Judit Szilvia Keserű

Dr. Judit Szilvia Keserű

Department of Human Genetics, University of Debrecen
orcid

Research Focus & Metrics

Academic Career Length

13Years (2014-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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Journal Article
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MSMelinda Szilágyi-Bónizs
Melinda Szilágyi-Bónizs
OPOndrej Pös
Ondrej Pös
ÉMÉva Márton
Éva Márton
GBGergely Buglyó
Gergely Buglyó
BSBeata Soltesz
Beata Soltesz
Bálint NagyBálint Nagy
Bálint Nagy
Liquid biopsy recently became a very promising diagnostic method that has several advantages over conventional invasive methods. Liquid biopsy may serve as a source of several important biomarkers including cell-free nucleic acids (cf-NAs). Cf-DNA is widely used in prenatal testing in order to characterize fetal genetic disorders. Analysis of cf-DNA may provide information about the mutation profile of tumor cells, while cell-free non-coding RNAs are promising biomarker candidates in the diagnosis and prognosis of cancer. Many of these markers have the potential to help clinicians in therapy selection and in the follow-up of patients. Thus, cf-NA-based diagnostics represent a new path in personalized medicine. Although several reviews are available in the field, most of them focus on a limited number of cf-NA types. In this review, we give an overview about all known cf-NAs including cf-DNA, cf-mtDNA and cell-free non-coding RNA (miRNA, lncRNA, circRNA, piRNA, YRNA, and vtRNA) by discussing their biogenesis, biological function and potential as biomarker candidates in liquid biopsy. We also outline possible future directions in the field.

1 June 2019 in Journal of Biotechnology
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Journal Article
Closed access
JKJudit Szilvia Keserű
Judit Szilvia Keserű
BSBeáta Soltész
Beáta Soltész
JLJános Lukács
János Lukács
ÉMÉva Márton
Éva Márton
MSMelinda Szilágyi-Bónizs
Melinda Szilágyi-Bónizs
Bálint NagyBálint Nagy
Bálint Nagy

14 January 2022 in Journal of Fungi
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Journal Article
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BGBarnabás Csaba Gila
Barnabás Csaba Gila
KAKaroly Antal
Karoly Antal
ZBZsuzsanna Birkó
Zsuzsanna Birkó
JKJudit Szilvia Keserű
Judit Szilvia Keserű
István PócsiIstván Pócsi
István Pócsi
TETamás Emri
Tamás Emri
Understanding the coordinated regulation of the hundreds of carbohydrate-active enzyme (CAZyme) genes occurring in the genomes of fungi has great practical importance. We recorded genome-wide transcriptional changes of Aspergillus nidulans cultivated on glucose, lactose, or arabinogalactan, as well as under carbon-starved conditions. We determined both carbon-stress-specific changes (weak or no carbon source vs. glucose) and carbon-source-specific changes (one type of culture vs. all other cultures). Many CAZyme genes showed carbon-stress-specific and/or carbon-source-specific upregulation on arabinogalactan (138 and 62 genes, respectively). Besides galactosidase and arabinan-degrading enzyme genes, enrichment of cellulolytic, pectinolytic, mannan, and xylan-degrading enzyme genes was observed. Fewer upregulated genes, 81 and 107 carbon stress specific, and 6 and 16 carbon source specific, were found on lactose and in carbon-starved cultures, respectively. They were enriched only in galactosidase and xylosidase genes on lactose and rhamnogalacturonanase genes in both cultures. Some CAZyme genes (29 genes) showed carbon-source-specific upregulation on glucose, and they were enriched in β-1,4-glucanase genes. The behavioral ecological background of these characteristics was evaluated to comprehensively organize our knowledge on CAZyme production, which can lead to developing new strategies to produce enzymes for plant cell wall saccharification.

18 December 2014 in Archives of Microbiology
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Journal Article
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ZSZsolt Spitzmüller
Zsolt Spitzmüller
NKNak-Jung Kwon
Nak-Jung Kwon
MSMelinda Szilágyi
Melinda Szilágyi
JKJudit Szilvia Keserű
Judit Szilvia Keserű
VTViktória Tóth
Viktória Tóth
TETamás Emri
Tamás Emri