Jeremie Rosain
@JRosain
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Immunologist @casanova_lab. Interest for rare genetic disorders affecting immunity. Located in @InstitutImagine @univ_paris_cite @hopital_necker
Paris, France
Joined October 2018
RT @casanova_lab: / I was honored to accept the 2025 Novo Nordisk Prize from @novonordiskfond at today’s award ceremony in Copenhagen, Denm….
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RT @casanova_lab: 1/ We are proud of our former trainees and will be highlighting their accomplishments from time-to-time. First up is @Sat….
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RT @RockUPress: We’re thrilled to announce our partnership with the International Alliance for Primary Immunodeficiency Societies (#IAPIDS)….
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RT @casanova_lab: I am thrilled to become the Editor of this new journal and grateful to both RUP and IAPIDS for their trust ! I also thank….
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RT @casanova_lab: 📢Join the Bukavu Scientific Days 🧬. 📅Jan 8-9, 2025. 🌍Genetic predisposition to infectious diseases. 📍On-site in Bukavu &….
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RT @BogunovicLab: What Happens When Some Cells Are More Dad Than Mom (and Vice Versa)? .Latest from us. Published today. News here https://….
cuimc.columbia.edu
A new study shows that some of our cells favor genes of one parent or the other and can explain a longstanding mystery of why some people with disease-causing genes experience no symptoms.
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RT @MasatoOgishi: 1/ We report @ImmunityCP that the PD-1:PD-L1 axis promotes the development of B-cell memory and antibody responses in mic….
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RT @KaanBoztug: Happy to announce the publication of our paper in Science Immunology. Here we describe the first patients with biallelic di….
science.org
Loss-of-function mutations in LTBR result in a stromal defect, leading to dysfunctional secondary lymphoid organs and combined immunodeficiency in humans.
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RT @AAlliance_SAID: Abstracts due Dec 18th! Register for the International Society of Systemic #Autoinflammatory Diseases (ISSAID) Congress….
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We also conducted a literature review on contiguous gene deletion syndromes involving at least one gene associated with inborn errors of immunity
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Here is our report on a nationwide study of patients with heterozygous 2q33 heterozygous deletions underlying syndromic and non syndromic CTLA4 deficiencies: Many thanks to all colleagues involved, including our cytogeneticist friends!.
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RT @casanova_lab: 1/ Delighted to share our review on Genetic Defects of Brain Immunity in Childhood Herpes Simplex Encephalitis (HSE), jus….
nature.com
Nature - This article reviews evidence that has emerged over the past two decades indicating that herpes simplex encephalitis in children can result from monogenic defects of brain immunity to...
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RT @RESIST_cluster: On 21 November, Jacinta Bustamante, @BustamanteJaci1 Université Paris Cité, Institut Imagine, INSERM, @casanova_lab , w….
resist-cluster.de
Spannende Themen, interessant präsentiert: Jeden ersten und dritten Donnerstag (außer während der Schulferien) stellen RESIST-Wissenschaftlerinnen oder -Wissenschaftler oder hochkarätige Forscherin...
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RT @doctorveera: GWAS of non-syndromic cleft palate in 228 cases and 300k controls from Finland. The striking signal in chromosome 1 is dri….
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RT @ImmunoEditor: Last week's @CytokineSociety #cytokines2024 meeting in Seoul was amazing! To celebrate, @SciImmunology has just released….
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Why do some patients present severe diseases when they meet Powassan, Usutu, and Ross River (arbo)viruses? Auto-antibodies to type I IFNs - again them ! Congrats to @grvsadrian et al.
1/ We are excited to share our new report in @JExpMed showing that auto-Abs neutralizing type I IFNs are strong, common, and global determinants of severe disease triggered by Powassan (POWV), Usutu (USUV), and Ross River (RRV) (arbo)viruses (.
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Very interesting review about kidney diseases caused by inborn errors of immunity, and their potential targeted therapies.
Now OA in @NDTsocial . Primary immunodeficiency (PID) as a cause of immune-mediated kidney diseases. 👉PIDs can cause autoimmunity.👉largely neglected in nephrology.👉many possibilities for research.👉PID as cause for infectious complications . ▶️
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