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            Human MCTS1-dependent translation of JAK2 is essential for IFN-γ immunity to mycobacteria
        
                            
                                                                                                            Jonathan Bohlen
                                                                ,
                                                                                                                                Qinhua Zhou
                                                                ,
                                                                                                                                Quentin Philippot
                                                                ,
                                                                                                                                Masato Ogishi
                                                                ,
                                                                                                                                Darawan Rinchai
                                                                                            et al.
                            
                 
                            
                 Article dans une revue
                    
        
        
            
                
                    hal-04968552
                                            v1
                                    
            
        
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            The immunopathological landscape of human pre-TCRα deficiency: From rare to common variants
        
                            
                                                                                                            Marie Materna
                                                                ,
                                                                                                                                Ottavia M Delmonte
                                                                ,
                                                                                                                                Marita Bosticardo
                                                                ,
                                                                                                                                Mana Momenilandi
                                                                ,
                                                                                                                                Peyton E Conrey
                                                                                            et al.
                            
                 
                            
                 Article dans une revue
                    
        
        
            
                
                    hal-04877280
                                            v1
                                    
            
        
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            FLT3L governs the development of partially overlapping hematopoietic lineages in humans and mice
        
                            
                                                                                                            Mana Momenilandi
                                                                ,
                                                                                                                                Romain Lévy
                                                                ,
                                                                                                                                Steicy Sobrino
                                                                ,
                                                                                                                                Jingwei Li
                                                                ,
                                                                                                                                Chantal Lagresle-Peyrou
                                                                                            et al.
                            
                 
                            
                 Article dans une revue
                    
        
        
            
                
                    pasteur-04589107
                                            v1
                                    
            
        
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            Human inherited CCR2 deficiency underlies progressive polycystic lung disease
        
                            
                                                                                                            Anna-Lena Neehus
                                                                ,
                                                                                                                                Brenna Carey
                                                                ,
                                                                                                                                Marija Landekic
                                                                ,
                                                                                                                                Patricia Panikulam
                                                                ,
                                                                                                                                Gail Deutsch
                                                                                            et al.
                            
                 
                            
                 Article dans une revue
                    
        
        
            
                
                    hal-04701934
                                            v1
                                    
            
        
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            Human germline gain-of-function in STAT6: from severe allergic disease to lymphoma and beyond
        
                            
                                                                                                            Mehul Sharma
                                                                ,
                                                                                                                                Narissara Suratannon
                                                                ,
                                                                                                                                Daniel Leung
                                                                ,
                                                                                                                                Safa Baris
                                                                ,
                                                                                                                                Ichiro Takeuchi
                                                                                            et al.
                            
                 
                            
                 Article dans une revue
                    
        
        
            
                
                    hal-04876482
                                            v1
                                    
            
        
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            Inherited human ZNF341 deficiency
        
                            
                                                                                                            Vivien Béziat
                                                                ,
                                                                                                                                Claire Fieschi
                                                                ,
                                                                                                                                Mana Momenilandi
                                                                ,
                                                                                                                                Mélanie Migaud
                                                                ,
                                                                                                                                Brahim Belaid
                                                                                            et al.
                            
                 
                            
                 Article dans une revue
                    
        
        
            
                
                    hal-04876430
                                            v1
                                    
            
        
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            Human CARMIL2 deficiency underlies a broader immunological and clinical phenotype than CD28 deficiency
        
                            
                                                                                                            Romain Lévy
                                                                ,
                                                                                                                                Florian Gothe
                                                                ,
                                                                                                                                Mana Momenilandi
                                                                ,
                                                                                                                                Thomas Magg
                                                                ,
                                                                                                                                Marie Materna
                                                                                            et al.
                            
                 
                            
                 Article dans une revue
                    
        
        
            
                
                    hal-04288101
                                            v1
                                    
            
        
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            Human IL-23 is essential for IFN-γ-dependent immunity to mycobacteria
        
                            
                                                                                                            Quentin Philippot
                                                                ,
                                                                                                                                Masato Ogishi
                                                                ,
                                                                                                                                Jonathan Bohlen
                                                                ,
                                                                                                                                Julia Puchan
                                                                ,
                                                                                                                                Andrés Augusto Arias
                                                                                            et al.
                            
                 
                            
                 Article dans une revue
                    
        
        
            
                
                    hal-04380991
                                            v1
                                    
            
        
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            Autoantibodies against type I IFNs in humans with alternative NF-κB pathway deficiency
        
                            
                                                                                                            Tom Le Voyer
                                                                ,
                                                                                                                                Audrey V Parent
                                                                ,
                                                                                                                                Xian Liu
                                                                ,
                                                                                                                                Axel Cederholm
                                                                ,
                                                                                                                                Adrian Gervais
                                                                                            et al.
                            
