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Tytuł:
PCNA Unloading Is Crucial for the Bypass of DNA Lesions Using Homologous Recombination.
Czasopismo naukowe
Tytuł:
PCNA Unloading Is Crucial for the Bypass of DNA Lesions Using Homologous Recombination.
Autorzy:
Arbel-Groissman M; The Shmunis School of Biomedicine and Cancer Research, The George S. Wise Faculty of Life Sciences, Tel Aviv University, Tel Aviv 69978, Israel.
Liefshitz B; The Shmunis School of Biomedicine and Cancer Research, The George S. Wise Faculty of Life Sciences, Tel Aviv University, Tel Aviv 69978, Israel.
Katz N; The Shmunis School of Biomedicine and Cancer Research, The George S. Wise Faculty of Life Sciences, Tel Aviv University, Tel Aviv 69978, Israel.
Kuryachiy M; The Shmunis School of Biomedicine and Cancer Research, The George S. Wise Faculty of Life Sciences, Tel Aviv University, Tel Aviv 69978, Israel.
Kupiec M; The Shmunis School of Biomedicine and Cancer Research, The George S. Wise Faculty of Life Sciences, Tel Aviv University, Tel Aviv 69978, Israel.
Źródło:
International journal of molecular sciences [Int J Mol Sci] 2024 Mar 15; Vol. 25 (6). Date of Electronic Publication: 2024 Mar 15.
Typ publikacji:
Journal Article
MeSH Terms:
Saccharomyces cerevisiae Proteins*/genetics
Saccharomyces cerevisiae Proteins*/metabolism
Proliferating Cell Nuclear Antigen/genetics ; Proliferating Cell Nuclear Antigen/metabolism ; Saccharomyces cerevisiae/metabolism ; DNA Damage ; DNA Helicases/genetics ; DNA Helicases/metabolism ; Homologous Recombination ; DNA Replication ; DNA/genetics ; DNA/metabolism ; Chromatin/genetics ; Chromatin/metabolism ; Carrier Proteins/metabolism
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Sequestrase chaperones protect against oxidative stress-induced protein aggregation and [PSI+] prion formation.
Czasopismo naukowe
Tytuł:
Sequestrase chaperones protect against oxidative stress-induced protein aggregation and [PSI+] prion formation.
Autorzy:
Carter Z; Faculty of Biology, Medicine and Health, School of Biological Sciences, The University of Manchester, Michael Smith Building, Oxford Road, Manchester, United Kingdom.
Creamer D; Faculty of Biology, Medicine and Health, School of Biological Sciences, The University of Manchester, Michael Smith Building, Oxford Road, Manchester, United Kingdom.
Kouvidi A; Faculty of Biology, Medicine and Health, School of Biological Sciences, The University of Manchester, Michael Smith Building, Oxford Road, Manchester, United Kingdom.
Grant CM; Faculty of Biology, Medicine and Health, School of Biological Sciences, The University of Manchester, Michael Smith Building, Oxford Road, Manchester, United Kingdom.
Źródło:
PLoS genetics [PLoS Genet] 2024 Feb 29; Vol. 20 (2), pp. e1011194. Date of Electronic Publication: 2024 Feb 29 (Print Publication: 2024).
Typ publikacji:
Journal Article
MeSH Terms:
Prions*/genetics
Prions*/metabolism
Saccharomyces cerevisiae Proteins*/genetics
Saccharomyces cerevisiae Proteins*/metabolism
Protein Aggregates/genetics ; Molecular Chaperones/genetics ; Molecular Chaperones/metabolism ; Saccharomyces cerevisiae/genetics ; Saccharomyces cerevisiae/metabolism ; Oxidative Stress/genetics ; Amyloid/metabolism ; Oxidants/pharmacology ; Oxidants/metabolism ; Peptide Termination Factors/genetics ; Peptide Termination Factors/metabolism
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Mapping of Prion Structures in the Yeast Rnq1.
Czasopismo naukowe
Tytuł:
Mapping of Prion Structures in the Yeast Rnq1.
Autorzy:
Galliamov AA; A.N. Bach Institute of Biochemistry, Federal Research Center 'Fundamentals of Biotechnology' of the Russian Academy of Sciences, Moscow 119071, Russia.
Malukhina AD; A.N. Bach Institute of Biochemistry, Federal Research Center 'Fundamentals of Biotechnology' of the Russian Academy of Sciences, Moscow 119071, Russia.; Department of Biology, Moscow State University, Moscow 119991, Russia.
Kushnirov VV; A.N. Bach Institute of Biochemistry, Federal Research Center 'Fundamentals of Biotechnology' of the Russian Academy of Sciences, Moscow 119071, Russia.
Źródło:
International journal of molecular sciences [Int J Mol Sci] 2024 Mar 17; Vol. 25 (6). Date of Electronic Publication: 2024 Mar 17.
Typ publikacji:
Journal Article
MeSH Terms:
Prions*/metabolism
Saccharomyces cerevisiae Proteins*/metabolism
Saccharomyces cerevisiae/genetics ; Saccharomyces cerevisiae/metabolism
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
The PP2A-like phosphatase Ppg1 mediates assembly of the Far complex to balance gluconeogenic outputs and enables adaptation to glucose depletion.
