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Journal Abstract Search

164 related items for PubMed ID: 30170160

  • 1. MHC-II Deficiency Among Egyptians: Novel Mutations and Unique Phenotypes.
    El Hawary RE, Mauracher AA, Meshaal SS, Eldash A, Abd Elaziz DS, Alkady R, Lotfy S, Opitz L, Galal NM, Boutros JA, Pachlopnik Schmid J, Elmarsafy AM.
    J Allergy Clin Immunol Pract; 2019 Mar; 7(3):856-863. PubMed ID: 30170160
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  • 2. MHC Class II Deficiency: Clinical, Immunological, and Genetic Insights in a Large Multicenter Cohort.
    Gulec Koksal Z, Bilgic Eltan S, Topyildiz E, Sezer A, Keles S, Celebi Celik F, Ozhan Kont A, Gemici Karaaslan B, Sefer AP, Karali Z, Arik E, Ozek Yucel E, Akcal O, Karakurt LT, Yorgun Altunbas M, Yalcin K, Uygun V, Ozek G, Babayeva R, Aydogmus C, Ozcan D, Cavkaytar O, Keskin O, Kilic SS, Kiykim A, Arikoglu T, Genel F, Gulez N, Guner SN, Karaca NE, Reisli I, Kutukculer N, Altintas DU, Ozen A, Karakoc Aydiner E, Baris S.
    J Allergy Clin Immunol Pract; 2024 Sep; 12(9):2490-2502.e6. PubMed ID: 38996837
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  • 3. Mutation of RFXAP, a regulator of MHC class II genes, in primary MHC class II deficiency.
    Villard J, Lisowska-Grospierre B, van den Elsen P, Fischer A, Reith W, Mach B.
    N Engl J Med; 1997 Sep 11; 337(11):748-53. PubMed ID: 9287230
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  • 4. A gene encoding a novel RFX-associated transactivator is mutated in the majority of MHC class II deficiency patients.
    Masternak K, Barras E, Zufferey M, Conrad B, Corthals G, Aebersold R, Sanchez JC, Hochstrasser DF, Mach B, Reith W.
    Nat Genet; 1998 Nov 11; 20(3):273-7. PubMed ID: 9806546
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  • 7. Clinical, Immunological, and Genetic Findings in Iranian Patients with MHC-II Deficiency: Confirmation of c.162delG RFXANK Founder Mutation in the Iranian Population.
    Mousavi Khorshidi MS, Seeleuthner Y, Chavoshzadeh Z, Behfar M, Hamidieh AA, Alimadadi H, Sherkat R, Momen T, Behniafard N, Eskandarzadeh S, Mansouri M, Behnam M, Mahdavi M, Heydarazad Zadeh M, Shokri M, Alizadeh F, Movahedi M, Momenilandi M, Keramatipour M, Casanova JL, Cobat A, Abel L, Shahrooei M, Parvaneh N.
    J Clin Immunol; 2023 Nov 11; 43(8):1941-1952. PubMed ID: 37584719
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  • 9. Mutation in the class II trans-activator leading to a mild immunodeficiency.
    Wiszniewski W, Fondaneche MC, Le Deist F, Kanariou M, Selz F, Brousse N, Steimle V, Barbieri G, Alcaide-Loridan C, Charron D, Fischer A, Lisowska-Grospierre B.
    J Immunol; 2001 Aug 01; 167(3):1787-94. PubMed ID: 11466404
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  • 10. MHC class II deficiency: Report of a novel mutation and special review.
    Farrokhi S, Shabani M, Aryan Z, Zoghi S, Krolo A, Boztug K, Rezaei N.
    Allergol Immunopathol (Madr); 2018 Aug 01; 46(3):263-275. PubMed ID: 28676232
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  • 14. [Research progress on regulation of class II MHC expression].
    Sun QH, Peng JP.
    Sheng Li Ke Xue Jin Zhan; 2004 Jan 01; 35(1):25-9. PubMed ID: 15127593
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  • 15. Founder effect for a 26-bp deletion in the RFXANK gene in North African major histocompatibility complex class II-deficient patients belonging to complementation group B.
    Wiszniewski W, Fondaneche MC, Lambert N, Masternak K, Picard C, Notarangelo L, Schwartz K, Bal J, Reith W, Alcaide C, de Saint Basile G, Fischer A, Lisowska-Grospierre B.
    Immunogenetics; 2000 Apr 01; 51(4-5):261-7. PubMed ID: 10803838
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  • 17. MHC Class II Deficiency with Normal CD4+ T Cell Counts: A Case Report.
    Abolnezhadian F, Saeedi-Boroujeni A, Iranparast S.
    Iran J Allergy Asthma Immunol; 2018 Dec 04; 17(6):594-600. PubMed ID: 30644704
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  • 18. A Novel RFXANK Mutation in a Chinese Child With MHC II Deficiency: Case Report and Literature Review.
    Cai YQ, Zhang H, Wang XZ, Xu C, Chao YQ, Shu Y, Tang LF.
    Open Forum Infect Dis; 2020 Aug 04; 7(8):ofaa314. PubMed ID: 32875002
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  • 19. Clinical, immunological and genetic findings of a large tunisian series of major histocompatibility complex class II deficiency patients.
    Ben-Mustapha I, Ben-Farhat K, Guirat-Dhouib N, Dhemaied E, Larguèche B, Ben-Ali M, Chemli J, Bouguila J, Ben-Mansour L, Mellouli F, Khemiri M, Béjaoui M, Barbouche MR.
    J Clin Immunol; 2013 May 04; 33(4):865-70. PubMed ID: 23314770
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