Results 171 to 180 of about 82,474 (317)
Autosomal dominant polycystic kidney disease. [PDF]
John C. Lieske, F. Gary Toback
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The pathogenesis of polycystic kidney disease.
Polycystic kidney disease (PKD) is a genetic or acquired disorder characterized by progressive distention of multiple tubular segments and manifested by fluid accumulation, growth of non-neoplastic epithelial cells and remodeling of the extracellular matrix resulting ultimately in some degree of renal functional impairment, with the potential for ...
Carone, F.A., Bacallao, R., Kanwar, Y.S.
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Abstract CEP162, a 162‐kDa centrosome protein, is a crucial centrosomal adapter, mediating cell differentiation and polarization. CEP162 maintains mitosis by dynamically stabilizing microtubules. CEP162 promotes the transition zone (TZ) assembly in the basal body through interaction with CEP131, CEP290, and axoneme microtubules as well as the distal ...
Jun Yin+7 more
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The second patient, a 37-year-old male with polycystic kidneys was grafted 10 months ago
NULL AUTHOR_ID
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Prenatal diagnosis by ultrasound in pregnancies at risk for autosomal recessive polycystic kidney disease [PDF]
A. Reuss+3 more
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Polycystin 2 is increased in disease to protect against stress-induced cell death [PDF]
Brill, Allison L.+13 more
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Ferroptosis, a controlled cell death, is driven by iron and characterized by reactive oxygen species and lipid peroxidation. The impact of lipid peroxides, GSH/GPX4, and iron metabolism–targeting small molecule inhibitors is discussed. Nucleic acids, proteins, and phytochemicals are implicated as inhibitors of ferroptosis.
Anwar Ali+10 more
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Adult polycystic kidney disease: Studies of the defect in urine concentration
Manuel Martínez–Maldonado+3 more
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Two step procedure for early diagnosis of polycystic kidney disease with polymorphic DNA markers on both sides of the gene. [PDF]
M.H. Breuning+6 more
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