Mgr. Tereza Omelková

Bachelor's thesis

Úloha genu pro PAX9 v patogenezi hypodoncie

The role of PAX9 gene in pathogenesis of hypodontia
Abstract:
Hypodoncie je nejčastější dědičnou poruchou dentice v lidské populaci. Agenezí zubů (vyjma třetího moláru) trpí 1,6–9,6 % populace. Toto onemocnění se vyskytuje v izolované nebo syndromické formě (Riegerův syndrom, anhidrotická ektodermální dysplazie, Witkopův syndrom). S izolovanou formou byly zatím asociovány pouze mutace ve třech genech (Pax9, Msx1, Axin2). Další geny pro syndromickou a izolovanou …more
Abstract:
Hypodontia is the most common developmental disorder in humans. From agenesis (exluding third molar) suffers from 1.6 to 9.6 % of the population. This disease appears in non-syndromic or syndromic form (Rieger syndrome, anhidrotic ectodermal dysplasia, Witkop syndrome). With the non-syndromic form there has been associated mutations only in three genes (Pax9, Msx1, Axin2). Other genes are examined …more
 
 
Language used: Czech
Date on which the thesis was submitted / produced: 10. 5. 2011

Thesis defence

  • Date of defence: 14. 6. 2011
  • Supervisor: prof. RNDr. Omar Šerý, Ph.D.

Citation record

Full text of thesis

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Institution archiving the thesis and making it accessible: Masarykova univerzita, Přírodovědecká fakulta

Masaryk University

Faculty of Science

Bachelor programme / field:
Biochemistry / Biochemistry

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