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Search life-sciences literature (45,104,145 articles, preprints and more)

Suggested authors matching "AUTH:Ellezam B" with an ORCID

Benjamin Ellezam
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FOXR2 targets LHX6+/DLX+ neural lineages to drive CNS neuroblastoma.
Jessa S, De Cola A, Chandarana B, McNicholas M, Hébert S, Ptack A, Faury D, Tsai JW, Korshunov A, Phoenix TN, Ellezam B, Jones DTW, Taylor MD, Bandopadhayay P, Pathania M, Jabado N, Kleinman CL
Cancer Res, 04 Nov 2024
Cited by: 0 articles | PMID: 39495206
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MADD-like pattern of acylcarnitines associated with sertraline use.
Ingoglia F, Tanfous M, Ellezam B, Anderson KJ, Pasquali M, Botto LD
Mol Genet Metab Rep, 41:101142, 16 Sep 2024
Cited by: 0 articles | PMID: 39318848 | PMCID: PMC11421287
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Immune landscape of oncohistone-mutant gliomas reveals diverse myeloid populations and tumor-promoting function.
Andrade AF, Annett A, Karimi E, Topouza DG, Rezanejad M, Liu Y, McNicholas M, Gonzalez Santiago EG, Llivichuzhca-Loja D, Gehlhaar A, Jessa S, De Cola A, Chandarana B, Russo C, Faury D, Danieau G, Puligandla E, Wei Y, Zeinieh M, [...] Jabado N
Nat Commun, 15(1):7769, 05 Sep 2024
Cited by: 0 articles | PMID: 39237515 | PMCID: PMC11377583
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IRF2BPL-Related Disorder, Causing Neurodevelopmental Disorder with Regression, Abnormal Movements, Loss of Speech and Seizures (NEDAMSS) Is Characterized by Pathology Consistent with DRPLA.
Venkateswaran S, Michaud J, Ito Y, Geraghty M, Lewis EC, Ellezam B, Boycott KM, Dyment DA, Kernohan KD, Care4Rare Canada Consortium
Mov Disord, 39(11):2102-2109, 03 Sep 2024
Cited by: 0 articles | PMID: 39224955
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TULIPs decorate the three-dimensional genome of PFA ependymoma.
Johnston MJ, Lee JJY, Hu B, Nikolic A, Hasheminasabgorji E, Baguette A, Paik S, Chen H, Kumar S, Chen CCL, Jessa S, Balin P, Fong V, Zwaig M, Michealraj KA, Chen X, Zhang Y, Varadharajan S, Billon P, [...] Gallo M
Cell, 187(18):4926-4945.e22, 09 Jul 2024
Cited by: 0 articles | PMID: 38986619
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Apelin stimulation of the vascular skeletal muscle stem cell niche enhances endogenous repair in dystrophic mice.
Le Moal E, Liu Y, Collerette-Tremblay J, Dumontier S, Fabre P, Molina T, Dort J, Orfi Z, Denault N, Boutin J, Michaud J, Giguère H, Desroches A, Trân K, Ellezam B, Vézina F, Bedard S, Raynaud C, Balg F, [...] Bentzinger CF
Sci Transl Med, 16(739):eabn8529, 20 Mar 2024
Cited by: 2 articles | PMID: 38507466
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Impact of trametinib on the neuropsychological profile of NF1 patients.
Lalancette E, Cantin É, Routhier MÈ, Mailloux C, Bertrand MC, Kiaei DS, Larouche V, Tabori U, Hawkins C, Ellezam B, Décarie JC, Théoret Y, Métras MÉ, McKeown T, Ospina LH, Vairy S, Ramaswamy V, Coltin H, Sultan S, [...] Lippé S
J Neurooncol, 167(3):447-454, 05 Mar 2024
Cited by: 0 articles | PMID: 38443693
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H3K27me3 spreading organizes canonical PRC1 chromatin architecture to regulate developmental programs
Krug B, Hu B, Chen H, Ptack A, Chen X, Gretarsson KH, Deshmukh S, Kabir N, Andrade AF, Jabbour E, Harutyunyan AS, Lee JJY, Hulswit M, Faury D, Russo C, Xu X, Johnston MJ, Baguette A, Dahl NA, [...] Lu C
bioRxiv, 28 Nov 2023
Cited by: 0 articles | PPR: PPR765796
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Decreased dystrophin expression and elevated dystrophin-targeting miRNAs in anti-HMGCR immune-mediated necrotizing myopathy.
Marmen MB, Orfi Z, Dort J, Proulx-Gauthier JP, Chrestian N, Dumont NA, Ellezam B
Acta Neuropathol, 146(4):655-658, 05 Aug 2023
Cited by: 2 articles | PMID: 37543531
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N-acetylneuraminate pyruvate lyase controls sialylation of muscle glycoproteins essential for muscle regeneration and function.
Da Silva A, Dort J, Orfi Z, Pan X, Huang S, Kho I, Heckel E, Muscarnera G, van Vliet PP, Sturiale L, Messina A, Romeo DA, van Karnebeek CDM, Wen XY, Hinek A, Molina T, Andelfinger G, Ellezam B, Yamanaka Y, [...] Pshezhetsky AV
Sci Adv, 9(26):eade6308, 30 Jun 2023
Cited by: 3 articles | PMID: 37390204 | PMCID: PMC10313170
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SCA34 caused by ELOVL4 L168F mutation is a lysosomal lipid storage disease sharing pathology features with neuronal ceroid lipofuscinosis and peroxisomal disorders.
Ellezam B, Kaseka ML, Nguyen DK, Michaud J
Acta Neuropathol, 146(2):337-352, 15 May 2023
Cited by: 1 article | PMID: 37184663
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Single substitution in H3.3G34 alters DNMT3A recruitment to cause progressive neurodegeneration.
Khazaei S, Chen CCL, Andrade AF, Kabir N, Azarafshar P, Morcos SM, França JA, Lopes M, Lund PJ, Danieau G, Worme S, Adnani L, Nzirorera N, Chen X, Yogarajah G, Russo C, Zeinieh M, Wong CJ, Bryant L, [...] Jabado N
Cell, 186(6):1162-1178.e20, 01 Mar 2023
Cited by: 23 articles | PMID: 36931244 | PMCID: PMC10112048
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Detection and genomic analysis of BRAF fusions in Juvenile Pilocytic Astrocytoma through the combination and integration of multi-omic data.
Zwaig M, Baguette A, Hu B, Johnston M, Lakkis H, Nakada EM, Faury D, Juretic N, Ellezam B, Weil AG, Karamchandani J, Majewski J, Blanchette M, Taylor MD, Gallo M, Kleinman CL, Jabado N, Ragoussis J
BMC Cancer, 22(1):1297, 12 Dec 2022
Cited by: 4 articles | PMID: 36503484 | PMCID: PMC9743522
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K27M in canonical and noncanonical H3 variants occurs in distinct oligodendroglial cell lineages in brain midline gliomas.
Jessa S, Mohammadnia A, Harutyunyan AS, Hulswit M, Varadharajan S, Lakkis H, Kabir N, Bashardanesh Z, Hébert S, Faury D, Vladoiu MC, Worme S, Coutelier M, Krug B, Faria Andrade A, Pathania M, Bajic A, Weil AG, Ellezam B, [...] Kleinman CL
Nat Genet, 54(12):1865-1880, 05 Dec 2022
Cited by: 34 articles | PMID: 36471070 | PMCID: PMC9742294
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Scleromyositis: A distinct novel entity within the systemic sclerosis and autoimmune myositis spectrum. Implications for care and pathogenesis.
Giannini M, Ellezam B, Leclair V, Lefebvre F, Troyanov Y, Hudson M, Senécal JL, Geny B, Landon-Cardinal O, Meyer A
Front Immunol, 13:974078, 26 Jan 2023
Cited by: 10 articles | PMID: 36776390 | PMCID: PMC9910219
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Myositis with prominent B cell aggregates may meet classification criteria for sporadic inclusion body myositis.
Meyer A, Troyanov Y, Korathanakhun P, Landon-Cardinal O, Leclair V, Allard-Chamard H, Bourré-Tessier J, Makhzoum JP, Isabelle C, Larue S, Grand'Maison F, Massie R, Page ML, Mansour AM, Routhier N, Zarka F, Roy F, Sonnen J, Satoh M, [...] O'Ferrall E
Neuromuscul Disord, 33(2):169-182, 05 Dec 2022
Cited by: 0 articles | PMID: 36649672
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Capillary pathology with prominent basement membrane reduplication is the hallmark histopathological feature of scleromyositis.
