A novel IL2RG mutation associated with maternal T lymphocyte engraftment in a patient with severe combined immunodeficiency
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概要
- 論文の詳細を見る
- Springer-Verlag Tokyoの論文
- 2006-05-01
著者
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Hsu Amy
Genetics And Molecular Biology Branch National Human Genome Research Institute Nih Dhhs
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Balogh Peter
Department Of Immunology And Biotechnology University Of Pecs
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Balogh Peter
Department Of Immunology And Biotechnology Faculty Of Medicine University Of Pecs
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KELLERMAYER Richard
Department of Medical Genetics and Child Development, University of Pecs
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STANKOVICS Jozsef
Department of Pediatrics, University of Pecs
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HADZSIEV Kinga
Department of Medical Genetics and Child Development, University of Pecs
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VOJCEK Agnes
Department of Pediatrics, University of Pecs
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MARODI Laszlo
Department of Infectious Diseases and Pediatric Immunology, University of Debrecen
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KAJTAR Pal
Department of Pediatrics, University of Pecs
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KOSZTOLANYI Gyorgy
Department of Medical Genetics and Child Development, University of Pecs
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PUCK Jennifer
Genetics and Molecular Biology Branch, National Human Genome Research Institute, NIH, DHHS
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Kajtar Pal
Department Of Pediatrics University Of Pecs
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Vojcek Agnes
Department Of Pediatrics University Of Pecs
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Puck Jennifer
Genetics And Molecular Biology Branch National Human Genome Research Institute Nih Dhhs
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Marodi Laszlo
Department Of Infectious Diseases And Pediatric Immunology University Of Debrecen
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Hadzsiev Kinga
Department Of Medical Genetics And Child Development University Of Pecs
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Stankovics Jozsef
Department Of Pediatrics University Of Pecs
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Kosztolanyi Gyorgy
Department Of Medical Genetics And Child Development University Of Pecs
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Kellermayer Richard
Department Of Medical Genetics And Child Development University Of Pecs
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- A novel IL2RG mutation associated with maternal T lymphocyte engraftment in a patient with severe combined immunodeficiency
- Analysis of Hungarian patients with Rett syndrome phenotype for MECP2, CDKL5 and FOXG1 gene mutations