mannose has been researched along with Genetic Predisposition in 11 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 4 (36.36) | 18.2507 |
| 2000's | 4 (36.36) | 29.6817 |
| 2010's | 2 (18.18) | 24.3611 |
| 2020's | 1 (9.09) | 2.80 |
| Authors | Studies |
|---|---|
| Bararpour, N; Darrous, L; Froguel, P; Gasser, M; Gilardi, F; Kutalik, Z; Marques-Vidal, P; Porcu, E; Thomas, A; Waeber, G; Yengo, L | 1 |
| Bonfert, M; Borggraefe, I; Kappler, M; Reiter, K; Schoen, C; Schroeder, AS | 1 |
| Wells, L | 1 |
| Ezekowitz, A | 1 |
| Foster, GR; Jack, DL; McIntosh, D; Sumiya, M; Summerfield, JA; Thomas, HC; Turner, MW | 1 |
| Amoroso, A; Berrino, M; Boniotto, M; Crovella, S; Palomba, E; Scarlatti, G; Serra, C; Tovo, PA; Vatta, S | 1 |
| Aerts, PC; Bartelink, AK; Bax, WA; Cluysenaer, OJ; Ezekowitz, RA; van Dijk, H | 1 |
| Hamvas, RM; Turner, MW | 1 |
| Besmond, C; Feingold, J; Gabolde, M; Guilloud-Bataille, M; Hubert, D; Lenaerts, C | 1 |
| Jack, DL; Klein, NJ; Turner, MW | 1 |
| Garred, P; Junker, P; Madsen, HO; Voss, A | 1 |
4 review(s) available for mannose and Genetic Predisposition
| Article | Year |
|---|---|
The o-mannosylation pathway: glycosyltransferases and proteins implicated in congenital muscular dystrophy.
Topics: Animals; Genetic Predisposition to Disease; Glycoproteins; Glycosylation; Glycosyltransferases; Humans; Mannose; Muscular Dystrophies; Mutation; Signal Transduction | 2013 |
Mannose-binding lectin: structure, function, genetics and disease associations.
Topics: Acute-Phase Reaction; Alleles; Alternative Splicing; Animals; Autoimmune Diseases; Bacteria; Calcium; Carrier Proteins; Chromosomes, Human, Pair 10; Collectins; Complement Activation; DNA Mutational Analysis; Ethnicity; Eukaryota; Evolution, Molecular; Exons; Fungi; Gene Frequency; Genes; Genetic Predisposition to Disease; Genotype; Humans; Infections; Macromolecular Substances; Mannose; Mannose-Binding Protein-Associated Serine Proteases; Models, Immunological; Models, Molecular; Mutation; Opsonin Proteins; Protein Binding; Protein Conformation; Protein Structure, Tertiary; Serine Endopeptidases; Species Specificity; Viruses | 2000 |
Mannose-binding lectin: targeting the microbial world for complement attack and opsonophagocytosis.
Topics: Bacterial Capsules; Bacterial Outer Membrane Proteins; Carbohydrate Metabolism; Carrier Proteins; Chromosomes, Human, Pair 10; Collectins; Complement Activation; Complement C3; Flow Cytometry; Genetic Predisposition to Disease; Gram-Negative Bacteria; Gram-Negative Bacterial Infections; Humans; Immunologic Deficiency Syndromes; Lipopolysaccharides; Mannose; Mannose-Binding Protein-Associated Serine Proteases; Opsonin Proteins; Phagocytosis; Point Mutation; Promoter Regions, Genetic; Protein Binding; Protein Conformation; Serine Endopeptidases; Substrate Specificity | 2001 |
Association of mannose-binding lectin gene variation with disease severity and infections in a population-based cohort of systemic lupus erythematosus patients.
Topics: Adolescent; Adult; Aged; Alleles; Carrier Proteins; Cohort Studies; Collectins; Disease Progression; Female; Gene Frequency; Genetic Predisposition to Disease; Genetic Variation; Humans; Infections; Lectins; Lupus Erythematosus, Systemic; Male; Mannose; Middle Aged; Promoter Regions, Genetic | 2001 |
7 other study(ies) available for mannose and Genetic Predisposition
| Article | Year |
|---|---|
Triangulating evidence from longitudinal and Mendelian randomization studies of metabolomic biomarkers for type 2 diabetes.
Topics: Adult; Aged; Betaine; Biomarkers; Carnitine; Case-Control Studies; Diabetes Mellitus, Type 2; Early Diagnosis; Female; Genetic Predisposition to Disease; Glutamic Acid; Humans; Leucine; Lysine; Male; Mannose; Mendelian Randomization Analysis; Metabolome; Middle Aged; Valine | 2021 |
Seizures and stupor during intravenous mannose therapy in a patient with CDG syndrome type 1b (MPI-CDG).
Topics: Adenosine Triphosphate; Biomarkers; Blood Glucose; Congenital Disorders of Glycosylation; Electroencephalography; Energy Metabolism; Genetic Predisposition to Disease; Glucose; Humans; Infusions, Intravenous; Injections, Intravenous; Magnetic Resonance Imaging; Male; Mannose; Mannose-6-Phosphate Isomerase; Phenotype; Seizures; Stupor; Time Factors; Treatment Outcome; Young Adult | 2010 |
Mannose-binding protein and susceptibility to chronic hepatitis B infection.
Topics: Acute-Phase Proteins; Alleles; Carrier Proteins; Genetic Predisposition to Disease; Hepatitis B; Humans; Mannose; Mannose-Binding Lectins | 1996 |
Mutation of gene of mannose-binding protein associated with chronic hepatitis B viral infection.
Topics: Acute Disease; Acute-Phase Proteins; Adult; Alleles; Asian People; Carrier Proteins; Chronic Disease; Codon; Enzyme-Linked Immunosorbent Assay; Female; Genetic Predisposition to Disease; Genotype; Hepatitis B; Humans; Male; Mannose; Mannose-Binding Lectins; Middle Aged; Mutation; Polymerase Chain Reaction; White People | 1996 |
Polymorphism at codon 54 of mannose-binding protein gene influences AIDS progression but not HIV infection in exposed children.
Topics: Acquired Immunodeficiency Syndrome; Alleles; Carrier Proteins; Child; Child, Preschool; Codon; Collectins; Disease Progression; Genetic Predisposition to Disease; HIV Infections; Humans; Infant; Mannose; Polymerase Chain Reaction; Polymorphism, Genetic | 1999 |
Association of familial deficiency of mannose-binding lectin and meningococcal disease.
Topics: Adolescent; Carrier Proteins; Collectins; Enzyme-Linked Immunosorbent Assay; Female; Genetic Predisposition to Disease; Humans; Lectins; Male; Mannose; Meningitis, Meningococcal; Neisseria meningitidis; Pedigree | 1999 |
The mannose binding lectin gene influences the severity of chronic liver disease in cystic fibrosis.
Topics: Alleles; Carrier Proteins; Chi-Square Distribution; Chronic Disease; Collectins; Cystic Fibrosis; Female; Genetic Predisposition to Disease; Genotype; Humans; Liver Diseases; Male; Mannose; Mutation; Odds Ratio; Phenotype; Sex Distribution | 2001 |