41 related articles for article (PubMed ID: 11134256)
1. Renal cell carcinoma in an adult-onset ESRD patient with nephronophthisis harboring
Li ZL; Wang FM; Wen Y; Ni HF; Zhang XL; Wang B
Heliyon; 2024 Apr; 10(7):e28985. PubMed ID: 38617907
[TBL] [Abstract][Full Text] [Related]
2. Lateral thinking in syndromic congenital cardiovascular disease.
Kocere A; Lalonde RL; Mosimann C; Burger A
Dis Model Mech; 2023 May; 16(5):. PubMed ID: 37125615
[TBL] [Abstract][Full Text] [Related]
3. Inactivation of
Li Y; Xu W; Makova S; Brueckner M; Sun Z
Elife; 2023 Mar; 12():. PubMed ID: 36920028
[TBL] [Abstract][Full Text] [Related]
4. Renal Ciliopathies: Sorting Out Therapeutic Approaches for Nephronophthisis.
Stokman MF; Saunier S; Benmerah A
Front Cell Dev Biol; 2021; 9():653138. PubMed ID: 34055783
[TBL] [Abstract][Full Text] [Related]
5. Lack of Benefit of Early Intervention with Dietary Flax and Fish Oil and Soy Protein in Orthologous Rodent Models of Human Hereditary Polycystic Kidney Disease.
Yamaguchi T; Devassy JG; Monirujjaman M; Gabbs M; Aukema HM
PLoS One; 2016; 11(5):e0155790. PubMed ID: 27213553
[TBL] [Abstract][Full Text] [Related]
6. Mouse Models of Rare Craniofacial Disorders.
Achilleos A; Trainor PA
Curr Top Dev Biol; 2015; 115():413-58. PubMed ID: 26589934
[TBL] [Abstract][Full Text] [Related]
7. NPHP3 mutations are associated with neonatal onset multiorgan polycystic disease in two siblings.
Leeman KT; Dobson L; Towne M; Dukhovny D; Joshi M; Stoler J; Agrawal PB
J Perinatol; 2014 May; 34(5):410-1. PubMed ID: 24776604
[TBL] [Abstract][Full Text] [Related]
8. Renal cyclooxygenase products are higher and lipoxygenase products are lower in early disease in the pcy mouse model of adolescent nephronophthisis.
Yamaguchi T; Lysecki C; Reid A; Nagao S; Aukema HM
Lipids; 2014 Jan; 49(1):39-47. PubMed ID: 24178445
[TBL] [Abstract][Full Text] [Related]
9. Senior-Løken syndrome: a syndromic form of retinal dystrophy associated with nephronophthisis.
Ronquillo CC; Bernstein PS; Baehr W
Vision Res; 2012 Dec; 75():88-97. PubMed ID: 22819833
[TBL] [Abstract][Full Text] [Related]
10. Loss of nephrocystin-3 function can cause embryonic lethality, Meckel-Gruber-like syndrome, situs inversus, and renal-hepatic-pancreatic dysplasia.
Bergmann C; Fliegauf M; Brüchle NO; Frank V; Olbrich H; Kirschner J; Schermer B; Schmedding I; Kispert A; Kränzlin B; Nürnberg G; Becker C; Grimm T; Girschick G; Lynch SA; Kelehan P; Senderek J; Neuhaus TJ; Stallmach T; Zentgraf H; Nürnberg P; Gretz N; Lo C; Lienkamp S; Schäfer T; Walz G; Benzing T; Zerres K; Omran H
Am J Hum Genet; 2008 Apr; 82(4):959-70. PubMed ID: 18371931
[TBL] [Abstract][Full Text] [Related]
11. Nephronophthisis complicated with hepatic fibrosis: an autopsy case with rupture of the splenic artery after renal transplantation.
Tsukamoto T; Tanaka M; Komiya T; Ueda S; Takasu K; Takahara S; Koizumi A; Muso E
Clin Exp Nephrol; 2008 Feb; 12(1):82-8. PubMed ID: 18175055
[TBL] [Abstract][Full Text] [Related]
12. Modulation of renal injury in pcy mice by dietary fat containing n-3 fatty acids depends on the level and type of fat.
Sankaran D; Lu J; Bankovic-Calic N; Ogborn MR; Aukema HM
Lipids; 2004 Mar; 39(3):207-14. PubMed ID: 15233398
[TBL] [Abstract][Full Text] [Related]
13. Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determination.
Otto EA; Schermer B; Obara T; O'Toole JF; Hiller KS; Mueller AM; Ruf RG; Hoefele J; Beekmann F; Landau D; Foreman JW; Goodship JA; Strachan T; Kispert A; Wolf MT; Gagnadoux MF; Nivet H; Antignac C; Walz G; Drummond IA; Benzing T; Hildebrandt F
Nat Genet; 2003 Aug; 34(4):413-20. PubMed ID: 12872123
[TBL] [Abstract][Full Text] [Related]
14. Human adolescent nephronophthisis: gene locus synteny with polycystic kidney disease in pcy mice.
Omran H; Häffner K; Burth S; Fernandez C; Fargier B; Villaquiran A; Nothwang HG; Schnittger S; Lehrach H; Woo D; Brandis M; Sudbrak R; Hildebrandt F
J Am Soc Nephrol; 2001 Jan; 12(1):107-113. PubMed ID: 11134256
[TBL] [Abstract][Full Text] [Related]
15. Evidence for further genetic heterogeneity in nephronophthisis.
Omran H; Häffner K; Burth S; Ala-Mello S; Antignac C; Hildebrandt F
Nephrol Dial Transplant; 2001 Apr; 16(4):755-8. PubMed ID: 11274269
[TBL] [Abstract][Full Text] [Related]
16. Mutations in a novel gene, NPHP3, cause adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis.
Olbrich H; Fliegauf M; Hoefele J; Kispert A; Otto E; Volz A; Wolf MT; Sasmaz G; Trauer U; Reinhardt R; Sudbrak R; Antignac C; Gretz N; Walz G; Schermer B; Benzing T; Hildebrandt F; Omran H
Nat Genet; 2003 Aug; 34(4):455-9. PubMed ID: 12872122
[TBL] [Abstract][Full Text] [Related]
17. Identification of a new gene locus for adolescent nephronophthisis, on chromosome 3q22 in a large Venezuelan pedigree.
Omran H; Fernandez C; Jung M; Häffner K; Fargier B; Villaquiran A; Waldherr R; Gretz N; Brandis M; Rüschendorf F; Reis A; Hildebrandt F
Am J Hum Genet; 2000 Jan; 66(1):118-27. PubMed ID: 10631142
[TBL] [Abstract][Full Text] [Related]
18. New insights: nephronophthisis-medullary cystic kidney disease.
Hildebrandt F; Omram H
Pediatr Nephrol; 2001 Feb; 16(2):168-76. PubMed ID: 11261687
[TBL] [Abstract][Full Text] [Related]
19. Nephronophthisis-associated ciliopathies.
Hildebrandt F; Zhou W
J Am Soc Nephrol; 2007 Jun; 18(6):1855-71. PubMed ID: 17513324
[TBL] [Abstract][Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]
