Luis Seabra

Imagine Institute for Genetic Diseases

France

Research Interests

Explore related searches

Professors in France Professors in Immunology Immunology professors in France

Contact this professor

Get a free first email built on one of their papers, ready for you to edit and send yourself.

Articles (17)

Year:

2024

Year:

2024

Year:

2024

Year:

2023

Year:

2023

Year:

2022

Year:

2022

Year:

2021

Year:

2021

Year:

2021

Year:

2020

Year:

2020

Year:

2020

Year:

2020

Year:

2020

Year:

2020

Year:

2020

Collaborators (15)

Carolina Uggenti

Institute of Molecular Genetics

UNITED KINGDOM

View details

Juan A. Botía

University College London

UNITED KINGDOM

View details

Lauren LaMonica

Rutgers Health

UNITED STATES

View details

Nicolas Manel

PSL Research University

FRANCE

View details

Sarah Clarke

University of Bristol

UNITED KINGDOM

View details

Ann Wheeler

Head of Advanced Microscopy Facility

University of Edinburgh

UNITED KINGDOM

View details

Marianna Parlato

INSERM

FRANCE

View details

Hugh J. McMillan

McGill University

CANADA

View details

Jan Rehwinkel

University of Oxford

UNITED KINGDOM

View details

Martin Reijns

Senior Lecturer

University of Edinburgh

UNITED KINGDOM

View details

Karen Mackenzie

ECAT SCREDS Clinical Lecturer in Clinical Genetics

University of Edinburgh

UNITED KINGDOM

View details

Andreas Ernst

Assistant Professor

University of California, San Diego

UNITED STATES

View details

Claire Pressiat

Université Paris-Est Créteil Val de Marne

FRANCE

View details

Anne HULIN

PH/ Head of pharmacology laboratory

Assistance Publique - Hôpitaux de Paris

FRANCE

View details

Alice Lepelley

FRANCE

View details

ApplyKite TwinLearns as you apply

Make your next move.

Prepare your application

Review drafts before you send them.

Luis Seabra

Research Interests

Explore related searches

Contact this professor

Articles (17)

Biallelic NAA60 variants with impaired n-terminal acetylation capacity cause autosomal recessive primary familial brain calcifications

Gain-of-function human UNC93B1 variants cause systemic lupus erythematosus and chilblain lupus

NOTCH1-Related Leukoencephalopathy: A Novel Variant and Literature Review

JAK Inhibition in Aicardi-Goutières Syndrome: a Monocentric Multidisciplinary Real-World Approach Study.

Type I Interferonopathy due to a Homozygous Loss-of-Inhibitory Function Mutation in STAT2.

Systemic inflammatory syndrome in children with <scp> <i>FARSA</i> </scp> deficiency

Juvenile Neuropsychiatric Systemic Lupus Erythematosus: Identification of Novel Central Neuroinflammation Biomarkers.

Enhanced cGAS-STING–dependent interferon signaling associated with mutations in ATAD3A

Differential Expression of Interferon-Alpha Protein Provides Clues to Tissue Specificity Across Type I Interferonopathies.

Novel compound heterozygous STN1 variants are associated with Coats Plus syndrome.

Mutations in COPA lead to abnormal trafficking of STING to the Golgi and interferon signaling

cGAS-mediated induction of type I interferon due to inborn errors of histone pre-mRNA processing

JAK Inhibition in the Aicardi-Goutières Syndrome.

Overview of STING-Associated Vasculopathy with Onset in Infancy (SAVI) Among 21 Patients.

Leukoencephalopathy with calcifications and cysts: Genetic and phenotypic spectrum.

A Novel Hypomorphic CSF1R Gene Mutation in the Biallelic State Leading to Fatal Childhood Neurodegeneration

Type 1 interferonopathy presenting as juvenile idiopathic arthritis with interstitial lung disease: report of a new phenotype.

Collaborators (15)

Carolina Uggenti

Juan A. Botía

Lauren LaMonica

Nicolas Manel

Sarah Clarke

Ann Wheeler

Marianna Parlato

Hugh J. McMillan

Jan Rehwinkel

Martin Reijns

Karen Mackenzie

Andreas Ernst

Claire Pressiat

Anne HULIN

Alice Lepelley

Make your next move.