| P50 | author | Balthasar A Heesters | Q83158491 |
| P2093 | author name string | Michel J Massaad | |
| | Raif S Geha | |
| | Claire Galand | |
| | Oliver T Burton | |
| | Hamid Mattoo | |
| | John Manis | |
| | Juhan Yoon | |
| | Jana L Mooster | |
| | Haifa Jabara | |
| | Severine Le Bras | |
| P2860 | cites work | X-linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane protein | Q24310290 |
| | RANK is essential for osteoclast and lymph node development | Q24598872 |
| | Follicular dendritic cells control engulfment of apoptotic bodies by secreting Mfge8 | Q24644725 |
| | Coordination between NF-kappaB family members p50 and p52 is essential for mediating LTbetaR signals in the development and organization of secondary lymphoid tissues | Q24685416 |
| | B cells from p50/NF-kappa B knockout mice have selective defects in proliferation, differentiation, germ-line CH transcription, and Ig class switching | Q70994054 |
| | The splenic marginal zone is absent in alymphoplastic aly mutant mice | Q71011987 |
| | A new mutation, aly, that induces a generalized lack of lymph nodes accompanied by immunodeficiency in mice | Q72753495 |
| | Essential role of RelB in germinal center and marginal zone formation and proper expression of homing chemokines | Q74321402 |
| | Transcription of the RelB gene is regulated by NF-kappaB | Q77378999 |
| | Preparation, culture, and immortalization of mouse embryonic fibroblasts | Q80674195 |
| | NF-κB, the first quarter-century: remarkable progress and outstanding questions | Q26822516 |
| | Phosphorylation meets ubiquitination: the control of NF-[kappa]B activity | Q27860643 |
| | Marginal zone B cells | Q28240061 |
| | NF-kappaB and the immune response | Q28271031 |
| | Germline mutations in NFKB2 implicate the noncanonical NF-κB pathway in the pathogenesis of common variable immunodeficiency | Q28300499 |
| | B cell antigen receptor signal strength and peripheral B cell development are regulated by a 9-O-acetyl sialic acid esterase | Q28304887 |
| | Abnormal development of peripheral lymphoid organs in mice deficient in lymphotoxin | Q28507630 |
| | Lymphotoxin-alpha-deficient mice. Effects on secondary lymphoid organ development and humoral immune responsiveness | Q28510392 |
| | Chemokine CXCL13 is essential for lymph node initiation and is induced by retinoic acid and neuronal stimulation | Q28585797 |
| | Distinct roles for lymphotoxin-alpha and tumor necrosis factor in organogenesis and spatial organization of lymphoid tissue | Q28586439 |
| | Abnormal development of secondary lymphoid tissues in lymphotoxin beta-deficient mice | Q28587099 |
| | Regulation of hair follicle development by the TNF signal ectodysplasin and its receptor Edar | Q28587214 |
| | Distinct roles in lymphoid organogenesis for lymphotoxins alpha and beta revealed in lymphotoxin beta-deficient mice | Q28587819 |
| | OPGL is a key regulator of osteoclastogenesis, lymphocyte development and lymph-node organogenesis | Q28589430 |
| | Immune and inflammatory responses in TNF alpha-deficient mice: a critical requirement for TNF alpha in the formation of primary B cell follicles, follicular dendritic cell networks and germinal centers, and in the maturation of the humoral immune re | Q28594116 |
| | Shared principles in NF-kappaB signaling | Q29547234 |
| | The two NF-kappaB activation pathways and their role in innate and adaptive immunity | Q29614355 |
| | Cdc42 interacting protein 4 (CIP4) is essential for integrin-dependent T-cell trafficking. | Q30496633 |
| | CD4+ Th1 and CD8+ type 1 cytotoxic T cells both play a crucial role in the full development of contact hypersensitivity | Q31713471 |
| | Autosomal dominant anhidrotic ectodermal dysplasia with immunodeficiency caused by a novel NFKBIA mutation, p.Ser36Tyr, presents with mild ectodermal dysplasia and non-infectious systemic inflammation | Q33409176 |
| | Development and maturation of secondary lymphoid tissues. | Q33652498 |
| | Ontogeny of stromal organizer cells during lymph node development. | Q33823116 |
| | The presentation and natural history of immunodeficiency caused by nuclear factor kappaB essential modulator mutation | Q33977713 |
| | Multiorgan inflammation and hematopoietic abnormalities in mice with a targeted disruption of RelB, a member of the NF-kappa B/Rel family | Q34317095 |
| | Infectious diseases in patients with IRAK-4, MyD88, NEMO, or IκBα deficiency | Q35090141 |
| | Organogenesis of lymphoid tissues | Q35096187 |
| | Dissecting the role of lymphotoxin in lymphoid organs by conditional targeting | Q35216954 |
| | A novel mutation in NFKBIA/IKBA results in a degradation-resistant N-truncated protein and is associated with ectodermal dysplasia with immunodeficiency | Q35231720 |
| | Inherited disorders of NF-kappaB-mediated immunity in man. | Q35634019 |
| | A hypermorphic IkappaBalpha mutation is associated with autosomal dominant anhidrotic ectodermal dysplasia and T cell immunodeficiency | Q36001303 |
| | Human disease resulting from gene mutations that interfere with appropriate nuclear factor-kappaB activation | Q36015009 |
| | Peyer's patch organogenesis is intact yet formation of B lymphocyte follicles is defective in peripheral lymphoid organs of mice deficient for tumor necrosis factor and its 55-kDa receptor | Q36184139 |
| | Regulation of peripheral lymph node genesis by the tumor necrosis factor family member TRANCE | Q36368551 |
| | Essential role of lymph nodes in contact hypersensitivity revealed in lymphotoxin-alpha-deficient mice. | Q36369156 |
| | Requirement for the NF-kappaB family member RelA in the development of secondary lymphoid organs | Q36369876 |
| | Distinct roles of lymphotoxin alpha and the type I tumor necrosis factor (TNF) receptor in the establishment of follicular dendritic cells from non-bone marrow-derived cells | Q36380985 |
| | The same IkappaBalpha mutation in two related individuals leads to completely different clinical syndromes. | Q36402422 |
| | TACI and BAFF-R mediate isotype switching in B cells | Q36402479 |
| | Abnormal lymphoid organ development in immunodeficient mutant mice. | Q36538837 |
| | Lymph node mapping in the mouse | Q36590616 |
| | Impaired CD19 expression and signaling, enhanced antibody response to type II T independent antigen and reduction of B-1 cells in CD81-deficient mice | Q36597251 |
| | Transcriptional regulation of NF-kappa B2: evidence for kappa B-mediated positive and negative autoregulation | Q36670738 |
| | Molecular basis of NF-κB signaling | Q36918115 |
| | Hypomorphic nuclear factor-kappaB essential modulator mutation database and reconstitution system identifies phenotypic and immunologic diversity | Q37262549 |
| | Dento-craniofacial phenotypes and underlying molecular mechanisms in hypohidrotic ectodermal dysplasia (HED): a review. | Q37333361 |
| | Noncanonical NF-κB signaling is limited by classical NF-κB activity | Q37651821 |
| | New insights into the development of lymphoid tissues | Q37779724 |
| | Stromal cell-immune cell interactions | Q37809072 |
| | A single NFκB system for both canonical and non-canonical signaling | Q37811890 |
| | Diagnosis and treatment in anhidrotic ectodermal dysplasia with immunodeficiency | Q38013562 |
| | Induction of the alternative NF-κB pathway by lymphotoxin αβ (LTαβ) relies on internalization of LTβ receptor | Q38960255 |
