Nadia Vasquez

发表

Faecalibacterium prausnitzii is an anti-inflammatory commensal bacterium identified by gut microbiota analysis of Crohn disease patients

J. Doré, H. Sokol, H. Blottière, 2008, Proceedings of the National Academy of Sciences.

Bone marrow failure in Fanconi anemia is triggered by an exacerbated p53/p21 DNA damage response that impairs hematopoietic stem and progenitor cells.

J. Soulier, M. Cavazzana‐Calvo, A. D’Andrea, 2012, Cell stem cell.

Myelodysplasia and leukemia of Fanconi anemia are associated with a specific pattern of genomic abnormalities that includes cryptic RUNX1/AML1 lesions.

F. Sigaux, J. Soulier, A. Baruchel, 2011, Blood.

Metronidazole effects on microbiota and mucus layer thickness in the rat gut.

Nadia Vasquez, P. Pochart, A. Suau, 2010, FEMS microbiology ecology.

Biallelic truncating FANCM mutations cause early-onset cancer but not Fanconi anemia

J. Soulier, D. Bluteau, J. Surrallés, 2017, Genetics in Medicine.

Patchy distribution of mucosal lesions in ileal Crohn's disease is not linked to differences in the dominant mucosa‐associated bacteria: A study using fluorescence in situ hybridization and temporal temperature gradient gel electrophoresis

J. Doré, P. Lepage, S. Blum, 2007, Inflammatory bowel diseases.

Germline DDX41 mutations define a significant entity within adult MDS/AML patients.

J. Soulier, E. Clappier, H. Dombret, 2019, Blood.

e- Blood Myelodysplasia and leukemia of Fanconi anemia are associated with a speciﬁc pattern of genomic abnormalities that includes cryptic RUNX1/AML1 lesions

F. Sigaux, J. Soulier, A. Baruchel, 2011 .

Heterogeneous telomere defects in patients with severe forms of dyskeratosis congenita.

A. Fischer, J. Soulier, P. Revy, 2012, The Journal of allergy and clinical immunology.

Differential Effects of Bifidobacterium pseudolongum Strain Patronus and Metronidazole in the Rat Gut

Nadia Vasquez, P. Pochart, A. Suau, 2008, Applied and Environmental Microbiology.

A landscape of germ line mutations in a cohort of inherited bone marrow failure patients.

J. Soulier, E. Clappier, A. Baruchel, 2018, Blood.

Spontaneous abrogation of the G₂DNA damage checkpoint has clinical benefits but promotes leukemogenesis in Fanconi anemia patients.

J. Soulier, Q. Waisfisz, D. Stoppa-Lyonnet, 2011, The Journal of clinical investigation.

Primary Microcephaly, Impaired DNA Replication, and Genomic Instability Caused by Compound Heterozygous ATR Mutations

A. Fischer, J. Soulier, P. Revy, 2013, Human mutation.

Clonal hematopoiesis driven by chromosome 1q/MDM4 trisomy defines a canonical route toward leukemia in Fanconi anemia.

E. Gilson, F. Sigaux, J. Soulier, 2023, Cell stem cell.

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

J. Soulier, P. Revy, N. Jabado, 2017, Oncotarget.

Crypt abscess-associated microbiota in inflammatory bowel disease and acute self-limited colitis.

H. Sokol, P. Marteau, Nadia Vasquez, 2010, World journal of gastroenterology.

Clonal evolution in hereditary thrombocytosis with MPL T487A mutation

E. Clappier, R. Favier, Nadia Vasquez, 2022, Pediatric blood & cancer.

A clickable melphalan for monitoring DNA interstrand crosslink accumulation and detecting ICL repair defects in Fanconi anemia patient cells

J. Soulier, Nadia Vasquez, C. Lachaud, 2023, Nucleic acids research.