Archives
- 2026-04
- 2026-03
- 2026-02
- 2026-01
- 2025-12
- 2025-11
- 2025-10
- 2025-09
- 2025-04
- 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
- 2023-07
- 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
- 2018-07
-
In addition to the receptor TGF also regulates the DDR
2020-07-28

In addition to the receptor, TGF-β1 also regulates the DDR1 ligand meaning the type I collagen and the enzyme involved in its maturation (LOXL2). We previously demonstrated that an increase of type I collagen concentration is associated with the presence of more linear invadosomes in L-703,664 succi
-
Bim is a pro apoptotic member
2020-07-28

Bim is a pro-apoptotic member of Bcl-2 family and has been found essential for ER stress-induced cell death in different types of glycine receptors in in vitro or in vivo studies. For example, thymocytes and macrophages from Bim-deficient mice are more resistant to ER stress caused cell death (Puth
-
In the inhibition study phenacetin O deethylation POD buprop
2020-07-28

In the inhibition study, phenacetin O-deethylation (POD), bupropion hydroxylation (BPOH), amodiaquine N-deethylation (AMND), diclofenac 4′-hydroxylation (DFOH), S-mephenytoin 4′-hydroxylation (SMOH), dextromethorphan O-demethylation (DMOD), and midazolam 1′-hydroxylation (MD1-OH) were selected as th
-
Listed in this section are several studies where
2020-07-28

Listed in this 5-alpha reductase inhibitors section are several studies where CRM1 inhibitors were used in combination with other cancer therapeutics and in drug-resistant/relapsed cancers. A table of current abstracts (Table 1) summarizes the latest findings in CRM1 combination therapies. In addit
-
The substrates carnitine L hydroxy N N N trimethylaminobutyr
2020-07-28

The substrates carnitine (L-3-hydroxy-4-N,N,N-trimethylaminobutyrate, C7H15NO3) and choline (2-hydroxy-N,N,N-trimethylethaneaminium, C5H14NO) are quite similar (Fig. 2). The major difference being the presence of a carboxyl unit in carnitine, and hence a quaternary carbon in position 3. Of the stere
-
Najafloo et al applied eSAFT HR
2020-07-28

Najafloo et al. [4] applied eSAFT-HR EoS to correlate the CO2 solubility in MDEA aqueous solutions in various conditions. In this work, 413 VLE data from different authors were utilized to model H2O + MDEA + CO2 system so that the overall overage absolute deviation (AAD) achieved was equal to 11.2.
-
Sex also influences COMT effects on cognition
2020-07-28

Sex also influences COMT effects on cognition. Women have 20%–30% less COMT activity than men (Chen et al., 2004, Fahndrich et al., 1980). Both Raz et al. (2011)O\'Hara et al. (2006) found that sex interacted with COMT genotype such that older men who had a Val allele showed greater negative effects
-
In summary the association of CK to tubulin and
2020-07-28

In summary, the association of CK1δ to α-tubulin and various proteins involved in mitosis points to a role of CK1δ in regulating key aspects of cell division and mitotic progression and by performing Michaelis–Menten kinetics we identified α-tubulin as the preferred interaction partner of CK1 isofor
-
To assess whether the described cooperation
2020-07-27

To assess whether the described cooperation between the EGFR and FGFR receptors was relevant at the clinical level, we determined the effect on progression-free survival of FGFR1 expression in patients with adenocarcinoma who were receiving erlotinib or gefitinib. As we had observed EGFR-FGFR1 coope
-
In line with findings reported for
2020-07-27

In line with findings reported for lipopolysaccharide activated macrophages [5] we have observed efficient secretion of 25-OHC into the cellular supernatant. In experiments analyzing free transfer of cholesterol or 25-OHC from erythrocytes and plasma, exchange of 25-OHC was found to occur about 2000
-
Genome wide screens to identify
2020-07-27

Genome-wide screens to identify host factors affecting TBSV RNA replication in yeast led to the identification of host genes known to be involved in various aspects of protein ubiquitination, such as BRE1, DOA4, RAD6, LGE1, UBP3 (Jiang et al., 2006, Panavas et al., 2005b, Serviene et al., 2005, Serv
-
infection CDI is typified by diarrhea intestinal
2020-07-27

infection (CDI) is typified by diarrhea, intestinal inflammation, and tissue damage, and in severe cases pseudomembranous colitis. Toxin-induced intestinal inflammation, a hallmark of CDI, is characterized by the production of proinflammatory cytokines/chemokines, neutrophil infiltration, and intest
-
fccp A series of monocarboxylated chalcones e g compounds
2020-07-27

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 fccp was not sensitive to
-
Mounting evidences show that the
2020-07-27

Mounting evidences show that the Quinidine glutamate metabolism plays an essential role in the pathophysiology of epilepsy. Administrating glutamate to experimental animals can contribute to seizure onset [3], by contrast, the symptom of seizures alleviated by coadministration of glutamate antagoni
-
Based on published reports and our own findings
2020-07-27

Based on published reports and our own findings, we propose to combine genetic inactivation with pharmacological inhibition in mechanistic studies because the selectivity of many commercially available inhibitors is often limited. Experiments with non-selective inhibitors easily lead to misleading c
14398 records 795/960 page Previous Next First page 上5页 791792793794795 下5页 Last page