Czasopismo naukowe
Tytuł:
The PP2A-like phosphatase Ppg1 mediates assembly of the Far complex to balance gluconeogenic outputs and enables adaptation to glucose depletion.
Autorzy:
Niphadkar S; Institute for Stem Cell Science and Regenerative Medicine (DBT-inStem) Bangalore, India.; Manipal Academy of Higher Education, Manipal, Karnataka, India.
Karinje L; Institute for Stem Cell Science and Regenerative Medicine (DBT-inStem) Bangalore, India.
Laxman S; Institute for Stem Cell Science and Regenerative Medicine (DBT-inStem) Bangalore, India.
Źródło:
PLoS genetics [PLoS Genet] 2024 Mar 07; Vol. 20 (3), pp. e1011202. Date of Electronic Publication: 2024 Mar 07 (Print Publication: 2024).
Typ publikacji:
Journal Article
MeSH Terms:
Glucose*/metabolism
Saccharomyces cerevisiae Proteins*/metabolism
Protein Phosphatase 2/metabolism ; Saccharomyces cerevisiae/genetics ; Saccharomyces cerevisiae/metabolism ; Signal Transduction ; Phosphorylation
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Functional analysis of chromatin-associated proteins in Sordaria macrospora reveals similar roles for RTT109 and ASF1 in development and DNA damage response.
Czasopismo naukowe
Tytuł:
Functional analysis of chromatin-associated proteins in Sordaria macrospora reveals similar roles for RTT109 and ASF1 in development and DNA damage response.
Autorzy:
Breuer J; Department of Molecular and Cellular Botany, Ruhr University Bochum, Universitätsstr. 150, 44801 Bochum, Germany.
Ferreira DEA; Department of Molecular and Cellular Botany, Ruhr University Bochum, Universitätsstr. 150, 44801 Bochum, Germany.
Kramer M; Department of Molecular and Cellular Botany, Ruhr University Bochum, Universitätsstr. 150, 44801 Bochum, Germany.
Bollermann J; Department of Molecular and Cellular Botany, Ruhr University Bochum, Universitätsstr. 150, 44801 Bochum, Germany.
Nowrousian M; Department of Molecular and Cellular Botany, Ruhr University Bochum, Universitätsstr. 150, 44801 Bochum, Germany.
Źródło:
G3 (Bethesda, Md.) [G3 (Bethesda)] 2024 Mar 06; Vol. 14 (3).
Typ publikacji:
Journal Article
MeSH Terms:
Histones*/metabolism
Saccharomyces cerevisiae Proteins*/genetics
Sordariales*
Methyl Methanesulfonate/pharmacology ; Molecular Chaperones/metabolism ; Saccharomyces cerevisiae/genetics ; DNA Repair ; DNA Damage ; Chromatin/genetics ; Chromatin/metabolism ; Cell Cycle Proteins/genetics ; Cell Cycle Proteins/metabolism ; Histone Acetyltransferases/metabolism ; Acetylation
SCR Organism:
Sordaria macrospora
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Meiotic prophase length modulates Tel1-dependent DNA double-strand break interference.
Czasopismo naukowe
Tytuł:
Meiotic prophase length modulates Tel1-dependent DNA double-strand break interference.
Autorzy:
López Ruiz LM; Genome Damage and Stability Centre, School of Life Sciences, University of Sussex, Brighton, United Kingdom.
Johnson D; Genome Damage and Stability Centre, School of Life Sciences, University of Sussex, Brighton, United Kingdom.
Gittens WH; Genome Damage and Stability Centre, School of Life Sciences, University of Sussex, Brighton, United Kingdom.
Brown GGB; Genome Damage and Stability Centre, School of Life Sciences, University of Sussex, Brighton, United Kingdom.
Allison RM; Genome Damage and Stability Centre, School of Life Sciences, University of Sussex, Brighton, United Kingdom.
Neale MJ; Genome Damage and Stability Centre, School of Life Sciences, University of Sussex, Brighton, United Kingdom.
Źródło:
PLoS genetics [PLoS Genet] 2024 Mar 01; Vol. 20 (3), pp. e1011140. Date of Electronic Publication: 2024 Mar 01 (Print Publication: 2024).
Typ publikacji:
Journal Article
MeSH Terms:
DNA Breaks, Double-Stranded*
Saccharomyces cerevisiae Proteins*/genetics
DNA ; DNA-Binding Proteins/genetics ; Endodeoxyribonucleases/genetics ; Intracellular Signaling Peptides and Proteins/genetics ; Meiosis/genetics ; Prophase/genetics ; Protein Serine-Threonine Kinases/genetics ; Saccharomyces cerevisiae/genetics
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Saccharomyces cerevisiae as a Model for Studying Human Neurodegenerative Disorders: Viral Capsid Protein Expression.
Czasopismo naukowe
Tytuł:
Saccharomyces cerevisiae as a Model for Studying Human Neurodegenerative Disorders: Viral Capsid Protein Expression.
Autorzy:
Bayandina SV; Vavilov Institute of General Genetics Russian Academy of Sciences, 119991 Moscow, Russia.
