يعرض 1 - 10 نتائج من 13 نتيجة بحث عن '"SBD, substrate binding domain"', وقت الاستعلام: 1.58s تنقيح النتائج
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    المصدر: Acta Pharmaceutica Sinica B, Vol 12, Iss 1, Pp 246-261 (2022)
    Acta Pharmaceutica Sinica. B

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    المصدر: Computational and Structural Biotechnology Journal
    COMPUTATIONAL AND STRUCTURAL BIOTECHNOLOGY JOURNAL
    Computational and Structural Biotechnology Journal, Vol 19, Iss, Pp 2905-2920 (2021)

    وصف الملف: application/pdf

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    المساهمون: Institute of Biotechnology, Molecular Systems Biology, Biosciences, Mart Saarma / Principal Investigator

    المصدر: Journal of Biological Chemistry
    The Journal of Biological Chemistry

    مصطلحات موضوعية: 0301 basic medicine, BiFC, bimolecular fluorescence complementation, MST, microscale thermophoresis, PDIA1, protein disulfide isomerase family A member 1, Apoptosis, NEUROTROPHIC FACTOR MANF, Endoplasmic Reticulum, Biochemistry, protein-protein interaction, Mice, Bimolecular fluorescence complementation, UPR, unfolded protein response, ENDOPLASMIC-RETICULUM STRESS, Mesencephalon, Neurotrophic factors, Insulin-Secreting Cells, Protein Interaction Mapping, BINDING, COMPREHENSIVE RESOURCE, ATF6, unfolded protein response (UPR), PDIA6, protein disulfide isomerase family A member 6, PPIs, protein-protein interactions, Endoplasmic Reticulum Chaperone BiP, Heat-Shock Proteins, NPTN, neuroplastin, biology, Chemistry, apoptosis, unfolded protein response, dopamine neurons, 3. Good health, Cell biology, GDNF, glial cell line–derived neurotrophic factor, IRE1-ALPHA, SBD, substrate-binding domain, endoplasmic reticulum stress, MANF, mesencephalic astrocyte-derived neurotrophic factor, Tm, tunicamycin, neuroprotection, Research Article, Protein Binding, Signal Transduction, GRP78, Protein Disulfide-Isomerase Family, Cell Survival, TH, tyrosine hydroxylase, Primary Cell Culture, SCG, superior cervical ganglion, Protein Disulfide-Isomerases, IRE1, inositol-requiring enzyme 1, ER-STRESS, ER, endoplasmic reticulum, 03 medical and health sciences, ohjelmoitunut solukuolema, C-MANF, C-terminal domain of MANF, CSPs, chemical shift perturbations, Animals, Humans, HSP70 Heat-Shock Proteins, Nerve Growth Factors, NBD, nucleotide-binding domain, NMR, nuclear magnetic resonance, Molecular Biology, 030102 biochemistry & molecular biology, BIP, Dopaminergic Neurons, Gene Expression Profiling, Binding protein, neuronal cell death, DISSOCIATION, Cell Biology, NEI, nucleotide exchange inhibitor, Embryo, Mammalian, adenosiinitrifosfaatti, ATP, hermosolut, mesencephalic astrocyte-derived neurotrophic factor, protein–protein interaction, PERK, protein kinase RNA-like ER kinase, HEK293 Cells, 030104 developmental biology, Gene Expression Regulation, Chaperone (protein), Tg, thapsigargin, biology.protein, Unfolded protein response, AP-MS, affinity purification mass spectrometry, 1182 Biochemistry, cell and molecular biology, GFP-SH, SH-tagged GFP, endoplasmic reticulum stress (ER stress), DA, dopamine, mesencephalic astrocyte-derived neurotrophic factor (MANF), proteiinit, Neuroplastin

    وصف الملف: application/pdf; fulltext

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    المصدر: European Journal of Pharmaceutical Sciences

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    المصدر: The Journal of biological chemistry, vol 297, iss 5
    The Journal of Biological Chemistry

    وصف الملف: application/pdf

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    المساهمون: Biotechnologie et signalisation cellulaire (BSC), Université de Strasbourg (UNISTRA)-Centre National de la Recherche Scientifique (CNRS)-Institut de recherche de l'Ecole de biotechnologie de Strasbourg (IREBS), Immunopathologie et chimie thérapeutique (ICT), Institut de biologie moléculaire et cellulaire (IBMC), Université de Strasbourg (UNISTRA)-Centre National de la Recherche Scientifique (CNRS)-Université de Strasbourg (UNISTRA)-Centre National de la Recherche Scientifique (CNRS)-Centre National de la Recherche Scientifique (CNRS)

