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Immunology Letters|May 13, 2009
TH1/TH2 balance in concomitant immediate and delayed-type hypersensitivity diseasesLuane Marques de Mello, Monique Isabel Silveira Bechara, Dirceu Solé, et al.Comparative Medicine|April 25, 2009
The spatial learning phenotype of heterozygous leaner mice is robust to systematic variation of the housing environmentJoana M Marques, Isabel Alonso, Cristina Santos, et al.American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|September 27, 2005
Haplotype diversity and somatic instability in normal and expanded SCA8 allelesSandra Martins, Ana I Seixas, Paula Magalhães, et al.Waste Management & Research : the Journal of the International Solid Wastes and Public Cleansing Association, ISWA|October 18, 2008
Report: new guidelines for characterization of municipal solid waste: the Portuguese caseMaria da Graça Madeira Martinho, Ana Isabel Silveira, Elsa Maria Fernandes Duarte BrancoArchives of Neurology|April 23, 2003
Phenotypes of spinocerebellar ataxia type 6 and familial hemiplegic migraine caused by a unique CACNA1A missense mutation in patients from a large familyIsabel Alonso, José Barros, Assunção Tuna, et al.Neurobiology of Aging|May 22, 2007
Motor and cognitive deficits in the heterozygous leaner mouse, a Cav2.1 voltage-gated Ca2+ channel mutantIsabel Alonso, Joana M Marques, Nuno Sousa, et al.American Journal of Human Genetics|December 4, 2018
Detecting Expansions of Tandem Repeats in Cohorts Sequenced with Short-Read Sequencing DataRick M Tankard, Mark F Bennett, Peter Degorski, et al.F1000Research|June 28, 2018
Recent advances in the detection of repeat expansions with short-read next-generation sequencingMelanie Bahlo, Mark F Bennett, Peter Degorski, et al.Colloids and Surfaces. B, Biointerfaces|November 9, 2016
Characterization of polymeric nanoparticles for intravenous delivery: Focus on stabilityClaudia L Oliveira, Francisco Veiga, Carla Varela, et al.Epilepsia|February 22, 2023
Genes4Epilepsy: An epilepsy gene resourceKaren L Oliver, Ingrid E Scheffer, Mark F Bennett, et al.Pageof 9