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saccharomyces cerevisiae - genetics (12) 12
apoptosis (11) 11
saccharomyces-cerevisiae (11) 11
oxidative stress (10) 10
saccharomyces cerevisiae - metabolism (9) 9
saccharomyces cerevisiae proteins - genetics (9) 9
humans (7) 7
index medicus (7) 7
saccharomyces cerevisiae - drug effects (7) 7
cell biology (6) 6
saccharomyces cerevisiae - cytology (6) 6
saccharomyces cerevisiae proteins - metabolism (6) 6
life-span (5) 5
mitochondria (5) 5
mitochondria - metabolism (5) 5
proteins (5) 5
saccharomyces cerevisiae (5) 5
animals (4) 4
biochemistry & molecular biology (4) 4
longevity (4) 4
microscopy, fluorescence (4) 4
mutation (4) 4
oxidants - pharmacology (4) 4
reactive oxygen species (4) 4
research article (4) 4
saccharomyces cerevisiae - growth & development (4) 4
saccharomyces cerevisiae - physiology (4) 4
yeast (4) 4
aging (3) 3
aging - physiology (3) 3
analysis (3) 3
apoptosis - genetics (3) 3
caenorhabditis-elegans (3) 3
cell proliferation (3) 3
cell size (3) 3
enzymes (3) 3
gene deletion (3) 3
gene-expression (3) 3
health aspects (3) 3
identification (3) 3
multidisciplinary sciences (3) 3
mutation - genetics (3) 3
oxidative stress - physiology (3) 3
reactive oxygen species - metabolism (3) 3
recombinant fusion proteins - genetics (3) 3
ribosomal proteins - genetics (3) 3
superoxides - metabolism (3) 3
active transport, cell nucleus - genetics (2) 2
aging - genetics (2) 2
amino acid sequence (2) 2
amino acid substitution (2) 2
base sequence (2) 2
biochemistry (2) 2
biology (2) 2
budding yeast (2) 2
caenorhabditis elegans - drug effects (2) 2
caenorhabditis elegans - genetics (2) 2
caenorhabditis elegans - physiology (2) 2
calorie restriction (2) 2
cell cycle (2) 2
cell cycle proteins - genetics (2) 2
cell cycle proteins - metabolism (2) 2
cell death (2) 2
cell division - genetics (2) 2
cells (2) 2
cellular senescence - genetics (2) 2
crosses, genetic (2) 2
dna, circular - genetics (2) 2
dna, circular - metabolism (2) 2
dna, ribosomal - genetics (2) 2
dna, ribosomal - metabolism (2) 2
dna-binding proteins - genetics (2) 2
dna-binding proteins - metabolism (2) 2
expression (2) 2
female (2) 2
genes (2) 2
genetic aspects (2) 2
geriatrics & gerontology (2) 2
green fluorescent proteins - genetics (2) 2
green fluorescent proteins - metabolism (2) 2
heat shock (2) 2
hydrogen peroxide (2) 2
hydrogen peroxide - pharmacology (2) 2
hydrogen-peroxide (2) 2
in-vivo (2) 2
inheritance (2) 2
male (2) 2
medicine (2) 2
microbiology (2) 2
microtubules (2) 2
mitochondrial proteins - genetics (2) 2
mitochondrial proteins - metabolism (2) 2
models, biological (2) 2
models, genetic (2) 2
molecular biology (2) 2
molecular sequence data (2) 2
mother cells (2) 2
organization (2) 2
oxidative stress - drug effects (2) 2
oxidative stress - genetics (2) 2
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1. Full Text Induction of autophagy by spermidine promotes longevity
by Tavernarakis, Nektarios and Kroemer, Guido and Herker, Eva and Madeo, Frank and Sinner, Frank and Magnes, Christoph and Laun, Peter and Knauer, Heide and Ring, Julia and Schraml, Elisabeth and Carmona-Gutierrez, Didac and Fröhlich, Kai-Uwe and Fahrenkrog, Birthe and Eisenberg, Tobias and Schroeder, Sabrina and Heeren, Gino and Breitenbach, Michael and Fussi, Heike and Weiskopf, Daniela and Hartl, Regina and Criollo, Alfredo and Megalou, Evgenia and Deszcz, Luiza and Grubeck-Loebenstein, Beatrix and Büttner, Sabrina and Minois, Nadege and Ruckenstuhl, Christoph and Schauer, Alexandra and Antonacci, Lucia
Nature Cell Biology, ISSN 1465-7392, 11/2009, Volume 11, Issue 11, pp. 1305 - 1314
Ageing results from complex genetically and epigenetically programmed processes that are elicited in part by noxious or stressful events that cause programmed... 
