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Profil bibliographique

Chiara Iannascoli

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

13Publications signalées
250Citations signalées
2Affiliations récentes

Les institutions déclarées

Les domaines associés

DNA Repair MechanismsCarcinogens and Genotoxicity AssessmentPlant Genetic and Mutation StudiesPorphyrin Metabolism and DisordersGenetic Neurodegenerative Diseases

Les publications récentes

Accès ouvert 2023 supplementary-materials OpenAlex

Supplementary Figures from Werner Syndrome Helicase Has a Critical Role in DNA Damage Responses in the Absence of a Functional Fanconi Anemia Pathway

Monika Aggarwal, Taraswi Banerjee, Joshua A. Sommers, Chiara Iannascoli et autres

PDF file, 1010K, Chemical structures of structurally related analogs of the previously identified parent compound NSC 19630 (S1); Effect of NSC 617145 on WRN catalytic functions and DNA unwinding by other helicases (S2); Effect of selected small molecules structurally related to NSC …

0 citations
Accès ouvert 2023 supplementary-materials OpenAlex

Supplementary Figures from Werner Syndrome Helicase Has a Critical Role in DNA Damage Responses in the Absence of a Functional Fanconi Anemia Pathway

Monika Aggarwal, Taraswi Banerjee, Joshua A. Sommers, Chiara Iannascoli et autres

PDF file, 1010K, Chemical structures of structurally related analogs of the previously identified parent compound NSC 19630 (S1); Effect of NSC 617145 on WRN catalytic functions and DNA unwinding by other helicases (S2); Effect of selected small molecules structurally related to NSC …

0 citations
Accès ouvert 2023 other OpenAlex

Data from Werner Syndrome Helicase Has a Critical Role in DNA Damage Responses in the Absence of a Functional Fanconi Anemia Pathway

Monika Aggarwal, Taraswi Banerjee, Joshua A. Sommers, Chiara Iannascoli et autres

Abstract Werner syndrome is genetically linked to mutations in WRN that encodes a DNA helicase-nuclease believed to operate at stalled replication forks. Using a newly identified small-molecule inhibitor of WRN helicase (NSC 617145), we investigated the role of WRN in the interstrand …

0 citations
Accès ouvert 2023 other OpenAlex

Data from Werner Syndrome Helicase Has a Critical Role in DNA Damage Responses in the Absence of a Functional Fanconi Anemia Pathway

Monika Aggarwal, Taraswi Banerjee, Joshua A. Sommers, Chiara Iannascoli et autres

Abstract Werner syndrome is genetically linked to mutations in WRN that encodes a DNA helicase-nuclease believed to operate at stalled replication forks. Using a newly identified small-molecule inhibitor of WRN helicase (NSC 617145), we investigated the role of WRN in the interstrand …

0 citations
Accès ouvert 2015 article OpenAlex

The WRN exonuclease domain protects nascent strands from pathological MRE11/EXO1-dependent degradation

Chiara Iannascoli, Valentina Palermo, Ivana Murfuni, Annapaola Franchitto et autres

The WRN helicase/exonuclease protein is required for proper replication fork recovery and maintenance of genome stability. However, whether the different catalytic activities of WRN cooperate to recover replication forks in vivo is unknown. Here, we show that, in response to replication perturbation …

it (code pays fourni par la source)

86 citations Nucleic Acids Research
Accès ouvert 2013 article OpenAlex

Werner Syndrome Helicase Has a Critical Role in DNA Damage Responses in the Absence of a Functional Fanconi Anemia Pathway

Monika Aggarwal, Taraswi Banerjee, Joshua A. Sommers, Chiara Iannascoli et autres

Werner syndrome is genetically linked to mutations in WRN that encodes a DNA helicase-nuclease believed to operate at stalled replication forks. Using a newly identified small-molecule inhibitor of WRN helicase (NSC 617145), we investigated the role of WRN in the interstrand cross-link …

it, us (code pays fourni par la source)

90 citations Cancer Research
2011 article OpenAlex

Novel and recurrent JAG1 mutations in patients with tetralogy of Fallot

Valentina Guida, Francesca Chiappe, Rosangela Ferese, Gianluca Usala et autres

Supporting Information The following Supporting information is available for this article: Fig. S1. Denaturing high-performance liquid chromatography electropherograms. (a) Electropherograms showing c.925G>C, predicting p.Gly309Arg in the JAGGED1 (JAG1) gene from a patient (TF4) with isolated tetralogy of Fallot (TOF) versus wild type. …

it (code pays fourni par la source)

12 citations Clinical Genetics

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