Learning from Job: A Rare Genetic Disease and Lessons of Biblical Proportions

por Milner, Joshua D.
Publicado 2018

TCR Signaling Abnormalities in Human Th2-Associated Atopic Disease

por Milner, Joshua D.
Publicado 2018

Primary atopic disorders

por Lyons, Jonathan J., Milner, Joshua D.
Publicado 2018

Editorial: Continued Fascination–A Tribute to a Giant in Immunology, Dr. William E. Paul

por Milner, Joshua D., Zhu, Jinfang, Paul, Marilyn
Publicado 2019

Impact of the COVID-19 pandemic on physical and mental health among individuals with primary immunodeficiency: results of a nationwide survey

por Deshpande, Deepti, Scalchunes, Christopher, Orange, Jordan, Milner, Joshua
Publicado 2021

Glycans Instructing Immunity: The Emerging Role of Altered Glycosylation in Clinical Immunology

por Lyons, Jonathan J., Milner, Joshua D., Rosenzweig, Sergio D.
Publicado 2015

Up, Down, and All Around: Diagnosis and Treatment of Novel STAT3 Variant

por Weinreich, Michael Alexander, Vogel, Tiphanie P., Rao, V. Koneti, Milner, Joshua D.
Publicado 2017

Measurement of serum tenascin-X in patients with congenital adrenal hyperplasia at risk for Ehlers–Danlos contiguous gene deletion syndrome CAH-X

por Kolli, Vipula, Kim, Hannah, Rao, Hamsini, Lao, Qizong, Gaynor, Alison, Milner, Joshua D., Merke, Deborah P.
Publicado 2019

The CBM-opathies—A Rapidly Expanding Spectrum of Human Inborn Errors of Immunity Caused by Mutations in the CARD11-BCL10-MALT1 Complex

por Lu, Henry Y., Bauman, Bradly M., Arjunaraja, Swadhinya, Dorjbal, Batsukh, Milner, Joshua D., Snow, Andrew L., Turvey, Stuart E.
Publicado 2018

Impact of naturally forming human α/β-tryptase heterotetramers in the pathogenesis of hereditary α-tryptasemia

por Le, Quang T., Lyons, Jonathan J., Naranjo, Andrea N., Olivera, Ana, Lazarus, Robert A., Metcalfe, Dean D., Milner, Joshua D., Schwartz, Lawrence B.
Publicado 2019

Potential mechanisms of anaphylaxis to COVID-19 mRNA vaccines

por Risma, Kimberly A., Edwards, Kathryn M., Hummell, Donna S., Little, Frederic F., Norton, Allison E., Stallings, Amy, Wood, Robert A., Milner, Joshua D.
Publicado 2021

De novo STAT3 Mutation in a Patient with Fatal, Treatment-Refractory Sino-orbital Aspergillosis

por Natarajan, Mukil, Hsu, Amy, Weinreich, Michael, Sugui, Janyce, Zangeneh, Tirdad, Carr, Tara, Oler, Andrew, Similuk, Morgan, Kwon-Chung, Kyung, Milner, Joshua, Lionakis, Michail S
Publicado 2017

Hereditary alpha-tryptasemia modifies clinical phenotypes among individuals with congenital hypermobility disorders

por Vazquez, Maribel, Chovanec, Jack, Kim, Jiwon, DiMaggio, Thomas, Milner, Joshua D., Francomano, Clair A., Gurnett, Christina A., Ritelli, Marco, Colombi, Marina, Lyons, Jonathan J.
Publicado 2022

Asthma among hospitalized patients with COVID-19 and related outcomes

por Lovinsky-Desir, Stephanie, Deshpande, Deepti R., De, Aliva, Murray, Laurie, Stingone, Jeanette A., Chan, Angela, Patel, Neha, Rai, Nooralam, DiMango, Emily, Milner, Joshua, Kattan, Meyer
Publicado 2020

Functional characterization of phospholipase C-γ(2) mutant protein causing both somatic ibrutinib resistance and a germline monogenic autoinflammatory disorder

por Walliser, Claudia, Wist, Martin, Hermkes, Elisabeth, Zhou, Yuan, Schade, Anja, Haas, Jennifer, Deinzer, Julia, Désiré, Laurent, Li, Shawn S.C., Stilgenbauer, Stephan, Milner, Joshua D., Gierschik, Peter
Publicado 2018

Risk Variants in the Exomes of Children With Critical Illness

por Motelow, Joshua E., Lippa, Natalie C., Hostyk, Joseph, Feldman, Evin, Nelligan, Matthew, Ren, Zhong, Alkelai, Anna, Milner, Joshua D., Gharavi, Ali G., Tang, Yingying, Goldstein, David B., Kernie, Steven G.
Publicado 2022

SARS-CoV-2–related MIS-C: A key to the viral and genetic causes of Kawasaki disease?

por Sancho-Shimizu, Vanessa, Brodin, Petter, Cobat, Aurélie, Biggs, Catherine M., Toubiana, Julie, Lucas, Carrie L., Henrickson, Sarah E., Belot, Alexandre, Tangye, Stuart G., Milner, Joshua D., Levin, Michael, Abel, Laurent, Bogunovic, Dusan, Casanova, Jean-Laurent, Zhang, Shen-Ying
Publicado 2021

A Novel Germline Heterozygous BCL11B Variant Causing Severe Atopic Disease and Immune Dysregulation

por Lu, Henry Y., Sertori, Robert, Contreras, Alejandra V., Hamer, Mark, Messing, Melina, Del Bel, Kate L., Lopez-Rangel, Elena, Chan, Edmond S., Rehmus, Wingfield, Milner, Joshua D., McNagny, Kelly M., Lehman, Anna, Wiest, David L., Turvey, Stuart E.
Publicado 2021

PD-L1 up-regulation restrains Th17 cell differentiation in STAT3 loss- and STAT1 gain-of-function patients

por Zhang, Yuan, Ma, Chi A., Lawrence, Monica G., Break, Timothy J., O’Connell, Michael P., Lyons, Jonathan J., López, Diego B., Barber, John S., Zhao, Yongge, Barber, Daniel L., Freeman, Alexandra F., Holland, Steven M., Lionakis, Michail S., Milner, Joshua D.
Publicado 2017

Ventricular Function and Tissue Characterization By Cardiac MRI in Children Following Hospitalization for Multisystem Inflammatory Syndrome in Children (MIS-C): A Prospective Study

por Dilorenzo, Michael P, Farooqi, Kanwal M, Shah, Amee M, Channing, Alexandra, Harrington, Jamie K, Connors, Thomas J, Martirosyan, Karen, Krishnan, Usha S, Ferris, Anne, Weller, Rachel J., Farber, Donna L, Milner, Joshua D., Gorelik, Mark, Rosenzweig, Erika B, Anderson, Brett R
Publicado 2022