    المصدر: Autophagy
    Autophagy, Taylor & Francis, 2015, 11 (3), pp.472-486. ⟨10.1080/15548627.2015.1017179⟩

    مصطلحات موضوعية: Phosphopeptides, Mice, Inbred MRL lpr, LC-MS, liquid chromatography-mass spectrometry, NBD, nucleotide binding domain, [SDV.BIO]Life Sciences [q-bio]/Biotechnology, T-Lymphocytes, Autoimmunity, CPZ: chlorpromazine, SLE, systemic lupus erythematosus, chemistry.chemical_compound, Mice, Chaperone-mediated autophagy, paraquat, 1, 1′-dimethyl-4, 4′-bipyridyldinium dichloride, qRT-PCR, quantitative reverse transcriptase-polymerase chain reaction, immune system diseases, Serine, Lupus Erythematosus, Systemic, antigen-presenting cells, ALF, artificial lysosomal fluid, RPL5, ribosomal protein L5, Phosphorylation, skin and connective tissue diseases, chaperone-mediated autophagy, HSPA8/HSC70, education.field_of_study, B-Lymphocytes, SBD, substrate binding domain, Sciences du Vivant [q-bio]/Biotechnologies, ELISA, enzyme-linked immunosorbent assay, MHCII, major histocompatibility complex class II, class II MHC molecules, Endocytosis, Basic Research Paper, CMA, chaperone-mediated autophagy, Cell biology, Lysosomal lumen, GAPDH, glyceraldehyde-3-phosphate dehydrogenase, bodipy: BODIPY FL C5 Lactosylceramide/bovine serum albumin, LAMP2A, lysosomal-associated membrane protein 2A, RP-HPLC, reversed-phase high-performance liquid chromatography, autophagy, CTSD, cathepsin D, PBS, phosphate-buffered saline, Endosomes, Biology, SEM, standard error of the mean, Ribosomal protein L5, Ribonucleoprotein, U1 Small Nuclear, lysosomal chaperones, TFA, trifluoroacetic acid, Sequestosome 1, lysosomes, CoIP, coimmunoprecipitation, Downregulation and upregulation, Animals, Humans, education, Antigen-presenting cell, Molecular Biology, SQSTM1/p62, sequestosome 1, iv, intravenous, SNRNP70/U170K: small nuclear ribonucleoprotein 70kDa, Autophagy, HSC70 Heat-Shock Proteins, Histocompatibility Antigens Class II, Cell Biology, lupus, HCQ, hydroxychloroquine, LC3-II, MAP1LC3-II, Molecular biology, Peptide Fragments, TF, transferrin, chemistry, APC, antigen-presenting cell, Phosphoserine, heat shock proteins, NIH 3T3 Cells, FCS, fetal calf serum, SD, standard deviation, DAPI, 4′, 6-diamidino-2-phenylindole, Molecular Chaperones, B lymphocytes

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    دورية أكاديمية

    المؤلفون: Shan S; Institute of Biotechnology, Key Laboratory of Chemical Biology and Molecular Engineering of National Ministry of Education, Shanxi University, Taiyuan 030006, China., Niu J; Institute of Biotechnology, Key Laboratory of Chemical Biology and Molecular Engineering of National Ministry of Education, Shanxi University, Taiyuan 030006, China., Yin R; Institute of Biotechnology, Key Laboratory of Chemical Biology and Molecular Engineering of National Ministry of Education, Shanxi University, Taiyuan 030006, China., Shi J; Institute of Biotechnology, Key Laboratory of Chemical Biology and Molecular Engineering of National Ministry of Education, Shanxi University, Taiyuan 030006, China., Zhang L; School of Life Science, Shanxi University, Taiyuan 030006, China., Wu C; Institute of Biotechnology, Key Laboratory of Chemical Biology and Molecular Engineering of National Ministry of Education, Shanxi University, Taiyuan 030006, China., Li H; School of Life Science, Shanxi University, Taiyuan 030006, China., Li Z; Institute of Biotechnology, Key Laboratory of Chemical Biology and Molecular Engineering of National Ministry of Education, Shanxi University, Taiyuan 030006, China.; School of Life Science, Shanxi University, Taiyuan 030006, China.

    المصدر: Acta pharmaceutica Sinica. B [Acta Pharm Sin B] 2022 Mar; Vol. 12 (3), pp. 1254-1270. Date of Electronic Publication: 2021 Oct 15.

    نوع المنشور: Journal Article

    بيانات الدورية: Publisher: Elsevier Country of Publication: Netherlands NLM ID: 101600560 Publication Model: Print-Electronic Cited Medium: Print ISSN: 2211-3835 (Print) Linking ISSN: 22113835 NLM ISO Abbreviation: Acta Pharm Sin B Subsets: PubMed not MEDLINE