Hypothesis

2 Matching Annotations

Nov 2021
www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov

Bi-allelic variants in OGDHL cause a neurodevelopmental spectrum disease featuring epilepsy, hearing loss, visual impairment, and ataxia

1
1. scibot 20 Nov 2021
  
  in Public
  
  17110-1-AP
  
  DOI: 10.1016/j.ajhg.2021.11.003
  
  Resource: (Proteintech Cat# 17110-1-AP, RRID:AB_2156767)
  
  Curator: @Naa003
  
  SciCrunch record: RRID:AB_2156767
  
  What is this?
  
  RRID:AB_2156767 RRIDCUR:Missing
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RRIDCUR:Missing

RRID:AB_2156767

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scibot

URL

ncbi.nlm.nih.gov/pmc/articles/PMC8715183/
www.sciencedirect.com www.sciencedirect.com

OGDHL Ameliorates Cognitive Impairment and Alzheimer's Disease-Like Pathology via Activating Wnt/β-catenin signaling in Alzheimer's Disease Mice

1
1. scibot 17 Nov 2021
  
  in Public
  
  17110-1-AP
  
  DOI: 10.1016/j.bbr.2021.113673
  
  Resource: (Proteintech Cat# 17110-1-AP, RRID:AB_2156767)
  
  Curator: @Naa003
  
  SciCrunch record: RRID:AB_2156767
  
  What is this?
  
  RRIDCUR:Missing RRID:AB_2156767
Visit annotations in context

Tags

RRIDCUR:Missing

RRID:AB_2156767

Annotators

scibot

URL

sciencedirect.com/science/article/pii/S0166432821005611