[HTML][HTML] The rise of genetically engineered mouse models of pancreatitis: A review of literature

TL Merry, MS Petrov - Biomolecular Concepts, 2018 - degruyter.com
Pancreatitis is increasingly recognized as not merely a local inflammation of the pancreas
but also a disease with high frequency of systemic sequelae. Current understanding of the …

Rapamycin treatment dose‐dependently improves the cystic kidney in a new ADPKD mouse model via the mTORC1 and cell‐cycle‐associated CDK1/cyclin axis

A Li, S Fan, Y Xu, J Meng, X Shen… - Journal of cellular …, 2017 - Wiley Online Library
Although translational research into autosomal dominant polycystic kidney disease
(ADPKD) and its pathogenesis has made considerable progress, there is presently lack of …

[HTML][HTML] Canonical Wnt inhibitors ameliorate cystogenesis in a mouse ortholog of human ADPKD

A Li, Y Xu, S Fan, J Meng, X Shen, Q Xiao, Y Li… - JCI insight, 2018 - ncbi.nlm.nih.gov
Autosomal dominant polycystic kidney disease (ADPKD) can be caused by mutations in the
PKD1 or PKD2 genes. The PKD1 gene product is a Wnt cell-surface receptor. We previously …

Bile acids as potential biomarkers to assess liver impairment in polycystic kidney disease

WJ Brock, JJ Beaudoin, JR Slizgi… - … journal of toxicology, 2018 - journals.sagepub.com
Polycystic kidney disease is characterized by the progressive development of kidney cysts
and declining renal function with frequent development of cysts in other organs including the …

SHCBP1 Overexpression Aggravates Pancreatitis by Triggering the Loss of Primary Cilia

L Li, H Zhao, Z Li, W Shi, Z Jiao - DNA and Cell Biology, 2024 - liebertpub.com
Primary cilia are microtubule-based organelles that mediate various biological processes.
Pancreatic cells are typically ciliated; however, the role of primary cilia in acute pancreatitis …

[HTML][HTML] Bacterial cholangitis in autosomal dominant polycystic kidney and liver disease

WP Martin, LE Vaughan, K Yoshida… - … : Innovations, Quality & …, 2019 - Elsevier
Objective To describe first episodes of bacterial cholangitis complicating autosomal
dominant polycystic kidney disease (ADPKD) and autosomal dominant polycystic liver …

Perspectives of gene therapies in autosomal dominant polycystic kidney disease

Y Xu, A Li, G Wu, C Liang - Current gene therapy, 2017 - ingentaconnect.com
Background: Autosomal dominant polycystic kidney disease (ADPKD) is the most common
inherited kidney disease in the clinic. The predominant clinical manifestation is bilateral and …

[HTML][HTML] Chronic pancreatitis with polycystic kidney disease: A rare coincidence?

G Hrčková, E Hegyi, K Skalická, I Čierna… - Nefrología (English …, 2020 - Elsevier
Introduction In children, chronic pancreatitis (CP) is usually associated with anatomical
anomalies of the pancreas and biliary tract or is genetically determined. Autosomal …

[HTML][HTML] Hepatointestinal complications in polycystic kidney disease

ST Huang, YW Chuang, TM Yu, CL Lin, LB Jeng - Oncotarget, 2017 - ncbi.nlm.nih.gov
Background The objective of this study was to determine the incidence of major
hepatointestinal complications in patients with polycystic kidney disease (PKD). Methods We …

N-acetilcisteína melhora os fenótipos renal e cardíaco e reduz o peso corpóreo em camundongos císticos deficientes em Pkd1

ZP Moyses - 2013 - teses.usp.br
Estudos experimentais e clínicos amparam a participação do estresse oxidativo na
progressão da doença renal na doença renal policística autossômica dominante (DRPAD) …