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

Year Number of Results
1985 1
1992 1
1994 1
1995 1
1997 1
1998 1
2002 1
2003 1
2004 3
2005 6
2006 4
2007 5
2008 6
2009 7
2010 4
2011 3
2012 6
2013 6
2014 13
2015 9
2016 11
2017 7
2018 12
2019 6
2020 3
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Similar Articles for PMID: 31537649

102 results
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Genome-Wide Association Study of Diabetic Kidney Disease Highlights Biology Involved in Glomerular Basement Membrane Collagen.
Salem RM, Todd JN, Sandholm N, Cole JB, Chen WM, Andrews D, Pezzolesi MG, McKeigue PM, Hiraki LT, Qiu C, Nair V, Di Liao C, Cao JJ, Valo E, Onengut-Gumuscu S, Smiles AM, McGurnaghan SJ, Haukka JK, Harjutsalo V, Brennan EP, van Zuydam N, Ahlqvist E, Doyle R, Ahluwalia TS, Lajer M, Hughes MF, Park J, Skupien J, Spiliopoulou A, Liu A, Menon R, Boustany-Kari CM, Kang HM, Nelson RG, Klein R, Klein BE, Lee KE, Gao X, Mauer M, Maestroni S, Caramori ML, de Boer IH, Miller RG, Guo J, Boright AP, Tregouet D, Gyorgy B, Snell-Bergeon JK, Maahs DM, Bull SB, Canty AJ, Palmer CNA, Stechemesser L, Paulweber B, Weitgasser R, Sokolovska J, Rovīte V, Pīrāgs V, Prakapiene E, Radzeviciene L, Verkauskiene R, Panduru NM, Groop LC, McCarthy MI, Gu HF, Möllsten A, Falhammar H, Brismar K, Martin F, Rossing P, Costacou T, Zerbini G, Marre M, Hadjadj S, McKnight AJ, Forsblom C, McKay G, Godson C, Maxwell AP, Kretzler M, Susztak K, Colhoun HM, Krolewski A, Paterson AD, Groop PH, Rich SS, Hirschhorn JN, Florez JC; SUMMIT Consortium, DCCT/EDIC Research Group, GENIE Consortium. Salem RM, et al. J Am Soc Nephrol. 2019 Oct;30(10):2000-2016. doi: 10.1681/ASN.2019030218. Epub 2019 Sep 19. J Am Soc Nephrol. 2019. PMID: 31537649 Free PMC article.
Association of kidney structure-related gene variants with type 2 diabetes-attributed end-stage kidney disease in African Americans.
Guan M, Ma J, Keaton JM, Dimitrov L, Mudgal P, Stromberg M, Bonomo JA, Hicks PJ, Freedman BI, Bowden DW, Ng MC. Guan M, et al. Hum Genet. 2016 Nov;135(11):1251-1262. doi: 10.1007/s00439-016-1714-2. Epub 2016 Jul 26. Hum Genet. 2016. PMID: 27461219 Free PMC article.
COL4A3 Gene Variants and Diabetic Kidney Disease in MODY.
Wang Y, Zhang J, Zhao Y, Wang S, Zhang J, Han Q, Zhang R, Guo R, Li H, Li L, Wang T, Tang X, He C, Teng G, Gu W, Liu F. Wang Y, et al. Clin J Am Soc Nephrol. 2018 Aug 7;13(8):1162-1171. doi: 10.2215/CJN.09100817. Epub 2018 Jul 16. Clin J Am Soc Nephrol. 2018. PMID: 30012629 Free PMC article.
Hypothesis as to How a Common Missense Mutation in COL4A3 May Confer Protection against Diabetic Kidney Disease.
Pieri M. Pieri M. J Am Soc Nephrol. 2020 Mar;31(3):663-664. doi: 10.1681/ASN.2019090966. Epub 2020 Jan 27. J Am Soc Nephrol. 2020. PMID: 31988270 No abstract available.
Autosomal dominant form of type IV collagen nephropathy exists among patients with hereditary nephritis difficult to diagnose clinicopathologically.
Imafuku A, Nozu K, Sawa N, Hasegawa E, Hiramatsu R, Kawada M, Hoshino J, Tanaka K, Ishii Y, Takaichi K, Fujii T, Ohashi K, Iijima K, Ubara Y. Imafuku A, et al. Nephrology (Carlton). 2018 Oct;23(10):940-947. doi: 10.1111/nep.13115. Nephrology (Carlton). 2018. PMID: 28704582 Free PMC article.
SNP in the genome-wide association study hotspot on chromosome 9p21 confers susceptibility to diabetic nephropathy in type 1 diabetes.
Fagerholm E, Ahlqvist E, Forsblom C, Sandholm N, Syreeni A, Parkkonen M, McKnight AJ, Tarnow L, Maxwell AP, Parving HH, Groop L, Groop PH; FinnDiane Study Group. Fagerholm E, et al. Diabetologia. 2012 Sep;55(9):2386-93. doi: 10.1007/s00125-012-2587-0. Epub 2012 May 29. Diabetologia. 2012. PMID: 22643932
Loss of alpha3/alpha4(IV) collagen from the glomerular basement membrane induces a strain-dependent isoform switch to alpha5alpha6(IV) collagen associated with longer renal survival in Col4a3-/- Alport mice.
Kang JS, Wang XP, Miner JH, Morello R, Sado Y, Abrahamson DR, Borza DB. Kang JS, et al. J Am Soc Nephrol. 2006 Jul;17(7):1962-9. doi: 10.1681/ASN.2006020165. Epub 2006 Jun 12. J Am Soc Nephrol. 2006. PMID: 16769745 Free article.
COL4A3/COL4A4 mutations producing focal segmental glomerulosclerosis and renal failure in thin basement membrane nephropathy.
Voskarides K, Damianou L, Neocleous V, Zouvani I, Christodoulidou S, Hadjiconstantinou V, Ioannou K, Athanasiou Y, Patsias C, Alexopoulos E, Pierides A, Kyriacou K, Deltas C. Voskarides K, et al. J Am Soc Nephrol. 2007 Nov;18(11):3004-16. doi: 10.1681/ASN.2007040444. Epub 2007 Oct 17. J Am Soc Nephrol. 2007. PMID: 17942953 Free article.
A unique evolution of the kidney phenotype in a patient with autosomal recessive Alport syndrome.
Vischini G, Kapp ME, Wheeler FC, Hopp L, Fogo AB. Vischini G, et al. Hum Pathol. 2018 Nov;81:229-234. doi: 10.1016/j.humpath.2018.02.024. Epub 2018 Mar 9. Hum Pathol. 2018. PMID: 29530752
Frequency of COL4A3/COL4A4 mutations amongst families segregating glomerular microscopic hematuria and evidence for activation of the unfolded protein response. Focal and segmental glomerulosclerosis is a frequent development during ageing.
Papazachariou L, Demosthenous P, Pieri M, Papagregoriou G, Savva I, Stavrou C, Zavros M, Athanasiou Y, Ioannou K, Patsias C, Panagides A, Potamitis C, Demetriou K, Prikis M, Hadjigavriel M, Kkolou M, Loukaidou P, Pastelli A, Michael A, Lazarou A, Arsali M, Damianou L, Goutziamani I, Soloukides A, Yioukas L, Elia A, Zouvani I, Polycarpou P, Pierides A, Voskarides K, Deltas C. Papazachariou L, et al. PLoS One. 2014 Dec 16;9(12):e115015. doi: 10.1371/journal.pone.0115015. eCollection 2014. PLoS One. 2014. PMID: 25514610 Free PMC article.
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