LIFE-SPAN EXTENSION | OXIDATIVE STRESS | CAENORHABDITIS-ELEGANS | BUDDING YEAST | REGULATES APOPTOSIS | GENE-EXPRESSION | NECROTIC CELL-DEATH | MURINE SKIN | SACCHAROMYCES-CEREVISIAE | CALORIE RESTRICTION | CELL BIOLOGY | Saccharomyces cerevisiae - physiology | Drosophila melanogaster - immunology | Drosophila melanogaster - physiology | Saccharomyces cerevisiae - immunology | Longevity - drug effects | Humans | Mice, Inbred C57BL | Male | Saccharomyces cerevisiae - drug effects | Caenorhabditis elegans - immunology | Autophagy - drug effects | Drosophila melanogaster - drug effects | Necrosis | Caenorhabditis elegans - physiology | Animals | Caenorhabditis elegans - drug effects | Spermidine - pharmacology | Adult | Female | Mice | Acetylation | HeLa Cells | Histones - metabolism | Hydrogen-Ion Concentration | Autophagy (Cytology) | Chromatin | Aging | Physiological aspects | Research | Polyamines | Health aspects
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2. Full Text Yno1p/Aim14p, a NADPH-oxidase ortholog, controls extramitochondrial reactive oxygen species generation, apoptosis, and actin cable formation in yeast
by Mark Rinnerthaler and Sabrina Büttner and Peter Laun and Gino Heeren and Thomas K. Felder and Harald Klinger and Martin Weinberger and Klaus Stolze and Tomas Grousl and Jiri Hasek and Oldrich Benada and Ivana Frydlova and Andrea Klocker and Birgit Simon-Nobbe and Bettina Jansko and Hannelore Breitenbach-Koller and Tobias Eisenberg and Campbell W. Gourlay and Frank Madeo and William C. Burhans and Michael Breitenbach
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 5/2012, Volume 109, Issue 22, pp. 8658 - 8663
The large protein superfamily of NADPH oxidases (NOX enzymes) is found in members of all eukaryotic kingdoms: animals, plants, fungi, and protists. The... 