Mukha DV; Vavilov Institute of General Genetics Russian Academy of Sciences, 119991 Moscow, Russia.
Źródło:
International journal of molecular sciences [Int J Mol Sci] 2023 Dec 07; Vol. 24 (24). Date of Electronic Publication: 2023 Dec 07.
Typ publikacji:
Journal Article; Review
MeSH Terms:
Saccharomyces cerevisiae Proteins*/genetics
Saccharomyces cerevisiae Proteins*/metabolism
Neurodegenerative Diseases*/metabolism
Humans ; Saccharomyces cerevisiae/genetics ; Saccharomyces cerevisiae/metabolism ; Capsid Proteins/genetics ; Capsid Proteins/metabolism ; Protein Aggregates ; Capsid/metabolism
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Collective production of hydrogen sulfide gas enables budding yeast lacking MET17 to overcome their metabolic defect.
Czasopismo naukowe
Tytuł:
Collective production of hydrogen sulfide gas enables budding yeast lacking MET17 to overcome their metabolic defect.
Autorzy:
Sonal; Centre for Life's Origins and Evolution, Department of Genetics, Evolution and Environment, University College London, London, United Kingdom.
Yuan AE; University of Washington, Seattle, Washington, United States of America.
Yang X; School of Environmental Science and Engineering, Sun Yat-sen University, Guangzhou, China.
Shou W; Centre for Life's Origins and Evolution, Department of Genetics, Evolution and Environment, University College London, London, United Kingdom.
Źródło:
PLoS biology [PLoS Biol] 2023 Dec 07; Vol. 21 (12), pp. e3002439. Date of Electronic Publication: 2023 Dec 07 (Print Publication: 2023).
Typ publikacji:
Journal Article
MeSH Terms:
Hydrogen Sulfide*/metabolism
Cysteine Synthase*/genetics
Cysteine Synthase*/metabolism
Saccharomyces cerevisiae Proteins*/genetics
Saccharomyces cerevisiae Proteins*/metabolism
Saccharomyces cerevisiae/genetics ; Saccharomyces cerevisiae/growth & development ; Saccharomyces cerevisiae/metabolism ; Gene Deletion ; Sulfates/metabolism ; Models, Biological
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Novel COX11 Mutations Associated with Mitochondrial Disorder: Functional Characterization in Patient Fibroblasts and Saccharomyces cerevisiae .
Czasopismo naukowe
Tytuł:
Novel COX11 Mutations Associated with Mitochondrial Disorder: Functional Characterization in Patient Fibroblasts and Saccharomyces cerevisiae .
Autorzy:
Caron-Godon CA; Department of Biology, University of Waterloo, Waterloo, ON N2L 3G1, Canada.
Della Vecchia S; Department of Neurosciences, Psychology, Drug Research and Child Health (NEUROFARBA), University of Florence, Viale Pieraccini, 6, 50139 Florence, Italy.; Molecular Medicine for Neurodegenerative and Neuromuscular Disease Unit, IRCCS Stella Maris Foundation, 56128 Pisa, Italy.
Romano A; Experimental Neuropathology Unit, Division of Neuroscience, Institute of Experimental Neurology, IRCCS Ospedale San Raffaele Scientific Institute, 20132 Milan, Italy.
Doccini S; Molecular Medicine for Neurodegenerative and Neuromuscular Disease Unit, IRCCS Stella Maris Foundation, 56128 Pisa, Italy.
Dal Canto F; Molecular Medicine for Neurodegenerative and Neuromuscular Disease Unit, IRCCS Stella Maris Foundation, 56128 Pisa, Italy.
Pasquariello R; Neuroradiology, IRCCS Stella Maris Foundation, 56128 Pisa, Italy.
Rubegni A; Molecular Medicine for Neurodegenerative and Neuromuscular Disease Unit, IRCCS Stella Maris Foundation, 56128 Pisa, Italy.
Battini R; Developmental Neurology and Neurorehabilitation Unit, IRCCS Stella Maris Foundation, 56128 Pisa, Italy.; Department of Clinical and Experimental Medicine, University of Pisa, 56126 Pisa, Italy.
Santorelli FM; Molecular Medicine for Neurodegenerative and Neuromuscular Disease Unit, IRCCS Stella Maris Foundation, 56128 Pisa, Italy.
Glerum DM; Department of Biology, University of Waterloo, Waterloo, ON N2L 3G1, Canada.; Waterloo Institute for Nanotechnology, University of Waterloo, Waterloo, ON N2L 3G1, Canada.
Nesti C; Molecular Medicine for Neurodegenerative and Neuromuscular Disease Unit, IRCCS Stella Maris Foundation, 56128 Pisa, Italy.
Źródło:
International journal of molecular sciences [Int J Mol Sci] 2023 Nov 23; Vol. 24 (23). Date of Electronic Publication: 2023 Nov 23.
Typ publikacji:
Journal Article
MeSH Terms:
Saccharomyces cerevisiae Proteins*/genetics
Saccharomyces cerevisiae Proteins*/metabolism
Mitochondrial Diseases*/genetics
Child ; Humans ; Saccharomyces cerevisiae/genetics ; Saccharomyces cerevisiae/metabolism ; Amino Acid Sequence ; Membrane Proteins/metabolism ; Electron Transport Complex IV/genetics ; Electron Transport Complex IV/metabolism ; Mitochondrial Proteins/genetics ; Mitochondrial Proteins/metabolism ; Mutation ; Fibroblasts/metabolism ; Copper Transport Proteins/metabolism ; Electron Transport Chain Complex Proteins/metabolism
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
A Protein-Protein Interaction Analysis Suggests a Wide Range of New Functions for the p21-Activated Kinase (PAK) Ste20.
Czasopismo naukowe
Tytuł:
A Protein-Protein Interaction Analysis Suggests a Wide Range of New Functions for the p21-Activated Kinase (PAK) Ste20.
Autorzy:
Joshua IM; Division of Biosciences, Brunel University London, Uxbridge UB8 3PH, UK.
Lin M; Institute of Biochemistry, Kiel University, 24118 Kiel, Germany.
Mardjuki A; Division of Biosciences, Brunel University London, Uxbridge UB8 3PH, UK.
Mazzola A; Division of Biosciences, Brunel University London, Uxbridge UB8 3PH, UK.; Department of Biopathology and Medical and Forensic Biotechnologies, University of Palermo, 90133 Palermo, Italy.
Höfken T; Division of Biosciences, Brunel University London, Uxbridge UB8 3PH, UK.; Institute of Biochemistry, Kiel University, 24118 Kiel, Germany.
Źródło:
International journal of molecular sciences [Int J Mol Sci] 2023 Nov 02; Vol. 24 (21). Date of Electronic Publication: 2023 Nov 02.
Typ publikacji:
Journal Article
MeSH Terms:
Protein Serine-Threonine Kinases*/metabolism
Saccharomyces cerevisiae Proteins*/metabolism
Humans ; MAP Kinase Kinase Kinases/metabolism ; p21-Activated Kinases/genetics ; p21-Activated Kinases/metabolism ; Saccharomyces cerevisiae/genetics ; Saccharomyces cerevisiae/metabolism
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Humanization reveals pervasive incompatibility of yeast and human kinetochore components.
Czasopismo naukowe
Tytuł:
Humanization reveals pervasive incompatibility of yeast and human kinetochore components.
Autorzy:
Ólafsson G; Institute for Systems Genetics and Department of Biochemistry and Molecular Pharmacology, NYU Langone Health, New York, NY 10016, USA.
Haase MAB; Institute for Systems Genetics and Department of Biochemistry and Molecular Pharmacology, NYU Langone Health, New York, NY 10016, USA.; Vilcek Institute of Graduate Biomedical Sciences, NYU School of Medicine, New York, NY 10016, USA.
Boeke JD; Institute for Systems Genetics and Department of Biochemistry and Molecular Pharmacology, NYU Langone Health, New York, NY 10016, USA.; Department of Biomedical Engineering, NYU Tandon School of Engineering, Brooklyn, NY 14 11201, USA.
Źródło:
G3 (Bethesda, Md.) [G3 (Bethesda)] 2023 Dec 29; Vol. 14 (1).
Typ publikacji:
Journal Article
MeSH Terms:
Kinetochores*/metabolism
Saccharomyces cerevisiae Proteins*/metabolism
Humans ; Histones/metabolism ; Centromere Protein A/genetics ; Centromere Protein A/metabolism ; Chromosomal Proteins, Non-Histone/metabolism ; Saccharomyces cerevisiae/genetics ; Saccharomyces cerevisiae/metabolism ; DNA-Binding Proteins/genetics ; DNA-Binding Proteins/metabolism ; Centromere/genetics ; Centromere/metabolism ; Nucleosomes/genetics ; Nucleosomes/metabolism ; Nuclear Proteins/genetics ; Nuclear Proteins/metabolism
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
A non-canonical Puf3p-binding sequence regulates CAT5/COQ7 mRNA under both fermentable and respiratory conditions in budding yeast.
Czasopismo naukowe
Tytuł:
A non-canonical Puf3p-binding sequence regulates CAT5/COQ7 mRNA under both fermentable and respiratory conditions in budding yeast.
Autorzy:
Hayashi S; Graduate School of Science, University of Hyogo, Ako-gun, Hyogo, Japan.
Iwamoto K; Graduate School of Life Science, University of Hyogo, Ako-gun, Hyogo, Japan.
Yoshihisa T; Graduate School of Science, University of Hyogo, Ako-gun, Hyogo, Japan.
Źródło:
PloS one [PLoS One] 2023 Dec 15; Vol. 18 (12), pp. e0295659. Date of Electronic Publication: 2023 Dec 15 (Print Publication: 2023).
Typ publikacji:
Journal Article
MeSH Terms:
Saccharomyces cerevisiae Proteins*/metabolism
Saccharomycetales*/genetics
Humans ; Glucose/metabolism ; RNA, Messenger/genetics ; RNA, Messenger/metabolism ; RNA-Binding Proteins/metabolism ; Saccharomyces cerevisiae/genetics ; Saccharomyces cerevisiae/metabolism
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Multiomics of GCN4 -Dependent Replicative Lifespan Extension Models Reveals Gcn4 as a Regulator of Protein Turnover in Yeast.
