Results 151 to 160 of about 42,420 (251)

Autosomal-dominante polyzystische Nierenerkrankung: Neue therapeutische Ansätze [PDF]

, 2018
Zusammenfassung: Die autosomal-dominante polyzystische Nierenerkrankung ("autosomal dominant polycystic kidney disease", ADPKD) ist die häufigste genetische Nierenerkrankung, sie betrifft weltweit etwa 6Mio. Menschen.
Poster, D., Serra, A.L., Wüthrich, R.P.
core  

The cAMP effectors Epac and protein kinase a (PKA) are involved in the hepatic cystogenesis of an animal model of autosomal recessive polycystic kidney disease (ARPKD) [PDF]

, 2008
Jesús M. Bañales, Tatyana V. Masyuk, Sergio A. Gradilone, Anatoliy I. Masyuk, Juan Francisco Medina Gallardo, Nicholas F. LaRusso   +5 more
openalex   +1 more source

Hyperinsulinemic Hypoglycemia Due to PMM2 Mutation in Two Siblings with Autosomal Recessive Polycystic Kidney Disease. [PDF]

Pediatr Rep, 2022
Acharya R, Upadhyay K.
europepmc   +1 more source

Effect of calcium-sensing receptor activation in models of autosomal recessive or dominant polycystic kidney disease [PDF]

, 2008
Xiaofang Wang, Peter C. Harris, Stefan Somlo, Daniel Batlle, Vicente E. Torres   +4 more
openalex   +1 more source

AI-Driven Predictive Analytics Approach for Early Prognosis of Chronic Kidney Disease Using Ensemble Learning and Explainable AI [PDF]

arXiv
Chronic Kidney Disease (CKD) is one of the widespread Chronic diseases with no known ultimo cure and high morbidity. Research demonstrates that progressive Chronic Kidney Disease (CKD) is a heterogeneous disorder that significantly impacts kidney structure and functions, eventually leading to kidney failure. With the progression of time, chronic kidney
arxiv  

MKS3-Related Ciliopathy with Features of Autosomal Recessive Polycystic Kidney Disease, Nephronophthisis, and Joubert Syndrome [PDF]

, 2009
Meral Gunay‐Aygun, Melissa A. Parisi, Dan Doherty, M. Tuchman, Ekaterini Tsilou, David E. Kleiner, Marjan Huizing, Barış Türkbey, Peter L. Choyke, Lisa M. Guay‐Woodford, Theo Heller, Katarzyna Szymańska, Colin A. Johnson, Ian Glass, William A. Gahl   +14 more
openalex   +1 more source

Characterizing the nuclear import and functions of cystin, the ciliary protein disrupted in the cpk mouse model of recessive polycystic kidney disease [PDF]

, 2015
Autosomal recessive polycystic kidney disease (ARPKD; MIM 263200) is a ma-jor cause of pediatric morbidity and mortality. Typically, orthologous animal models are the mainstay for pathogenic studies of human diseases.
Watts, Jacob Asher
core   +1 more source

Na Transport in Autosomal Recessive Polycystic Kidney Disease (ARPKD) Cyst Lining Epithelial Cells

, 2003
Rajeev Rohatgi, Andrew S. Greenberg, Christopher R. Burrow, Patricia D. Wilson, Lisa M. Satlin   +4 more
openalex   +1 more source

Transcription factor Ap2b regulates the mouse autosomal recessive polycystic kidney disease genes, Pkhd1 and Cys1. [PDF]

Front Mol Biosci, 2022
Wu M, Harafuji N, O'Connor AK, Caldovic L, Guay-Woodford LM.   +4 more
europepmc   +1 more source

PKHD1mutations in families requesting prenatal diagnosis for autosomal recessive polycystic kidney disease (ARPKD)

, 2004
Carsten Bergmann, Jan Senderek, Frank Schneider, Christian Dornia, Fabian Küpper, Thomas Eggermann, Sabine Rudnik‐Schöneborn, Jutta Kirfel, Markus Moser, Reinhard Büttner, Klaus Zerres   +10 more
openalex   +1 more source