Oxidases | Enzymes | Yeasts | Reactive oxygen species | Steepest descent method | Superoxides | Cell cycle | Actins | Gene expression regulation | Apoptosis | Latrunculin | Wiskostatin | Integral membrane reductase | SUPEROXIDE | cell cycle | MULTIDISCIPLINARY SCIENCES | MOLECULAR EVOLUTION | MITOCHONDRIA | SACCHAROMYCES-CEREVISIAE | ORGANIZATION | wiskostatin | NOX FAMILY | GENES | integral membrane reductase | REDUCTASE | latrunculin | CELL-DIFFERENTIATION | INHERITANCE | Endoplasmic Reticulum - enzymology | NADPH Oxidases - classification | Amino Acid Sequence | Green Fluorescent Proteins - metabolism | Reactive Oxygen Species - metabolism | Caspases - genetics | Microscopy, Phase-Contrast | Saccharomyces cerevisiae - genetics | Actins - metabolism | NADPH Oxidases - metabolism | Molecular Sequence Data | Green Fluorescent Proteins - genetics | Phylogeny | Saccharomyces cerevisiae Proteins - genetics | Open Reading Frames - genetics | Saccharomyces cerevisiae - metabolism | Caspases - metabolism | Saccharomyces cerevisiae Proteins - metabolism | Superoxides - metabolism | Cytoskeleton - metabolism | NADPH Oxidases - genetics | Mutation | Microscopy, Fluorescence | Mitochondria | Yeast fungi | NADP (Coenzyme) | Physiological aspects | Genetic aspects | Health aspects | Biological Sciences
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3. Full Text Dynamic rerouting of the carbohydrate flux is key to counteracting oxidative stress
by Ralser, Markus and Wamelink, Mirjam M and Kowald, Axel and Gerisch, Birgit and Heeren, Gino and Struys, Eduard A and Klipp, Edda and Jakobs, Cornelis and Breitenbach, Michael and Lehrach, Hans and Krobitsch, Sylvia
Journal of Biology, ISSN 1475-4924, 2007, Volume 6, Issue 4, pp. 10 - 10
Eukaryotic cells have evolved various response mechanisms to counteract the deleterious consequences of oxidative stress. Among these processes, metabolic... 
Carbohydrate Metabolism - drug effects | Pentose Phosphate Pathway - drug effects | Oxidants - pharmacology | Saccharomyces cerevisiae - genetics | Humans | Oxidative Stress - physiology | Recombinant Fusion Proteins - physiology | Saccharomyces cerevisiae - drug effects | Glycolysis - drug effects | Glyceraldehyde 3-Phosphate Dehydrogenase (NADP+) - physiology | Gene Knockdown Techniques | Saccharomyces cerevisiae - metabolism | Triose-Phosphate Isomerase - genetics | Glycolysis - physiology | Computer Simulation | Superoxides - metabolism | Kluyveromyces - enzymology | NADP - metabolism | Drug Resistance | Glyceraldehyde 3-Phosphate Dehydrogenase (NADP+) - genetics | Caenorhabditis elegans - metabolism | Caenorhabditis elegans - genetics | Triose-Phosphate Isomerase - physiology | Saccharomyces cerevisiae Proteins - genetics | Animals | Caenorhabditis elegans - drug effects | Aging - physiology | Caenorhabditis elegans Proteins - antagonists & inhibitors | Models, Biological | Recombinant Fusion Proteins - genetics | Oxidative Stress - drug effects | Kluyveromyces - genetics | Caenorhabditis elegans Proteins - genetics | Amino Acid Substitution | Oxidative stress | Carbohydrate metabolism | Control | Research | Health aspects
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4. Full Text Mmi1, the Yeast Homologue of Mammalian TCTP, Associates with Stress Granules in Heat-Shocked Cells and Modulates Proteasome Activity
by Rinnerthaler, Mark and Lejskova, Renata and Grousl, Tomas and Stradalova, Vendula and Heeren, Gino and Richter, Klaus and Breitenbach-Koller, Lore and Malinsky, Jan and Hasek, Jiri and Breitenbach, Michael
PLoS ONE, ISSN 1932-6203, 10/2013, Volume 8, Issue 10, p. e77791
As we have shown previously, yeast Mmi1 protein translocates from the cytoplasm to the outer surface of mitochondria when vegetatively growing yeast cells are... 
