Format
Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 123

Similar articles for PubMed (Select 19118152)

1.

Nephronophthisis: disease mechanisms of a ciliopathy.

Hildebrandt F, Attanasio M, Otto E.

J Am Soc Nephrol. 2009 Jan;20(1):23-35. doi: 10.1681/ASN.2008050456. Epub 2008 Dec 31. Review.

2.

Ciliopathies and DNA damage: an emerging nexus.

Attanasio M.

Curr Opin Nephrol Hypertens. 2015 Jul;24(4):366-70. doi: 10.1097/MNH.0000000000000134.

PMID:
26050124
3.

Non-invasive sources of cells with primary cilia from pediatric and adult patients.

Ajzenberg H, Slaats GG, Stokman MF, Arts HH, Logister I, Kroes HY, Renkema KY, van Haelst MM, Terhal PA, van Rooij IA, Keijzer-Veen MG, Knoers NV, Lilien MR, Jewett MA, Giles RH.

Cilia. 2015 Jun 1;4:8. doi: 10.1186/s13630-015-0017-x. eCollection 2015.

4.

Cilia and Diseases.

Brown JM, Witman GB.

Bioscience. 2014 Dec 1;64(12):1126-1137.

5.

Are renal ciliopathies (replication) stressed out?

Slaats GG, Giles RH.

Trends Cell Biol. 2015 Jun;25(6):317-9. doi: 10.1016/j.tcb.2015.03.005. Epub 2015 Apr 27.

PMID:
25937400
6.

Nephronophthisis and related syndromes.

Wolf MT.

Curr Opin Pediatr. 2015 Apr;27(2):201-11. doi: 10.1097/MOP.0000000000000194.

PMID:
25635582
7.

Proteomic analysis of isolated ciliary transition zones reveals the presence of ESCRT proteins.

Diener DR, Lupetti P, Rosenbaum JL.

Curr Biol. 2015 Feb 2;25(3):379-84. doi: 10.1016/j.cub.2014.11.066. Epub 2015 Jan 8.

PMID:
25578910
8.

The role of cilia in the pathogenesis of cystic kidney disease.

Dell KM.

Curr Opin Pediatr. 2015 Apr;27(2):212-8. doi: 10.1097/MOP.0000000000000187.

PMID:
25575298
9.

DCDC2 mutations cause a renal-hepatic ciliopathy by disrupting Wnt signaling.

Schueler M, Braun DA, Chandrasekar G, Gee HY, Klasson TD, Halbritter J, Bieder A, Porath JD, Airik R, Zhou W, LoTurco JJ, Che A, Otto EA, Böckenhauer D, Sebire NJ, Honzik T, Harris PC, Koon SJ, Gunay-Aygun M, Saunier S, Zerres K, Bruechle NO, Drenth JP, Pelletier L, Tapia-Páez I, Lifton RP, Giles RH, Kere J, Hildebrandt F.

Am J Hum Genet. 2015 Jan 8;96(1):81-92. doi: 10.1016/j.ajhg.2014.12.002. Epub 2014 Dec 31.

PMID:
25557784
10.

Atypical retinopathy in patients with nephronophthisis type 1: an uncommon ophthalmological finding.

Kang HG, Ahn YH, Kim JH, Ha IS, Yu YS, Park YH, Cheong HI.

Clin Experiment Ophthalmol. 2014 Nov 17. doi: 10.1111/ceo.12469. [Epub ahead of print]

PMID:
25401970
11.

Nephronophthisis-associated CEP164 regulates cell cycle progression, apoptosis and epithelial-to-mesenchymal transition.

Slaats GG, Ghosh AK, Falke LL, Le Corre S, Shaltiel IA, van de Hoek G, Klasson TD, Stokman MF, Logister I, Verhaar MC, Goldschmeding R, Nguyen TQ, Drummond IA, Hildebrandt F, Giles RH.

PLoS Genet. 2014 Oct 23;10(10):e1004594. doi: 10.1371/journal.pgen.1004594. eCollection 2014 Oct.

