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  2. Autosomal recessive polycystic kidney disease - Wikipedia

    en.wikipedia.org/wiki/Autosomal_recessive...

    Autosomal recessive polycystic kidney disease (ARPKD) is the recessive form of polycystic kidney disease. It is associated with a group of congenital fibrocystic syndromes. [5] Mutations in the PKHD1 (chromosomal locus 6p12.2) cause ARPKD. [6] [7]

  3. Polycystic kidney disease - Wikipedia

    en.wikipedia.org/wiki/Polycystic_kidney_disease

    PKD is caused by abnormal genes which produce a specific abnormal protein which has an adverse effect on tubule development. PKD is a general term for two types, each having their own pathology and genetic cause: autosomal dominant polycystic kidney disease (ADPKD) and autosomal recessive polycystic kidney disease (ARPKD). [10] [11]

  4. Fibrocystin - Wikipedia

    en.wikipedia.org/wiki/Fibrocystin

    Fibrocystin is a large, receptor-like protein that is thought to be involved in the tubulogenesis and/or maintenance of duct-lumen architecture of epithelium. [5] FPC associates with the primary cilia of epithelial cells and co-localizes with the Pkd2 gene product polycystin-2 (PC2), suggesting that these two proteins may function in a common molecular pathway.

  5. Polycystin cation channel family - Wikipedia

    en.wikipedia.org/wiki/Polycystin_cation_channel...

    Human polycystin 1 is a huge protein of 4303 amino acyl residues (aas). Its repeated leucine-rich (LRR) segment is found in many proteins. According to the UniProt description, polycystin 1 contains 16 polycystic kidney disease (PKD) domains, one LDL-receptor class A domain, one C-type lectin family domain, and 16-18 putative TMSs in positions between residues 2200 and 4100. [2]

  6. Polycystin 1 - Wikipedia

    en.wikipedia.org/wiki/Polycystin_1

    Polycystin 1 (PC1) is a protein that in humans is encoded by the PKD1 gene. [5] [6] Mutations of PKD1 are associated with most cases of autosomal dominant polycystic kidney disease, a severe hereditary disorder of the kidneys characterised by the development of renal cysts and severe kidney dysfunction. [7]

  7. Autosomal dominant polycystic kidney disease - Wikipedia

    en.wikipedia.org/wiki/Autosomal_dominant...

    Autosomal dominant polycystic kidney disease (ADPKD) is one of the most common, life-threatening inherited human disorders and the most common hereditary kidney disease. [ 1 ] [ 2 ] It is associated with large interfamilial and intrafamilial variability, which can be explained to a large extent by its genetic heterogeneity and modifier genes ...

  8. C H E L S E A G R E E N P U B L I S H I N G W H I T E R I V E ...

    images.huffingtonpost.com/2007-09-10-EOA...

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  9. PKD domain - Wikipedia

    en.wikipedia.org/wiki/PKD_domain

    Polycystin-1 is a large cell-surface glycoprotein involved in adhesive proteinprotein and protein–carbohydrate interactions; however it is not clear if the PKD domain mediates any of these interactions. PKD domains are also found in other proteins, usually in the extracellular parts of proteins involved in interactions with other proteins.