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The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|January 29, 2000
Structured long-range connections can provide a scaffold for orientation mapsH Z Shouval, D H Goldberg, J P Jones, et al.
Human Mutation|December 24, 2002
Meta-analysis of indels causing human genetic disease: mechanisms of mutagenesis and the role of local DNA sequence complexityNadia A Chuzhanova, Emmanuel J Anassis, Edward V Ball, et al.
Gene|September 7, 2000
Promoter shuffling has occurred during the evolution of the vertebrate growth hormone geneN A Chuzhanova, M Krawczak, L A Nemytikova, et al.
Learning & Memory (Cold Spring Harbor, N.Y.)|July 20, 2005
A model of bidirectional synaptic plasticity: from signaling network to channel conductanceGastone C Castellani, Elizabeth M Quinlan, Ferdinando Bersani, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|August 1, 1993
A novel point mutation (Val 297-->Met) in the serine proteinase domain of protein C in a patient with both venous and arterial thromboembolic diseaseD S Millar, A I Wacey, J Voke, et al.
Current Hematologic Malignancy Reports|December 11, 2012
CARs in chronic lymphocytic leukemia -- ready to driveChitra Hosing, Partow Kebriaei, William Wierda, et al.
Injury Epidemiology|January 25, 2021
Impact of ICD-9-CM to ICD-10-CM coding transition on trauma hospitalization trends among young adults in 12 statesYuri V Sebastião, Gregory A Metzger, Deena J Chisolm, et al.
Acta Crystallographica. Section E, Structure Reports Online|January 24, 2014
N (1)-(Thio-phen-2-ylmeth-yl)-N (3),N (3)-bis-[3-(thio-phen-2-yl-methyl-ammonio)-prop-yl]propane-1,3-di-ammonium hexa-fluorido-silicate methanol tris-olvateSyed A Haque, Dominique N Cooper, Douglas R Powell, et al.
The Journal of Cardiovascular Surgery|July 1, 1987
Initial clinical experience with a more efficient hollow fiber oxygenator of unique designK E Karlson, R Massimino, A K Singh, et al.
Human Genomics|September 18, 2010
Methylation-mediated deamination of 5-methylcytosine appears to give rise to mutations causing human inherited disease in CpNpG trinucleotides, as well as in CpG dinucleotidesDavid N Cooper, Matthew Mort, Peter D Stenson, et al.
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