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Profil bibliographique

Michelle de la Vega

Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.

21Publications signalées
736Citations signalées
0Affiliations récentes

Les domaines associés

Ubiquitin and proteasome pathwaysCancer, Hypoxia, and MetabolismRNA modifications and cancerCell death mechanisms and regulationMuscle Physiology and Disorders

Les publications récentes

Accès ouvert 2023 other OpenAlex

Data from The Deubiquitinating Enzyme USP17 Is Highly Expressed in Tumor Biopsies, Is Cell Cycle Regulated, and Is Required for G1-S Progression

Cheryl McFarlane, Alyson A. Kelvin, Michelle de la Vega, Ureshnie Govender et autres

Abstract Ubiquitination is a reversible posttranslational modification that is essential for cell cycle control, and it is becoming increasingly clear that the removal of ubiquitin from proteins by deubiquitinating enzymes (DUB) is equally important. In this study, we have identified high levels …

0 citations
Accès ouvert 2023 other OpenAlex

Data from The Deubiquitinating Enzyme USP17 Is Highly Expressed in Tumor Biopsies, Is Cell Cycle Regulated, and Is Required for G1-S Progression

Cheryl McFarlane, Alyson A. Kelvin, Michelle de la Vega, Ureshnie Govender et autres

Abstract Ubiquitination is a reversible posttranslational modification that is essential for cell cycle control, and it is becoming increasingly clear that the removal of ubiquitin from proteins by deubiquitinating enzymes (DUB) is equally important. In this study, we have identified high levels …

0 citations
Accès ouvert 2017 article OpenAlex

PTRH2 gene mutation causes progressive congenital skeletal muscle pathology

Jinger Doe, Angela M. Kaindl, Mayumi Jijiwa, Michelle de la Vega et autres

Peptidyl-tRNA hydrolase 2 (PTRH2) regulates integrin-mediated pro-survival and apoptotic signaling. PTRH2 is critical in muscle development and regulates myogenic differentiation. In humans a biallelic mutation in the PTRH2 gene causes infantile-onset multisystem disease with progressive muscle weakness. We report here that the …

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15 citations Human Molecular Genetics
Accès ouvert 2015 article OpenAlex

Bit-1 is an essential regulator of myogenic differentiation

Genevieve S. Griffiths, Jinger Doe, Mayumi Jijiwa, Pam Van Ry et autres

Muscle differentiation requires a complex signaling cascade that leads to the production of multinucleated myofibers. Genes regulating the intrinsic mitochondrial apoptotic pathway also function in controlling cell differentiation. How such signaling pathways are regulated during differentiation is not fully understood. Bit-1 (also …

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19 citations Journal of Cell Science
Accès ouvert 2014 article OpenAlex

Mutations in PTRH2 cause novel infantile‐onset multisystem disease with intellectual disability, microcephaly, progressive ataxia, and muscle weakness

Hao Hu, Michelle L. Matter, Lina Issa‐Jahns, Mayumi Jijiwa et autres

OBJECTIVE: To identify the cause of a so-far unreported phenotype of infantile-onset multisystem neurologic, endocrine, and pancreatic disease (IMNEPD). METHODS: We characterized a consanguineous family of Yazidian-Turkish descent with IMNEPD. The two affected children suffer from intellectual disability, postnatal microcephaly, growth retardation, …

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38 citations Annals of Clinical and Translational Neurology

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