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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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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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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
|
|
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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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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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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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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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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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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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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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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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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Potential of rare actinomycetes in the production of metabolites against multiple oxidant agents
Fatemeh Mohammadipanah
,
Mana Momenilandi
Article dans une revue
hal-04968662
v1
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