Human - Page 2 | DATOSPDF

Application of transcranial magnetic stimulation in treatment of drug-resistant major depression?a report of two cases

Psychology / Cognitive Science / Transcranial Magnetic Stimulation / Human / Drug Resistance / Major Depression

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ICSI in cases of sperm DNA damage: beneficial effect of oral antioxidant treatment

DNA damage / Human / Antioxidants / Pregnancy / Humans / vitamin C / Female / Male / Vitamin E / Incidence / Male Infertility / Human reproduction / Ascorbic Acid / Adult / Spermatozoa / Embryos / Pregnancy Outcome / DNA fragmentation / vitamin C / Female / Male / Vitamin E / Incidence / Male Infertility / Human reproduction / Ascorbic Acid / Adult / Spermatozoa / Embryos / Pregnancy Outcome / DNA fragmentation

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ICSI in cases of sperm DNA damage: beneficial effect of oral antioxidant treatment

DNA damage / Human / Antioxidants / Pregnancy / Humans / vitamin C / Female / Male / Vitamin E / Incidence / Male Infertility / Human reproduction / Ascorbic Acid / Adult / Spermatozoa / Embryos / Pregnancy Outcome / DNA fragmentation / vitamin C / Female / Male / Vitamin E / Incidence / Male Infertility / Human reproduction / Ascorbic Acid / Adult / Spermatozoa / Embryos / Pregnancy Outcome / DNA fragmentation

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Chemical chaperone therapy: chaperone effect on mutant enzyme and cellular pathophysiology in β-galactosidase deficiency

Genetics / Gene expression / Human / Humans / Mice / Animals / Clinical Sciences / Human Fibroblasts / Structure activity Relationship / Hexosamines / Animals / Clinical Sciences / Human Fibroblasts / Structure activity Relationship / Hexosamines

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A double mutant [N543H+2393del9] allele in the LDL receptor gene in familial hypercholesterolemia: effect on plasma cholesterol levels and cardiovascular disease

Genetics / Cardiovascular disease / Human / DNA / Humans / Mutation / Cholesterol / Female / Male / Pedigree / Phenotype / Triglycerides / Clinical Sciences / Aged / Middle Aged / Genotype / Adult / Cardiovascular Diseases / Familial Hypercholesterolemia / Amino Acid Substitution Rates / Mutation / Cholesterol / Female / Male / Pedigree / Phenotype / Triglycerides / Clinical Sciences / Aged / Middle Aged / Genotype / Adult / Cardiovascular Diseases / Familial Hypercholesterolemia / Amino Acid Substitution Rates

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Estradiol induces heparanase-1 expression and heparan sulphate proteoglycan degradation in human endometrium

Flow Cytometry / Fluorescence Microscopy / Immunohistochemistry / Gene expression / Human / Humans / Basement Membrane / Female / Glucuronidase / Menstrual Cycle / Human reproduction / Adult / Heparan Sulphate / Enzymatic Activity / Cell Surface Markers / Endometrium / Enzyme Linked Immunosorbent Assay / Estradiol / Follicle stimulating hormone / Differential expression / Humans / Basement Membrane / Female / Glucuronidase / Menstrual Cycle / Human reproduction / Adult / Heparan Sulphate / Enzymatic Activity / Cell Surface Markers / Endometrium / Enzyme Linked Immunosorbent Assay / Estradiol / Follicle stimulating hormone / Differential expression

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Pulse pressure and peripheral arterial vasoreactivity

Human / Humans / Blood Pressure / Clinical Medicine / Female / Male / Vascular endothelium / Clinical Sciences / Aged / Middle Aged / Pulse Pressure / Coronary Artery Disease / Vasodilation / Case Control Studies / Brachial artery / Male / Vascular endothelium / Clinical Sciences / Aged / Middle Aged / Pulse Pressure / Coronary Artery Disease / Vasodilation / Case Control Studies / Brachial artery

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Seminal plasma alpha-glucosidase activity and male infertility

Colorimetry / Human / Humans / Male / Vasectomy / Male Infertility / ROC Curve / Human reproduction / Semen / Sensitivity and Specificity / Male Infertility / ROC Curve / Human reproduction / Semen / Sensitivity and Specificity

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Molecular characterization of novel progranulin ( GRN ) mutations in frontotemporal dementia

