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Dissecting the phenotypic and functional heterogeneity of mouse inflammatory osteoclasts by the expression of Cx3cr1

eLife, 2020-05, Vol.9

2020

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Mapping interactions between complement C3 and regulators using mutations in atypical hemolytic uremic syndrome

Blood, 2015-04, Vol.125 (15), p.2359-2369

2015

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Microbial-Host Co-metabolites Are Prodromal Markers Predicting Phenotypic Heterogeneity in Behavior, Obesity, and Impaired Glucose Tolerance

Cell reports (Cambridge), 2017-07, Vol.20 (1), p.136-148

2017

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Complement Factor B Mutations in Atypical Hemolytic Uremic Syndrome—Disease-Relevant or Benign?

Journal of the American Society of Nephrology, 2014-09, Vol.25 (9), p.2053-2065

2014

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A prevalent C3 mutation in aHUS patients causes a direct C3 convertase gain of function

Blood, 2012-05, Vol.119 (18), p.4182-4191

2012

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Monocyte transcriptomes from patients with axial spondyloarthritis reveal dysregulated monocytopoiesis and a distinct inflammatory imprint

Arthritis research & therapy, 2021-09, Vol.23 (1), p.246-246, Article 246

2021

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Sustained Correction of X-Linked Severe Combined Immunodeficiency by ex Vivo Gene Therapy

The New England journal of medicine, 2002-04, Vol.346 (16), p.1185-1193

2002

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Vector integration is nonrandom and clustered and influences the fate of lymphopoiesis in SCID-X1 gene therapy

The Journal of clinical investigation, 2007-08, Vol.117 (8), p.2225-2232

2007

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Molecular genetics of the transcription factor GLIS3 identifies its dual function in beta cells and neurons

Genomics (San Diego, Calif.), 2018-03, Vol.110 (2), p.98-111

2018

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Nutrigenomics of high fat diet induced obesity in mice suggests relationships between susceptibility to fatty liver disease and the proteasome

PloS one, 2013-12, Vol.8 (12), p.e82825-e82825

2013

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Gene Therapy of Human Severe Combined Immunodeficiency (SCID)-X1 Disease

Science (American Association for the Advancement of Science), 2000-04, Vol.288 (5466), p.669-672

2000

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Adaptive expression of microRNA-125a in adipose tissue in response to obesity in mice and men

PloS one, 2014-03, Vol.9 (3), p.e91375-e91375

2014

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Transcriptome Profiling in Rat Inbred Strains and Experimental Cross Reveals Discrepant Genetic Architecture of Genome-Wide Gene Expression

G3 : genes - genomes - genetics, 2016-11, Vol.6 (11), p.3671-3683

2016

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Mir-342-3p regulates ostoclastogenesis in arthritis-associated osteoclast precursors

Bone Reports, 2020-10, Vol.13, p.100458, Article 100458

2020

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Protective effect of Saccharomyces boulardii CNCM I-745 on the development of inflammatory osteoclasts and inflammatory bone destruction

Bone Reports, 2020-10, Vol.13, p.100622, Article 100622

2020

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Epigenetics of spondyloarthritis

Joint, bone, spine : revue du rhumatisme, 2020-12, Vol.87 (6), p.565-571

2020

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Targeted resequencing of the 13q13 spondyloarthritis-linked locus identifies a rare variant in FREM2 possibly associated with familial spondyloarthritis

Joint, bone, spine : revue du rhumatisme, 2022-11, Vol.89 (6), p.105419-105419, Article 105419

2022

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Épigénétique de la spondyloarthrite

Revue du rhumatisme (Ed. française : 1993), 2021-01, Vol.88 (1), p.32-39

2021

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Modulatory role of the anti-apoptotic protein kinase CK2 in the sub-cellular localization of Fas associated death domain protein (FADD)

Biochimica et biophysica acta, 2015-11, Vol.1853 (11), p.2885-2896

2015

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Eculizumab in an anephric patient with atypical haemolytic uraemic syndrome and advanced vascular lesions

Nephrology, dialysis, transplantation, 2013-11, Vol.28 (11), p.2899-2907

2013

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Topological analysis of metabolic networks integrating co-segregating transcriptomes and metabolomes in type 2 diabetic rat congenic series

Genome medicine, 2016-09, Vol.8 (1), p.101-101, Article 101

2016

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Failure of SCID-X1 gene therapy in older patients

Blood, 2005-06, Vol.105 (11), p.4255-4257

2005

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Restoration of Human B-cell Differentiation Into NOD-SCID Mice Engrafted With Gene-corrected CD34+ Cells Isolated From Artemis or RAG1-deficient Patients

Molecular therapy, 2008-02, Vol.16 (2), p.396-403

2008

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Dissecting the phenotypic and functional heterogeneity of mouse inflammatory osteoclasts by the expression of Cx3cr1

Mapping interactions between complement C3 and regulators using mutations in atypical hemolytic uremic syndrome

Microbial-Host Co-metabolites Are Prodromal Markers Predicting Phenotypic Heterogeneity in Behavior, Obesity, and Impaired Glucose Tolerance

Complement Factor B Mutations in Atypical Hemolytic Uremic Syndrome—Disease-Relevant or Benign?

A prevalent C3 mutation in aHUS patients causes a direct C3 convertase gain of function

Monocyte transcriptomes from patients with axial spondyloarthritis reveal dysregulated monocytopoiesis and a distinct inflammatory imprint

Specific targeting of inflammatory osteoclastogenesis by the probiotic yeast S. boulardii CNCM I-745 reduces bone loss in osteoporosis

Sustained Correction of X-Linked Severe Combined Immunodeficiency by ex Vivo Gene Therapy

Vector integration is nonrandom and clustered and influences the fate of lymphopoiesis in SCID-X1 gene therapy

Molecular genetics of the transcription factor GLIS3 identifies its dual function in beta cells and neurons

Nutrigenomics of high fat diet induced obesity in mice suggests relationships between susceptibility to fatty liver disease and the proteasome

Hyperfunctional C3 convertase leads to complement deposition on endothelial cells and contributes to atypical hemolytic uremic syndrome

Gene Therapy of Human Severe Combined Immunodeficiency (SCID)-X1 Disease

Adaptive expression of microRNA-125a in adipose tissue in response to obesity in mice and men

Transcriptome Profiling in Rat Inbred Strains and Experimental Cross Reveals Discrepant Genetic Architecture of Genome-Wide Gene Expression

Mir-342-3p regulates ostoclastogenesis in arthritis-associated osteoclast precursors

Protective effect of Saccharomyces boulardii CNCM I-745 on the development of inflammatory osteoclasts and inflammatory bone destruction

Epigenetics of spondyloarthritis

Targeted resequencing of the 13q13 spondyloarthritis-linked locus identifies a rare variant in FREM2 possibly associated with familial spondyloarthritis

Épigénétique de la spondyloarthrite

Modulatory role of the anti-apoptotic protein kinase CK2 in the sub-cellular localization of Fas associated death domain protein (FADD)

Eculizumab in an anephric patient with atypical haemolytic uraemic syndrome and advanced vascular lesions

Topological analysis of metabolic networks integrating co-segregating transcriptomes and metabolomes in type 2 diabetic rat congenic series

Failure of SCID-X1 gene therapy in older patients

Restoration of Human B-cell Differentiation Into NOD-SCID Mice Engrafted With Gene-corrected CD34+ Cells Isolated From Artemis or RAG1-deficient Patients

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