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1. Full Text The 3′ end formation in small RNAs
by Perumal, Karthika and Reddy, Ram
Gene Expression, ISSN 1052-2166, 2002, Volume 10, Issue 1-2, pp. 59 - 78
Small RNAs are a major class of RNAs along with transfer RNAs, ribosomal RNAs, and messenger RNAs. They vary in size from less than 100 nucleotides to several... 
3′ Uridylation | 3′ End formation | 3′ Adenylation | Small RNAs | 3 ' uridylation | SMALL NUCLEAR-RNA | HELA-CELL EXTRACT | 3'-TERMINAL PHOSPHATE CYCLASE | 3 ' adenylation | small RNAs | INTRONIC U14 SNORNA | MESSENGER-RNA | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | SMALL NUCLEOLAR RNAS | GENETICS & HEREDITY | 3 ' end formation | SIGNAL RECOGNITION PARTICLE | TRYPANOSOMA-BRUCEI MITOCHONDRIA | EXOSOME SUBUNIT RRP43P | 5.8S RIBOSOMAL-RNA | RNA 3' End Processing - physiology | Saccharomyces cerevisiae - genetics | Humans | Multienzyme Complexes - metabolism | Eukaryotic Cells - metabolism | RNA, Ribosomal, 5.8S - metabolism | RNA Polymerase II - metabolism | RNA Caps - metabolism | Spliceosomes - metabolism | Telomerase - metabolism | Transcription, Genetic | Telomere - metabolism | Exonucleases - metabolism | RNA - metabolism | RNA Processing, Post-Transcriptional | RNA Polymerase III - metabolism | RNA, Fungal - metabolism | RNA, Small Nucleolar - chemistry | Animals | Prokaryotic Cells - metabolism | Escherichia coli - genetics | Polyadenylation | Saccharomyces cerevisiae Proteins - metabolism | RNA, Small Nuclear - chemistry | Uridine - metabolism | Mice | Models, Genetic
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2. Full Text Origins and activities of the eukaryotic exosome
by Lykke-Andersen, Søren and Brodersen, Ditiev E and Jensen, Torben Heick
Journal of Cell Science, ISSN 0021-9533, 05/2009, Volume 122, Issue 10, pp. 1487 - 1494
The exosome is a multi-subunit 3'-5' exonucleolytic complex that is conserved in structure and function in all eukaryotes studied to date. The complex is... 
RNA exosome | Exosome structure | Exosome function | RNA-POLYMERASE-II | CRYPTIC UNSTABLE TRANSCRIPTS | SMALL NUCLEAR-RNA | ESCHERICHIA-COLI | HUMAN PM-SCL | PRE-RIBOSOMAL-RNA | SACCHAROMYCES-CEREVISIAE | CELL BIOLOGY | HUMAN POLYNUCLEOTIDE PHOSPHORYLASE | MESSENGER-RNA | BINDING PROTEINS NRD1 | Eukaryotic Cells - enzymology | Exosomes - metabolism | Polynucleotide Adenylyltransferase - metabolism | RNA Helicases - metabolism | RNA Processing, Post-Transcriptional | Humans | Ribosomes - metabolism | Cytoplasm - metabolism | Eukaryotic Cells - metabolism | Endonucleases - metabolism | RNA, Messenger - metabolism | RNA, Fungal - metabolism | Animals | Prokaryotic Cells - metabolism | Saccharomyces cerevisiae Proteins - metabolism | Exosomes - enzymology | Transcription, Genetic | Exonucleases - metabolism | Exosome Multienzyme Ribonuclease Complex | RNA, Bacterial - metabolism | RNA - metabolism
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3. Full Text mRNA Deadenylation Is Coupled to Translation Rates by the Differential Activities of Ccr4-Not Nucleases
by Webster, Michael W and Chen, Ying-Hsin and Stowell, James A.W and Alhusaini, Najwa and Sweet, Thomas and Graveley, Brenton R and Coller, Jeff and Passmore, Lori A
Molecular Cell, ISSN 1097-2765, 06/2018, Volume 70, Issue 6, pp. 1089 - 1100.e8
Translation and decay of eukaryotic mRNAs is controlled by shortening of the poly(A) tail and release of the poly(A)-binding protein Pab1/PABP. The Ccr4-Not... 
