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1994 1
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Page 1
Deep Learning-Based Algorithm for the Detection and Characterization of MRI Safety of Cardiac Implantable Electronic Devices on Chest Radiographs.
Kim UH, Kim MY, Park EA, Lee W, Lim WH, Kim HL, Oh S, Jin KN. Kim UH, et al. Korean J Radiol. 2021 Nov;22(11):1918-1928. doi: 10.3348/kjr.2021.0201. Epub 2021 Aug 19. Korean J Radiol. 2021. PMID: 34431249 Free PMC article.
XCID demonstrated a higher accuracy (88.1%; 141/160) than PPMnn (80.0%; 128/160) in identifying model groups (p < 0.001). ...Further studies are warranted to guarantee the safe use of XCID in clinical practice....
XCID demonstrated a higher accuracy (88.1%; 141/160) than PPMnn (80.0%; 128/160) in identifying model groups (p < 0.001). ...Furth
Interaction of IL-2R beta and gamma c chains with Jak1 and Jak3: implications for XSCID and XCID.
Russell SM, Johnston JA, Noguchi M, Kawamura M, Bacon CM, Friedmann M, Berg M, McVicar DW, Witthuhn BA, Silvennoinen O, et al. Russell SM, et al. Science. 1994 Nov 11;266(5187):1042-5. doi: 10.1126/science.7973658. Science. 1994. PMID: 7973658
Truncations of gamma c, and a gamma c, point mutation causing moderate X-linked combined immunodeficiency (XCID), decreased gamma c-Jak3 association. Thus, gamma c mutations in at least some XSCID and XCID patients prevent normal Jak3 activation, suggesting that mut …
Truncations of gamma c, and a gamma c, point mutation causing moderate X-linked combined immunodeficiency (XCID), decreased gamma c-J …
Immune consequences of mutations in the human common gamma-chain gene.
Schmalstieg FC, Goldman AS. Schmalstieg FC, et al. Mol Genet Metab. 2002 Jul;76(3):163-71. doi: 10.1016/s1096-7192(02)00042-2. Mol Genet Metab. 2002. PMID: 12126929 Review.
A mutation (c.878T>A) in the common gamma chain (gamma(c)) causes an X-linked combined immunodeficiency (XCID) in a large kindred of British origin. In the disease, gamma(c) is expressed, but its binding to Jak3 is reduced. The immune deficiencies and clinical course we …
A mutation (c.878T>A) in the common gamma chain (gamma(c)) causes an X-linked combined immunodeficiency (XCID) in a large kindred …
Missense mutation in exon 7 of the common gamma chain gene causes a moderate form of X-linked combined immunodeficiency.
Schmalstieg FC, Leonard WJ, Noguchi M, Berg M, Rudloff HE, Denney RM, Dave SK, Brooks EG, Goldman AS. Schmalstieg FC, et al. J Clin Invest. 1995 Mar;95(3):1169-73. doi: 10.1172/JCI117765. J Clin Invest. 1995. PMID: 7883965 Free PMC article.
Clinical and immunologic features of a recently recognized X-linked combined immunodeficiency disease (XCID) suggested that XCID and X-linked severe combined immunodeficiency (XSCID) might arise from different genetic defects. ...As in XSCID, X-chromosome inactivati …
Clinical and immunologic features of a recently recognized X-linked combined immunodeficiency disease (XCID) suggested that XCID
Genesis of progressive T-cell deficiency owing to a single missense mutation in the common gamma chain gene.
Goldman AS, Palkowetz KH, Rudloff HE, Dallas DV, Schmalstieg FC. Goldman AS, et al. Scand J Immunol. 2001 Dec;54(6):582-91. doi: 10.1046/j.1365-3083.2001.01006.x. Scand J Immunol. 2001. PMID: 11902333 Free article.
Patients with a moderate X-linked combined immunodeficiency (XCID) owing to a single missense mutation in the common gamma chain (gammac) gene (L-->Q271) were found to have a progressive T-cell deficiency. ...
Patients with a moderate X-linked combined immunodeficiency (XCID) owing to a single missense mutation in the common gamma chain (gam …
Novel Hemizygous IL2RG p.(Pro58Ser) Mutation Impairs IL-2 Receptor Complex Expression on Lymphocytes Causing X-Linked Combined Immunodeficiency.
Tuovinen EA, Grönholm J, Öhman T, Pöysti S, Toivonen R, Kreutzman A, Heiskanen K, Trotta L, Toiviainen-Salo S, Routes JM, Verbsky J, Mustjoki S, Saarela J, Kere J, Varjosalo M, Hänninen A, Seppänen MRJ. Tuovinen EA, et al. J Clin Immunol. 2020 Apr;40(3):503-514. doi: 10.1007/s10875-020-00745-2. Epub 2020 Feb 19. J Clin Immunol. 2020. PMID: 32072341 Free PMC article.