Menkes and wilson disease proteins. Medical search. Frequent questions

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Anatomy7

Extrapyramidal Tracts Chromosomes, Human, Pair 13 Golgi Apparatus Cell Line Liver Inclusion Bodies Hepatocytes

Organisms3

Rats, Inbred LEC Rats, Mutant Strains Saccharomyces cerevisiae

Diseases12

Hepatolenticular Degeneration Menkes Kinky Hair Syndrome Heavy Chain Disease Machado-Joseph Disease Heredodegenerative Disorders, Nervous System Brain Diseases, Metabolic Neurodegenerative Diseases Metal Metabolism, Inborn Errors Proteostasis Deficiencies Disease Models, Animal Huntington Disease Spinocerebellar Ataxias

Chemicals and Drugs25

Metallochaperones Cation Transport Proteins Copper Adenosine Triphosphatases Ceruloplasmin Trientine Carrier Proteins Penicillamine Chelating Agents Recombinant Fusion Proteins Nerve Tissue Proteins Immunoglobulin gamma-Chains Molecular Chaperones Carboxylesterase DNA Primers Peptides Nuclear Proteins Dimethyldithiocarbamate Zinc DNA, Complementary Repressor Proteins Ubiquitin TRPP Cation Channels Genetic Markers Iron

Analytical, Diagnostic and Therapeutic Techniques and Equipment6

Chelation Therapy DNA Mutational Analysis Models, Molecular Disease Models, Animal Liver Function Tests Pedigree

Psychiatry and Psychology1

Huntington Disease

Phenomena and Processes15

Mutation Chromosomes, Human, Pair 13 Amino Acid Sequence Base Sequence Protein Transport Protein Structure, Tertiary Protein Binding Biological Transport Phenotype Mutation, Missense Protein Conformation Trinucleotide Repeat Expansion Binding Sites Genetic Markers Sequence Homology, Amino Acid

Information Science3

Molecular Sequence Data Amino Acid Sequence Base Sequence

Anatomy Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Psychiatry and Psychology Phenomena and Processes Information Science

Hepatolenticular Degeneration Metallochaperones Cation Transport Proteins Copper Menkes Kinky Hair Syndrome Adenosine Triphosphatases Rats, Inbred LEC Ceruloplasmin Heavy Chain Disease Trientine Carrier Proteins Machado-Joseph Disease Penicillamine Extrapyramidal Tracts Mutation Heredodegenerative Disorders, Nervous System Chelating Agents Chromosomes, Human, Pair 13 Chelation Therapy Rats, Mutant Strains Molecular Sequence Data Recombinant Fusion Proteins Nerve Tissue Proteins Immunoglobulin gamma-Chains Amino Acid Sequence Golgi Apparatus Molecular Chaperones Brain Diseases, Metabolic Neurodegenerative Diseases Carboxylesterase Base Sequence Protein Transport DNA Primers Cell Line DNA Mutational Analysis Protein Structure, Tertiary Metal Metabolism, Inborn Errors Peptides Models, Molecular Proteostasis Deficiencies Nuclear Proteins Disease Models, Animal Liver Huntington Disease Protein Binding Spinocerebellar Ataxias Saccharomyces cerevisiae Biological Transport Phenotype Liver Function Tests Mutation, Missense Inclusion Bodies Dimethyldithiocarbamate Zinc Hepatocytes Protein Conformation DNA, Complementary Repressor Proteins Ubiquitin TRPP Cation Channels Trinucleotide Repeat Expansion Pedigree Binding Sites Genetic Markers Iron Sequence Homology, Amino Acid

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