Mutations hydroxylase. Medical search. Frequent questions

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Anatomy17

Cell Line Cells, Cultured Liver COS Cells Neurons Microsomes, Liver Substantia Nigra Adrenal Glands Fibroblasts Brain Locus Coeruleus Cell Line, Tumor Adrenal Medulla Tumor Cells, Cultured Corpus Striatum HeLa Cells Mesencephalon

Organisms12

Escherichia coli Saccharomyces cerevisiae Mice, Inbred C57BL Mice, Mutant Strains Mice, Transgenic Cricetinae Pseudomonas Drosophila melanogaster Cercopithecus aethiops Mice, Knockout Pseudomonas fluorescens Caenorhabditis elegans

Diseases13

Adrenal Hyperplasia, Congenital Phenylketonurias Syndrome Genetic Predisposition to Disease Xanthomatosis, Cerebrotendinous Pheochromocytoma Genetic Diseases, X-Linked Disease Models, Animal Retinitis Pigmentosa Abnormalities, Multiple Chromosome Deletion Eye Abnormalities Ehlers-Danlos Syndrome

Chemicals and Drugs93

Phenylalanine Hydroxylase Steroid 21-Hydroxylase Tryptophan Hydroxylase Tyrosine 3-Monooxygenase Mixed Function Oxygenases Procollagen-Proline Dioxygenase Steroid Hydroxylases Cholestanetriol 26-Monooxygenase Benzopyrene Hydroxylase 4-Hydroxybenzoate-3-Monooxygenase Cytochrome P-450 Enzyme System Hypoxia-Inducible Factor-Proline Dioxygenases Codon, Nonsense DNA Primers Aniline Hydroxylase RNA, Messenger Trans-Cinnamate 4-Monooxygenase DNA Transcription Factors DNA-Binding Proteins Phenylalanine Codon Recombinant Proteins Aryl Hydrocarbon Hydroxylases Dopamine gamma-Butyrobetaine Dioxygenase Pterins Bacterial Proteins Dopamine beta-Hydroxylase Oxygenases 17-alpha-Hydroxyprogesterone Membrane Proteins 25-Hydroxyvitamin D3 1-alpha-Hydroxylase Mutant Proteins Nuclear Proteins DNA, Complementary Carrier Proteins Biopterin Alkane 1-Monooxygenase Hydroxybenzoates Ketoglutaric Acids DNA, Mitochondrial Proto-Oncogene Proteins B-raf Catecholamines Fenclonine Recombinant Fusion Proteins DNA, Neoplasm Proteins Proline Phenol Parabens Mutagens Flavin-Adenine Dinucleotide Repressor Proteins Amino Acids, Dicarboxylic Proto-Oncogene Proteins Eye Proteins Nerve Tissue Proteins DNA, Bacterial Saccharomyces cerevisiae Proteins Ethylnitrosourea RNA Splice Sites Fungal Proteins Hypoxia-Inducible Factor 1, alpha Subunit Methylcholanthrene Dihydroxyphenylalanine Serine Escherichia coli Proteins Tumor Suppressor Protein p53 Drosophila Proteins DNA Transposable Elements Genetic Markers BRCA2 Protein Dioxygenases Homeodomain Proteins Benz(a)Anthracenes ras Proteins Trans-Activators Benzopyrenes Steroid 17-alpha-Hydroxylase Membrane Transport Proteins Arginine Serotonin Isoenzymes Alanine Hydroxylysine Iron Collagen Tyrosine Pteridines Homogentisic Acid Lysine Phenylethanolamine N-Methyltransferase

Analytical, Diagnostic and Therapeutic Techniques and Equipment27

Pedigree Amino Acid Substitution Polymerase Chain Reaction DNA Mutational Analysis Mutagenesis, Site-Directed Sequence Analysis, DNA Cloning, Molecular Models, Molecular Genetic Testing Chromosome Mapping Sequence Alignment Genetic Complementation Test Transfection Heterozygote Detection Models, Genetic Mutagenesis, Insertional Immunohistochemistry Restriction Mapping Reverse Transcriptase Polymerase Chain Reaction Blotting, Western Crosses, Genetic Electrophoresis, Polyacrylamide Gel Disease Models, Animal Chromatography, High Pressure Liquid Models, Biological Genetic Association Studies Enzyme Stability

