Yoshino et al., 2017 - Google Patents
DNA methylation changes in intron 1 of Triggering receptor expressed on myeloid cell 2 in Japanese schizophrenia subjectsYoshino et al., 2017
View HTML- Document ID
- 7436457563282441494
- Author
- Yoshino Y
- Ozaki Y
- Yamazaki K
- Sao T
- Mori Y
- Ochi S
- Iga J
- Ueno S
- Publication year
- Publication venue
- Frontiers in Neuroscience
External Links
Snippet
A hypothesis for schizophrenia (SCZ) called the “microglia hypothesis” has been suggested. In SCZ, expression of triggering receptor expressed on myeloid cell 2 (TREM2) mRNA is higher in leukocytes than in healthy individuals. Here, the methylation rates of four CpG sites …
- 201000000980 schizophrenia 0 title abstract description 72
Classifications
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES OR MICRO-ORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or micro-organisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or micro-organisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
- C12Q1/6876—Hybridisation probes
- C12Q1/6883—Hybridisation probes for diseases caused by alterations of genetic material
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by the preceding groups
- G01N33/48—Investigating or analysing materials by specific methods not covered by the preceding groups biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/68—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving proteins, peptides or amino acids
- G01N33/6893—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving proteins, peptides or amino acids related to diseases not provided for elsewhere
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by the preceding groups
- G01N33/48—Investigating or analysing materials by specific methods not covered by the preceding groups biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/5005—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES OR MICRO-ORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q2600/00—Oligonucleotides characterized by their use
- C12Q2600/158—Expression markers
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES OR MICRO-ORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q2600/00—Oligonucleotides characterized by their use
- C12Q2600/156—Polymorphic or mutational markers
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Gauthier et al. | De novo mutations in the gene encoding the synaptic scaffolding protein SHANK3 in patients ascertained for schizophrenia | |
Vona et al. | Genetics of tinnitus: still in its infancy | |
Walton et al. | Correspondence of DNA methylation between blood and brain tissue and its application to schizophrenia research | |
Labonté et al. | Genome-wide epigenetic regulation by early-life trauma | |
Blumen et al. | A rare recessive distal hereditary motor neuropathy with HSJ1 chaperone mutation | |
Hirata et al. | Study of the Catechol‐O‐Methyltransferase (COMT) gene with high aggression in children | |
Daoud et al. | Resequencing of 29 candidate genes in patients with familial and sporadic amyotrophic lateral sclerosis | |
Gingnell et al. | Neuroticism-related personality traits are related to symptom severity in patients with premenstrual dysphoric disorder and to the serotonin transporter gene-linked polymorphism 5-HTTPLPR | |
Yoshino et al. | DNA methylation changes in intron 1 of Triggering receptor expressed on myeloid cell 2 in Japanese schizophrenia subjects | |
Lin et al. | Genetic biomarkers on age-related cognitive decline | |
Gao et al. | DNA methylation and gene expression of matrix metalloproteinase 9 gene in deficit and non-deficit schizophrenia | |
Singh et al. | Differential expression of matrix metalloproteinase-9 gene in wounds of type 2 diabetes mellitus cases with susceptible-1562C> T genotypes and wound severity | |
Lepeta et al. | A normal genetic variation modulates synaptic MMP‐9 protein levels and the severity of schizophrenia symptoms | |
Stefanis et al. | Variation in psychosis gene ZNF804A is associated with a refined schizotypy phenotype but not neurocognitive performance in a large young male population | |
Mise et al. | TOMM40 and APOE gene expression and cognitive decline in Japanese Alzheimer’s disease subjects | |
Choe et al. | Serotonergic genes (5-HTT and HTR1A) and separation life events: gene-by-environment interaction for panic disorder | |
Guerini et al. | Vitamin D receptor polymorphisms associated with autism spectrum disorder | |
Corrado et al. | The length of SNCA Rep1 microsatellite may influence cognitive evolution in Parkinson’s disease | |
de Nijs et al. | DNA methyltransferase isoforms expression in the temporal lobe of epilepsy patients with a history of febrile seizures | |
França Jr et al. | Normal ATXN3 allele but not CHIP polymorphisms modulates age at onset in Machado–Joseph disease | |
Matsuno et al. | A naturally occurring null variant of the NMDA type glutamate receptor NR3B subunit is a risk factor of schizophrenia | |
Ludwig et al. | Influence of CRHR1 polymorphisms and childhood abuse on suicide attempts in affective disorders: a GxE approach | |
Alfimova et al. | Methylation of the reelin gene promoter in peripheral blood and its relationship with the cognitive function of schizophrenia patients | |
Liu et al. | Association study of candidate gene polymorphisms with amnestic mild cognitive impairment in a Chinese population | |
Ershova et al. | Copy number variation of satellite III (1q12) in patients with schizophrenia |