249 related articles for article (PubMed ID: 28798345)
1. NEDD4-family E3 ligase dysfunction due to PKHD1/Pkhd1 defects suggests a mechanistic model for ARPKD pathobiology.
Kaimori JY; Lin CC; Outeda P; Garcia-Gonzalez MA; Menezes LF; Hartung EA; Li A; Wu G; Fujita H; Sato Y; Nakanuma Y; Yamamoto S; Ichimaru N; Takahara S; Isaka Y; Watnick T; Onuchic LF; Guay-Woodford LM; Germino GG
Sci Rep; 2017 Aug; 7(1):7733. PubMed ID: 28798345
[TBL] [Abstract][Full Text] [Related]
2. Cystin is required for maintaining fibrocystin (FPC) levels and safeguarding proteome integrity in mouse renal epithelial cells: A mechanistic connection between the kidney defects in cpk mice and human ARPKD.
Zhang YJ; Yang C; Wang W; Harafuji N; Stasiak P; Bell PD; Caldovic L; Sztul E; Guay-Woodford LM; Bebok Z
FASEB J; 2023 Jul; 37(7):e23008. PubMed ID: 37318790
[TBL] [Abstract][Full Text] [Related]
3. Cystogenesis in ARPKD results from increased apoptosis in collecting duct epithelial cells of Pkhd1 mutant kidneys.
Hu B; He X; Li A; Qiu Q; Li C; Liang D; Zhao P; Ma J; Coffey RJ; Zhan Q; Wu G
Exp Cell Res; 2011 Jan; 317(2):173-87. PubMed ID: 20875407
[TBL] [Abstract][Full Text] [Related]
4. Kidney cysts, pancreatic cysts, and biliary disease in a mouse model of autosomal recessive polycystic kidney disease.
Williams SS; Cobo-Stark P; James LR; Somlo S; Igarashi P
Pediatr Nephrol; 2008 May; 23(5):733-41. PubMed ID: 18286309
[TBL] [Abstract][Full Text] [Related]
5. PKHD1 gene silencing may cause cell abnormal proliferation through modulation of intracellular calcium in autosomal recessive polycystic kidney disease.
Yang J; Zhang S; Zhou Q; Guo H; Zhang K; Zheng R; Xiao C
J Biochem Mol Biol; 2007 Jul; 40(4):467-74. PubMed ID: 17669261
[TBL] [Abstract][Full Text] [Related]
6. A mouse model for cystic biliary dysgenesis in autosomal recessive polycystic kidney disease (ARPKD).
Moser M; Matthiesen S; Kirfel J; Schorle H; Bergmann C; Senderek J; Rudnik-Schöneborn S; Zerres K; Buettner R
Hepatology; 2005 May; 41(5):1113-21. PubMed ID: 15830394
[TBL] [Abstract][Full Text] [Related]
7. Tissue-specific regulation of the mouse Pkhd1 (ARPKD) gene promoter.
Williams SS; Cobo-Stark P; Hajarnis S; Aboudehen K; Shao X; Richardson JA; Patel V; Igarashi P
Am J Physiol Renal Physiol; 2014 Aug; 307(3):F356-68. PubMed ID: 24899057
[TBL] [Abstract][Full Text] [Related]
8. Molecular genetics of autosomal recessive polycystic kidney disease.
Harris PC; Rossetti S
Mol Genet Metab; 2004 Feb; 81(2):75-85. PubMed ID: 14741187
[TBL] [Abstract][Full Text] [Related]
9. A novel model of autosomal recessive polycystic kidney questions the role of the fibrocystin C-terminus in disease mechanism.
