| scholarly article | Q13442814 |
| P6179 | Dimensions Publication ID | 1005420491 |
| P356 | DOI | 10.1038/SJ.GENE.6364116 |
| P698 | PubMed publication ID | 15306844 |
| P50 | author | James Taylor | Q42322786 |
| P2093 | author name string | Chanock SJ | |
| Foster CB | |||
| Yeager M | |||
| Bernig T | |||
| Staats B | |||
| P2860 | cites work | A second serine protease associated with mannan-binding lectin that activates complement | Q24311275 |
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| Complex signatures of natural selection at the Duffy blood group locus | Q24561910 | ||
| Active conservation of noncoding sequences revealed by three-way species comparisons | Q24623668 | ||
| Human microRNA genes are frequently located at fragile sites and genomic regions involved in cancers | Q24625794 | ||
| Genetics and the population history of Europe | Q24633591 | ||
| The human mannose-binding protein gene. Exon structure reveals its evolutionary relationship to a human pulmonary surfactant gene and localization to chromosome 10 | Q24681840 | ||
| A New Statistical Method for Haplotype Reconstruction from Population Data | Q27860495 | ||
| The structure of haplotype blocks in the human genome | Q27860500 | ||
| MEGA2: molecular evolutionary genetics analysis software | Q27860788 | ||
| MicroRNAs: genomics, biogenesis, mechanism, and function | Q27861070 | ||
| High frequencies in African and non-African populations of independent mutations in the mannose binding protein gene | Q28118760 | ||
| Intensely punctate meiotic recombination in the class II region of the major histocompatibility complex | Q28190352 | ||
| Mannose-binding lectin polymorphisms in clinical tuberculosis | Q28203157 | ||
| A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms | Q28203288 | ||
| On the number of segregating sites in genetical models without recombination | Q28206543 | ||
| Crossover clustering and rapid decay of linkage disequilibrium in the Xp/Yp pseudoautosomal gene SHOX | Q28207843 | ||
| The mannan-binding lectin pathway of complement activation: biology and disease association | Q28214987 | ||
| The human ortholog of rhesus mannose-binding protein-A gene is an expressed pseudogene that localizes to chromosome 10 | Q28264648 | ||
| Differential recognition of obligate anaerobic bacteria by human mannose-binding lectin | Q28367585 | ||
| Molecular determinants of oligomer formation and complement fixation in mannose-binding proteins | Q28575621 | ||
| Structure of human steroid 21-hydroxylase genes | Q28646488 | ||
| A comparison of bayesian methods for haplotype reconstruction from population genotype data | Q29547566 | ||
| VISTA : visualizing global DNA sequence alignments of arbitrary length | Q29614270 | ||
| DnaSP version 3: an integrated program for molecular population genetics and molecular evolution analysis | Q29615363 | ||
| Linkage disequilibrium in the human genome | Q29616097 | ||
| Evolution of the mammalian MHC: natural selection, recombination, and convergent evolution | Q33630613 | ||
| Association of mannose-binding lectin gene heterogeneity with severity of lung disease and survival in cystic fibrosis | Q33857510 | ||
| Determination of ancestral alleles for human single-nucleotide polymorphisms using high-density oligonucleotide arrays | Q33864868 | ||
| The 3' untranslated region of messenger RNA: A molecular 'hotspot' for pathology? | Q33903996 | ||
| Assessing the performance of the haplotype block model of linkage disequilibrium | Q33906300 | ||
| Adjusting the focus on human variation | Q33945651 | ||
| Mannan-binding lectin enhances susceptibility to visceral leishmaniasis | Q34008749 | ||
| Gene conversion and different population histories may explain the contrast between polymorphism and linkage disequilibrium levels | Q34020571 | ||
| Sequence variation and linkage disequilibrium in the human T-cell receptor beta (TCRB) locus | Q34044334 | ||
| Lower-than-expected linkage disequilibrium between tightly linked markers in humans suggests a role for gene conversion | Q34044608 | ||
| A dynamic programming algorithm for haplotype block partitioning | Q34063575 | ||
| Human genome sequence variation and the influence of gene history, mutation and recombination | Q34142742 | ||
| Linkage disequilibrium and allele-frequency distributions for 114 single-nucleotide polymorphisms in five populations | Q34146133 | ||
| Intense and highly localized gene conversion activity in human meiotic crossover hot spots | Q34287628 | ||
| Haplotype structure and population genetic inferences from nucleotide-sequence variation in human lipoprotein lipase | Q34386645 | ||
| Population genomics: a bridge from evolutionary history to genetic medicine | Q34416664 | ||
| Mannose-binding lectin gene polymorphisms are associated with major infection following allogeneic hemopoietic stem cell transplantation. | Q34621964 | ||
| Using genetic variation to study immunomodulation | Q34750497 | ||
