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Publications by Bruna P. Brylawski
Mapping of an Origin of DNA Replication in the Promoter of Fragile X Gene FMR1
Experimental and Molecular Pathology
Forensic Medicine
Pathology
Clinical Biochemistry
Molecular Biology
Related publications
Reevaluation of FMR1 Hypermethylation Timing in Fragile X Syndrome
Frontiers in Molecular Neuroscience
Molecular Neuroscience
Molecular Biology
Cellular
Specific Effect of the Fragile-X Mental Retardation-1 Gene (FMR1) on White Matter Microstructure
British Journal of Psychiatry
Medicine
Psychiatry
Mental Health
Fine Mapping of a Replication Origin of Human DNA.
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
AGG Interruptions Within the Maternal FMR1 Gene Reduce the Risk of Offspring With Fragile X Syndrome
Genetics in Medicine
Medicine
Genetics
Establishment of Reporter Lines for Detecting Fragile X Mental Retardation (FMR1) Gene Reactivation in Human Neural Cells
Stem Cells
Medicine
Molecular Medicine
Developmental Biology
Cell Biology
Fine Mapping of Secondary Structures of Fd Phage DNA in the Region of the Replication Origin
Nucleic Acids Research
Genetics
Static and Dynamic Postural Control Deficits in Aging Fragile X Mental Retardation 1 (FMR1) Gene Premutation Carriers
Journal of Neurodevelopmental Disorders
Pediatrics
Cognitive Neuroscience
Perinatology
Neurology
Forensic Medicine
Child Health
Pathology
Binding of the Herpes Simplex Virus Type 1 UL9 Gene Product to an Origin of Viral DNA Replication
Nucleic Acids Research
Genetics
Antipurinergic Therapy Corrects the Autism-Like Features in the Fragile X (Fmr1 Knockout) Mouse Model
Molecular Autism
Psychiatry
Mental Health
Developmental Neuroscience
Developmental Biology
Molecular Biology