Czasopismo naukowe
Tytuł:
Multiomics of GCN4 -Dependent Replicative Lifespan Extension Models Reveals Gcn4 as a Regulator of Protein Turnover in Yeast.
Autorzy:
Mariner BL; Department of Biochemistry and Molecular Biology, School of Medicine, University of New Mexico Health Sciences Center, Albuquerque, NM 87131, USA.; Department of Chemical and Biological Engineering, University of New Mexico, Albuquerque, NM 87131, USA.
Felker DP; Department of Biochemistry and Molecular Biology, School of Medicine, University of New Mexico Health Sciences Center, Albuquerque, NM 87131, USA.
Cantergiani RJ; Department of Biochemistry and Molecular Biology, School of Medicine, University of New Mexico Health Sciences Center, Albuquerque, NM 87131, USA.
Peterson J; Department of Biochemistry and Molecular Biology, School of Medicine, University of New Mexico Health Sciences Center, Albuquerque, NM 87131, USA.
McCormick MA; Department of Biochemistry and Molecular Biology, School of Medicine, University of New Mexico Health Sciences Center, Albuquerque, NM 87131, USA.; Autophagy, Inflammation, and Metabolism Center of Biomedical Research Excellence, University of New Mexico, Albuquerque, NM 87131, USA.
Źródło:
International journal of molecular sciences [Int J Mol Sci] 2023 Nov 10; Vol. 24 (22). Date of Electronic Publication: 2023 Nov 10.
Typ publikacji:
Journal Article
MeSH Terms:
Saccharomyces cerevisiae Proteins*/genetics
Saccharomyces cerevisiae Proteins*/metabolism
Amino Acyl-tRNA Synthetases*/genetics
Animals ; Saccharomyces cerevisiae/metabolism ; Longevity/genetics ; Proteolysis ; Caenorhabditis elegans/genetics ; Caenorhabditis elegans/metabolism ; Multiomics ; Proteomics ; Transcription Factors/metabolism ; Ubiquitin/metabolism ; Proteasome Endopeptidase Complex/metabolism ; Fungal Proteins/metabolism ; Gene Expression Regulation, Fungal ; Protein Biosynthesis
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
In Vivo and In Vitro Characterization of the RNA Binding Capacity of SETD1A (KMT2F).
Czasopismo naukowe
Tytuł:
In Vivo and In Vitro Characterization of the RNA Binding Capacity of SETD1A (KMT2F).
Autorzy:
Amin HM; Institute of Enzymology, HUN-REN Research Centre for Natural Sciences, H-1117 Budapest, Hungary.; Doctoral School of Biology, Institute of Biology, ELTE Eötvös Loránd University, H-1117 Budapest, Hungary.; Department of Biology, College of Science, University of Sulaimani, Sulaymaniyah 46001, Kurdistan Region, Iraq.
Szabo B; Institute of Enzymology, HUN-REN Research Centre for Natural Sciences, H-1117 Budapest, Hungary.
Abukhairan R; Institute of Enzymology, HUN-REN Research Centre for Natural Sciences, H-1117 Budapest, Hungary.
Zeke A; Institute of Enzymology, HUN-REN Research Centre for Natural Sciences, H-1117 Budapest, Hungary.
Kardos J; ELTE NAP Neuroimmunology Research Group, Department of Biochemistry, Institute of Biology, ELTE Eötvös Loránd University, H-1117 Budapest, Hungary.
Schad E; Institute of Enzymology, HUN-REN Research Centre for Natural Sciences, H-1117 Budapest, Hungary.
Tantos A; Institute of Enzymology, HUN-REN Research Centre for Natural Sciences, H-1117 Budapest, Hungary.
Źródło:
International journal of molecular sciences [Int J Mol Sci] 2023 Nov 07; Vol. 24 (22). Date of Electronic Publication: 2023 Nov 07.
Typ publikacji:
Journal Article
MeSH Terms:
RNA*/metabolism
Saccharomyces cerevisiae Proteins*/metabolism
Humans ; HEK293 Cells ; Methylation ; Saccharomyces cerevisiae/genetics ; Saccharomyces cerevisiae/metabolism
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Exportin-mediated nucleocytoplasmic transport maintains Pch2 homeostasis during meiosis.
Czasopismo naukowe
Tytuł:
Exportin-mediated nucleocytoplasmic transport maintains Pch2 homeostasis during meiosis.
Autorzy:
Herruzo E; Instituto de Biología Funcional y Genómica (IBFG), CSIC-USAL, Salamanca, Spain.
Sánchez-Díaz E; Instituto de Biología Funcional y Genómica (IBFG), CSIC-USAL, Salamanca, Spain.
González-Arranz S; Instituto de Biología Funcional y Genómica (IBFG), CSIC-USAL, Salamanca, Spain.
Santos B; Instituto de Biología Funcional y Genómica (IBFG), CSIC-USAL, Salamanca, Spain.; Departamento de Microbiología y Genética. University of Salamanca. Salamanca, Spain.
Carballo JA; Instituto de Biología Funcional y Genómica (IBFG), CSIC-USAL, Salamanca, Spain.
