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Adult Myopathic CPT-2 Deficiency The adult form of CPT2 deficiency, the myopathic form, is the most common form of CPT2 deficiency
This dimerization process is dependent upon a short HGF domain located between its N-terminal and first kringle domain referred to as the hinge region [83] ( Figure 2 )
However, these mice develop early-onset cataracts and exhibit defects in muscle satellite cell proliferation, highlighting a protective role under specific physiological stresses
(2023, Sep 27)
The family of NF-B consists of five structurally similar members, involving p50/p105 (NF-B1), p52/p100 (NF-B2), RelA (p65), RelB, and c-Rel (Liu et al
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