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We aimed to determine the genetic basis of migraine and its association with syncope in a cohort of migraineurs at a tertiary hospital in Taiwan.
ORGANISM(S): Homo Sapiens 
2023-07-22 | PRJEB64467 | EVA
To identify additional genomic targets that are enriched in the Chinese population, we carried out the CHOICE study to perform Exome Sequencing of 241 Chinese NSCLC patients.
ORGANISM(S): Homo Sapiens 
2019-02-26 | PRJEB31315 | EVA
Kernel development is accompanied by complex gene networks. Expression quantitative trait loci (eQTL) analysis is an efficient way to detect the regulatory elements of genes, especially the trans-eQTLs help to construct the regulatory networks of genes and contribute to a better understanding of the...
ORGANISM(S): Zea Mays 
2018-10-10 | PRJEB24974 | EVA
A FAM8A1 frameshift variant is associated with REM sleep behaviour disorder, urinary retention and mydriasis in Russian Blue cats
ORGANISM(S): Felis Catus 
2026-01-22 | PRJEB87525 | EVA
Ion AmpliSeq Comprehensive Cancer Panel sequencing to identify somatic single nucleotide variants and copy number variations in 409 cancer-related genes from gastric cancer patient samples. Clinical samples provided by Chang Gung Memorial Hospital.
ORGANISM(S): Homo Sapiens 
2026-01-23 | PRJEB106877 | EVA
An Investigation into the associations of variants in genes associated with angiogenesis with markers of metabolic syndrome
ORGANISM(S): Homo Sapiens 
2026-01-25 | PRJEB107010 | EVA
This project determine the genome sequence of Naked mole rat in Kumamoto University, and detected the intra-specific variation of genomes in this species.
ORGANISM(S): Heterocephalus Glaber 
2026-01-25 | PRJEB106988 | EVA
The early pregnancy probability (OPP) in heifers is a trait of high economic value for Nellore. However, the variability among heifers is not always detected because most breeders do not expose heifers while still young. The aim of this study was identify polymorphisms in the genes XKR-4, ESRRG, PAP...
ORGANISM(S): Bos Indicus 
2019-07-02 | PRJEB30522 | EVA
An investigation to determine the genotypes of VEGFA SNPs and their link to MS development
ORGANISM(S): Homo Sapiens 
2025-10-19 | PRJEB100861 | EVA
We report a patient that presented the typical clinical features of FRDA and genetic analysis of FXN intron 1 led to the assumption that the patient carried the common biallelic expansion. Subsequently, parental sample testing led to the identification of a novel intragenic deletion involving the 5?...
ORGANISM(S): Homo Sapiens 
2023-09-03 | PRJEB65722 | EVA
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