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The impact of the CACNA1C risk allele on limbic structures and facial emotions recognition in bipolar disorder subjects and healthy controls
(ELSEVIER SCIENCE BVAMSTERDAM, 2012-12-01)
Introduction: Impairments in facial emotion recognition (PER) have been reported in bipolar disorder (BD) during all mood states. FER has been the focus of functional magnetic resonance imaging studies evaluating differential ...
The Drosophila ortholog of the schizophrenia-associated CACNA1A and CACNA1B voltage-gated calcium channels regulate memory, sleep and circadian rhythms
(Academic Press Inc., 2021)
© 2021 The AuthorsSchizophrenia exhibits up to 80% heritability. A number of genome wide association studies (GWAS) have repeatedly shown common variants in voltage-gated calcium (Cav) channel genes CACNA1C, CACNA1I and ...
Canalopatía De Calcio CACNA1E: Nueva Encefalopatía Epiléptica En Un Paciente Pediátrico
(Sociedad Médica Ecuatoriana de Neurología, 2022)
Analysing an allelic series of rare missense variants of 1 CACNA1I in a Swedish schizophrenia cohort
(2021)
CACNA1I is implicated in the susceptibility to schizophrenia by large-scale genetic association studies of single nucleotide polymorphisms. However, the channelopathy of CACNA1I in schizophrenia is unknown. CACNA1I encodes ...
Analysing an allelic series of rare missense variants of CACNA1I in a Swedish schizophrenia cohort
(2021)
CACNA1I is implicated in the susceptibility to schizophrenia by large-scale genetic association studies of single nucleotide polymorphisms. However, the channelopathy of CACNA1I in schizophrenia is unknown. CACNA1I encodes ...
Distribution of the CAG Triplet Repeat in ATXN1, ATXN3, and CACNA1A Loci in Peruvian Population
(Springer, 2020)
Spinocerebellar ataxia subtypes 1, 3, and 6 (SCA1, MJD/SCA3, and SCA6) are among the most prevalent autosomal dominant cerebellar ataxias worldwide, but their relative frequencies in Peru are low. Frequency of large normal ...
Novel CACNA1S mutation causes autosomal dominant hypokalemic periodic paralysis in a South American family
Hypokalaemic periodic paralysis (HypoPP) is an autosomal dominant disorder, which is characterized by periodic attacks of muscle weakness associated with a decrease in the serum potassium level. A major disease-causing ...
A genética comportamental do transtorno bipolar
(UniCEUB, 2021)