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S M Ring

Showing results (11-20 of 21) with videos related to

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Biochemical Society Transactions|October 10, 1998
Studies on the structure of a transmembrane region and a cytoplasmic loop of the human red cell anion exchanger (band 3, AE1)E J Chambers, D Askin, G B Bloomberg, et al.
Blood|January 15, 1995
Changes in the blood group Wright antigens are associated with a mutation at amino acid 658 in human erythrocyte band 3: a site of interaction between band 3 and glycophorin A under certain conditionsL J Bruce, S M Ring, D J Anstee, et al.
Thorax|September 1, 2010
Maternal Nrf2 and gluthathione-S-transferase polymorphisms do not modify associations of prenatal tobacco smoke exposure with asthma and lung function in school-aged childrenA J Henderson, R B Newson, M Rose-Zerilli, et al.
Transfusion Medicine (Oxford, England)|June 3, 1999
Glycophorin A mutation Ala65 --> Pro gives rise to a novel pair of MNS alleles ENEP (MNS39) and HAG (MNS41) and altered Wrb expression: direct evidence for GPA/band 3 interaction necessary for normal Wrb expressionJ Poole, J Banks, L J Bruce, et al.
Journal of Thrombosis and Haemostasis : JTH|August 30, 2008
Factor V Leiden is associated with pre-eclampsia but not with fetal growth restriction: a genetic association study and meta-analysisT Dudding, J Heron, A Thakkinstian, et al.
British Journal of Cancer|March 28, 2007
New germline mutations in the hypervariable minisatellite CEB1 in the parents of children with leukaemiaB G Davies, A Hussain, S M Ring, et al.
Biochimica Et Biophysica Acta|January 16, 1999
South-east asian ovalocytic (SAO) erythrocytes have a cold sensitive cation leak: implications for in vitro studies on stored SAO red cellsL J Bruce, S M Ring, K Ridgwell, et al.
Diabetologia|March 5, 2008
Association analysis of the IGF1 gene with childhood growth, IGF-1 concentrations and type 1 diabetesA Vella, N Bouatia-Naji, B Heude, et al.
Genes, Brain, and Behavior|February 28, 2014
Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairmentR Nudel, N H Simpson, G Baird, et al.
Genes, Brain, and Behavior|September 13, 2013
Genome-wide association study of shared components of reading disability and language impairmentJ D Eicher, N R Powers, L L Miller, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
Biochemical Society Transactions|October 10, 1998
Studies on the structure of a transmembrane region and a cytoplasmic loop of the human red cell anion exchanger (band 3, AE1)E J Chambers, D Askin, G B Bloomberg, et al.
Blood|January 15, 1995
Changes in the blood group Wright antigens are associated with a mutation at amino acid 658 in human erythrocyte band 3: a site of interaction between band 3 and glycophorin A under certain conditionsL J Bruce, S M Ring, D J Anstee, et al.
Thorax|September 1, 2010
Maternal Nrf2 and gluthathione-S-transferase polymorphisms do not modify associations of prenatal tobacco smoke exposure with asthma and lung function in school-aged childrenA J Henderson, R B Newson, M Rose-Zerilli, et al.
Transfusion Medicine (Oxford, England)|June 3, 1999
Glycophorin A mutation Ala65 --> Pro gives rise to a novel pair of MNS alleles ENEP (MNS39) and HAG (MNS41) and altered Wrb expression: direct evidence for GPA/band 3 interaction necessary for normal Wrb expressionJ Poole, J Banks, L J Bruce, et al.
Journal of Thrombosis and Haemostasis : JTH|August 30, 2008
Factor V Leiden is associated with pre-eclampsia but not with fetal growth restriction: a genetic association study and meta-analysisT Dudding, J Heron, A Thakkinstian, et al.
British Journal of Cancer|March 28, 2007
New germline mutations in the hypervariable minisatellite CEB1 in the parents of children with leukaemiaB G Davies, A Hussain, S M Ring, et al.
Biochimica Et Biophysica Acta|January 16, 1999
South-east asian ovalocytic (SAO) erythrocytes have a cold sensitive cation leak: implications for in vitro studies on stored SAO red cellsL J Bruce, S M Ring, K Ridgwell, et al.
Diabetologia|March 5, 2008
Association analysis of the IGF1 gene with childhood growth, IGF-1 concentrations and type 1 diabetesA Vella, N Bouatia-Naji, B Heude, et al.
Genes, Brain, and Behavior|February 28, 2014
Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairmentR Nudel, N H Simpson, G Baird, et al.
Genes, Brain, and Behavior|September 13, 2013
Genome-wide association study of shared components of reading disability and language impairmentJ D Eicher, N R Powers, L L Miller, et al.
Pageof 3