Phenomena and Processes96

Point Mutation Mutation, Missense Mutation Frameshift Mutation Germ-Line Mutation Base Sequence Mutation Rate Exons Amino Acid Sequence Heterozygote Hydroxylation Amino Acid Substitution Alleles Genotype Polymorphism, Single-Stranded Conformational Homozygote Mutagenesis Kinetics Codon, Nonsense Genes, Recessive Phenotype Sequence Deletion Binding Sites Sequence Homology, Amino Acid Protein Structure, Tertiary Genes, Dominant Protein Binding Suppression, Genetic Codon Gene Deletion Plasmids Transfection Genetic Linkage Transcription, Genetic Substrate Specificity Consanguinity Founder Effect Polymorphism, Genetic Genes, p53 Promoter Regions, Genetic Genetic Predisposition to Disease Protein Conformation Structure-Activity Relationship Genes, Bacterial Gene Frequency Genes Mutagenesis, Insertional Introns Enzyme Induction Gene Expression Genetic Variation Catalysis Gene Expression Regulation, Enzymologic Genes, Lethal Signal Transduction Polymorphism, Restriction Fragment Length Exome Genes, BRCA1 Gene Expression Regulation Conserved Sequence Phosphorylation Recombination, Genetic Temperature Microsatellite Repeats Time Factors Drug Resistance, Viral RNA Splicing Protein Structure, Secondary Genes, Suppressor Evolution, Molecular Polymorphism, Single Nucleotide INDEL Mutation Penetrance Species Specificity Enzyme Activation Genes, BRCA2 RNA Splice Sites Selection, Genetic Genes, Fungal Gene Expression Regulation, Bacterial Sequence Homology, Nucleic Acid Catalytic Domain Chromosome Deletion DNA Transposable Elements Genetic Markers Amino Acid Motifs DNA Repair Phylogeny Genetic Heterogeneity Protein Biosynthesis Enzyme Stability Gene Expression Regulation, Developmental Drug Resistance, Microbial Protein Transport Genes, Regulator Alternative Splicing

Disciplines and Occupations1

Immunohistochemistry

Information Science4

Base Sequence Molecular Sequence Data Amino Acid Sequence Phylogeny

Named Groups2

Jews Asian Continental Ancestry Group

Health Care4

Genetic Testing Family Health Temperature Age of Onset

Anatomy Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Phenomena and Processes Disciplines and Occupations Information Science Named Groups Health Care

Point Mutation Phenylalanine Hydroxylase Mutation, Missense Steroid 21-Hydroxylase Mutation Tryptophan Hydroxylase Tyrosine 3-Monooxygenase Mixed Function Oxygenases Procollagen-Proline Dioxygenase Frameshift Mutation Germ-Line Mutation Steroid Hydroxylases Pedigree Cholestanetriol 26-Monooxygenase Base Sequence Molecular Sequence Data Benzopyrene Hydroxylase Adrenal Hyperplasia, Congenital 4-Hydroxybenzoate-3-Monooxygenase Mutation Rate Exons Amino Acid Sequence Heterozygote Hydroxylation Amino Acid Substitution Polymerase Chain Reaction Alleles DNA Mutational Analysis Mutagenesis, Site-Directed Phenylketonurias Cytochrome P-450 Enzyme System Genotype Polymorphism, Single-Stranded Conformational Homozygote Sequence Analysis, DNA Mutagenesis Hypoxia-Inducible Factor-Proline Dioxygenases Kinetics Codon, Nonsense Genes, Recessive Cloning, Molecular Escherichia coli Phenotype Cell Line DNA Primers Aniline Hydroxylase Sequence Deletion Binding Sites Sequence Homology, Amino Acid Protein Structure, Tertiary Models, Molecular RNA, Messenger Trans-Cinnamate 4-Monooxygenase Genes, Dominant Genetic Testing Chromosome Mapping DNA Transcription Factors DNA-Binding Proteins Phenylalanine Protein Binding Suppression, Genetic Codon Gene Deletion Sequence Alignment Recombinant Proteins Genetic Complementation Test Plasmids Aryl Hydrocarbon Hydroxylases Dopamine gamma-Butyrobetaine Dioxygenase Pterins Bacterial Proteins Transfection Genetic Linkage Transcription, Genetic Dopamine beta-Hydroxylase Oxygenases Substrate Specificity Consanguinity Syndrome Founder Effect Saccharomyces cerevisiae Polymorphism, Genetic Genes, p53 Promoter Regions, Genetic 17-alpha-Hydroxyprogesterone Genetic Predisposition to Disease Protein Conformation Membrane Proteins 25-Hydroxyvitamin D3 1-alpha-Hydroxylase Structure-Activity Relationship Heterozygote Detection Mutant Proteins Xanthomatosis, Cerebrotendinous Cells, Cultured Genes, Bacterial Models, Genetic Nuclear Proteins Gene Frequency

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