ORGANIZATION | OXIDATIVE STRESS | MICROTUBULES | MEMBRANE | MULTIDISCIPLINARY SCIENCES | IDENTIFICATION | SACCHAROMYCES-CEREVISIAE | EXPRESSION | FORTILIN | CONTROLLED TUMOR PROTEIN | REVEALS | Endopeptidases - metabolism | Saccharomyces cerevisiae - genetics | Valosin Containing Protein | Cell Cycle Proteins - metabolism | Ubiquitin - metabolism | Adenosine Triphosphatases - metabolism | Hot Temperature | Saccharomyces cerevisiae Proteins - genetics | Microscopy, Electron | Saccharomyces cerevisiae - metabolism | Heat-Shock Response | Cell Nucleus - metabolism | Endopeptidases - genetics | Cytoplasmic Granules - metabolism | Saccharomyces cerevisiae Proteins - metabolism | Cell Cycle Proteins - genetics | Adenosine Triphosphatases - genetics | Proteasome Endopeptidase Complex - metabolism | Microscopy, Fluorescence | Saccharomyces cerevisiae - growth & development | Ubiquitin | Cell death | Analysis | Oxidative stress | Yeast | Laboratories | Homology | Biology | Machinery | Nuclei | Machinery and equipment | Degradation | Proteins | Mitochondria | Ubiquitination | Proteolysis | Cell cycle | Genetics | Immunoelectron microscopy | Heat stress | Trends | Localization | Stress response | Biodegradation | Stress concentration | Shock resistance | Granule cells | Cell division | Substrates | Microscopy | Granular materials | Protein synthesis | Proteasomes | Heat tolerance | Nuclei (cytology) | Protein structure | Cytoplasm | Heat shock | Apoptosis
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5. Full Text Triose phosphate isomerase deficiency is caused by altered dimerization-not catalytic inactivity-of the mutant enzymes
by Ralser, Markus and Heeren, Gino and Breitenbach, Michael and Lehrach, Hans and Krobitsch, Sylvia
PLoS ONE, ISSN 1932-6203, 12/2006, Volume 1, Issue 1, p. e30
Triosephosphate isomerase (TPI) deficiency is an autosomal recessive disorder caused by various mutations in the gene encoding the key glycolytic enzyme TPI. A... 
MULTIDISCIPLINARY SCIENCES | Saccharomyces cerevisiae - genetics | Humans | Protein Multimerization | Cercopithecus aethiops | Diamide - pharmacology | Peptide Chain Initiation, Translational | Mutation, Missense | RNA, Messenger - metabolism | Genetic Complementation Test | Recombinant Fusion Proteins - metabolism | Triose-Phosphate Isomerase - genetics | Base Sequence | Protein Structure, Quaternary | Triose-Phosphate Isomerase - deficiency | Triose-Phosphate Isomerase - chemistry | RNA, Messenger - genetics | Models, Molecular | Recombinant Fusion Proteins - chemistry | Drug Resistance - genetics | Two-Hybrid System Techniques | Animals | Recombinant Fusion Proteins - genetics | Saccharomyces cerevisiae - enzymology | Sulfhydryl Reagents - pharmacology | Mutation | COS Cells | Amino Acid Substitution | Phosphates | Enzymes | Analysis | Genetic aspects | Genetic translation | Cells | Sugars | Monosaccharides | Oxidative stress | Deregulation | Populations | Yeast | Dehydrogenases | Hydrogen peroxide | Dihydroxyacetone | Pathogenesis | Genes | Dihydroxyacetone phosphate | Catalytic activity | Inactivation | Triose-phosphate isomerase | Population genetics | Blood | Mammalian cells | Human populations | Proteins | Oxidation resistance | Catalysis | Stress response | Dimerization | Deactivation | Translation initiation | Cystic fibrosis | Metabolism | Hereditary diseases | Tpi gene | Plasmids | Protein synthesis | Alleles | Glycolysis | Regulation | Aberration | Apoptosis
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6. Full Text Superoxide radicals have a protective role during H2O 2 stress
by Thorpe, Geoffrey W and Reodica, Mayfebelle and Davies, Michael J and Heeren, Gino and Jarolim, Stefanie and Pillay, Bethany and Breitenbach, Michael and Higgins, Vincent J and Dawes, Ian W
Molecular Biology of the Cell, ISSN 1059-1524, 09/2013, Volume 24, Issue 18, pp. 2876 - 2884
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7. Full Text Superoxide radicals have a protective role during H2O2 stress
by Thorpe, GW and Reodica, M and Davies, MJ and Heeren, G and Jarolim, S and Pillay, B and Breitenbach, M and Higgins, VJ and Dawes, IW
MOLECULAR BIOLOGY OF THE CELL, ISSN 1059-1524, 09/2013, Volume 24, Issue 18, pp. 2876 - 2884
Reactive oxygen species (ROS) consist of potentially toxic, partly reduced oxygen species and free radicals. After H2O2 treatment, yeast cells significantly... 
