Literature DB >> 20086307

Genetic diversity among old Portuguese bread wheat cultivars and botanical varieties evaluated by ITS rDNA PCR-RFLP markers.

A Carvalho1, H Guedes-Pinto, J Lima-Brito.   

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Year:  2009        PMID： 20086307     DOI： 10.1007/s12041-009-0055-5

Source DB:  PubMed          Journal:  J Genet        ISSN： 0022-1333            Impact factor:   1.166


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  8 in total

Review 1.  Ribosomal ITS sequences and plant phylogenetic inference.

Authors:  I Alvarez; J F Wendel
Journal:  Mol Phylogenet Evol       Date:  2003-12       Impact factor: 4.286

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3.  A COMPARISON OF THREE INDIRECT METHODS FOR ESTIMATING AVERAGE LEVELS OF GENE FLOW.

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Authors:  R F Barker; N P Harberd; M G Jarvis; R B Flavell
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6.  Analysis of gene diversity in subdivided populations.

Authors:  M Nei
Journal:  Proc Natl Acad Sci U S A       Date:  1973-12       Impact factor: 11.205

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8.  Intra-individual and intra-species heterogeneity in nuclear rDNA ITS region of Vigna species from subgenus Ceratotropis.

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  8 in total
  5 in total

1.  Polymorphism of the simple sequence repeat (AAC)5 in the nucleolar chromosomes of Old Portuguese wheat cultivars.

Authors:  Ana Carvalho; Henrique Guedes-Pinto; José Lima-Brito
Journal:  J Genet       Date:  2013-12       Impact factor: 1.166

2.  Physical localization of NORs and ITS length variants in old Portuguese durum wheat cultivars.

Authors:  Ana Carvalho; Henrique Guedes-Pinto; José Lima-Brito
Journal:  J Genet       Date:  2011-04       Impact factor: 1.166

3.  Molecular characterization of Vigna radiata (L.) Wilczek genotypes based on nuclear ribosomal DNA and RAPD polymorphism.

Authors:  Aparna Raturi; S K Singh; Vinay Sharma; Rakesh Pathak
Journal:  Mol Biol Rep       Date:  2011-06-11       Impact factor: 2.316

4.  Intergenic spacer length variants in Old Portuguese bread wheat cultivars.

Authors:  Ana Carvalho; Henrique Guedes-Pinto; José Lima-Brito
Journal:  J Genet       Date:  2011-08       Impact factor: 1.166

5.  Taxonomic and ecological discrimination of Fagaceae species based on internal transcribed spacer polymerase chain reaction-restriction fragment length polymorphism.

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