[HTML][HTML] Emerging therapies for autosomal dominant polycystic kidney disease with a focus on cAMP signaling

X Zhou, VE Torres - Frontiers in Molecular Biosciences, 2022 - frontiersin.org
Autosomal dominant polycystic kidney disease (ADPKD), with an estimated genetic
prevalence between 1: 400 and 1: 1,000 individuals, is the third most common cause of end …

Modulation of polycystic kidney disease by G-protein coupled receptors and cyclic AMP signaling

CR Sussman, X Wang, FT Chebib, VE Torres - Cellular signalling, 2020 - Elsevier
Abstract Autosomal Dominant Polycystic Kidney Disease (ADPKD) is a systemic disorder
associated with polycystic liver disease (PLD) and other extrarenal manifestations, the most …

[HTML][HTML] Cystin genetic variants cause autosomal recessive polycystic kidney disease associated with altered Myc expression

C Yang, N Harafuji, AK O'Connor, RA Kesterson… - Scientific Reports, 2021 - nature.com
Mutation of the Cys1 gene underlies the renal cystic disease in the Cys1 cpk/cpk (cpk)
mouse that phenocopies human autosomal recessive polycystic kidney disease (ARPKD) …

[HTML][HTML] Ppia is the most stable housekeeping gene for qRT-PCR normalization in kidneys of three Pkd1-deficient mouse models

JJ Muñoz, AC Anauate, AG Amaral, FM Ferreira… - Scientific Reports, 2021 - nature.com
Abstract Autosomal Dominant Polycystic Kidney Disease (ADPKD) is the most common
inherited renal disorder, characterized by renal cyst development leading to end-stage renal …

JNK signaling prevents biliary cyst formation through a CASPASE-8–dependent function of RIPK1 during aging

K Müller, H Honcharova-Biletska… - Proceedings of the …, 2021 - National Acad Sciences
The c-Jun N-terminal kinase (JNK) signaling pathway mediates adaptation to stress signals
and has been associated with cell death, cell proliferation, and malignant transformation in …

The cellular pathways and potential therapeutics of Polycystic Kidney Disease

T Richards, K Modarage, SA Malik… - Biochemical Society …, 2021 - portlandpress.com
Polycystic Kidney Disease (PKD) refers to a group of disorders, driven by the formation of
cysts in renal tubular cells and is currently one of the leading causes of end-stage renal …

Protein kinase A downregulation delays the development and progression of polycystic kidney disease

X Wang, L Jiang, K Thao, CR Sussman… - Journal of the …, 2022 - journals.lww.com
Background Upregulation of cAMP-dependent and cAMP-independent PKA signaling is
thought to promote cystogenesis in polycystic kidney disease (PKD). PKA-I regulatory …

Nrf2 knockout attenuates the astragaloside IV therapeutic effect on kidney fibrosis from liver cancer by regulating pSmad3C/3L pathways

Q Wang, J Xu, M Li, Y Chen, Y Xu, L Li, Y Gong… - Naunyn-Schmiedeberg's …, 2024 - Springer
Fibrotic kidney injury from hepatocarcinogenesis seriously impacts treatment effect.
Astragaloside IV (AS-IV), an extract of Astragalus membranaceus, has several …

Cystin gene mutations cause autosomal recessive polycystic kidney disease associated with altered Myc expression

C Yang, AK O'Connor, RA Kesterson, JA Watts… - bioRxiv, 2020 - biorxiv.org
Mutation of the Cys1 gene underlies the renal cystic disease in the Cys1 cpk/cpk (cpk)
mouse that phenocopies human autosomal recessive polycystic kidney disease (ARPKD) …

Role of C-JUN terminal kinases (JNK1/2) in the development of cancer of the biliary tract

C Chen - 2021 - docta.ucm.es
Role of-JUN N-terminal kinases (JNK1/2) in the development of cancer of the biliary tract Page
1 UNIVERSIDAD COMPLUTENSE DE MADRID FACULTAD DE MEDICINA © Chaobo Chen …