YEAST SACCHAROMYCES-CEREVISIAE | OXYGEN | CHRONOLOGICAL LIFE-SPAN | OXIDATIVE-STRESS | IN-VIVO | DISMUTASE | CYTOCHROME BC COMPLEX | HYDROGEN-PEROXIDE | TRANSCRIPTION FACTOR | HEART-MITOCHONDRIA | CELL BIOLOGY | Hydrogen Peroxide - toxicity | Gene Expression Regulation, Enzymologic - drug effects | Superoxide Dismutase - genetics | Electron Transport - drug effects | Microbial Viability - drug effects | RNA, Messenger - genetics | Superoxides - pharmacology | Adaptation, Physiological - drug effects | Saccharomyces cerevisiae - drug effects | Mitochondria - metabolism | Cytochromes b - metabolism | Mitochondria - drug effects | Mutation - genetics | RNA, Messenger - metabolism | Saccharomyces cerevisiae - cytology | Saccharomyces cerevisiae - metabolism | Cytoprotection - drug effects | Stress, Physiological - drug effects | Oxidative Stress - drug effects | Superoxide Dismutase - metabolism
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8. Full Text Ribosomal proteins Rpl10 and Rps6 are potent regulators of yeast replicative life span
by Chiocchetti, Andreas and Zhou, Jia and Zhu, Huashun and Karl, Thomas and Haubenreisser, Olaf and Rinnerthaler, Mark and Heeren, Gino and Oender, Kamil and Bauer, Johann and Hintner, Helmut and Breitenbach, Michael and Breitenbach-Koller, Lore
Experimental Gerontology, ISSN 0531-5565, 2007, Volume 42, Issue 4, pp. 275 - 286
The yeast ribosome is composed of two subunits, the large 60S subunit (LSU) and the small 40S subunit (SSU) and harbors 78 ribosomal proteins (RPs), 59 of... 
Yeast replicative aging | Translational capacity | Rps18 | Rpl10 | Rps6 | Longevity | Ribosomal protein | Cell Division - genetics | Ribosomal Proteins - genetics | Saccharomyces cerevisiae - genetics | Cell Count | Cell Size | Saccharomyces cerevisiae Proteins - genetics | Ribosomal Protein S6 - genetics | Ribosomes - genetics | Gene Deletion | Heterozygote | Gene Expression Regulation, Fungal - genetics | Models, Genetic | Protein Biosynthesis - genetics | Genes, Fungal - genetics | Saccharomyces cerevisiae - growth & development | Proteins
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9. Full Text Quantitation of (a)symmetric inheritance of functional and of oxidatively damaged mitochondrial aconitase in the cell division of old yeast mother cells
by Klinger, Harald and Rinnerthaler, Mark and Lam, Yuen T and Laun, Peter and Heeren, Gino and Klocker, Andrea and Simon-Nobbe, Birgit and Dickinson, J. Richard and Dawes, Ian W and Breitenbach, Michael
Experimental Gerontology, ISSN 0531-5565, 08/2010, Volume 45, Issue 7-8, pp. 533 - 542
Asymmetric segregation of oxidatively damaged proteins is discussed in the literature as a mechanism in cell division cycles which at the same time causes... 
