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

Year Number of Results
1999 1
2001 1
2004 4
2005 4
2006 8
2007 6
2008 6
2009 4
2010 4
2011 13
2012 11
2013 11
2014 9
2015 8
2016 10
2017 12
2018 11
2019 5
2020 6
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Similar Articles for PMID: 23723427

123 results
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Laminin β2 gene missense mutation produces endoplasmic reticulum stress in podocytes.
Chen YM, Zhou Y, Go G, Marmerstein JT, Kikkawa Y, Miner JH. Chen YM, et al. J Am Soc Nephrol. 2013 Jul;24(8):1223-33. doi: 10.1681/ASN.2012121149. Epub 2013 May 30. J Am Soc Nephrol. 2013. PMID: 23723427 Free PMC article.
Laminin-521 Protein Therapy for Glomerular Basement Membrane and Podocyte Abnormalities in a Model of Pierson Syndrome.
Lin MH, Miller JB, Kikkawa Y, Suleiman HY, Tryggvason K, Hodges BL, Miner JH. Lin MH, et al. J Am Soc Nephrol. 2018 May;29(5):1426-1436. doi: 10.1681/ASN.2017060690. Epub 2018 Feb 22. J Am Soc Nephrol. 2018. PMID: 29472414 Free PMC article.
Pathogenicity of a Human Laminin β2 Mutation Revealed in Models of Alport Syndrome.
Funk SD, Bayer RH, Malone AF, McKee KK, Yurchenco PD, Miner JH. Funk SD, et al. J Am Soc Nephrol. 2018 Mar;29(3):949-960. doi: 10.1681/ASN.2017090997. Epub 2017 Dec 20. J Am Soc Nephrol. 2018. PMID: 29263159 Free PMC article.
Forced expression of laminin beta1 in podocytes prevents nephrotic syndrome in mice lacking laminin beta2, a model for Pierson syndrome.
Suh JH, Jarad G, VanDeVoorde RG, Miner JH. Suh JH, et al. Proc Natl Acad Sci U S A. 2011 Sep 13;108(37):15348-53. doi: 10.1073/pnas.1108269108. Epub 2011 Aug 29. Proc Natl Acad Sci U S A. 2011. PMID: 21876163 Free PMC article.
Alport syndrome and Pierson syndrome: Diseases of the glomerular basement membrane.
Funk SD, Lin MH, Miner JH. Funk SD, et al. Matrix Biol. 2018 Oct;71-72:250-261. doi: 10.1016/j.matbio.2018.04.008. Epub 2018 Apr 16. Matrix Biol. 2018. PMID: 29673759 Free PMC article. Review.
First Japanese case of Pierson syndrome with mutations in LAMB2.
Togawa H, Nakanishi K, Mukaiyama H, Hama T, Shima Y, Nakano M, Fujita N, Iijima K, Yoshikawa N. Togawa H, et al. Pediatr Int. 2013 Apr;55(2):229-31. doi: 10.1111/j.1442-200X.2012.03629.x. Pediatr Int. 2013. PMID: 23679161
Skeletal impairment in Pierson syndrome: Is there a role for lamininβ2 in bone physiology?
Beaufils C, Farlay D, Machuca-Gayet I, Fassier A, Zenker M, Freychet C, Bonnelye E, Bertholet-Thomas A, Ranchin B, Bacchetta J. Beaufils C, et al. Bone. 2018 Jan;106:187-193. doi: 10.1016/j.bone.2017.10.015. Epub 2017 Oct 16. Bone. 2018. PMID: 29051055
LAMB2 mutation with different phenotypes in China
Zhang H, Cui J, Wang F, Xiao H, Ding J, Yao Y. Zhang H, et al. Clin Nephrol. 2017 Jan;87 (2017)(1):33-38. doi: 10.5414/CN108979. Clin Nephrol. 2017. PMID: 27925579
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