Publications by authors named "Jan Jencik"

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Use of Dicyclopentadiene and Methyl Dicyclopentadiene for the Synthesis of Unsaturated Polyester Resins.
Alexandre Perrot, Jan Hyršl, Jan Bandžuch, Simona Waňousová, Jiří Hájek

Polymers (Basel)· September 2021

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Lignocellulosic Bioethanol and Biobutanol as a Biocomponent for Diesel Fuel.
Michal Obergruber, Vladimír Hönig, Jan Jenčík, Jiří Hájek, Dominik Schlehöfer

Materials (Basel)· September 2021

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Advanced Biofuels Based on Fischer-Tropsch Synthesis for Applications in Diesel Engines.
Jan Jenčík, Vladimír Hönig, Michal Obergruber, Jiří Hájek, Aleš Vráblík

Materials (Basel)· June 2021

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Advanced Biofuels Based on Fischer-Tropsch Synthesis for Applications in Gasoline Engines.
Jiří Hájek, Vladimír Hönig, Michal Obergruber, Jan Jenčík, Aleš Vráblík

Materials (Basel)· June 2021

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Spectrum and frequencies of non GJB2 gene mutations in Czech patients with early non-syndromic hearing loss detected by gene panel NGS and whole-exome sequencing.
Dana Safka Brozkova, Simona Poisson Marková, Anna Uhrová Mészárosová, Ján Jenčík, Vlasta Čejnová

Clin Genet· December 2020

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Variant c.2158-2A>G in MANBA is an important and frequent cause of hereditary hearing loss and beta-mannosidosis among the Czech and Slovak Roma population- evidence for a new ethnic-specific variant.
Dana Safka Brozkova, Lukas Varga, Anna Uhrova Meszarosova, Zuzana Slobodova, Martina Skopkova, Jan Jencik

Orphanet J Rare Dis· August 2020

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Two types of recessive hereditary spastic paraplegia in Roma patients in compound heterozygous state; no ethnically prevalent variant found.
Anna Uhrova Meszarosova, Pavel Seeman, Jan Jencik, Jana Drabova, Renata Cibochova

Neurosci Lett· March 2020

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Moderate sensorineural hearing loss is typical for DFNB16 caused by various types of mutations affecting the STRC gene.
Zdeněk Čada, Dana Šafka Brožková, Zuzana Balatková, Pavlína Plevová, Dagmar Rašková

Eur Arch Otorhinolaryngol· December 2019

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Fanconi anemia with biallelic FANCD1/BRCA2 mutations - Case report of a family with three affected children.
Karel Svojgr, David Sumerauer, Alena Puchmajerova, Ales Vicha, Ondrej Hrusak, Jan Jencik

Eur J Med Genet· March 2016

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