                 
                            
                 Article dans une revue
                    
        
        
            
                
                    hal-04815868
                                            v1
                                    
            
        
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            Clinical, Immunological, and Genetic Findings in Iranian Patients with MHC-II Deficiency: Confirmation of c.162delG RFXANK Founder Mutation in the Iranian Population
        
                            
                                                                                                            Mohadese Sadat Mousavi Khorshidi
                                                                ,
                                                                                                                                Yoann Seeleuthner
                                                                ,
                                                                                                                                Zahra Chavoshzadeh
                                                                ,
                                                                                                                                Maryam Behfar
                                                                ,
                                                                                                                                Amir Ali Hamidieh
                                                                                            et al.
                            
                 
                            
                 Article dans une revue
                    
        
        
            
                
                    hal-04968582
                                            v1
                                    
            
        
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            Human inherited complete STAT2 deficiency underlies inflammatory viral diseases
        
                            
                                                                                                            Giorgia Bucciol
                                                                ,
                                                                                                                                Leen Moens
                                                                ,
                                                                                                                                Masato Ogishi
                                                                ,
                                                                                                                                Darawan Rinchai
                                                                ,
                                                                                                                                Daniela Matuozzo
                                                                                            et al.
                            
                 
                            
                 Article dans une revue
                    
        
        
            
                
                    hal-04945238
                                            v1
                                    
            
        
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            Delayed Diagnosis of Chronic Necrotizing Granulomatous Skin Lesions due to TAP2 Deficiency
        
                            
                                                                                                            Ilad Alavi Darazam
                                                                ,
                                                                                                                                Atousa Hakamifard
                                                                ,
                                                                                                                                Mana Momenilandi
                                                                ,
                                                                                                                                Marie Materna
                                                                ,
                                                                                                                                Farid Javandoust Gharehbagh
                                                                                            et al.
                            
                 
                            
                 Article dans une revue
                    
        
        
            
                
                    hal-04968615
                                            v1
                                    
            
        
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            Two Novel Biallelic RASGRP1 Mutations Presenting with Immunodeficiency, Hodgkin’s Lymphoma, and Autoimmunity
        
                            
                                                                                                            Mana Momenilandi
                                                                ,
                                                                                                                                Ali Pourvali
                                                                ,
                                                                                                                                Leen Moens
                                                                ,
                                                                                                                                Nima Parvaneh
                                                                ,
                                                                                                                                Greet Wuyts
                                                                                            et al.
                            
                 
                            
                 Article dans une revue
                    
        
        
            
                
                    hal-04968619
                                            v1
                                    
            
        
     | 
                                                                                
    | 
        
                            
                    
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            Human CARMIL2 deficiency underlies a broader immunological and clinical phenotype than CD28 deficiency
        
                            
                                                                                                            Romain Lévy
                                                                ,
                                                                                                                                Florian Gothe
                                                                ,
                                                                                                                                Mana Momenilandi
                                                                ,
                                                                                                                                Thomas Magg
                                                                ,
                                                                                                                                Marie Materna
                                                                                            et al.
                            
                 
                            
                 Article dans une revue
                    
        
        
            
                
                    hal-04119583
                                            v1
                                    
            
        
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    | 
        
                            
                    
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            Humans with inherited T cell CD28 deficiency are susceptible to skin papillomaviruses but are otherwise healthy
        
                            
                                                                                                            Vivien Béziat
                                                                ,
                                                                                                                                Franck Rapaport
                                                                ,
                                                                                                                                Jiafen Hu
                                                                ,
                                                                                                                                Matthias Titeux
                                                                ,
                                                                                                                                Mathilde Bonnet Des Claustres
                                                                                            et al.
                            
                 
                            
                 Article dans une revue
                    
        
        
            
                
                    hal-04602284
                                            v1
                                    
            
        
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            Inherited IFNAR1 deficiency in otherwise healthy patients with adverse reaction to measles and yellow fever live vaccines
        
                            
                                                                                                            Nicholas Hernandez
                                                                ,
                                                                                                                                Giorgia Bucciol
                                                                ,
                                                                                                                                Leen Moens
                                                                ,
                                                                                                                                Jérémie Le Pen
                                                                ,
                                                                                                                                Mohammad Shahrooei
                                                                                            et al.
                            
                 
                            
                 Article dans une revue
                    
        
        
            
                
                    hal-04968630
                                            v1
                                    
            
        
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            A novel homozygous LRRK1 stop gain mutation in a patient suspected with osteosclerotic metaphyseal dysplasia
        
                            
                                                                                                            Mohammad Miryounesi
                                                                ,
                                                                                                                                Ali Nikfar
                                                                ,
                                                                                                                                Majid Changi-Ashtiani
                                                                ,
                                                                                                                                Mohammad Shahrooei
                                                                ,
                                                                                                                                Hossein Dinmohammadi
                                                                                            et al.
                            
                 
                            
                 Article dans une revue
                    
        
        
            
                
                    hal-04968623
                                            v1
                                    
            
        
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            Potential of rare actinomycetes in the production of metabolites against multiple oxidant agents
        
                            
                                                                                                            Fatemeh Mohammadipanah
                                                                ,
                                                                                                                                Mana Momenilandi
                                                                                    
                 
                            
                 Article dans une revue
                    
        
        
            
                
                    hal-04968662
                                            v1
                                    
            
        
     |