poly(A) tail | exonuclease | RNA binding protein | translation | deadenylation | gene expression | mRNA decay | CODON OPTIMALITY | YEAST | POLY(A) BINDING-PROTEIN | DECAY | STABILITY | BIOCHEMISTRY & MOLECULAR BIOLOGY | POLY(A)-BINDING PROTEIN | SACCHAROMYCES-CEREVISIAE | DOMAINS | REVEALS | SUBUNIT | CELL BIOLOGY | RNA-Binding Proteins - genetics | Exoribonucleases - genetics | Schizosaccharomyces pombe Proteins - genetics | RNA, Messenger - genetics | Poly(A)-Binding Protein I - metabolism | Transcriptome | Cytoplasm - metabolism | Endonucleases - metabolism | Transcription Factors - genetics | RNA Stability | RNA, Messenger - metabolism | Ribonucleases - metabolism | RNA, Fungal - metabolism | Schizosaccharomyces - genetics | Transcription Factors - metabolism | Schizosaccharomyces - metabolism | Poly A - metabolism | Polyadenylation | Schizosaccharomyces pombe Proteins - metabolism | Schizosaccharomyces - enzymology | RNA, Fungal - genetics | Exoribonucleases - metabolism | RNA-Binding Proteins - metabolism | Messenger RNA | Codon | Developmental biology | Exonucleases | DNA binding proteins | Molecular biology | Genetic translation | Protein binding
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4. Full Text A role for the Perlman syndrome exonuclease Dis3l2 in the Lin28-let-7 pathway
by Chang, Hao-Ming and Triboulet, Robinson and Thornton, James E and Gregory, Richard I
Nature, ISSN 0028-0836, 2013, Volume 497, Issue 7448, pp. 244 - 248
The pluripotency factor Lin28 blocks the expression of let-7 microRNAs in undifferentiated cells during development, and functions as an oncogene in a subset... 
ZCCHC11 | MESSENGER-RNA | MICRORNA BIOGENESIS | MULTIDISCIPLINARY SCIENCES | 3' URIDYLATION | EXOSOME | LET-7 | RECRUITS | MATURATION | EXPRESSION | RNA DEGRADATION | Uridine Monophosphate - metabolism | Embryonic Stem Cells - metabolism | Fetal Macrosomia - metabolism | Wilms Tumor - genetics | Humans | Substrate Specificity | MicroRNAs - metabolism | Ribonucleases - metabolism | HEK293 Cells | RNA Precursors - metabolism | Exonucleases - metabolism | Wilms Tumor - metabolism | RNA Processing, Post-Transcriptional | Cells, Cultured | Fetal Macrosomia - genetics | Fetal Macrosomia - enzymology | RNA Precursors - genetics | RNA Stability | Animals | Wilms Tumor - enzymology | Uridine Monophosphate - analogs & derivatives | Wilms Tumor - etiology | Mice | MicroRNAs - genetics | Exoribonucleases - metabolism | RNA-Binding Proteins - metabolism | Proteins | Cloning | Cytoplasm | Cell cycle | uridylation | let-7 | microRNA (miRNA) | exonuclease | Lin28 | Lin-28 | Embryonic Stem Cells | TUTase | Dis3l2
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5. Full Text Regulation of the p53-MDM2 pathway by 14-3-3 sigma and other proteins
by Lee, MH and Lozano, G
SEMINARS IN CANCER BIOLOGY, ISSN 1044-579X, 06/2006, Volume 16, Issue 3, pp. 225 - 234
The 14-3-3 sigma (sigma) protein, a unique member of 14-3-3 family, is a negative regulator of the cell cycle and is induced by p53 to initiate cell cycle... 
