Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Kelly Capuder"'
Publikováno v:
The Foot. 39:88-91
The process of repeated handling and steam sterilization of bone screws and allows debris to deposit on the surface and inside cannulated screws. Individually packaged screws could alleviate these potential problems. This research intended to evaluat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::47a43822f011fe435a065e83d35f708e
https://doi.org/10.1016/j.foot.2019.02.010
https://doi.org/10.1016/j.foot.2019.02.010
Autor:
Douglas Ryan, Nicole Luche, Sevgi Keles, Maria K. Lehtinen, Luigi D. Notarangelo, Kelly Capuder, Melody P. Lun, Ismail Reisli, Morgan L. Shannon
Publikováno v:
Am J Pathol
Cells of the developing central nervous system are particularly susceptible to formation of double-stranded DNA breaks (DSBs) arising from physiological and/or environmental insults. Therefore, efficient repair of DSBs is especially vital for maintai
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::613e5d1f3384bfae5309f6fbccee5308
https://pubmed.ncbi.nlm.nih.gov/31541646
https://pubmed.ncbi.nlm.nih.gov/31541646
Autor:
Beryl Royer-Bertrand, Fabienne E. Poulain, Pietro Luigi Poliani, Luigi D. Notarangelo, Ellen van Rooijen, Ileana Bortolomai, Hye Sun Kuehn, Elliott J. Hagedorn, Robert J. Linhardt, Leonard I. Zon, Luisa Imberti, Pyong Woo Park, Genni Enza Marcovecchio, Atsuko Hayashida, Anne Slavotinek, George Freedman, Kerry Dobbs, Stefano Volpi, Prisni Rath, Patrick M. Brauer, Yasuhiro Yamazaki, Maja Di Rocco, Alberto Martini, Kazutaka Hayashida, Kelly Capuder, Juan Carlos Zúñiga-Pflücker, Sergio D. Rosenzweig, Marita Bosticardo, John P. Manis, Silvia Giliani, Andrea Superti-Furga, Jennifer M. Puck, Carlo Rivolta, Kerstin Felgentreff, Lisa Ott de Bruin, Nicole Luche, Antonella Buoncompagni, Hane Lee, Likun Du
Publikováno v:
The Journal of experimental medicine, vol 214, iss 3
The Journal of experimental medicine, vol. 214, no. 3, pp. 623-637
The Journal of Experimental Medicine
The Journal of experimental medicine, vol. 214, no. 3, pp. 623-637
The Journal of Experimental Medicine
Volpi et al. demonstrate that hypomorphic EXTL3 mutations cause abnormalities of heparan sulfate composition, affect signaling in response to growth factors and cytokines, and perturb thymopoiesis, resulting in a novel genetic disease associating ske
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::89ebb94df5b44febc6eafe227af51d7c
https://escholarship.org/uc/item/7bg3j769
https://escholarship.org/uc/item/7bg3j769
Autor:
Marina Cella, Susan Gilfillan, Marco Colonna, Alexander D. Barrow, Lih-Ling Lin, Michelle L. Robinette, Tyler K. Ulland, Jean Baptiste Telliez, Luigi D. Notarangelo, Kelly Capuder
Publikováno v:
Mucosal immunology
Loss-of-function mutations in the tyrosine kinase JAK3 cause autosomal recessive severe combined immunodeficiency (SCID). Defects in this form of SCID are restricted to the immune system, which led to the development of immunosuppressive JAK inhibito
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9044f0ac36202e4823686a6adc45159b
https://pubmed.ncbi.nlm.nih.gov/28513593
https://pubmed.ncbi.nlm.nih.gov/28513593
Autor:
Kerry Dobbs, Roshini S. Abraham, Michel J. Masaad, Raif S. Geha, Morton J. Cowan, Mehdi Adeli, Karin Chen, Joao Bosco Oliveira, Kari C. Nadeau, Divij Mathew, Jolan E. Walter, Paolo Palma, Rima Wakim, Jack J. Bleesing, Antonio Condino-Neto, Yu Nee Lee, Janet Chou, Paul J. Utz, Lindsey B. Rosen, David Buchbinder, Catharina Schuetz, Chiara Azzari, Jennifer M. Puck, Sarah K. Browne, Michael Grimley, Boglarka Ujhazi, Harry L. Malech, Javeed Akhter, Imelda Balboni, Tim Niehues, Mike Recher, Steven M. Holland, Chaim M. Roifman, Caterina Cancrini, Kathleen E. Sullivan, Luigi D. Notarangelo, Irit Tirosh, Ghassan Dbaibo, Beatriz Tavares Costa-Carvalho, Andrew R. Gennery, Rebecca Gelman, Jacob M. Rosenberg, José Luis Franco, Christina S.K. Yee, Dalia H. El-Ghoneimy, Attila Kumánovics, Waleed Al-Herz, Manish J. Butte, Marton Keszei, Reem Elfeky, Suk See De Ravin, Gulbu Uzel, Kelly Capuder, Avni Y. Joshi, Krisztian Csomos, Taco W. Kuijpers, Thomas G. Boyce
