Aller au contenu principal
Profil bibliographique

Roxane Lahmi

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

14Publications signalées
248Citations signalées
0Affiliations récentes

Les domaines associés

Microtubule and mitosis dynamicsPhotosynthetic Processes and MechanismsCancer-related Molecular PathwaysUbiquitin and proteasome pathwaysPlant Stress Responses and Tolerance

Les publications récentes

Accès ouvert 2024 article OpenAlex

Cell cycle oscillators underlying orderly proteolysis of E2F8

Sapir Nachum, Evelin Sheinberger-Chorni, Sarit Zomer-Polak, Meital Cohen et autres

E2F8 is a transcriptional repressor that antagonizes E2F1 at the crossroads of the cell cycle, apoptosis, and cancer. Previously, we discovered that E2F8 is a direct target of the APC/C ubiquitin ligase. Nevertheless, it remains unknown how E2F8 is dynamically controlled throughout …

us (code pays fourni par la source)

0 citations Carolina Digital Repository (University of North Carolina at Chapel Hill)
Accès ouvert 2020 article OpenAlex

Cell cycle oscillators underlying orderly proteolysis of E2F8

Danit Wasserman, Sapir Nachum, Meital Cohen, Taylor P. Enrico et autres

We uncovered interlocking mechanisms regulating the temporal proteolysis of the transcriptional repressor E2F8 in cycling cells including SCF Cyclin F in G2, dephosphorylation of Cdk1 sites, and activation of APC/C Cdh1 , but not APC/C Cdc20 during mitotic exit and G1. Differential …

il, us (code pays fourni par la source)

20 citations Molecular Biology of the Cell
Accès ouvert 2019 preprint OpenAlex

Cell cycle oscillators underlying orderly proteolysis of E2F8

Danit Wasserman, Sapir Nachum, Meital Cohen, Taylor P. Enrico et autres

Abstract E2F8 is a transcriptional repressor that antagonizes the canonical cell cycle transcription factor E2F1. Despite the importance of this atypical E2F family member in cell cycle, apoptosis and cancer, we lack a complete description of the mechanisms that control its dynamics. …

il, us (code pays fourni par la source)

6 citations bioRxiv (Cold Spring Harbor Laboratory)
Accès ouvert 2019 article OpenAlex

A high-throughput integrated microfluidics method enables tyrosine autophosphorylation discovery

Hadas Nevenzal, Meirav Noach-Hirsh, Or Skornik-Bustan, Lev Brio et autres

Autophosphorylation of receptor and non-receptor tyrosine kinases is a common molecular switch with broad implications for pathogeneses and therapy of cancer and other human diseases. Technologies for large-scale discovery and analysis of autophosphorylation are limited by the inherent difficulty to distinguish between …

il (code pays fourni par la source)

14 citations Communications Biology
Accès ouvert 2013 article OpenAlex

Gas2l3, a Novel Constriction Site-Associated Protein Whose Regulation Is Mediated by the APC/CCdh1 Complex

Tal Pe’er, Roxane Lahmi, Yaara Sharaby, Evelin Chorni et autres

Growth arrest-specific 2-like protein 3 (Gas2l3) was recently identified as an Actin/Tubulin cross-linker protein that regulates cytokinesis. Using cell-free systems from both frog eggs and human cells, we show that the Gas2l3 protein is targeted for ubiquitin-mediated proteolysis by the APC/C(Cdh1) complex, …

il, us (code pays fourni par la source)

24 citations PLoS ONE
Accès ouvert 2009 article OpenAlex

Codanin-1, the protein encoded by the gene mutated in congenital dyserythropoietic anemia type I (CDAN1), is cell cycle-regulated

S. Noy-Lotan, Orly Dgany, Roxane Lahmi, Nathaly Marcoux et autres

BACKGROUND: Congenital dyserythropoietic anemia type I is an inherited autosomal recessive macrocytic anemia associated with ineffective erythropoiesis and the development of secondary hemochromatosis. Distinct erythroid precursors with internuclear chromatin bridges and spongy heterochromatin are pathognomonic for the disease. The mutated gene (CDAN1) …

il, us (code pays fourni par la source)

43 citations Haematologica
2008 article OpenAlex

Codanin-1, the Protein Encoded by the Gene Mutated in Congenital Dyserythropoietic Anemia Type I (CDAN1), Is Cell Cycle Regulated

Sharon Noy‐Lotan, Orly Dgany, Roxane Lahmi, Nathaly Marcoux et autres

Abstract Congenital dyserythropoietic anemia (CDA) type I is an inherited autosomal recessive macrocytic anemia associated with ineffective erythropoiesis and the development of secondary hemochromatosis. Distinct erythroid precursors with inter-nuclear chromatin bridges and spongy heterochromatin are pathognomonic for the disease. The mutated gene …

il, us (code pays fourni par la source)

2 citations Blood

BNTIC News n’est pas le producteur de ces données. Les publications sont interrogées à la demande dans Crossref, OpenAIRE, DOAJ, Europe PMC, HAL, DataCite, AfricArXiv, ROR et la Banque mondiale, sans clé d’accès. OpenAlex reste optionnel. Aucun service payant n’est nécessaire et aucune donnée externe n’est enregistrée en base. Consulter les sources et leurs limites.