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Status |
Public on Aug 09, 2019 |
Title |
N6-methyladenosine (m6A) profiling of type II diabetes islets |
Organism |
Homo sapiens |
Experiment type |
Methylation profiling by high throughput sequencing
|
Summary |
In type 2 diabetes, pancreatic beta-cells fail to compensate for the presence of insulin resistance in target tissues and represent a central player in the disease development. Identifying and studying innovative molecular mechanisms that lead to beta-cell failure in diabetes represent an interesting line of research and are necessary. N6-Methyladenosine (m6A) is the most abundant modification in mRNA and is found virtually in all mammals. Through m6A-profiling, we aim to characterize the dynamic RNA methylation changes in islets obtained from patients with type 2 diabetes.
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Overall design |
MeRIP-seq profiling of T2D islets
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Web link |
https://www.nature.com/articles/s42255-019-0089-9
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Contributor(s) |
Zhang Z, DeJesus D, Kulkarni R, He C |
Citation(s) |
31867565 |
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Submission date |
Sep 17, 2018 |
Last update date |
Feb 11, 2022 |
Contact name |
Zijie Zhang |
E-mail(s) |
scottzjzhang@uchicago.edu
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Phone |
7738083212
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Organization name |
University of Chicago
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Department |
Chemistry
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Lab |
He, Chuan
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Street address |
919E 57th
|
City |
CHICAGO |
State/province |
IL |
ZIP/Postal code |
60637 |
Country |
USA |
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Platforms (1) |
GPL20301 |
Illumina HiSeq 4000 (Homo sapiens) |
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Samples (30)
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Relations |
BioProject |
PRJNA491415 |
SRA |
SRP161883 |