14-3-3 | FORKHEAD TRANSCRIPTION FACTOR | SUPPRESSES TUMOR-GROWTH | P53 UBIQUITINATION | cell cycle | CRYSTAL-STRUCTURE | DNA-DAMAGE | DOWN-REGULATION | tumor suppressor | ATM-DEPENDENT PHOSPHORYLATION | p53 | NEGATIVE REGULATOR | GENETIC INSTABILITY | ONCOLOGY | STRUCTURAL BASIS | Mdm2 | Exoribonucleases | Humans | Neoplasm Proteins - metabolism | Tripartite Motif-Containing Protein 28 | DNA-Binding Proteins - metabolism | Exonucleases - genetics | Biomarkers, Tumor - metabolism | Exonucleases - metabolism | Neoplasm Proteins - genetics | Proto-Oncogene Proteins c-akt - metabolism | Gene Expression Regulation, Neoplastic - physiology | Proto-Oncogene Proteins c-mdm2 - metabolism | Protein-Serine-Threonine Kinases - metabolism | Repressor Proteins - metabolism | Proto-Oncogene Proteins - metabolism | Endopeptidases - metabolism | Tumor Suppressor Proteins - metabolism | Cell Cycle Proteins - metabolism | Tumor Suppressor Protein p53 - metabolism | Ubiquitin-Protein Ligases - metabolism | PTEN Phosphohydrolase - metabolism | Neoplasm Proteins - chemistry | Ataxia Telangiectasia Mutated Proteins | Exonucleases - chemistry | Animals | Signal Transduction - physiology | 14-3-3 Proteins | Biomarkers, Tumor - genetics | Proteasome Endopeptidase Complex - metabolism | Biomarkers, Tumor - chemistry | Tumor Suppressor Protein p14ARF - metabolism | Ubiquitin Thiolesterase | Ubiquitin-Specific Peptidase 7 | Protein Binding - physiology
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6. Full Text Cutting edge: CGAS is required for lethal autoimmune disease in the Trex1-deficient mouse model of Aicardi-Goutières syndrome
by Gray, Elizabeth E and Treuting, Piper M and Woodward, Joshua J and Stetson, Daniel B
Journal of Immunology, ISSN 0022-1767, 09/2015, Volume 195, Issue 5, pp. 1939 - 1943
Detection of intracellular DNA triggers activation of the stimulator of IFN genes dependent IFN-stimulatory DNA (ISD) pathway, which is essential for antiviral... 
CYCLIC GMP-AMP | INTRACELLULAR DNA | LUPUS | DENDRITIC CELLS | GENE | DNA EXONUCLEASE TREX1 | CYTOSOLIC DNA | INNATE IMMUNE SENSOR | MUTATIONS | IMMUNOLOGY | RETROVIRUSES | Nucleotides, Cyclic - metabolism | Phosphoproteins - immunology | Exodeoxyribonucleases - immunology | Interferon-beta - immunology | Nervous System Malformations - immunology | Gene Expression - drug effects | Autoantibodies - blood | Humans | Immunoblotting | Interferons - immunology | Phosphoproteins - metabolism | Inflammation - metabolism | Nervous System Malformations - metabolism | Autoimmune Diseases of the Nervous System - genetics | Gene Expression - immunology | Interferon-beta - genetics | Exodeoxyribonucleases - genetics | Nucleotidyltransferases - metabolism | Autoimmune Diseases of the Nervous System - metabolism | Nervous System Malformations - genetics | Macrophages - immunology | Disease Models, Animal | Fibroblasts - metabolism | Interferons - pharmacology | Mice, Inbred C57BL | Cells, Cultured | Inflammation - immunology | Phosphoproteins - genetics | Reverse Transcriptase Polymerase Chain Reaction | Mice, Knockout | Autoimmune Diseases of the Nervous System - immunology | Autoantibodies - immunology | Macrophages - metabolism | Animals | Interferon-beta - metabolism | Embryo, Mammalian - cytology | Fibroblasts - drug effects | Exodeoxyribonucleases - metabolism | Inflammation - genetics | Nucleotidyltransferases - genetics | Fibroblasts - immunology | Macrophages - drug effects | Nucleotidyltransferases - immunology | Nucleotides, Cyclic - immunology
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7. Full Text Aicardi-Goutie'res syndrome and related phenotypes: Linking nucleic acid metabolism with autoimmunity
by Crow, Yanick J and Rehwinkel, Jan
Human Molecular Genetics, ISSN 0964-6906, 10/2009, Volume 18, Issue 2, pp. R130 - R136
Aicardi-Goutieres syndrome (AGS) is a genetically determined encephalopathy demonstrating phenotypic overlap both with the sequelae of congenital infection and... 