12.

Nephronophthisis and retinal degeneration in tmem218-/- mice: a novel mouse model for Senior-Løken syndrome?

Vogel P, Gelfman CM, Issa T, Payne BJ, Hansen GM, Read RW, Jones C, Pitcher MR, Ding ZM, DaCosta CM, Shadoan MK, Vance RB, Powell DR.

Vet Pathol. 2015 May;52(3):580-95. doi: 10.1177/0300985814547392. Epub 2014 Aug 26.

PMID:
25161209
13.

Murine Joubert syndrome reveals Hedgehog signaling defects as a potential therapeutic target for nephronophthisis.

Hynes AM, Giles RH, Srivastava S, Eley L, Whitehead J, Danilenko M, Raman S, Slaats GG, Colville JG, Ajzenberg H, Kroes HY, Thelwall PE, Simmons NL, Miles CG, Sayer JA.

Proc Natl Acad Sci U S A. 2014 Jul 8;111(27):9893-8. doi: 10.1073/pnas.1322373111. Epub 2014 Jun 19.

14.

Sensing a sensor: identifying the mechanosensory function of primary cilia.

Prasad RM, Jin X, Nauli SM.

Biosensors (Basel). 2014;4(1):47-62. doi: 10.3390/bios4010047.

15.

Loss of cilia causes embryonic lung hypoplasia, liver fibrosis, and cholestasis in the talpid3 ciliopathy mutant.

Davey MG, McTeir L, Barrie AM, Freem LJ, Stephen LA.

Organogenesis. 2014 Apr-Jun;10(2):177-85. doi: 10.4161/org.28819. Epub 2014 Apr 17.

16.

Renal-retinal ciliopathy gene Sdccag8 regulates DNA damage response signaling.

Airik R, Slaats GG, Guo Z, Weiss AC, Khan N, Ghosh A, Hurd TW, Bekker-Jensen S, Schrøder JM, Elledge SJ, Andersen JS, Kispert A, Castelli M, Boletta A, Giles RH, Hildebrandt F.

J Am Soc Nephrol. 2014 Nov;25(11):2573-83. doi: 10.1681/ASN.2013050565. Epub 2014 Apr 10.

PMID:
24722439
17.

Downregulating hedgehog signaling reduces renal cystogenic potential of mouse models.

Tran PV, Talbott GC, Turbe-Doan A, Jacobs DT, Schonfeld MP, Silva LM, Chatterjee A, Prysak M, Allard BA, Beier DR.

J Am Soc Nephrol. 2014 Oct;25(10):2201-12. doi: 10.1681/ASN.2013070735. Epub 2014 Apr 3.

PMID:
24700869
18.

The challenges and surprises of a definitive molecular genetic diagnosis.

Sayer JA, Simms RJ.

Kidney Int. 2014 Apr;85(4):748-9. doi: 10.1038/ki.2013.432.

PMID:
24682124
19.

Early presentation of cystic kidneys in a family with a homozygous INVS mutation.

Oud MM, van Bon BW, Bongers EM, Hoischen A, Marcelis CL, de Leeuw N, Mol SJ, Mortier G, Knoers NV, Brunner HG, Roepman R, Arts HH.

Am J Med Genet A. 2014 Jul;164A(7):1627-34. doi: 10.1002/ajmg.a.36501. Epub 2014 Mar 26.

PMID:
24677454
20.

Mutations in WDR19 encoding the intraflagellar transport component IFT144 cause a broad spectrum of ciliopathies.

Fehrenbach H, Decker C, Eisenberger T, Frank V, Hampel T, Walden U, Amann KU, Krüger-Stollfuß I, Bolz HJ, Häffner K, Pohl M, Bergmann C.

Pediatr Nephrol. 2014 Aug;29(8):1451-6. doi: 10.1007/s00467-014-2762-2. Epub 2014 Feb 7.

PMID:
24504730
Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk