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Identification of a transient state during the acquisition of temozolomide resistance in glioblastoma.
Rabé M(1), Dumont S(1)(2), Álvarez-Arenas A(3), Janati H(4), Belmonte-Beitia J(3), Calvo GF(3), Thibault-Carpentier C(5), Séry Q(1)(6), Chauvin C(1), Joalland N(1), Briand F(1), Blandin S(7), Scotet E(1), Pecqueur C(1), Clairambault J(4), Oliver L(1)(8), Perez-Garcia V(3), Nadaradjane A(1)(6), Cartron PF(1)(6), Gratas C(9)(10), Vallette FM(11)(12).
Cell Death Dis Jan. 6, 2020
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In utero exposure to acetaminophen and ibuprofen leads to intergenerational accelerated reproductive aging in female mice.
Rossitto M(1), Ollivier M(1)(2), Déjardin S(1), Pruvost A(3), Brun C(4), Marchive C(1), Nguyen AL(3), Ghettas A(3), Keime C(5), de Massy B(4), Poulat F(1), Philibert P(1)(6), Boizet-Bonhoure B(7).
Commun Biol Aug. 13, 2019
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Unstable TTTTA/TTTCA expansions in MARCH6 are associated with Familial Adult Myoclonic Epilepsy type 3.
Florian RT(1), Kraft F(2), Leitao E(1), Kaya S(1), Klebe S(3), Magnin E(4), van Rootselaar AF(5), Buratti J(6), Kuhnel T(1), Schroder C(1), Giesselmann S(2), Tschernoster N(7), Altmueller J(7), Lamiral A(4), Keren B(6), Nava C(6)(8), Bouteiller D(8), Forlani S(8), Jornea L(8), Kubica R(1), Ye T(9), Plassard D(9), Jost B(9), Meyer V(10), Deleuze JF(10), Delpu Y(11), Avarello MDM(11), Vijfhuizen LS(12), Rudolf G(9)(13), Hirsch E(13), Kroes T(14), Reif PS(15)(16), Rosenow F(15)(16), Ganos C(17), Vidailhet M(8)(18), Thivard L(18), Mathieu A(19), Bourgeron T(19), Kurth I(2), Rafehi H(20)(21)(22), Steenpass L(1), Horsthemke B(1); FAME consortium, LeGuern E(6)(8), Klein KM(15)(16)(23), Labauge P(24), Bennett MF(20)(21)(22), Bahlo M(20)(21), Gecz J(14)(25), Corbett MA(14), Tijssen MAJ(26), van den Maagdenberg AMJM(12)(27), Depienne C(28)(29)(30).
Nat Commun Oct. 29, 2019
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Hypoxic Environment and Paired Hierarchical 3D and 2D Models of Pediatric H3.3-Mutated Gliomas Recreate the Patient Tumor Complexity.
Blandin AF(1), Durand A(1), Litzler M(1), Tripp A(1), Guerin E(1), Ruhland E(2), Obrecht A(3), Keime C(4), Fuchs Q(5), Reita D(1)(5), Lhermitte B(5)(6)(7), Coca A(8), Jones C(9), Rebel IL(5), Villa P(3), Namer IJ(3), Dontenwill M(5), Guenot D(1), Entz-Werle N(5)(10).
Cancers (Basel) Nov. 26, 2019
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Longitudinal transcriptomic analysis of altered pathways in a CHMP2Bintron5-based model of ALS-FTD.
Waegaert R(1), Dirrig-Grosch S(1), Parisot F(1), Keime C(2), Henriques A(1), Loeffler JP(1), Rene F(3).
Neurobiol Dis Dec. 16, 2019
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Rfx6 promotes the differentiation of peptide-secreting enteroendocrine cells while repressing genetic programs controlling serotonin production.
Piccand J(1), Vagne C(1), Blot F(1), Meunier A(1), Beucher A(1), Strasser P(1), Lund ML(2), Ghimire S(1), Nivlet L(1), Lapp C(1), Petersen N(2), Engelstoft MS(2), Thibault-Carpentier C(1), Keime C(1), Correa SJ(1), Schreiber V(1), Molina N(1), Schwartz TW(2), De Arcangelis A(3), Gradwohl G(4).
Mol Metab Nov 2019
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Exacerbation of C1q dysregulation, synaptic loss and memory deficits in tau pathology linked to neuronal adenosine A2A receptor.
Carvalho K(1), Faivre E(1), Pietrowski MJ(2), Marques X(3), Gomez-Murcia V(1), Deleau A(1), Huin V(1), Hansen JN(2), Kozlov S(2), Danis C(1)(4), Temido-Ferreira M(5), Coelho JE(5), Meriaux C(1), Eddarkaoui S(1), Gras SL(6), Dumoulin M(7), Cellai L(1); NeuroCEB Brain Bank, Landrieu I(4), Chern Y(8), Hamdane M(1), Buee L(1), Boutillier AL(9), Levi S(3), Halle A(2)(10), Lopes LV(5), Blum D(1).
Brain Oct. 10, 2019
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Novel IQCE variations confirm its role in postaxial polydactyly and cause ciliary defect phenotype in zebrafish.
Estrada-Cuzcano A(1), Etard C(2), Delvallee C(1), Stoetzel C(1), Schaefer E(1)(3), Scheidecker S(1)(4), Geoffroy V(1), Schneider A(1), Studer F(5), Mattioli F(6), Chennen K(1)(7), Sigaudy S(8), Plassard D(9), Poch O(7), Piton A(4)(6), Strahle U(2), Muller J(1)(4), Dollfus H(1)(3)(5).
Hum Mutat Sept. 24, 2019
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Attitudes towards Genetic Information Delivered by High-Throughput Sequencing among Molecular Geneticists, Genetic Counselors, Medical Advisors and Students in France.
Titerlea V(1), Dembele D(2), Mandel JL(3), Laporte J(2).
Eur J Med Genet Sep 16:103770 2019
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Interleukin-32 Contributes to Human Nonalcoholic Fatty Liver Disease and Insulin Resistance.
Dali-Youcef N(1)(2), Vix M(3), Costantino F(3), El-Saghire H(4), Lhermitte B(5), Callari C(3), D'Agostino J(3), Perretta S(3), Paveliu S(3), Gualtierotti M(3), Dumeny E(6), Oudot MA(4), Jaulin A(2), Dembele D(7), Zeisel MB(4), Tomasetto C(2), Baumert TF(4)(8), Doffoel M(8).
Hepatol Commun July 19, 2019
