Zobrazeno 1 - 10
of 643
pro vyhledávání: '"Michael S, Hershfield"'
Autor:
Federica Barzaghi, Maria Pia Cicalese, Matteo Zoccolillo, Immacolata Brigida, Matteo Barcella, Ivan Merelli, Claudia Sartirana, Monica Zanussi, Valeria Calbi, Maria Ester Bernardo, Francesca Tucci, Maddalena Migliavacca, Fabio Giglio, Matteo Doglio, Daniele Canarutto, Francesca Ferrua, Giulia Consiglieri, Giulia Prunotto, Francesco Saettini, Sonia Bonanomi, Patrizia Rovere-Querini, Giulia Di Colo, Tatiana Jofra, Georgia Fousteri, Federica Penco, Marco Gattorno, Michael S. Hershfield, Lucia Bongiovanni, Maurilio Ponzoni, Sarah Marktel, Raffaella Milani, Jacopo Peccatori, Fabio Ciceri, Alessandra Mortellaro, Alessandro Aiuti
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
Deficiency of adenosine deaminase 2 (DADA2) is an autosomal recessive disease associated with a highly variable clinical presentation, including vasculitis, immunodeficiency, and hematologic manifestations, potentially progressing over time. The pres
Externí odkaz:
https://doaj.org/article/90dfc8d0b666457dafde9ab89f41de11
Autor:
Imran Ozer, Garrett Kelly, Renpeng Gu, Xinghai Li, Nikita Zakharov, Parul Sirohi, Smita K. Nair, Joel H. Collier, Michael S. Hershfield, Angus M. Hucknall, Ashutosh Chilkoti
Publikováno v:
Advanced Science, Vol 9, Iss 11, Pp n/a-n/a (2022)
Abstract Protein therapeutics, except for antibodies, have a short plasma half‐life and poor stability in circulation. Covalent coupling of polyethylene glycol (PEG) to protein drugs addresses this limitation. However, unlike previously thought, PE
Externí odkaz:
https://doaj.org/article/25fd6625ae81428db034482f847d8104
Autor:
Deepti Suri, Amit Rawat, Ankur Kumar Jindal, Pandiarajan Vignesh, Anju Gupta, Rakesh Kumar Pilania, Vibhu Joshi, Kanika Arora, Rajni Kumrah, Gummadi Anjani, Amita Aggarwal, Shubha Phadke, Fouzia N. Aboobacker, Biju George, Eunice Sindhuvi Edison, Mukesh Desai, Prasad Taur, Vijaya Gowri, Ambreen Abdulwahab Pandrowala, Sagar Bhattad, Swati Kanakia, Marco Gottorno, Isabella Ceccherini, Adriana Almeida de Jesus, Raphaela Goldbach-Mansky, Michael S. Hershfield, Surjit Singh
Publikováno v:
Frontiers in Immunology, Vol 12 (2021)
Background: Systemic autoinflammatory diseases (SAID) are rare inherited disorders involving genes regulating innate immune signaling and are characterized by periodic or chronic multi-systemic inflammation.Objective: To describe spectrum of clinical
Externí odkaz:
https://doaj.org/article/a93420f803dd40d082f9ff6cd12c0cbc
Autor:
Caridad Martinez, Brent Logan, Xuerong Liu, Christopher C. Dvorak, Lisa Madden, Lyndsay Molinari, Morton J. Cowan, Sung-Yun Pai, Elie Haddad, Jennifer Puck, Donald B. Kohn, Linda M. Griffith, Michael Pulsipher, Jennifer W. Leiding, Luigi D. Notarangelo, Troy Torgerson, Rebecca A. Marsh, Geoff D.E. Cuvelier, Susan Prockop, Rebecca H. Buckley, Caroline Y. Kuo, Alison Yip, Michael S. Hershfield, Roberta E Parrott, Christen L. Ebens, Theodore B. Moore, Richard J. O’Reilly, Malika Kapadia, Neena Kapoor, Lisa Forbes Satter, Lauri M. Burroughs, Aleksandra Petrovic, Monica S. Thakar, Deepak Chellapandian, Jennifer R. Heimall, David C. Shyr, Jeffrey J Bednarski, Ahmad Rayes, Shanmuganathan Chandrakasan, Troy C. Quigg, Blachy J Davila, Kenneth DeSantes, Hesham Eissa, Frederick Goldman, Jacob Rozmus, Ami J Shah, Mark Vander Lugt, Michael D. Keller, Kathleen E. Sullivan, Soma Jyonouchi, Christine Seroogy, Helene Decaluwe, Pierre Teira, Alan P. Knutsen, Morris Kletzel, Victor Aquino, Jeffrey H Davis, Paul Szabolcs
Publikováno v:
Transplantation and Cellular Therapy. 29:S91-S93
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0824a310f115e5aa7f4a806f6f069dfa
https://doi.org/10.1016/s2666-6367(23)00185-9
https://doi.org/10.1016/s2666-6367(23)00185-9
Autor:
Chia-Jung Chang, Chien-Hsiun Chen, Bing-Mae Chen, Yu-Cheng Su, Ying-Ting Chen, Michael S. Hershfield, Ming-Ta Michael Lee, Tian-Lu Cheng, Yuan-Tsong Chen, Steve R. Roffler, Jer-Yuarn Wu
Publikováno v:
Nature Communications, Vol 8, Iss 1, Pp 1-7 (2017)
Some individuals develop antibodies against the polyethylene glycol that is commonly used in therapeutic preparations. Here the authors conduct a GWAS in Han Chinese and find the IGH locus is associated with anti-PEG IgM.
