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D Curtis

Showing results (431-440 of 561) with videos related to

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Annals of Human Genetics|October 11, 2001
Coeliac disease: follow-up linkage study provides further support for existence of a susceptibility locus on chromosome 11p11A L King, J S Fraser, S J Moodie, et al.
Neuropediatrics|February 1, 1994
Linkage analysis of idiopathic generalised epilepsy in families of probands with Juvenile Myoclonic Epilepsy and marker loci in the region of EPM 1 on chromosome 21 q: Unverricht-Lundborg disease and JME are not allelic variantsM Rees, D Curtis, K Parker, et al.
Archives of Disease in Childhood|September 1, 1988
Neonatal seizures: the Dublin Collaborative StudyP D Curtis, T G Matthews, T A Clarke, et al.
European Journal of Immunogenetics : Official Journal of the British Society for Histocompatibility and Immunogenetics|July 18, 2002
Analysis of candidate genes on chromosome 19 in coeliac disease: an association study of the KIR and LILR gene clustersS J Moodie, P J Norman, A L King, et al.
Human Molecular Genetics|April 1, 1993
A silent A to G mutation in exon 11 of the medium-chain acyl-CoA dehydrogenase (MCAD) geneB S Andresen, S Kølvraa, P Bross, et al.
Nature Communications|July 5, 2022
Spatial regulation of AMPK signaling revealed by a sensitive kinase activity reporterDanielle L Schmitt, Stephanie D Curtis, Anne C Lyons, et al.
Nature Medicine|May 4, 2010
Memory CD4+ T cells induce innate responses independently of pathogenTara M Strutt, K Kai McKinstry, John P Dibble, et al.
Cancer Letters|September 30, 1999
Macromolecular adduct formation and metabolism of heterocyclic amines in humans and rodents at low dosesK W Turteltaub, K H Dingley, K D Curtis, et al.
Human Mutation|January 1, 1992
Mutations in the medium chain acyl-CoA dehydrogenase (MCAD) geneK Tanaka, I Yokota, P M Coates, et al.
Neuroreport|December 29, 1995
Association between clozapine response and allelic variation in the 5-HT2C receptor geneM S Sodhi, M J Arranz, D Curtis, et al.
Pageof 57

Showing results (431-440 of 561) with videos related to

Sort By:
Pageof 57
Annals of Human Genetics|October 11, 2001
Coeliac disease: follow-up linkage study provides further support for existence of a susceptibility locus on chromosome 11p11A L King, J S Fraser, S J Moodie, et al.
Neuropediatrics|February 1, 1994
Linkage analysis of idiopathic generalised epilepsy in families of probands with Juvenile Myoclonic Epilepsy and marker loci in the region of EPM 1 on chromosome 21 q: Unverricht-Lundborg disease and JME are not allelic variantsM Rees, D Curtis, K Parker, et al.
Archives of Disease in Childhood|September 1, 1988
Neonatal seizures: the Dublin Collaborative StudyP D Curtis, T G Matthews, T A Clarke, et al.
European Journal of Immunogenetics : Official Journal of the British Society for Histocompatibility and Immunogenetics|July 18, 2002
Analysis of candidate genes on chromosome 19 in coeliac disease: an association study of the KIR and LILR gene clustersS J Moodie, P J Norman, A L King, et al.
Human Molecular Genetics|April 1, 1993
A silent A to G mutation in exon 11 of the medium-chain acyl-CoA dehydrogenase (MCAD) geneB S Andresen, S Kølvraa, P Bross, et al.
Nature Communications|July 5, 2022
Spatial regulation of AMPK signaling revealed by a sensitive kinase activity reporterDanielle L Schmitt, Stephanie D Curtis, Anne C Lyons, et al.
Nature Medicine|May 4, 2010
Memory CD4+ T cells induce innate responses independently of pathogenTara M Strutt, K Kai McKinstry, John P Dibble, et al.
Cancer Letters|September 30, 1999
Macromolecular adduct formation and metabolism of heterocyclic amines in humans and rodents at low dosesK W Turteltaub, K H Dingley, K D Curtis, et al.
Human Mutation|January 1, 1992
Mutations in the medium chain acyl-CoA dehydrogenase (MCAD) geneK Tanaka, I Yokota, P M Coates, et al.
Neuroreport|December 29, 1995
Association between clozapine response and allelic variation in the 5-HT2C receptor geneM S Sodhi, M J Arranz, D Curtis, et al.
Pageof 57