Human Genome Epidemiology Literature Finder
Records 1 - 13 (of 13 Records) |
Query Trace: RAG2[original query] |
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Mutations in genes required for T-cell development: IL7R, CD45, IL2RG, JAK3, RAG1, RAG2, ARTEMIS, and ADA and severe combined immunodeficiency: HuGE review. Genetics in medicine : official journal of the American College of Medical Genetics 0 6 (1): 16-26. Kalman Lisa, Lindegren Mary Lou, Kobrynski Lisa, Vogt Robert, Hannon Harry, Howard Joelyn Tonkin, Buckley Rebec |
IL7R and RAG1/2 genes mutations/polymorphisms in patients with SCID. Iranian journal of allergy, asthma, and immunology 2011 Jun 10 (2): 129-32. Safaei Sepideh, Pourpak Zahra, Moin Mostafa, Houshmand Masso |
Sprague Dawley Rag2-Null Rats Created from Engineered Spermatogonial Stem Cells Are Immunodeficient and Permissive to Human Xenografts. Molecular cancer therapeutics 2018 9 17 (11): 2481-2489. Noto Fallon K, Adjan-Steffey Valeriya, Tong Min, Ravichandran Kameswaran, Zhang Wei, Arey Angela, McClain Christopher B, Ostertag Eric, Mazhar Sahar, Sangodkar Jaya, DiFeo Analisa, Crawford Jack, Narla Goutham, Jamling Tseten |
Genetic mutations and immunological features of severe combined immunodeficiency patients in Iran. Immunology letters 2019 Oct . Shahbazi Zahra, Yazdani Reza, Shahkarami Sepideh, Shahbazi Shirin, Hamid Mohammad, Sadeghi-Shabestari Mahnaz, Momen Tooba, Aleyasin Soheila, Esmaeilzadeh Hossein, Darougar Sepideh, Delavari Sama, Mahdaviani Seyed Alireza, Ahanchian Hamid, Behmanesh Fatemeh, Kiaee Fatemeh, Chavoshzade Zahra, Shariat Mansoureh, Keramatipour Mohammad, Rezaei Nima, Abolhassani Hassan, Parvaneh Nima, Mahdian Reza, Aghamohammadi Asgh |
Variation in genes implicated in B-cell development and antibody production affects susceptibility to pemphigus. Immunology 2020 Sep . Calonga-Solís Verónica, Amorim Leonardo M, Farias Ticiana D J, Petzl-Erler Maria Luiza, Malheiros Danielle, Augusto Danillo |
Clinical Manifestations, Mutational Analysis, and Immunological Phenotype in Patients with RAG1/2 Mutations: First Cases Series from Mexico and Description of Two Novel Mutations. Journal of clinical immunology 2021 5 41 (6): 1291-1302. Lugo-Reyes Saul Oswaldo, Pastor Nina, González-Serrano Edith, Yamazaki-Nakashimada Marco Antonio, Scheffler-Mendoza Selma, Berron-Ruiz Laura, Wakida Guillermo, Nuñez-Nuñez Maria Enriqueta, Macias-Robles Ana Paola, Staines-Boone Aide Tamara, Venegas-Montoya Edna, Alaez-Verson Carmen, Molina-Garay Carolina, Flores-Lagunes Luis Leonardo, Carrillo-Sanchez Karol, Niemela Julie, Rosenzweig Sergio D, Gaytan Paul, Yañez Jorge A, Martinez-Duncker Ivan, Notarangelo Luigi D, Espinosa-Padilla Sara, Cruz-Munoz Mario Ernes |
Chronic Refractory Immune Thrombocytopenia Is Associated With Variants in Immune Genes. Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis 2021 11 27 10760296211059813. Zhao Shasha, Ma Jingyao, Zhu Xiaojing, Zhang Jialu, Wu Runh |
Clinical, Immunological, and Molecular Variability of RAG Deficiency: A Retrospective Analysis of 22 RAG Patients. Journal of clinical immunology 2021 10 42 (1): 130-145. Cifaldi Cristina, Rivalta Beatrice, Amodio Donato, Mattia Algeri, Pacillo Lucia, Di Cesare Silvia, Chiriaco Maria, Ursu Giorgiana Madalina, Cotugno Nicola, Giancotta Carmela, Manno Emma C, Santilli Veronica, Zangari Paola, Federica Galaverna, Palumbo Giuseppe, Merli Pietro, Palma Paolo, Rossi Paolo, Di Matteo Gigliola, Locatelli Franco, Finocchi Andrea, Cancrini Cateri |
Hypomorphic RAG deficiency: impact of disease burden on survival and thymic recovery argues for early diagnosis and HSCT. Blood 2022 10 . Schuetz C, Gerke J, Ege M, Walter J, Kusters M, Worth A, Kanakry J A, Dimitrova D, Wolska-Ku?nierz B, Chen K, Unal E, Karakukcu M, Pashchenko O, Leiding J, Kawai T, Amrolia P J, Berghuis D, Buechner J, Buchbinder D, Cowan M J, Gennery A R, Güngör T, Heimall J, Miano M, Meyts I, Morris E C, Rivière J, Sharapova S O, Shaw P J, Slatter M, Honig M, Veys P, Fischer A, Cavazzana M, Moshous D, Schulz A, Albert M H, Puck J M, Lankester A C, Notarangelo L D, Neven |
Multiple genetic variants involved in both autoimmunity and autoinflammation detected in Chinese patients with sporadic Meniere's disease: a preliminary study. Frontiers in neurology 2023 6 14 1159658. Jing Zou, Guoping Zhang, Hongbin Li, Zikai Zhao, Qing Zhang, Ilmari Pyykkö, Antti Mäkit |
Waldenström macroglobulinemia and non-IgM-type lymphoplasmacytic lymphoma are genetically similar. Acta haematologica 2023 3 . Awata-Shiraiwa Maaya, Yokohama Akihiko, Kanai Yukihiro, Gotoh Nanami, Kasamatsu Tetsuhiro, Handa Hiroshi, Saitoh Takayuki, Murakami Hirokazu, Hirato Junko, Ikota Hayato, Tsukamoto Norifu |
Immunological and molecular study in children with combined immunodeficiency. European annals of allergy and clinical immunology 2023 2 . Kholoussi S, Ramadan A, Kholoussi N, Ashaat E A, Fayez A G, Raouf H A, Helwa I, Esmaiel N N, Ghorab R, Abo-Shanab A |
DNA Copy Number Alterations and Copy Neutral Loss of Heterozygosity in Adult Ph-Negative Acute B-Lymphoblastic Leukemia: Focus on the Genes Involved. International journal of molecular sciences 2023 12 24 (24): . Natalya Risinskaya, Maria Gladysheva, Abdulpatakh Abdulpatakhov, Yulia Chabaeva, Valeriya Surimova, Olga Aleshina, Anna Yushkova, Olga Dubova, Nikolay Kapranov, Irina Galtseva, Sergey Kulikov, Tatiana Obukhova, Andrey Sudarikov, Elena Parovichniko |
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