| SNP500Cancer: a public resource for sequence validation and assay development for genetic variation in candidate genes | Q34922555 | ||
| Structural and functional aspects of complement activation by mannose-binding protein. | Q34978572 | ||
| AVID: A global alignment program | Q35023871 | ||
| SNP and haplotype variation in the human genome | Q35114507 | ||
| Anti-microbial activities of mannose-binding lectin | Q35187396 | ||
| Haplotype blocks and linkage disequilibrium in the human genome | Q35191477 | ||
| Patterns of Human Genetic Diversity: Implications for Human Evolutionary History and Disease | Q35550637 | ||
| Impact of mannose-binding lectin on susceptibility to infectious diseases. | Q35582450 | ||
| Haplotype and linkage disequilibrium architecture for human cancer-associated genes | Q35806728 | ||
| Association of mutations in mannose binding protein gene with childhood infection in consecutive hospital series | Q36244208 | ||
| Host defense molecule polymorphisms influence the risk for immune-mediated complications in chronic granulomatous disease | Q37388319 | ||
| Haplotype structure, LD blocks, and uneven recombination within the LRP5 gene. | Q40952708 | ||
| The collectins in innate immunity | Q41053677 | ||
| The Gly-54-->Asp allelic form of human mannose-binding protein (MBP) fails to bind MBP-associated serine protease | Q42160405 | ||
| Association of mannose-binding lectin gene variation with disease severity and infections in a population-based cohort of systemic lupus erythematosus patients. | Q43848180 | ||
| Mannan-binding lectin in the sub-Saharan HIV and tuberculosis epidemics | Q43953062 | ||
| Lack of mannose-binding lectin-A enhances survival in a mouse model of acute septic peritonitis | Q44149324 | ||
| Mannose-binding lectin plasma levels and gene polymorphisms in Plasmodium falciparum malaria | Q44164008 | ||
| Enhancement of complement activation and opsonophagocytosis by complexes of mannose-binding lectin with mannose-binding lectin-associated serine protease after binding to Staphylococcus aureus | Q44172221 | ||
| A comprehensive haplotype analysis of CYP19 and breast cancer risk: the Multiethnic Cohort | Q44307819 | ||
| Restricted polymorphism of the mannose-binding lectin gene of indigenous Australians | Q46733770 | ||
| Mannose-binding protein B allele confers protection against tuberculous meningitis | Q46869254 | ||
| DNA variability of human genes. | Q46876583 | ||
| Mutations in the human mannose-binding protein gene: frequencies in several population groups | Q46896178 | ||
| Defining haplotype blocks and tag single-nucleotide polymorphisms in the human genome | Q47313992 | ||
| Characterization of human serum mannan-binding protein promoter | Q47906897 | ||
| Sequence variation in the human angiotensin converting enzyme | Q47964948 | ||
| DNA sequence diversity in a 9.7-kb region of the human lipoprotein lipase gene | Q48036374 | ||
| Binding of mannan-binding protein to various bacterial pathogens of meningitis | Q50147158 | ||
| Disease-associated mutations in human mannose-binding lectin compromise oligomerization and activity of the final protein. | Q51829664 | ||
| Further evidence for role of a promoter variant in the TNFRSF6 gene in Alzheimer disease. | Q51951518 | ||
| Blocks of limited haplotype diversity revealed by high-resolution scanning of human chromosome 21. | Q52051237 | ||
| A new frequent allele is the missing link in the structural polymorphism of the human mannan-binding protein | Q56702159 | ||
| Chromosome-wide distribution of haplotype blocks and the role of recombination hot spots | Q56879657 | ||
| A first-generation linkage disequilibrium map of human chromosome 22 | Q56879659 | ||
| Juxtaposed regions of extensive and minimal linkage disequilibrium in human Xq25 and Xq28 | Q57232777 | ||
| Increased frequency of homozygosity of abnormal mannan-binding-protein alleles in patients with suspected immunodeficiency | Q63728163 | ||
| Molecular basis of opsonic defect in immunodeficient children | Q68303831 | ||
| Cytoplasmic regulation of mRNA function: The importance of the 3′ untranslated region | Q72088073 | ||
| Mannose binding protein gene mutations associated with unusual and severe infections in adults | Q72135612 | ||
| Mannose-binding lectin is a component of innate mucosal defense against Cryptosporidium parvum in AIDS | Q73130760 | ||
| Association of functional mutant homozygotes of the mannose binding protein gene with susceptibility to pulmonary tuberculosis in India | Q73488670 | ||
| Variation is the spice of life | Q73594237 | ||
| Evolution of introns and exons of class II major histocompatibility complex genes of vertebrates | Q73922623 | ||
| Differential binding of mannose-binding lectin to respiratory pathogens in cystic fibrosis | Q73923265 | ||
| Deficiency of mannose-binding lectin and burden of infection in children with malignancy: a prospective study | Q74446395 | ||
