نتایج جستجو برای: مدل l meb
تعداد نتایج: 736688 فیلتر نتایج به سال:
The two ion pairs [(4,7-Me(2)indenyl)(2)ZrMe](+)[MeB(C(6)F(5))(3)](-) (1 b) and [(indenyl)(2)ZrMe](+) [MeB(C(6)F(5))(3)](-) (2 b) have been generated in situ by reaction of stoichiometric B(C(6)F(5))(3) with the corresponding dimethyl zirconocenes. It has been shown that molecular mechanics computations, guided by experimental (1)H/(1)H NOE correlations, can provide information on the conformer...
This assessment report is published by the MEB pursuant Article 21 (3) and (4) of Directive 2001/83/EC. The report comments on the registration dossier that was submitted to the MEB and its fellow –organisations in all concerned EU member states. It reflects the scientific conclusion reached by the MEB and all concerned member states at the end of the evaluation process and provides a summary o...
In this paper we study a new variant of the Minimum Energy Broadcast (MEB) problem, namely the Probabilistic MEB (PMEB). The objective of the classic MEB problem is to assign transmission powers to the nodes of a wireless network is such a way that the total energy dissipated on the network is minimized, while a connected broadcasting structure is guaranteed by the assigned transmission powers....
Protein O-mannose beta1,2-N-acetyglucosaminyltransferase 1 (POMGnT1) is an enzyme involved in the synthesis of O-mannosyl glycans. Mutations of POMGnT1 in humans result in the muscle-eye-brain (MEB) disease. In this study, we have characterized a null mutation generated by gene trapping with a retroviral vector inserted into the second exon of the mouse POMGnT1 locus. Expression of POMGnT1 mRNA...
In this paper, we address the minimum energy broadcast (MEB) problem in wireless ad-hoc networks (WANETs). The researches in WANETs have attracted significant attentions, and one of the most critical issues in WSNs is minimization of energy consumption. In WANETs the packets have to be transported from a given source node to all other nodes in the network, and the objective of the MEB problem i...
Muscle-Eye-Brain disease (MEB) is a disorder with an autosomal recessive inheritance characterised by congenital muscle dystrophy, eye and brain abnormalities (Cormand et al., 1999). The onset is usually in the first 6 months of life. MEB presents with marked delay in development resulting in severe or profound learning disability, epilepsy, hypotonia and muscular contractures. A high prominent...
Fukuyama-type congenital muscular dystrophy (FCMD), Walker-Warburg syndrome (WWS), and muscle-eye-brain (MEB) disease are clinically similar autosomal recessive disorders characterized by congenital muscular dystrophy, lissencephaly, and eye anomalies. We identified the gene for FCMD and MEB, which encodes the fukutin protein and the protein O-linked mannose β1, 2-N-acetylglucosaminyltransferas...
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