Molecular basis of opsonic defect in immunodeficient children

M. Sumiya, P Tabona, T Arai, +4

The Lancet

Primary ImmunodeficiencyAutoimmune DiseaseImmunodeficienciesPathogenesisImmunology +5

High frequencies in African and non-African populations of independent mutations in the mannose binding protein gene

Richard Lipscombe, M. Sumiya, Adrian V. S. Hill, +4

Human Molecular Genetics

GeneticsGlycobiologyMolecular BiologyMolecular GeneticsGenomics +18

Association of variants of the gene for mannose-binding lectin with susceptibility to meningococcal disease

Martin L. Hibberd, M. Sumiya, John A. Summerfield, +2

The Lancet

Meningococcal DiseasePathogenesisImmunologyMannose-binding LectinMicrobiology +2

Mannose binding protein gene mutations associated with unusual and severe infections in adults

John A. Summerfield, Stephen Ryder, M. Sumiya, +4

The Lancet

Medical MicrobiologySevere InfectionsPathogenesisImmunologyPathogen Characterization +6

Distinct physicochemical characteristics of human mannose binding protein expressed by individuals of differing genotype.

Richard Lipscombe, M. Sumiya, John A. Summerfield, +1

PubMed

GlycobiologyImmunologyMolecular BiologyProtein GeneticsProtein Expression +14

Mutation of gene for mannose-binding protein associated with chronic hepatitis B viral infection

Thomas Hc, Graham R. Foster, M. Sumiya, +4

The Lancet

Molecular VirologyViral PersistenceViral HepatitisPathogenesisImmunology +7

Mutations in the HumanMannose-Binding Protein Gene:Frequencies in Several PopulationGroups

Richard Lipscombe, David Beatty, Mary Ganczakowski, +7

European Journal of Human Genetics

Recurrent miscarriage and variant alleles of mannose binding lectin, tumour necrosis factor and lymphotoxin<i>α</i>genes

Nancy N. Baxter, M. Sumiya, S Cheng, +3

Clinical & Experimental Immunology

Molecular genetics of a receptor protein for D-xylose, encoded by the gene xylF, in Escherichia coli.

M. Sumiya, E. O. Davis, Leonard C. Packman, +2

PubMed

EngineeringGeneticsMolecular BiologyEscherichia ColiXylose Transport Activity +20

Identical point mutation leading to low levels of mannose binding protein and poor C3b mediated opsonisation in Chinese and Caucasian populations

Richard Lipscombe, YL Lau, R J Levinsky, +3

Immunology Letters

Allelic VariantGenetic DisorderNatural SciencesGeneticsHuman Polymorphism +9