نتایج جستجو برای: 1103؟ ق.

تعداد نتایج: 3540  

2004
İlyas Eker

حي ت يو جذومنلأا ىلع يطخلا ريغ أ ،ءاملا ةمدص رث جاوملأاو يلاقتنلاا ه ، ةفاضإ ىلإ ضيف ءا ملا . مب ا نمق ه تءافآو ما ظنلا ة ناتم ة ساردلو أ ة شقان تاز يمملاو تابارط ضلاا ر ث (Parameters) ملا ر يغت ة بُ لطتيو ، مُيم صت ةَ فرعم ما ظنلا اذ ه ي ف ر يغتلا ىد م هذ ه مي ق تازيمملا . ةُقيرط تمدخُتسا دقو H ∞ يف دودحلا ةد يدع ميمصتلا . تا نارتقلاا را بتخا م ت ا مآ لا ة يكيمانيدلا ة ننقملا مكحت لل ة بولطملا ...

2007
Turhan Canli Klaus-Peter Lesch

The gene encoding the serotonin transporter (5-HTT) contains a regulatory variation that has been associated with anxiety-related traits and susceptibility for depression. Here we highlight recent discoveries related to allelic variation of 5-HTT function with respect to emotion regulation and social behavior, drawing from an interdisciplinary perspective of behavioral genetics and cognitive ne...

2013
Xiaoyan Qin Lynn M. Teesch Michael W. Duffel

The human cytosolic sulfotransferase hSULT2A1 catalyzes the sulfation of a broad range of xenobiotics, as well as endogenous hydroxysteroids and bile acids. Reversible modulation of the catalytic activity of this enzyme could play important roles in its physiologic functions. Whereas other mammalian sulfotransferases are known to be reversibly altered by changes in their redox environment, this...

2014

Esterases catalyze the hydrolysis of therapeutic drugs containing esters or amides in their structures. Human carboxylesterase (CES) and arylacetamide deacetylase (AADAC) are the major enzymes that catalyze the hydrolysis of drugs in the liver. Characterization of the enzyme(s) responsible for drug metabolism is required in drug development and to realize optimal drug therapy. Because multiple ...

2014

Esterases catalyze the hydrolysis of therapeutic drugs containing esters or amides in their structures. Human carboxylesterase (CES) and arylacetamide deacetylase (AADAC) are the major enzymes that catalyze the hydrolysis of drugs in the liver. Characterization of the enzyme(s) responsible for drug metabolism is required in drug development and to realize optimal drug therapy. Because multiple ...

2017
Vanessa Porrini Ilenia Sarnico Marina Benarese Caterina Branca Mariana Mota Annamaria Lanzillotta Arianna Bellucci Edoardo Parrella Lara Faggi Pierfranco Spano Bruno Pietro Imbimbo Marina Pizzi

CSP-1103 (formerly CHF5074) has been shown to reverse memory impairment and reduce amyloid plaque as well as inflammatory microglia activation in preclinical models of Alzheimer's disease. Moreover, it was found to improve cognition and reduce brain inflammation in patients with mild cognitive impairment. Recent evidence suggests that CSP-1103 acts through a single molecular target, the amyloid...

2015
Miyeon Jue Cheol-Woon Kim Seoung-Hun Kang Hansub Yoon Dongsoo Jang Young-Kyun Kwon Chinkyo Kim

Epitaxial lateral overgrowth in tandem with the first-principles calculation was employed to investigate the determining factor of a preferred orientation of GaN on SiO2-patterned m-plane sapphire substrates. We found that the (1100)-orientation is favored over the (1103)-orientation in the region with a small filling factor of SiO2, while the latter orientation becomes preferred in the region ...

2014

Esterases catalyze the hydrolysis of therapeutic drugs containing esters or amides in their structures. Human carboxylesterase (CES) and arylacetamide deacetylase (AADAC) are the major enzymes that catalyze the hydrolysis of drugs in the liver. Characterization of the enzyme(s) responsible for drug metabolism is required in drug development and to realize optimal drug therapy. Because multiple ...

2004
David J. Smith

. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1103 1. Components of Performance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1104 1.1 Factors Associated with Sport Performance . . . . . . . . . . . . . . ...

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