Externí odkaz:
https://doaj.org/article/df2dcbdf3ece4077a9f03be585cdb8d7
Autor:
Federica Barzaghi, Federica Minniti, Margherita Mauro, Massimiliano De Bortoli, Rita Balter, Elisa Bonetti, Ada Zaccaron, Virginia Vitale, Maryam Omrani, Matteo Zoccolillo, Immacolata Brigida, Maria Pia Cicalese, Massimo Degano, Michael S. Hershfield, Alessandro Aiuti, Anastasiia V. Bondarenko, Matteo Chinello, Simone Cesaro
Publikováno v:
Frontiers in Immunology, Vol 9 (2019)
Adenosine deaminase 2 (ADA2) deficiency is an auto-inflammatory disease due to mutations in cat eye syndrome chromosome region candidate 1 (CECR1) gene, currently named ADA2. The disease has a wide clinical spectrum encompassing early-onset vasculopa
Externí odkaz:
https://doaj.org/article/47f65f0e0e954a7a959df3bccfcbee78
Autor:
Liang Chen, Anna Mamutova, Anna Kozlova, Elena Latysheva, Frolov Evgeny, Tatiana Latysheva, Kirill Savostyanov, Alexander Pushkov, Ilya Zhanin, Elena Raykina, Maria Kurnikova, Irina Mersiyanova, Craig D. Platt, Hyuk Jee, Kailey Brodeur, Yan Du, Meng Liu, Aaron Weiss, Grant S. Schulert, Jackeline Rodriguez-Smith, Michael S. Hershfield, Ivona Aksentijevich, Qing Zhou, Peter A. Nigrovic, Anna Shcherbina, Ekaterina Alexeeva, Pui Y. Lee
Publikováno v:
Journal of Allergy and Clinical Immunology.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::91db7472918fb7dcaf7cae15565418e1
https://doi.org/10.1016/j.jaci.2023.04.014
https://doi.org/10.1016/j.jaci.2023.04.014
Autor:
Luis Murguia-Favela, Sneha Suresh, Nicola A.M. Wright, Saima Alvi, Sarah Tehseen, Vivian Hernandez-Trujillo, Christine M. Seroogy, Elie Haddad, Daime Nieves, Michael S. Hershfield, Jolan E. Walter, Leah Pettiford, Naynesh R. Kamani, Michael D. Keller, Anne Pham-Huy, Eyal Grunebaum
Publikováno v:
The Journal of Allergy and Clinical Immunology: In Practice.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e088afb8c3dacf395848c34d050d6f72
https://doi.org/10.1016/j.jaip.2023.01.028
https://doi.org/10.1016/j.jaip.2023.01.028
Publikováno v:
Expert Opinion on Orphan Drugs. 9:257-264
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::535b11ccc98c2e6d67463de003080bb3
https://doi.org/10.1080/21678707.2021.2050367
https://doi.org/10.1080/21678707.2021.2050367
Autor:
Giorgia Bucciol, Cindy S. Ma, Ming-Wei Lin, Jin Yan Yap, Anthony D. Kelleher, Leen Moens, Georgina E Hollway, Isabelle Meyts, Michael S. Hershfield, Kathy H C Wu, Paul Gray, William A. Sewell, Stuart G. Tangye, Karen Enthoven, Alisa Kane, Jose Casas-Martin, Tri Giang Phan, Selket Delafontaine, Lien De Somer, Catherine Toong, Carine Wouters
Publikováno v:
Journal of Clinical Immunology
Journal of Clinical Immunology, volume 41, pages1915–1935 (2021)
Journal of Clinical Immunology, volume 41, pages1915–1935 (2021)
Purpose Deficiency of adenosine deaminase type 2 (ADA2) (DADA2) is a rare inborn error of immunity caused by deleterious biallelic mutations in ADA2. Clinical manifestations are diverse, ranging from severe vasculopathy with lacunar strokes to immuno
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::413bcd88ba039078d84e5f8e6b3f683c
http://europepmc.org/articles/PMC8604888
http://europepmc.org/articles/PMC8604888