These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

214 related articles for article (PubMed ID: 37584738)

  • 1. 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]  

  • 2. Differential regulation of MYC expression by
    Harafuji N; Yang C; Wu M; Thiruvengadam G; Gordish-Dressman H; Thompson RG; Bell PD; Rosenberg AZ; Dafinger C; Liebau MC; Bebok Z; Caldovic L; Guay-Woodford LM
    Front Cell Dev Biol; 2023; 11():1270980. PubMed ID: 38125876
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. PKHD1 mutations in autosomal recessive polycystic kidney disease (ARPKD).
    Bergmann C; Senderek J; Küpper F; Schneider F; Dornia C; Windelen E; Eggermann T; Rudnik-Schöneborn S; Kirfel J; Furu L; Onuchic LF; Rossetti S; Harris PC; Somlo S; Guay-Woodford L; Germino GG; Moser M; Büttner R; Zerres K
    Hum Mutat; 2004 May; 23(5):453-63. PubMed ID: 15108277
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 9. Intragenic motifs regulate the transcriptional complexity of Pkhd1/PKHD1.
    Boddu R; Yang C; O'Connor AK; Hendrickson RC; Boone B; Cui X; Garcia-Gonzalez M; Igarashi P; Onuchic LF; Germino GG; Guay-Woodford LM
    J Mol Med (Berl); 2014 Oct; 92(10):1045-56. PubMed ID: 24984783
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Spectrum of mutations in the gene for autosomal recessive polycystic kidney disease (ARPKD/PKHD1).
    Bergmann C; Senderek J; Sedlacek B; Pegiazoglou I; Puglia P; Eggermann T; Rudnik-Schöneborn S; Furu L; Onuchic LF; De Baca M; Germino GG; Guay-Woodford L; Somlo S; Moser M; Büttner R; Zerres K
    J Am Soc Nephrol; 2003 Jan; 14(1):76-89. PubMed ID: 12506140
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Molecular genetic analysis of PKHD1 by next-generation sequencing in Czech families with autosomal recessive polycystic kidney disease.
    Obeidova L; Seeman T; Elisakova V; Reiterova J; Puchmajerova A; Stekrova J
    BMC Med Genet; 2015 Dec; 16():116. PubMed ID: 26695994
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Challenges in establishing genotype-phenotype correlations in ARPKD: case report on a toddler with two severe PKHD1 mutations.
    Ebner K; Dafinger C; Ortiz-Bruechle N; Koerber F; Schermer B; Benzing T; Dötsch J; Zerres K; Weber LT; Beck BB; Liebau MC
    Pediatr Nephrol; 2017 Jul; 32(7):1269-1273. PubMed ID: 28364132
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Predominant Liver Cystic Disease in a New Heterozygotic PKHD1 Variant: A Case Report.
    Van Buren JD; Neuman JT; Sidlow R
    Am J Case Rep; 2023 Jan; 24():e938507. PubMed ID: 36691356
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Molecular and cellular pathogenesis of autosomal recessive polycystic kidney disease.
    Menezes LF; Onuchic LF
    Braz J Med Biol Res; 2006 Dec; 39(12):1537-48. PubMed ID: 17160262
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Algorithm for efficient PKHD1 mutation screening in autosomal recessive polycystic kidney disease (ARPKD).
    Bergmann C; Küpper F; Dornia C; Schneider F; Senderek J; Zerres K
    Hum Mutat; 2005 Mar; 25(3):225-31. PubMed ID: 15706593
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Clinical consequences of PKHD1 mutations in 164 patients with autosomal-recessive polycystic kidney disease (ARPKD).
    Bergmann C; Senderek J; Windelen E; Küpper F; Middeldorf I; Schneider F; Dornia C; Rudnik-Schöneborn S; Konrad M; Schmitt CP; Seeman T; Neuhaus TJ; Vester U; Kirfel J; Büttner R; Zerres K;
    Kidney Int; 2005 Mar; 67(3):829-48. PubMed ID: 15698423
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. 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]  

  • 20. Clinical and genetic characteristics of autosomal recessive polycystic kidney disease in Oman.
    Al Alawi I; Molinari E; Al Salmi I; Al Rahbi F; Al Mawali A; Sayer JA
    BMC Nephrol; 2020 Aug; 21(1):347. PubMed ID: 32799815
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.