ID

45535

Description

Principal Investigator: Kendall Van Keuren-Jensen, PhD, The Translational Genomics Research Institute (TGen), Phoenix, AZ, USA MeSH: Alzheimer Disease,Parkinson Disease https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000727 We profiled the miRNA contents from cerebrospinal fluid and serum (using next generation sequencing) from postmortem patients diagnosed with Alzheimer's or Parkinson's disease, and neurologically normal controls. All biofluids were cell-free and patient matched, there was one cerebrospinal fluid and one serum sample from each of 70 patients with Alzheimer's disease, 67 patients with Parkinson's disease and 78 age-similar controls. We correlated the miRNA changes with measurements of neuropathology such as plaques, tangles and Lewy bodies.

Lien

dbGaP-study=phs000727

Mots-clés

  1. 28/12/2022 28/12/2022 - Chiara Middel
Détendeur de droits

Kendall Van Keuren-Jensen, PhD, The Translational Genomics Research Institute (TGen), Phoenix, AZ, USA

Téléchargé le

28 décembre 2022

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

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dbGaP phs000727 miRNA profiles in serum and CSF of Parkinson's and Alzheimer's patients

Eligibility Criteria

Inclusion and exclusion criteria
Description

Inclusion and exclusion criteria

Alias
UMLS CUI [1,1]
C1512693
UMLS CUI [1,2]
C0680251
For inclusion in the study, the participants had to be diagnosed with Alzheimer's disease or Parkinson's disease based on postmortem neuropathological criteria or to be neuropathologically normal.
Description

Elig.phs000727.v1.p1.1

Type de données

boolean

Alias
UMLS CUI [1,1]
C1512693
UMLS CUI [1,2]
C0030567
UMLS CUI [1,3]
C0002395
UMLS CUI [1,4]
C0332145
UMLS CUI [1,5]
C0876934
UMLS CUI [1,6]
C0679228
UMLS CUI [2,1]
C0027853
UMLS CUI [2,2]
C0205307

Similar models

Eligibility Criteria

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
Inclusion and exclusion criteria
C1512693 (UMLS CUI [1,1])
C0680251 (UMLS CUI [1,2])
Elig.phs000727.v1.p1.1
Item
For inclusion in the study, the participants had to be diagnosed with Alzheimer's disease or Parkinson's disease based on postmortem neuropathological criteria or to be neuropathologically normal.
boolean
C1512693 (UMLS CUI [1,1])
C0030567 (UMLS CUI [1,2])
C0002395 (UMLS CUI [1,3])
C0332145 (UMLS CUI [1,4])
C0876934 (UMLS CUI [1,5])
C0679228 (UMLS CUI [1,6])
C0027853 (UMLS CUI [2,1])
C0205307 (UMLS CUI [2,2])

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