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Profil bibliographique

Joseph Martin Dalloul

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

3Publications signalées
19Citations signalées
3Affiliations récentes

Les institutions déclarées

Les domaines associés

Ubiquitin and proteasome pathwaysGenetics and Neurodevelopmental DisordersGlaucoma and retinal disordersEndoplasmic Reticulum Stress and DiseaseRNA modifications and cancer

Les publications récentes

Accès ouvert 2024 article OpenAlex

Inhibition of pterygium cell fibrosis by the Rho kinase inhibitor

Jiannong Dai, Naga Pradeep Rayana, Michael Peng, Chenna Kesavulu Sugali et autres

Pterygium is an ocular disease in which the conjunctival tissue invades the cornea. When the pterygium tissue reaches the pupillary region, the visual function of the patient is affected. Currently, surgical removal is the only effective treatment. However, the recurrence rate of …

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3 citations Scientific Reports
Accès ouvert 2023 article OpenAlex

Systemic proteome phenotypes reveal defective metabolic flexibility in Mecp2 mutants

Stephanie A. Zlatic, Erica Werner, Veda Surapaneni, Chelsea E. Lee et autres

Genes mutated in monogenic neurodevelopmental disorders are broadly expressed. This observation supports the concept that monogenic neurodevelopmental disorders are systemic diseases that profoundly impact neurodevelopment. We tested the systemic disease model focusing on Rett syndrome, which is caused by mutations in MECP2. …

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13 citations Human Molecular Genetics
Accès ouvert 2023 preprint OpenAlex

Systemic Proteome Phenotypes Reveal Defective Metabolic Flexibility in Mecp2 Mutants

Stephanie A. Zlatic, Erica Werner, Veda Surapaneni, Chelsea E. Lee et autres

Genes mutated in monogenic neurodevelopmental disorders are broadly expressed. This observation supports the concept that monogenic neurodevelopmental disorders are systemic diseases that profoundly impact neurodevelopment. We tested the systemic disease model focusing on Rett syndrome, which is caused by mutations in MECP2. …

us (code pays fourni par la source)

3 citations bioRxiv (Cold Spring Harbor Laboratory)

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