Genetics

USO DE RAPD PARA ANÁLISE DE DIVERSIDADE GENÉTICA EM ARROZ

Genetics / Genetic Diversity / Oryza Sativa / Enzyme / Molecular Marker / Enzyme activity / Genetic Variability / Enzyme activity / Genetic Variability

Estimativas de parâmetros genéticos para características de desempenho de suínos em fase de crescimento e terminação

Genetics / Breeding / China / Aquaculture / Animal Production / Female / Animals / Male / Genetic Association Studies / Fisheries Sciences / Floresta / Veterinary Sciences / Oncorhynchus Mykiss / Female / Animals / Male / Genetic Association Studies / Fisheries Sciences / Floresta / Veterinary Sciences / Oncorhynchus Mykiss

Estimação de parâmetros genéticos para produção de leite de cabras da raça Alpina

Genetics / Animal Model / Milk Yield / Dairy Cattle / Veterinary Sciences / Genetic Variability / Restricted Maximum Likelihood / Fixed Effects / Genetic Correlation / Genetic Variability / Restricted Maximum Likelihood / Fixed Effects / Genetic Correlation

Avaliação genética de bovinos da raça holandesa usando a produção de leite no dia do controle

Genetics / Seasonality / Animal Model / Repeated Measures / Milk Yield / Restricted Maximum Likelihood / Environmental Parameter / Genetic Correlation / Restricted Maximum Likelihood / Environmental Parameter / Genetic Correlation

Types of PCR | Daniel Apeh Academia.edu

Bioengineering / Genetics / Molecular Biology / Genomics / Biotechnology

Rhizobial extrachromosomal replicon variability, stability and expression in natural niches

Genetics / Rhizobium / Plasmids / Plant Roots / Phaseolus / Rhizosphere / Zea mays / Sinorhizobium / Agrobacterium / Plasmid / Rhizosphere / Zea mays / Sinorhizobium / Agrobacterium / Plasmid

Deoxyguanosine kinase deficiency presenting as neonatal hemochromatosis

Genetics / Molecular Genetics / Mitochondrial DNA / Humans / African American / Liver / Mutation / Female / Phenotype / Hemochromatosis / Clinical Sciences / Newborn Infant / Autopsy / Liver Failure / Liver / Mutation / Female / Phenotype / Hemochromatosis / Clinical Sciences / Newborn Infant / Autopsy / Liver Failure

MTRR A66G polymorphism among two caste groups of Uttar Pradesh (India)

Bioinformatics / Genetics / Epidemiology / Immunology / Molecular Biology / Genomics / Computational Biology / Cancer / Cancer Biology / Social Class / India / Humans / Female / Male / Genotype / Genomics / Computational Biology / Cancer / Cancer Biology / Social Class / India / Humans / Female / Male / Genotype

Mouse autosomal trisomy: two’s company, three’s a crowd

Genetics / Down Syndrome / Biological Sciences / Pregnancy / Humans / Mice / Female / Animals / Male / Pregnancy Loss / Trisomy 21 / Syndrome / Mice / Female / Animals / Male / Pregnancy Loss / Trisomy 21 / Syndrome

Genome sequencing reveals widespread virulence gene exchange among human Neisseria species

Genetics / Human Development / Horizontal Gene Transfer / Multidisciplinary / Virulence / Humans / Neisseria / PLoS one / Genome sequence / Neisseria gonorrhoeae / Humans / Neisseria / PLoS one / Genome sequence / Neisseria gonorrhoeae

An Ethical Analysis of Embryonic Stem Cell Research

Genetics / Stem Cells

Molecular structure in peripheral dog breeds: Portuguese native breeds as a case study

Genetics / Zoology / Portugal / Dogs / Animal Genetics / Animal / Case Study / Female / Animals / Cluster Analysis / Population Density / Genotype / Veterinary Sciences / Bayes Theorem / Genetic Markers / Molecular Structure / Animal / Case Study / Female / Animals / Cluster Analysis / Population Density / Genotype / Veterinary Sciences / Bayes Theorem / Genetic Markers / Molecular Structure

Echocardiographic Features of Genetic Diseases: Part 6. Complex Cardiovascular Defects

Genetics / Adolescent / Williams Syndrome / Down Syndrome / Echocardiography / Spleen / Congenital Heart Defects / Humans / Child / Female / Inborn errors of metabolism / Connective tissue / Marfan syndrome / Differential Diagnosis / Pheochromocytoma / Hemochromatosis / Fabry Disease / Aged / L-carnitine / Adult / Tuberous sclerosis / Genetic Disorder / Neoplasms / Ehlers-Danlos Syndrome / Reproducibility of Results / Noonan syndrome / Cardiomyopathies / Pericardium / Hypertrophic Cardiomyopathy / Aorta / Turner Syndrome / Gaucher Disease / Friedreich Ataxia / Myxoma / Heart Diseases / Spleen / Congenital Heart Defects / Humans / Child / Female / Inborn errors of metabolism / Connective tissue / Marfan syndrome / Differential Diagnosis / Pheochromocytoma / Hemochromatosis / Fabry Disease / Aged / L-carnitine / Adult / Tuberous sclerosis / Genetic Disorder / Neoplasms / Ehlers-Danlos Syndrome / Reproducibility of Results / Noonan syndrome / Cardiomyopathies / Pericardium / Hypertrophic Cardiomyopathy / Aorta / Turner Syndrome / Gaucher Disease / Friedreich Ataxia / Myxoma / Heart Diseases

Echocardiographic features of genetic diseases: Part 1. Cardiomyopathy

Genetics / Adolescent / Williams Syndrome / Down Syndrome / Echocardiography / Spleen / Congenital Heart Defects / Humans / Child / Female / Inborn errors of metabolism / Connective tissue / Marfan syndrome / Differential Diagnosis / Pheochromocytoma / Hemochromatosis / Fabry Disease / Aged / L-carnitine / Adult / Tuberous sclerosis / Genetic Disorder / Neoplasms / Ehlers-Danlos Syndrome / Reproducibility of Results / Noonan syndrome / Cardiomyopathies / Pericardium / Hypertrophic Cardiomyopathy / Aorta / Turner Syndrome / Gaucher Disease / Friedreich Ataxia / Myxoma / Heart Diseases / Spleen / Congenital Heart Defects / Humans / Child / Female / Inborn errors of metabolism / Connective tissue / Marfan syndrome / Differential Diagnosis / Pheochromocytoma / Hemochromatosis / Fabry Disease / Aged / L-carnitine / Adult / Tuberous sclerosis / Genetic Disorder / Neoplasms / Ehlers-Danlos Syndrome / Reproducibility of Results / Noonan syndrome / Cardiomyopathies / Pericardium / Hypertrophic Cardiomyopathy / Aorta / Turner Syndrome / Gaucher Disease / Friedreich Ataxia / Myxoma / Heart Diseases

Echocardiographic Features of Genetic Diseases: Part 4. Connective Tissue

Genetics / Adolescent / Williams Syndrome / Down Syndrome / Echocardiography / Spleen / Congenital Heart Defects / Humans / Child / Female / Inborn errors of metabolism / Connective tissue / Marfan syndrome / Differential Diagnosis / Pheochromocytoma / Hemochromatosis / Fabry Disease / Aged / L-carnitine / Adult / Tuberous sclerosis / Genetic Disorder / Neoplasms / Ehlers-Danlos Syndrome / Reproducibility of Results / Noonan syndrome / Cardiomyopathies / Pericardium / Hypertrophic Cardiomyopathy / Aorta / Turner Syndrome / Gaucher Disease / Friedreich Ataxia / Myxoma / Heart Diseases / Spleen / Congenital Heart Defects / Humans / Child / Female / Inborn errors of metabolism / Connective tissue / Marfan syndrome / Differential Diagnosis / Pheochromocytoma / Hemochromatosis / Fabry Disease / Aged / L-carnitine / Adult / Tuberous sclerosis / Genetic Disorder / Neoplasms / Ehlers-Danlos Syndrome / Reproducibility of Results / Noonan syndrome / Cardiomyopathies / Pericardium / Hypertrophic Cardiomyopathy / Aorta / Turner Syndrome / Gaucher Disease / Friedreich Ataxia / Myxoma / Heart Diseases

comH, a Novel Gene Essential for Natural Transformation of Helicobacter pylori

Genetics / Bacteriology / Helicobacter pylori / Horizontal Gene Transfer / Biological Sciences / Gram-negative bacteria / Genome sequence / Peptic Ulcer / Natural Transformation / H Pylori / Gene Transfer / DNA fragmentation / Gram-negative bacteria / Genome sequence / Peptic Ulcer / Natural Transformation / H Pylori / Gene Transfer / DNA fragmentation

Copyright © 2017 DADOSPDF Inc.