[HTML][HTML] Clinical and Immunological Phenotype of Patients With Primary Immunodeficiency Due to Damaging Mutations in NFKB2
C Klemann, N Camacho-Ordonez, L Yang… - Frontiers in …, 2019 - frontiersin.org
Non-canonical NF-κB-pathway signaling is integral in immunoregulation. Heterozygous
mutations in NFKB2 have recently been established as a molecular cause of common …
mutations in NFKB2 have recently been established as a molecular cause of common …
[PDF][PDF] Clinical and Immunological Phenotype of Patients With Primary Immunodeficiency Due to Damaging Mutations in NFKB2
SG Tangye, VL Bryant, MJ Massaad, B Grimbacher… - freidok.uni-freiburg.de
NFKB2-associated disease. In addition, an array of lymphocyte subpopulations, such as
regulatory T cell, Th17-, cTFH-, NKT-, and MAIT-cell numbers were decreased. We conclude …
regulatory T cell, Th17-, cTFH-, NKT-, and MAIT-cell numbers were decreased. We conclude …
Clinical and Immunological Phenotype of Patients With Primary Immunodeficiency Due to Damaging Mutations in NFKB2
C Klemann, N Camacho-Ordonez… - Frontiers in …, 2019 - pubmed.ncbi.nlm.nih.gov
Non-canonical NF-κB-pathway signaling is integral in immunoregulation. Heterozygous
mutations in NFKB2 have recently been established as a molecular cause of common …
mutations in NFKB2 have recently been established as a molecular cause of common …
Clinical and Immunological Phenotype of Patients With Primary Immunodeficiency Due to Damaging Mutations in NFKB2
C Klemann, N Camacho-Ordonez, L Yang… - Frontiers in …, 2019 - discovery.ucl.ac.uk
Non-canonical NF-κB-pathway signaling is integral in immunoregulation. Heterozygous
mutations in NFKB2 have recently been established as a molecular cause of common …
mutations in NFKB2 have recently been established as a molecular cause of common …
[PDF][PDF] Clinical and Immunological Phenotype of Patients With Primary Immunodeficiency Due to Damaging Mutations in NFKB2
SG Tangye, VL Bryant, MJ Massaad, B Grimbacher… - scienceopen.com
NFKB2-associated disease. In addition, an array of lymphocyte subpopulations, such as
regulatory T cell, Th17-, cTFH-, NKT-, and MAIT-cell numbers were decreased. We conclude …
regulatory T cell, Th17-, cTFH-, NKT-, and MAIT-cell numbers were decreased. We conclude …
Clinical and Immunological Phenotype of Patients With Primary Immunodeficiency Due to Damaging Mutations in NFKB2
C Klemann, N Camacho-Ordonez, L Yang… - … in Immunology (Web), 2019 - jglobal.jst.go.jp
Clinical and Immunological Phenotype of Patients With Primary Immunodeficiency Due to
Damaging Mutations in NFKB2 | Article Information | J-GLOBAL Art J-GLOBAL ID:201902291289434957 …
Damaging Mutations in NFKB2 | Article Information | J-GLOBAL Art J-GLOBAL ID:201902291289434957 …
[HTML][HTML] Clinical and Immunological Phenotype of Patients With Primary Immunodeficiency Due to Damaging Mutations in NFKB2
C Klemann, N Camacho-Ordonez, L Yang… - Frontiers in …, 2019 - ncbi.nlm.nih.gov
Non-canonical NF-κB-pathway signaling is integral in immunoregulation. Heterozygous
mutations in NFKB2 have recently been established as a molecular cause of common …
mutations in NFKB2 have recently been established as a molecular cause of common …
Clinical and Immunological Phenotype of Patients With Primary Immunodeficiency Due to Damaging Mutations in NFKB2.
C Klemann, N Camacho-Ordonez, L Yang… - Frontiers in …, 2019 - europepmc.org
Non-canonical NF-κB-pathway signaling is integral in immunoregulation. Heterozygous
mutations in NFKB2 have recently been established as a molecular cause of common …
mutations in NFKB2 have recently been established as a molecular cause of common …
[PDF][PDF] Clinical and Immunological Phenotype of Patients With Primary Immunodeficiency Due to Damaging Mutations in NFKB2
SG Tangye, VL Bryant, MJ Massaad, B Grimbacher… - scholar.archive.org
NFKB2-associated disease. In addition, an array of lymphocyte subpopulations, such as
regulatory T cell, Th17-, cTFH-, NKT-, and MAIT-cell numbers were decreased. We conclude …
regulatory T cell, Th17-, cTFH-, NKT-, and MAIT-cell numbers were decreased. We conclude …
[引用][C] Clinical and Immunological Phenotype of Patients With Primary Immunodeficiency Due to Damaging Mutations in NFKB2
C Klemann, N Camacho-Ordonez, L Yang… - Frontiers in …, 2019 - cir.nii.ac.jp
Clinical and Immunological Phenotype of Patients With Primary Immunodeficiency Due to
Damaging Mutations in NFKB2 | CiNii Research CiNii 国立情報学研究所 学術情報ナビゲータ[サイニィ …
Damaging Mutations in NFKB2 | CiNii Research CiNii 国立情報学研究所 学術情報ナビゲータ[サイニィ …