Výsledky vyhledávání - "Olga Karicheva"

Autor: Olga Karicheva, Bernardo Reina San Martin, Valérie Schreiber, Françoise Dantzer, Isabelle Robert

Publikováno v: Mol Aspects Med
Mol Aspects Med, 2013, 34 (6), pp.1138-52. ⟨10.1016/j.mam.2013.02.001⟩

To cope with the devastating insults constantly inflicted to their genome by intrinsic and extrinsic DNA damaging sources, cells have evolved a sophisticated network of interconnected DNA caretaking mechanisms that will detect, signal and repair the

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::50290f8181c5f6fc0a57e52d2ff9d814
https://doi.org/10.1016/j.mam.2013.02.001

Zobrazit plný text záznamu

PARP3 controls TGFβ and ROS driven epithelial-to-mesenchymal transition and stemness by stimulating a TG2-Snail-E-cadherin axis

Autor: Françoise Dantzer, Najat Magroun, Valérie Schreiber, Agnès Tissier, Nadège Wadier, Kathline Martin-Hernandez, Olga Karicheva, Romain Vauchelles, José Manuel Rodríguez-Vargas

Publikováno v: Oncotarget
Oncotarget, Impact journals, 2016, 7 (39), pp.64109-64123. ⟨10.18632/oncotarget.11627⟩

// Olga Karicheva 1 , Jose Manuel Rodriguez-Vargas 1 , Nadege Wadier 1 , Kathline Martin-Hernandez 1 , Romain Vauchelles 2 , Najat Magroun 1 , Agnes Tissier 3 , Valerie Schreiber 1 , Francoise Dantzer 1 1 Poly(ADP-ribosyl)ation and Genome Integrity,

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::968873ed55d506e058bda37969850174
https://www.oncotarget.com/lookup/doi/10.18632/oncotarget.11627

Zobrazit plný text záznamu

Correction of the consequences of mitochondrial 3243A>G mutation in the MT-TL1 gene causing the MELAS syndrome by tRNA import into mitochondria

Autor: Abdeldjalil Boucheham, Anne-Marie Mager-Heckel, Tom Schirtz, Olga Karicheva, Robert P. Martin, Nina Entelis, Olga Kolesnikova, Mikhail Y. Vysokikh, Igor A. Krasheninnikov, Anne Lombès, Ivan Tarassov

Publikováno v: Nucleic Acids Research

Mutations in human mitochondrial DNA are often associated with incurable human neuromuscular diseases. Among these mutations, an important number have been identified in tRNA genes, including 29 in the gene MT-TL1 coding for the tRNA(Leu(UUR)). The m

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::be6f8eab79c213f15268dc8dc8c2fb5e
http://europepmc.org/articles/PMC3185436

Zobrazit plný text záznamu

Acute Infantile Liver Failure Due to Mutations in the TRMU Gene

Autor: Avraham Shaag, Daphna Marom, Anne-Marie Mager-Heckel, Hanna Mandel, Reeval Segel, Marine Beinat, Orly Elpeleg, Agnès Rötig, Olga Karicheva, Ivan Tarassov, Ann Saada, Orit Pappo, Avraham Zeharia, Noa Ofek

Acute liver failure in infancy accompanied by lactic acidemia was previously shown to result from mtDNA depletion. We report on 13 unrelated infants who presented with acute liver failure and lactic acidemia with normal mtDNA content. Four died durin

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1cd39137ac66337caf1c39ca6276dd63
https://europepmc.org/articles/PMC2820182/

Zobrazit plný text záznamu

Import of nuclear DNA-encoded RNAs into mitochondria and mitochondrial translation

Autor: Olga Karicheva, Piotr Kamenski, Robert P. Martin, Olga Kolesnikova, Nina Entelis, Ivan Tarassov, Igor A. Krasheninnikov

Publikováno v: ResearcherID
Scopus-Elsevier

Targeting nuclear DNA-encoded tRNA into mitochondria is a quasi-ubiquitous process, found in a variety of species, although the mechanisms of this pathway seem to differ from one system to another. In all cases reported, this import concerns small no

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::715291280408c08843ea211f8cf2736b
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=ORCID&SrcApp=OrcidOrg&DestLinkType=FullRecord&DestApp=WOS_CPL&KeyUT=WOS:000251085800009&KeyUID=WOS:000251085800009

Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání