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1. Full Text Mannose-binding lectin and mannose-binding protein-associated serine protease 2 levels and infection in very-low-birth-weight infants
by Hartz, Annika and Schreiter, Lena and Pagel, Julia and Moser, Katja and Wieg, Christian and Grotheer, Anneke and Rupp, Jan and Herting, Egbert and Göpel, Wolfgang and Härtel, Christoph
Pediatric Research, ISSN 0031-3998, 07/2018, Volume 84, Issue 1, pp. 134 - 138
OBJECTIVE: The aim of this study was to explore the role of the lectin pathway in neonatal sepsis through the study of MBL and MASP2 levels and their... 
IMMUNITY | COMPLEMENT | POLYMORPHISMS | PATHWAY | PEDIATRICS | SEPSIS | LARGE COHORT | CHILDREN | Genetic Predisposition to Disease | Mannose-Binding Lectin - blood | Premature Birth | Prospective Studies | Exons | Infant, Very Low Birth Weight | Humans | Genotype | Male | Gestational Age | Mannose-Binding Lectin - genetics | Sepsis - genetics | Mannose-Binding Protein-Associated Serine Proteases - analysis | Polymorphism, Genetic | Birth Weight | Mannose-Binding Protein-Associated Serine Proteases - genetics | Female | Polymorphism, Single Nucleotide | Sepsis - blood | Infant, Newborn | Sepsis | Infections | Birth weight
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2. Full Text Mannan‐binding lectin (MBL)‐associated serine protease‐1 (MASP‐1), a serine protease associated with humoral pattern‐recognition molecules: normal and acute‐phase levels in serum and stoichiometry of lectin pathway components
by Thiel, S and Jensen, L and Degn, S. E and Nielsen, H. J and Gál, P and Dobó, J and Jensenius, J. C
Clinical & Experimental Immunology, ISSN 0009-9104, 07/2012, Volume 169, Issue 1, pp. 38 - 48
Summary The pattern‐recognition molecules mannan‐binding lectin (MBL) and the three ficolins circulate in blood in complexes with MBL‐associated serine... 
innate immunity | complement | inflammation | lectin pathway | Innate immunity | Complement | Inflammation | Lectin pathway | ACTIVATION | MAP44 | 2ND | IMMUNOLOGY | COMPLEMENT-SYSTEM | H-FICOLIN | GENES | MUTATIONS | MAP19 | Immunoglobulin G - isolation & purification | Mannose-Binding Protein-Associated Serine Proteases - immunology | Blotting, Western - methods | Chromatography, Gel - methods | Mannose-Binding Lectin - blood | Complement Pathway, Mannose-Binding Lectin - immunology | Age Factors | Lectins - immunology | Rats, Wistar | Acute-Phase Reaction - immunology | Colorectal Neoplasms - blood | Humans | Rats | Infant | Mannose-Binding Protein-Associated Serine Proteases - analysis | Immunity, Innate - immunology | Animals | Acute-Phase Reaction - blood | Adult | C-Reactive Protein - analysis | Lectins - analysis | Infant, Newborn | Original
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3. Full Text Plasma levels of mannan‐binding lectin (MBL)‐associated serine proteases (MASPs) and MBL‐associated protein in cardio‐ and cerebrovascular diseases
by Frauenknecht, V and Thiel, S and Storm, L and Meier, N and Arnold, M and Schmid, J.‐P and Saner, H and Schroeder, V
Clinical & Experimental Immunology, ISSN 0009-9104, 07/2013, Volume 173, Issue 1, pp. 112 - 120
Summary Growing evidence suggests a prominent role of the complement system in the pathogenesis of cardio‐ and cerebrovascular diseases (CVD). Mannan‐binding... 
MAp44 | ischaemic stroke | MASP | coronary heart disease | complement system | Complement system | Coronary heart disease | Ischaemic stroke | PATTERN-RECOGNITION MOLECULES | MYOCARDIAL-INFARCTION | PROTECTION | ATHEROSCLEROSIS | IMMUNOLOGY | PATHWAY ACTIVATION | COMPLEMENT-SYSTEM | ACUTE ISCHEMIC-STROKE | FACTOR-XIII | COAGULATION | MUTATIONS | Diabetes Mellitus - blood | Myocardial Infarction - blood | Humans | Middle Aged | Male | Brain Ischemia - immunology | Myocardial Infarction - immunology | Hypertension - blood | Dyslipidemias - blood | Brain Ischemia - blood | Overweight - epidemiology | Female | Hypertension - epidemiology | Complement Pathway, Mannose-Binding Lectin | Severity of Illness Index | Coronary Disease - blood | Acute Disease | Coronary Disease - immunology | Enzyme-Linked Immunosorbent Assay | Smoking - blood | Risk Factors | Mannose-Binding Protein-Associated Serine Proteases - analysis | Pilot Projects | Dyslipidemias - epidemiology | Overweight - blood | Smoking - epidemiology | Diabetes Mellitus - epidemiology | Aged | Lectins | Plasma | Cardiovascular disease | Stroke | Animal models | Translational Studies
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4. Full Text Mannose-binding lectin and mannose-binding lectin–associated serine protease 2 in susceptibility, severity, and outcome of pneumonia in adults
by Garcia-Laorden, M. Isabel, BSc and Sole-Violan, Jordi, PhD and de Castro, Felipe Rodriguez, PhD and Aspa, Javier, PhD and Briones, M. Luisa, PhD and Garcia-Saavedra, Ayoze, BSc and Rajas, Olga, PhD and Blanquer, Jose, PhD and Caballero-Hidalgo, Araceli, BEc and Marcos-Ramos, J. Alberto, MD and Hernandez-Lopez, Javier, BSc and Rodriguez-Gallego, Carlos, PhD
Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2008, Volume 122, Issue 2, pp. 368 - 374.e2
Background Community-acquired pneumonia (CAP) is the leading cause of death from infection in developed countries. Mannose-binding lectin (MBL) and... 
Allergy and Immunology | primary immunodeficiency | Community-acquired pneumonia | sepsis | mannose-binding lectin | mannose-binding lectin–associated serine protease 2 | mannose-binding lectin-associated serine protease 2 | L-FICOLIN | INFLAMMATORY RESPONSE SYNDROME | MODULATING FACTOR | PHASE-I SAFETY | DEFICIENT MICE | IMMUNOLOGY | community-acquired pneumonia | INVASIVE PNEUMOCOCCAL INFECTION | ALLERGY | CANARY-ISLANDS | CLASSICAL PATHWAY | INNATE IMMUNITY | Mannose-Binding Lectin - physiology | Prospective Studies | Humans | Middle Aged | Male | Pneumonia, Bacterial - metabolism | Mannose-Binding Lectin - genetics | Case-Control Studies | Pneumonia, Pneumococcal - genetics | Pneumonia, Pneumococcal - physiopathology | Mannose-Binding Protein-Associated Serine Proteases - genetics | Adult | Female | Pneumonia, Bacterial - genetics | Pneumonia, Bacterial - physiopathology | Severity of Illness Index | Genetic Predisposition to Disease | Mannose-Binding Lectin - blood | Gene Frequency | Kaplan-Meier Estimate | Genotype | Mannose-Binding Protein-Associated Serine Proteases - deficiency | Mannose-Binding Protein-Associated Serine Proteases - analysis | Polymorphism, Genetic | Community-Acquired Infections - genetics | Pneumonia, Pneumococcal - metabolism | Alleles | Aged | Mannose-Binding Lectin - deficiency | Lectins | Pneumonia | Disease susceptibility | Proteases | Serine | Bacterial pneumonia | Chronic obstructive pulmonary disease | Respiratory distress syndrome | Drug therapy | Mortality
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5. Full Text Plasma levels of MASP‐1, MASP‐3 and MAp44 in patients with type 2 diabetes: influence of glycaemic control, body composition and polymorphisms in the MASP1 gene
by Krogh, S. S and Holt, C. B and Steffensen, R and Funck, K. L and Høyem, P and Laugesen, E and Poulsen, P. L and Thiel, S and Hansen, T. K
Clinical & Experimental Immunology, ISSN 0009-9104, 07/2017, Volume 189, Issue 1, pp. 103 - 112
Summary Mounting evidence indicates that adverse activation of the complement system plays a role in the development of diabetic vascular complications. Plasma... 
type 2 diabetes mellitus | mannan‐binding lectin‐associated serine proteases | complement | single nucleotide polymorphism | mannan-binding lectin-associated serine proteases | SYSTEM | MORTALITY | PROTEIN | COMPLEMENT ACTIVATION | IMMUNOLOGY | MANNAN-BINDING LECTIN | VASCULAR COMPLICATIONS | DISEASES | SERINE PROTEASES MASPS | PATHWAY | ASSOCIATION | Body Composition | Mannose-Binding Lectin - blood | Streptozocin | Humans | Mice, Inbred C57BL | Middle Aged | Blood Glucose | Genotype | Linear Models | Male | Case-Control Studies | Mannose-Binding Protein-Associated Serine Proteases - analysis | Diabetes Mellitus, Type 2 - blood | Animals | Diabetes Mellitus, Experimental | Mannose-Binding Protein-Associated Serine Proteases - genetics | Denmark | Female | Aged | Mice | Polymorphism, Single Nucleotide | Type 2 diabetes | Proteases | Analysis | Genes | Physiological aspects | Lectins | Genetic aspects | Single nucleotide polymorphisms | Protein binding | Diabetes therapy | Plasma | Serine | Sex | Activation | Complement | Single-nucleotide polymorphism | Assaying | Body composition | Mannan | Proteins | Body composition (biology) | Rodents | Mannose-binding lectin | Age | Binding | Complications | Diabetes mellitus | Patients | MASP-2 protein | Complement activation | Genotyping | Plasma levels | Diabetes | MASP-1 protein | Original
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6. Full Text Pentraxin 3, ficolin-2 and lectin pathway associated serine protease MASP-3 as early predictors of myocardial infarction - The HUNT2 study
by Vengen, Inga Thorsen and Enger, Tone Bull and Videm, Vibeke and Garred, Peter
Scientific Reports, ISSN 2045-2322, 02/2017, Volume 7, Issue 1, p. 43045
The lectin complement pathway is suggested to play a role in atherogenesis. Pentraxin-3 (PTX3), ficolin-1, ficolin-2, ficolin-3,... 
SYSTEM | COMPLEMENT ACTIVATION | MARKER | INFLAMMATION | MBL | MULTIDISCIPLINARY SCIENCES | CARDIOVASCULAR-DISEASE | ATHEROSCLEROSIS | PTX3 | PREVALENCE | DEFICIENCY | Myocardial Infarction - diagnosis | Myocardial Infarction - blood | Prognosis | Humans | Middle Aged | Male | Inflammation | Biomarkers - blood | Myocardial Infarction - metabolism | Case-Control Studies | Serum Amyloid P-Component - analysis | Mannose-Binding Protein-Associated Serine Proteases - analysis | Lectins - blood | Adult | Female | C-Reactive Protein - analysis | Complement Pathway, Mannose-Binding Lectin | Cohort Studies | Myocardial infarction | Serum levels | Atherogenesis | Complement activation | Heart attacks | Serine | Lectins | Serine proteinase | Health risk assessment | Risk factors | Pentraxins
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7. Full Text Low MBL‐associated serine protease 2 (MASP‐2) levels correlate with urogenital schistosomiasis in Nigerian children
by Ojurongbe, Olusola and Antony, Justin S and Van Tong, Hoang and Meyer, Christian G and Akindele, Akeem A and Sina‐Agbaje, Olawumi R and Kremsner, Peter G and Velavan, Thirumalaisamy P
Tropical Medicine & International Health, ISSN 1360-2276, 10/2015, Volume 20, Issue 10, pp. 1311 - 1319
Objectives The human mannose‐binding lectin (MBL) and ficolins (FCN) are involved in pathogen recognition in the first line of defence. They support activation... 
