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Thap11 Protein Expression Summary The Human Protein Atlas.

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The High Encapsulation Barrier For Thpa11 215 Kcal Mol1 Is In Line With The Reported Conditions Of Synthesis.

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Mutations In Thap11 Cause An Inborn Error Of Cobalamin Metabolism.

Mutations in thap11 cause an inborn error of cobalamin metabolism. Effects of thap11 on erythroid differentiation and megakaryocytic. Thap11 mutations in a patient with a cblxlike phenotype implicates.
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Tha11 Recombinant Protein Thap Domaincontaining Protein 11.

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Thap11 is the most recently described member of this human protein family.

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Thpa11 shared by jumhan pikpak.

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The cterminal region of the transcriptional regulator thap11 forms.

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Thap11 is a recently discovered pluripotency factor and described as an important gene that involved in embryonic stem cells selfrenewal and embryo development, which works independently with other known pluripotency factors.

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