Ellezam B, Leclair V, Troyanov Y, Bersali I, Giannini M, Hoa S, Bourré-Tessier J, Nadon V, Drouin J, Karamchandani J, O'Ferrall E, Lannes B, Satoh M, Fritzler MJ, Senécal JL, Hudson M, Meyer A, Landon-Cardinal O
Neuropathol Appl Neurobiol, 48(7):e12840, 12 Aug 2022
Cited by: 6 articles | PMID: 35894636
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Anti-synthetase syndrome occurring after SARS-CoV-2 infection.
Bouchard Marmen M, Ellezam B, Fritzler MJ, Troyanov Y, Gould PV, Satoh M, Meyer A, Mahjoub Z, Landon-Cardinal O
Scand J Rheumatol, 51(3):255-257, 09 Feb 2022
Cited by: 4 articles | PMID: 35138215
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Autoantibody profiles delineate distinct subsets of scleromyositis.
Leclair V, D'Aoust J, Gyger G, Landon-Cardinal O, Meyer A, O'Ferrall E, Karamchandani J, Massie R, Ellezam B, Satoh M, Troyanov Y, Fritzler MJ, Hudson M, Canadian Inflammatory Myopathy Study Group
Rheumatology (Oxford), 61(3):1148-1157, 01 Mar 2022
Cited by: 11 articles | PMID: 34146090
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Myositis with prominent B-cell aggregates causing shrinking lung syndrome in systemic lupus erythematosus: a case report.
Roy F, Korathanakhun P, Karamchandani J, Dubé BP, Landon-Cardinal O, Routhier N, Peyronnard C, Massie R, Leclair V, Meyer A, Bourré-Tessier J, Satoh M, Fritzler MJ, Senécal JL, Hudson M, O'Ferrall EK, Troyanov Y, Ellezam B, Makhzoum JP
BMC Rheumatol, 6(1):11, 16 Feb 2022
Cited by: 0 articles | PMID: 35168668 | PMCID: PMC8848966
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Upfront BRAF/MEK inhibitors for treatment of high-grade glioma: A case report and review of the literature.
Arbour G, Ellezam B, Weil AG, Cayrol R, Vanan MI, Coltin H, Larouche V, Erker C, Jabado N, Perreault S
Neurooncol Adv, 4(1):vdac174, 01 Jan 2022
Cited by: 4 articles | PMID: 36567957 | PMCID: PMC9772816
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French-Canadian families from Saguenay-Lac-Saint-Jean: a new founder population for APECED.
Cruz Marino T, Villeneuve H, Leblanc J, Duranceau C, Caron P, Morin C, Milot M, Chrétien R, Gagnon MM, Mathieu J, Ellezam B, Buhas D
Endocrine, 75(1):48-58, 30 Nov 2021
Cited by: 0 articles | PMID: 34846681
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Autologous humanized mouse models of iPSC-derived tumors enable characterization and modulation of cancer-immune cell interactions.
Moquin-Beaudry G, Benabdallah B, Maggiorani D, Le O, Li Y, Colas C, Raggi C, Ellezam B, M'Callum MA, Dal Soglio D, Guimond JV, Paganelli M, Haddad E, Beauséjour C
Cell Rep Methods, 2(1):100153, 14 Jan 2022
Cited by: 12 articles | PMID: 35474871 | PMCID: PMC9017190
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Clinical phenotypes and prognostic features of embryonal tumours with multi-layered rosettes: a Rare Brain Tumor Registry study.
Khan S, Solano-Paez P, Suwal T, Lu M, Al-Karmi S, Ho B, Mumal I, Shago M, Hoffman LM, Dodgshun A, Nobusawa S, Tabori U, Bartels U, Ziegler DS, Hansford JR, Ramaswamy V, Hawkins C, Dufour C, André N, [...] Rare Brain Tumor Registry
Lancet Child Adolesc Health, 5(11):800-813, 30 Sep 2021
Cited by: 9 articles | PMID: 34599879
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Capillary basement membrane reduplication in myositis patients with mild clinical features of systemic sclerosis supports the concept of 'scleromyositis'.
Ellezam B, Leclair V, Troyanov Y, Meyer A, Hudson M, Landon-Cardinal O
Acta Neuropathol, 142(2):395-397, 11 Jun 2021
Cited by: 4 articles | PMID: 34115197
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