| scholarly article | Q13442814 |
| P50 | author | Shigeo Horie | Q28691693 |
| P2093 | author name string | Jing Zhou | |
| Kenichi Ishibashi | |||
| Sei Sasaki | |||
| Eisei Sohara | |||
| Yuichi Inoue | |||
| Xuefeng Su | |||
| Shinichi Uchida | |||
| Tatemitsu Rai | |||
| Motoko Chiga | |||
| Katsuki Kobayashi | |||
| P2860 | cites work | Cleavage of polycystin-1 requires the receptor for egg jelly domain and is disrupted by human autosomal-dominant polycystic kidney disease 1-associated mutations. | Q24336734 |
| Simple and highly efficient BAC recombineering using galK selection | Q24794075 | ||
| Water permeability and characterization of aquaporin-11. | Q28000039 | ||
| Mechanical stimuli induce cleavage and nuclear translocation of the polycystin-1 C terminus | Q28506516 | ||
| Disruption of aquaporin-11 produces polycystic kidneys following vacuolization of the proximal tubule | Q28507564 | ||
| Aquaporin-11 containing a divergent NPA motif has normal water channel activity | Q28509017 | ||
| Cardiac defects and renal failure in mice with targeted mutations in Pkd2 | Q28510555 | ||
| Single amino acid substitution in aquaporin 11 causes renal failure | Q28513171 | ||
| Nek8 regulates the expression and localization of polycystin-1 and polycystin-2 | Q28513278 | ||
| A genetic interaction network of five genes for human polycystic kidney and liver diseases defines polycystin-1 as the central determinant of cyst formation | Q28590393 | ||
| Chlamydomonas IFT88 and its mouse homologue, polycystic kidney disease gene tg737, are required for assembly of cilia and flagella | Q28593253 | ||
| Identification, characterization, and localization of a novel kidney polycystin-1-polycystin-2 complex | Q28594213 | ||
| The polycystic kidney disease proteins, polycystin-1, polycystin-2, polaris, and cystin, are co-localized in renal cilia | Q29615732 | ||
| Pkd1 transgenic mice: adult model of polycystic kidney disease with extrarenal and renal phenotypes | Q30435066 | ||
| Liver-specific Aquaporin 11 knockout mice show rapid vacuolization of the rough endoplasmic reticulum in periportal hepatocytes after amino acid feeding | Q30583631 | ||
| A loss-of-function model for cystogenesis in human autosomal dominant polycystic kidney disease type 2. | Q33868896 | ||
| Impaired urea accumulation in the inner medulla of mice lacking the urea transporter UT-A2. | Q33924881 | ||
| Acute insulin stimulation induces phosphorylation of the Na-Cl cotransporter in cultured distal mpkDCT cells and mouse kidney | Q34016466 | ||
| Polycystin-1 surface localization is stimulated by polycystin-2 and cleavage at the G protein-coupled receptor proteolytic site | Q34408468 | ||
| The NPC motif of aquaporin-11, unlike the NPA motif of known aquaporins, is essential for full expression of molecular function. | Q34536847 | ||
| Kidney-specific inactivation of the KIF3A subunit of kinesin-II inhibits renal ciliogenesis and produces polycystic kidney disease | Q34982718 | ||
| Pathogenesis and treatment of autosomal-dominant nephrogenic diabetes insipidus caused by an aquaporin 2 mutation | Q35080543 | ||
| Polycystin: in vitro synthesis, in vivo tissue expression, and subcellular localization identifies a large membrane-associated protein | Q36185189 | ||
| Essential role of cleavage of Polycystin-1 at G protein-coupled receptor proteolytic site for kidney tubular structure. | Q36276959 | ||
| Functional polycystin-1 dosage governs autosomal dominant polycystic kidney disease severity | Q36357916 | ||
| A polycystin-1 multiprotein complex is disrupted in polycystic kidney disease cells | Q36781051 | ||
| Aquaporin 11 insufficiency modulates kidney susceptibility to oxidative stress. | Q36836209 | ||
| Polycystins and primary cilia: primers for cell cycle progression | Q37538766 | ||
