Search Results - (Author, Cooperation:A. S. Graphodatsky)
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1O. Thalmann ; B. Shapiro ; P. Cui ; V. J. Schuenemann ; S. K. Sawyer ; D. L. Greenfield ; M. B. Germonpre ; M. V. Sablin ; F. Lopez-Giraldez ; X. Domingo-Roura ; H. Napierala ; H. P. Uerpmann ; D. M. Loponte ; A. A. Acosta ; L. Giemsch ; R. W. Schmitz ; B. Worthington ; J. E. Buikstra ; A. Druzhkova ; A. S. Graphodatsky ; N. D. Ovodov ; N. Wahlberg ; A. H. Freedman ; R. M. Schweizer ; K. P. Koepfli ; J. A. Leonard ; M. Meyer ; J. Krause ; S. Paabo ; R. E. Green ; R. K. Wayne
American Association for the Advancement of Science (AAAS)
Published 2013Staff ViewPublication Date: 2013-11-16Publisher: American Association for the Advancement of Science (AAAS)Print ISSN: 0036-8075Electronic ISSN: 1095-9203Topics: BiologyChemistry and PharmacologyComputer ScienceMedicineNatural Sciences in GeneralPhysicsKeywords: Animals ; Animals, Domestic/*genetics ; Base Sequence ; Breeding ; Dogs/*genetics ; Europe ; Genome, Mitochondrial/*genetics ; Molecular Sequence Data ; Phylogeny ; Wolves/geneticsPublished by: -
2Protopopov, A. I. ; Gizatullin, R. Z. ; Vorobieva, N. V. ; Protopopova, M. V. ; Kiss, C. ; Kashuba, V. I. ; Klein, G. ; Kisselev, L. L. ; Graphodatsky, A. S. ; Zabarovsky, E. R.
Springer
Published 1996Staff ViewISSN: 1573-6849Keywords: fluorescencein situ hybridization ; human chromosome 3 ; localization of genes ; Notl linking clonesSource: Springer Online Journal Archives 1860-2000Topics: BiologyNotes: Abstract Forty newNotl linking clones representing sequence tagged sites (STSs) were mapped by fluorescencein situ hybridization (FISH) to different regions of human chromosome 3 (HSA3). Clone NL1-245, containing human aminoacylase 1, was localized to 3p21.2–p21.1. Our previous localization of the CLC-2 chloride channel protein gene was refined to 3q27. Clone NL2-316 most likely contains a translocon-associated protein γ-subunit gene and was mapped to 3q23–q24. To our knowledge, this is the first time this gene has been mapped. OneNoti linking clone (NL1-229) probably contains a new protein phosphatase gene. This clone was mapped to 3p25. FiveNoti linking clones probably contain human expressed sequence tags (ESTs), as they possess sequences with a high level of identity (〉90%) to cDNA clones. Other clones show 56–85% homology to known mammalian and human genes with various functions, including oncogenes and tumour-suppressor genes. These clones might represent new genes.Type of Medium: Electronic ResourceURL: -
3Graphodatsky, A. S. ; Yang, F. ; O'Brien, P. C. M. ; Serdukova, N. ; Milne, B. S. ; Trifonov, V. ; Ferguson-Smith, M. A.
Springer
Published 2000Staff ViewISSN: 1573-6849Keywords: Comparative mapping ; dog ; red fox ; Arctic fox ; karyotype evolution ; G-bandingSource: Springer Online Journal Archives 1860-2000Topics: BiologyNotes: Abstract A complete set of paint probes, with each probe specific for a single type of dog chromosome, was generated by DOP-PCR amplification of flow-sorted chromosomes. These probes have been assigned to high-resolution G-banded chromosomes of the dog and Arctic fox by fluorescence in-situ hybridization. On the basis of these results we propose improved nomenclature for the G-banded karyotypes of the dog and Artic fox. A comparative map between the Arctic fox, red fox and dog has been established based on results from chromosome painting and high-resolution G-banding. This map demonstrates that the euchromatic complements of these three canid species consists of 42 conserved segments. Thirty-four of these 42 segments are each represented by a single dog chromosome with dog chromosomes 1, 13, 18 and 19 each retaining two segments, respectively. The autosomes of the Arctic fox and red fox could be reconstructed from these 42 blocks in different combinations through chromosomal fusions. Our findings suggest that chromosome fusion has been the principal mechanism of karyotype evolution occuring during speciation in canids.Type of Medium: Electronic ResourceURL: