Keywords: AC; anterior cingulum; ACE; adverse childhood experiences; ACG; anterior cingulate gyrus; ALIC; anterior limb of internal capsule; ANK3; ankyrin 3; BD; bipolar disorder; BDNF; brain-derived neurotrophic factor; BOLD; blood oxygen level dependent; CACNA1C;
مقالات ISI (ترجمه نشده)
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Keywords: Fetal hydrops; Fetal bradychardia; Atrioventricular block; Long QT; Syndactyly; Amitriptyline; CACNA1C
Keywords: Bipolar disorder; Schizophrenia; MRI; Genetics; CACNA1C; ANK3;
Replication of GWAS identified miR-137 and its target gene polymorphisms in Schizophrenia of South Indian population and meta-analysis with Psychiatric Genomics Consortium
Keywords: Replication of GWAS; Schizophrenia; Meta-analysis; mir137 and its target; CACNA1C; rs4765905; PRS;
YY1-induced upregulation of lncRNA KCNQ1OT1 regulates angiotensin II-induced atrial fibrillation by modulating miR-384b/CACNA1C axis
Keywords: KCNQ1OT1; miR-384; CACNA1C; YY1; Atrial fibrillation;
Overexpression of miR-135b attenuates pathological cardiac hypertrophy by targeting CACNA1C
Keywords: microRNA-135b; Cardiac hypertrophy; CACNA1C; L-type Ca2+ channels;
Association of CACNA1C with bipolar disorder among the Pakistani population
Keywords: BD; bipolar disorder; SNPs; single nucleotide polymorphisms; ORs; odds ratios; GWAS; genome-wide association studies; NHGRI; National Human Genome Research Institute; ANK3; Ankyrin G; CACNA1C; L-type voltage-dependent calcium channel; PCR; polymerase chai
Interactive effects of early life stress and CACNA1C genotype on cortisol awakening response
Keywords: CACNA1C; Calcium channel; Early life stress; Childhood trauma; Cortisol awakening response;
Mn2+ dynamics in manganese-enhanced MRI (MEMRI): Cav1.2 channel-mediated uptake and preferential accumulation in projection terminals
Keywords: Manganese enhanced MRI; Functional imaging; Connectomics; Activity-dependent; CACNA1C; Calcium channels;
Regulation of cardiac CACNB2 by microRNA-499: Potential role in atrial fibrillation
Keywords: AF; atrial fibrillation; Ago; Argonaute; GAPDH; glyceraldehyde-3-phosphate dehydrogenase; LTCC; L-type calcium channel; miR-499; microRNA-499; miRISC; microRNA-inducing silencing complex; CACNA1C; voltage-dependent calcium channel α-1C subunit; CACNB2; v
Novel long QT syndrome-associated missense mutation, L762F, in CACNA1C-encoded L-type calcium channel imparts a slower inactivation tau and increased sustained and window current
Keywords: CACNA1C; the CACNA1C-encoded α1c α-subunit of the L-type calcium channel; COTS; cardiac-only Timothy syndrome; LQTS; long QT syndrome; LTCC; L-type calcium channel; SCD; sudden cardiac death; SIDS; sudden infant death syndrome; TS; Timothy syndrome; CAC
Association of CACNA1C and SYNE1 in offspring of patients with psychiatric disorders
Keywords: Schizophrenia; Bipolar disorder; Offspring; CACNA1C; SYNE1; Polymorphism;
Meta-analysis of data from the Psychiatric Genomics Consortium and additional samples supports association of CACNA1C with risk for schizophrenia
Keywords: Schizophrenia; Genome-wide association study; PGC; Follow-up study; Meta-analysis; CACNA1C;
Association study between polymorphisms in the CACNA1A, CACNA1C, and CACNA1H genes and drug-resistant epilepsy in the Chinese Han population
Keywords: Drug-resistant epilepsy; Single nucleotide polymorphism; CACNA1A; CACNA1C; CACNA1H; Association study
CACNA1C rs1006737 genotype and bipolar disorder: Focus on intermediate phenotypes and cardiovascular comorbidity
Keywords: CACNA1C; Bipolar disorder; Magnetic resonance imaging; Cognition; Calcium channel blockers;
Genotype–phenotype relationship in a child with 2.3 Mb de novo interstitial 12p13.33-p13.32 deletion
Keywords: 12p13.33 Deletion; CACNA1C; Speech delay; Array-CGH; Interstitial deletion; Microcephaly
Further evidence for genetic association of CACNA1C and schizophrenia: New risk loci in a Han Chinese population and a meta-analysis
Keywords: CACNA1C; rs1006737; Schizophrenia; Genetic association; Case-control study; Meta-analysis;
The impact of a CACNA1C gene polymorphism on learning and hippocampal formation in healthy individuals: A diffusion tensor imaging study
Keywords: CACNA1C; Diffusion tensor imaging; White matter; Hippocampal formation; Learning;
