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Status |
Public on May 31, 2018 |
Title |
Transcriptome sequencing of differentially expressed genes in acne inversa (AI) patients with NCSTN mutation and healthy individuals |
Organism |
Homo sapiens |
Experiment type |
Expression profiling by high throughput sequencing
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Summary |
To elucidate the relationship between NCSTN mutations and familial AI pathogenesis by investigating differential gene expression, we have employed transcriptome sequencing profiling as a discovery platform to identify genes with the potential to be involved in familial AI pathogenesis. Skin biopsies were obtained from the lesions of AI patients with NCSTN mutations . Control skin tissues were obtained from healthy individuals undergoing cosmetic surgery procedures
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Overall design |
Two groups, AI patients with NCSTN mutations vs. healthy individuals. Each group contains 4 samples.
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Contributor(s) |
He Y |
Citation missing |
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Submission date |
May 30, 2018 |
Last update date |
Mar 20, 2019 |
Contact name |
Yanyan He |
E-mail(s) |
[email protected]
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Organization name |
hinese Academy of Medical Sciences and Peking Union Medical College
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Department |
Institute of Dermatology
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Street address |
Jiangwangmiao Street
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City |
Nanjing |
ZIP/Postal code |
210042 |
Country |
China |
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Platforms (1) |
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Samples (8)
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This SubSeries is part of SuperSeries: |
GSE115101 |
Transcriptome sequencing of differentially expressed genes in mouse and human skin with and without NCSTN mutation |
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Relations |
BioProject |
PRJNA473795 |
SRA |
SRP149349 |