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Year | Number of Results |
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1999 | 2 |
2003 | 1 |
2004 | 1 |
2005 | 1 |
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2024 | 0 |
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Structural impact of human and Escherichia coli biotin carboxyl carrier proteins on biotin attachment.
Biochemistry. 2010 Jun 8;49(22):4687-94. doi: 10.1021/bi901612y.
Biochemistry. 2010.
PMID: 20443544
Mitochondrial targeting signals and mature peptides of 3-methylcrotonyl-CoA carboxylase.
Stadler SC, Polanetz R, Meier S, Mayerhofer PU, Herrmann JM, Anslinger K, Roscher AA, Röschinger W, Holzinger A.
Stadler SC, et al.
Biochem Biophys Res Commun. 2005 Sep 2;334(3):939-46. doi: 10.1016/j.bbrc.2005.06.190.
Biochem Biophys Res Commun. 2005.
PMID: 16023992
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Mutation spectrum of the PCCA and PCCB genes in Japanese patients with propionic acidemia.
Yang X, Sakamoto O, Matsubara Y, Kure S, Suzuki Y, Aoki Y, Yamaguchi S, Takahashi Y, Nishikubo T, Kawaguchi C, Yoshioka A, Kimura T, Hayasaka K, Kohno Y, Iinuma K, Ohura T.
Yang X, et al.
Mol Genet Metab. 2004 Apr;81(4):335-42. doi: 10.1016/j.ymgme.2004.01.003.
Mol Genet Metab. 2004.
PMID: 15059621
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Propionic acidemia: identification of twenty-four novel mutations in Europe and North America.
Pérez B, Desviat LR, Rodríguez-Pombo P, Clavero S, Navarrete R, Perez-Cerdá C, Ugarte M.
Pérez B, et al.
Mol Genet Metab. 2003 Jan;78(1):59-67. doi: 10.1016/s1096-7192(02)00197-x.
Mol Genet Metab. 2003.
PMID: 12559849
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Coding sequence mutations in the alpha subunit of propionyl-CoA carboxylase in patients with propionic acidemia.
Campeau E, Dupuis L, León-Del-Rio A, Gravel R.
Campeau E, et al.
Mol Genet Metab. 1999 May;67(1):11-22. doi: 10.1006/mgme.1999.2850.
Mol Genet Metab. 1999.
PMID: 10329019
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Genetic heterogeneity in propionic acidemia patients with alpha-subunit defects. Identification of five novel mutations, one of them causing instability of the protein.
Richard E, Desviat LR, Pérez B, Pérez-Cerdá C, Ugarte M.
Richard E, et al.
Biochim Biophys Acta. 1999 Mar 30;1453(3):351-8. doi: 10.1016/s0925-4439(99)00008-3.
Biochim Biophys Acta. 1999.
PMID: 10101253
Free article.
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