SYSTEMIC-LUPUS-ERYTHEMATOSUS | FAMILIAL CHILBLAIN LUPUS | SUBSTRATE-SPECIFICITY | DENDRITIC CELLS | BIOCHEMISTRY & MOLECULAR BIOLOGY | DNA EXONUCLEASE TREX1 | ESCHERICHIA-COLI | GENETICS & HEREDITY | INNATE IMMUNE-RESPONSE | GAMMA-INDUCED PROTEIN | CONGENITAL INFECTION | MEDIATED CELL-DEATH | Abnormalities, Multiple - metabolism | Abnormalities, Multiple - pathology | Humans | Nucleic Acids - metabolism | Phosphoproteins - genetics | Abnormalities, Multiple - immunology | Phosphoproteins - chemistry | Syndrome | Phenotype | Autoimmunity - immunology | Exodeoxyribonucleases - chemistry | Exodeoxyribonucleases - genetics | Abnormalities, Multiple - genetics | Reviews
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8. Full Text Idling by DNA polymerase δ maintains a ligatable nick during lagging-strand DNA replication
by Garg, Parie and Stith, Carrie M and Sabouri, Nasim and Johansson, Erik and Burgers, Peter M and Medicinska fakulteten and Institutionen för medicinsk kemi och biofysik and Umeå universitet
Genes and Development, ISSN 0890-9369, 11/2004, Volume 18, Issue 22, pp. 2764 - 2773
During each yeast cell cycle, similar to100,000 nicks are generated during lagging-strand DNA replication. Efficient nick processing during Okazaki fragment... 
DNA replication | Exonuclease | Nick translation | DNA polymerase | Okazaki fragment | PROTEIN-A | COMPLEX | CELL NUCLEAR ANTIGEN | exonuclease | nick translation | DEVELOPMENTAL BIOLOGY | SACCHAROMYCES-CEREVISIAE | EPSILON | YEAST | GENETICS & HEREDITY | OKAZAKI FRAGMENT MATURATION | FLAP ENDONUCLEASE-1 | DISPLACEMENT | DNA Helicases - metabolism | Oligonucleotides - metabolism | Saccharomyces cerevisiae - genetics | Saccharomyces cerevisiae - enzymology | DNA Replication | DNA - metabolism | DNA Polymerase III - metabolism | DNA Primers | Exonucleases - metabolism | Flap Endonucleases - metabolism | Research Papers | DNA/metabolism | Oligonucleotides/metabolism | DNA Helicases/metabolism | Exonucleases/metabolism | Saccharomyces cerevisiae/enzymology/genetics | Flap Endonucleases/metabolism | DNA Polymerase III/metabolism
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9. Full Text Argonaute and Triman Generate Dicer-Independent priRNAs and Mature siRNAs to Initiate Heterochromatin Formation
by Marasovic, Mirela and Zocco, Manuel and Halic, Mario
Molecular Cell, ISSN 1097-2765, 10/2013, Volume 52, Issue 2, pp. 173 - 183
RNAi is a conserved mechanism in which small RNAs induce silencing of complementary targets. We have previously identified priRNAs, a class of... 
BIOGENESIS PATHWAY | GENOME DEFENSE | FISSION YEAST | GERMLINE | EPIGENETIC MEMORY | BIOCHEMISTRY & MOLECULAR BIOLOGY | PIRNAS | PROTEINS | C. ELEGANS | DROSOPHILA | PIWI-INTERACTING RNAS | CELL BIOLOGY | RNA, Small Interfering - genetics | Endoribonucleases - genetics | Exoribonucleases - genetics | Molecular Sequence Data | Centromere - metabolism | Schizosaccharomyces - genetics | Heterochromatin - metabolism | RNA Interference | Exonucleases - genetics | Schizosaccharomyces pombe Proteins - metabolism | Exosome Multienzyme Ribonuclease Complex - metabolism | RNA Precursors - metabolism | RNA, Fungal - genetics | Exonucleases - metabolism | Exosome Multienzyme Ribonuclease Complex - genetics | Amino Acid Sequence | Argonaute Proteins - metabolism | Argonaute Proteins - genetics | Schizosaccharomyces pombe Proteins - genetics | Endoribonucleases - metabolism | Electrophoresis, Polyacrylamide Gel | RNA Precursors - genetics | Blotting, Western | RNA, Fungal - metabolism | Sequence Homology, Amino Acid | Schizosaccharomyces - metabolism | Heterochromatin - genetics | Centromere - genetics | Protein Binding | Models, Genetic | Mutation | Exoribonucleases - metabolism | RNA, Small Interfering - metabolism | RNA | Genomics
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10. Full Text DCAMKL-1 regulates epithelial-mesenchymal transition in human pancreatic cells through a miR-200a-dependent mechanism
by Sureban, Sripathi M and May, Randal and Lightfoot, Stan A and Hoskins, Aimee B and Lerner, Megan and Brackett, Daniel J and Postier, Russell G and Ramanujam, Rama and Mohammed, Altaf and Rao, Chinthalapally V and Wyche, James H and Anant, Shrikant and Houchen, Courtney W
Cancer Research, ISSN 0008-5472, 03/2011, Volume 71, Issue 6, pp. 2328 - 2338
Pancreatic cancer is an exceptionally aggressive disease in great need of more effective therapeutic options. Epithelial-mesenchymal transition (EMT) plays a... 
