يعرض 1 - 10 نتائج من 13 نتيجة بحث عن '"Hutchinson Gilford progeria syndrome"', وقت الاستعلام: 1.99s تنقيح النتائج
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    المصدر: Computational and Structural Biotechnology Journal
    Computational and Structural Biotechnology Journal, Vol 17, Iss, Pp 1265-1277 (2019)

    مصطلحات موضوعية: Aging, Review Article, Disease, Aging disorders, Biochemistry, vascular smooth muscle cells, (VSMC), cyclin-dependent kinase inhibitor 1, (cdkn1A/p21), 0302 clinical medicine, Structural Biology, HutchinsonGilford progeria syndrome, (HGPS), purinergic receptors family, (P2Y), protein kinases, (PK), beta2-adrenergic receptor, (β2AR), Receptor, endothelial cell differentiation gene, (Edg), nuclear factor kappa-light-chain-enhancer of activated B cells, (NF- κβ), senescence associated secretory phenotype, (SASP), 0303 health sciences, Relaxin family receptor 3, (RXFP3), tumor suppressor gene PTEN, (PTEN), transcription factor E2F3, (E2F3), Computer Science Applications, Cell biology, retinoblastoma, (RB), Chemistry, 030220 oncology & carcinogenesis, G protein-coupled receptor kinase, (GRK), latent semantic indexing, (LSI), Lysophosphatidic acid, (LPA), G protein-coupled receptors (GPCRs), G protein-coupled receptor kinase interacting protein 2 (GIT2), mitogen-activated protein kinase, (MAPK), Regulator of G-protein signaling, (RGS), Engineering sciences. Technology, AT1R blockers, (ARB), Biotechnology, Cell signaling, lcsh:Biotechnology, renin-angiotensin system, (RAS), Biophysics, Cellular senescence, tumor suppressor protein 53, (p53), Biology, 03 medical and health sciences, Cell surface receptor, lcsh:TP248.13-248.65, angiotensin type 2 receptor, (AT2R), Genetics, G protein-coupled receptor kinase interacting protein 2, (GIT2), Ataxia telangiectasia mutated, (ATM), Angiotensin II, (Ang II), 030304 developmental biology, G protein-coupled receptor, inactive state, (R), angiotensin type 1 receptor, (AT1R), G protein-coupled receptors, (GPCRs), β-Arrestin, ADP-ribosylation factor GTPase-activating protein, (Arf-GAP), cyclin-dependent kinase 2, (CDK2), Apoptosis, transmembrane, (TM), stress-induced premature senescence, (SIPS), active state, (R*)

    وصف الملف: pdf

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    المصدر: Seminars in Cell & Developmental Biology

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    المساهمون: Ministerio de Economía y Competitividad (España), Instituto de Salud Carlos III, Progeria Research Foundation, Comunidad de Madrid (España), Ministerio de Educación (España), Fundación ProCNIC, Fundación Cajastur

    المصدر: Repisalud
    Instituto de Salud Carlos III (ISCIII)

    مصطلحات موضوعية: Male, Proteomics, Ribosomal protein S6 kinase, 70kDa, polypeptide 1, ATP synthase, H+ transporting, mitochondrial F1 complex, beta polypeptide, ATP5B, Molecular biology of aging, ENO2, Pyruvate kinase, muscle, ATP5F1, Zoledronic Acid, SILAC, Biochemistry, Progerin, LMNA, Mice, Adenosine Triphosphate, Methionine, Progeria, cytochrome c oxidase, Amino Acids, Stable isotope labeling with amino acids in cell culture, Child, p70S6K, Pravastatin, Skin, Mammalian target of rapamycin, Diphosphonates, integumentary system, Imidazoles, ATP5O, Nuclear Proteins, Lamin Type A, MAF, OXPHOS, PKM, Mitochondria, Cell biology, ATP5A1, FTI, mTOR, HGPS, eIF2, Female, eIF4, Flavoprotein subunit of succinate dehydrogenase, CS, Accelerated aging, Premature aging, Senescence, congenital, hereditary, and neonatal diseases and abnormalities, Adolescent, Biophysics, Mouse adult fibroblast, ATP synthase, H+ transporting, mitochondrial F1 complex, gamma polypeptide, Biology, ATP synthase, H+ transporting, mitochondrial F1 complex, O subunit, ATP synthase, H+ transporting, mitochondrial F0 complex, subunit B1, Oxygen Consumption, Eukaryotic translation initiation factor 2, Zinc metalloproteinase STE24 homolog, Eukaryotic translation initiation factor 4, ATP5C1, medicine, Animals, Humans, Zmpste24, Oxidative phosphorylation, Protein Precursors, HutchinsonGilford progeria syndrome, Enolase 2, COX, Galactose, nutritional and metabolic diseases, Fibroblasts, medicine.disease, Molecular biology, Glucose, ATP synthase, H+ transporting, mitochondrial F1 complex, alpha subunit 1, Farnesyltransferase inhibitor, Gene Expression Regulation, Mutation, Lamin A, FpSDH, Hydroxymethylglutaryl-CoA Reductase Inhibitors, Mitochondrial dysfunction, citrate synthase

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