Oxidative stress | Yeast mitochondria | Yeast mother cell-specific aging | Reactive oxygen species (ROS) | Asymmetric segregation/inheritance | Aconitase | Saccharomyces cerevisiae | PROTEIN | BUDDING YEAST | CENTROSOME | MECHANISMS | SACCHAROMYCES-CEREVISIAE | MAMMALIAN-CELLS | GERIATRICS & GERONTOLOGY | LONGEVITY | ASYMMETRIC SEGREGATION | DAUGHTER CELLS | GENE-EXPRESSION | Aconitate Hydratase - metabolism | Cell Division - genetics | Green Fluorescent Proteins - metabolism | Reactive Oxygen Species - metabolism | Oxidative Stress | Mitosis | Saccharomyces cerevisiae - genetics | DNA Primers - genetics | Green Fluorescent Proteins - genetics | Mitochondria - metabolism | Saccharomyces cerevisiae Proteins - genetics | Recombinant Fusion Proteins - metabolism | Cell Division - physiology | Saccharomyces cerevisiae - cytology | Saccharomyces cerevisiae - metabolism | Base Sequence | Saccharomyces cerevisiae Proteins - metabolism | Recombinant Fusion Proteins - genetics | Genes, Fungal | Aconitate Hydratase - genetics | Microscopy, Fluorescence | Apoptosis | Aconitate hydratase
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10. Full Text Yeast mother cell-specific ageing, genetic (in)stability, and the somatic mutation theory of ageing
by Laun, Peter and Bruschi, Carlo V and Dickinson, J. Richard and Rinnerthaler, Mark and Heeren, Gino and Schwimbersky, Richard and Rid, Raphaela and Breitenbach, Michael
Nucleic Acids Research, ISSN 0305-1048, 12/2007, Volume 35, Issue 22, pp. 7514 - 7526
Yeast mother cell-specific ageing is characterized by a limited capacity to produce daughter cells. The replicative lifespan is determined by the number of... 
MITOCHONDRIAL-DNA MUTATIONS | LIFE-SPAN | INTRACELLULAR-LOCALIZATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | RIBOSOMAL DNA | SACCHAROMYCES-CEREVISIAE | FORK BLOCK PROTEIN | MITOTIC RECOMBINATION | NUCLEOTIDE EXCISION-REPAIR | TRANSCRIPTION-COUPLED REPAIR | REPLICATIVE SENESCENCE | Cellular Senescence - genetics | Genomic Instability | Yeasts - genetics | Recombination, Genetic | DNA Repair | Models, Genetic | Telomere - metabolism | Genome, Mitochondrial | Mutation | DNA, Ribosomal - chemistry | Survey and Summary
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11. Full Text Superoxide radicals have a protective role during H2O2 stress
by Thorpe, Geoffrey W and Reodica, Mayfebelle and Davies, Michael J and Heeren, Gino and Jarolim, Stefanie and Pillay, Bethany and Breitenbach, Michael and Higgins, Vincent J and Dawes, Ian W
Molecular Biology of the Cell, ISSN 1059-1524, 09/2013, Volume 24, Issue 18, pp. 2876 - 2884
Reactive oxygen species (ROS) consist of potentially toxic, partly reduced oxygen species and free radicals. After H2O2 treatment, yeast cells significantly... 
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12. Full Text Partial uncoupling of oxidative phosphorylation induces premature senescence in human fibroblasts and yeast mother cells
by Stöckl, Petra and Zankl, Christina and Hütter, Eveline and Unterluggauer, Hermann and Laun, Peter and Heeren, Gino and Bogengruber, Edith and Herndler-Brandstetter, Dietmar and Breitenbach, Michael and Jansen-Dürr, Pidder
Free Radical Biology and Medicine, ISSN 0891-5849, 2007, Volume 43, Issue 6, pp. 947 - 958
The mitochondrial theory of aging predicts that functional alterations in mitochondria leading to reactive oxygen species (ROS) production contribute to the... 
