| Accession |
PRJCA009655 |
| Title |
Mitochondrial Mutation in Cholecystolithiasis Pedigrees |
| Relevance |
Medical |
| Data types |
Genome sequencing
|
| Organisms |
Homo sapiens
|
| Description |
Cholecystolithiasis and its associated complications (e.g., cholecystitis and pancreatitis) have become an increasingly significant public health problem around the globe. 20%-30% of adults in developed countries have been diagnosed with cholecystolithiasis.In particular, cholecystolithiasis has a strong genetic predisposition, and ethnic differences indicate that genetic factors play an important role in the occurrence of cholecystolithiasis. the association between mitochondrial DNA (mtDNA) and the onset of cholecystolithiasis still remains to be unraveled. To further elucidate the molecular basis of cholecystolithiasis in the Chinese population, we conformed a systematic and extended mutational screening of mtDNA. |
| Sample scope |
Multiisolate |
| Release date |
2022-05-18 |
| Grants |
| Agency |
program |
Grant ID |
Grant title |
| National Natural Science Foundation of China (NSFC)
|
Young Scientists Fund
|
81600769
|
Mitochondrial primary and secondary mutations
|
| The Natural Science Foundation of Zhejiang Province
|
Young Scientists Fund
|
LQ19H120004
|
Study on the function of new mitochondrial mutation sites
|
| The grant qnyc-077 from the First Affiliated Hospital of Wenzhou Medical University
|
In-hospital Fund
|
qnyc-077
|
Study on the function of new mitochondrial mutation sites
|
| the Science and Technology Bureau of Wenzhou
|
Young Scientists Fund
|
Y20190475
|
Functional study of mitochondrial RNA mutation sites
|
|
|
| Submitter |
Wu
Zhou (gonewithwind95@163.com)
|
| Organization |
Wenzhou Medical University |
| Submission date |
2022-05-18 |
