نتائج البحث - "Jannier, S"

1

دورية أكاديمية

Bevacizumab, Irinotecan, or Topotecan Added to Temozolomide for Children With Relapsed and Refractory Neuroblastoma: Results of the ITCC-SIOPEN BEACON-Neuroblastoma Trial

المؤلفون: Moreno, L., Weston, R., Owens, C., Valteau-Couanet, D., Gambart, M., Castel, V., Zwaan, C.M., Nysom, K., Gerber, N., Castellano, A., Laureys, G., Ladenstein, R., Rössler, J., Makin, G., Murphy, D., Morland, B., Vaidya, S., Thebaud, E., van Eijkelenburg, N., Tweddle, D.A., Barone, G., Tandonnet, J., Corradini, N., Chastagner, P., Paillard, C., Bautista, F.J., Gallego Melcon, S., De Wilde, B., Marshall, L., Gray, J., Burchill, S.A., Schleiermacher, G., Chesler, L., Peet, A., Leach, M.O., McHugh, K., Hayes, R., Jerome, N., Caron, H., Laidler, J., Fenwick, N., Holt, G., Moroz, V., Kearns, P., Gates, S., Pearson, A.D.J., Wheatley, K., José Bautista, F., Thebaut, E., Hobin, D., Elliott, M., Tweddle, D., Jannier, S., Gallego, S., Coze, C., Auvrignon, A., Sophie Defachelles, A., Lopez Almaraz, R., Brichard, B., Luksch, R., Zwaan, M., Popovic Maja, B., Willis, C., Hettmer, S., Schweigerer, L., Kontny, U., Christiansen, H., Garaventa, A., Ng, A., Howell, L., Yeomanson, D.

وصف الملف: text

العلاقة: https://eprints.whiterose.ac.uk/212436/1/moreno-et-al-2024-bevacizumab-irinotecan-or-topotecan-added-to-temozolomide-for-children-with-relapsed-and-refractory.pdfTest; Moreno, L. orcid.org/0000-0002-0708-1670 , Weston, R. orcid.org/0000-0002-7884-1884 , Owens, C. et al. (87 more authors) (2024) Bevacizumab, Irinotecan, or Topotecan Added to Temozolomide for Children With Relapsed and Refractory Neuroblastoma: Results of the ITCC-SIOPEN BEACON-Neuroblastoma Trial. Journal of Clinical Oncology, 42 (10). pp. 1135-1145. ISSN 0732-183X

الإتاحة: https://eprints.whiterose.ac.uk/212436Test/
https://eprints.whiterose.ac.uk/212436/1/moreno-et-al-2024-bevacizumab-irinotecan-or-topotecan-added-to-temozolomide-for-children-with-relapsed-and-refractory.pdfTest

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2

دورية أكاديمية

Characterization of the transcriptional and metabolic responses of pediatric high grade gliomas to mTOR-HIF-1α axis inhibition.

المؤلفون: Nguyen, A, Moussallieh, FM, Mackay, A, Cicek, AE, Coca, A, Chenard, MP, Weingertner, N, Lhermitte, B, Letouzé, E, Guérin, E, Pencreach, E, Jannier, S, Guenot, D, Namer, IJ, Jones, C, Entz-Werlé, N

المساهمون: Mackay, Alan, Jones, Chris

وصف الملف: Electronic-eCollection; 71617; application/pdf

العلاقة: Oncotarget, 2017, 8 (42), pp. 71597 - 71617; https://repository.icr.ac.uk/handle/internal/4302Test

الإتاحة: https://doi.org/10.18632/oncotarget.16500Test
https://repository.icr.ac.uk/handle/internal/4302Test

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النص الكامل

3

دورية أكاديمية

Characterization of the transcriptional and metabolic responses of pediatric high grade gliomas to mTOR-HIF-1α axis inhibition.

