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Disease Info Card
Pyridoxine-responsive Sideroblastic Anemia
Information about Pyridoxine-responsive Sideroblastic Anemia: characteristics, related genes and pathways, plus antibodies you can use for research. This page is being enriched constantly, if you see some information you would like this page to include please send your suggestions to us.
Overview of Pyridoxine-responsive Sideroblastic Anemia
Most recent studies have shown that Pyridoxine-responsive Sideroblastic Anemia shares some biological mechanisms with anemia, ataxia, chronic-graft-versus-host-disease, dysplasia, fibrosis, hereditary-sideroblastic-anemia, hypochromia, iron-overload, leukemia, leukemia-myelocytic-acute, microcytic-anemia, microcytic-hypochromic-anemia-(disorder), myeloid-leukemia, myeloid-leukemia-chronic, refractory-anemias, sideroblastic-anemia, tuberculosis-pulmonary.
Among the many pathways, these few ones have gauged particular interests from scientists studying Pyridoxine-responsive Sideroblastic Anemia, and have been seen in publications frequently: Localization, Pathogenesis, Translation
Quite a number of genes have been found to play important roles in Pyridoxine-responsive Sideroblastic Anemia, such as ALAS1, ALAS2, FECH, HMBS, TF, TFE3. See what Boster has to offer for the research of these genes by clicking the gene name links below and view a more detailed info card/product listing for that gene.
In a later update, we will include information such as current drugs and therapy solutions as well as on-going and past clinical trials for this disease. Plesae stay updated.
Pathways Related to Pyridoxine-responsive Sideroblastic Anemia
This information is being compiled and will come in a future update
| Localization | Pathogenesis | Translation |