human | Q5 |
P8446 | Gateway to Research person ID | 79E3B557-4507-44C3-BE54-4EA9DD0AAA30 |
P496 | ORCID iD | 0000-0001-7764-577X |
P1153 | Scopus author ID | 8982438100 |
P69 | educated at | Osaka University | Q651233 |
P108 | employer | University of Cambridge | Q35794 |
P734 | family name | Narita | Q20189031 |
Narita | Q20189031 | ||
Narita | Q20189031 | ||
P735 | given name | Masashi | Q3297184 |
Masashi | Q3297184 | ||
P106 | occupation | researcher | Q1650915 |
Q28214507 | 14-3-3 Interacts directly with and negatively regulates pro-apoptotic Bax |
Q43184738 | 14-3-3 interacts directly with and negatively regulates pro-apoptotic Bax. |
Q38694968 | A 'synthetic-sickness' screen for senescence re-engagement targets in mutant cancer backgrounds |
Q57580301 | A Case Report of Celiac Axis Compression Syndrome Combined with Gastric Cancer. Diagnosis by Doppler Ultrasonography |
Q57580298 | A Case of Lactic Acidosis from Vitamin B1 Deficiency during Total Parenteral Nutrition |
Q57580291 | A case of microangiopathic hemolytic anemia associated with breast cancer: Improvement with chemoendocrine therapy |
Q89589492 | A novel Atg5-shRNA mouse model enables temporal control of Autophagy in vivo |
Q24299446 | A novel role for high-mobility group a proteins in cellular senescence and heterochromatin formation |
Q57580204 | Abstract SY02-03: Chromatin architecture and gene regulation in oncogene-induced senescence |
Q57580176 | Abstract SY10-01: Chromatin structure change and aberrant gene expression during senescence |
Q57580178 | Abstract SY10-04: Histone tail alterations in cellular senescence |
Q57580249 | Analysis of Apaf-1 and Caspase 9 in Tumorigenesis |
Q57580260 | Analysis of Apaf-1 and Caspase 9 in Tumorigenesis |
Q57580271 | Analysis of Apaf-1 and Caspase 9 in Tumorigenesis |
Q57580273 | Apoptotic cytosol facilitates Bax translocation to mitochondria that involves cytosolic factor regulated by Bcl-2 |
Q47999212 | Autophagy Detection During Oncogene-Induced Senescence Using Fluorescence Microscopy |
Q57580194 | Autophagy facilitates oncogene-induced senescence |
Q37938309 | Autophagy in cancer: having your cake and eating it. |
Q24320401 | Autophagy mediates the mitotic senescence transition |
Q22008484 | Bax interacts with the permeability transition pore to induce permeability transition and cytochrome c release in isolated mitochondria |
Q22009974 | Bcl-2 family proteins regulate the release of apoptogenic cytochrome c by the mitochondrial channel VDAC |
Q28267760 | CELL BIOLOGY. GATA get a hold on senescence |
Q37982201 | Cancer cell senescence: a new frontier in drug development. |
Q45864651 | Cancer gene therapy using a pro-apoptotic gene, caspase-3. |
Q38072349 | Cell senescence as both a dynamic and a static phenotype |
Q36609955 | Cellular senescence and chromatin organisation |
Q38180648 | Cellular senescence and its effector programs |
Q43203449 | Connecting autophagy to senescence in pathophysiology. |
Q91297526 | Crisis management by autophagy |
Q40695864 | Direct coupling of the cell cycle and cell death machinery by E2F. |
Q33929054 | Dissecting the unique role of the retinoblastoma tumor suppressor during cellular senescence |
Q99566207 | Dynamic modulation of autophagy: implications for aging and cancer |
Q96641338 | Epigenetic priming by Dppa2 and 4 in pluripotency facilitates multi-lineage commitment |
Q57580197 | Executing Cell Senescence |
Q57580253 | Executing cell senescence |
Q38746800 | G-quadruplex structures mark human regulatory chromatin |
Q21996341 | Guidelines for the use and interpretation of assays for monitoring autophagy |
Q22676705 | Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition) |
Q35615694 | HMGA2 overexpression-induced ovarian surface epithelial transformation is mediated through regulation of EMT genes |
Q42223650 | High-order chromatin structure and the epigenome in SAHFs |
Q34533167 | Histone H3.3 and its proteolytically processed form drive a cellular senescence programme |