Outeda P; Menezes L; Hartung EA; Bridges S; Zhou F; Zhu X; Xu H; Huang Q; Yao Q; Qian F; Germino GG; Watnick T
Kidney Int; 2017 Nov; 92(5):1130-1144. PubMed ID: 28729032
[TBL] [Abstract][Full Text] [Related]
10. Pkhd1
Yang C; Harafuji N; Caldovic L; Yu W; Boddu R; Bhattacharya S; Barseghyan H; Gordish-Dressman H; Foreman O; Bebok Z; Eicher EM; Guay-Woodford LM
J Mol Med (Berl); 2023 Sep; 101(9):1141-1151. PubMed ID: 37584738
[TBL] [Abstract][Full Text] [Related]
11. Defects in cholangiocyte fibrocystin expression and ciliary structure in the PCK rat.
Masyuk TV; Huang BQ; Ward CJ; Masyuk AI; Yuan D; Splinter PL; Punyashthiti R; Ritman EL; Torres VE; Harris PC; LaRusso NF
Gastroenterology; 2003 Nov; 125(5):1303-10. PubMed ID: 14598246
[TBL] [Abstract][Full Text] [Related]
12. Therapeutic Potential for CFTR Correctors in Autosomal Recessive Polycystic Kidney Disease.
Yanda MK; Tomar V; Cebotaru L
Cell Mol Gastroenterol Hepatol; 2021; 12(5):1517-1529. PubMed ID: 34329764
[TBL] [Abstract][Full Text] [Related]
13. Atmin modulates Pkhd1 expression and may mediate Autosomal Recessive Polycystic Kidney Disease (ARPKD) through altered non-canonical Wnt/Planar Cell Polarity (PCP) signalling.
Richards T; Modarage K; Dean C; McCarthy-Boxer A; Hilton H; Esapa C; Norman J; Wilson P; Goggolidou P
Biochim Biophys Acta Mol Basis Dis; 2019 Feb; 1865(2):378-390. PubMed ID: 30414501
[TBL] [Abstract][Full Text] [Related]
14. Biliary and pancreatic dysgenesis in mice harboring a mutation in Pkhd1.
Gallagher AR; Esquivel EL; Briere TS; Tian X; Mitobe M; Menezes LF; Markowitz GS; Jain D; Onuchic LF; Somlo S
Am J Pathol; 2008 Feb; 172(2):417-29. PubMed ID: 18202188
[TBL] [Abstract][Full Text] [Related]
15. Fibrocystin/polyductin modulates renal tubular formation by regulating polycystin-2 expression and function.
Kim I; Fu Y; Hui K; Moeckel G; Mai W; Li C; Liang D; Zhao P; Ma J; Chen XZ; George AL; Coffey RJ; Feng ZP; Wu G
J Am Soc Nephrol; 2008 Mar; 19(3):455-68. PubMed ID: 18235088
[TBL] [Abstract][Full Text] [Related]
16. Ameliorating liver disease in an autosomal recessive polycystic kidney disease mouse model.
Yanda MK; Zeidan A; Cebotaru L
Am J Physiol Gastrointest Liver Physiol; 2023 May; 324(5):G404-G414. PubMed ID: 36880660
[TBL] [Abstract][Full Text] [Related]
17. A mouse model of autosomal recessive polycystic kidney disease with biliary duct and proximal tubule dilatation.
Woollard JR; Punyashtiti R; Richardson S; Masyuk TV; Whelan S; Huang BQ; Lager DJ; vanDeursen J; Torres VE; Gattone VH; LaRusso NF; Harris PC; Ward CJ
Kidney Int; 2007 Aug; 72(3):328-36. PubMed ID: 17519956
[TBL] [Abstract][Full Text] [Related]
18. Molecular and cellular pathophysiology of autosomal recessive polycystic kidney disease (ARPKD).
Sweeney WE; Avner ED
Cell Tissue Res; 2006 Dec; 326(3):671-85. PubMed ID: 16767405
[TBL] [Abstract][Full Text] [Related]
19. A novel gene encoding a TIG multiple domain protein is a positional candidate for autosomal recessive polycystic kidney disease.
Xiong H; Chen Y; Yi Y; Tsuchiya K; Moeckel G; Cheung J; Liang D; Tham K; Xu X; Chen XZ; Pei Y; Zhao ZJ; Wu G
Genomics; 2002 Jul; 80(1):96-104. PubMed ID: 12079288
[TBL] [Abstract][Full Text] [Related]
20. Analysis of missense variants in the PKHD1-gene in patients with autosomal recessive polycystic kidney disease (ARPKD).
Losekoot M; Haarloo C; Ruivenkamp C; White SJ; Breuning MH; Peters DJ
Hum Genet; 2005 Nov; 118(2):185-206. PubMed ID: 16133180
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
