tuning the gut-liver-axis
    Maiju Myllys · 2020 · Archives of Toxicology
  52. DRUG TRANSPORT IN THE LIVER
    Noora Sjöstedt, Jeffry Adiwidjaja, William A. Murphy, Kim L. R. Brouwer · 2022
  53. Liver disease in infants and children
    Joseph DiNorcia, John C. Bucuvalas, Irini D. Batsis, Rachel W. Smith · 2024 · Elsevier eBooks
  54. Klinische Genetik der Gallenwegserkrankungen
    M. Reichert, F. Lammert, Christoph Jüngst · 2016 · Die Gastroenterologie
  55. Co nowego w cholestazie – część 2. Cholestaza z podwyższoną aktywnością gamma-glutamylotranspeptydazy
    Patryk Lipiński, Irena Jankowska · 2017 · Pediatria Polska
  56. İlaca Bağlı Karaciğer Hasarı
    Melek Akıncı · 2023
  57. Cholestases hépatocytaires génétiques
    Emmanuel M. Gonzales, Anne Spraul · 2018 · Elsevier eBooks
  58. Genetic Cholestatic Disorders
    Emanuele Nicastro, Lorenzo D’Antiga · 2019 · Springer eBooks
  59. Rheumatologie und Hepatologie: Diagnostik und Therapie von autoimmunen Lebererkrankungen
    Alexander Zipprich · 2019 · Aktuelle Rheumatologie
  60. Mice Lacking FXR Are Susceptible to Liver Ischemia-Reperfusion Injury
    Yuxin Li, Rui‐Hua Xu, Prahlad Rao, Charles Gomes, E. Richard Moran, Michelle Puchowicz, Eugene B. Chang, D. Yin, Joseph F. Pierre · 2019 · bioRxiv (Cold Spring Harbor Laboratory)
  61. Clinical Genetics of Cholangiopathies
    Matthias Reichert, Frank Lammert · 2020 · Encyclopedia of Life Sciences
  62. [Clinical and genetic analysis of an infant with progressive familial intrahepatic cholestasis type II].
    Gui‐Zhi Lin, Jian‐Wu Qiu, Ying Cheng, Wei‐Xia Lin, Yuan‐Zong Song · 2018 · PubMed Central
  63. Gallengangatresie und angeborene Cholestasesyndrome: Besonderheiten vor, nach und während der Transition
    Norman Junge, Jens Dingemann, Claus Petersen, M.P. Manns, Nicolas Richter, J. Klempnauer, Ulrich Baumann, Armin Schneider · 2018 · Der Internist
  64. Differential Diagnosis of Biliary Atresia
    Daiki Abukawa · 2021 · Springer eBooks
  65. MODELO DE CALIDAD APLICADO A LA INVESTIGACIÓN SOFTWARE
    Adriana Llamosa Ardila, Sandra Milena Vera Arciniegas · 2003 · Revista gerencia tecnológica informática/Gerenc. tecnol. inform. GTI
  66. A study of exons 14, 15, and 24 of the ABCB11 gene in Egyptian children with normal GGT cholestasis
    Nora Mahmoud Selim, Heba Omair, Hanaa Mostafa El-Karaksy, Marianne Fathy, Enas H. Mahmoud, Sherif Baroudy, Mona Mohamed Fathy, Noha Adel Yassin · 2022 · Arab Journal of Gastroenterology
  67. Hereditäre Lebererkrankungen
    Carolin Lackner, Alexander S. Knisely · 2020 · Pathologie
  68. Vitamin D3 deficiency in babies and children with cholestasis
    Mustafa Mohammed Albassam · 2022 · Medical Science
  69. Pediatric hepatobiliary disease: Genetic and clinical manifestations
    Nguyen Thi Kim Lien, Nguyen Pham Anh Hoa, Nguyen Huy Hoang · 2022 · Vietnam Journal of Biotechnology
  70. The Role of FXR-Signaling Variability in the Development and Course of Non-Alcoholic Fatty Liver Disease in Children
    Yu.M. Stepanov, N.Yu. Zavhorodnia, І.А. Кленіна, O. I. Hrabovska, Viktoria Yagmur · 2022 · Acta Medica (Hradec Kralove Czech Republic)
  71. Impaired transitioning of the FXR ligand binding domain to an active state underlies an FXR-associated PFIC phenotype