المؤلفون: Nguyen, A, Moussallieh, FM, Mackay, A, Cicek, AE, Coca, A, Chenard, MP, Weingertner, N, Lhermitte, B, Letouzé, E, Guérin, E, Pencreach, E, Jannier, S, Guenot, D, Namer, IJ, Jones, C, Entz-Werlé, N

المساهمون: Jones, Chris, Mackay, Alan

مصطلحات موضوعية: HIF1alpha, high grade glioma, mTor, pediatric, targets

جغرافية الموضوع: United States

وصف الملف: 71617; application/pdf

العلاقة: https://www.ncbi.nlm.nih.gov/pubmed/29069732Test; 16500; Oncotarget, 2017, 8 (42), pp. 71597 - 71617; https://repository.icr.ac.uk/handle/internal/930Test

الإتاحة: https://doi.org/10.18632/oncotarget.16500Test
https://www.ncbi.nlm.nih.gov/pubmed/29069732Test
https://repository.icr.ac.uk/handle/internal/930Test

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النص الكامل

4

دورية أكاديمية

Prise en charge des adolescents jeunes adultes dans les déficits immunitaires primitifs et les maladies auto-immunes : expérience monocentrique et évaluation des attentes des patients par auto-questionnaire dans l’Est de la France

المؤلفون: Guffroy, A., Jannier, S., Humbert, S., Servettaz, A., Cheikh, N., Vogler-Finck, M., Guillet, S., Presta, V., Moog, C., Entz-Werlé, N., Martin, T., Korganow, A.S.

المصدر: La Revue de Médecine Interne ; volume 39, page A107-A108 ; ISSN 0248-8663

مصطلحات موضوعية: Gastroenterology, Internal Medicine

الإتاحة: https://doi.org/10.1016/j.revmed.2018.03.355Test
https://api.elsevier.com/content/article/PII:S0248866318304533?httpAccept=text/xmlTest
https://api.elsevier.com/content/article/PII:S0248866318304533?httpAccept=text/plainTest

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5

دورية أكاديمية

Heterozygous STAT1 gain-of-function mutations underlie an unexpectedly broad clinical phenotype

المؤلفون: Toubiana, J., Okada, S., Hiller, J., Oleastro, M., Lagos Gomez, M., Aldave Becerra, J. C., Ouachee-Chardin, M., Fouyssac, F., Girisha, K. M., Etzioni, A., Van Montfrans, J., Camcioglu, Y., Kerns, L. A., Belohradsky, B., Blanche, S., Bousfiha, A., Rodriguez-Gallego, C., Meyts, I., Kisand, K., Reichenbach, J., Renner, E. D., Rosenzweig, S., Grimbacher, B., van de Veerdonk, F. L., Traidl-Hoffmann, C., Picard, C., Marodi, L., Morio, T., Kobayashi, M., Lilic, D., Milner, J. D., Holland, S., Casanova, J. -L., Puel A, Cypowyj S, Thumerelle C, Toulon A, Bustamante J, Tahuil N, SALHI, DALILA, Boiu S, Chopra C, Di Giovanni D, Bezrodnik L, Boutros J, Thomas C, Lacuesta G, Jannier S, Korganow AS, Paillard C, Boutboul, Bué M, Marie-Cardine A, Bayart S, Migaud M, Weiss, Karmochkine M, Garcia-Martinez JM, Stephan JL, Bensaid P, Jeannoel GP, Witte T, Baumann U, Harrer T, Navarrete C, ACOSTA HUGHES, BENJAMIN, Firinu, Pignata C, Picco P, Mendoza D, Lugo Reyes SO, Torres Lozano C, Ortega-Cisneros M, Cortina M, Mesdaghi M, Nabavi M, Español T, Martínez-Saavedra MT, Rezaei N, Zoghi S, Pac M, Barlogis V, Revon-Rivière G, Haimi-Cohen Y, Spiegel R, Miron D, Bouchaib J, Blancas-Galicia L, Toth B, Drexel B, Rohrlich PS, Lesens O, Hoernes M, Drewe E, Abinum M, Sawalle-Belohradsky J, Kindle G, Depner M, Milani L, Nikopensius T, Remm M, Talas UG, Tucker M, Willis M, Leonard S, Meuwissen H, Ferdman RM, CORBO UGULINO, WALLACE, Desai MM, Taur P, Badolato R, Soltesz B, Schnopp C, Jansson AF, Ayvaz D, Shabashova N, Chernyshova L, Bondarenko A, Moshous D, Neven B, Boubidi C, Ailal F, Giardino G, Del Giacco S, Bougnoux ME, Imai K, Okawa T, Mizoguchi Y, Ozaki Y, Takeuchi M, Hayakawa A, Lögering B, Reich K, Buhl T, Eyerich K, Schaller M, Arkwright PD, Gennery AR, Cant AJ, Warris A, Henriet S, Mekki N, Barbouche R, Ben Mustapha I, Bodemer, Polak M, Grimprel E, Burgel PR, Fischer A, Hermine O, Debré M, Kocacyk D, Dhalla F, Patel SY, Moens L, Haerynck F, Dullaers, Hoste L, Sanal O, Kilic SS, Roesler J, Lanternier F, Lortholary O, Fieschi C, Church JA, Roifman C, Yuenyongviwat A, Peterson P, Boisson-Dupuis S, Abel L, Marciano BE, Netea MG.

