Associated Papers
Recurrent somatic mutations of FAT family cadherins induce an aggressive phenotype and poor prognosis in anaplastic large cell lymphoma.
Villa M et al.
British Journal of Cancer, 2024
39478125 (PubMed )
Supplement: 41416_2024_2881_MOESM1_ESM.pdf
ACE Phenotyping in Human Blood and Tissues: Revelation of ACE Outliers and Sex Differences in ACE Sialylation.
Enyedi EE et al.
Biomedicines, 2024
38790902 (PubMed )
Supplement: biomedicines-12-00940-s001.zip › biomedicines-2930173-supplementary.pdf
Exome variants associated with asthma and allergy.
Wjst M
Scientific Reports, 2022
36470944 (PubMed )
Supplement: 41598_2022_24960_MOESM1_ESM.pdf
Identification of ultra-rare missense mutations associated with familial schizophrenia by whole-exome sequencing.
Wang YC et al.
Schizophrenia Research, 2021
Heat Shock Protein 70 Gene Single Nucleotide Polymorphism and Diabetic Foot Ulcer. Is There Any Relationship?
Zubair M et al.
Journal of Clinical Medicine, 2018
De novo and rare mutations in the HSPA1L heat shock gene associated with inflammatory bowel disease.
Takahashi S et al.
Genome Medicine, 2017
Heat Shock 70 Protein Genes and Genetic Susceptibility to Apical Periodontitis.
Maheshwari K et al.
Journal of Endodontics, 2016
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-A2-A0CT-01A.domain
Heat shock protein 70 gene polymorphisms in sudden sensorineural hearing loss.
Chien CY et al.
Audiology & Neuro-otology, 2012
A genetic association analysis of cognitive ability and cognitive ageing using 325 markers for 109 genes associated with oxidative stress or cognition.
Harris SE et al.
Bmc Genetics, 2007
17601350 (PubMed )
Supplement: 1471-2156-8-43-S1.doc
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