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Search Results - Jenčík, Ján
Search Results - Jenčík, Ján
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Evaluation of High-Viscosity Residual Fractions by Hot Filtration
by
Schlehöfer, Dominik
,
Vráblík, Aleš
,
Chrudimská, Kateřina
,
Jenčík, Jan
,
Hradecká, Ivana
Published in
Energy & fuels
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Hydrocracking of a Heavy Vacuum Gas Oil with Fischer–Tropsch Wax
by
Pleyer, Olga
,
Vrtiška, Dan
,
Straka, Petr
,
Vráblík, Aleš
,
Jenčík, Jan
,
Šimáček, Pavel
Published in
Energies (Basel)
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A comparative study of a modified unsaturated polyester resin with dicyclopentadiene and methyl dicyclopentadiene blends
by
Perrot, Alexandre
,
Hyršl, Jan
,
Bandžuch, Jan
,
Waňousová, Simona
,
Hájek, Jiří
,
Jenčík, Jan
,
Herink, Tomáš
Published in
Polymer (Guilford)
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Use of Dicyclopentadiene and Methyl Dicyclopentadiene for the Synthesis of Unsaturated Polyester Resins
by
Perrot, Alexandre
,
Hyršl, Jan
,
Bandžuch, Jan
,
Waňousová, Simona
,
Hájek, Jiří
,
Jenčík, Jan
,
Herink, Tomáš
Published in
Polymers
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Lignocellulosic Bioethanol and Biobutanol as a Biocomponent for Diesel Fuel
by
Obergruber, Michal
,
Hönig, Vladimír
,
Jenčík, Jan
,
Hájek, Jiří
,
Schlehöfer, Dominik
,
Herink, Tomáš
Published in
Materials
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Advanced Biofuels Based on Fischer-Tropsch Synthesis for Applications in Diesel Engines
by
Jenčík, Jan
,
Hönig, Vladimír
,
Obergruber, Michal
,
Hájek, Jiří
,
Vráblík, Aleš
,
Černý, Radek
,
Schlehöfer, Dominik
,
Herink, Tomáš
Published in
Materials
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Advanced Biofuels Based on Fischer–Tropsch Synthesis for Applications in Gasoline Engines
by
Hájek, Jiří
,
Hönig, Vladimír
,
Obergruber, Michal
,
Jenčík, Jan
,
Vráblík, Aleš
,
Černý, Radek
,
Pšenička, Martin
,
Herink, Tomáš
Published in
Materials
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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
by
Safka Brozkova, Dana
,
Poisson Marková, Simona
,
Mészárosová, Anna Uhrová
,
Jenčík, Ján
,
Čejnová, Vlasta
,
Čada, Zdeněk
,
Laštůvková, Jana
,
Rašková, Dagmar
,
Seeman, Pavel
Published in
Clinical genetics
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Moderate sensorineural hearing loss is typical for DFNB16 caused by various types of mutations affecting the STRC gene
by
Čada, Zdeněk
,
Šafka Brožková, Dana
,
Balatková, Zuzana
,
Plevová, Pavlína
,
Rašková, Dagmar
,
Laštůvková, Jana
,
Černý, Rudolf
,
Bandúrová, Veronika
,
Koucký, Vladimír
,
Hrubá, Silvie
,
Komarc, Martin
,
Jenčík, Ján
,
Poisson Marková, Simona
,
Plzák, Jan
,
Kluh, Jan
,
Seeman, Pavel
Published in
European archives of oto-rhino-laryngology
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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 ethn...
by
Safka Brozkova, Dana
,
Varga, Lukas
,
Uhrova Meszarosova, Anna
,
Slobodova, Zuzana
,
Skopkova, Martina
,
Soltysova, Andrea
,
Ficek, Andrej
,
Jencik, Jan
,
Lastuvkova, Jana
,
Gasperikova, Daniela
,
Seeman, Pavel
Published in
Orphanet journal of rare diseases
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Two types of recessive hereditary spastic paraplegia in Roma patients in compound heterozygous state; no ethnically prevalent variant found
by
Meszarosova, Anna Uhrova
,
Seeman, Pavel
,
Jencik, Jan
,
Drabova, Jana
,
Cibochova, Renata
,
Stellmachova, Julia
,
Safka Brozkova, Dana
Published in
Neuroscience letters
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Variant c.2158-2AG 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 ethni...
by
Safka Brozkova, Dana
,
Varga, Lukas
,
Uhrova Meszarosova, Anna
,
Slobodova, Zuzana
,
Skopkova, Martina
,
Soltysova, Andrea
,
Ficek, Andrej
,
Jencik, Jan
,
Lastuvkova, Jana
,
Gasperikova, Daniela
,
Seeman, Pavel
Published in
Orphanet journal of rare diseases
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