haplotipos | genotypes | esquistosomiasis | genotipos | MASP‐2 | Schistosomiasis | schistosomiase | haplotypes | complemento | complément | MBL | génotypes | complement | Haplotypes | Complement | MASP-2 | Genotypes | COMPLEMENT ACTIVATION | SUSCEPTIBILITY | MANSONI | GENE POLYMORPHISM | TROPICAL MEDICINE | MANNAN-BINDING LECTIN | SURFACE GLYCOPROTEINS | PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH | PATHWAY | NEGLECTED TROPICAL DISEASES | INFECTION | AGE | Schistosoma haematobium - isolation & purification | Humans | Middle Aged | Schistosomiasis haematobia - genetics | Child, Preschool | Genotype | Male | Schistosomiasis haematobia - blood | Case-Control Studies | Mannose-Binding Protein-Associated Serine Proteases - analysis | Polymorphism, Genetic | Young Adult | Schistosoma haematobium - genetics | Animals | Adolescent | Adult | Female | Nigeria | Child | Lectins | Thrombin | Serine | Sugars | Monosaccharides | Parasitic diseases | Proteases | Urogenital system | Polymorphism | Children & youth
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8. Full Text Biological variations of MASP-3 and MAp44, two splice products of the MASP1 gene involved in regulation of the complement system
by Degn, Søren E and Jensen, Lisbeth and Gál, Péter and Dobó, József and Holmvad, Steffen H and Jensenius, Jens C and Thiel, Steffen
Journal of Immunological Methods, ISSN 0022-1759, 09/2010, Volume 361, Issue 1-2, pp. 37 - 50
The lectin pathway of complement is part of the innate immune system. The complement-activating pattern-recognition molecules (for which we suggest the... 
Mannan-binding lectin | MAp44 | Lectin pathway | MASP-3 | Complement | Ficolin | MAP-1 | INNATE IMMUNE DEFENSE | PATTERN-RECOGNITION MOLECULES | CATALYTIC REGION | M-FICOLIN | BIOCHEMICAL RESEARCH METHODS | IMMUNOLOGY | ACETYL GROUPS | PATHWAY | MBL | ACTIVATES COMPLEMENT | SERINE-PROTEASE | Amino Acid Sequence | Mannose-Binding Protein-Associated Serine Proteases - immunology | Blotting, Western - methods | Antibodies, Monoclonal - biosynthesis | Humans | Complement System Proteins - immunology | Molecular Sequence Data | Adult | Complement Activation - immunology | Infant, Newborn | Mannose-Binding Protein-Associated Serine Proteases - analysis | C-reactive protein | Immunoglobulin G | Monoclonal antibodies | Lectins | Thrombin | Chromophores | Genetic engineering
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9. Full Text Lectin‐complement pathway molecules are decreased in patients with cirrhosis and constitute the risk of bacterial infections
by Foldi, Ildiko and Tornai, Tamas and Tornai, David and Sipeki, Nora and Vitalis, Zsuzsanna and Tornai, Istvan and Dinya, Tamas and Antal‐Szalmas, Peter and Papp, Maria
Liver International, ISSN 1478-3223, 07/2017, Volume 37, Issue 7, pp. 1023 - 1031
Background & Aims Lectin pathway molecules of the complement system are synthesized by hepatocytes and have pivotal role in innate host defence against... 
