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  1. ...of humans and chimpanzees. Am. J. Hum. Genet. 68 : 444 -456. ↵ Crosier, M., Viggiano, L., Guy, J., Misceo, D., Stones, R., Wei, W., Hearn, T., Ventura, M., Archidiacono, N., Rocchi, M., et al. 2002 . Human paralogs of KIAA0187 were created through independent pericentromeric-directed and chromosome-specific...
  2. ....1 and Xq28: A novel pericentromeric-directed mechanism for paralogous evolution. Hum. Mol. Genet. 5 : 899 – 912 . ↵ Eichler E.E. , Budarf M.L. , Rocchi M. , Deaven L.L. , Doggett N.A. , Baldini A. , Nelson D.L. , Mohrenweiser H.W. ( 1997 ) Interchromosomal duplications of the adrenoleukodystrophy locus...
  3. ...of the human Yp11.2/Yp11.1 region were already present in the macaque–human ancestor as multiple paralogs located predominantly in subtelomeric regions. In contrast, duplicons from the Yq11.1/Yq11.21, Yq11.23/Yq12, and Yq12/PAR2 regions show no evidence of duplication in rhesus macaque, but map...
  4. ...satellite-associated pericentromeric-directed duplication events. Consistent with this, one or both termini of identity between 10p11 and the majority of paralogs falls within the satellite 3 sequence or the short CATTT repeat at position 168–170 kb (Fig. 4 A). Furthermore, all paralogs are linked...
  5. ...for evidence that a transposition and/or duplication event has generated a new transcript. RESULTS Clustering of Gene-Derived Sequences in Euchromatic Regions of HSA5 To first determine the precise chromosomal localization of all the paralogous copies of the gene segments, we used a combination of mono...
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