CD28 costimulatory signal induces protein arginine methylation in T cells

por Blanchet, Fabien, Cardona, Ana, Letimier, Fabrice A., Hershfield, Michael S., Acuto, Oreste
Publicado 2005

Combined immunodeficiencies: twenty years experience from a single center in Turkey

por Akar, H. Haluk, Patiroglu, Turkan, Hershfield, Michael, van der Burg, Mirjam
Publicado 2016

Control of hyperuricemia in subjects with refractory gout, and induction of antibody against poly(ethylene glycol) (PEG), in a phase I trial of subcutaneous PEGylated urate oxidase

por Ganson, Nancy J, Kelly, Susan J, Scarlett, Edna, Sundy, John S, Hershfield, Michael S
Publicado 2006

Purine nucleoside phosphorylase deficiency in two unrelated Saudi patients

por Alangari, Abdullah, Al-Harbi, Abdullah, Al-Ghonaium, Abdulaziz, Santisteban, Ines, Hershfield, Michael
Publicado 2009

The Binding Site of Human Adenosine Deaminase for Cd26/Dipeptidyl Peptidase IV: The Arg142gln Mutation Impairs Binding to Cd26 but Does Not Cause Immune Deficiency

por Richard, Eva, Arredondo-Vega, Francisco X., Santisteban, Ines, Kelly, Susan J., Patel, Dhavalkumar D., Hershfield, Michael S.
Publicado 2000

Induced and pre-existing anti-polyethylene glycol antibody in a trial of every 3-week dosing of pegloticase for refractory gout, including in organ transplant recipients

por Hershfield, Michael S, Ganson, Nancy J, Kelly, Susan J, Scarlett, Edna L, Jaggers, Denise A, Sundy, John S
Publicado 2014

Impulse oscillometry identifies peripheral airway dysfunction in children with adenosine deaminase deficiency

por Komarow, Hirsh D., Sokolic, Robert, Hershfield, Michael S., Kohn, Donald B., Young, Michael, Metcalfe, Dean D., Candotti, Fabio
Publicado 2015

Autoimmune phenotype with type I interferon signature in two brothers with ADA2 deficiency carrying a novel CECR1 mutation

por Skrabl-Baumgartner, Andrea, Plecko, Barbara, Schmidt, Wolfgang M., König, Nadja, Hershfield, Michael, Gruber-Sedlmayr, Ursula, Lee-Kirsch, Min Ae
Publicado 2017

A brush-polymer conjugate of exendin-4 reduces blood glucose for up to five days and eliminates poly(ethylene glycol) antigenicity

por Qi, Yizhi, Simakova, Antonina, Ganson, Nancy J., Li, Xinghai, Luginbuhl, Kelli M., Özer, Imran, Liu, Wenge, Hershfield, Michael S., Matyjaszewski, Krzysztof, Chilkoti, Ashutosh
Publicado 2016

Mitochondrial Basis for Immune Deficiency: Evidence from Purine Nucleoside Phosphorylase–Deficient Mice

por Arpaia, Enrico, Benveniste, Patricia, Di Cristofano, Antonio, Gu, Yiping, Dalal, Ilan, Kelly, Susan, Hershfield, Michael, Pandolfi, Pier Paolo, Roifman, Chaim M., Cohen, Amos
Publicado 2000

Pre-existing anti–polyethylene glycol antibody linked to first-exposure allergic reactions to pegnivacogin, a PEGylated RNA aptamer

por Ganson, Nancy J., Povsic, Thomas J., Sullenger, Bruce A., Alexander, John H., Zelenkofske, Steven L., Sailstad, Jeffrey M., Rusconi, Christopher P., Hershfield, Michael S.
Publicado 2015

Complexities of genetic diagnosis illustrated by an atypical case of congenital hypoplastic anemia

por Claassen, David, Boals, Michelle, Bowling, Kevin M., Cooper, Gregory M., Cox, Jennifer, Hershfield, Michael, Lewis, Sara, Wlodarski, Marcin, Weiss, Mitchell J., Estepp, Jeremie H.
Publicado 2018

Polyethylene Glycol‐Like Brush Polymer Conjugate of a Protein Drug Does Not Induce an Antipolymer Immune Response and Has Enhanced Pharmacokinetics than Its Polyethylene Glycol Cou...

por Ozer, Imran, Kelly, Garrett, Gu, Renpeng, Li, Xinghai, Zakharov, Nikita, Sirohi, Parul, Nair, Smita K., Collier, Joel H., Hershfield, Michael S., Hucknall, Angus M., Chilkoti, Ashutosh
Publicado 2022

Hematopoietic stem cell transplantation rescues the immunologic phenotype and prevents vasculopathy in patients with adenosine deaminase 2 deficiency

por Van Eyck, Lien, Hershfield, Michael S., Pombal, Diana, Kelly, Susan J., Ganson, Nancy J., Moens, Leen, Frans, Glynis, Schaballie, Heidi, De Hertogh, Gert, Dooley, James, Bossuyt, Xavier, Wouters, Carine, Liston, Adrian, Meyts, Isabelle
Publicado 2015

