Pages that link to "Q34325839"

The following pages link to Early myoclonic encephalopathy caused by a disruption of the neuregulin-1 receptor ErbB4 (Q34325839):

Displaying 22 items.

• Specific regulation of NRG1 isoform expression by neuronal activity (Q24618674) (← links)
• Recent developments in the genetics of childhood epileptic encephalopathies: impact in clinical practice (Q26777746) (← links)
• Fusion of large-scale genomic knowledge and frequency data computationally prioritizes variants in epilepsy (Q30000781) (← links)
• Association study of neuregulin-1 gene polymorphisms in a North Indian schizophrenia sample (Q33692336) (← links)
• Mutations in DOCK7 in individuals with epileptic encephalopathy and cortical blindness (Q34000883) (← links)
• A de novo missense mutation of GABRB2 causes early myoclonic encephalopathy (Q34543571) (← links)
• Copy number variants and infantile spasms: evidence for abnormalities in ventral forebrain development and pathways of synaptic function (Q35591685) (← links)
• Neurological dysfunctions associated with altered BACE1-dependent Neuregulin-1 signaling (Q36804007) (← links)
• Targeted sequencing of 351 candidate genes for epileptic encephalopathy in a large cohort of patients. (Q37257128) (← links)
• The relationship between genes affecting the development of epilepsy and approaches to epilepsy therapy (Q38187700) (← links)
• Considering specific clinical features as evidence of pathogenic copy number variants (Q38188895) (← links)
• Clinical management of epileptic encephalopathies of childhood and infancy (Q38213837) (← links)
• Neuregulin-ERBB signaling in the nervous system and neuropsychiatric diseases (Q38225912) (← links)
• ErbB4 modulates tubular cell polarity and lumen diameter during kidney development (Q40777975) (← links)
• Calpain-Dependent ErbB4 Cleavage Is Involved in Brain Ischemia-Induced Neuronal Death (Q40817583) (← links)
• Contribution of NRG1 Gene Polymorphisms in Temporal Lobe Epilepsy (Q40839066) (← links)
• Molecular cytogenetic characterisation of a mosaic add(12)(p13.3) with an inv dup(3)(q26.31 --> qter) detected in an autistic boy. (Q42143538) (← links)
• Neuregulin 1 represses limbic epileptogenesis through ErbB4 in parvalbumin-expressing interneurons (Q48204966) (← links)
• A new single gene deletion on 2q34: ERBB4 is associated with intellectual disability. (Q54261485) (← links)
• Neuregulin 1-induced AKT and ERK phosphorylation in patients with fragile X syndrome (FXS) and intellectual disability associated with obstetric complications. (Q54375474) (← links)
• Two-stage genome-wide association study identifies variants in CAMSAP1L1 as susceptibility loci for epilepsy in Chinese (Q57233954) (← links)
• New avenues in molecular genetics for the diagnosis and application of therapeutics to the epilepsies (Q92542992) (← links)