Associated Papers
Functional mutation, splice, distribution, and divergence analysis of impactful genes associated with heart failure and other cardiovascular diseases.
Mhatre I et al.
Scientific Reports, 2023
37798313 (PubMed )
Supplement: 41598_2023_44127_MOESM2_ESM.pdf
Deep Resequencing of Ulcerative Colitis-Associated Genes Identifies Novel Variants in Candidate Genes in the Korean Population.
Moon CM et al.
Inflammatory Bowel Diseases, 2018
29733354 (PubMed )
Supplement: izy122_suppl_supporting_data.pdf
The eSNV-detect: a computational system to identify expressed single nucleotide variants from transcriptome sequencing data.
Tang X et al.
Nucleic Acids Research, 2014
25352556 (PubMed )
Supplement: supp_gku1005_nar-01266-met-n-2014-File012.xlsx › TCGA-AN-A0FW-01A.domain
Genome-wide analysis to predict protein sequence variations that change phosphorylation sites or their corresponding kinases.
Ryu GM et al.
Nucleic Acids Research, 2009
19139070 (PubMed )
Supplement: gkn1008_nar-01723-s-2008-File009.xls › TypeI-
[Role of urotensin II gene in the genetic susceptibility to gestational diabetes mellitus in northern Chinese women].
Tan YJ et al.
Zhonghua Fu Chan Ke Za Zhi, 2006
Role of urotensin II gene in genetic susceptibility to Type 2 diabetes mellitus in Japanese subjects.
Wenyi Z et al.
Diabetologia, 2003
[The role of urotensin II gene in the genetic susceptibility to type 2 diabetes in Chinese population].
Zhu F et al.
Zhonghua Yi Xue Za Zhi, 2002
[Mitochondrial gene mutations in diabetes mellitus].
Hinokio Y et al.
Nihon Rinsho. Japanese Journal of Clinical Medicine, 2002
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