Biliary Dysgenesis in the PCK Rat, an Orthologous Model of Autosomal Recessive Polycystic Kidney Disease-Reference-Cited by-同舟云学术

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Biliary Dysgenesis in the PCK Rat, an Orthologous Model of Autosomal Recessive Polycystic Kidney Disease

Published:2004-11 Issue:5 Volume:165 Page:1719-1730
ISSN:0002-9440
Container-title:The American Journal of Pathology
language:en
Short-container-title:The American Journal of Pathology

Author:

Masyuk Tatyana V.,Huang Bing Q.,Masyuk Anatoliy I.,Ritman Erik L.,Torres Vicente E.,Wang Xiaofang,Harris Peter C.,LaRusso Nicholas F.

Publisher

Elsevier BV

Subject

Pathology and Forensic Medicine

Reference49 articles.

1. Isolated polycystic liver disease not linked to polycystic kidney disease 1 and 2;Iglesias;Dig Dis Sci,1999

2. Isolated polycystic liver disease as a distinct genetic disease, unlinked to polycystic kidney disease 1 and polycystic kidney disease 2;Pirson;Hepatology,1996

3. Mutations in PRKCSH cause isolated autosomal dominant polycystic liver disease;Li;Am J Hum Genet,2003

4. Germline mutations in PRKCSH are associated with autosomal dominant polycystic liver disease;Drenth;Nat Genet,2003

5. The genetic and physiology of polycystic kidney disease;Calvet;Semin Nephrol,2001

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1. Classic Lesions of the Biliary Tree;Toxicologic Pathology;2024-08-27

2. Differential regulation of MYC expression by PKHD1/Pkhd1 in human and mouse kidneys: phenotypic implications for recessive polycystic kidney disease;Frontiers in Cell and Developmental Biology;2023-11-17

3. Transcriptomics of Congenital Hepatic Fibrosis in Autosomal Recessive Polycystic Kidney Disease Using PCK Rats;Livers;2023-07-21

4. Global Transcriptomics of Congenital Hepatic Fibrosis in Autosomal Recessive Polycystic Kidney Disease using PCK rats;2023-01-20

5. Genetics, pathobiology and therapeutic opportunities of polycystic liver disease;Nature Reviews Gastroenterology & Hepatology;2022-05-13

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