Q35811361 | Identification of a Selective G1-Phase Benzimidazolone Inhibitor by a Senescence-Targeted Virtual Screen Using Artificial Neural Networks |
Q37800219 | Impact of cellular senescence signature on ageing research |
Q57580185 | Improving Literature-Based Discovery with Advanced Text Mining |
Q34337209 | Independence of repressive histone marks and chromatin compaction during senescent heterochromatic layer formation |
Q57580283 | Independent Prognostic Factors in Breast Cancer Patients |
Q38230319 | Inside and out: the activities of senescence in cancer. |
Q57580165 | Late cornified envelope (LCE) proteins: distinct expression patterns of LCE2 and LCE3 members suggest nonredundant roles in human epidermis and other epithelia |
Q28251930 | Let-7 repression leads to HMGA2 overexpression in uterine leiomyosarcoma |
Q40403745 | Metabolomic changes during cellular transformation monitored by metabolite-metabolite correlation analysis and correlated with gene expression |
Q37681644 | Multiple expression cassette exchange via TP901-1, R4, and Bxb1 integrase systems on a mouse artificial chromosome |
Q35133431 | NG2 expression in glioblastoma identifies an actively proliferating population with an aggressive molecular signature. |
Q42317186 | NOTCH and the 2 SASPs of senescence |
Q54965975 | NOTCH-mediated non-cell autonomous regulation of chromatin structure during senescence. |
Q30806890 | NOTCH1 mediates a switch between two distinct secretomes during senescence. |
Q104584551 | Neuron type-specific increase in lamin B1 contributes to nuclear dysfunction in Huntington's disease |
Q30796282 | Normalization of metabolomics data with applications to correlation maps |
Q26750501 | Old cells, new tricks: chromatin structure in senescence |
Q36702441 | Oncogenes and senescence: breaking down in the fast lane |
Q36808432 | Oncogenic HMGA2: short or small? |
Q35196159 | Phenotype specific analyses reveal distinct regulatory mechanism for chronically activated p53 |
Q57580278 | Prognostic Factors in Breast Cancer and their Limitations |
Q41815721 | Psoriasis risk genes of the late cornified envelope-3 group are distinctly expressed compared with genes of other LCE groups. |
Q37762358 | Quality and quantity control of proteins in senescence |
Q29029578 | Quantitation and Identification of Thousands of Human Proteoforms below 30 kDa |
Q39395750 | Quantitative assessment of higher-order chromatin structure of the INK4/ARF locus in human senescent cells |
Q57580211 | Rags connect mTOR and autophagy |
Q37138585 | Redistribution of the Lamin B1 genomic binding profile affects rearrangement of heterochromatic domains and SAHF formation during senescence |
Q35935196 | Retinoblastoma protein promotes oxidative phosphorylation through upregulation of glycolytic genes in oncogene-induced senescent cells |
Q35561999 | Reversal of human cellular senescence: roles of the p53 and p16 pathways |
Q34945503 | SASP reflects senescence. |
Q57580244 | Senescence comes of age |
Q113816146 | Senescence-induced endothelial phenotypes underpin immune-mediated senescence surveillance |
Q91311854 | Short-term gain, long-term pain: the senescence life cycle and cancer |
Q52758554 | Spatial and Temporal Control of Senescence. |
Q54571094 | Spatio-temporal association between mTOR and autophagy during cellular senescence. |
Q92711500 | Temporal inhibition of autophagy reveals segmental reversal of ageing with increased cancer risk |
Q42977333 | The expanding territories of condensin II. |
Q57580223 | The tumor suppressor ING1 contributes to epigenetic control of cellular senescence |
Q42805018 | Three nonsense mutations responsible for group A xeroderma pigmentosum |
Q103027719 | Transcription-dependent cohesin repositioning rewires chromatin loops in cellular senescence |
Q54243358 | Translating the effects of mTOR on secretory senescence. |
Q44368039 | Transmitting senescence to the cell neighbourhood |
Q57580233 | [Dynamism of chromatin-structural changes in cellular senescence] |
Q34399239 | p400 is required for E1A to promote apoptosis |
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