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HLA-DRB1 Alleles as Genetic Risk Factors for the Development of Anti-MDA5 Antibodies in Patients with Dermatomyositis.
- Published in:
- 2017
- By:
- Publication type:
- journal article
A novel de novo mutation of β-cardiac myosin heavy chain gene found in a twelve-year-old boy with hypertrophic cardiomyopathy.
- Published in:
- Journal of Genetics, 2014, v. 93, n. 2, p. 557, doi. 10.1007/s12041-014-0414-8
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- Publication type:
- Article
Killer cell immunoglobulin‐like receptor three domains long cytoplasmic tail 1 gene *007 may modulate disease progression of human immunodeficiency virus‐1 infection in the Japanese population.
- Published in:
- International Journal of Immunogenetics, 2023, v. 50, n. 2, p. 48, doi. 10.1111/iji.12617
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- Publication type:
- Article
Apelin is a positive regulator of ACE2 in failing hearts.
- Published in:
- Journal of Clinical Investigation, 2013, v. 123, n. 12, p. 5203, doi. 10.1172/JCI69608
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- Publication type:
- Article
Reference strand-mediated conformation analysis-based typing of multiple alleles in the rhesus macaque MHC class I Mamu-A and Mamu-B loci.
- Published in:
- Electrophoresis, 2007, v. 28, n. 6, p. 918, doi. 10.1002/elps.200600586
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- Publication type:
- Article
Viral load of SARS‐CoV‐2 Omicron is not high despite its high infectivity.
- Published in:
- Journal of Medical Virology, 2022, v. 94, n. 11, p. 5543, doi. 10.1002/jmv.27974
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- Publication type:
- Article
Viral loads and profile of the patients infected with SARS‐CoV‐2 Delta, Alpha, or R.1 variants in Tokyo.
- Published in:
- Journal of Medical Virology, 2022, v. 94, n. 4, p. 1707, doi. 10.1002/jmv.27479
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- Publication type:
- Article
SARS‐CoV‐2 R.1 lineage variants that prevailed in Tokyo in March 2021.
- Published in:
- Journal of Medical Virology, 2021, v. 93, n. 12, p. 6833, doi. 10.1002/jmv.27240
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- Publication type:
- Article
Barth syndrome associated with triple mutation.
- Published in:
- 2018
- By:
- Publication type:
- Case Study
Screening of sarcomere gene mutations in young athletes with abnormal findings in electrocardiography: identification of a MYH7 mutation and MYBPC3 mutations.
- Published in:
- Journal of Human Genetics, 2015, v. 60, n. 10, p. 641, doi. 10.1038/jhg.2015.81
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- Publication type:
- Article
A single nucleotide polymorphism in the 3′-untranslated region of MyD88 gene is associated with Buerger disease but not with Takayasu arteritis in Japanese.
- Published in:
- Journal of Human Genetics, 2011, v. 56, n. 7, p. 545, doi. 10.1038/jhg.2011.44
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- Publication type:
- Article
Association of HLA-A<sup>*</sup>02:06 and HLA-DRB1<sup>*</sup>04:05 with clinical subtypes of juvenile idiopathic arthritis.
- Published in:
- Journal of Human Genetics, 2011, v. 56, n. 3, p. 196, doi. 10.1038/jhg.2010.159
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- Publication type:
- Article
HLA and CTLA4 polymorphisms may confer a synergistic risk in the susceptibility to Graves’ disease.
- Published in:
- Journal of Human Genetics, 2010, v. 55, n. 5, p. 323, doi. 10.1038/jhg.2010.20
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- Publication type:
- Article
Molecular basis of hereditary cardiomyopathy: abnormalities in calcium sensitivity, stretch response, stress response and beyond.
- Published in:
- Journal of Human Genetics, 2010, v. 55, n. 2, p. 81, doi. 10.1038/jhg.2009.138
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- Publication type:
- Article
Validation of eight genetic risk factors in East Asian populations replicated the association of BRAP with coronary artery disease.
- Published in:
- Journal of Human Genetics, 2009, v. 54, n. 11, p. 642, doi. 10.1038/jhg.2009.87
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- Publication type:
- Article
Validation of the association between AGTRL1 polymorphism and coronary artery disease in the Japanese and Korean populations.
- Published in:
- Journal of Human Genetics, 2009, v. 54, n. 9, p. 554, doi. 10.1038/jhg.2009.78
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- Publication type:
- Article
Complex divergence at a microsatellite marker C1_2_5 in the lineage of HLA-Cw/-B haplotype.
- Published in:
- Journal of Human Genetics, 2009, v. 54, n. 4, p. 224, doi. 10.1038/jhg.2009.15
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- Publication type:
- Article
Replication studies for the association of PSMA6 polymorphism with coronary artery disease in East Asian populations.
