About: Detection of RET proto-oncogene mutations in families with medullary thyroid cancer, syndrome MEN 2 - predictive molecular genetic analysis     Goto   Sponge   NotDistinct   Permalink

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Description
  • The project objective is to reveal the RET proto-oncogene mutations that cause the hereditary forms of medullary thyroid cancer (FMTC, MEN 2A, MEN 2B) and thus to contribute to the early presymptomatic diagnosis in predictive persons. (en)
  • MTC je u familiární varianty (FMTC, MEN2A, MEN2B) nádorem s autozomálně dominantním typem dědičnosti. Detekce mutací v RET proto-onkogenu přispěje významnou měrou k včasné predikci onemocnění u osob ještě bez zjevných klinických příznaků.
Title
  • Detection of RET proto-oncogene mutations in families with medullary thyroid cancer, syndrome MEN 2 - predictive molecular genetic analysis (en)
  • Detekce mutací RET proto-onkogenu u rodin s medulárním karcinomem štítné žlázy,syndromem MEN 2 - prediktivní molekulárně genetická diagnostika
skos:notation
  • NC6650
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  • Medullary thyroid carcinoma;Ret proto-oncogene;MEn 2A;FMTC;Molecular genetic diagnostics;Cancer prediction;TGGE (en)
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  • Detekce mutací RET onkogenu u rodin s medulárním karcinomem štítné žlázy. (cs)
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  • Cancer prediction
  • FMTC
  • MEn 2A
  • Medullary thyroid carcinoma
  • Molecular genetic diagnostics
  • Ret proto-oncogene
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