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20 Mar 2018: The corresponding val-ues for ParM and AlfA are 746 and 808 Å.

1 Nov 2018: 806 hlpArr[3] = pow( this->_so3InvCoeffs[newIter][0], 2.0 ) pow( this->_so3InvCoeffs[newIter][1], 2.0 );. 807 if ( hlpArr[3] > tmpVal ) { breakPeak = true; break; }. 808 hlpInterp[0] = hlpArr[0];

31 Oct 2005: 01Eichler(Hedge)

453:797-808. 2006. Kang, S. W.,. Rane, N. S., Kim, S. J., Garrison, J.

t},"")},!1)))}(window,document); / ]]> / </script> https://www2.mrc-lmb.cam.ac.uk/wordpress/wp-content/uploads/LMB365_TwoColour.jpg 1325 808 The LMB’s first, purpose built laboratory was officially handed

22 Jul 2008: Structure. Article. Single Copies of Sec61 and TRAP Associatewith a Nontranslating Mammalian RibosomeJean-François Ménétret,1 Ramanujan S. Hegde,2 Mike Aguiar,3 Steven P. Gygi,3 Eunyong Park,3 Tom A. Rapoport,3,4,and Christopher W.

2 Aug 2010: Helix αC 808–827 811–830 785–804 839–858. Hinge Val851 , Glu849 Val854 , Glu852 Val828 , Glu826 Val882 , Glu880.

1 Aug 2010: Structure of the signal recognition particle interacting with theelongation-arrested ribosome. Nature 427, 808–814 (2004).

14 Jun 2007: Many plasma-membrane proteins are in a constant flux throughout the internal trafficking pathways of the cell. Some receptors, such as that for transferrin, are continuously internalized into recycling endosomes and returned to the cell surface.

12 Jun 2020: For correspondence:. rhegde@mrc-lmb.cam.ac.uk. †These authors contributed. equally to this work. Competing interest: See. page 25. Funding: See page 25. Received: 15 April 2020. Accepted: 26 May 2020. Published: 27 May 2020. Reviewing editor: