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Author Correction: Identifying antibiotics based on structural differences in the conserved allostery from mitochondrial heme-copper oxidases.
- Published in:
- 2022
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- Publication type:
- Correction Notice
rs10924104 in the expression enhancer motif of CD58 confers susceptibility to human autoimmune diseases.
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- Human Genetics, 2024, v. 143, n. 1, p. 19, doi. 10.1007/s00439-023-02617-2
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- Article
Disease susceptibility genes shared by primary biliary cirrhosis and Crohn's disease in the Japanese population.
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- Journal of Human Genetics, 2015, v. 60, n. 9, p. 525, doi. 10.1038/jhg.2015.59
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- Article
De novo mutations in ATP1A3 cause alternating hemiplegia of childhood.
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- Nature Genetics, 2012, v. 44, n. 9, p. 1030, doi. 10.1038/ng.2358
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- Article
Human CD72 splicing isoform responsible for resistance to systemic lupus erythematosus regulates serum immunoglobulin level and is localized in endoplasmic reticulum.
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- BMC Immunology, 2012, v. 13, n. 1, p. 1, doi. 10.1186/1471-2172-13-72
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- Article
Fine-mapping analysis revealed complex pleiotropic effect and tissue-specific regulatory mechanism of TNFSF15 in primary biliary cholangitis, Crohn's disease and leprosy.
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- Scientific Reports, 2016, p. 31429, doi. 10.1038/srep31429
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- Publication type:
- Article
Human primary biliary cirrhosis-susceptible allele of rs4979462 enhances TNFSF15 expression by binding NF-1.
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- Human Genetics, 2015, v. 134, n. 7, p. 737, doi. 10.1007/s00439-015-1556-3
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- Publication type:
- Article
Mapping of susceptible variants for cold medicine-related Stevens–Johnson syndrome by whole-genome resequencing.
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- NPJ Genomic Medicine, 2021, v. 6, n. 1, p. 1, doi. 10.1038/s41525-021-00171-2
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- Article
The ubiquinone synthesis pathway is a promising drug target for Chagas disease.
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- PLoS ONE, 2021, v. 16, n. 2, p. 1, doi. 10.1371/journal.pone.0243855
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- Publication type:
- Article
Thymic Stromal Lymphopoietin Gene Promoter Polymorphisms Are Associated with Susceptibility to Bronchial Asthma.
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- American Journal of Respiratory Cell & Molecular Biology, 2011, v. 44, n. 6, p. 787, doi. 10.1165/rcmb.2009-0418OC
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- Publication type:
- Article
Identification of HLA-A*02:06:01 as the primary disease susceptibility HLA allele in cold medicine-related Stevens-Johnson syndrome with severe ocular complications by high-resolution NGS-based HLA typing.
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- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-52619-2
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- Publication type:
- Article
The association of integration patterns of human papilloma virus and single nucleotide polymorphisms on immune- or DNA repair-related genes in cervical cancer patients.
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- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-49523-0
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- Publication type:
- Article
Support Vector Machine model for hERG inhibitory activities based on the integrated hERG database using descriptor selection by NSGA-II.
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- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-47536-3
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- Publication type:
- Article
Analysis of whole Y-chromosome sequences reveals the Japanese population history in the Jomon period.
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- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-44473-z
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- Article
Novel HLA allele associations with susceptibility, staging, symptomatic state, autoimmune hepatitis and hepatocellular carcinoma events for primary biliary cholangitis in the Japanese population.
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- Frontiers in Immunology, 2023, p. 1, doi. 10.3389/fimmu.2023.1151502
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- Article
Genomic Heritabilities and Correlations of 17 Traits Related to Obesity and Associated Conditions in the Japanese Population.
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- G3: Genes | Genomes | Genetics, 2020, v. 10, n. 7, p. 2221, doi. 10.1534/g3.120.401242
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- Article
Mutations in TNK2 in severe autosomal recessive infantile onset epilepsy.
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- Annals of Neurology, 2013, v. 74, n. 3, p. 496, doi. 10.1002/ana.23934
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- Publication type:
- Article
rs2013278 in the multiple immunological-trait susceptibility locus CD28 regulates the production of non-functional splicing isoforms.
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- Human Genomics, 2022, v. 16, n. 1, p. 1, doi. 10.1186/s40246-022-00419-7
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- Article
HLA-VBSeq v2: improved HLA calling accuracy with full-length Japanese class-I panel.