- Published in:
- Journal of Human Genetics, 2009, v. 54, n. 4, p. 248, doi. 10.1038/jhg.2009.22
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- Publication type:
- Article
HLA-DPB1 and NFKBIL1 may confer the susceptibility to chronic thromboembolic pulmonary hypertension in the absence of deep vein thrombosis.
- Published in:
- Journal of Human Genetics, 2009, v. 54, n. 2, p. 108, doi. 10.1038/jhg.2008.15
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- Publication type:
- Article
Role of HCN4 channel in preventing ventricular arrhythmia.
- Published in:
- Journal of Human Genetics, 2009, v. 54, n. 2, p. 115, doi. 10.1038/jhg.2008.16
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- Publication type:
- Article
Replication of the association between a chromosome 9p21 polymorphism and coronary artery disease in Japanese and Korean populations.
- Published in:
- Journal of Human Genetics, 2008, v. 53, n. 4, p. 357, doi. 10.1007/s10038-008-0248-4
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- Publication type:
- Article
The role of a common TNNT2 polymorphism in cardiac hypertrophy.
- Published in:
- Journal of Human Genetics, 2004, v. 49, n. 3, p. 129, doi. 10.1007/s10038-003-0121-4
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- Publication type:
- Article
Induction of expression of MHC-class-II antigen on human thyroid carcinoma by wild-type p53.
- Published in:
- International Journal of Cancer, 1998, v. 75, n. 3, p. 391, doi. 10.1002/(SICI)1097-0215(19980130)75:3<391::AID-IJC11>3.0.CO;2-C
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- Publication type:
- Article
The CCR4-NOT deadenylase complex controls Atg7-dependent cell death and heart function.
- Published in:
- Science Signaling, 2018, v. 11, n. 516, p. 1, doi. 10.1126/scisignal.aan3638
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- Publication type:
- Article
Arthroscopic fixation with EndoButton for tibial eminence fractures visualised through a proximal superomedial portal: a surgical technique.
- Published in:
- 2016
- By:
- Publication type:
- journal article
High-Contrast Fluorescence Imaging of Tumors In Vivo Using Nanoparticles of Amphiphilic Brush-Like Copolymers Produced by ROMP.
- Published in:
- Angewandte Chemie, 2011, v. 123, n. 29, p. 6697, doi. 10.1002/ange.201101005
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- Publication type:
- Article
Association of lymph-node antigens with lower Gag-specific central-memory and higher Env-specific effector-memory CD8<sup>+</sup> T-cell frequencies in a macaque AIDS model.
- Published in:
- Scientific Reports, 2016, p. 30153, doi. 10.1038/srep30153
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- Publication type:
- Article
Clinical significance of prediabetes, undiagnosed diabetes and diagnosed diabetes on critical outcomes in COVID‐19: Integrative analysis from the Japan COVID‐19 task force.
- Published in:
- Diabetes, Obesity & Metabolism, 2023, v. 25, n. 1, p. 144, doi. 10.1111/dom.14857
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- Publication type:
- Article
Influence of Side Chain Length on Fluorescence Intensity of ROMP-Based Polymeric Nanoparticles and Their Tumor Specificity in In-Vivo Tumor Imaging.
- Published in:
- Small, 2011, v. 7, n. 24, p. 3536, doi. 10.1002/smll.201101637
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- Publication type:
- Article
Limited Impact of Passive Non-Neutralizing Antibody Immunization in Acute SIV Infection on Viremia Control in Rhesus Macaques.
- Published in:
- PLoS ONE, 2013, v. 8, n. 9, p. 1, doi. 10.1371/journal.pone.0073453
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- Publication type:
- Article
A Novel Protective MHC-I Haplotype Not Associated with Dominant Gag-Specific CD8<sup>+</sup> T-Cell Responses in SIVmac239 Infection of Burmese Rhesus Macaques.
- Published in:
- PLoS ONE, 2013, v. 8, n. 1, p. 1, doi. 10.1371/journal.pone.0054300
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- Publication type:
- Article
Protection of Macaques with Diverse MHC Genotypes against a Heterologous SIV by Vaccination with a Deglycosylated Live-Attenuated SIV.
- Published in:
- PLoS ONE, 2010, v. 5, n. 7, p. 1, doi. 10.1371/journal.pone.0011678
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- Publication type:
- Article
No Evidence of an Association between the APOBEC3B Deletion Polymorphism and Susceptibility to HIV Infection and AIDS in Japanese and Indian Populations.
- Published in:
- Journal of Infectious Diseases, 2010, v. 202, n. 5, p. 815, doi. 10.1086/655227
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- Publication type:
- Article
Losartan inhibits LPS-induced inflammatory signaling through a PPARγ-dependent mechanism in human THP-1 macrophages.
- Published in:
- Hypertension Research, 2010, v. 33, n. 8, p. 831, doi. 10.1038/hr.2010.79
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- Publication type:
- Article
Characterization of a newly established human gallbladder carcinoma cell line.
- Published in:
- 1994
- By:
- Publication type:
- Letter
Polymorphisms in the Platelet-Endothelial Cell Adhesion Molecule-1 (PECAM-1) Gene, Asn563Ser and Gly670Arg, Associated with Myocardial Infarction in the Japanese.
- Published in:
- Annals of the New York Academy of Sciences, 2001, v. 947, n. 1, p. 259, doi. 10.1111/j.1749-6632.2001.tb03948.x
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- Publication type:
- Article
Susceptibility to chronic thromboembolic pulmonary hypertension may be conferred by miR- 759 via its targeted interaction with polymorphic fibrinogen alpha gene.
- Published in:
- Human Genetics, 2010, v. 128, n. 4, p. 443, doi. 10.1007/s00439-010-0866-8
- By:
- Publication type:
- Article
Megakaryoblastic leukemia factor-1 gene in the susceptibility to coronary artery disease.
- Published in:
- Human Genetics, 2009, v. 126, n. 4, p. 539, doi. 10.1007/s00439-009-0698-6
- By:
- Publication type:
- Article
Synergistic contribution of CD14 and HLA loci in the susceptibility to Buerger disease.
- Published in:
- Human Genetics, 2007, v. 122, n. 3/4, p. 367, doi. 10.1007/s00439-007-0408-1
- By:
- Publication type:
- Article
Characterization of the human nebulette gene: a polymorphism in an actin-binding motif is associated with nonfamilial idiopathic dilated cardiomyopathy.
- Published in:
- Human Genetics, 2000, v. 107, n. 5, p. 440, doi. 10.1007/s004390000389
- By:
- Publication type:
- Article
A Novel Mutation in KCNQ1 Associated with a Potent Dominant Negative Effect as the Basis for the LQT1 Form of the Long QT Syndrome.
- Published in:
- Journal of Cardiovascular Electrophysiology, 2007, v. 18, n. 9, p. 972, doi. 10.1111/j.1540-8167.2007.00889.x
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- Publication type:
- Article
Spontaneous T Wave Alternans in a Patient with Brugada Syndrome—Responses to Intravenous Administration of Class I Antiarrhythmic Drug, Glucose Tolerance Test, and Atrial Pacing.
- Published in:
- Journal of Cardiovascular Electrophysiology, 2005, v. 16, n. 2, p. 217, doi. 10.1046/j.1540-8167.2004.40411.x
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- Publication type:
- Article
ELABELA-APJ axis protects from pressure overload heart failure and angiotensin II-induced cardiac damage.
- Published in:
- Cardiovascular Research, 2017, v. 113, n. 7, p. 760, doi. 10.1093/cvr/cvx061
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- Publication type:
- Article
Impaired binding of ZASP/Cypher with phosphoglucomutase 1 is associated with dilated cardiomyopathy.
- Published in:
- Cardiovascular Research, 2009, v. 83, n. 1, p. 80, doi. 10.1093/cvr/cvp119
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- Publication type:
- Article
A mutant cardiac sodium channel with multiple biophysical defects associated with overlapping clinical features of Brugada syndrome and cardiac conduction disease
- Published in:
- Cardiovascular Research, 2002, v. 53, n. 2, p. 348, doi. 10.1016/S0008-6363(01)00494-1
- By:
- Publication type:
- Article
Fatal transfusion-associated graft-versus-host disease.
- Published in:
- 1994
- By:
- Publication type:
- Case Study
Reciprocal expression of MRTF-A and myocardin is crucial for pathological vascular remodelling in mice.
- Published in:
- EMBO Journal, 2012, v. 31, n. 23, p. 4428, doi. 10.1038/emboj.2012.296
- By:
- Publication type:
- Article
Glutathione S-transferase μ1 null genotype is associated with K-ras gene mutation in lung adenocarcinoma among smokers.
- Published in:
- Carcinogenesis, 2001, v. 22, n. 8, p. 1327, doi. 10.1093/carcin/22.8.1327
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- Publication type:
- Article
A DFNA5 Mutation Identified in Japanese Families with Autosomal Dominant Hereditary Hearing Loss.
- Published in:
- Annals of Human Genetics, 2014, v. 78, n. 2, p. 83, doi. 10.1111/ahg.12053
- By:
- Publication type:
- Article
Dilated cardiomyopathy-linked heat shock protein family D member 1 mutations cause up-regulation of reactive oxygen species and autophagy through mitochondrial dysfunction.
- Published in:
- Cardiovascular Research, 2021, v. 117, n. 4, p. 1118, doi. 10.1093/cvr/cvaa158
- By:
- Publication type:
- Article