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Profil bibliographique

Nathan J. Brown

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

4Publications signalées
95Citations signalées
1Affiliations récentes

Les institutions déclarées

Les domaines associés

T-cell and B-cell ImmunologyParkinson's Disease Mechanisms and TreatmentsAlzheimer's disease research and treatmentsImmune Response and InflammationImmunotherapy and Immune Responses

Les publications récentes

Accès ouvert 2024 article OpenAlex

Structural basis of MPL activation by thrombopoietin

Amirhossein Mafi, Matthew A. Bratkowski, Jiefei Geng, Alyssa Brito et autres

Myeloproliferative leukemia protein (MPL), also known as thrombopoietin (TPO) receptor, is a class I cytokine receptor that is expressed on hematopoietic progenitors, promoting growth and differentiation toward the megakaryocyte lineage and is critical for normal platelet production. Mutations in MPL, TPO, or …

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6 citations Blood Vessels Thrombosis & Hemostasis
Accès ouvert 2024 article OpenAlex

Broad proteomics analysis of seeding-induced aggregation of α-synuclein in M83 neurons reveals remodeling of proteostasis mechanisms that might contribute to Parkinson’s disease pathogenesis

Casey J. Lumpkin, Hiral S. Patel, Gregory K. Potts, Shilpi Chaurasia et autres

Aggregation of misfolded α-synuclein (α-syn) is a key characteristic feature of Parkinson's disease (PD) and related synucleinopathies. The nature of these aggregates and their contribution to cellular dysfunction is still not clearly elucidated. We employed mass spectrometry-based total and phospho-proteomics to characterize …

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5 citations Molecular Brain
2024 article OpenAlex

An anti–TNF–glucocorticoid receptor modulator antibody-drug conjugate is efficacious against immune-mediated inflammatory diseases

Michael J. McPherson, Adrian D. Hobson, Axel Hernández, Christopher C. Marvin et autres

Glucocorticoids (GCs) are efficacious drugs used for treating many inflammatory diseases, but the dose and duration of administration are limited because of severe side effects. We therefore sought to identify an approach to selectively target GCs to inflamed tissue. Previous work identified …

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30 citations Science Translational Medicine

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