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Comparative effectiveness of biological disease-modifying antirheumatic drugs and Janus kinase inhibitor monotherapy in rheumatoid arthritis.
- Published in:
- Rheumatology, 2024, v. 63, n. 11, p. 3065, doi. 10.1093/rheumatology/kead620
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- Article
Real-world comparative study of the efficacy of Janus kinase inhibitors in patients with rheumatoid arthritis: the ANSWER cohort study.
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- Rheumatology, 2024, v. 63, n. 11, p. 3033, doi. 10.1093/rheumatology/kead543
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- Article
Vaginal microbiome as a tool for prediction of chorioamnionitis in preterm labor: a pilot study.
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- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-98587-4
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- Article
Human cytomegalovirus downregulates SLITRK6 expression through IE2.
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- Journal of NeuroVirology, 2017, v. 23, n. 1, p. 79, doi. 10.1007/s13365-016-0475-y
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- Publication type:
- Article
Exploring the unique function of imprinting control centers in the PWS/AS-responsible region: finding from array-based methylation analysis in cases with variously sized microdeletions.
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- Clinical Epigenetics, 2019, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13148-019-0633-1
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- Publication type:
- Article
Wiskott-Aldrich Syndrome in a Girl Caused by Heterozygous WASP Mutation and Extremely Skewed X-Chromosome Inactivation: A Novel Association with Maternal Uniparental Isodisomy 6.
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- Neonatology (16617800), 2015, v. 107, n. 3, p. 185, doi. 10.1159/000370059
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- Article
Fluorescent-Ligand-Mediated Screening of G-Quadruplex Structures Using a DNA Microarray.
- Published in:
- Angewandte Chemie International Edition, 2013, v. 52, n. 46, p. 12052, doi. 10.1002/anie.201305366
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- Publication type:
- Article
Inside Cover: Fluorescent-Ligand-Mediated Screening of G-Quadruplex Structures Using a DNA Microarray (Angew. Chem. Int. Ed. 46/2013).
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- Angewandte Chemie International Edition, 2013, v. 52, n. 46, p. 11944, doi. 10.1002/anie.201308949
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- Publication type:
- Article
Prognostic Factors Affecting Death in Patients with Rheumatoid Arthritis Complicated by Pneumocystis jirovecii Pneumonia and One-Year Clinical Course: The ANSWER Cohort Study.
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- International Journal of Molecular Sciences, 2023, v. 24, n. 8, p. 7399, doi. 10.3390/ijms24087399
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- Article
The DNA methylation profile of liver tumors in C3H mice and identification of differentially methylated regions involved in the regulation of tumorigenic genes.
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- 2018
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- Publication type:
- journal article
Clinical features of fetal hydrothorax associated with mucopolysaccharidosis‐VII.
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- Journal of Obstetrics & Gynaecology Research, 2023, v. 49, n. 10, p. 2538, doi. 10.1111/jog.15744
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- Article
Novel Nonsense Mutation in the NLRP7 Gene Associated with Recurrent Hydatidiform Mole.
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- 2016
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- Publication type:
- journal article
Physical Properties of Ultrafine Bubbles Generated Using a Generator System.
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- In Vivo, 2023, v. 37, n. 6, p. 2555, doi. 10.21873/invivo.13363
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- Article
Genetic features of B‐cell lymphoblastic lymphoma with TCF3‐PBX1.
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- Cancer Reports, 2022, v. 5, n. 9, p. 1, doi. 10.1002/cnr2.1559
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- Publication type:
- Article
Genetic features of precursor B‐cell phenotype Burkitt leukemia with IGH‐MYC rearrangement.
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- Cancer Reports, 2022, v. 5, n. 7, p. 1, doi. 10.1002/cnr2.1545
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- Publication type:
- Article
Monochorionic diamniotic twins of discordant external genitalia with 45,X/46,XY mosaicism.
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- Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 9, p. 1, doi. 10.1002/mgg3.1382
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- Article
Donor cord blood aging accelerates in recipients after transplantation.
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- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-29912-2
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- Publication type:
- Article
Dynamics of genomic 5-hydroxymethylcytosine during mouse oocyte growth.
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- Genes to Cells, 2014, v. 19, n. 8, p. 629, doi. 10.1111/gtc.12164
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- Publication type:
- Article
Compilation of copy number variants identified in phenotypically normal and parous Japanese women.
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- Journal of Human Genetics, 2014, v. 59, n. 6, p. 326, doi. 10.1038/jhg.2014.27
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- Publication type:
- Article
Epigenomics comes of age with expanding roles in biological understanding and clinical application.
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- Journal of Human Genetics, 2013, v. 58, n. 7, p. 395, doi. 10.1038/jhg.2013.70
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- Article
Identification of independent risk loci for Graves' disease within the MHC in the Japanese population.
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- Journal of Human Genetics, 2011, v. 56, n. 11, p. 772, doi. 10.1038/jhg.2011.99
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- Publication type:
- Article
Androgenetic/biparental mosaicism in a girl with Beckwith-Wiedemann syndrome-like and upd(14)pat-like phenotypes.
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- Journal of Human Genetics, 2011, v. 56, n. 1, p. 91, doi. 10.1038/jhg.2010.142
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- Publication type:
- Article
Identification of novel candidate loci for anorexia nervosa at 1q41 and 11q22 in Japanese by a genome-wide association analysis with microsatellite markers.
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- Journal of Human Genetics, 2009, v. 54, n. 9, p. 531, doi. 10.1038/jhg.2009.74
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- Publication type:
- Article
Imprinting control regions (ICRs) are marked by mono-allelic bivalent chromatin when transcriptionally inactive.
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- Nucleic Acids Research, 2016, v. 44, n. 2, p. 621, doi. 10.1093/nar/gkv960
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- Article
Two unrelated pedigrees with achondrogenesis type 1b carrying a Japan‐specific pathogenic variant in SLC26A2.
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- American Journal of Medical Genetics. Part A, 2020, v. 182, n. 4, p. 735, doi. 10.1002/ajmg.a.61469
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- Publication type:
- Article
Macrothrombocytopenia and developmental delay with a de novo CDC42 mutation: Yet another locus for thrombocytopenia and developmental delay.
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- American Journal of Medical Genetics. Part A, 2015, v. 167A, n. 11, p. 2822, doi. 10.1002/ajmg.a.37275
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- Article
Progressive hip joint subluxation in Saul-Wilson syndrome.
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- American Journal of Medical Genetics. Part A, 2015, v. 167A, n. 11, p. 2834, doi. 10.1002/ajmg.a.37278
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- Publication type:
- Article
Mosaic overgrowth with fibroadipose hyperplasia due to AKT1 mutation.
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- American Journal of Medical Genetics. Part A, 2015, v. 167A, n. 4, p. 907, doi. 10.1002/ajmg.a.36947
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- Publication type:
- Article
Somatic CTNNB1 mutation in hepatoblastoma from a patient with Simpson-Golabi-Behmel syndrome and germline GPC3 mutation.
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- American Journal of Medical Genetics. Part A, 2014, v. 164A, n. 4, p. 993, doi. 10.1002/ajmg.a.36364
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- Publication type:
- Article
Aberrant methylation of H19-DMR acquired after implantation was dissimilar in soma versus placenta of patients with Beckwith-Wiedemann syndrome.
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- American Journal of Medical Genetics. Part A, 2012, v. 158A, n. 7, p. 1670, doi. 10.1002/ajmg.a.35335
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- Article
Targeted DNA demethylation in vivo using dCas9-peptide repeat and scFv-TET1 catalytic domain fusions.
- Published in:
- Nature Biotechnology, 2016, v. 34, n. 10, p. 1060, doi. 10.1038/nbt.3658
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- Article
Characteristics of genetic alterations of peripheral T‐cell lymphoma in childhood including identification of novel fusion genes: the Japan Children's Cancer Group (JCCG).
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- British Journal of Haematology, 2021, v. 194, n. 4, p. 718, doi. 10.1111/bjh.17639
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- Article
ATF7 IP as a novel PDGFRB fusion partner in acute lymphoblastic leukaemia in children.
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- British Journal of Haematology, 2014, v. 165, n. 6, p. 836, doi. 10.1111/bjh.12834
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- Article
Dynamic CpG island methylation landscape in oocytes and preimplantation embryos.
