heme has been researched along with Ataxias, Hereditary in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (50.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Kishi, F; Miura, K; Yanatori, I; Yasui, Y | 1 |
| Fujiwara, T; Horie, M; Kanemoto, N; Kawai, A; Nishino, N; Okuno, S; Omori, Y; Saito, A; Shimada, Y; Shinomiya, H; Suzuki, M; Takahashi, E | 1 |
2 other study(ies) available for heme and Ataxias, Hereditary
| Article | Year |
|---|---|
Mutations of FLVCR1 in posterior column ataxia and retinitis pigmentosa result in the loss of heme export activity.
Topics: Amino Acid Substitution; Animals; Biological Transport, Active; Cell Line; Dogs; Heme; Humans; Lysosomes; Membrane Transport Proteins; Mutation; Protein Folding; Protein Structure, Tertiary; Proteolysis; Receptors, Virus; Retinitis Pigmentosa; Sensation Disorders; Spinocerebellar Degenerations | 2012 |
Cloning and chromosomal mapping of a novel ABC transporter gene (hABC7), a candidate for X-linked sideroblastic anemia with spinocerebellar ataxia.
Topics: 5-Aminolevulinate Synthetase; Amino Acid Sequence; Anemia, Sideroblastic; Animals; ATP-Binding Cassette Transporters; Base Sequence; Biological Transport; Blood Proteins; Brain; Chromosome Banding; Chromosome Mapping; Cloning, Molecular; Cytosol; DNA, Complementary; Erythrocytes; Genes; Heme; Humans; In Situ Hybridization, Fluorescence; Intracellular Membranes; Isoenzymes; Mice; Mitochondria; Molecular Sequence Data; Nerve Tissue Proteins; Saccharomyces cerevisiae; Sequence Alignment; Sequence Homology, Amino Acid; Species Specificity; Spinocerebellar Degenerations; X Chromosome | 1998 |