| | Acute hypoxia induces HIF-independent monocyte adhesion to endothelial cells through increased intercellular adhesion molecule-1 expression: the role of hypoxic inhibition of prolyl hydroxylase activity for the induction of NF-kappa B. | Q39688881 |
| | Finding NEMO: genetic disorders of NF-κB activation | Q39912726 |
| | Genetic analysis of NF- B/Rel transcription factors defines functional specificities | Q39962410 |
| | LTbetaR signaling induces cytokine expression and up-regulates lymphangiogenic factors in lymph node anlagen | Q39986041 |
| | Artificial lymph nodes induce potent secondary immune responses in naive and immunodeficient mice | Q40233488 |
| | Disseminated BCG infection mimicking metastatic nasopharyngeal carcinoma in an immunodeficient child with a novel hypomorphic NEMO mutation | Q40318502 |
| | The ligands and receptors of the lymphotoxin system | Q40541150 |
| | The lymphotoxin-beta receptor induces different patterns of gene expression via two NF-kappaB pathways | Q40696432 |
| | Alymphoplasia is caused by a point mutation in the mouse gene encoding Nf-kappa b-inducing kinase | Q40954925 |
| | Clonal selection and learning in the antibody system | Q41002744 |
| | Essential role of nuclear factor (NF)-kappaB-inducing kinase and inhibitor of kappaB (IkappaB) kinase alpha in NF-kappaB activation through lymphotoxin beta receptor, but not through tumor necrosis factor receptor I | Q42015911 |
| | Roles of IKK-beta, IRF1, and p65 in the activation of chemokine genes by interferon-gamma | Q42021111 |
| | Surface lymphotoxin alpha/beta complex is required for the development of peripheral lymphoid organs | Q42196937 |
| | BAFF mediates survival of peripheral immature B lymphocytes | Q42944182 |
| | Ectodysplasin-A1 is sufficient to rescue both hair growth and sweat glands in Tabby mice | Q43829636 |
| | CD4+ T cells regulate CD8+ T cell-mediated cutaneous immune responses by restricting effector T cell development through a Fas ligand-dependent mechanism | Q44757009 |
| | Targeting the NF-kappaB pathway through pharmacological inhibition of IKK2 prevents human cytomegalovirus replication and virus-induced inflammatory response in infected endothelial cells | Q45286181 |
| | A novel gain-of-function IKBA mutation underlies ectodermal dysplasia with immunodeficiency and polyendocrinopathy | Q45345436 |
| | The lymphotoxin beta receptor controls organogenesis and affinity maturation in peripheral lymphoid tissues | Q47713235 |
| | A rapid screening method to detect autosomal-dominant ectodermal dysplasia with immune deficiency syndrome. | Q50335729 |
| | Heterozygous N-terminal deletion of IkappaBalpha results in functional nuclear factor kappaB haploinsufficiency, ectodermal dysplasia, and immune deficiency. | Q51733159 |
| | Blood dendritic cells interact with splenic marginal zone B cells to initiate T-independent immune responses. | Q52114309 |
| | A novel mutation in the Nfkb2 gene generates an NF-kappa B2 "super repressor". | Q52583526 |
| | BAFF-induced NEMO-independent processing of NF-kappa B2 in maturing B cells. | Q53664665 |
| | Successful Allogeneic Hemopoietic Stem Cell Transplantation in a Child Who Had Anhidrotic Ectodermal Dysplasia With Immunodeficiency | Q56940834 |
| | A hypermorphic IκBα mutation is associated with autosomal dominant anhidrotic ectodermal dysplasia and T cell immunodeficiency | Q56941191 |
| P4510 | describes a project that uses | ImageJ | Q1659584 |
| P433 | issue | 2 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | heterozygosity | Q124059385 |
| P304 | page(s) | 185-202 | |
| P577 | publication date | 2015-01-19 | |
| P1433 | published in | Journal of Experimental Medicine | Q3186912 |
| P1476 | title | Defective lymphoid organogenesis underlies the immune deficiency caused by a heterozygous S32I mutation in IκBα | |
| P478 | volume | 212 | |