about
A marked effect of electroconvulsive stimulation on behavioral aberration of mice with neuron-specific mitochondrial DNA defectsExome sequencing identifies a novel missense variant in RRM2B associated with autosomal recessive progressive external ophthalmoplegiaAbnormal behavior in a chromosome-engineered mouse model for human 15q11-13 duplication seen in autismGuideline for treatment of bipolar disorder by the Japanese Society of Mood Disorders, 2012Neurobiological basis of bipolar disorder: Mitochondrial dysfunction hypothesis and beyondRNA editing of serotonin 2C receptor in human postmortem brains of major mental disordersAltered RNA editing of serotonin 2C receptor in a rat model of depressionA family-based association study and gene expression analyses of netrin-G1 and -G2 genes in schizophreniaMeasurement of brain phosphoinositide metabolism in bipolar patients using in vivo 31P-MRSGenetic variation of melatonin productivity in laboratory mice under domesticationMicroendophenotypes of psychiatric disorders: phenotypes of psychiatric disorders at the level of molecular dynamics, synapses, neurons, and neural circuitsA role of ADAR2 and RNA editing of glutamate receptors in mood disorders and schizophreniaNeurons show distinctive DNA methylation profile and higher interindividual variations compared with non-neurons.Transport Response is a filial-specific behavioral response to maternal carrying in C57BL/6 mice.The International Society for Bipolar Disorders (ISBD) task force report on antidepressant use in bipolar disordersBiological predictors of lithium response in bipolar disorder.Replication and cross-phenotype study based upon schizophrenia GWASs data in the Japanese population: support for association of MHC region with psychosis.Mitochondrial dysfunction in bipolar disorder: from 31P-magnetic resonance spectroscopic findings to their molecular mechanisms.Mitochondrial dysfunction as the molecular basis of bipolar disorder: therapeutic implications.Identification of mitochondrial DNA polymorphisms that alter mitochondrial matrix pH and intracellular calcium dynamicsDetection of chromosomal structural alterations in single cells by SNP arrays: a systematic survey of amplification bias and optimized workflow.Valproate, a mood stabilizer, induces WFS1 expression and modulates its interaction with ER stress protein GRP94Voxel-based analyses of gray/white matter volume and diffusion tensor data in major depression.Exome sequencing for bipolar disorder points to roles of de novo loss-of-function and protein-altering mutations.The International Consortium on Lithium Genetics (ConLiGen): an initiative by the NIMH and IGSLI to study the genetic basis of response to lithium treatment.Molecular genetics of bipolar disorder.Nutritional biochemistry: A new redox-cofactor vitamin for mammals.Association of mitochondrial complex I subunit gene NDUFV2 at 18p11 with bipolar disorder.Association of mitochondrial complex I subunit gene NDUFV2 at 18p11 with bipolar disorder in Japanese and the National Institute of Mental Health pedigrees.Mitochondrial DNA 3243A>G mutation and increased expression of LARS2 gene in the brains of patients with bipolar disorder and schizophrenia.Genome-wide DNA methylation and gene expression analyses of monozygotic twins discordant for intelligence levels.Association of mitochondrial complex I subunit gene NDUFV2 at 18p11 with schizophrenia in the Japanese population.Proteomic analysis of lymphoblastoid cells derived from monozygotic twins discordant for bipolar disorder: a preliminary study.A promoter haplotype of the inositol monophosphatase 2 gene (IMPA2) at 18p11.2 confers a possible risk for bipolar disorder by enhancing transcription.A population-specific uncommon variant in GRIN3A associated with schizophrenia.Heterozygous Polg mutation causes motor dysfunction due to mtDNA deletions.Assessment of Response to Lithium Maintenance Treatment in Bipolar Disorder: A Consortium on Lithium Genetics (ConLiGen) ReportGenetic variants on 3q21 and in the Sp8 transcription factor gene (SP8) as susceptibility loci for psychotic disorders: a genetic association study.Identification of Rare, Single-Nucleotide Mutations in NDE1 and Their Contributions to Schizophrenia Susceptibility.Hypermethylation of serotonin transporter gene in bipolar disorder detected by epigenome analysis of discordant monozygotic twins.