INITIATING CELLS | ONCOLOGY | GROWTH | GENES | NOTCH | ACUTE MYELOID-LEUKEMIA | IDENTIFICATION | EXPRESSION | PROGRESSION | CANCER STEM-CELLS | BRAIN-TUMORS | Immunohistochemistry | ras Proteins - genetics | Pancreatic Neoplasms - metabolism | Exoribonucleases | Vimentin - metabolism | Humans | ras Proteins - metabolism | Intracellular Signaling Peptides and Proteins - metabolism | Epithelial-Mesenchymal Transition - genetics | Zinc Finger E-box Binding Homeobox 2 | RNA Interference | Biomarkers, Tumor - metabolism | Exonucleases - metabolism | Intracellular Signaling Peptides and Proteins - genetics | Protein-Serine-Threonine Kinases - metabolism | Gene Expression | Pancreatic Neoplasms - pathology | Protein-Serine-Threonine Kinases - genetics | Repressor Proteins - genetics | Mice, Transgenic | Pancreatic Neoplasms - genetics | Receptor, Notch1 - metabolism | Transcription Factors - genetics | Reverse Transcriptase Polymerase Chain Reaction | Proto-Oncogene Proteins c-myc - metabolism | Homeodomain Proteins - genetics | 14-3-3 Proteins - metabolism | Animals | Twist-Related Protein 1 - genetics | Cell Line, Tumor | Mice | MicroRNAs - genetics | Proto-Oncogene Proteins c-myc - genetics | Mutation | Receptor, Notch1 - genetics | Zinc Finger E-box-Binding Homeobox 1 | epithelial-mesenchymal transition (EMT) | pancreatic intraepithelial neoplasia (PanIN) | Cancer Stem Cell Marker | miR-144 | 14-3-3 σ | Let-7a | vimentin | miR-200a | DCAMKL-1 | Dclk-1 | Notch-1
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11. Combined gene expression analysis of whole-tissue and microdissected pancreatic ductal adenocarcinoma identifies genes specifically overexpressed in tumor epithelia
by Badea, Liviu and Herlea, Vlad and Dima, Simona Olimpia and Dumitrascu, Traian and Popescu, Irinel
Hepato-Gastroenterology, ISSN 0172-6390, 11/2008, Volume 55, Issue 88, pp. 2016 - 2027
Background/Aims: The precise details of pancreatic ductal adenocarcinoma (PDAC) pathogenesis are still insufficiently known, requiring the use of... 
Combined gene expression analysis | Genes correlated with survival | Microarrays | Pancreatic Ductal Adenocarcinoma (PDAC) | Cancer genomics | SURGERY | PROFILES | CANCER CELLS | CDNA MICROARRAY | Combined Gene Expression Analysis | PERIOSTIN | MESENCHYMAL TRANSFORMATION | BREAST-CANCER | Cancer Genomics | GROWTH | BIOLOGY | Genes Correlated with Survival | HOMOZYGOUS DELETIONS | CARCINOMA | Exoribonucleases | Microdissection | Oligonucleotide Array Sequence Analysis - methods | Humans | Gene Expression Regulation, Neoplastic | Pancreatic Neoplasms - genetics | Intracellular Signaling Peptides and Proteins - metabolism | Neoplasm Proteins - metabolism | Keratin-7 - metabolism | Biomarkers, Tumor - metabolism | 14-3-3 Proteins | Adenocarcinoma - genetics | Membrane Proteins - metabolism | Laminin - metabolism | Exonucleases - metabolism | Annexin A2 - metabolism | Protein-Serine-Threonine Kinases - metabolism | Phosphofructokinases - metabolism
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12. Full Text SAMHD1 acts at stalled replication forks to prevent interferon induction
by Coquel, Flavie and Silva, Maria-Joao and Técher, Hervé and Zadorozhny, Karina and Sharma, Sushma and Nieminuszczy, Jadwiga and Mettling, Clément and Dardillac, Elodie and Barthe, Antoine and Schmitz, Anne-Lyne and Promonet, Alexy and Cribier, Alexandra and Sarrazin, Amélie and Niedzwiedz, Wojciech and Lopez, Bernard and Costanzo, Vincenzo and Krejci, Lumir and Chabes, Andrei and Benkirane, Monsef and Lin, Yea-Lih and Pasero, Philippe and Medicinska fakulteten and Institutionen för medicinsk kemi och biofysik and Molekylär Infektionsmedicin, Sverige (MIMS) and Umeå universitet
Nature, ISSN 0028-0836, 05/2018, Volume 557, Issue 7703, pp. 57 - 61
SAMHD1 was previously characterized as a dNTPase that protects cells from viral infections. Mutations in SAMHD1 are implicated in cancer development and in a... 
