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The PDZ domains of DLG interact with
2024-04-24
The PDZ domains of DLG interact with tumor suppressor proteins, APC and PTEN, as well as with several viral oncoproteins such as the E6 protein present in oncogenic human papillomavirus (reviewed in [177]). It has been reported that overexpression of DLG in fibroblasts impairs the events in the G0/G
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carnitine palmitoyltransferase Interestingly metabolic dysfu
2024-04-24
Interestingly, metabolic dysfunction is also observed in amyotrophic lateral sclerosis (ALS). Patients and mouse models of familial ALS exhibit higher levels of resting carnitine palmitoyltransferase expenditure and lower fat-free mass, indicating a hypermetabolic phenotype. Lim et al. (2012) found
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The expanding catalog of glutamate receptor auxiliary subuni
2024-04-24
The expanding catalog of glutamate receptor auxiliary subunits and associated transmembrane proteins underscores the importance and complexity of the receptor complexes. Whereas the interactions described here specifically control AMPARs, distinct auxiliary subunits, Neto-1/2, modulate neuronal kain
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In this study using pure
2024-04-24
In this study, using pure enzyme preparations of human placental recombinant AR (hAR) and of AR isolated from bovine lens (bAR), which behave as Michaelis Milrinone with glyceraldehyde as substrate, is shown that an apparent negative cooperativity action for glucose still occurs. We present evidenc
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Differentiation of skeletal myoblasts is
2024-04-24
Differentiation of skeletal myoblasts is a tightly orchestrated process that involves myoblast proliferation, hexokinase inhibitor withdrawal, expression of muscle-specific genes, and fusion into multinucleated myofibers (Horsley and Pavlath, 2004; Krauss, 2010). The maintenance of muscle mass is im
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dhfr inhibitor br Theoretical mechanism of ABCA activity in
2024-04-24
Theoretical mechanism of ABCA2 activity in LE/LY in modulation of cholesterol trafficking It is important to confirm that ABCA2 is a lipid transporter and identify the substrates that are mechanistic in its cholesterol sequestering activity. We hypothesize that ABCA2 modulates cholesterol seques
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We now present a series of
2024-04-24
We now present a series of findings obtained in heterologous expression systems, brain slices, and living animals that suggest that any interaction between mGlu7 and α1-adrenergic receptors exists, is specific, and is physiologically and behaviourally relevant. Materials and methods Norepinephri
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br Conclusion br Conflict of Interest br Author Contribution
2024-04-24
Conclusion Conflict of Interest Author Contributions Acknowledgements This work was supported by a research grant (SR/50/AS-14/2012) from the Department of Science and Technology, New Delhi, India to CMC and CSIR Senior Research Fellowship (09/013(0339)/2010-EMR-I) to SB. Introduction
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The activation of the A BR subtype
2024-04-24
The activation of the A2BR subtype triggers different intracellular metabolic pathways, often linked to the activation of adenylyl cyclase and increased levels of intracellular cAMP (Lynge et al., 2003, Bernareggi et al., 2015). The nAChR-channel brompheniramine maleate receptor mediated by the cAM
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br Introduction Epilepsy is characterized by
2024-04-24
Introduction Epilepsy is characterized by spontaneous recurrent seizures and represents one of the most frequent neurological diseases affecting about 60 million people worldwide (McNamara, 1999). It is estimated that up to 50% of all cases are triggered by “initial precipitating injuries”, such
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br Conflict of interest br
2024-04-24
Conflict of interest Financial support Acknowledgments This work was supported by the Japanese Millennium project. We thank all members of the Center for Genomic Medicine of RIKEN and Dainippon-Sumitomo Pharma Co., Ltd. for supporting this study. We are also grateful to members of the Hiros
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Our initial approach to identify hits
2024-04-24
Our initial approach to identify hits was two-pronged and included a high-throughput screening (HTS) campaign of the OSI 3-Deazaneplanocin library as well as a virtual screening (VS) campaign, utilizing a publically available crystal structure of ACK1 (PDB code: ). A tolerance for protein flexibili
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The discovery of acetylsalicylic acid aspirin in
2024-04-24
The discovery of acetylsalicylic sorafenib tosylate (aspirin) in 1897 paved the way for the development of classical NSAIDs as first-line therapeutics for anti-inflammatory, anti-pyretic and analgesic therapy. Large efforts have been made in the following decades to improve the efficacy and in part
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br Funding This work was supported by
2024-04-24
Funding This work was supported by Arena Pharmaceuticals, Inc, San Diego, CA, USA. Introduction 5-hydroxytryptamine 1B (5-HT1B) receptors are widely distributed in the central nervous system (CNS); they have various modulatory functions in drug reinforcement, appetitive behaviors, stress, moo
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MOG (35-55) During the year study period of men in the
2024-04-24
During the 4-year study period, 19.9% of men in the dutasteride group developed prostate cancer as compared to 25.1% in the placebo group, which represents an absolute risk MOG (35-55) of 5.1% for men taking dutasteride (Pe weighed against the prospect of undesirable sexual side effects and decreas
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