    Annika Behrendt, Alex Bastianelli, Jan Stindt, Eva‐Doreen Pfister, Malte Sgodda, Tobias Cantz, Sebastian Hook, Kathrin Grau, Stefanie Brands, Carola Dröge et al. · 2024 · bioRxiv (Cold Spring Harbor Laboratory)
  72. Additional file 1 of Identification of two novel pathogenic variants of the NR1H4 gene in intrahepatic cholestasis of pregnancy patients
    Hua Lai, Xianxian Liu, Siming Xin, Jiusheng Zheng, Huai Liu, Yu Ouyang, Huoxiu Yang, Yang Zeng, Yang Zou, Xiaoming Zeng · 2022 · Figshare
  73. Behandlung progressiv-familiärer intrahepatischer Cholestasen (PFIC)
    Verena Keitel, Carola Dröge, Jan Stindt · 2024 · Elsevier eBooks
  74. Reviewer #1 (Public Review): Sex differences in bile acid homeostasis and excretion underlie the disparity in liver cancer incidence between males and females
    2024 · eLife
  75. Reviewer #2 (Public Review): Sex differences in bile acid homeostasis and excretion underlie the disparity in liver cancer incidence between males and females
    2024 · eLife
  76. eLife Assessment: Sex differences in bile acid homeostasis and excretion underlie the disparity in liver cancer incidence between males and females
    Edward A A Fisher · 2024 · eLife
  77. Hepatic Expression of Fibroblast Growth Factor 19 Significantly Correlates With Serum Bile Acids in Neonatal Cholestasis
    Ola Ahmed Fouad, Doaa F. Zaghlol, Dina Sweed, Magdy Anwar Saber, Mostafa Mohamed Sıra · 2025 · Pediatric and Developmental Pathology
  78. PROGRESSIVE FAMILIAL INTRAHEPATIC CHOLESTASIS IN CHILDREN
    R. A. Gudkov, A.V. DMITRIEV, Natalia V. Fedina, V. I. Petrova · 2024 · Avicenna Bulletin
  79. Clinical Diversity and Outcomes of Progressive Familial Intrahepatic Cholestasis Diagnosed by Whole Genome Sequencing in Pakistani Children
    Huma Arshad Cheema, Aliaksandr Skrahin, Anjum Saeed, Zafar Fayyaz, Muhammad Arshad Alvi, Muhammad Nadeem Anjum, Nadia Khalida Waheed, Khalil Ur Rehman, Ahmad Malik, Volha Skrahina et al. · 2025 · GenoMed Connect
  80. Bile Acid Physiology and Alterations in the Enterohepatic Circulation
    Gregory J. Guthrie, Sanjiv Harpavat · 2025 · Elsevier eBooks
  81. Pediatric Cholestatic Liver Disease
    Tamir Diamond, Kathleen M. Loomes · 2025 · Elsevier eBooks
  82. Sex differences in bile acid homeostasis and excretion underlie the disparity in liver cancer incidence between males and females
    Megan E Patton, Sherwin Kelekar, Lauren J Taylor, Angela Elizabeth Dean, Qianying Zuo, Rhishikesh N. Thakare, Sung-Hwan Lee, Emily C. Gentry, Morgan W. Panitchpakdi, Pieter C. Dorrestein et al. · 2025 · eLife
  83. Pediatric and Neonatal Cholestatic and Bile Duct Diseases
    Iván González · 2025 · Pracatical anatomic pathology
  84. Sex differences in bile acid homeostasis and excretion underlie the disparity in liver cancer incidence between males and females
    Megan E Patton, Sherwin Kelekar, Lauren J Taylor, Angela Elizabeth Dean, Qianying Zuo, Rhishikesh N. Thakare, Sung-Hwan Lee, Emily C. Gentry, Morgan W. Panitchpakdi, Pieter C. Dorrestein et al. · 2025 · eLife
  85. Rodent-specific induction of cholestasis and cholangioma through the reduction of bile salt export pump by bardoxolone methyl
    Hironori Otsuki, Tetsuro Araki, Atsuko Takami, Koji Inomata, Masanori Hiura, Ken‐ichiro Nan‐ya, Kouichi Yoshinari · 2025 · The Journal of Toxicological Sciences
