نتایج جستجو برای: abetalipoproteinemia

تعداد نتایج: 433  

Journal: :Physiology & behavior 1984
F Borsini E T Rolls

First, it was confirmed that bilateral lesions in the basolateral region of the amygdala (ABL) of the rat increased the time spent eating novel as compared to familiar food in a food preference test, and that the lesions impaired learned taste aversion to a sucrose solution which had been paired with lithium chloride. Then the roles of noradrenaline and serotonin in the amygdala in these aspect...

Journal: :The Journal of Cell Biology 1997
David M. Farschon Clément Couture Tomas Mustelin Donald D. Newmeyer

We have begun to explore the mechanisms of apoptosis using a cell-free system based on extracts from Xenopus eggs. Nuclei assembled or placed in these extracts undergo the morphological changes typical of apoptosis and eventually disintegrate. We used this system to investigate the potential involvement in apoptosis of proteins containing Src homology 2 (SH2) domains, which are known to interac...

Journal: :Neuron 2005
Michael P. Saddoris Michela Gallagher Geoffrey Schoenbaum

Certain goal-directed behaviors depend upon interactions between basolateral amygdala (ABL) and orbitofrontal cortex (OFC). Here we describe neurophysiological evidence of this cooperative function. We recorded from ABL in intact and OFC-lesioned rats during learning of odor discrimination problems and reversals. During learning, rats with ipsilateral OFC lesions exhibited a marked decline in t...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2009
Roxana E Iacob Teodora Pene-Dumitrescu Jianming Zhang Nathanael S Gray Thomas E Smithgall John R Engen

Protein dynamics are inextricably linked to protein function but there are few techniques that allow protein dynamics to be conveniently interrogated. For example, mutations and translocations give rise to aberrant proteins such as Bcr-Abl where changes in protein conformation and dynamics are believed to result in deregulated kinase activity that provides the oncogenic signal in chronic myelog...

2012
Igor A. Kozlov Elliot R. Thomsen Sarah E. Munchel Patricia Villegas Petr Capek Austin J. Gower Stephanie J. K. Pond Eugene Chudin Mark S. Chee

We report a scalable and cost-effective technology for generating and screening high-complexity customizable peptide sets. The peptides are made as peptide-cDNA fusions by in vitro transcription/translation from pools of DNA templates generated by microarray-based synthesis. This approach enables large custom sets of peptides to be designed in silico, manufactured cost-effectively in parallel, ...

Journal: :Biochimica et biophysica acta 2010
Doriano Fabbro Paul W Manley Wolfgang Jahnke Janis Liebetanz Alexandra Szyttenholm Gabriele Fendrich Andre Strauss Jianming Zhang Nathanael S Gray Francisco Adrian Markus Warmuth Xavier Pelle Robert Grotzfeld Frederic Berst Andreas Marzinzik Sandra W Cowan-Jacob Pascal Furet Jürgen Mestan

The ATP-competitive inhibitors dasatinib and nilotinib, which bind to catalytically different conformations of the Abl kinase domain, have recently been approved for the treatment of imatinib-resistant CML. These two new drugs, albeit very efficient against most of the imatinib-resistant mutants of Bcr-Abl, fail to effectively suppress the Bcr-Abl activity of the T315I (or gatekeeper) mutation....

Journal: :Blood 1989
C M Redman T Huima E Robbins S Lee W L Marsh

The rare McLeod blood group phenotype is characterized by weak Kell antigens, lack of the common Kx antigen, and acanthocytic morphology. Previous studies that did not detect membrane or cytoskeletal protein abnormalities suggested a lipid disturbance. In normal red cells, dimyristoyl phosphatidylserine (DMPS) is transported across the membrane by an enzymatic process and accumulates in the inn...

Journal: :Cancer cell 2011
Leisl M Packer Sareena Rana Robert Hayward Thomas O'Hare Christopher A Eide Ana Rebocho Sonja Heidorn Matthew S Zabriskie Ion Niculescu-Duvaz Brian J Druker Caroline Springer Richard Marais

We show that imatinib, nilotinib, and dasatinib possess weak off-target activity against RAF and, therefore, drive paradoxical activation of BRAF and CRAF in a RAS-dependent manner. Critically, because RAS is activated by BCR-ABL, in drug-resistant chronic myeloid leukemia (CML) cells, RAS activity persists in the presence of these drugs, driving paradoxical activation of BRAF, CRAF, MEK, and E...

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