Zobrazeno 1 - 10
of 439
pro vyhledávání: '"A. Zikánová"'
Autor:
Binter, Jakub, Klapilová, Kateřina, Zikánová, Tereza, Nilsson, Tommy, Bártová, Klára, Krejcová, Lucie, Androvicová, Renata, Lindová, Jitka, Prušová, Denisa, Wells, Timothy, Riha, Daniel
There are many reasons for utilising 3D animation and virtual reality in sexuality research. Apart from providing a mean with which to (re)experience certain situations there are four main advantages: a) bespoke animated stimuli can be created and cu
Externí odkaz:
http://arxiv.org/abs/1611.01817
Autor:
Ilaria Dutto, Julian Gerhards, Antonio Herrera, Olga Souckova, Václava Škopová, Jordann A Smak, Alexandra Junza, Oscar Yanes, Cedric Boeckx, Martin D Burkhalter, Marie Zikánová, Sebastian Pons, Melanie Philipp, Jens Lüders, Travis H Stracker
Publikováno v:
eLife, Vol 11 (2022)
Adenylosuccinate lyase (ADSL) functions in de novo purine synthesis (DNPS) and the purine nucleotide cycle. ADSL deficiency (ADSLD) causes numerous neurodevelopmental pathologies, including microcephaly and autism spectrum disorder. ADSLD patients ha
Externí odkaz:
https://doaj.org/article/5ef7d8baa9df4de681a7f4e9f3e46c1a
Autor:
Nabil El-Lababidi, Marie Zikánová, Alice Baxová, Lenka Nosková, Alena Leiská, Lukáš Lambert, Tomáš Honzík, Jiří Zeman
Publikováno v:
Prague Medical Report, Vol 121, Iss 3, Pp 153-162 (2020)
Dominantly inherited mutations in COMP gene encoding cartilage oligomeric matrix protein may cause two dwarfing skeletal dysplasias, milder multiple epiphyseal dysplasia (MED) and more severe pseudoachondroplasia (PSACH). We studied the phenotype and
Externí odkaz:
https://doaj.org/article/d450c9a33fe74e548b3b0623d87dfce2
Autor:
Giada Zurlo, Xijuan Liu, Mamoru Takada, Cheng Fan, Jeremy M. Simon, Travis S. Ptacek, Javier Rodriguez, Alex von Kriegsheim, Juan Liu, Jason W. Locasale, Adam Robinson, Jing Zhang, Jessica M. Holler, Baek Kim, Marie Zikánová, Jörgen Bierau, Ling Xie, Xian Chen, Mingjie Li, Charles M. Perou, Qing Zhang
Publikováno v:
Nature Communications, Vol 10, Iss 1, Pp 1-15 (2019)
The hydroxylase EgIN2 contributes to triple negative breast cancers. Here, using an enzyme-substrate trapping strategy, the authors identify ASDL as a bona fide substrate of EgIN2 promoting aggressive properties of TNBC via the activation of cMYC sig
Externí odkaz:
https://doaj.org/article/4f3b6b5738bf4496a2ce34dde8289124
Autor:
Crible, Ludivine, Abuczki, Ágnes, Burkšaitienė, Nijolė, Furkó, Péter, Nedoluzhko, Anna, Rackevičienė, Sigita, Oleškevičienė, Giedrė Valūnaitė, Zikánová, Šárka
Publikováno v:
In Journal of Pragmatics March 2019 142:139-155
Akademický článek
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Autor:
Randall C Mazzarino, Veronika Baresova, Marie Zikánová, Nathan Duval, Terry G Wilkinson, David Patterson, Guido N Vacano
Publikováno v:
PLoS ONE, Vol 16, Iss 7, p e0247227 (2021)
In humans, GART [phosphoribosylglycinamide formyltransferase (EC 2.1.2.2) / phosphoribosylglycinamide synthetase (EC 6.3.4.13) / phosphoribosylaminoimidazole synthetase (EC 6.3.3.1)] is a trifunctional protein which catalyzes the second, third, and f
Externí odkaz:
https://doaj.org/article/54ef6066cb6c430fa7cef10f019684ac
Autor:
Randall C. Mazzarino, Veronika Baresova, Marie Zikánová, Nathan Duval, Terry G. Wilkinson, II, David Patterson, Guido N. Vacano
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 25, Iss , Pp 100642- (2020)
In de novo purine biosynthesis (DNPS), 5-aminoimidazole-4-carboxamide ribonucleotide formyltransferase (EC 2.1.2.3)/inosine monophosphate cyclohydrolase (EC 3.5.4.10) (ATIC) catalyzes the last two reactions of the pathway: conversion of 5-aminoimidaz
Externí odkaz:
https://doaj.org/article/9d371210153f41a2a86d1a26c04d6739
Autor:
Lucie Mádrová, Olga Součková, Radana Brumarová, Dana Dobešová, Jan Václavík, Štěpán Kouřil, Julie de Sousa, Jaroslava Friedecká, David Friedecký, Veronika Barešová, Marie Zikánová, Tomáš Adam
Publikováno v:
Metabolites, Vol 12, Iss 3, p 241 (2022)
Three genetically determined enzyme defects of purine de novo synthesis (PDNS) have been identified so far in humans: adenylosuccinate lyase (ADSL) deficiency, 5-amino-4-imidazole carboxamide-ribosiduria (AICA-ribosiduria), and deficiency in bifuncti
Externí odkaz:
https://doaj.org/article/c5b3d625bd1947d688de40048b640354
Publikováno v:
Écho des études romanes. 18:99-115