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Nature genetics, ISSN 1546-1718, 2014, Volume 46, Issue 5, pp. 492 - 497
Common multi-allelic copy number variants (CNVs) appear enriched for phenotypic associations compared to their biallelic counterparts(1-4). Here we... 
VARIANTS | GENETICS & HEREDITY | EARLY-ONSET | BODY-MASS INDEX | SEGMENTAL DUPLICATIONS | MICROBIOTA | POLYMORPHISM | DELETIONS | HERITABILITY | GENOME-WIDE ASSOCIATION | ACCURACY | Body Mass Index | Gene Dosage - genetics | Genetic Predisposition to Disease - genetics | Salivary alpha-Amylases - genetics | Microarray Analysis | Humans | Salivary alpha-Amylases - blood | Carbohydrate Metabolism - genetics | Genomics - methods | Odds Ratio | Obesity - genetics | Obesity | Amylases | Genetic susceptibility | Salivary glands | Genetic research | Genetic aspects | Research | Health aspects | Saliva | Risk factors | secretions | Studies | Medical research | Hospitals | Biomedical research | Genomes | Grants | Gene expression | Deoxyribonucleic acid--DNA | Life Sciences | Genetics | Human genetics | body mass | major clinical study | Genomics | genetic association | gene cluster | heritability | copy number variation | enzyme activity | gene mapping | genetic risk | genetic predisposition | sugar intake | female | obesity | Genetic Predisposition to Disease | Salivary alpha-Amylases | adipose tissue | European | article | Clinical Medicine | alpha amylase saliva isoenzyme | adult | gene expression | male | carbohydrate metabolism | fat mass | gene identification | Klinisk medicin | insulin release | subcutaneous fat | priority journal | saliva level | human | gene replication | enzyme blood level | human tissue | gene linkage disequilibrium | Gene Dosage | genetic variability | nucleotide sequence | controlled study | Chinese | overlapping gene | alpha amylase pancreas isoenzyme | principal component analysis
Journal Article
Journal Article
Brain pathology (Zurich, Switzerland), ISSN 1015-6305, 2018, Volume 28, Issue 6, pp. 920 - 932
Reduced glucose metabolism and formation of polyglucosan bodies (PGB) are, beside amyloid beta plaques and neurofibrillary tangles, well-known pathological... 
Journal Article | α‐amylase | polyglucosan bodies | astrocytes | Alzheimer's disease | dendritic spines | amyloid beta | α-amylase | TAU | PATHOLOGY | GLYCOGEN ACCUMULATION | NEUROSCIENCES | CLINICAL NEUROLOGY | HIRANO BODIES | alpha-amylase | METABOLISM | MEMORY | GENE-EXPRESSION | NEURONS | HEALTH | CONTRIBUTES | Salivary alpha-Amylases - genetics | Glucans - biosynthesis | Humans | Middle Aged | Male | Astrocytes - enzymology | Pericytes - enzymology | Alzheimer Disease - pathology | Pancreatic alpha-Amylases - metabolism | Glycogen - metabolism | Amyloid beta-Peptides - metabolism | Aged, 80 and over | Female | Neurofibrillary Tangles - pathology | CA1 Region, Hippocampal - enzymology | Gene Expression | Plaque, Amyloid - pathology | Dendritic Spines - enzymology | Alzheimer Disease - enzymology | Salivary alpha-Amylases - metabolism | Energy Metabolism | Glucose - metabolism | Aged | Pancreatic alpha-Amylases - genetics | Cohort Studies | Immunohistochemistry | Glucose metabolism | Medical research | Brain | Amylases | Glycogen | Physiological aspects | Medicine, Experimental | Glucose | Gene expression | Dextrose | Enzymes | Neurodegenerative diseases | Astrocytes | Gastrointestinal tract | Metabolism | Patients | Degradation | Proteins | Dendritic spines | Polysaccharides | Neurofibrillary tangles | Isotypes | Gastrointestinal system | Pericytes | Alzheimers disease | Plaques | Hippocampus
Journal Article