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A CpG island-encoded mechanism protects genes from premature transcription termination
by
Hughes, Amy L
,
Szczurek, Aleksander T
,
Kelley, Jessica R
,
Lastuvkova, Anna
,
Turberfield, Anne H
,
Dimitrova, Emilia
,
Blackledge, Neil P
,
Klose, Robert J
Published in
Nature communications
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CDK-Mediator and FBXL19 prime developmental genes for activation by promoting atypical regulatory interactions
by
Feldmann, Angelika
,
Dimitrova, Emilia
,
Kenney, Alexander
,
Lastuvkova, Anna
,
Klose, Robert J
Published in
Nucleic acids research
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BAP1 constrains pervasive H2AK119ub1 to control the transcriptional potential of the genome
by
Fursova, Nadezda A
,
Turberfield, Anne H
,
Blackledge, Neil P
,
Findlater, Emma L
,
Lastuvkova, Anna
,
Huseyin, Miles K
,
Dobrinić, Paula
,
Klose, Robert J
Published in
Genes & development
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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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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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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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Autosomal recessive hereditary spastic paraplegia type SPG35 due to a novel variant in the FA2H gene in a Czech patient
by
Uhrova Meszarosova, Anna
,
Safka Brozkova, Dana
,
Vyhnalek, Martin
,
Mazanec, Radim
,
Lastuvkova, Jana
,
Trkova, Marie
,
Bittoova, Martina
,
Soldatova, Inna
,
Seeman, Pavel
Published in
Journal of clinical neuroscience
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The Cause of Hereditary Hearing Loss in GJB2 Heterozygotes—A Comprehensive Study of the GJB2/DFNB1 Region
by
Safka Brozkova, Dana
,
Uhrova Meszarosova, Anna
,
Lassuthova, Petra
,
Varga, Lukáš
,
Staněk, David
,
Borecká, Silvia
,
Laštůvková, Jana
,
Čejnová, Vlasta
,
Rašková, Dagmar
,
Lhota, Filip
,
Gašperíková, Daniela
,
Seeman, Pavel
Published in
Genes
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