A pilot study conducted in the Czech Republic relating to the molecular analysis of the RET and GDNF genes in patients with cakut, predominantly unilateral renal agenesis

Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00023761%3A_____%2F15%3A%230000548" target="_blank" >RIV/00023761:_____/15:#0000548 - isvavai.cz</a>
Výsledek na webu
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DOI - Digital Object Identifier
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Jazyk výsledku
angličtina
Název v původním jazyce
A pilot study conducted in the Czech Republic relating to the molecular analysis of the RET and GDNF genes in patients with cakut, predominantly unilateral renal agenesis
Popis výsledku v původním jazyce
Renal anomalies are quite a common medical condition thought to be genetically influenced. The subject of this work was to conduct molecular genetic analysis of two human renal agenesis causing candidate genes encoding the RET receptor thyrosin kinase and GDNF neutrophic factor. The mutational analysis of twenty RET exons and three GDNF exons in twenty patients diagnosed with unilateral renal agenesis was carried out.
Název v anglickém jazyce
A pilot study conducted in the Czech Republic relating to the molecular analysis of the RET and GDNF genes in patients with cakut, predominantly unilateral renal agenesis
Popis výsledku anglicky
Renal anomalies are quite a common medical condition thought to be genetically influenced. The subject of this work was to conduct molecular genetic analysis of two human renal agenesis causing candidate genes encoding the RET receptor thyrosin kinase and GDNF neutrophic factor. The mutational analysis of twenty RET exons and three GDNF exons in twenty patients diagnosed with unilateral renal agenesis was carried out.

Druh
J<sub>x</sub> - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)
CEP obor
EB - Genetika a molekulární biologie
OECD FORD obor
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Rok uplatnění
2015
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

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