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Results by year

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

Year Number of Results
2006 1
2007 1
2008 2
2009 1
2010 2
2011 2
2012 2
2013 4
2014 2
2015 1
2016 1
2017 2
2019 1
2021 3
2022 2
2023 0

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PubMed for id: 888362

25 results

Results by year

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Page 1
Heterozygous missense variant in TRPC6 in a boy with rapidly progressive infantile nephrotic syndrome associated with diffuse mesangial sclerosis.
Hanafusa H, Hidaka Y, Yamaguchi T, Shimojo H, Tsukahara T, Murase T, Matsuoka D, Chiba N, Shimada S, Morokawa H, Omori N, Minoura H, Nagano C, Takano K, Nakamura K, Wakui K, Fukushima Y, Uehara T, Nakazawa Y, Iijima K, Nozu K, Kosho T. Hanafusa H, et al. Am J Med Genet A. 2021 Jul;185(7):2175-2179. doi: 10.1002/ajmg.a.62216. Epub 2021 Apr 21. Am J Med Genet A. 2021. PMID: 33884742
A disease-causing mutation illuminates the protein membrane topology of the kidney-expressed prohibitin homology (PHB) domain protein podocin.
Schurek EM, Völker LA, Tax J, Lamkemeyer T, Rinschen MM, Ungrue D, Kratz JE 3rd, Sirianant L, Kunzelmann K, Chalfie M, Schermer B, Benzing T, Höhne M. Schurek EM, et al. J Biol Chem. 2014 Apr 18;289(16):11262-11271. doi: 10.1074/jbc.M113.521773. Epub 2014 Mar 4. J Biol Chem. 2014. PMID: 24596097 Free PMC article.
25 results