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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1951 1
1964 1
1967 1
1971 1
1975 1
1976 1
1977 1
1980 1
1996 1
1997 4
1998 1
1999 1
2000 4
2001 5
2002 5
2003 3
2004 3
2005 3
2006 6
2007 8
2008 5
2009 5
2010 9
2011 8
2012 4
2013 10
2014 8
2015 8
2016 7
2017 9
2018 15
2019 14
2020 13
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Similar Articles for PMID: 17855640

149 results
Results by year
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Page 1
Evidence of oligogenic inheritance in nephronophthisis.
Hoefele J, Wolf MT, O'Toole JF, Otto EA, Schultheiss U, Dêschenes G, Attanasio M, Utsch B, Antignac C, Hildebrandt F. Hoefele J, et al. J Am Soc Nephrol. 2007 Oct;18(10):2789-95. doi: 10.1681/ASN.2007020243. Epub 2007 Sep 12. J Am Soc Nephrol. 2007. PMID: 17855640 Free article.
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. Olbrich H, et al. Nat Genet. 2003 Aug;34(4):455-9. doi: 10.1038/ng1216. Nat Genet. 2003. PMID: 12872122
The gene mutated in juvenile nephronophthisis type 4 encodes a novel protein that interacts with nephrocystin.
Mollet G, Salomon R, Gribouval O, Silbermann F, Bacq D, Landthaler G, Milford D, Nayir A, Rizzoni G, Antignac C, Saunier S. Mollet G, et al. Nat Genet. 2002 Oct;32(2):300-5. doi: 10.1038/ng996. Epub 2002 Sep 9. Nat Genet. 2002. PMID: 12244321
High mutation rate of NPHP3 in 18 Chinese infantile nephronophthisis patients.
Sun L, Tong H, Wang H, Yue Z, Liu T, Lin H, Li J, Wang C. Sun L, et al. Nephrology (Carlton). 2016 Mar;21(3):209-16. doi: 10.1111/nep.12563. Nephrology (Carlton). 2016. PMID: 26184788
Mutation analysis in nephronophthisis using a combined approach of homozygosity mapping, CEL I endonuclease cleavage, and direct sequencing.
Otto EA, Helou J, Allen SJ, O'Toole JF, Wise EL, Ashraf S, Attanasio M, Zhou W, Wolf MT, Hildebrandt F. Otto EA, et al. Hum Mutat. 2008 Mar;29(3):418-26. doi: 10.1002/humu.20669. Hum Mutat. 2008. PMID: 18076122 Free article.
High NPHP1 and NPHP6 mutation rate in patients with Joubert syndrome and nephronophthisis: potential epistatic effect of NPHP6 and AHI1 mutations in patients with NPHP1 mutations.
Tory K, Lacoste T, Burglen L, Morinière V, Boddaert N, Macher MA, Llanas B, Nivet H, Bensman A, Niaudet P, Antignac C, Salomon R, Saunier S. Tory K, et al. J Am Soc Nephrol. 2007 May;18(5):1566-75. doi: 10.1681/ASN.2006101164. Epub 2007 Apr 4. J Am Soc Nephrol. 2007. PMID: 17409309 Free article.
Mutational analysis of the NPHP4 gene in 250 patients with nephronophthisis.
Hoefele J, Sudbrak R, Reinhardt R, Lehrack S, Hennig S, Imm A, Muerb U, Utsch B, Attanasio M, O'Toole JF, Otto E, Hildebrandt F. Hoefele J, et al. Hum Mutat. 2005 Apr;25(4):411. doi: 10.1002/humu.9326. Hum Mutat. 2005. PMID: 15776426 Free article.
Wolf MT, Hildebrandt F. Wolf MT, et al. Pediatr Nephrol. 2011 Feb;26(2):181-94. doi: 10.1007/s00467-010-1585-z. Epub 2010 Jul 22. Pediatr Nephrol. 2011. PMID: 20652329 Free PMC article. Review.
[Identification of a new mutation of the NPHP1 gene].
La Russa A, Cifarelli RA, Perri A, Saracino A, Santarsia G, Bonofiglio R. La Russa A, et al. G Ital Nefrol. 2018 May;35(3):2018-vol3. G Ital Nefrol. 2018. PMID: 29786190 Italian.
Genotype-phenotype correlation in 440 patients with NPHP-related ciliopathies.
Chaki M, Hoefele J, Allen SJ, Ramaswami G, Janssen S, Bergmann C, Heckenlively JR, Otto EA, Hildebrandt F. Chaki M, et al. Kidney Int. 2011 Dec;80(11):1239-45. doi: 10.1038/ki.2011.284. Epub 2011 Aug 24. Kidney Int. 2011. PMID: 21866095 Free PMC article.
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