San-Segundo PA; Instituto de Biología Funcional y Genómica (IBFG), CSIC-USAL, Salamanca, Spain.
Źródło:
PLoS genetics [PLoS Genet] 2023 Nov 10; Vol. 19 (11), pp. e1011026. Date of Electronic Publication: 2023 Nov 10 (Print Publication: 2023).
Typ publikacji:
Journal Article
MeSH Terms:
Saccharomyces cerevisiae Proteins*/genetics
Meiosis/genetics ; Saccharomyces cerevisiae/genetics ; Active Transport, Cell Nucleus/genetics ; Nuclear Proteins/genetics ; Nuclear Proteins/metabolism ; DNA-Binding Proteins/genetics ; Karyopherins/genetics ; Karyopherins/metabolism ; Homeostasis
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Predictive Potential of RNA Polymerase B (II) Subunit 1 (RPB1) Cytoplasmic Aggregation for Neoadjuvant Chemotherapy Failure.
Czasopismo naukowe
Tytuł:
Predictive Potential of RNA Polymerase B (II) Subunit 1 (RPB1) Cytoplasmic Aggregation for Neoadjuvant Chemotherapy Failure.
Autorzy:
Nagy-Mikó B; Department of Biochemistry and Molecular Biology, University of Szeged, 52 Középfasor, H-6726 Szeged, Hungary.
Németh-Szatmári O; Department of Biochemistry and Molecular Biology, University of Szeged, 52 Középfasor, H-6726 Szeged, Hungary.
Faragó-Mészáros R; Department of Biochemistry and Molecular Biology, University of Szeged, 52 Középfasor, H-6726 Szeged, Hungary.
Csókási A; Department of Biochemistry and Molecular Biology, University of Szeged, 52 Középfasor, H-6726 Szeged, Hungary.; Department of Pathology, Albert Szent-Györgyi Medical School, University of Szeged, Állomás utca 1, H-6725 Szeged, Hungary.
Bognár B; Department of Biochemistry and Molecular Biology, University of Szeged, 52 Középfasor, H-6726 Szeged, Hungary.
Ördög N; Department of Pathology, Albert Szent-Györgyi Medical School, University of Szeged, Állomás utca 1, H-6725 Szeged, Hungary.
Borsos BN; Department of Pathology, Albert Szent-Györgyi Medical School, University of Szeged, Állomás utca 1, H-6725 Szeged, Hungary.
Majoros H; Department of Pathology, Albert Szent-Györgyi Medical School, University of Szeged, Állomás utca 1, H-6725 Szeged, Hungary.; Competence Centre of the Life Sciences Cluster of the Centre of Excellence for Interdisciplinary Research, Development and Innovation, University of Szeged, Dugonics tér 13, H-6720 Szeged, Hungary.
Ujfaludi Z; Department of Pathology, Albert Szent-Györgyi Medical School, University of Szeged, Állomás utca 1, H-6725 Szeged, Hungary.; Competence Centre of the Life Sciences Cluster of the Centre of Excellence for Interdisciplinary Research, Development and Innovation, University of Szeged, Dugonics tér 13, H-6720 Szeged, Hungary.
Oláh-Németh O; Department of Pathology, Albert Szent-Györgyi Medical School, University of Szeged, Állomás utca 1, H-6725 Szeged, Hungary.
Nikolényi A; Department of Oncotherapy, Albert Szent-Györgyi Health Centre, University of Szeged, 12 Korányi Fasor, H-6720 Szeged, Hungary.
Dobi Á; Department of Oncotherapy, Albert Szent-Györgyi Health Centre, University of Szeged, 12 Korányi Fasor, H-6720 Szeged, Hungary.
Kószó R; Department of Oncotherapy, Albert Szent-Györgyi Health Centre, University of Szeged, 12 Korányi Fasor, H-6720 Szeged, Hungary.
Sántha D; Department of Oncotherapy, Albert Szent-Györgyi Health Centre, University of Szeged, 12 Korányi Fasor, H-6720 Szeged, Hungary.
Lázár G; Department of Surgery, Albert Szent-Györgyi Health Centre, University of Szeged, 8 Semmelweis Street, H-6725 Szeged, Hungary.
Simonka Z; Department of Surgery, Albert Szent-Györgyi Health Centre, University of Szeged, 8 Semmelweis Street, H-6725 Szeged, Hungary.
Paszt A; Department of Surgery, Albert Szent-Györgyi Health Centre, University of Szeged, 8 Semmelweis Street, H-6725 Szeged, Hungary.
Ormándi K; Department of Radiology, Albert Szent-Györgyi Health Centre, University of Szeged, 6 Semmelweis Street, H-6725 Szeged, Hungary.
Pankotai T; Department of Pathology, Albert Szent-Györgyi Medical School, University of Szeged, Állomás utca 1, H-6725 Szeged, Hungary.; Competence Centre of the Life Sciences Cluster of the Centre of Excellence for Interdisciplinary Research, Development and Innovation, University of Szeged, Dugonics tér 13, H-6720 Szeged, Hungary.; Genome Integrity and DNA Repair Core Group, Hungarian Centre of Excellence for Molecular Medicine (HCEMM), University of Szeged, Budapesti út 9, H-6728 Szeged, Hungary.