P50
Q21090096-829565AC-8BCC-4C6B-BD0E-1E39A7DBFEE6Q21184016-DE9E771D-65F7-4D71-8C33-A4466E81542FQ24599984-DF796D1D-9285-470F-AEEA-DE4EE291DB8BQ26824955-744DAB08-4E80-482A-B497-7A7D5A243A35Q28079086-5AC5BF40-4100-42FE-93F0-EFFBC0DCA813Q28186174-C7602947-60CC-4A86-BFD5-F5A60EC9F612Q28260669-D93F26E0-E5E8-4E7B-B317-0ADF980E0899Q28306895-FAD9F223-E5AF-484F-87DB-63FC97A8C5EBQ28321813-BD46482F-1512-4CB4-8800-71F7CEA70509Q28588823-F6F2904C-54F1-4B79-A678-EA00617D7482Q30409099-FEF71153-04EB-4499-A881-A99731DFF43AQ30444005-2515105A-5DF3-4DA8-B431-5616FD765E96Q30473263-882E818D-CCE0-4DF3-927F-4A244C79C14EQ30543417-07189911-E89B-4184-8F9B-C84ACAD8A7A4Q30583384-C816B16A-B187-4040-9E5A-E63423BC629AQ30794691-50B825C7-9B06-4385-AADA-68C1D46AA5F0Q30828357-B7825011-1637-47EA-AA7C-85D9C2650011Q30985980-C6686014-EB3A-419C-9854-70EAB4E1B632Q31088436-CD575D2B-A412-468E-9F9D-7F482E4B1C00Q33253241-EBC23621-0232-4D82-9BBE-190227D5D2A1Q33309953-B6EB25E7-58C5-4FDD-9BAD-430BFEFE81A8Q33397723-34713501-53FA-420D-88DA-DDA4607705E7Q33517201-B3A6CBD1-3106-45C0-974D-C34F3067999BQ33629413-67C36B1E-573F-4FF6-A7C0-FC5DC351405FQ33929926-20D50D8E-7920-4388-9DD7-2854ED568688Q33948623-21ECB23C-69C7-4CD3-BFA5-A1DB88785340Q33965649-E61B9F04-EE77-44B3-828E-7E9BD760852CQ34207223-5521035D-1C77-48BC-A7C0-AC16973338A1Q34353407-9A080CDE-69CD-4D07-AA60-F9C09AE10328Q34398757-3ECDDA56-B354-4235-9B24-E2BA845C5E29Q34451972-45A07B1D-C2E3-48A4-996E-DE977B274A8AQ34498492-FD64125D-CE31-49A8-AF1C-F7C95A3B19E0Q34585836-AE261A70-7FE1-4101-BB58-0BC8A42CACE0Q34605987-7F0C99A0-2D62-4C54-91E7-52C60A459B79Q34646384-B451ABC1-74F6-4436-B421-E957B45AB655Q34692062-15B9A4DE-36BA-4056-AC3E-7F9A4D89D664Q34804607-3D7DD8B6-0EE0-40F7-9EF0-3C04CF6A3E7DQ34963267-06F85AC9-0938-4233-9FFC-C9DBA9884976Q35369750-2B3B1241-9FE9-47AB-B95A-02721D6B4998Q35844206-E04AAAF2-DDFE-4F06-8B12-6F1BFC477E9E
P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Tadafumi Kato
@ast
Tadafumi Kato
@de
Tadafumi Kato
@en
Tadafumi Kato
@es
Tadafumi Kato
@nl
Tadafumi Kato
@sl
type
label
Tadafumi Kato
@ast
Tadafumi Kato
@de
Tadafumi Kato
@en
Tadafumi Kato
@es
Tadafumi Kato
@nl
Tadafumi Kato
@sl
prefLabel
Tadafumi Kato
@ast
Tadafumi Kato
@de
Tadafumi Kato
@en
Tadafumi Kato
@es
Tadafumi Kato
@nl
Tadafumi Kato
@sl
P1053
J-3583-2014
P106
P21
P31
P3829
P496
0000-0001-7856-3952
P569
2000-01-01T00:00:00Z