NUCLEASE ACTIVITY | REPAIR | PROTEIN | HIV-1 RESTRICTION | AICARDI-GOUTIERES SYNDROME | STABILITY | MULTIDISCIPLINARY SCIENCES | CYTOSOLIC DNA SENSOR | END RESECTION | RESTRICTION FACTOR SAMHD1 | MAMMALIAN-CELLS | SAM Domain and HD Domain-Containing Protein 1 - metabolism | RecQ Helicases - metabolism | DNA, Single-Stranded - metabolism | Humans | DNA Replication | Inflammation - immunology | SAM Domain and HD Domain-Containing Protein 1 - deficiency | Interferon Type I - immunology | Checkpoint Kinase 1 - metabolism | Inflammation - metabolism | HEK293 Cells | Interferon Type I - metabolism | Cytosol - metabolism | Inflammation - prevention & control | Membrane Proteins - metabolism | HeLa Cells | Nucleotidyltransferases - metabolism | MRE11 Homologue Protein - metabolism | Physiological aspects | DNA replication | Interferon | Observations | Cytokines | Single-stranded DNA | DNA damage | CHK1 protein | Genomes | Kinases | DNA repair | Cytosol | Replication forks | DNA biosynthesis | Exonuclease | Microscopy | MRE11 protein | Cell lines | Replication | Mutation | Deoxyribonucleic acid--DNA | Cellular stress response | Cancer | Life Sciences | Genetics | Cell and Molecular Biology | Basic Medicine | Medical and Health Sciences | Medicin och hälsovetenskap | Cell- och molekylärbiologi | Medicinska och farmaceutiska grundvetenskaper
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13. Full Text BLM-DNA2-RPA-MRN and EXO1-BLM-RPA-MRN constitute two DNA end resection machineries for human DNA break repair
by Nimonkar, Amitabh V and Genschel, Jochen and Kinoshita, Eri and Polaczek, Piotr and Campbell, Judith L and Wyman, Claire and Modrich, Paul and Kowalczykowski, Stephen C
Genes and Development, ISSN 0890-9369, 02/2011, Volume 25, Issue 4, pp. 350 - 362
Repair of dsDNA breaks requires processing to produce 3'-terminated ssDNA. We biochemically reconstituted DNA end resection using purified human proteins:... 
BLM helicase | DNA2 nuclease | DNA break repair | EXO1 nuclease | DNA end resection | Homologous recombination | NUCLEASE ACTIVITY | PROTEIN | HUMAN EXONUCLEASE 1 | MISMATCH REPAIR | DEVELOPMENTAL BIOLOGY | CELL BIOLOGY | XENOPUS DNA2 | homologous recombination | SGS1 | GENETICS & HEREDITY | BLOOM-SYNDROME | 5' STRAND RESECTION | MRE11 NUCLEASE | RecQ Helicases - metabolism | Humans | DNA Repair Enzymes - genetics | Replication Protein A - physiology | Multiprotein Complexes - genetics | RecQ Helicases - genetics | DNA Repair - genetics | DNA Breaks, Double-Stranded | DNA Breaks, Single-Stranded | DNA-Binding Proteins - metabolism | MRE11 Homologue Protein | Multiprotein Complexes - metabolism | Replication Protein A - genetics | DNA Repair Enzymes - metabolism | Cell Cycle Proteins - genetics | Exodeoxyribonucleases - genetics | Nuclear Proteins - genetics | DNA Helicases - genetics | RecQ Helicases - physiology | DNA Repair Enzymes - physiology | DNA-Binding Proteins - physiology | Cell Cycle Proteins - metabolism | Nuclear Proteins - metabolism | Replication Protein A - metabolism | DNA-Binding Proteins - genetics | Multiprotein Complexes - physiology | DNA Helicases - metabolism | Models, Biological | Exodeoxyribonucleases - metabolism | Exodeoxyribonucleases - physiology | Nuclear Proteins - physiology | In Vitro Techniques | Cell Cycle Proteins - physiology | DNA Helicases - physiology | Protein Binding - physiology | Research Paper
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14. Full Text Endoribonucleases – enzymes gaining spotlight in mRNA metabolism
by Li, Wai Ming and Barnes, Tavish and Lee, Chow H
The FEBS Journal, ISSN 1742-464X, 02/2010, Volume 277, Issue 3, pp. 627 - 641
The efficient turnover of messenger RNA represents an important mechanism that allows the cell to control gene expression. Until recently, the mechanism of... 
