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AT132 Rabbit Polyclonal Antibody, 20ul Cell Senescence Mutations in CTNNB1 are a

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AT132 Rabbit Polyclonal Antibody, 20ul Cell Senescence Mutations in CTNNB1 are aThis gene encodes a member of the P5 subfamily of ATPases which transports inorganic cations as well as other substrates. Mutations in this gene are associated with Kufor Rakeb syndrome (KRS), also referred to as Parkinson disease 9. Multiple transcript variants encoding different isoforms have been found for this gene.

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Description

Mutations in CTNNB1 are a cause of colorectal cancer (CRC)

can unbiquitinate and induce the degradation of this protein

Its ligand

Alternate splicing of this gene results in multiple transcript variants

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AT132 Rabbit Polyclonal Antibody, 20ul Cell Senescence Mutations in CTNNB1 are aThis gene encodes a member of the P5 subfamily of ATPases which transports inorganic cations as well as other substrates. Mutations in this gene are associated with Kufor Rakeb syndrome (KRS), also referred to as Parkinson disease 9. Multiple transcript variants encoding different isoforms have been found for this gene.

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