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https://www2.mrc-lmb.cam.ac.uk/groups/hmm/F-BAR_proteins/2009BARprogram.pdf20 May 2009: 11:00-11:25 Andrew Craig, Kingston, Canada 11:30-11:55 Richard Stanley, New York, USA 12:00-12:25 Presentation selected from the abstracts 12:45-14:00 Lunch -
318-320 News Feat Curves MH.indd
https://www2.mrc-lmb.cam.ac.uk/groups/hmm/publica/Papers/NatureAheadCurve.pdf17 Jul 2009: The pictures came from an experiment carried out by Kohji Takei, De Camilli’s postdoc at Yale University in New Haven, Connecticut. ... The new helix “is a start to explaining why the Golgi has this beautiful architecture”, says Antonny. -
cell4855sup
https://www2.mrc-lmb.cam.ac.uk/groups/JYL/PDF/cell%202009%20dynamin%20supp.pdf20 Nov 2009: A new GTPase dimer was created by superimposing the BDLP domain onto the hGBP1 dimer (Ghosh et al., 2006) (see Fig. -
Science Magazine
https://www2.mrc-lmb.cam.ac.uk/groups/JYL/PDF/Salje%20et%20al%20Science%202009%20N&V.pdf23 Jan 2009: Unfortunately, although these advances. have opened a completely new window into. ... These findings point the way toward new. questions and opportunities. It is unclear, for. -
DOI: 10.1126/science.1164346 , 509 (2009); 323Science et al.Jeanne…
https://www2.mrc-lmb.cam.ac.uk/groups/JYL/PDF/Salje%20et%20al%20Science%202009.pdf23 Jan 2009: The title. CopyrightAmerican Association for the Advancement of Science, 1200 New York Avenue NW, Washington, DC 20005. ... 2Department of Biochemistryand Molecular Biophysics, Columbia University, and HowardHughes Medical Institute, New York, NY 10032, -
The MORPHEUS protein crystallization screen
https://www2.mrc-lmb.cam.ac.uk/groups/JYL/PDF/morpheus%202009.pdf12 Nov 2009: LMB). The concept integrates several innovative approaches,such as chemically compatible mixes of potential ligands, new buffer systems andprecipitant mixes that also act as cryoprotectants. ... Both assumptions were a driving force behind my attemptsto -
doi:10.1016/j.tibs.2009.03.001
https://www2.mrc-lmb.cam.ac.uk/groups/hegde/download/58_Chakrabarti_O_TIBS_2009.pdf13 Jun 2009: Recent advances in our understanding of normalPrP biosynthesis and degradation might have unexpect-edly shed new light on this complex problem. ... Cell 93, 337–3484 Wickner, R.B. et al. (2004) Prion genetics: new rules for a new kind of. -
Structure of a Bacterial Dynamin-like Protein Lipid Tube Provides a…
https://www2.mrc-lmb.cam.ac.uk/groups/JYL/PDF/cell%202009%20dynamin.pdf19 Dec 2009: body, so slight movements indicated by the new density. have not been adjusted. -
ARTICLES ; The structural basis of tail-anchoredmembrane protein…
https://www2.mrc-lmb.cam.ac.uk/groups/hegde/download/61_Mateja_A_Nature_2009.pdf3 Aug 2009: Subsequently, Get3 revertstowards the open dimer state, lowering its affinity for the Get1/2receptor, and returning it to the cytosol to initiate a new round oftargeting. ... PHENIX: building new software for automated crystallographicstructure -
Molecular Biology of the CellVol. 19, 5093–5103, December 2008 ...
https://www2.mrc-lmb.cam.ac.uk/groups/hmm/publica/Papers/LynchMBC5093.pdf24 Jan 2009: Molecular Biology of the CellVol. 19, 5093–5103, December 2008. Synaptotagmin-1 Utilizes Membrane Bending and SNAREBinding to Drive Fusion Pore ExpansionKara L. Lynch, Roy R.L. Gerona, Dana M. Kielar, Sascha Martens,†Harvey T. McMahon,† and -
Functional Depletion of Mahogunin by Cytosolically Exposed Prion…
https://www2.mrc-lmb.cam.ac.uk/groups/hegde/download/59_Chakrabarti_O_Cell_2009.pdf13 Jun 2009: of diseases associated with aberrant PrP metabolism. These findings provide a qualitatively new direction for. -
ppat.1000479 1..19
https://www2.mrc-lmb.cam.ac.uk/groups/hegde/download/60_Ashok_A_PLoS_Path_2009.pdf20 Jun 2009: Selective Processing and Metabolism of Disease-CausingMutant Prion ProteinsAarthi Ashok, Ramanujan S. Hegde. Cell Biology and Metabolism Program, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of -
ANRV378-BI78-31.tex
https://www2.mrc-lmb.cam.ac.uk/groups/hmm/publica/DohertyMcMahonAnnRevBiochem09.pdf27 Apr 2009: However, it should be notedat this stage that using methods that inhibitCME as tools to discover new constitutive up-take pathways (that ordinarily exist and that areprevalent) is far from ideal
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