mortality | bacterial infection | ficolin | mannan‐binding lectin serine protease | cirrhosis | mannan-binding lectin serine protease | IMMUNE DYSFUNCTION | PREVALENCE | DEFICIENCY | PERITONITIS | MANNAN-BINDING LECTIN | LIVER-CIRRHOSIS | PROPHYLAXIS | H-FICOLIN | MBL | GASTROENTEROLOGY & HEPATOLOGY | Multivariate Analysis | Prognosis | Complement Activation | Follow-Up Studies | Humans | Middle Aged | Liver Cirrhosis - mortality | Male | Time Factors | Female | Retrospective Studies | Bacterial Infections - microbiology | Liver Cirrhosis - diagnosis | Enzyme-Linked Immunosorbent Assay | Risk Assessment | Liver Cirrhosis - complications | Down-Regulation | Risk Factors | Kaplan-Meier Estimate | Proportional Hazards Models | Glycoproteins - blood | Liver Cirrhosis - blood | Biomarkers - blood | Chi-Square Distribution | Mannose-Binding Protein-Associated Serine Proteases - analysis | Lectins - blood | Bacterial Infections - blood | Bacterial Infections - diagnosis | Bacterial Infections - mortality | Care and treatment | Bacterial infections | Lectins | Thrombin | Health aspects | Liver cirrhosis | Risk factors | Pathogens | Serine | Risk | Infections | Complement | Pattern recognition | Assaying | Patients | Low level | Ficolins | Mannan | Mannose-binding protein-associated serine proteinase | Cirrhosis | MASP-2 protein | Hepatocytes | Mannose-binding lectin | Bacteria | Chemical synthesis | Enzyme-linked immunosorbent assay
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10. Full Text MAp19, the alternative splice product of the MASP2 gene
by Degn, Søren E and Thiel, Steffen and Nielsen, Ole and Hansen, Annette G and Steffensen, Rudi and Jensenius, Jens C
Journal of Immunological Methods, ISSN 0022-1759, 10/2011, Volume 373, Issue 1-2, pp. 89 - 101
The lectin pathway of complement is a central part of innate immunity, but as a powerful inducer of inflammation it needs to be tightly controlled. The gene... 
Mannan-binding lectin | MAp19 | Complement | Lectin pathway | sMAP | MASP-2 | SMAP | L-FICOLIN | PROTEIN | PATTERN-RECOGNITION MOLECULES | SERINE PROTEASES | COMPLEMENT ACTIVATION | BIOCHEMICAL RESEARCH METHODS | COMPONENTS | IMMUNOLOGY | ACETYL GROUPS | PATHWAY | MBL | Immunohistochemistry | Mannose-Binding Protein-Associated Serine Proteases - immunology | Alternative Splicing | Mannose-Binding Lectin - immunology | Humans | Antibody Affinity - immunology | Cytoplasm - metabolism | Gene Expression Profiling | Hepatocytes - metabolism | Protein Isoforms - blood | Lectins - metabolism | Kidney - metabolism | Protein Isoforms - metabolism | Mannose-Binding Protein-Associated Serine Proteases - genetics | HEK293 Cells | Protein Isoforms - urine | Antibodies, Monoclonal - immunology | Lectins - immunology | Rats | Reverse Transcriptase Polymerase Chain Reaction | Blotting, Western | Mannose-Binding Protein-Associated Serine Proteases - analysis | Mannose-Binding Lectin - metabolism | Animals | Hybridomas | Protein Binding | Mice | Macrophages, Alveolar - metabolism | Lectins | Thrombin | Immunoglobulins | Chromophores | Genetic engineering | Genes
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11. Full Text MBL-associated serine protease-3 circulates in high serum concentrations predominantly in complex with Ficolin-3 and regulates Ficolin-3 mediated complement activation
by Skjoedt, Mikkel-Ole and Palarasah, Yaseelan and Munthe-Fog, Lea and Jie Ma, Ying and Weiss, Gudrun and Skjodt, Karsten and Koch, Claus and Garred, Peter
Immunobiology, ISSN 0171-2985, 2009, Volume 215, Issue 11, pp. 921 - 931
Abstract Background The human lectin complement pathway (LCP) involves circulating complexes consisting of mannose-binding lectin (MBL) or ficolins in... 
