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Publications by Dario De Cesare
Mutation Analysis of the RSK2 Gene in Coffin-Lowry Patients: Extensive Allelic Heterogeneity and a High Rate of De Novo Mutations
American Journal of Human Genetics
Genetics
Role of Distinct Mitogen-Activated Protein Kinase Pathways and Cooperation Between Ets-2, ATF-2, and Jun Family Members in Human Urokinase-Type Plasminogen Activator Gene Induction by Interleukin-1 and Tetradecanoyl Phorbol Acetate
Molecular and Cellular Biology
Cell Biology
Molecular Biology
Related publications
Unreported RSK2 Missense Mutation in Two Male Sibs With an Unusually Mild Form of Coffin-Lowry Syndrome
Journal of Medical Genetics
Genetics
Síndrome De Coffin-Lowry
Universitas Médica
X-Linked Coffin-Lowry Syndrome (CLS, MIM 303600, RPS6KA3 Gene, Protein Product Known Under Various Names: Pp90rsk2, RSK2, ISPK, MAPKAP1)
European Journal of Human Genetics
Genetics
Stimulus-Induced Drop Episodes in Coffin-Lowry Syndrome
Pediatrics
Child Health
Pediatrics
Perinatology
Extensive Natural Epigenetic Variation at a De Novo Originated Gene
PLoS Genetics
Evolution
Ecology
Genetics
Molecular Biology
Cancer Research
Systematics
Behavior
Clinical Features and Outcome of 6 New Patients Carrying De Novo KCNB1 Gene Mutations
Neurology: Genetics
Neurology
Genetics
Phenotypic Heterogeneity in British Patients With a Founder Mutation in the FHL1 Gene
European Journal of Human Genetics
Genetics
De Novo Mutations in the Gene Encoding the Synaptic Scaffolding proteinSHANK3in Patients Ascertained for Schizophrenia
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Enhanced Accumulation of Hyaluronate in the Culture of Skin Fibroblasts From Two Patients With Coffin-Lowry Syndrome.
Tohoku Journal of Experimental Medicine
Biochemistry
Medicine
Genetics
Molecular Biology