Replication of brain function effects of a genome-wide supported psychiatric risk variant in the CACNA1C gene and new multi-locus effects
Keywords: fMRI; Imaging genetics; CACNA1C; Hippocampus; Perigenual anterior cingulate; Dorsolateral prefrontal cortex;
Genetic variation in CACNA1C affects neural processing in major depression
Keywords: Major depression; CACNA1C; Verbal fluency; fMRI; Left inferior frontal gyrus; Cerebellum;
Hippocampal and Frontolimbic Function as Intermediate Phenotype for Psychosis: Evidence from Healthy Relatives and a Common Risk Variant in CACNA1C
Keywords: CACNA1C; episodic memory; functional magnetic resonance imaging; hippocampus; imaging genetics; perigenual cingulate cortex
Association of genetic variation in CACNA1C with bipolar disorder in Han Chinese
Keywords: Major depressive disorder; Bipolar disorder; CACNA1C; Polymorphism; Age at onset;
Lessons from the gene expression pattern of the rat zona glomerulosa
Keywords: zG; zona glomerulosa; zF; zona fasciculata; zR; zona reticularis; Cyp11b1; steroid 11β-hydroxylase; Cyp11b2; aldosterone synthase; TGF-β; transforming growth factor β; Gpc3; glypican 3; Kcnn2; potassium intermediate/small conductance calcium-activated
Analysis of association between common SNPs in ErbB4 and bipolar affective disorder, major depressive disorder and schizophrenia in the Han Chinese population
Keywords: NRG1; Neuregulin-1; ErbB4; v-erb-a erythroblastic leukemia viral oncogene homolog 4; SNPs; single nucleotide polymorphisms; CHB; Han Chinese in Beijing, China; JPT; Japanese in Tokyo, Japan; CEU; Utah residents with ancestry from northern and western Euro
ANK3 and CACNA1C – Missing genetic link for bipolar disorder and major depressive disorder in two German case-control samples
Keywords: Depression; Genetics; Bipolar disorder; CACNA1C; ANK3
The impact of the CACNA1C risk allele on limbic structures and facial emotions recognition in bipolar disorder subjects and healthy controls
Keywords: Bipolar disorder; Calcium channel; CACNA1C; Social cognition; Facial emotions recognition
Calcium regulates caveolin-1 expression at the transcriptional level
Keywords: Cacna1; L-type calcium channel alpha-1 subunit (c, etc.); HBSS; Hank's buffered salt solution; NFAT; nuclear factor of activated T-cells; PI; propidium iodide; qPCR; quantitative real-time PCR; RT-PCR; reverse transcriptase-polymerase chain reaction; St
Lack of association between translin-associated factor X gene (TSNAX) and methamphetamine dependence in the Japanese population
Keywords: GWAS; whole genome association study; ZNF804A; Zinc finger binding protein 804A; CACNA1C; calcium channel, voltage-dependent, L type, alpha 1C subunits; BP; bipolar disorder; MDD; major depressive disorder; TSNAX; translin-associated factor X gene; DISC1;
Effect of CACNA1C rs1006737 on neural correlates of verbal fluency in healthy individuals
Keywords: CACNA1C; fMRI; Verbal fluency; Inferior frontal gyrus; Bipolar disorder;
Mood Disorder Susceptibility Gene CACNA1C Modifies Mood-Related Behaviors in Mice and Interacts with Sex to Influence Behavior in Mice and Diagnosis in Humans
Keywords: Animal model; bipolar disorder; CACNA1C; CaV1.2; gender; major depression; sex differences
2.3 Mb terminal deletion in 12p13.33 associated with oculoauriculovertebral spectrum and evaluation of WNT5B as a candidate gene
Keywords: Goldenhar syndrome; Oculoauriculovertebral spectrum; 12p13.33 deletion; WNT5B; CACNA1C
An intronic mutation leading to incomplete skipping of exon-2 in KCNQ1 rescues hearing in Jervell and Lange-Nielsen syndrome
Keywords: Long QT syndrome; KCNQ1; Intronic mutation; Hearing rescue; SCN5A; sodium channel, voltage-gated, type V, alpha subunit; KCNH2; potassium voltage-gated channel, subfamily H (eag-related), member 2; KCNQ1; potassium voltage-gated channel, KQT-like subfamil
Molecular aspects of the congenital and acquired Long QT Syndrome: Clinical implications
Keywords: Ion channel; Long QT Syndrome; Arrhythmia; Sudden cardiac death; hERG; KCNQ1; SCN5A; KCNE1; KCNE2; CACNA1c; KCNJ2; Genotype; Phenotype; Congenital; Acquired; Torsade de pointes
Syndactyly and long QT syndrome (CaV1.2 missense mutation G406R) is associated with hypertrophic cardiomyopathy
Keywords: Long QT syndrome; Infants; Sudden death; Hypertrophic cardiomyopathy; CACNA1C; Implantable cardioverter-defibrillator therapy;