A genome-wide association study identifies a novel susceptibility locus for the immunogenicity of polyethylene glycol

por Chang, Chia-Jung, Chen, Chien-Hsiun, Chen, Bing-Mae, Su, Yu-Cheng, Chen, Ying-Ting, Hershfield, Michael S., Lee, Ming-Ta Michael, Cheng, Tian-Lu, Chen, Yuan-Tsong, Roffler, Steve R., Wu, Jer-Yuarn
Publicado 2017

ALPS-Like Phenotype Caused by ADA2 Deficiency Rescued by Allogeneic Hematopoietic Stem Cell Transplantation

por Barzaghi, Federica, Minniti, Federica, Mauro, Margherita, Bortoli, Massimiliano De, Balter, Rita, Bonetti, Elisa, Zaccaron, Ada, Vitale, Virginia, Omrani, Maryam, Zoccolillo, Matteo, Brigida, Immacolata, Cicalese, Maria Pia, Degano, Massimo, Hershfield, Michael S., Aiuti, Alessandro, Bondarenko, Anastasiia V., Chinello, Matteo, Cesaro, Simone
Publicado 2019

Intrinsic Defects in B Cell Development and Differentiation, T Cell Exhaustion and Altered Unconventional T Cell Generation Characterize Human Adenosine Deaminase Type 2 Deficiency

por Yap, Jin Yan, Moens, Leen, Lin, Ming-Wei, Kane, Alisa, Kelleher, Anthony, Toong, Catherine, Wu, Kathy H.C., Sewell, William A., Phan, Tri Giang, Hollway, Georgina E., Enthoven, Karen, Gray, Paul E., Casas-Martin, Jose, Wouters, Carine, De Somer, Lien, Hershfield, Michael, Bucciol, Giorgia, Delafontaine, Selket, Ma, Cindy S., Tangye, Stuart G., Meyts, Isabelle
Publicado 2021

Spectrum of Systemic Auto-Inflammatory Diseases in India: A Multi-Centric Experience

por Suri, Deepti, Rawat, Amit, Jindal, Ankur Kumar, Vignesh, Pandiarajan, Gupta, Anju, Pilania, Rakesh Kumar, Joshi, Vibhu, Arora, Kanika, Kumrah, Rajni, Anjani, Gummadi, Aggarwal, Amita, Phadke, Shubha, Aboobacker, Fouzia N., George, Biju, Edison, Eunice Sindhuvi, Desai, Mukesh, Taur, Prasad, Gowri, Vijaya, Pandrowala, Ambreen Abdulwahab, Bhattad, Sagar, Kanakia, Swati, Gottorno, Marco, Ceccherini, Isabella, Almeida de Jesus, Adriana, Goldbach-Mansky, Raphaela, Hershfield, Michael S., Singh, Surjit
Publicado 2021

Case Report: Consistent disease manifestations with a staggered time course in two identical twins affected by adenosine deaminase 2 deficiency

por Barzaghi, Federica, Cicalese, Maria Pia, Zoccolillo, Matteo, Brigida, Immacolata, Barcella, Matteo, Merelli, Ivan, Sartirana, Claudia, Zanussi, Monica, Calbi, Valeria, Bernardo, Maria Ester, Tucci, Francesca, Migliavacca, Maddalena, Giglio, Fabio, Doglio, Matteo, Canarutto, Daniele, Ferrua, Francesca, Consiglieri, Giulia, Prunotto, Giulia, Saettini, Francesco, Bonanomi, Sonia, Rovere-Querini, Patrizia, Di Colo, Giulia, Jofra, Tatiana, Fousteri, Georgia, Penco, Federica, Gattorno, Marco, Hershfield, Michael S., Bongiovanni, Lucia, Ponzoni, Maurilio, Marktel, Sarah, Milani, Raffaella, Peccatori, Jacopo, Ciceri, Fabio, Mortellaro, Alessandra, Aiuti, Alessandro
Publicado 2022

Clinical, Immunological, and Molecular Features of Severe Combined Immune Deficiency: A Multi-Institutional Experience From India

por Vignesh, Pandiarajan, Rawat, Amit, Kumrah, Rajni, Singh, Ankita, Gummadi, Anjani, Sharma, Madhubala, Kaur, Anit, Nameirakpam, Johnson, Jindal, Ankur, Suri, Deepti, Gupta, Anju, Khadwal, Alka, Saikia, Biman, Minz, Ranjana Walker, Sharma, Kaushal, Desai, Mukesh, Taur, Prasad, Gowri, Vijaya, Pandrowala, Ambreen, Dalvi, Aparna, Jodhawat, Neha, Kambli, Priyanka, Madkaikar, Manisha Rajan, Bhattad, Sagar, Ramprakash, Stalin, CP, Raghuram, Jayaram, Ananthvikas, Sivasankaran, Meena, Munirathnam, Deenadayalan, Balaji, Sarath, Rajendran, Aruna, Aggarwal, Amita, Singh, Komal, Na, Fouzia, George, Biju, Mehta, Ankit, Lashkari, Harsha Prasada, Uppuluri, Ramya, Raj, Revathi, Bartakke, Sandip, Gupta, Kirti, Sreedharanunni, Sreejesh, Ogura, Yumi, Kato, Tamaki, Imai, Kohsuke, Chan, Koon Wing, Leung, Daniel, Ohara, Osamu, Nonoyama, Shigeaki, Hershfield, Michael, Lau, Yu-Lung, Singh, Surjit
Publicado 2021