Boros IM; Department of Biochemistry and Molecular Biology, University of Szeged, 52 Középfasor, H-6726 Szeged, Hungary.
Villányi Z; Department of Biochemistry and Molecular Biology, University of Szeged, 52 Középfasor, H-6726 Szeged, Hungary.
Vörös A; Department of Pathology, Albert Szent-Györgyi Medical School, University of Szeged, Állomás utca 1, H-6725 Szeged, Hungary.
Źródło:
International journal of molecular sciences [Int J Mol Sci] 2023 Nov 01; Vol. 24 (21). Date of Electronic Publication: 2023 Nov 01.
Typ publikacji:
Journal Article
MeSH Terms:
RNA Polymerase II*/genetics
Saccharomyces cerevisiae Proteins*/metabolism
Humans ; Neoadjuvant Therapy ; Protein Aggregates ; Saccharomyces cerevisiae/metabolism
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Regulatory and pathogenic mechanisms in response to iron deficiency and excess in fungi.
Czasopismo naukowe
Tytuł:
Regulatory and pathogenic mechanisms in response to iron deficiency and excess in fungi.
Autorzy:
Pijuan J; Laboratory of Neurogenetics and Molecular Medicine, Institut de Recerca Sant Joan de Déu, Barcelona, Spain.; Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), ISCIII, Madrid, Spain.
Moreno DF; Department of Molecular Cellular and Developmental Biology, Yale University, New Haven, Connecticut, USA.; Systems Biology Institute, Yale University, West Haven, Connecticut, USA.; Institut de Génétique et de Biologie Moléculaire et Cellulaire, Illkirch, France.
Yahya G; Department of Microbiology and Immunology, Faculty of Pharmacy, Zagazig University, Al Sharqia, Egypt.
Moisa M; Faculty of Medicine and Pharmacy, University of Oradea, Oradea, Romania.
Ul Haq I; Department of Physical Chemistry and Polymers Technology, Silesian University of Technology, Gliwice, Poland.; Programa de Pós-graduação em Inovação Tecnológica, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
Krukiewicz K; Department of Physical Chemistry and Polymers Technology, Silesian University of Technology, Gliwice, Poland.; Centre for Organic and Nanohybrid Electronics, Silesian University of Technology, Gliwice, Poland.
Mosbah R; Infection Control Unit, Hospitals of Zagazig University, Zagazig, Egypt.
Metwally K; Department of Medicinal Chemistry, Faculty of Pharmacy, University of Tabuk, Tabuk, Saudi Arabia.; Department of Pharmaceutical Medicinal Chemistry, Faculty of Pharmacy, Zagazig University, Zagazig, Egypt.
Cavalu S; Faculty of Medicine and Pharmacy, University of Oradea, Oradea, Romania.
Źródło:
Microbial biotechnology [Microb Biotechnol] 2023 Nov; Vol. 16 (11), pp. 2053-2071. Date of Electronic Publication: 2023 Oct 07.
Typ publikacji:
Journal Article; Review
MeSH Terms:
Iron Deficiencies*
Saccharomyces cerevisiae Proteins*/metabolism
Humans ; Transcription Factors/metabolism ; Iron/metabolism ; Saccharomyces cerevisiae/genetics ; Biological Transport ; Gene Expression Regulation, Fungal ; Trans-Activators/genetics ; Basic-Leucine Zipper Transcription Factors/genetics ; Basic-Leucine Zipper Transcription Factors/metabolism
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Systematic profiling of subtelomeric silencing factors in budding yeast.
Czasopismo naukowe
Tytuł:
Systematic profiling of subtelomeric silencing factors in budding yeast.
Autorzy:
Juárez-Reyes A; Unidad de Genómica Avanzada (Langebio), Centro de Investigación y de Estudios Avanzados, 36824 Irapuato, Guanajuato, Mexico.; Departamento de Ingeniería Genética, Unidad Irapuato, Centro de Investigación y de Estudios Avanzados, 36824 Irapuato, Guanajuato, Mexico.
Avelar-Rivas JA; Unidad de Genómica Avanzada (Langebio), Centro de Investigación y de Estudios Avanzados, 36824 Irapuato, Guanajuato, Mexico.
Hernandez-Valdes JA; Unidad de Genómica Avanzada (Langebio), Centro de Investigación y de Estudios Avanzados, 36824 Irapuato, Guanajuato, Mexico.; Nouryon Chemicals Research Centre, Expert Capability Center Deventer, 7418AJ Deventer, Netherlands.
Hua B; Department of Systems Biology, Harvard Medical School, Boston, MA 02115, USA.
Campos SE; Unidad de Genómica Avanzada (Langebio), Centro de Investigación y de Estudios Avanzados, 36824 Irapuato, Guanajuato, Mexico.
González J; Instituto de Fisiología Celular, Universidad Nacional Autónoma de México, 04510 Ciudad de México, Mexico.; Departamento de Biología Celular, Facultad de Ciencias, Universidad Nacional Autónoma de México, 04510 Ciudad de México, Mexico.
González A; Instituto de Fisiología Celular, Universidad Nacional Autónoma de México, 04510 Ciudad de México, Mexico.