Primary human fibroblasts | Senescence | Mitochondria | Mother-cell-specific life span | Yeast | Aging | Mitochondrial inhibitors | FCCP | Reactive Oxygen species | Coupling state | LIFE-SPAN | MITOCHONDRIAL THEORY | DROSOPHILA-MELANOGASTER | mitochondria | BIOCHEMISTRY & MOLECULAR BIOLOGY | coupling state | mitochondrial inhibitors | primary human fibroblasts | CYANIDE META-CHLOROPHENYLHYDRAZONE | SACCHAROMYCES-CEREVISIAE | CELLULAR SENESCENCE | yeast | senescence | CAENORHABDITIS-ELEGANS | reactive oxygen species | IN-VIVO | ENDOCRINOLOGY & METABOLISM | mother-cell-specific life span | HYDROGEN-PEROXIDE | aging | SUPEROXIDE-DISMUTASE | Aging, Premature - chemically induced | Cell Proliferation | Reactive Oxygen Species - metabolism | Uncoupling Agents - pharmacology | Humans | Cells, Cultured | Acetylcysteine - metabolism | Saccharomyces cerevisiae - drug effects | Oxidative Phosphorylation - drug effects | Saccharomyces cerevisiae - metabolism | Cell Respiration | Cellular Senescence | Aging, Premature - etiology | Fibroblasts - drug effects | Carbonyl Cyanide p-Trifluoromethoxyphenylhydrazone - pharmacology | Aging, Premature - metabolism | Fibroblasts - metabolism
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13. Full Text Yeast as a model for chronological and reproductive aging – A comparison
by Laun, Peter and Rinnerthaler, Mark and Bogengruber, Edith and Heeren, Gino and Breitenbach, Michael
Experimental Gerontology, ISSN 0531-5565, 2006, Volume 41, Issue 12, pp. 1208 - 1212
LIFE-SPAN | LONGEVITY | CELLS | APOPTOSIS | OXIDATIVE STRESS | PATHWAY | TOR | GROWTH | MARKERS | SACCHAROMYCES-CEREVISIAE | GERIATRICS & GERONTOLOGY | Saccharomyces cerevisiae - cytology | Phenotype | Saccharomyces cerevisiae - physiology | Aging - genetics | Aging - physiology | Genome, Fungal - genetics | Models, Biological | Saccharomyces cerevisiae - genetics | Humans | Reproduction - genetics | Reproduction - physiology | Apoptosis Regulatory Proteins - physiology
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14. Full Text MMI1 ( YKL056c, TMA19), the yeast orthologue of the translationally controlled tumor protein (TCTP) has apoptotic functions and interacts with both microtubules and mitochondria
by Rinnerthaler, Mark and Jarolim, Stefanie and Heeren, Gino and Palle, Elfriede and Perju, Simona and Klinger, Harald and Bogengruber, Edith and Madeo, Frank and Braun, Ralf J and Breitenbach-Koller, Lore and Breitenbach, Michael and Laun, Peter
BBA - Bioenergetics, ISSN 0005-2728, 2006, Volume 1757, Issue 5, pp. 631 - 638
The yeast orthologue of mammalian TCTP is here proposed to be named Mmi1p ( icrotubule and itochondria nteracting protein). This protein displays about 50%... 
Oxidative stress | Mitochondria | TCTP | Ageing, heat shock | Microtubules | Apoptosis | ageing | TRANSCRIPTOME | mitochondria | BIOCHEMISTRY & MOLECULAR BIOLOGY | BINDING-PROTEIN | apoptosis | heat shock | microtubules | IDENTIFICATION | SACCHAROMYCES-CEREVISIAE | CELL-DEATH | POLYACRYLAMIDE-GELS | BIOPHYSICS | MESSENGER-RNA | ACTIN CYTOSKELETON | EXPRESSION | oxidative stress | Proteins | Histamine | Cysteine | Hydrogen peroxide | Mitochondrial DNA | Tumors
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