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Publications by F. Brenet
SRSF2-p95 Hotspot Mutation Is Highly Associated With Advanced Forms of Mastocytosis and Mutations in Epigenetic Regulator Genes
Haematologica
Hematology
Related publications
Advanced Systemic Mastocytosis: The Impact of KIT Mutations in Diagnosis, Treatment, and Progression
European Journal of Haematology
Medicine
Hematology
Growth Disrupting Mutations in Epigenetic Regulatory Molecules Are Associated With Abnormalities of Epigenetic Aging
Genome Research
Genetics
The p.Phe174Ser Mutation Is Associated With Mild Forms of Smith Lemli Opitz Syndrome
BMC Medical Genetics
Genetics
"Occult" Mastocytosis With Activating C-Kit Point Mutation Evolving Into Systemic Mastocytosis Associated With Plasma Cell Myeloma and Secondary Amyloidosis
Journal of Clinical Pathology
Medicine
Forensic Medicine
Pathology
SRSF2 Mutations in Myelodysplasia/Myeloproliferative Neoplasms
Biomarker Research
Biochemistry
Molecular Medicine
Clinical Biochemistry
SRSF2 and U2AF1 Mutations in Primary Myelofibrosis Are Associated With JAK2 and MPL but Not Calreticulin Mutation and May Independently Reoccur After Allogeneic Stem Cell Transplantation
Leukemia
Cancer Research
Oncology
Anesthesiology
Pain Medicine
Hematology
Activating and Dominant Inactivating C-Kit Catalytic Domain Mutations in Distinct Clinical Forms of Human Mastocytosis
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
ABCG5/G8 Gene Is Associated With Hypercholesterolemias Without Mutation in Candidate Genes and Noncholesterol Sterols
Journal of Clinical Lipidology
Internal Medicine
Nutrition
Cardiology
Endocrinology
Cardiovascular Medicine
Dietetics
Metabolism
Diabetes
Genetic and Epigenetic Mutations of Tumor Suppressive Genes in Sporadic Pituitary Adenoma
Molecular and Cellular Endocrinology
Biochemistry
Endocrinology
Molecular Biology
