JPWO2021177447A5 - - Google Patents

Download PDF

Info

Publication number
JPWO2021177447A5
JPWO2021177447A5 JP2022504476A JP2022504476A JPWO2021177447A5 JP WO2021177447 A5 JPWO2021177447 A5 JP WO2021177447A5 JP 2022504476 A JP2022504476 A JP 2022504476A JP 2022504476 A JP2022504476 A JP 2022504476A JP WO2021177447 A5 JPWO2021177447 A5 JP WO2021177447A5
Authority
JP
Japan
Prior art keywords
determination
risk
absence
degree
impairment
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP2022504476A
Other languages
English (en)
Japanese (ja)
Other versions
JPWO2021177447A1 (de
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/JP2021/008722 external-priority patent/WO2021177447A1/ja
Publication of JPWO2021177447A1 publication Critical patent/JPWO2021177447A1/ja
Publication of JPWO2021177447A5 publication Critical patent/JPWO2021177447A5/ja
Pending legal-status Critical Current

Links

JP2022504476A 2020-03-06 2021-03-05 Pending JPWO2021177447A1 (de)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2020038991 2020-03-06
PCT/JP2021/008722 WO2021177447A1 (ja) 2020-03-06 2021-03-05 認知症又は脳機能の判定のためのキット及び方法

Publications (2)

Publication Number Publication Date
JPWO2021177447A1 JPWO2021177447A1 (de) 2021-09-10
JPWO2021177447A5 true JPWO2021177447A5 (de) 2022-11-04

Family

ID=77614329

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2022504476A Pending JPWO2021177447A1 (de) 2020-03-06 2021-03-05

Country Status (2)

Country Link
JP (1) JPWO2021177447A1 (de)
WO (1) WO2021177447A1 (de)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2024085246A1 (ja) * 2022-10-21 2024-04-25 株式会社カネカ 認知症の罹患の有無の判定のためのキット及び方法

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1303537B1 (de) * 2000-07-25 2006-09-27 The Sir Mortimer B. Davis-Jewish General Hospital Ho-1 suppressor als diagnostischer und prognostischer test für demenz-krankheiten
FI20075320A0 (fi) * 2007-05-07 2007-05-07 Panu Jaakkola Uusia käyttökelpoisia inhibiittoreita

Similar Documents

Publication Publication Date Title
Dos Santos et al. miRNA-based signatures in cerebrospinal fluid as potential diagnostic tools for early stage Parkinson’s disease
Kovarik et al. Measuring enzyme activity in single cells
Galimberti et al. Circulating miRNAs as potential biomarkers in Alzheimer's disease
Leidinger et al. A blood based 12-miRNA signature of Alzheimer disease patients
Piehl et al. Cerebrospinal fluid immune dysregulation during healthy brain aging and cognitive impairment
EP2293069A3 (de) Verfahren und Zusammensetzungen zum Nachweis von zervikalen Erkrankungen
EP2893039B1 (de) Marker und verfahren zum nachweis einer posttraumatischen belastungsstörung
CN102869791A (zh) 用于脆性x染色体综合征(fxs)治疗的预测标记
Zischka et al. Differential Analysis of Saccharomyces cerevisiae Mitochondria by Free Flow Electrophoresis* S
CN102762986A (zh) 阿尔茨海默病的诊断方法
JPWO2021177447A5 (de)
Nishitani et al. Cross-tissue correlations of genome-wide DNA methylation in Japanese live human brain and blood, saliva, and buccal epithelial tissues
Cuevas-González et al. Expression of microRNAs in periodontal disease: a systematic review
Qin et al. Exome sequencing revealed PDE11A as a novel candidate gene for early-onset Alzheimer’s disease
Kamath et al. A molecular census of midbrain dopaminergic neurons in Parkinson’s disease
Yoshioka et al. Fluorescence laser microdissection reveals a distinct pattern of gene activation in the mouse hippocampal region
NO20074882L (no) En fremgangsmate og kit for bestemmelse av tymidin kinaseaktivitet og deres anvendelse
CN104087671A (zh) 一种用于检测人21号染色体数目的试剂盒
Alinaghi et al. Expression analysis and genotyping of dgkz: a gwas-derived risk gene for schizophrenia
Gootjes et al. Novel mutations in the PEX12 gene of patients with a peroxisome biogenesis disorder
Wiles et al. Activated CD90/Thy-1 fibroblasts co-express the Δ133p53β isoform and are associated with highly inflamed rheumatoid arthritis
KR101947141B1 (ko) 산성 스핑고미엘리나제를 이용한 근위축성측삭경화증 진단용 조성물과 진단 마커 검출 방법
JP6715526B2 (ja) ストレスバイオマーカー
Kadena et al. Amyotrophic lateral sclerosis: current status in diagnostic biomarkers
US11497817B2 (en) Senile dementia treatment formulation and application thereof