Publikováno v:
Walter, JE; Rosen, LB; Csomos, K; Rosenberg, JM; Mathew, D; Keszei, M; et al.(2015). Broad-spectrum antibodies against self-antigens and cytokines in RAG deficiency. Journal of Clinical Investigation, 125(11), 4135-4148. doi: 10.1172/JCI80477. UCSF: Retrieved from: http://www.escholarship.org/uc/item/2zw8w5m6
The Journal of clinical investigation
The Journal of clinical investigation, vol 125, iss 11
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Journal of clinical investigation, 125(11), 4135-4148. The American Society for Clinical Investigation
The Journal of clinical investigation
The Journal of clinical investigation, vol 125, iss 11
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Journal of clinical investigation, 125(11), 4135-4148. The American Society for Clinical Investigation
Patients with mutations of the recombination-activating genes (RAG) present with diverse clinical phenotypes, including severe combined immune deficiency (SCID), autoimmunity, and inflammation. However, the incidence and extent of immune dysregulatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f01e415942f0e22afb80ccf523547145
https://hdl.handle.net/2108/314369
https://hdl.handle.net/2108/314369
Autor:
Ergin Çiftçi, Kerry Dobbs, David Goldstein, Roberta E. Parrott, Samuli Rounioja, Cecilia Domínguez Conde, Ornella Patrizi, Kaan Boztug, Satoshi Okada, Janna Saarela, Emma Haapaniemi, Janet Chou, Yuval Itan, Mikael Knip, Talal A. Chatila, Berna Savaş, Luigi D. Notarangelo, Axel Schambach, Anne Marie Comeau, Michael Schuster, Sule Haskologlu, Merja Helminen, Michel J. Massaad, Alessandro Moretta, Pierre Lebon, Ivan Bilic, Flore Rozenberg, Silvia Parolini, Raif S. Geha, Sevgi Keles, Jean-Laurent Casanova, Rebecca H. Buckley, Giovanna Tabellini, Figen Dogu, Toshiro K. Ohsumi, Kerstin Felgentreff, Laurent Abel, Magali Audry, Christoph Bock, Aydan Ikinciogullari, Nina K. Serwas, Shen-Ying Zhang, Waleed Al-Herz, Bertrand Boisson, Adel M Alwahadneh, Vincent Pedergnana, Arzu Ensari, Kelly Capuder, Slavé Petrovski
Publikováno v:
New England Journal of Medicine
New England Journal of Medicine, 2015, 372 (25), pp.2409-2422. ⟨10.1056/NEJMoa1413462⟩
New England Journal of Medicine, 2015, 372 (25), pp.2409-2422. ⟨10.1056/NEJMoa1413462⟩
International audience; Background Combined immunodeficiencies are marked by inborn errors of T-cell immunity in which the T cells that are present are quantitatively or functionally deficient. Impaired humoral immunity is also common. Patients have
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb181f2c65b7ef2344103cd88e9f7315
http://hdl.handle.net/11567/815623
http://hdl.handle.net/11567/815623
Autor:
Divij Mathew, Douglas Ryan, Fabio Candotti, Katrina Abernethy, Eva Csizmadia, Adrian J. Thrasher, Kelly Capuder, Mike Recher, Scott B. Snapper, Stefano Volpi, Carin I. M. Dahlberg, Luigi D. Notarangelo, Masayuki Mizui, Elettra Santori, Lisa S. Westerberg, George C. Tsokos
Publikováno v:
Blood
Mutations of the Wiskott-Aldrich syndrome gene (WAS) are responsible for Wiskott-Aldrich syndrome (WAS), a disease characterized by thrombocytopenia, eczema, immunodeficiency, and autoimmunity. Mice with conditional deficiency of Was in B lymphocytes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::36bb509fb1169961b0c4e0af4f568bae
http://hdl.handle.net/11567/894993
http://hdl.handle.net/11567/894993