| Association between deficiency of mannose-binding lectin and severe infections after chemotherapy | Q74446408 | ||
| Direct measurement of the male recombination fraction in the human beta-globin hot spot | Q77584232 | ||
| Molecular Evolutionary Genetics | Q104203812 | ||
| P433 | issue | 6 | |
| P921 | main subject | heterozygosity | Q124059385 |
| P304 | page(s) | 461-476 | |
| P577 | publication date | 2004-09-01 | |
| P1433 | published in | Genes and Immunity | Q15745246 |
| P1476 | title | Sequence analysis of the mannose-binding lectin (MBL2) gene reveals a high degree of heterozygosity with evidence of selection | |
| P478 | volume | 5 |
| Q81318250 | An analysis of genetic variation across the MBL2 locus in Dutch Caucasians indicates that 3' haplotypes could modify circulating levels of mannose-binding lectin |
| Q38913656 | Association of a new mannose-binding lectin variant with severe malaria in Gabonese children |
| Q38320019 | Association of mannose-binding lectin gene (MBL2) polymorphisms with rheumatoid arthritis in an Indian cohort of case-control samples |
| Q36481104 | Challenges of SNP genotyping and genetic variation: its future role in diagnosis and treatment of cancer |
| Q30350759 | Effects of natural selection on interpopulation divergence at polymorphic sites in human protein-coding Loci |
| Q38335440 | Evolution of the mannose-binding lectin gene in primates. |
| Q92666194 | Exploring association between MBL2 gene polymorphisms and the occurrence of clinical blackwater fever through a case-control study in Congolese children |
| Q35330085 | Extreme high prevalence of a defective mannose-binding lectin (MBL2) genotype in native South American West Andean populations. |
| Q37642585 | From evolutionary genetics to human immunology: how selection shapes host defence genes |
| Q33401966 | Genetic and other factors determining mannose-binding lectin levels in American Indians: the Strong Heart Study |
| Q37144998 | Genetic polymorphisms of mannose-binding lectin do not influence placental malaria but are associated with preterm deliveries |
| Q33799136 | Genome-wide association study SNPs in the human genome diversity project populations: does selection affect unlinked SNPs with shared trait associations? |
| Q37209510 | Haplotype specific-sequencing reveals MBL2 association with asymptomatic Plasmodium falciparum infection |
| Q38164341 | If there is an evolutionary selection pressure for the high frequency of MBL2 polymorphisms, what is it? |
| Q36232275 | Increased plasma mannose binding lectin levels are associated with bronchiolitis obliterans after lung transplantation |
| Q37184715 | Independent effects of genetic variations in mannose-binding lectin influence the course of HIV disease: the advantage of heterozygosity for coding mutations |
| Q33359581 | Intriguing balancing selection on the intron 5 region of LMBR1 in human population |
| Q21090770 | Lectin-dependent enhancement of Ebola virus infection via soluble and transmembrane C-type lectin receptors |
| Q27486245 | MBL2and Hepatitis C Virus Infection among Injection Drug Users |
| Q35153921 | Mannose binding lectin and susceptibility to rheumatoid arthritis in Brazilian patients and their relatives. |
| Q34170265 | Mannose-binding lectin 2 polymorphisms do not influence frequency or type of infection in adults with chemotherapy induced neutropaenia |
| Q36361610 | Mannose-binding lectin and its genetic variants. |
| Q33577516 | Phylogenetic nomenclature and evolution of mannose-binding lectin (MBL2) haplotypes |
| Q27001032 | Population genetic tools for dissecting innate immunity in humans |
| Q25257137 | SNP500Cancer: a public resource for sequence validation, assay development, and frequency analysis for genetic variation in candidate genes |
| Q34393517 | Serum mannose-binding lectin concentration, but not genotype, is associated with Clostridium difficile infection recurrence: a prospective cohort study |
| Q34400153 | The MBL2 'LYQA secretor' haplotype is an independent predictor of postoperative myocardial infarction in whites undergoing coronary artery bypass graft surgery |
| Q57191722 | The Role of Complement Activating Collectins and Associated Serine Proteases in Patients With Hematological Malignancies, Receiving High-Dose Chemotherapy, and Autologous Hematopoietic Stem Cell Transplantations (Auto-HSCT) |
| Q61798413 | The association of mannose binding lectin genotype and immune response to Chlamydia pneumoniae: The Strong Heart Study |
| Q34991781 | The lectin pathway of complement and rheumatic heart disease. |
| Q27692121 | Toll-like receptors (TLRs) and mannan-binding lectin (MBL): on constant alert in a hostile environment |
| Q33939617 | Variant G57E of Mannose Binding Lectin Associated with Protection against Tuberculosis Caused by Mycobacterium africanum but not by M. tuberculosis |
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