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Publications by Nasséra Abermil
Somatic NF1 Inactivation Is a Frequent Event in Sporadic Pheochromocytoma
Human Molecular Genetics
Medicine
Genetics
Molecular Biology
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Somatic Inactivation of Nf1 in Hematopoietic Cells Results in a Progressive Myeloproliferative Disorder
Blood
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Immunology
Cell Biology
Hematology
Deletion of SPRY4 Is a Frequent Event in Secondary Acute Myeloid Leukemia
Annals of Hematology
Medicine
Hematology
LKB1 Somatic Mutations in Sporadic Tumors
American Journal of Pathology
Forensic Medicine
Pathology
A Search for Evidence of Somatic Mutations in the NF1 Gene
Journal of Medical Genetics
Genetics
Amyloid Accumulation Is a Late Event in Sporadic Alzheimer’s Disease-Like Pathology in Nontransgenic Rats
Oncotarget
Oncology
Somatic SMARCB1 Mutation in Sporadic Multiple Meningiomas: Case Report
Frontiers in Neurology
Neurology
Proteasomal and Genetic Inactivation of the NF1 Tumor Suppressor in Gliomagenesis
Cancer Cell
Cancer Research
Oncology
Cell Biology
Frequent EPAS1/HIF2 Exons 9 and 12 Mutations in Non-Familial Pheochromocytoma
Endocrine-Related Cancer
Cancer Research
Endocrinology
Oncology
Metabolism
Diabetes
Somatic Recombination Underlies Frequent Revertant Mosaicism in Loricrin Keratoderma
Life Science Alliance
Plant Science
Ecology
Genetics
Molecular Biology
Biochemistry
Mutagenesis
Health
Toxicology