Résultat de recherche

PROMIDISα: A T-cell receptor α signature associated with immunodeficiencies caused by V(D)J recombination defects.

Jean-Pierre De Villartay

Source :

Pmid / DOI:

Reduced recruitment of 53BP1 during interstrand crosslink repair is associated with genetically inherited attenuation of mitomycin C sensitivity in a family with Fanconi anemia.

Jean-Pierre De Villartay

Source :

Pmid / DOI:

Chromosomal Translocation Formation Is Sufficient to Produce Fusion Circular RNAs Specific to Patient Tumor Cells.

Source :

Pmid / DOI:

PAXX and Xlf interplay revealed by impaired CNS development and immunodeficiency of double KO mice.

Jean-Pierre De Villartay

Source :

Pmid / DOI:

Single-Molecule Analysis of mtDNA Replication Uncovers the Basis of the Common Deletion.

Source :

Pmid / DOI:

Interleukin-15-Dependent T-Cell-like Innate Intraepithelial Lymphocytes Develop in the Intestine and Transform into Lymphomas in Celiac Disease.

Nadine CERF-BENSUSSAN

Source :

Pmid / DOI:

NKp46 is a diagnostic biomarker and may be a therapeutic target in gastrointestinal T-cell lymphoproliferative diseases: a CELAC study.

Olivier Hermine

Source :

Pmid / DOI:

Diagnostic Yield of Next-Generation Sequencing in Very Early-Onset Inflammatory Bowel Diseases: A Multicenter Study.

Nadine CERF-BENSUSSAN

Source :

Pmid / DOI:

Efficacy of Ruxolitinib Therapy in a Patient With Severe Enterocolitis Associated With a STAT3 Gain-of-Function Mutation.

Nadine CERF-BENSUSSAN

Source :

Pmid / DOI:

Human ALPI deficiency causes inflammatory bowel disease and highlights a key mechanism of gut homeostasis.

Nadine CERF-BENSUSSAN

Source :

Pmid / DOI:

Effect of Cell-Free DNA Screening vs Direct Invasive Diagnosis on Miscarriage Rates in Women With Pregnancies at High Risk of Trisomy 21: A Randomized Clinical Trial.

Yves Ville

Source :

Pmid / DOI: