MeSH term
Frequency | Condition_Probility | Animals | 37 | 0.0 |
Humans | 62 | 0.0 |
Cation Transport Proteins/*metabolism | 2 | 25.0 |
Copper/*metabolism | 13 | 14.0 |
Research Support, Non-U.S. Gov't | 40 | 0.0 |
Research Support, U.S. Gov't, Non-P.H.S. | 4 | 0.0 |
Research Support, U.S. Gov't, P.H.S. | 21 | 0.0 |
Adenosinetriphosphatase/chemistry/*genetics/metabolism | 3 | 42.0 |
Amino Acid Motifs | 3 | 0.0 |
Amino Acid Sequence | 13 | 0.0 |
Base Sequence | 14 | 0.0 |
Carrier Proteins/chemistry/*genetics/metabolism | 2 | 6.0 |
*Cation Transport Proteins | 36 | 16.0 |
Child | 2 | 0.0 |
DNA Mutational Analysis | 8 | 0.0 |
Female | 15 | 0.0 |
Fibroblasts | 4 | 0.0 |
Infant | 3 | 0.0 |
Male | 13 | 0.0 |
Molecular Sequence Data | 17 | 0.0 |
Pedigree | 8 | 0.0 |
Phenotype | 8 | 0.0 |
*Recombinant Fusion Proteins | 35 | 57.0 |
Copper/metabolism/*pharmacology | 2 | 25.0 |
Hepatolenticular Degeneration/*genetics | 2 | 7.0 |
Kinetics | 3 | 0.0 |
Menkes Kinky Hair Syndrome/*genetics | 17 | 77.0 |
Models, Molecular | 3 | 0.0 |
Phosphorylation | 6 | 0.0 |
Protein Structure, Secondary | 4 | 0.0 |
Adenosinetriphosphatase/*genetics | 16 | 16.0 |
Alleles | 2 | 0.0 |
Carrier Proteins/*genetics | 12 | 0.0 |
Disease Models, Animal | 4 | 0.0 |
Exons | 7 | 0.0 |
*Gene Deletion | 4 | 0.0 |
Mice | 14 | 0.0 |
Mice, Inbred C3H | 3 | 0.0 |
Mice, Inbred C57BL | 3 | 0.0 |
Mutation | 10 | 0.0 |
Reverse Transcriptase Polymerase Chain Reaction | 2 | 0.0 |
Sequence Analysis, DNA | 4 | 0.0 |
Adult | 2 | 0.0 |
Amino Acid Substitution | 3 | 0.0 |
DNA/chemistry/genetics | 2 | 0.0 |
Family Health | 2 | 0.0 |
Point Mutation | 2 | 0.0 |
Pregnancy | 5 | 0.0 |
Cells, Cultured | 4 | 0.0 |
Dose-Response Relationship, Drug | 2 | 0.0 |
Rats | 7 | 0.0 |
Adenosinetriphosphatase/genetics/*metabolism | 5 | 17.0 |
Biological Transport | 7 | 0.0 |
Carrier Proteins/genetics/*metabolism | 2 | 0.0 |
Cell Line | 7 | 0.0 |
Fluorescent Antibody Technique | 6 | 0.0 |
Mutation/genetics | 3 | 0.0 |
Protein Transport | 3 | 0.0 |
Transfection | 4 | 0.0 |
English Abstract | 2 | 0.0 |
Liver/metabolism | 2 | 0.0 |
Adenosinetriphosphatase/*metabolism | 3 | 7.0 |
Carrier Proteins/*metabolism | 2 | 0.0 |
Protein Binding | 2 | 0.0 |
Alternative Splicing | 2 | 0.0 |
CHO Cells | 8 | 0.0 |
DNA, Complementary | 4 | 0.0 |
Hamsters | 10 | 0.0 |
Tumor Cells, Cultured | 4 | 0.0 |
Frameshift Mutation | 2 | 0.0 |
Genotype | 2 | 0.0 |
*Mutation | 4 | 0.0 |
Polymerase Chain Reaction | 8 | 0.0 |
Polymorphism, Single-Stranded Conformational | 2 | 0.0 |
Sequence Deletion | 3 | 0.0 |
Genes, Dominant/genetics | 2 | 1.0 |
Circular Dichroism | 2 | 0.0 |
Mutagenesis, Site-Directed | 3 | 0.0 |
Protein Structure, Tertiary | 2 | 0.0 |
Temperature | 2 | 0.0 |
Copper/metabolism | 10 | 15.0 |
Immunohistochemistry | 3 | 0.0 |
Menkes Kinky Hair Syndrome/genetics/*metabolism | 3 | 100.0 |
Adenosinetriphosphatase/*genetics/metabolism | 4 | 15.0 |
Carrier Proteins/*genetics/metabolism | 3 | 1.0 |
Copper/pharmacology | 2 | 3.0 |
CHO Cells/cytology/drug effects/metabolism | 2 | 100.0 |
Copper/*metabolism/pharmacology | 3 | 33.0 |
DNA, Complementary/genetics | 3 | 0.0 |
Fluorescent Antibody Technique, Indirect | 2 | 0.0 |
Mice, Mutant Strains | 4 | 0.0 |
Menkes Kinky Hair Syndrome/*enzymology/*genetics | 2 | 100.0 |
Cation Transport Proteins/*genetics | 4 | 11.0 |
Codon/genetics | 2 | 0.0 |
Recombinant Fusion Proteins/*genetics | 3 | 8.0 |
Sequence Deletion/*genetics | 2 | 1.0 |
Cloning, Molecular | 7 | 0.0 |
Microscopy, Fluorescence | 2 | 0.0 |
Blotting, Northern | 3 | 0.0 |
Sequence Alignment | 3 | 0.0 |
Sequence Homology, Nucleic Acid | 2 | 0.0 |
Binding Sites | 4 | 0.0 |
Gene Expression | 2 | 0.0 |
Adenosinetriphosphatase/*genetics/*metabolism | 3 | 42.0 |
COS Cells | 2 | 0.0 |
Golgi Apparatus/*metabolism | 2 | 2.0 |
Recombinant Proteins/genetics/metabolism | 2 | 0.0 |
Blotting, Western | 6 | 0.0 |
Immunoenzyme Techniques | 2 | 0.0 |
Adenosinetriphosphatase/chemistry/*genetics | 2 | 28.0 |
Carrier Proteins/chemistry/*genetics | 2 | 3.0 |
Comparative Study | 3 | 0.0 |
DNA Primers | 6 | 0.0 |
Linkage (Genetics) | 2 | 0.0 |
*X Chromosome | 2 | 0.0 |
*Point Mutation | 2 | 0.0 |
Sequence Homology, Amino Acid | 2 | 0.0 |
Adenosinetriphosphatase/metabolism | 2 | 1.0 |
Homeostasis | 4 | 1.0 |
Menkes Kinky Hair Syndrome/genetics | 2 | 40.0 |
In Situ Hybridization/methods | 2 | 1.0 |
Tissue Distribution | 3 | 0.0 |
Mice, Inbred BALB C | 2 | 0.0 |
*DNA Mutational Analysis | 2 | 1.0 |
*Disease Models, Animal | 3 | 0.0 |
Electrophoresis, Polyacrylamide Gel | 3 | 0.0 |
Heterozygote | 2 | 0.0 |
Polymorphism, Genetic | 2 | 0.0 |
RNA Splicing/genetics | 2 | 1.0 |
Brefeldin A | 2 | 4.0 |
Cyclopentanes/pharmacology | 2 | 4.0 |
Hepatolenticular Degeneration/genetics/metabolism | 3 | 75.0 |
Introns | 5 | 0.0 |
Cell Membrane/metabolism | 4 | 0.0 |
Chromosome Mapping | 3 | 0.0 |
Restriction Mapping | 2 | 0.0 |
Culture Media | 2 | 0.0 |
X Chromosome | 3 | 0.0 |
Time Factors | 3 | 0.0 |
RNA, Messenger/analysis | 2 | 0.0 |
*Polymorphism, Genetic | 2 | 0.0 |
Cation Transport Proteins/genetics/*metabolism | 3 | 25.0 |
Hela Cells | 3 | 0.0 |
Models, Biological | 2 | 0.0 |
Cation Transport Proteins/*genetics/*metabolism | 2 | 25.0 |
Subcellular Fractions/enzymology | 2 | 2.0 |
Menkes Kinky Hair Syndrome/*diagnosis/genetics | 3 | 100.0 |
Mental Retardation, X-Linked/diagnosis/genetics | 2 | 100.0 |
