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Publications by Gabrielle de Courten-Myers

Region-Specific Astrogliosis in Brains of Mice Heterozygous for Mutations in the Neurofibromatosis Type 1 (Nf1) Tumor Suppressor

Developmental Biology

Molecular Biology

English

Related publications

Neurofibromatosis Type 1 (NF1)

Atlas of Genetics and Cytogenetics in Oncology and Haematology

Cancer Research

English

Molecular Genetics of Neurofibromatosis Type 1 (NF1).

Journal of Medical Genetics

English

Clinical and Molecular Characterization of Patients With Heterozygous Mutations in Wilms Tumor Suppressor Gene 1

Clinical Journal of the American Society of Nephrology

Transplantation

Intensive Care Medicine

English

Differential MSH2 Promoter Methylation in Blood Cells of Neurofibromatosis Type 1 (NF1) Patients

European Journal of Human Genetics

English

NF1 Gene Mutations Are the Major Molecular Event in Neurofibromatosis-Noonan Syndrome

Journal of Neurology & Stroke

English

Autism Spectrum Disorder in an Unselected Cohort of Children With Neurofibromatosis Type 1 (NF1)

Journal of Autism and Developmental Disorders

Educational Psychology

English

Neurofibromatosis Type 1 (NF1) With an Unusually Severe Phenotype Due to Digeny for NF1 and Ryanodine Receptor 1 Associated Myopathy

European Journal of Pediatrics

English

Proteasomal and Genetic Inactivation of the NF1 Tumor Suppressor in Gliomagenesis

Cancer Research

English

Molecular Characterization of NF1 and Neurofibromatosis Type 1 Genotype-Phenotype Correlations in a Chinese Population

Scientific Reports

Multidisciplinary

English