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

Year Number of Results
1954 1
1983 1
1992 1
1994 4
1995 3
1996 2
1997 5
1998 4
1999 7
2000 8
2001 2
2002 5
2003 4
2004 1
2005 2
2006 1
2008 3
2009 3
2010 3
2011 7
2012 6
2013 5
2014 4
2015 4
2016 7
2017 6
2018 3
2019 4
2020 10
2021 10
2022 9
2023 3
2024 0

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Similar articles for PMID: 9529363

122 results

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Page 1
Molecular analyses of the HGO gene mutations in Turkish alkaptonuria patients suggest that the R58fs mutation originated from central Asia and was spread throughout Europe and Anatolia by human migrations.
Uyguner O, Goicoechea de Jorge E, Cefle A, Baykal T, Kayserili H, Cefle K, Demirkol M, Yuksel-Apak M, Rodriguez de Córdoba S, Wollnik B. Uyguner O, et al. J Inherit Metab Dis. 2003;26(1):17-23. doi: 10.1023/a:1024063126954. J Inherit Metab Dis. 2003. PMID: 12872836 Clinical Trial.
Mutational analysis of the HGO gene in Finnish alkaptonuria patients.
Beltrán-Valero de Bernabé D, Peterson P, Luopajärvi K, Matintalo P, Alho A, Konttinen Y, Krohn K, Rodríguez de Córdoba S, Ranki A. Beltrán-Valero de Bernabé D, et al. J Med Genet. 1999 Dec;36(12):922-3. J Med Genet. 1999. PMID: 10594001 Free PMC article.
The human homogentisate 1,2-dioxygenase (HGO) gene.
Granadino B, Beltrán-Valero de Bernabé D, Fernández-Cañón JM, Peñalva MA, Rodríguez de Córdoba S. Granadino B, et al. Genomics. 1997 Jul 15;43(2):115-22. doi: 10.1006/geno.1997.4805. Genomics. 1997. PMID: 9244427
Structural and functional analysis of mutations in alkaptonuria.
Rodríguez JM, Timm DE, Titus GP, Beltrán-Valero De Bernabé D, Criado O, Mueller HA, Rodríguez De Córdoba S, Peñalva MA. Rodríguez JM, et al. Hum Mol Genet. 2000 Sep 22;9(15):2341-50. doi: 10.1093/oxfordjournals.hmg.a018927. Hum Mol Genet. 2000. PMID: 11001939
The molecular basis of alkaptonuria.
Fernández-Cañón JM, Granadino B, Beltrán-Valero de Bernabé D, Renedo M, Fernández-Ruiz E, Peñalva MA, Rodríguez de Córdoba S. Fernández-Cañón JM, et al. Nat Genet. 1996 Sep;14(1):19-24. doi: 10.1038/ng0996-19. Nat Genet. 1996. PMID: 8782815
122 results