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E is the key components of Ub transfer pathway
2020-08-03
E2 is the key components of Ub transfer pathway in ubiquitination, which is responsible for E3 selection and substrate modification as well as the diversity of Ub cellular signaling (Huang et al., 2009; Sakata et al., 2010). E2s can be easily identified by their evolutionarily conserved ‘Ubc’ cataly
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The UPP broadly involves proteolysis in biochemical processe
2020-08-03
The UPP broadly involves proteolysis in biochemical processes and is a potential target for cancer therapy. The UPP degrades unfolding or damaged proteins by an ATP-dependent mechanism (Ciechanover, Elias, Heller, Ferber, & Hershko, 1980). It also plays an important role in IWP-L6 regulation, DNA d
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Venous thromboembolism VTE either deep vein thrombosis or
2020-08-03
Venous thromboembolism (VTE), either deep vein thrombosis or pulmonary embolism, is a main harmful effect of HT among postmenopausal women [2], [3], [4]. For about 10 years, epidemiological data have shown a differential association of oral and transdermal estrogens with the VTE risk among postmenop
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EWS FLI is the most heterogeneous gene fusion in cancer
2020-08-03
EWS-FLI-1 is the most heterogeneous gene fusion in cancer. The 2 most common fusions join EWS r78 sale 7 in frame with either exon 6 (type 1 fusion) or exon 5 (type 2 fusion) of FLI-1. Other types of fusion transcript are designated by different exons involved (eg, type 10-5). Similarly, at least 4
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br Materials and methods br Results br Discussion Imatinib
2020-08-03
Materials and methods Results Discussion Imatinib inhibits the tyrosine kinase activities of ABL, as well as the c-KIT and PDGF (platelet derived growth factor) atp enzyme mg kinases, and is an effective therapy for chronic myeloid leukemia and c-KIT and PDGF receptor-dependent gastrointest
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br Experimental br Results and discussions br
2020-08-03
Experimental Results and discussions Conclusion Introduction The joining of DNA fragments using Metabolism Compound Library receptor is an essential process in gene cloning. One of the important parameters for performing DNA ligation efficiently is the temperature [1]. In the case of DNA
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Phosphoramidon Disodium Salt The DDR gene is located in q
2020-08-03
The DDR2 gene is located in 1q23.3, and its product is a tyrosine kinase receptor for fibrillar collagen [7], [8], [9], [10]. Under normal physiological conditions, it acts in cutaneous wound healing mediated by proliferation, chemotactic migration, and secretion of metalloproteinases and collagen b
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br Material and methods br Results
2020-07-31
Material and methods Results Discussion Acknowledgements This work was supported by grants from the Agence Nationale de la Recherche (ANR) (ANR07-PHYSIO-008-2 and BLAN 2010-111201), and by a grant from the BHFZ (Bayerisch-Französisches Hochschulzentrum; FK-13/09). S. L\'Hoste and O. Andr
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br DUBs in immunotherapy P is
2020-07-31
DUBs in immunotherapy P53 is a well known tumor repressor protein involves in CGP 42112 synthesis control and frequently mutated in tumor cells (Harris and Levine, 2005). Many of the USPs involve in P53 regulation. USP7 and USP15 involve in the control of P53-MDM2 pathway by regulating the stabil
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br Structural and biochemical features of
2020-07-31
Structural and biochemical features of pol X family polymerases The X-family DNA polymerase (polX) is specialized in DNA repair. This family is composed of four different DNA polymerases: pol β, pol λ, pol μ and TdT. Only three members of the polX family possess an N-terminal BRCT (BRCA1 carboxy
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Bafilomycin A1 br Regulation of DGK activity Activation of t
2020-07-31
Regulation of DGK activity Activation of the DGKs is complex and unique for each DGK isotype. In most cases, DGKs must translocate to a membrane compartment to access DAG. However, translocation does not necessarily activate the enzyme [57]. In addition, DGK activity can be modified by other cofa
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To determine whether serine phosphorylation could influence
2020-07-31
To determine whether serine 15 Lopinavir could influence the ability of CK1 to phosphorylate p53, the GST-p53 fusion proteins (both murine and human) were phosphorylated stoichiometrically using recombinant DNA-PK and excess unlabelled ATP as phosphate donor. The proteins were bound to glutathione-
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We have shown that the glycation of collagen
2020-07-30
We have shown that the glycation of collagen hinders collagen-DDR2 binding. McCarthy et al. previously showed reduced binding of rat osteosarcoma-derived cells (UMR106) to glycated collagen. The authors speculated that glycation of collagen attenuates collagen binding to collagen-specific integrins
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Next we tried to specifically inhibit DDR
2020-07-30
Next, we tried to specifically inhibit DDR2 function in endochondral proliferation and ossification in vivo. We used competitive inhibition with KD-Ddr2 overexpression specifically in cartilage cells, because it is generally difficult to regulate genes by miRNA in vivo. We constructed a transgenic v
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phosphodiesterase inhibitors br Conclusion Several classes o
2020-07-30
Conclusion Several phosphodiesterase inhibitors of models have successively emerged since the 1970s. Three main models describing Ca2+ binding to CaM are now surviving: All three models explain most of the experimental results obtained up to now. However, the two first ones, due to the symmetri
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