neurofibromatosis 2/arginine

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The distribution of constitutional and somatic mutations in the neurofibromatosis 2 gene.

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Ingia / Ingia

Constitutional heterozygous inactivating mutations in the neurofibromatosis 2 (NF2) tumor suppressor gene cause the autosomal dominant disease NF2, and biallelic inactivating somatic NF2 mutations are found in a high proportion of unilateral sporadic vestibular schwannoma (USVS) and sporadic

Regulation of cell proliferation and adhesion by means of a novel region of drosophila merlin interacting with Sip1.

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Ingia / Ingia

BACKGROUND The tumor suppressor protein merlin is thought to regulate cell proliferation and cell adhesion through interaction with protein partners. Loss of merlin is associated with Neurofibromatosis Type 2 (NF2) tumors. NHERF1 or EBP50 is a scaffolding protein that functions in apical

A role for the p53 pathway in the pathology of meningiomas with NF2 loss.

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Ingia / Ingia

The neurofibromatosis 2 locus (NF2) is inactivated through mutation and loss of heterozygosity (LOH) in 40-65% of all sporadic meningiomas, while the role of the p53 tumor suppression pathway in meningioma initiation and progression is still unclear. This study aims to determine if a p53 codon 72

Merlin sumoylation is required for its tumor suppressor activity.

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Ingia / Ingia

Merlin, encoded by the Neurofibromatosis 2 (NF2) gene, is a multifunctional tumor suppressor that integrates and regulates extracellular cues and intracellular signaling pathways, both at the plasma membrane and in the nucleus, to control cell proliferation, migration and invasion. Molecular

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Herbal & Natural Medicine

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Panga maslahi yako na fanya tarehe ya utafiti wa habari, majaribio ya kliniki na ruhusu

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