eukaryotes | decay | degradation | mRNA | endoribonucleases | RNA metabolism | Degradation | Eukaryotes | Decay | Endoribonucleases | BASE-EXCISION-REPAIR | CRYSTAL-STRUCTURE | BIOCHEMISTRY & MOLECULAR BIOLOGY | QUALITY-CONTROL | UNFOLDED PROTEIN RESPONSE | REF-1 NUCLEAR TRANSLOCATION | STRUCTURAL BASIS | ENDOPLASMIC-RETICULUM | DNA-REPAIR | LUNG-CANCER RISK | HUMAN APURINIC/APYRIMIDINIC ENDONUCLEASE | Ribonuclease III - metabolism | Endoribonucleases - metabolism | Humans | Phosphoprotein Phosphatases - metabolism | RNA Stability | RNA, Messenger - metabolism | Poly-ADP-Ribose Binding Proteins | DNA Helicases | RNA Helicases | Animals | Carrier Proteins - metabolism | DNA-(Apurinic or Apyrimidinic Site) Lyase - metabolism | Ribonuclease, Pancreatic - metabolism | Saccharomyces cerevisiae Proteins - metabolism | Argonaute Proteins | Eukaryotic Initiation Factor-2 - metabolism | Telomerase - metabolism | Membrane Proteins - metabolism | Fructose-Bisphosphate Aldolase - metabolism | Exosome Multienzyme Ribonuclease Complex | RNA Recognition Motif Proteins | Protein-Serine-Threonine Kinases - metabolism | RNA-Binding Proteins - metabolism | Physiological aspects | Exonucleases | Messenger RNA | Ribonuclease | Gene expression | Proteins | Enzymes | Ribozymes | Ribonucleic acid--RNA
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15. Full Text Keratin 17 Expression Correlates with Tumor Progression and Poor Prognosis in Gastric Adenocarcinoma
by Ide, Munenori and Kato, Toshihide and Ogata, Kyoichi and Mochiki, Erito and Kuwano, Hiroyuki and Oyama, Tetsunari
Annals of Surgical Oncology, ISSN 1068-9265, 10/2012, Volume 19, Issue 11, pp. 3506 - 3514
Keratin 17 (K17) is regarded as a basal/myoepithelial cell keratin and is known to be inducible in activated keratinocytes. The high frequency of K17... 
Oncology | Medicine & Public Health | Surgical Oncology | Surgery | SURGERY | CELLS | IN-VITRO | ONCOLOGY | CYTOKERATIN-17 | PANCREATICOBILIARY | PATTERNS | SKIN | IDENTIFICATION | CARCINOMA | NEGATIVE BREAST-CANCER | BASAL | Multivariate Analysis | Prognosis | Exoribonucleases | Homeodomain Proteins - metabolism | Humans | Middle Aged | Stomach Neoplasms - metabolism | Ki-67 Antigen - metabolism | Male | Stomach Neoplasms - pathology | Adenocarcinoma - metabolism | Biomarkers, Tumor - metabolism | Female | Exonucleases - metabolism | Kaplan-Meier Estimate | Proportional Hazards Models | Tumor Suppressor Protein p53 - metabolism | Lymphatic Metastasis | Neprilysin - metabolism | Adenocarcinoma - secondary | Disease Progression | 14-3-3 Proteins - metabolism | Keratin-17 - metabolism | Mucin 5AC - metabolism | Aged | CDX2 Transcription Factor | Neoplasm Staging | Mucin-6 - metabolism
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