المساهمون: Toubiana, J., Okada, S., Hiller, J., Oleastro, M., Lagos Gomez, M., Aldave Becerra, J. C., Ouachee-Chardin, M., Fouyssac, F., Girisha, K. M., Etzioni, A., Van Montfrans, J., Camcioglu, Y., Kerns, L. A., Belohradsky, B., Blanche, S., Bousfiha, A., Rodriguez-Gallego, C., Meyts, I., Kisand, K., Reichenbach, J., Renner, E. D., Rosenzweig, S., Grimbacher, B., van de Veerdonk, F. L., Traidl-Hoffmann, C., Picard, C., Marodi, L., Morio, T., Kobayashi, M., Lilic, D., Milner, J. D., Holland, S., Casanova, J. -L., Puel, A, Cypowyj, S, Thumerelle, C, Toulon, A, Bustamante, J, Tahuil, N, Salhi, Dalila, Boiu, S, Chopra, C, Di Giovanni, D, Bezrodnik, L, Boutros, J, Thomas, C, Lacuesta, G, Jannier, S, Korganow, A, Paillard, C, Boutboul, Bué, M, Marie-Cardine, A, Bayart, S, Migaud, M, Weiss, Karmochkine, M, Garcia-Martinez, Jm, Stephan, Jl, Bensaid, P, Jeannoel, Gp, Witte, T, Baumann, U, Harrer, T, Navarrete, C, ACOSTA HUGHES, Benjamin, Firinu, Pignata, C, Picco, P, Mendoza, D, Lugo Reyes, So, Torres Lozano, C, Ortega-Cisneros, M, Cortina, M, Mesdaghi, M, Nabavi, M, Español, T, Martínez-Saavedra, Mt, Rezaei, N, Zoghi, S, Pac, M, Barlogis, V, Revon-Rivière, G, Haimi-Cohen, Y, Spiegel, R, Miron, D, Bouchaib, J, Blancas-Galicia, L, Toth, B, Drexel, B, Rohrlich, P, Lesens, O, Hoernes, M, Drewe, E, Abinum, M, Sawalle-Belohradsky, J, Kindle, G, Depner, M, Milani, L, Nikopensius, T

مصطلحات موضوعية: Key Points AD STAT1 GOF is the most common genetic cause of inherited CMC and is not restricted to a specific age or ethnic group. STAT1 GOF underlies a variety of infectious and autoimmune features, as well as carcinomas and aneurysms associated with a poor outcome.

العلاقة: info:eu-repo/semantics/altIdentifier/wos/WOS:000378337700009; volume:127; issue:25; firstpage:3154; lastpage:3164; numberofpages:11; journal:BLOOD; http://hdl.handle.net/11588/721177Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84977482520

الإتاحة: https://doi.org/10.1182/blood-2015-11-679902Test
http://hdl.handle.net/11588/721177Test

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