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

Year Number of Results
1928 1
1951 2
1955 2
1957 1
1958 1
1959 1
1960 2
1963 1
1964 2
1968 1
1970 1
1973 1
1975 1
1979 1
1983 1
1988 1
1992 1
1993 1
1994 4
1995 3
1996 6
1997 6
1998 5
1999 7
2000 6
2001 5
2002 5
2003 4
2004 2
2005 2
2006 2
2008 3
2009 4
2010 2
2011 4
2012 4
2013 3
2014 2
2015 3
2016 3
2017 3
2018 1
2019 3
2020 4
2021 5
2022 3
2023 4
2024 3

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Similar articles for PMID: 9154114

123 results

Results by year

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Page 1
Molecular defects in alkaptonuria.
Gehrig A, Schmidt SR, Müller CR, Srsen S, Srsnova K, Kress W. Gehrig A, et al. Cytogenet Cell Genet. 1997;76(1-2):14-6. doi: 10.1159/000134501. Cytogenet Cell Genet. 1997. PMID: 9154114
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
The genetic defect of the alkaptonuric mouse (aku).
Kress W, Schmidt SR, Halliger-Keller B, Montagutelli X, Müller CR. Kress W, et al. Mamm Genome. 1999 Jan;10(1):68-70. doi: 10.1007/s003359900945. Mamm Genome. 1999. PMID: 9892737 No abstract available.
Crystal structure of human homogentisate dioxygenase.
Titus GP, Mueller HA, Burgner J, Rodríguez De Córdoba S, Peñalva MA, Timm DE. Titus GP, et al. Nat Struct Biol. 2000 Jul;7(7):542-6. doi: 10.1038/76756. Nat Struct Biol. 2000. PMID: 10876237
123 results