  86. Adult Cholestatic and Bile Duct Diseases
    Byoung Uk Park, Zongming Eric Chen · 2025 · Pracatical anatomic pathology
  87. Differenzialdiagnostik der Cholestase bei Erwachsenen
    Carola Dröge, Thomas Berg, Verena Keitel-Anselmino · 2025 · Gastroenterologie up2date
  88. Sex differences in bile acid homeostasis and excretion underlie the disparity in liver cancer incidence between males and females
    Megan E Patton, Sherwin Kelekar, Lauren J Taylor, Angela Elizabeth Dean, Qianying Zuo, Rhishikesh N. Thakare, Sung Hwan Lee, Emily C. Gentry, Morgan W. Panitchpakdi, Pieter C. Dorrestein et al. · 2025 · eLife
  89. Activation of farnesoid X receptor inhibits TMEM16A-mediated chloride secretion in renal collecting duct cells and retards renal cyst progression
    Nipitpon Srimai, Kanlayanee Tonum, Sanya Sureram, Alisa Tubsuwan, Prasat Kittakoop, Sunhapas Soodvilai · 2026 · American Journal of Physiology-Renal Physiology
  90. Régulation de l'expression membranaire du transporteur de phospholipides biliaires ABCB4 : effet de mutations
    Alix Bruneau · 2019
  91. Analyse de la régulation de l'homéostasie des acides biliaires au sein des testicules
    Hélène Holota · 2024 · theses.fr (ABES)
  92. Farnesoid x Receptor Deficiency Promotes Hepatocytic Injury in Cyp2c70 ‐Deficient Mice With a Human‐Like Bile Acid Composition
    Hilde D. de Vries, Jinxiao Li, Kirill Ustyantsev, Milaine V. Hovingh, Niels L. Mulder, Rick Havinga, Anna Palmiotti, Krisztina de Bruyn, Brecht J. Attema, Ellen Weersing et al. · 2026 · Liver International
  93. A Mechanistic Framework of Genetic Liver Diseases: From Developmental Defects to Functional Disorders
    Angelo Corso Faini, Alberto Calleri, Michele Pinon, Cristina Chiadò, Pier Luigi Calvo, Tiziana Vaisitti, Silvia Deaglio · 2026 · Livers
  94. FXR’s double life in bile ducts
    Shogo Takahashi, Frank J. Gonzalez · 2026 · Nature Metabolism
  95. Genetic testing in liver diseases: Clinical applications
    Verena Keitel, Anne Mentzinger, Carola Dröge, Sílvia Vilarinho · 2026 · JHEP Reports
  96. Decoding the bile acid–mitochondria axis: Implications for disease management and therapeutic opportunities
    Xueru Jia, Zehan Zhang, Xiaoyu Lin, Xiangyue Dong, Ruixue Chen, Nan Liang, He Ding, Feng Li · 2026 · Pharmacological Research
  97. Genetic and Familial Forms of Pediatric Intrahepatic Cholestasis
    Maria Amendola, Lara E. Berklite, Simon Peter Horslen, James E. Squires · 2026 · Clinics in Liver Disease
  98. Pediatric Cholestatic Liver Disease: A Contemporary Review of Etiology, Diagnostics, and Management
    Minoti Vather, Jasmine Lee, Jennifer Vittorio · 2026 · Current Treatment Options in Pediatrics
  99. Bile Biochemistry as a Therapeutic Target in Biliary Surgery: Disease-Specific Evidence and Clinical Limits
    Zelimkhan G. M. Berikkhanov, Zakhar A. Akulov, M. A. Emtsev, E. А. Tarabrin, Alexey Shestakov, Aleksey Kotelnikov, Andrey Nikolaev, Vadim Sergeevich Razumovsky, M. Yu. Ivanova, Mehrshad Ebrahimnezhad et al. · 2026 · Metabolites
  100. Genetic hepatocellular cholestasis: an update
    Antoine Gardin, William Pouillot, Marion Almes, Charlotte Mussini, Emmanuel M. Gonzales, Emmanuel Jacquemin · 2026 · Clinics and Research in Hepatology and Gastroenterology