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searching for USP9X 8 found (24 total)

alternate case: uSP9X

Ectoderm specification (2,122 words) [view diff] case mismatch in snippet view article find links to article

TIF1-γ, TRIM33); later, it was found that the deubiquitinating enzyme, FAM/USP9x, is able to overcome the effects of ubiquitination made by Ectodermin in

BRSK1 (601 words) [view diff] exact match in snippet view article find links to article

M, Peggie M, Alessi DR (Apr 2008). "Control of AMPK-related kinases by USP9X and atypical Lys(29)/Lys(33)-linked polyubiquitin chains" (PDF). The Biochemical

Xenopus (5,805 words) [view diff] case mismatch in snippet view article find links to article

Cordenonsi M, Montagner M, Zacchigna L, Adorno M, et al. (January 2009). "FAM/USP9x, a deubiquitinating enzyme essential for TGFbeta signaling, controls Smad4

Stress granule (12,548 words) [view diff] exact match in snippet view article find links to article

PMID 23912948. Narayanan N, Wang Z, Li L, Yang Y (2017). "Arginine methylation of USP9X promotes its interaction with TDRD3 and its anti-apoptotic activities in

USP27X (2,080 words) [view diff] exact match in snippet view article find links to article

Besides, other proteins from the same peptidase C19 family such as the USP9X have been linked to several neurologic disorders. "USP27X - Ubiquitin carboxyl-terminal

Ubiquitin C (4,261 words) [view diff] exact match in snippet view article find links to article

Peggie M, Alessi DR (April 2008). "Control of AMPK-related kinases by USP9X and atypical Lys(29)/Lys(33)-linked polyubiquitin chains" (PDF). The Biochemical

Nodal signaling pathway (3,355 words) [view diff] case mismatch in snippet view article find links to article

Moro S, Modena N, Argenton F, Newfeld SJ, Piccolo S (January 2009). "FAM/USP9x, a deubiquitinating enzyme essential for TGFbeta signaling, controls Smad4

X-chromosome reactivation (5,094 words) [view diff] exact match in snippet view article find links to article

Pfundt R, et al. (February 2016). "De Novo Loss-of-Function Mutations in USP9X Cause a Female-Specific Recognizable Syndrome with Developmental Delay and