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

Year Number of Results
1984 1
1985 1
1996 1
1997 1
2000 1
2003 2
2004 1
2005 1
2006 1
2009 3
2010 4
2011 9
2012 10
2013 10
2014 11
2015 13
2016 13
2017 10
2018 9
2019 9
2020 4
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Similar Articles for PMID: 32444357

98 results
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A Deregulated Stress Response Underlies Distinct INF2-Associated Disease Profiles.
Bayraktar S, Nehrig J, Menis E, Karli K, Janning A, Struk T, Halbritter J, Michgehl U, Krahn MP, Schuberth CE, Pavenstädt H, Wedlich-Söldner R. Bayraktar S, et al. J Am Soc Nephrol. 2020 Jun;31(6):1296-1313. doi: 10.1681/ASN.2019111174. J Am Soc Nephrol. 2020. PMID: 32444357
INF2 mutations in Charcot-Marie-Tooth disease with glomerulopathy.
Boyer O, Nevo F, Plaisier E, Funalot B, Gribouval O, Benoit G, Huynh Cong E, Arrondel C, Tête MJ, Montjean R, Richard L, Karras A, Pouteil-Noble C, Balafrej L, Bonnardeaux A, Canaud G, Charasse C, Dantal J, Deschenes G, Deteix P, Dubourg O, Petiot P, Pouthier D, Leguern E, Guiochon-Mantel A, Broutin I, Gubler MC, Saunier S, Ronco P, Vallat JM, Alonso MA, Antignac C, Mollet G. Boyer O, et al. N Engl J Med. 2011 Dec 22;365(25):2377-88. doi: 10.1056/NEJMoa1109122. N Engl J Med. 2011. PMID: 22187985 Free article.
Mutational screening of inverted formin 2 in adult-onset focal segmental glomerulosclerosis or minimal change patients from the Czech Republic.
Safarikova M, Stekrova J, Honsova E, Horinova V, Tesar V, Reiterova J. Safarikova M, et al. BMC Med Genet. 2018 Aug 20;19(1):147. doi: 10.1186/s12881-018-0667-9. BMC Med Genet. 2018. PMID: 30126379 Free PMC article.
Inverted formin 2-related Charcot-Marie-Tooth disease: extension of the mutational spectrum and pathological findings in Schwann cells and axons.
Roos A, Weis J, Korinthenberg R, Fehrenbach H, Häusler M, Züchner S, Mache C, Hubmann H, Auer-Grumbach M, Senderek J. Roos A, et al. J Peripher Nerv Syst. 2015 Mar;20(1):52-9. doi: 10.1111/jns.12106. J Peripher Nerv Syst. 2015. PMID: 25676889
Novel INF2 mutations in an Italian cohort of patients with focal segmental glomerulosclerosis, renal failure and Charcot-Marie-Tooth neuropathy.
Caridi G, Lugani F, Dagnino M, Gigante M, Iolascon A, Falco M, Graziano C, Benetti E, Dugo M, Del Prete D, Granata A, Borracelli D, Moggia E, Quaglia M, Rinaldi R, Gesualdo L, Ghiggeri GM. Caridi G, et al. Nephrol Dial Transplant. 2014 Sep;29 Suppl 4:iv80-6. doi: 10.1093/ndt/gfu071. Nephrol Dial Transplant. 2014. PMID: 25165188
A complex containing lysine-acetylated actin inhibits the formin INF2.
A M, Fung TS, Kettenbach AN, Chakrabarti R, Higgs HN. A M, et al. Nat Cell Biol. 2019 May;21(5):592-602. doi: 10.1038/s41556-019-0307-4. Epub 2019 Apr 8. Nat Cell Biol. 2019. PMID: 30962575 Free PMC article.
De novo INF2 mutations expand the genetic spectrum of hereditary neuropathy with glomerulopathy.
Mademan I, Deconinck T, Dinopoulos A, Voit T, Schara U, Devriendt K, Meijers B, Lerut E, De Jonghe P, Baets J. Mademan I, et al. Neurology. 2013 Nov 26;81(22):1953-8. doi: 10.1212/01.wnl.0000436615.58705.c9. Epub 2013 Oct 30. Neurology. 2013. PMID: 24174593
The formin INF2 in disease: progress from 10 years of research.
Labat-de-Hoz L, Alonso MA. Labat-de-Hoz L, et al. Cell Mol Life Sci. 2020 May 25. doi: 10.1007/s00018-020-03550-7. Online ahead of print. Cell Mol Life Sci. 2020. PMID: 32451589 Review.
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