Genetics / Dementia / Human / Cell line / Brain / Humans / Mutation / Female / Male / Clinical Sciences / Introns / Aged / Middle Aged / Molecular Characterization / Frontotemporal Dementia / Transfection / Base Sequence / Subcellular Fractions / Age of Onset / Founder Effect / Case Control Studies / Humans / Mutation / Female / Male / Clinical Sciences / Introns / Aged / Middle Aged / Molecular Characterization / Frontotemporal Dementia / Transfection / Base Sequence / Subcellular Fractions / Age of Onset / Founder Effect / Case Control Studies

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Baculovirus complementation restores a novel NDUFAF2 mutation causing complex I deficiency

Genetics / Human / Molecular chaperones / Mitochondrial DNA / Humans / Female / Infant / Skin / Clinical Sciences / Genomic DNA / Human Fibroblasts / Female / Infant / Skin / Clinical Sciences / Genomic DNA / Human Fibroblasts

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Functional PMS2 hybrid alleles containing a pseudogene-specific missense variant trace back to a single ancient intrachromosomal recombination event

Genetics / Human / Humans / Mutation / Haplotypes / Polymerase Chain Reaction / Clinical Sciences / Chimera / Genetic Recombination / Base Sequence / Pseudogenes / DNA binding proteins / Polymerase Chain Reaction / Clinical Sciences / Chimera / Genetic Recombination / Base Sequence / Pseudogenes / DNA binding proteins

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Potential impact of hormonal male contraception: cross-cultural implications for development of novel preparations

Research Methodology / Contraception / Behavior / Culture / Developing Countries / China / Adolescent / Human / Knowledge / Cross-Cultural Comparison / South Africa / Population / Humans / Comparative studies / Female / Male / Attitudes / Great Britain / Middle Aged / Developed Countries / Questionnaires / Human reproduction / Adult / Spermatozoa / China / Adolescent / Human / Knowledge / Cross-Cultural Comparison / South Africa / Population / Humans / Comparative studies / Female / Male / Attitudes / Great Britain / Middle Aged / Developed Countries / Questionnaires / Human reproduction / Adult / Spermatozoa

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Sporadic heteroplasmic single 5.5 Kb mitochondrial DNA deletion associated with cerebellar ataxia, hypogonadotropic hypogonadism, choroidal dystrophy, and mitochondrial respiratory chain complex I deficiency

Genetics / Skeletal muscle biology / Human / Mitochondrial DNA / Humans / Female / Cerebellar ataxia / Mitochondrial Respiratory Chain / Electron Transport / Pedigree / Clinical Sciences / Late onset hypogonadism / Adult / Female / Cerebellar ataxia / Mitochondrial Respiratory Chain / Electron Transport / Pedigree / Clinical Sciences / Late onset hypogonadism / Adult

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A double mutant [N543H+2393del9] allele in the LDL receptor gene in familial hypercholesterolemia: effect on plasma cholesterol levels and cardiovascular disease

Genetics / Cardiovascular disease / Human / DNA / Humans / Mutation / Cholesterol / Female / Male / Pedigree / Phenotype / Triglycerides / Clinical Sciences / Aged / Middle Aged / Genotype / Adult / Cardiovascular Diseases / Familial Hypercholesterolemia / Amino Acid Substitution Rates / DNA mutational analysis / Mutation / Cholesterol / Female / Male / Pedigree / Phenotype / Triglycerides / Clinical Sciences / Aged / Middle Aged / Genotype / Adult / Cardiovascular Diseases / Familial Hypercholesterolemia / Amino Acid Substitution Rates / DNA mutational analysis

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Drospirenone increases endothelial nitric oxide synthesis via a combined action on progesterone and mineralocorticoid receptors

Flavonoids / Cardiovascular disease / Signal Transduction / Human / Progesterone / Humans / Aldosterone / Nitric oxide / Vascular endothelium / Human reproduction / Endothelial cell / Time Factors / Mineralocorticoid Receptor / Estradiol / Medroxyprogesterone Acetate / Humans / Aldosterone / Nitric oxide / Vascular endothelium / Human reproduction / Endothelial cell / Time Factors / Mineralocorticoid Receptor / Estradiol / Medroxyprogesterone Acetate

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Lactase Persistence in Central Asia: Phenotype, Genotype, and Evolution

Genetics / Polymorphism / Molecular Evolution / Life Style / Low Frequency / Natural Selection / Human / Human Biology / Humans / Blood Glucose / Lactose intolerance / Pastoralism / Phenotype / Ethnic Groups / Questionnaires / Genotype / Ethnic Group / Genetic variation / Statistics as Topic / Natural Selection / Human / Human Biology / Humans / Blood Glucose / Lactose intolerance / Pastoralism / Phenotype / Ethnic Groups / Questionnaires / Genotype / Ethnic Group / Genetic variation / Statistics as Topic

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