Results 111 to 120 of about 2,905 (217)

Functional correction of renal defects in a mouse model for ARPKD through expression of the cloned wild-type Tg737 cDNA

, 1996
Bradley K. Yoder, William G. Richards, Carla S. Sommardahl, William E. Sweeney, Edward J. Michaud, John E. Wilkinson, Ellis D. Avner, Richard P. Woychik   +7 more
openalex   +1 more source

Novel ARPKD mouse model with near complete deletion of Polycystic Kidney and Hepatic Disease 1 (Pkhd1) genomic locus has multiple phenotypes but no renal cysts.

Kidney International, 2023
Y. Ishimoto, L. Menezes, Fang Zhou, Teruhiko Yoshida, Taishi Komori, Jiahe Qiu, Marian F Young, Huiyan Lu, Svetlana Potapova, Patricia Outeda, T. Watnick, G. Germino   +11 more
semanticscholar   +1 more source

UEG Week 2024 Moderated Posters

United European Gastroenterology Journal, Volume 12, Issue S8, Page 201-664, October 2024.
wiley   +1 more source

Clinical manifestations of autosomal recessive polycystic kidney disease (ARPKD): kidney-related and non-kidney-related phenotypes [PDF]

, 2013
Rainer Büscher, Anja Büscher, Stefanie Weber, Julia Mohr, Bianca Hegen, Udo Vester, Peter F. Hoyer   +6 more
openalex   +1 more source

Liver and spleen volume and stiffness in patients post-Fontan procedure and patients with ARPKD compared to normal controls.

Clinical imaging, 2022
S. Serai, M. Elsingergy, Erum A. Hartung, Hansel J. Otero   +3 more
semanticscholar   +1 more source

Generation of an induced pluripotent stem cell line (DHMCi007-A) from a patient with autosomal recessive polycystic kidney disease (ARPKD) carrying a homozygous missense mutation in the fibrocystin-encoding PKHD1 gene

, 2021
Mansoureh Tabatabaeifar, Theresa Leonie Fluhr, Hanna Syring, Gudrun Göhring, Franz Schaefer, Sabine Jung‐Klawitter   +5 more
openalex   +1 more source

Atmin modulates Pkhd1 expression and may mediate Autosomal Recessive Polycystic Kidney Disease (ARPKD) through altered non-canonical Wnt/Planar Cell Polarity (PCP) signalling

, 2018
Taylor Richards, Kavindiya Modarage, Charlotte Dean, Aidan McCarthy-Boxer, Helen Hilton, Chris Esapa, Jill T. Norman, Patricia D. Wilson, Paraskevi Goggolidou   +8 more
openalex   +2 more sources

Role of genetic modifiers in an orthologous rat model of ARPKD

, 2012
Caitlin C. O’Meara, Matthew Hoffman, William E. Sweeney, Shirng‐Wern Tsaih, Bing Xiao, Howard J. Jacob, Ellis D. Avner, Carol Moreno   +7 more
openalex   +2 more sources

Two-dimensional (2D) morphologic measurements can quantify the severity of liver disease in children with autosomal recessive polycystic kidney disease (ARPKD)

Abdominal Radiology, 2021
A. Ghosh, S. Serai, S. S. B. Venkatakrishna, Mohini Dutt, Erum A. Hartung   +4 more
semanticscholar   +1 more source

Congenital Hepatic Fibrosis and/or Autosomal Recessive Polycystic Kidney Disease: A Single-center Experience. [PDF]

Pediatr Gastroenterol Hepatol Nutr
Altay D, Yel S, Dursun İ, Arslan D.
europepmc   +1 more source