Archives
- 2026-02
- 2026-01
- 2025-12
- 2025-11
- 2025-10
- 2025-09
- 2025-03
- 2025-02
- 2025-01
- 2024-12
- 2024-11
- 2024-10
- 2024-09
- 2024-08
- 2024-07
- 2024-06
- 2024-05
- 2024-04
- 2024-03
- 2024-02
- 2024-01
- 2023-12
- 2023-11
- 2023-10
- 2023-09
- 2023-08
- 2023-06
- 2023-05
- 2023-04
- 2023-03
- 2023-02
- 2023-01
- 2022-12
- 2022-11
- 2022-10
- 2022-09
- 2022-08
- 2022-07
- 2022-06
- 2022-05
- 2022-04
- 2022-03
- 2022-02
- 2022-01
- 2021-12
- 2021-11
- 2021-10
- 2021-09
- 2021-08
- 2021-07
- 2021-06
- 2021-05
- 2021-04
- 2021-03
- 2021-02
- 2021-01
- 2020-12
- 2020-11
- 2020-10
- 2020-09
- 2020-08
- 2020-07
- 2020-06
- 2020-05
- 2020-04
- 2020-03
- 2020-02
- 2020-01
- 2019-12
- 2019-11
- 2019-10
- 2019-09
- 2019-08
- 2019-07
- 2019-06
- 2019-05
- 2019-04
- 2018-11
- 2018-10
- 2018-07
-
Because some evidence has shown doses of levodopa in
2020-08-03

Because some evidence has shown doses of levodopa in patients with PD can be influenced by specific COMT haplotypes [20] and doses of levodopa itself might also affect the rate of cognitive decline, although the results were inconsistent [21,22], we therefore examined the mean LEDD per day in patien
-
br Acknowledgments This work was financially supported by th
2020-08-03

Acknowledgments This work was financially supported by the National Natural Science Foundation of China (Nos. 21362026, 21867016), Young Talent Program of NingXia medical University and Ningxia Medical University Key Project (XZ2018002). Introduction Bidirectional DNA replication is initiated
-
As a measure of target inhibition
2020-08-03

As a measure of target inhibition in vivo, a triglyceride tolerance test in mice was carried out with . Since DGAT-1 is highly expressed in the small intestine and catalyzes the rate determining step in triglyceride synthesis, co-dosing of an inhibitor with an oral SLIGKV-NH2 mg of lipid provides a
-
β-Sitosterol Decreased spreading and formation of actin stre
2020-08-03

Decreased spreading and formation of β-Sitosterol stress fibers by DDR2 silenced cells could reflect a link between DDR2 activation and of focal adhesion kinase. Other studies have suggested that DDR1 signaling affects myosin function activation [29] or inhibition [17], [29] depending on cell type
-
br Acknowledgements br Introduction Protein tyrosine kinases
2020-07-31

Acknowledgements Introduction Protein–tyrosine kinases are found in all multicellular eukaryotic organisms and play important roles in a variety of intracellular signal-transduction pathways. Receptor-type tyrosine kinases, a subclass of transmembrane-spanning receptors, transmit signals acros
-
Several reasons may explain that other studies using PDE
2020-07-31

Several reasons may explain that other studies using PDE-5-Is yielded negative or contradictory results [30], [31], [32]. Lee [30] applied 50mg sildenafil to seven patients with liver cirrhosis. NO and cGMP in the hepatic Milrinone significantly increased, hepatic and pulmonary resistance decrease
-
br Introduction Evolutionary conservation has become more an
2020-07-31

Introduction Evolutionary conservation has become more and more a powerful tool to identify functionally important sequences in the genome (Dermitzakis et al., 2005). In this context, the ultraconserved elements (UCEs) are 481 genomic segments longer than 200 A23187, free acid pairs (bp), which
-
DDR kinases are linked to
2020-07-31

DDR kinases are linked to the progression of various human diseases, including fibrotic disorders, atherosclerosis and cancer [9], [12], [13]. Significantly, they are identified as indicators of poor prognosis in ovarian, breast and lung cancer [14], [15], [16]. DDR1 overexpression is associated wit
-
The termini of the substrate recognition
2020-07-31

The termini of the substrate recognition and catalytic modules are anchored to opposite sides of the scaffold so that they face each other. Within the substrate recognition module, the coactivators CDC20 and CDH1 have three domains: intrinsically disordered N- and C-terminal regions containing so-ca
-
We also extended our observations
2020-07-31

We also extended our observations with Ube2E1 to other members of Ube2E class of E2s to show that self-ubiquitination-mediated activity attenuation is preserved across the Ube2E family. Sequence analysis revealed that this chk1 inhibitor preservation is a consequence of perfectly conserved lysines
-
br Restenosis after angioplasty remains a remarkable
2020-07-31

Restenosis after angioplasty remains a remarkable challenge, although drug-eluting stents have reduced the incidence of restenosis considerably . Vascular smooth muscle CGS 35066 (VSMCs) play a pivotal role in the development of intimal thickening and restenosis. VSMCs proliferate and migrate fro
-
Ubiquitination is a reversible posttranslational modificatio
2020-07-31

Ubiquitination is a reversible posttranslational modification. The removal of Ub is carried out by enzymes known as deubiquitinases (DUBs). The antagonistic role played by these enzymes in the Ub pathway regulates the function of the ubiquitinated proteins, while maintaining the free Ub pool in euka
-
Tamoxifen was approved by the US Food and Drug Administratio
2020-07-31

Tamoxifen was approved by the US Food and Drug Administration in 1977 (Del Re et al., 2012) and it has been used as an agent of choice in the treatment of hormone responsive breast tumors for over four decades. Furthermore, this drug is prescribed as a chemo-preventive agent for high-risk women who
-
DGK type II DGK has a separated catalytic domain
2020-07-31

DGKη1 (type II DGK) has a separated catalytic domain [10], [13], whereas the domains of DGKα, ε and ζ are not split [1], [2], [3], [4], [5]. Therefore, the structural difference may cause the distinct affinity for DG among these isozymes. Because other type II DGKs (η2, δ1, δ2 and κ) also have the s
-
On the basis of the SAR findings a phenyl
2020-07-31

On the basis of the SAR1 findings, a phenyl group or heteroaromatic ring was necessary for the activity, which is supported by the existence of a π-π interaction between the aromatic moiety and His-160 in the Docking model. The different substituents at para- or meta-position modulate the CK2 inhibi
16009 records 801/1068 page Previous Next First page 上5页 801802803804805 下5页 Last page