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Bioorganic & Medicinal Chemistry|October 13, 2001
Immobilisation on polystyrene of diazirine derivatives of mono- and disaccharides: biological activities of modified surfacesY Chevolot, J Martins, N Milosevic, et al.
Biomaterials|June 13, 2006
Chemistry and the biological response against immunoisolating alginate-polycation capsules of different compositionSara Ponce, Gorka Orive, Rosa Hernández, et al.
Travel Medicine and Infectious Disease|January 17, 2012
A model-based tool to predict the propagation of infectious disease via airportsGrace M Hwang, Paula J Mahoney, John H James, et al.
American Journal of Human Genetics|January 1, 1996
The gene responsible for a severe form of peripheral neuropathy and agenesis of the corpus callosum maps to chromosome 15qL K Casaubon, M Melanson, I Lopes-Cendes, et al.
Neurology|February 1, 1990
Tight linkage of creatine kinase (CKMM) to myotonic dystrophy on chromosome 19L H Yamaoka, M A Pericak-Vance, M C Speer, et al.
Social Science & Medicine (1982)|March 1, 1996
Alzheimer's disease: preliminary study of spatial distribution at birth placeH Jean, J F Emard, J P Thouez, et al.
Brain : a Journal of Neurology|May 5, 2006
A new autosomal recessive spastic ataxia associated with frequent white matter changes maps to 2q33-34I Thiffault, M F Rioux, M Tetreault, et al.
American Journal of Human Genetics|March 3, 1999
Location score and haplotype analyses of the locus for autosomal recessive spastic ataxia of Charlevoix-Saguenay, in chromosome region 13q11A Richter, J D Rioux, J P Bouchard, et al.
Nature Genetics|February 2, 2000
ARSACS, a spastic ataxia common in northeastern Québec, is caused by mutations in a new gene encoding an 11.5-kb ORFJ C Engert, P Bérubé, J Mercier, et al.
Frontiers in Tuberculosis|June 3, 2026
Dose optimization of inhaled tigecycline in humans to overcome inherent adverse events and maximize bacterial clearance using a physiologically-based pharmacokinetic modeling approachHyunseo Park, Amarinder Singh, Ashish Srivastava, et al.
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