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Codon usage and genome evolution.
Sharp PM, Matassi G. Sharp PM, et al. Among authors: matassi g. Curr Opin Genet Dev. 1994 Dec;4(6):851-60. doi: 10.1016/0959-437x(94)90070-1. Curr Opin Genet Dev. 1994. PMID: 7888755 Review.
Chromosomal location effects on gene sequence evolution in mammals.
Matassi G, Sharp PM, Gautier C. Matassi G, et al. Curr Biol. 1999 Jul 29-Aug 12;9(15):786-91. doi: 10.1016/s0960-9822(99)80361-3. Curr Biol. 1999. PMID: 10469563
BACKGROUND: Nucleotide substitution rates and G + C content vary considerably among mammalian genes. It has been proposed that the mammalian genome comprises a mosaic of regions - termed isochores - with differing G + C content. ...Moreover, we demonstrated that the …
BACKGROUND: Nucleotide substitution rates and G + C content vary considerably among mammalian genes. It has been proposed that the ma …
DNA sequence evolution: the sounds of silence.
Sharp PM, Averof M, Lloyd AT, Matassi G, Peden JF. Sharp PM, et al. Among authors: matassi g. Philos Trans R Soc Lond B Biol Sci. 1995 Sep 29;349(1329):241-7. doi: 10.1098/rstb.1995.0108. Philos Trans R Soc Lond B Biol Sci. 1995. PMID: 8577834 Review.
However, it now appears that natural selection shapes codon usage in some multicellular species (e.g. Drosophila and Caenorhabditis), and that regional variations in mutation biases occur in yeast. ...
However, it now appears that natural selection shapes codon usage in some multicellular species (e.g. Drosophila and Caenorhabditis), …
The members of the RH gene family (RH50 and RH30) followed different evolutionary pathways.
Matassi G, Chérif-Zahar B, Pesole G, Raynal V, Cartron JP. Matassi G, et al. J Mol Evol. 1999 Feb;48(2):151-9. doi: 10.1007/pl00006453. J Mol Evol. 1999. PMID: 9929383
Interestingly, this event seems to coincide with the appearance in these species of a G-to-T mutation in the RH50 gene which created a stop codon in the corresponding transcript. ...
Interestingly, this event seems to coincide with the appearance in these species of a G-to-T mutation in the RH50 gene which created …
Organization of the human RH50A gene (RHAG) and evolution of base composition of the RH gene family.
Matassi G, Chérif-Zahar B, Raynal V, Rouger P, Cartron JP. Matassi G, et al. Genomics. 1998 Jan 15;47(2):286-93. doi: 10.1006/geno.1997.5112. Genomics. 1998. PMID: 9479501
., different isochores) that are likely to drive the evolution of these genes, the base compositions (G + C content) of which differ drastically. ...
., different isochores) that are likely to drive the evolution of these genes, the base compositions (G + C content) of which differ …
Evolution and functional characterization of the RH50 gene from the ammonia-oxidizing bacterium Nitrosomonas europaea.
Cherif-Zahar B, Durand A, Schmidt I, Hamdaoui N, Matic I, Merrick M, Matassi G. Cherif-Zahar B, et al. Among authors: matassi g. J Bacteriol. 2007 Dec;189(24):9090-100. doi: 10.1128/JB.01089-07. Epub 2007 Oct 5. J Bacteriol. 2007. PMID: 17921289 Free PMC article.
Rh-deficiency of the regulator type caused by splicing mutations in the human RH50 gene.
Chérif-Zahar B, Matassi G, Raynal V, Gane P, Delaunay J, Arrizabalaga B, Cartron JP. Chérif-Zahar B, et al. Among authors: matassi g. Blood. 1998 Oct 1;92(7):2535-40. Blood. 1998. PMID: 9746795
The first mutation affected the invariant G residue of the 3' acceptor splice-site of intron 6, causing the skipping of the downstream exon and the premature termination of translation. ...
The first mutation affected the invariant G residue of the 3' acceptor splice-site of intron 6, causing the skipping of the downstrea …
Insights into the structure and function of membrane polypeptides carrying blood group antigens.
Cartron JP, Bailly P, Le Van Kim C, Cherif-Zahar B, Matassi G, Bertrand O, Colin Y. Cartron JP, et al. Among authors: matassi g. Vox Sang. 1998;74 Suppl 2:29-64. doi: 10.1111/j.1423-0410.1998.tb05397.x. Vox Sang. 1998. PMID: 9704424 Review.
Molecular defects of the RHCE gene in Rh-deficient individuals of the amorph type.
Chérif-Zahar B, Matassi G, Raynal V, Gane P, Mempel W, Perez C, Cartron JP. Chérif-Zahar B, et al. Among authors: matassi g. Blood. 1998 Jul 15;92(2):639-46. Blood. 1998. PMID: 9657766
Molecular characterization of a new urea transporter in the human kidney.
Olivès B, Martial S, Mattei MG, Matassi G, Rousselet G, Ripoche P, Cartron JP, Bailly P. Olivès B, et al. Among authors: matassi g. FEBS Lett. 1996 May 20;386(2-3):156-60. doi: 10.1016/0014-5793(96)00425-5. FEBS Lett. 1996. PMID: 8647271
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