| scholarly article | Q13442814 |
| P50 | author | Didier Raoult | Q915676 |
| Lluís Quintana-Murci | Q3257549 | ||
| Antoine Guérin | Q88050442 | ||
| Gaspard Kerner | Q88050444 | ||
| Erika Della Mina | Q88050446 | ||
| Danielle T Avery | Q90292203 | ||
| Salim Bougarn | Q90319249 | ||
| Tomi Lazarov | Q90711646 | ||
| Sophie Edouard | Q91286374 | ||
| Benedetta Bigio | Q99710543 | ||
| Lisa Worley | Q125310157 | ||
| Jean-Laurent Casanova | Q17322542 | ||
| Florence Fenollar | Q21337920 | ||
| Laurent Abel | Q30503755 | ||
| Cindy S Ma | Q37830704 | ||
| Jacinta Bustamante | Q41112850 | ||
| Vivien Béziat | Q41489611 | ||
| Etienne Patin | Q41561223 | ||
| Soraya Boucherit | Q42290217 | ||
| Nico Marr | Q45358099 | ||
| Damien Chaussabel | Q46313612 | ||
| Guillaume Vogt | Q56435794 | ||
| Caroline Deswarte | Q56810370 | ||
| Janet G Markle | Q56878987 | ||
| Sabri Boughorbel | Q57421112 | ||
| Vimel Rattina | Q58509316 | ||
| Carmen Oleaga-Quintas | Q59552398 | ||
| Stuart Tangye | Q71045268 | ||
| P2093 | author name string | Frédéric Geissmann | |
| Stéphanie Boisson-Dupuis | |||
| Xavier Ayral | |||
| Natalie Wong | |||
| Tina Nguyen | |||
| Matthieu Bouaziz | |||
| Rubén Martinez-Barricarte | |||
| P2860 | cites work | Whipple's disease in a father-son pair | Q79375921 |
| IFN regulatory factor-4 and -8 govern dendritic cell subset development and their functional diversity | Q81434870 | ||
| Mycobacterial disease and impaired IFN-γ immunity in humans with inherited ISG15 deficiency | Q24294718 | ||
| Human Trypanosoma evansi infection linked to a lack of apolipoprotein L-I | Q24338417 | ||
| Assembly requirements of PU.1-Pip (IRF-4) activator complexes: inhibiting function in vivo using fused dimers | Q24533589 | ||
| Fast and accurate short read alignment with Burrows-Wheeler transform | Q24653853 | ||
| PLINK: a tool set for whole-genome association and population-based linkage analyses | Q24677407 | ||
| Interferon regulatory factor subcellular localization is determined by a bipartite nuclear localization signal in the DNA-binding domain and interaction with cytoplasmic retention factors | Q24682160 | ||
| Severe infectious diseases of childhood as monogenic inborn errors of immunity | Q26775891 | ||
| Human genetic basis of interindividual variability in the course of infection | Q26775894 | ||
| Analysis of protein-coding genetic variation in 60,706 humans | Q26831376 | ||
| Population genetic tools for dissecting innate immunity in humans | Q27001032 | ||
| The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data | Q27860742 | ||
| Merlin--rapid analysis of dense genetic maps using sparse gene flow trees | Q27860829 | ||
| The Sequence Alignment/Map format and SAMtools | Q27860966 | ||
| Exploration, normalization, and summaries of high density oligonucleotide array probe level data | Q27861098 | ||
| Identification of the uncultured bacillus of Whipple's disease | Q28187530 | ||
| BATF-JUN is critical for IRF4-mediated transcription in T cells | Q28590152 | ||
| Critical roles of interferon regulatory factor 4 in CD11bhighCD8alpha- dendritic cell development | Q28591631 | ||
| ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data | Q29547161 | ||
| affy--analysis of Affymetrix GeneChip data at the probe level | Q29547353 | ||
| Whipple endocarditis without overt gastrointestinal disease: report of four cases | Q78037602 | ||
| Crystal structure of PU.1/IRF-4/DNA ternary complex | Q78578334 | ||
| Development of Th1 and not Th2 immune responses in mice lacking IFN-regulatory factor-4 | Q78720007 | ||
| Combined electron and light microscopy in Whipple's disease. Demonstration of "bacillary bodies" in the intestine | Q79116162 | ||
| A general framework for estimating the relative pathogenicity of human genetic variants | Q29615730 | ||
| False positive PCR detection of Tropheryma whipplei in the saliva of healthy people | Q33286091 | ||
| Cultivation of the bacillus of Whipple's disease | Q33891998 | ||
| Detection of Tropheryma whipplei DNA in feces by PCR using a target capture method | Q33961198 | ||
| Dysregulated T helper cell differentiation in the absence of interferon regulatory factor 4. | Q34154407 | ||
| Human TRAF3 adaptor molecule deficiency leads to impaired Toll-like receptor 3 response and susceptibility to herpes simplex encephalitis | Q34158815 | ||
| Whole-exome sequencing-based discovery of STIM1 deficiency in a child with fatal classic Kaposi sarcoma | Q34243449 | ||
| Whipple's endocarditis: review of the literature and comparisons with Q fever, Bartonella infection, and blood culture-positive endocarditis | Q34374844 | ||
| Infectious disease. Life-threatening influenza and impaired interferon amplification in human IRF7 deficiency | Q34468857 | ||
| SnIPRE: selection inference using a Poisson random effects model | Q34510133 | ||
| Whipple's disease: new aspects of pathogenesis and treatment | Q34753203 | ||
| A narrow repertoire of transcriptional modules responsive to pyogenic bacteria is impaired in patients carrying loss-of-function mutations in MYD88 or IRAK4 | Q34795980 | ||
| Functional STAT3 deficiency compromises the generation of human T follicular helper cells. | Q35970620 | ||
| Functional IRF3 deficiency in a patient with herpes simplex encephalitis. | Q35992221 | ||
| The human gene damage index as a gene-level approach to prioritizing exome variants | Q36268400 | ||
