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Year | Number of Results |
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2019 | 1 |
2020 | 1 |
2021 | 2 |
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2024 | 1 |
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Human inherited PD-L1 deficiency is clinically and immunologically less severe than PD-1 deficiency.
J Exp Med. 2024 Jun 3;221(6):e20231704. doi: 10.1084/jem.20231704. Epub 2024 Apr 18.
J Exp Med. 2024.
PMID: 38634869
Free PMC article.
New Dominant-Negative IL6ST Variants Expand the Immunological and Clinical Spectrum of GP130-Dependent Hyper-IgE Syndrome.
Arlabosse T, Materna M, Riccio O, Schnider C, Angelini F, Perreau M, Rochat I, Superti-Furga A, Campos-Xavier B, Héritier S, Pereira A, Deswarte C, Lévy R, Distefano M, Bustamante J, Roelens M, Borie R, Le Brun M, Crestani B, Casanova JL, Puel A, Hofer M, Fieschi C, Theodoropoulou K, Béziat V, Candotti F.
Arlabosse T, et al.
J Clin Immunol. 2023 Oct;43(7):1566-1580. doi: 10.1007/s10875-023-01517-4. Epub 2023 Jun 5.
J Clin Immunol. 2023.
PMID: 37273120
Free PMC article.
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Inborn errors of TLR3- or MDA5-dependent type I IFN immunity in children with enterovirus rhombencephalitis.
Chen J, Jing H, Martin-Nalda A, Bastard P, Rivière JG, Liu Z, Colobran R, Lee D, Tung W, Manry J, Hasek M, Boucherit S, Lorenzo L, Rozenberg F, Aubart M, Abel L, Su HC, Soler Palacin P, Casanova JL, Zhang SY.
Chen J, et al.
J Exp Med. 2021 Dec 6;218(12):e20211349. doi: 10.1084/jem.20211349. Epub 2021 Nov 2.
J Exp Med. 2021.
PMID: 34726731
Free PMC article.
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Biochemically deleterious human NFKB1 variants underlie an autosomal dominant form of common variable immunodeficiency.
Li J, Lei WT, Zhang P, Rapaport F, Seeleuthner Y, Lyu B, Asano T, Rosain J, Hammadi B, Zhang Y, Pelham SJ, Spaan AN, Migaud M, Hum D, Bigio B, Chrabieh M, Béziat V, Bustamante J, Zhang SY, Jouanguy E, Boisson-Dupuis S, El Baghdadi J, Aimanianda V, Thoma K, Fliegauf M, Grimbacher B, Korganow AS, Saunders C, Rao VK, Uzel G, Freeman AF, Holland SM, Su HC, Cunningham-Rundles C, Fieschi C, Abel L, Puel A, Cobat A, Casanova JL, Zhang Q, Boisson B.
Li J, et al.
J Exp Med. 2021 Nov 1;218(11):e20210566. doi: 10.1084/jem.20210566. Epub 2021 Sep 2.
J Exp Med. 2021.
PMID: 34473196
Free PMC article.
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The genetic basis of pneumococcal and staphylococcal infections: inborn errors of human TLR and IL-1R immunity.
Boisson B.
Boisson B.
Hum Genet. 2020 Jun;139(6-7):981-991. doi: 10.1007/s00439-020-02111-z. Epub 2020 Jan 24.
Hum Genet. 2020.
PMID: 31980906
Free PMC article.
Review.
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Novel immune signatures associated with dysplastic naevi and primary cutaneous melanoma in human skin.
Yan BY, Garcet S, Gulati N, Kiecker F, Fuentes-Duculan J, Gilleaudeau P, Sullivan-Whalen M, Shemer A, Mitsui H, Krueger JG.
Yan BY, et al.
Exp Dermatol. 2019 Jan;28(1):35-44. doi: 10.1111/exd.13805. Epub 2018 Dec 21.
Exp Dermatol. 2019.
PMID: 30326165
Free PMC article.
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