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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2008 | 2 |
2013 | 1 |
2014 | 2 |
2022 | 1 |
2024 | 0 |
PubMed (GeneRIF) for id: 203286
6 results
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Page 1
Biallelic ANKS6 mutations cause late-onset ciliopathy with chronic kidney disease through YAP dysregulation.
Hum Mol Genet. 2022 May 4;31(9):1357-1369. doi: 10.1093/hmg/ddab322.
Hum Mol Genet. 2022.
PMID: 34740236
Characterization of the SAM domain of the PKD-related protein ANKS6 and its interaction with ANKS3.
Leettola CN, Knight MJ, Cascio D, Hoffman S, Bowie JU.
Leettola CN, et al.
BMC Struct Biol. 2014 Jul 7;14:17. doi: 10.1186/1472-6807-14-17.
BMC Struct Biol. 2014.
PMID: 24998259
Free PMC article.
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Mutations in ANKS6 cause a nephronophthisis-like phenotype with ESRD.
Taskiran EZ, Korkmaz E, Gucer S, Kosukcu C, Kaymaz F, Koyunlar C, Bryda EC, Chaki M, Lu D, Vadnagara K, Candan C, Topaloglu R, Schaefer F, Attanasio M, Bergmann C, Ozaltin F.
Taskiran EZ, et al.
J Am Soc Nephrol. 2014 Aug;25(8):1653-61. doi: 10.1681/ASN.2013060646. Epub 2014 Mar 7.
J Am Soc Nephrol. 2014.
PMID: 24610927
Free PMC article.
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ANKS6 is a central component of a nephronophthisis module linking NEK8 to INVS and NPHP3.
Hoff S, Halbritter J, Epting D, Frank V, Nguyen TM, van Reeuwijk J, Boehlke C, Schell C, Yasunaga T, Helmstädter M, Mergen M, Filhol E, Boldt K, Horn N, Ueffing M, Otto EA, Eisenberger T, Elting MW, van Wijk JA, Bockenhauer D, Sebire NJ, Rittig S, Vyberg M, Ring T, Pohl M, Pape L, Neuhaus TJ, Elshakhs NA, Koon SJ, Harris PC, Grahammer F, Huber TB, Kuehn EW, Kramer-Zucker A, Bolz HJ, Roepman R, Saunier S, Walz G, Hildebrandt F, Bergmann C, Lienkamp SS.
Hoff S, et al.
Nat Genet. 2013 Aug;45(8):951-6. doi: 10.1038/ng.2681. Epub 2013 Jun 23.
Nat Genet. 2013.
PMID: 23793029
Free PMC article.
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Candidate gene/loci studies in cleft lip/palate and dental anomalies finds novel susceptibility genes for clefts.
Vieira AR, McHenry TG, Daack-Hirsch S, Murray JC, Marazita ML.
Vieira AR, et al.
Genet Med. 2008 Sep;10(9):668-74. doi: 10.1097/gim.0b013e3181833793.
Genet Med. 2008.
PMID: 18978678
Free PMC article.
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Genomic organization and mutation screening of the human ortholog of Pkdr1 associated with polycystic kidney disease in the rat.
Kaisaki PJ, Bergmann C, Brown JH, Outeda P, Lens XM, Peters DJ, Gretz N, Gauguier D, Bihoreau MT.
Kaisaki PJ, et al.
Eur J Med Genet. 2008 Jul-Aug;51(4):325-31. doi: 10.1016/j.ejmg.2008.02.007. Epub 2008 Mar 16.
Eur J Med Genet. 2008.
PMID: 18434273
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