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UnknownPorphyrin accumulation in humans with common dysfunctional variants of ABCG2, a porphyrin transporter: potential association with acquired photosensitivity.
Not available
S-EPMC8197704 | biostudies-literature
UnknownNotch interaction with RUNX factors regulates initiation of the T-lineage program.
Not available
S-EPMC12677141 | biostudies-literature
UnknownBiallelic null variants in PNPLA8 cause microcephaly by reducing the number of basal radial glia.
Not available
S-EPMC11531855 | biostudies-literature
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