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Genotyping Glycogen Storage Disease Type II and Type V in Cattle Reared in the Czech Republic

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60076658%3A12220%2F07%3A00008180" target="_blank" >RIV/60076658:12220/07:00008180 - isvavai.cz</a>

  • Alternative codes found

    RIV/60076658:12220/07:8P001640 RIV/00027162:_____/07:#0000447

  • Result on the web

  • DOI - Digital Object Identifier

Alternative languages

  • Result language

    angličtina

  • Original language name

    Genotyping Glycogen Storage Disease Type II and Type V in Cattle Reared in the Czech Republic

  • Original language description

    Genotyping was carried out for glycogen storage disease type II and type V in seven cattle breeds. The analysis was carried out using the polymerase chain reaction/restriction fragment length polymorphism (PCR/RFLP) method. In the breeds analysed (Charolais, Czech Spotted - Czech Simmental, Belgian Blue, Limousine, Blonde d'Aquitaine, Aberdeen Angus and beef Simmental sires reared in the Czech Republic), the recessive allele was not found in the PYGM (phosphorylase glycogen, muscle) responsible for theglycogen storage disease type V. In the same apnel, the recessive allele in exon 7, exon 9 and exon 13 of the GAA (glucosidase alpha, acid), causing the glycogen storage disease type II was not found. Therefore, we have not revealed the recessive outsideprevious reported breeds. The knowledge of the breed specific occurrence of inherited disorders facilitates focusing and reduces the costs of detecting the heterozygous carriers of recessive inherited disorders.

  • Czech name

    Genotypizace glycogen storage disease typu II a typu V u skotu chovaného v České republice

  • Czech description

    U sedmi plemen skotu jsme genotypizovali lokus pro glycogen storage disease typu II a typu V. Analýza byla provedena s využitím PCR/RFLP. U býků plemen charolais, české strakaté, belgické modré, limousin, plavé akvitánské, aberdeen angus a masný simentáljsme nenalezli recesivní alelu PYGM (phosphorylase glycogen, muscle) zodpovědnou za glycogen storage disease typu V. Ve stejném panelu nebyla nalezena ani recesivní alela GAA (glucosidase alpha, acid) v exonu 7, 9 a 13, která zapříčiňuje vznik glycogenstorage disease typu II. U analyzovaných plemen jsme tedy nenalezli žádné skryté přenašeče. Znalost plemenně specifického výskytu dědičných chorob usnadňuje zaměření a redukuje náklady na detekci heterozygotních přenašečů recesivně podmíněných dědičnýchchorob.

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    EB - Genetics and molecular biology

  • OECD FORD branch

Result continuities

  • Project

    Result was created during the realization of more than one project. More information in the Projects tab.

  • Continuities

    Z - Vyzkumny zamer (s odkazem do CEZ)

Others

  • Publication year

    2007

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Journal of Veterinary Medicine Series A

  • ISSN

    0931-184X

  • e-ISSN

  • Volume of the periodical

    54

  • Issue of the periodical within the volume

    5

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    3

  • Pages from-to

    257-259

  • UT code for WoS article

  • EID of the result in the Scopus database