Springer M; Department of Systems Biology, Harvard Medical School, Boston, MA 02115, USA.
Mancera E; Departamento de Ingeniería Genética, Unidad Irapuato, Centro de Investigación y de Estudios Avanzados, 36824 Irapuato, Guanajuato, Mexico.
DeLuna A; Unidad de Genómica Avanzada (Langebio), Centro de Investigación y de Estudios Avanzados, 36824 Irapuato, Guanajuato, Mexico.
Źródło:
G3 (Bethesda, Md.) [G3 (Bethesda)] 2023 Sep 30; Vol. 13 (10).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Saccharomyces cerevisiae Proteins*/genetics
Saccharomyces cerevisiae Proteins*/metabolism
Saccharomycetales*/genetics
Saccharomycetales*/metabolism
Silent Information Regulator Proteins, Saccharomyces cerevisiae/genetics ; Silent Information Regulator Proteins, Saccharomyces cerevisiae/metabolism ; Saccharomyces cerevisiae/genetics ; Saccharomyces cerevisiae/metabolism ; Telomere/genetics ; Telomere/metabolism ; Heterochromatin/metabolism ; Gene Expression Regulation, Fungal
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Poly(dA:dT) Tracts Differentially Modulate Nucleosome Remodeling Activity of RSC and ISW1a Complexes, Exerting Tract Orientation-Dependent and -Independent Effects.
Czasopismo naukowe
Tytuł:
Poly(dA:dT) Tracts Differentially Modulate Nucleosome Remodeling Activity of RSC and ISW1a Complexes, Exerting Tract Orientation-Dependent and -Independent Effects.
Autorzy:
Amigo R; Laboratory of Transcriptional Regulation, Department of Biochemistry and Molecular Biology, Faculty of Biological Sciences, University of Concepción, Concepción 4070043, Chile.
Raiqueo F; Laboratory of Transcriptional Regulation, Department of Biochemistry and Molecular Biology, Faculty of Biological Sciences, University of Concepción, Concepción 4070043, Chile.
Tarifeño E; Laboratory of Transcriptional Regulation, Department of Biochemistry and Molecular Biology, Faculty of Biological Sciences, University of Concepción, Concepción 4070043, Chile.
Farkas C; Biomedical Sciences Research Laboratory, Department of Basic Sciences and Morphology, Faculty of Medicine, Universidad Católica de la Santísima Concepción, Concepción 4090541, Chile.
Gutiérrez JL; Laboratory of Transcriptional Regulation, Department of Biochemistry and Molecular Biology, Faculty of Biological Sciences, University of Concepción, Concepción 4070043, Chile.
Źródło:
International journal of molecular sciences [Int J Mol Sci] 2023 Oct 17; Vol. 24 (20). Date of Electronic Publication: 2023 Oct 17.
Typ publikacji:
Journal Article
MeSH Terms:
Nucleosomes*
Saccharomyces cerevisiae Proteins*/genetics
Saccharomyces cerevisiae Proteins*/metabolism
Poly dA-dT ; Chromatin/genetics ; DNA/genetics ; Saccharomyces cerevisiae/genetics ; Saccharomyces cerevisiae/metabolism ; Chromatin Assembly and Disassembly
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Structure-function analysis of histone H2B and PCNA ubiquitination dynamics using deubiquitinase-deficient strains.
Czasopismo naukowe
Tytuł:
Structure-function analysis of histone H2B and PCNA ubiquitination dynamics using deubiquitinase-deficient strains.
Autorzy:
Radmall KS; Department of Radiation Oncology and Huntsman Cancer Institute, University of Utah School of Medicine, Salt Lake City, UT, 84112, USA.
Shukla PK; Department of Radiation Oncology and Huntsman Cancer Institute, University of Utah School of Medicine, Salt Lake City, UT, 84112, USA.
Leng AM; Department of Radiation Oncology and Huntsman Cancer Institute, University of Utah School of Medicine, Salt Lake City, UT, 84112, USA.
Chandrasekharan MB; Department of Radiation Oncology and Huntsman Cancer Institute, University of Utah School of Medicine, Salt Lake City, UT, 84112, USA. .; Huntsman Cancer Institute, University of Utah School of Medicine, 2000, Circle of Hope, Room 3715, Salt Lake City, UT, 84112, USA. .
Źródło:
Scientific reports [Sci Rep] 2023 Oct 04; Vol. 13 (1), pp. 16731. Date of Electronic Publication: 2023 Oct 04.
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:
Histones*/genetics
Histones*/metabolism
Saccharomyces cerevisiae Proteins*/metabolism
Saccharomyces cerevisiae/genetics ; Saccharomyces cerevisiae/metabolism ; Proliferating Cell Nuclear Antigen/genetics ; Proliferating Cell Nuclear Antigen/metabolism ; Ubiquitination ; Ubiquitin/genetics ; Ubiquitin/metabolism ; Deubiquitinating Enzymes/genetics ; Deubiquitinating Enzymes/metabolism ; Ubiquitin-Conjugating Enzymes/metabolism ; Ubiquitin Thiolesterase/metabolism ; Transcription Factors/metabolism
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Wyświetlanie 1-20 z 156557

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