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In conclusion our data represents a step forward
2019-10-15
In conclusion, our data represents a step forward in terms of clarifying the role of I/D polymorphism of ACE and VNTR polymorphism of eNOS and G1793A, C677T and A1298C polymorphism of MTHFR in pathophysiology of psoriasis in Pakistani patients. It will help in better understanding of the disease pro
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br Results br Discussion In this paper we
2019-10-14
Results Discussion In this paper we present insights into the observed specificities of inhibitors targeting the ubiquitin-activating and related E1 DL-AP5 Sodium salt pathway via crystal structures of the specific NEDD8-E1 inhibitor MLN4924, the dual NEDD8/Ub E1 inhibitor ABPA3, and the selec
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ATP dependent DNA ligases in vertebrates
2019-10-14
ATP-dependent DNA ligases in vertebrates are divided in three families [7]. Family I DNA ligases are responsible for sealing the nicks during DNA replication and in long-patch base excision repair (BER). Family III DNA ligases are involved in short-patch BER. Lastly, family IV DNA ligases are involv
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Given the importance of cysteine cathepsin inhibitors as
2019-10-14
Given the importance of cysteine cathepsin inhibitors as putative therapeutic molecules and microbial virulence factors, we chose to investigate whether Yersinia enterocolitica may be a potent producer of such inhibitors. Y. enterocolitica is the most heterogeneous species within the genus Yersinia.
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The absence of an observable time dependence of kobs on
2019-10-14
The absence of an observable time dependence of kobs on inhibitor concentration for MLN9708 3 with AChE and compounds 1, 3 and 4 with BuChE parallels a similar absence of time dependence for some related fluoro ketones with AChE. Nair et al. found that trifluoromethyl acetophenones with small meta-s
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Kinetic isotope effects KIEs inform on bond vibrational chan
2019-10-14
Kinetic isotope effects (KIEs) inform on bond vibrational changes between the ground state (GS) and TS of a chemical reaction and remain one of the most powerful experimental techniques for interrogating TS structure. KIEs on enzyme reactions measured by the internal gonadotropin releasing hormone r
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gw501516 Our study found a significant association between
2019-10-14
Our study found a significant association between the degree of primary tumor lobulation and EGFR mutations status (P EGFR gw501516 status. However, only a small portion of these previous studies included the evaluation of lobulation, and almost all of them reported no association between EGFR muta
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5-Carboxymethylester-UTP pathway A potential weakness of the
2019-10-14
A potential weakness of the present study is that it involved population controls rather than family controls, which are a better way of controlling the effects of population stratification (e.g. ethnic group differences in allele frequencies). On the other hand, general population samples do have t
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br Acknowledgement br Introduction Human
2019-10-14
Acknowledgement Introduction Human dihydroorotate dehydrogenase (hDHODH), a flavin-dependent mitochondrial enzyme involved in de novo 1-NM-PP1 biosynthesis, is a validated therapeutic target for the treatment of autoimmune diseases such as rheumatoid arthritis and cancer [1], [2], [3]. Leflun
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The discoidin domain receptors DDR and
2019-10-14
The discoidin domain receptors, DDR1 and DDR2, are receptor tyrosine kinases (RTKs) that are stimulated by collagen in the extracellular matrix (ECM). Unlike most other RTKs, they form ligand-independent stable dimers that are non-covalently linked. This ECM activation induces receptor phosphorylati
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br Introduction Sphingolipids are ubiquitous membrane compon
2019-10-14
Introduction Sphingolipids are ubiquitous membrane components of all eukaryotic cells belonging to a group of complex lipids. The basic structure of sphingolipids is composed of a sphingoid long chain base (LCB) linked to a fatty Anastrozole via an amide bond to form a ceramide [1]. In animals,
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A series of monocarboxylated chalcones
2019-10-14
A series of monocarboxylated chalcones (e.g. compounds 7 and 8, Fig. 2A) was previously identified as good CysLT1 antagonists [20], and none of them exhibited CysLT2 antagonistic activities (Supplementary Table S1). This study was consistent with reported result that CysLT2 Amyloid Beta-Peptide (1-4
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MK-3207 HCl kinase ARA metabolites which are produced throug
2019-10-14
ARA metabolites, which are produced through cytochrome P450 (CYP450) enzymes influence cardiovascular homeostasis. Human CYP4A11 and CYP1A2 metabolize ARA to 20-hydroxyecostearonic MK-3207 HCl kinase (20-HETE) [11], which is a vasoconstrictor [12], platelet activator [13] and naturetic in the kidne
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Intriguingly one E residue may serve
2019-10-12
Intriguingly, one E2 residue may serve as a molecular ‘gate’ to allow the C-terminus of ubiquitin to access the closed E2~Ub conformations favorable for ubiquitin transfer. This residue, Asp87 in UbcH5 family members, resides on one side of the opening that leads to the active site Cys (Fig. 4D). In
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br Conformational properties of DGK br
2019-10-12
Conformational properties of DGKϵ Interaction of DGKϵ with its lipid substrate A major component of the interaction between DGKϵ and lipid bilayers is the insertion of the hydrophobic segment comprising residues 20–42 into the membrane, as discussed above. However, this is not the only interac
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