Allergy and Immunology | Advanced Basic Science | Complement | MBL-associated serine proteases | Lectin pathway | Mannose-binding lectin | Ficolins | CELLS | PROTEIN | IMMUNOLOGY | DEFICIENCY | MANNAN-BINDING LECTIN | POLYMORPHISMS | CONVERTASE | PATHWAY | MASP-1 | MONOCLONAL-ANTIBODIES | FIBRINOGEN | Mannose-Binding Protein-Associated Serine Proteases - immunology | Cricetinae | Glycoproteins - immunology | Lectins - blood | Animals | Complement Pathway, Mannose-Binding Lectin - immunology | Lectins - immunology | Humans | Glycoproteins - blood | Mice | Complement C4 - immunology | Mannose-Binding Protein-Associated Serine Proteases - analysis | Monoclonal antibodies | Lectins | Thrombin | Universities and colleges | Serine | Biochemical characteristics
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12. Full Text Genetic polymorphisms of mannan binding lectin (MBL), serum levels of MBL, the MBL associated serine protease and H-ficolin in patients with Crohn's disease [10]
by Nielsen, Rasmus Gaardskaer and Vind, I and Munkholm, P and Jensenius, J.C and Thiel, S and Husby, S
Gut, ISSN 0017-5749, 02/2007, Volume 56, Issue 2, pp. 311 - 312
  Age at onset of Crohn's disease, localisation and disease behaviour were classified according to the Vienna classification. 3 Plasma levels of MBL were... 
GASTROENTEROLOGY & HEPATOLOGY | Crohn Disease - genetics | Mannose-Binding Lectin - blood | Humans | Genotype | Male | Glycoproteins - blood | Mannose-Binding Lectin - genetics | Mannose-Binding Protein-Associated Serine Proteases - analysis | Lectins - blood | Crohn Disease - blood | Sex Factors | Female | Polymorphism, Genetic - genetics | Physiological aspects | Crohn's disease | Research | Genetic polymorphisms | Prescription drugs | Genotype & phenotype | Pathogenesis | Bowel disease | Genes | Classification | Lectins | Females | Crohns disease | Letter
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13. Full Text AmpliSeq screening of genes encoding the C-type lectin receptors and their signaling components reveals a common variant in MASP1 associated with pulmonary tuberculosis in an Indian population
by Klassert, Tilman E and Goyal, Surabhi and Stock, Magdalena and Driesch, Dominik and Hussain, Abid and Berrocal-Almanza, Luis Carlos and Myakala, Rajashekar and Sumanlatha, Gaddam and Valluri, Vijayalakshmi and Ahmed, Niyaz and Schumann, Ralf R and Flores, Carlos and Slevogt, Hortense
Frontiers in Immunology, ISSN 1664-3224, 02/2018, Volume 9, p. 242
Tuberculosis (TB) is a multifactorial disease governed by bacterial, host and environmental factors. On the host side, growing evidence shows the crucial role... 
C-type lectin receptor | Complement | AmpliSeq | MASP1 | Pulmonary tuberculosis | MYCOBACTERIUM-TUBERCULOSIS | IMMUNE-RESPONSE | ACTIVATION | MANNOSE-BINDING LECTIN | PROTEASE MASP-1 | SUSCEPTIBILITY | IMMUNOLOGY | pulmonary tuberculosis | POLYMORPHISMS | INFECTION | complement | DNA-SEQUENCING DATA | Tuberculosis, Pulmonary - microbiology | Complement Pathway, Mannose-Binding Lectin - immunology | Host Microbial Interactions - genetics | Mannose-Binding Lectin - immunology | Humans | Lectins, C-Type - immunology | Mycobacterium tuberculosis - immunology | Male | Disease Resistance - immunology | Lectins, C-Type - genetics | Tuberculosis, Pulmonary - genetics | Case-Control Studies | Tuberculosis, Pulmonary - blood | Young Adult | Lectins, C-Type - metabolism | DNA Mutational Analysis | Mannose-Binding Protein-Associated Serine Proteases - genetics | Adult | Female | Host Microbial Interactions - immunology | Disease Resistance - genetics | European Continental Ancestry Group - genetics | Complement Pathway, Mannose-Binding Lectin - genetics | Biomarkers - blood | Mycobacterium tuberculosis - isolation & purification | India | Mannose-Binding Protein-Associated Serine Proteases - analysis | Mannose-Binding Lectin - metabolism | Tuberculosis, Pulmonary - immunology | Mass Screening | Adolescent | Polymorphism, Single Nucleotide | Multigene Family - immunology | Lectins | Physiological aspects | Genetic aspects | Research | Genetic polymorphisms
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