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SRB4D Rabbit Polyclonal Antibody, 100ul 3D Culture Mutations in this gene cause

SKU: 28634344861

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SRB4D Rabbit Polyclonal Antibody, 100ul 3D Culture Mutations in this gene cause

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Description

Mutations in this gene cause primary ciliary dyskinesia type 3| as well as Kartagener syndrome| which are both diseases due to ciliary defects

This gene encodes a member of the phosphatase and actin regulator protein family

PER2 is upregulated by CLOCK/ARNTL heterodimers but then represses this upregulation in a feedback loop using PER/CRY heterodimers to interact with CLOCK/ARNTL

They form a three-tiered signaling module composed of MAPKKKs

SRB4D Rabbit Polyclonal Antibody, 100ul 3D Culture Mutations in this gene cause

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