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- Human Genome Variation, 2019, v. 6, n. 1, p. N.PAG, doi. 10.1038/s41439-019-0061-y
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- Article
rs1944919 on chromosome 11q23.1 and its effector genes COLCA1/COLCA2 confer susceptibility to primary biliary cholangitis.
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- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-84042-x
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- Article
Genome-wide association studies identify PRKCB as a novel genetic susceptibility locus for primary biliary cholangitis in the Japanese population.
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- Human Molecular Genetics, 2017, v. 26, n. 3, p. 650, doi. 10.1093/hmg/ddw406
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- Publication type:
- Article
A Pyrrolo-Pyrimidine Derivative Targets Human Primary AML Stem Cells in Vivo.
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- Science Translational Medicine, 2013, v. 5, n. 181, p. 1, doi. 10.1126/scitranslmed.3004387
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- Article
De novo mutations in epileptic encephalopathies.
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- Nature, 2013, v. 501, n. 7466, p. 217, doi. 10.1038/nature12439
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- Article
Discovery of the novel HLA‐B allele, HLA‐B*51:01:01:36 in a Japanese individual.
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- HLA: Immune Response Genetics, 2019, v. 94, n. 5, p. 445, doi. 10.1111/tan.13658
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- Article
Detection of the novel HLA‐A allele, HLA‐A*02:01:01:58, in a Japanese individual.
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- HLA: Immune Response Genetics, 2019, v. 94, n. 5, p. 435, doi. 10.1111/tan.13657
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- Publication type:
- Article
Identification of the novel HLA‐DQB1 allele, HLA‐DQB1*05:03:01:04, in a Japanese individual.
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- HLA: Immune Response Genetics, 2019, v. 94, n. 5, p. 466, doi. 10.1111/tan.13654
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- Article
Genome-Wide Association Study for Chronic Hepatitis B Infection in the Thai Population.
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- Frontiers in Genetics, 2022, v. 13, p. 1, doi. 10.3389/fgene.2022.887121
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- Article
Implementation of π-π interactions in molecular dynamics simulation.
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- Journal of Computational Chemistry, 2007, v. 28, n. 6, p. 1091, doi. 10.1002/jcc.20557
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- Article
POGLUT1, the putative effector gene driven by rs2293370 in primary biliary cholangitis susceptibility locus chromosome 3q13.33.
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- Scientific Reports, 2019, v. 9, n. 1, p. 1, doi. 10.1038/s41598-018-36490-1
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- Article
Identification of a two-SNP PLA2R1 Haplotype and HLA-DRB1 Alleles as Primary Risk Associations in Idiopathic Membranous Nephropathy.
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- Scientific Reports, 2018, v. 8, n. 1, p. 1, doi. 10.1038/s41598-018-33612-7
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- Publication type:
- Article
Increased expression and altered localization of cathepsin Z are associated with progression to jaundice stage in primary biliary cholangitis.
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- Scientific Reports, 2018, v. 8, n. 1, p. 1, doi. 10.1038/s41598-018-30146-w
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- Publication type:
- Article
CD72 polymorphisms associated with alternative splicing modify susceptibility to human systemic lupus erythematosus through epistatic interaction with FCGR2B.
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- Human Molecular Genetics, 2004, v. 13, n. 23, p. 2907, doi. 10.1093/hmg/ddh318
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- Article
The Genetics of Primary Biliary Cholangitis: A GWAS and Post-GWAS Update.
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- Genes, 2023, v. 14, n. 2, p. 405, doi. 10.3390/genes14020405
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- Article
Construction of an integrated database for hERG blocking small molecules.
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- PLoS ONE, 2018, p. 1, doi. 10.1371/journal.pone.0199348
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- Article
Molecular and morphological evidence of hybridization between native Ruditapes philippinarum and the introduced Ruditapes form in Japan.
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- Conservation Genetics, 2013, v. 14, n. 3, p. 717, doi. 10.1007/s10592-013-0467-x
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- Article
Mechanism of the decrease in catalytic activity of human cytochrome P450 2C9 polymorphic variants investigated by computational analysis.
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- Journal of Computational Chemistry, 2010, v. 31, n. 15, p. 2746, doi. 10.1002/jcc.21568
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- Publication type:
- Article
Significance of functional disease-causal/susceptible variants identified by whole-genome analyses for the understanding of human diseases.
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- Proceedings of the Japan Academy, Series B Physical & biological sciences, 2017, v. 93, n. 9, p. 657, doi. 10.2183/pjab.93.042
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- Article