| Whole-exome sequencing to analyze population structure, parental inbreeding, and familial linkage | Q37021842 | ||
| Unique and shared signaling pathways cooperate to regulate the differentiation of human CD4+ T cells into distinct effector subsets. | Q37178987 | ||
| IRF4: Immunity. Malignancy! Therapy? | Q37454043 | ||
| From evolutionary genetics to human immunology: how selection shapes host defence genes | Q37642585 | ||
| New insights into Whipple's disease and Tropheryma whipplei infections. | Q37779838 | ||
| The IRF family transcription factors at the interface of innate and adaptive immune responses | Q38149074 | ||
| Whipple's disease: clinical, biochemical, and histopathologic features and assessment of treatment in 29 patients | Q38188932 | ||
| Tropheryma whipplei and Whipple's disease | Q38216060 | ||
| Inborn errors in RNA polymerase III underlie severe varicella zoster virus infections | Q38637282 | ||
| Tropheryma whipplei infection and Whipple's disease | Q38726452 | ||
| Whipple's disease: a review of 19 patients from one hospital and a review of the literature since 1950. | Q39878643 | ||
| BACH2 immunodeficiency illustrates an association between super-enhancers and haploinsufficiency. | Q40055997 | ||
| Fluorescence In Situ Hybridization for Diagnosis of Whipple's Disease in Formalin-Fixed Paraffin-Embedded Tissue | Q40142200 | ||
| Recurrent rhinovirus infections in a child with inherited MDA5 deficiency. | Q40162658 | ||
| Human Adaptive Immunity Rescues an Inborn Error of Innate Immunity. | Q40318735 | ||
| Whipple's arthritis | Q40583894 | ||
| The mutation significance cutoff: gene-level thresholds for variant predictions | Q40814517 | ||
| Genomics is rapidly advancing precision medicine for immunological disorders | Q40993323 | ||
| Whipple's disease: neurological relapse presenting as headache for two years | Q41172246 | ||
| Whipple disease. Clinical review of 52 cases. The SNFMI Research Group on Whipple Disease. Société Nationale Française de Médecine Interne | Q41507470 | ||
| The rise of Tropheryma whipplei: a 12-year retrospective study of PCR diagnoses in our reference center | Q41640198 | ||
| Immunology. Autoimmunity by haploinsufficiency | Q41725536 | ||
| Failure and relapse after treatment with trimethoprim/sulfamethoxazole in classic Whipple's disease | Q42966714 | ||
| Value of Tropheryma whipplei quantitative polymerase chain reaction assay for the diagnosis of Whipple disease: usefulness of saliva and stool specimens for first-line screening | Q44734196 | ||
| Immunosuppressive therapy in Whipple's disease patients is associated with the appearance of gastrointestinal manifestations | Q44968838 | ||
| Acquired resistance to trimethoprim-sulfamethoxazole during Whipple disease and expression of the causative target gene | Q46577793 | ||
| International Union of Immunological Societies: 2017 Primary Immunodeficiency Diseases Committee Report on Inborn Errors of Immunity. | Q46948758 | ||
| Transcriptional and functional profiling defines human small intestinal macrophage subsets. | Q47256407 | ||
| Inborn Errors of RNA Lariat Metabolism in Humans with Brainstem Viral Infection | Q50422132 | ||
| Transcription factor IRF4 controls plasma cell differentiation and class-switch recombination. | Q51981842 | ||
| Genotyping reveals a wide heterogeneity of Tropheryma whipplei. | Q54549162 | ||
| Prevalence of Tropheryma whipplei DNA in patients with various gastrointestinal diseases and in healthy controls. | Q54779182 | ||
| Whipple's Disease | Q55933942 | ||
| Evidence of lifetime susceptibility to Tropheryma whipplei in patients with Whipple's disease | Q56574344 | ||
| A ParadoxicalTropheryma whippleiWestern Blot Differentiates Patients with Whipple Disease from Asymptomatic Carriers | Q56588313 | ||
| Prevalence of Asymptomatic Tropheryma whipplei Carriage among Humans and Nonhuman Primates | Q56596695 | ||
| Requirement for the transcription factor LSIRF/IRF4 for mature B and T lymphocyte function | Q71984887 | ||
| Is there an immune deficit in Whipple's disease? | Q72636213 | ||
| Tropheryma whippelii DNA in saliva of healthy people | Q73064879 | ||
| PCR-positive tests for Tropheryma whippelii in patients without Whipple's disease | Q77958532 | ||
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | haploinsufficiency | Q852654 |
| P577 | publication date | 2018-03-14 | |
| P1433 | published in | eLife | Q2000008 |
| P1476 | title | IRF4 haploinsufficiency in a family with Whipple's disease | |
| P478 | volume | 7 |
| Q53821619 | Back from the brink of obscurity. |
| Q89601652 | CD8+ T Cells Require ITK-Mediated TCR Signaling for Migration to the Intestine |
| Q92742012 | Human Inborn Errors of Immunity: 2019 Update on the Classification from the International Union of Immunological Societies Expert Committee |
| Q90740614 | Lessons learned from the study of human inborn errors of innate immunity |
| Q64097605 | Peripheral-blood b-cell subset disturbances in inflammatory joint diseases induced by Tropheryma whipplei |
| Q60142481 | PopViz: a webserver for visualizing minor allele frequencies and damage prediction scores of human genetic variations |
| Q92065173 | Recent advances in understanding inherited deficiencies in immunity to infections |
| Q96022920 | Tumour predisposition and cancer syndromes as models to study gene-environment interactions |
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