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Prevalence of fibrosis in hepatic explants and biopsies from individuals with urea cycle disorders.

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Title: Prevalence of fibrosis in hepatic explants and biopsies from individuals with urea cycle disorders.
Authors: Ali S; Department of Molecular & Human Genetics, Baylor College of Medicine, United States of America., Nisar A; Department of Pediatrics-Medical Genetics and Center for Academic Medicine, Stanford University School of Medicine, United States of America., Zhang A; Division of Biostatistics and Study Methodology, Children's National Medical Center, United States of America., Nagamani S; Department of Molecular & Human Genetics, Baylor College of Medicine, United States of America; Texas Children's Hospital, United States of America., Aceves-Ewing NM; Department of Molecular & Human Genetics, Baylor College of Medicine, United States of America., Rawls B; Texas Children's Hospital, United States of America., Quan T; Department of Pediatrics-Medical Genetics and Center for Academic Medicine, Stanford University School of Medicine, United States of America., Enns G; Department of Pediatrics-Medical Genetics and Center for Academic Medicine, Stanford University School of Medicine, United States of America., Goss J; Division of Abdominal Transplantation, Department of Surgery, Baylor College of Medicine, United States of America., Leung DH; Division of Pediatric Gastroenterology, Hepatology, and Nutrition, Texas Children's Hospital, United States of America; Department of Pediatrics, Baylor College of Medicine, United States of America., Shneider BL; Division of Pediatric Gastroenterology, Hepatology, and Nutrition, Texas Children's Hospital, United States of America; Department of Pediatrics, Baylor College of Medicine, United States of America., Jain S; Department of Pathology and Immunology, Baylor College of Medicine, United States of America., Hazard FK; Department of Pathology, Stanford University School of Medicine, United States of America., Schady D; Department of Pathology and Immunology, Baylor College of Medicine, United States of America., Burrage LC; Department of Molecular & Human Genetics, Baylor College of Medicine, United States of America; Texas Children's Hospital, United States of America. Electronic address: burrage@bcm.edu.
Source: Molecular genetics and metabolism [Mol Genet Metab] 2025 Aug; Vol. 145 (4), pp. 109175. Date of Electronic Publication: 2025 Jun 13.
Publication Type: Journal Article
Journal Info: Publisher: Academic Press Country of Publication: United States NLM ID: 9805456 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1096-7206 (Electronic) Linking ISSN: 10967192 NLM ISO Abbreviation: Mol Genet Metab Subsets: MEDLINE
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  Data: Prevalence of fibrosis in hepatic explants and biopsies from individuals with urea cycle disorders.
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  Data: <searchLink fieldCode="AU" term="%22Ali+S%22">Ali S</searchLink>; Department of Molecular & Human Genetics, Baylor College of Medicine, United States of America.<br /><searchLink fieldCode="AU" term="%22Nisar+A%22">Nisar A</searchLink>; Department of Pediatrics-Medical Genetics and Center for Academic Medicine, Stanford University School of Medicine, United States of America.<br /><searchLink fieldCode="AU" term="%22Zhang+A%22">Zhang A</searchLink>; Division of Biostatistics and Study Methodology, Children's National Medical Center, United States of America.<br /><searchLink fieldCode="AU" term="%22Nagamani+S%22">Nagamani S</searchLink>; Department of Molecular & Human Genetics, Baylor College of Medicine, United States of America; Texas Children's Hospital, United States of America.<br /><searchLink fieldCode="AU" term="%22Aceves-Ewing+NM%22">Aceves-Ewing NM</searchLink>; Department of Molecular & Human Genetics, Baylor College of Medicine, United States of America.<br /><searchLink fieldCode="AU" term="%22Rawls+B%22">Rawls B</searchLink>; Texas Children's Hospital, United States of America.<br /><searchLink fieldCode="AU" term="%22Quan+T%22">Quan T</searchLink>; Department of Pediatrics-Medical Genetics and Center for Academic Medicine, Stanford University School of Medicine, United States of America.<br /><searchLink fieldCode="AU" term="%22Enns+G%22">Enns G</searchLink>; Department of Pediatrics-Medical Genetics and Center for Academic Medicine, Stanford University School of Medicine, United States of America.<br /><searchLink fieldCode="AU" term="%22Goss+J%22">Goss J</searchLink>; Division of Abdominal Transplantation, Department of Surgery, Baylor College of Medicine, United States of America.<br /><searchLink fieldCode="AU" term="%22Leung+DH%22">Leung DH</searchLink>; Division of Pediatric Gastroenterology, Hepatology, and Nutrition, Texas Children's Hospital, United States of America; Department of Pediatrics, Baylor College of Medicine, United States of America.<br /><searchLink fieldCode="AU" term="%22Shneider+BL%22">Shneider BL</searchLink>; Division of Pediatric Gastroenterology, Hepatology, and Nutrition, Texas Children's Hospital, United States of America; Department of Pediatrics, Baylor College of Medicine, United States of America.<br /><searchLink fieldCode="AU" term="%22Jain+S%22">Jain S</searchLink>; Department of Pathology and Immunology, Baylor College of Medicine, United States of America.<br /><searchLink fieldCode="AU" term="%22Hazard+FK%22">Hazard FK</searchLink>; Department of Pathology, Stanford University School of Medicine, United States of America.<br /><searchLink fieldCode="AU" term="%22Schady+D%22">Schady D</searchLink>; Department of Pathology and Immunology, Baylor College of Medicine, United States of America.<br /><searchLink fieldCode="AU" term="%22Burrage+LC%22">Burrage LC</searchLink>; Department of Molecular & Human Genetics, Baylor College of Medicine, United States of America; Texas Children's Hospital, United States of America. Electronic address: burrage@bcm.edu.
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  Data: <searchLink fieldCode="JN" term="%229805456%22">Molecular genetics and metabolism</searchLink> [Mol Genet Metab] 2025 Aug; Vol. 145 (4), pp. 109175. <i>Date of Electronic Publication: </i>2025 Jun 13.
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              Text: 2025 Aug
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