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PLoS Genetics, ISSN 1553-7390, 09/2010, Volume 6, Issue 9, p. e1001130
Journal Article
Journal Article
BMC Evolutionary Biology, ISSN 1471-2148, 2012, Volume 12, Issue 1, pp. 237 - 237
Background: HIV-1 derives from multiple independent transfers of simian immunodeficiency virus (SIV) strains from chimpanzees to human populations. We... 
Single nucleotide polymorphisms | Mbuti pygmies | Biaka pygmies | HIV dependency factors | VARIANTS | AIDS | RESTRICTION | FOAMY VIRUS | EVOLUTIONARY BIOLOGY | GENETICS & HEREDITY | CHEMOKINE RECEPTOR | RETROVIRUS | PYGMY HUNTER-GATHERERS | INFECTION | DIVERSITY | PROGRESSION | African Continental Ancestry Group - ethnology | Humans | Endosomal Sorting Complexes Required for Transport - genetics | Molecular Sequence Data | Mutation, Missense | Receptors, Virus - genetics | Aminohydrolases - genetics | Africa, Central | Simian Acquired Immunodeficiency Syndrome - virology | Ethnic Groups - genetics | HIV-1 - physiology | Simian Acquired Immunodeficiency Syndrome - transmission | African Continental Ancestry Group - genetics | Receptors, Chemokine - genetics | Genetic Predisposition to Disease - genetics | Pan troglodytes - virology | HIV Infections - genetics | HIV Infections - virology | Selection, Genetic | Genotype | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Sequence Analysis, DNA | Simian Immunodeficiency Virus - physiology | Cullin Proteins - genetics | Host-Pathogen Interactions | Carrier Proteins - genetics | Animals | Polymorphism, Single Nucleotide | HLA-C Antigens - genetics | Africa, Western | Receptors, CXCR6 | Genetic susceptibility | Demographic aspects | Physiological aspects | Genetic aspects | Research | HIV infection | Chemokine receptors | Risk factors | Epidemics | United States | Genes | Genomics | HLA histocompatibility antigens | Development and progression | Disease susceptibility | HIV (Viruses) | Histocompatibility antigens | Comparative analysis | Health aspects | Biotechnology industry | Medical research | Genetics | Cancer | Antiviral agents | CCR5 protein | Immunodeficiency | Genomes | Single-nucleotide polymorphism | Population genetics | Infection | Acquired immune deficiency syndrome | genomics | Histocompatibility antigen HLA | Mutation | Budding | pandemics | Genotypes
Journal Article
PLoS Pathogens, ISSN 1553-7366, 2014, Volume 10, Issue 7, pp. e1004281 - e1004281
Journal Article
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 1/2013, Volume 110, Issue 2, pp. 549 - 554
Maternal supplementation with folic acid is known to reduce the incidence of neural tube defects (NTDs) by as much as 70%. Despite the strong clinical link... 
Enzymes | Phenotypes | Mitochondria | Dams | Sodium | Exons | Neural tube defects | Alleles | Formates | Embryos | CELLS | MESSENGER-RNA | MOUSE MUTANTS | RAT EMBRYOS | MULTIDISCIPLINARY SCIENCES | DEPENDENT METHYLENETETRAHYDROFOLATE DEHYDROGENASE | METHENYLTETRAHYDROFOLATE CYCLOHYDROLASE | CLOSURE | MITOCHONDRIAL C-1-TETRAHYDROFOLATE SYNTHASE | FOLIC ACID METABOLISM | KNOCKOUT MICE | Methylenetetrahydrofolate Dehydrogenase (NADP) - deficiency | Aminohydrolases - deficiency | Embryonic Development - genetics | Formate-Tetrahydrofolate Ligase - deficiency | Neural Tube Defects - genetics | Genotype | Immunoblotting | DNA Primers - genetics | Multienzyme Complexes - genetics | Aminohydrolases - genetics | Reverse Transcriptase Polymerase Chain Reaction | Mice, Knockout | Multienzyme Complexes - deficiency | Animals | Formates - pharmacology | Gene Deletion | Formate-Tetrahydrofolate Ligase - genetics | Metabolic Networks and Pathways - physiology | Mice | Embryonic Development - drug effects | Formates - administration & dosage | Abnormalities, Multiple - genetics | Craniofacial Abnormalities - genetics | Methylenetetrahydrofolate Dehydrogenase (NADP) - genetics | Embryonic development | Phenotype | Neural tube | Physiological aspects | Genetic aspects | Research | Gene expression | Health aspects | Biological Sciences
Journal Article
PLoS ONE, ISSN 1932-6203, 03/2014, Volume 9, Issue 3, p. e89029
Background and Aims: The methylene-tetrahydrofolate dehydrogenase (NADP+ dependent) 1-like (MTHFD1L) gene is involved in mitochondrial tetrahydrofolate... 
MORTALITY | STROKE | GENOTYPE | MULTIDISCIPLINARY SCIENCES | DISEASE | ACUTE MYOCARDIAL-INFARCTION | RISK | Myocardial Infarction - blood | Myocardial Infarction - genetics | Myocardial Infarction - mortality | Prognosis | Follow-Up Studies | Genetic Association Studies | Humans | Acute Coronary Syndrome - mortality | Genotype | Multienzyme Complexes - genetics | Vitamin B 12 - blood | Aminohydrolases - genetics | Acute Coronary Syndrome - blood | Polymorphism, Genetic | Time Factors | Alleles | Survival Analysis | Biomarkers | Formate-Tetrahydrofolate Ligase - genetics | Acute Coronary Syndrome - genetics | Methylenetetrahydrofolate Dehydrogenase (NADP) - genetics | Cohort Studies | Medical research | Hospital patients | Patient outcomes | Mortality | Genes | Research | Heart attack | Risk factors | Vitamins | Genetic polymorphisms | Analysis | Physiological aspects | Medicine, Experimental | Genetic aspects | Dihydrofolate reductase | Homocysteine | Myocardial infarction | Immunoassay | Disorders | Cardiovascular disease | Vitamin B12 | Multivariate analysis | Gene polymorphism | Mitochondria | NADP | Heart diseases | Genotypes | Deoxyribonucleic acid--DNA | Tetrahydrofolic acid | Coronary artery | Health risks | Metabolism | Risk analysis | Coronary artery disease | Patients | Survival | Cyanocobalamin | Studies | Infarction | Cardiovascular diseases | Health risk assessment | Polymorphism | Deoxyribonucleic acid | DNA
Journal Article
Journal of Clinical Investigation, ISSN 0021-9738, 05/2017, Volume 127, Issue 5, pp. 1856 - 1872
Journal Article
BMC Medical Genetics, ISSN 1471-2350, 11/2011, Volume 12, Issue 1, pp. 150 - 150
Journal Article