Neurodevelopmental Defects and Neurodegenerative P... (ID 635098) - BioProject

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Accession: PRJNA635098 ID: 635098

Neurodevelopmental Defects and Neurodegenerative Phenotypes in Human Brain Organoids Carrying Parkinson Disease-Linked DNAJC6 Mutations (human)

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In this study, human isogenic model of juvenile onset PD caused by DNAJC6 mutation were made. More...

Accession	PRJNA635098; GEO: GSE151190
Data Type	Transcriptome or Gene expression
Scope	Multiisolate
Organism	Homo sapiens[Taxonomy ID: 9606] Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo; Homo sapiens
Publications	Wulansari N et al., "Neurodevelopmental defects and neurodegenerative phenotypes in human brain organoids carrying Parkinson's disease-linked DNAJC6 mutations.", Sci Adv, 2021 Feb;7(8)
Submission	Registration date: 26-May-2020 Lee Sang-Hun Lab, Department of Biochemistry and Molecular Biology, Hanyang University
Relevance	Medical

Project Data:

Parameter	Value
Data volume, Supplementary Mbytes	1

Parameter	Value
Data volume, Gbases	35
Data volume, Mbytes	16749

Supplemental Content

Neurodevelopmental Defects and Neurodegenerative Phenotypes in Human Brain Organ...
Neurodevelopmental Defects and Neurodegenerative Phenotypes in Human Brain Organoids Carrying Parkinson Disease-Linked DNAJC6 Mutations
Neurodevelopmental Defects and Neurodegenerative Phenotypes in Human Brain Organoids Carrying Parkinson Disease-Linked DNAJC6 Mutations

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