| Congenital disorders of glycosylation in hepatology: the example of polycystic liver disease | Q37688598 | ||
| Polycystin-1, STAT6, and P100 function in a pathway that transduces ciliary mechanosensation and is activated in polycystic kidney disease | Q40332825 | ||
| Phosphatidylinositol 3-kinase/Akt signaling pathway activates the WNK-OSR1/SPAK-NCC phosphorylation cascade in hyperinsulinemic db/db mice | Q42135510 | ||
| PKD1 haploinsufficiency causes a syndrome of inappropriate antidiuresis in mice | Q42512106 | ||
| Pancreas-specific aquaporin 12 null mice showed increased susceptibility to caerulein-induced acute pancreatitis | Q43281809 | ||
| Pioglitazone improves the phenotype and molecular defects of a targeted Pkd1 mutant | Q44049169 | ||
| In vivo protein biotinylation for identification of organ-specific antigens accessible from the vasculature | Q46396196 | ||
| Polycystic kidneys caused by sustained expression of Cux1 isoform p75. | Q46690342 | ||
| Polycystin-1 distribution is modulated by polycystin-2 expression in mammalian cells | Q47785642 | ||
| Development of polycystic kidney disease in juvenile cystic kidney mice: insights into pathogenesis, ciliary abnormalities, and common features with human disease. | Q51789472 | ||
| Defects in cholangiocyte fibrocystin expression and ciliary structure in the PCK rat. | Q52552433 | ||
| Aquaporin-11 knockout mice and polycystic kidney disease animals share a common mechanism of cyst formation. | Q52587924 | ||
| Somatic inactivation of Pkd2 results in polycystic kidney disease | Q74502174 | ||
| Somatic PKD2 mutations in individual kidney and liver cysts support a "two-hit" model of cystogenesis in type 2 autosomal dominant polycystic kidney disease | Q77998428 | ||
| P433 | issue | 12 | |
| P921 | main subject | glycosylation | Q898365 |
| Aquaporin 11 | Q21982760 | ||
| P304 | page(s) | 2789-2799 | |
| P577 | publication date | 2014-05-22 | |
| P1433 | published in | Journal of the American Society of Nephrology | Q17123893 |
| P1476 | title | Aberrant glycosylation and localization of polycystin-1 cause polycystic kidney in an AQP11 knockout model | |
| P478 | volume | 25 |
| Q26800974 | A polycystin-centric view of cyst formation and disease: the polycystins revisited |
| Q37719527 | Abnormal glycosylation in Joubert syndrome type 10. |
| Q36828975 | Aquaporin 11, a regulator of water efflux at retinal Müller glial cell surface decreases concomitant with immune-mediated gliosis |
| Q42115780 | Aquaporin-11 (AQP11) Expression in the Mouse Brain |
| Q61815142 | Aquaporins in Renal Diseases |
| Q51112302 | Aquaporins in Urinary System. |
| Q52689816 | Deficient transient receptor potential vanilloid type 4 function contributes to compromised [Ca2+]i homeostasis in human autosomal-dominant polycystic kidney disease cells. |
| Q37534564 | Enhanced Autophagy in Polycystic Kidneys of AQP11 Null Mice |
| Q36061872 | Genetic predisposition of donors affects the allograft outcome in kidney transplantation: Single-nucleotide polymorphism of aquaporin-11 |
| Q64103262 | Inhibitors of Mammalian Aquaporin Water Channels |
| Q60910381 | Involvement of the NADPH oxidase 2 pathway in renal oxidative stress in mice |
| Q51112320 | Molecular Biology of Aquaporins. |
| Q50211745 | Polycystic Kidney Disease with Hyperinsulinemic Hypoglycemia Caused by a Promoter Mutation in Phosphomannomutase 2. |
| Q47103366 | Proteomic analysis of AQP11-null kidney: Proximal tubular type polycystic kidney disease |
| Q49922693 | Renal involvement in PMM2-CDG, a mini-review. |
| Q48374920 | Temporal deletion of Aqp11 in mice is linked to the severity of cyst-like disease. |
| Q38707517 | The distribution and function of aquaporins in the kidney: resolved and unresolved questions |
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