Genetic linkage analysis - Page 2

Lewy body pathology is a frequent co-pathology in familial Alzheimer\'s disease

Genetics / Immunohistochemistry / Alpha Synuclein / Humans / Female / Male / Genetic linkage analysis / Clinical Sciences / Aged / Middle Aged / Autopsy / ACTA / Genetic variation / Alzheimer Disease / Neurosciences / Dementia With Lewy Bodies / Male / Genetic linkage analysis / Clinical Sciences / Aged / Middle Aged / Autopsy / ACTA / Genetic variation / Alzheimer Disease / Neurosciences / Dementia With Lewy Bodies

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A new locus (RP31) for autosomal dominant retinitis pigmentosa maps to chromosome 9p

Genetics / Human Genetics / Complementary and Alternative Medicine / Humans / Retinitis pigmentosa / Pedigree / Genetic linkage analysis / Genetic distance / Linkage Analysis / Age of Onset / Inheritance Patterns / Pedigree / Genetic linkage analysis / Genetic distance / Linkage Analysis / Age of Onset / Inheritance Patterns

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Exact tandem repeats analyzer (E-TRA): A new program for DNA sequence mining

Genetics / Software / Cell line / Humans / Expressed Sequence Tags / Regulation of Gene Expression / Genetic linkage analysis / Short Tandem Repeat / Nucleotides / Simple Sequence Repeat / DNA sequence / Regulation of Gene Expression / Genetic linkage analysis / Short Tandem Repeat / Nucleotides / Simple Sequence Repeat / DNA sequence

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HLA-association of serum levels of natural antibodies

Genetics / Immunology / Immune response / Polymorphism / Family / Molecular / Molecular Immunology / Humans / Child / Adaptive Immunity / Female / Male / Genetic linkage analysis / Adult / Major histocompatibility complex / Heat Shock Protein / Family Study / Citrate Synthase / Autoantibodies / Chondroitin Sulphate / Molecular / Molecular Immunology / Humans / Child / Adaptive Immunity / Female / Male / Genetic linkage analysis / Adult / Major histocompatibility complex / Heat Shock Protein / Family Study / Citrate Synthase / Autoantibodies / Chondroitin Sulphate

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Esterase D assay in Brazilian retinoblastoma families

Genetics / Brazil / Humans / American / Pedigree / Genetic linkage analysis / Clinical Sciences / Retinoblastoma / Biological markers / Genetic Markers / Genetic linkage analysis / Clinical Sciences / Retinoblastoma / Biological markers / Genetic Markers

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A Discordant-Sibship Test for Disequilibrium and Linkage: No Need for Parental Data

Genetics / Methodology / Nonparametric Statistics / Biological Sciences / Humans / Genetic Testing / Female / Male / Linkage / Genetic determinism / Gene / Sample Size / Genetic linkage analysis / Association / Parents / Gen / Genotype / Hum / Nuclear Family / Linkage Disequilibrium / Statistical Test / Genetic Mapping / Locus / J / Genetic Markers / Genetic Testing / Female / Male / Linkage / Genetic determinism / Gene / Sample Size / Genetic linkage analysis / Association / Parents / Gen / Genotype / Hum / Nuclear Family / Linkage Disequilibrium / Statistical Test / Genetic Mapping / Locus / J / Genetic Markers

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CAMOS, a nonprogressive, autosomal recessive, congenital cerebellar ataxia, is caused by a mutant zinc-finger protein, ZNF592

Genetics / Human Genetics / Lebanon / Molecular Genetics / Intellectual Disability / Mental Retardation / Cytogenetics / Humans / Clinical Genetics / C2H2 zinc fingers / Cerebellar ataxia / Genetic linkage analysis / European / Zinc Finger / Family Health / DNA binding / Disease Progression / Amino Acid Profile / Amino Acid Sequence / Autosomal Recessive / DNA binding proteins / Genetic Markers / Gene Expression Regulation / Zinc Finger Protein / Molecular Sequence Data / Mental Retardation / Cytogenetics / Humans / Clinical Genetics / C2H2 zinc fingers / Cerebellar ataxia / Genetic linkage analysis / European / Zinc Finger / Family Health / DNA binding / Disease Progression / Amino Acid Profile / Amino Acid Sequence / Autosomal Recessive / DNA binding proteins / Genetic Markers / Gene Expression Regulation / Zinc Finger Protein / Molecular Sequence Data

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Mitochondrial DNA Sequence Diversity in Bipolar Affective Disorder

Bipolar Disorder / Adolescent / Mitochondrial DNA / Humans / Child / Haplotypes / Female / Male / Polymerase Chain Reaction / American / Genetic linkage analysis / Middle Aged / Adult / Genetic variation / X chromosome / Bipolar Affective Disorder / Genetic Markers / Case Control Studies / Haplotypes / Female / Male / Polymerase Chain Reaction / American / Genetic linkage analysis / Middle Aged / Adult / Genetic variation / X chromosome / Bipolar Affective Disorder / Genetic Markers / Case Control Studies

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HLA-association of serum levels of natural antibodies

Genetics / Immunology / Immune response / Polymorphism / Family / Regulation / Molecular / Molecular Immunology / Humans / Child / MHC / HLA / Adaptive Immunity / Female / Male / Genetic linkage analysis / Adult / Major histocompatibility complex / Heat Shock Proteins / Heat Shock Protein / Family Study / Citrate Synthase / Autoantibodies / Chondroitin Sulphate / Regulation / Molecular / Molecular Immunology / Humans / Child / MHC / HLA / Adaptive Immunity / Female / Male / Genetic linkage analysis / Adult / Major histocompatibility complex / Heat Shock Proteins / Heat Shock Protein / Family Study / Citrate Synthase / Autoantibodies / Chondroitin Sulphate

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Cardiomyocyte-mediated contact programs human mesenchymal stem cells to express cardiogenic phenotype

Stem Cells / Immunohistochemistry / Stem Cell / Signal Transduction / Mitosis / Cell Differentiation / Humans / Phenotype / Genetic linkage analysis / Clinical Sciences / Adult / CARDİOVASCULAR SURGERY / Protein isoforms / Cell communication / Troponin I / Human Mesenchymal Stem Cells / Troponin T / Thoracic and cardiovascular surgery / Cell Differentiation / Humans / Phenotype / Genetic linkage analysis / Clinical Sciences / Adult / CARDİOVASCULAR SURGERY / Protein isoforms / Cell communication / Troponin I / Human Mesenchymal Stem Cells / Troponin T / Thoracic and cardiovascular surgery

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Tau is a candidate gene for chromosome 17 frontotemporal dementia

Dementia / Temporal Lobe / Humans / Female / Male / Pedigree / Genetic linkage analysis / Clinical Sciences / Family Health / Frontotemporal Dementia / Annals / Neurosciences / Frontal Lobe / Molecular Sequence Data / Pedigree / Genetic linkage analysis / Clinical Sciences / Family Health / Frontotemporal Dementia / Annals / Neurosciences / Frontal Lobe / Molecular Sequence Data

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A New Locus for Autosomal Recessive Retinitis Pigmentosa (RP19) Maps to 1p13–1p21

Information Systems / Genetics / Genomics / Polymorphism / Humans / Retinitis pigmentosa / Female / Male / Linkage / Gene / Pedigree / Genetic linkage analysis / Phosphodiesterase Inhibitors / Aged / Gen / Genetic Mapping / Linkage Analysis / Molecular Sequence Data / Retinitis pigmentosa / Female / Male / Linkage / Gene / Pedigree / Genetic linkage analysis / Phosphodiesterase Inhibitors / Aged / Gen / Genetic Mapping / Linkage Analysis / Molecular Sequence Data

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A new locus for autosomal recessive retinitis pigmentosa (RP19) maps to 1p13-1p21

Information Systems / Genetics / Genomics / Polymorphism / Humans / Retinitis pigmentosa / Female / Male / Linkage / Gene / Pedigree / Genetic linkage analysis / Phosphodiesterase Inhibitors / Aged / Gen / Genetic Mapping / Linkage Analysis / Molecular Sequence Data / Retinitis pigmentosa / Female / Male / Linkage / Gene / Pedigree / Genetic linkage analysis / Phosphodiesterase Inhibitors / Aged / Gen / Genetic Mapping / Linkage Analysis / Molecular Sequence Data

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Genetic control of resistance to trypanosomiasis

Genetics / Zoology / Innate immunity / Cell line / Mice / Animals / Genetic linkage analysis / Trypanosomiasis / Veterinary Sciences / Species Specificity / Linkage Analysis / Animals / Genetic linkage analysis / Trypanosomiasis / Veterinary Sciences / Species Specificity / Linkage Analysis

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Genetics of Photosensitivity (Photoparoxysmal Response): A Review

Genetics / Humans / Animals / Photosensitivity / Phenotype / Genetic linkage analysis / Epilepsia / Clinical Sciences / Neurosciences / Genetic linkage analysis / Epilepsia / Clinical Sciences / Neurosciences

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