- Published in:
- Nature Genetics, 2011, v. 43, n. 8, p. 811, doi. 10.1038/ng.864
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- Publication type:
- Article
Innentitelbild: Fluorescent-Ligand-Mediated Screening of G-Quadruplex Structures Using a DNA Microarray (Angew. Chem. 46/2013).
- Published in:
- Angewandte Chemie, 2013, v. 125, n. 46, p. 12162, doi. 10.1002/ange.201308949
- By:
- Publication type:
- Article
Fluorescent-Ligand-Mediated Screening of G-Quadruplex Structures Using a DNA Microarray.
- Published in:
- Angewandte Chemie, 2013, v. 125, n. 46, p. 12274, doi. 10.1002/ange.201305366
- By:
- Publication type:
- Article
Acute promyelocytic leukemia with a cryptic insertion of RARA into TBL1XR1.
- Published in:
- Genes, Chromosomes & Cancer, 2019, v. 58, n. 11, p. 820, doi. 10.1002/gcc.22791
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- Publication type:
- Article
Whole transcriptome sequencing reveals a KMT2A‐USP2 fusion in infant acute myeloid leukemia.
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- Genes, Chromosomes & Cancer, 2019, v. 58, n. 9, p. 669, doi. 10.1002/gcc.22751
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- Publication type:
- Article
Elucidation of the developmental mechanism of ovarian mature cystic teratomas using B allele‐frequency plots of single nucleotide polymorphism array data.
- Published in:
- Genes, Chromosomes & Cancer, 2018, v. 57, n. 8, p. 409, doi. 10.1002/gcc.1
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- Publication type:
- Article
Deleterious fibronectin type III-related gene variants may induce a spinal extradural arachnoid cyst: an exome sequencing study of identical twin cases.
- Published in:
- Child's Nervous System, 2021, v. 37, n. 7, p. 2329, doi. 10.1007/s00381-021-05137-4
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- Publication type:
- Article
Rare sequence variants associated with the risk of non‐syndromic biliary atresia.
- Published in:
- Hepatology Research, 2023, v. 53, n. 11, p. 1134, doi. 10.1111/hepr.13946
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- Publication type:
- Article
Distinctive features of single nucleotide alterations in induced pluripotent stem cells with different types of DNA repair deficiency disorders.
- Published in:
- Scientific Reports, 2016, p. 26342, doi. 10.1038/srep26342
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- Article
Gene expression profiling of white adipose tissue reveals paternal transmission of proneness to obesity.
- Published in:
- Scientific Reports, 2016, p. 21693, doi. 10.1038/srep21693
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- Publication type:
- Article
Increased epigenetic alterations at the promoters of transcriptional regulators following inadequate maternal gestational weight gain.
- Published in:
- Scientific Reports, 2015, p. 14224, doi. 10.1038/srep14224
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- Publication type:
- Article
Clinical and genetic characteristics of abnormal glucose tolerance in Japanese women in the first year after gestational diabetes mellitus.
- Published in:
- Journal of Diabetes Investigation, 2019, v. 10, n. 3, p. 817, doi. 10.1111/jdi.12935
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- Publication type:
- Article
Nucleotide substitutions in CD101, the human homolog of a diabetes susceptibility gene in non-obese diabetic mouse, in patients with type 1 diabetes.
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- Journal of Diabetes Investigation, 2017, v. 8, n. 3, p. 286, doi. 10.1111/jdi.12586
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- Publication type:
- Article
Aberrant hypomethylation at imprinted differentially methylated regions is involved in biparental placental mesenchymal dysplasia.
- Published in:
- Clinical Epigenetics, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13148-022-01280-0
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- Publication type:
- Article
Increased Serum LIGHT Levels Correlate with Disease Progression and Severity of Interstitial Pneumonia in Patients with Dermatomyositis: A Case Control Study.
- Published in:
- PLoS ONE, 2015, v. 10, n. 10, p. 1, doi. 10.1371/journal.pone.0140117
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- Article
An Insulator Element Located at the Cyclin B1 Interacting Protein 1 Gene Locus Is Highly Conserved among Mammalian Species.
- Published in:
- PLoS ONE, 2015, v. 10, n. 6, p. 1, doi. 10.1371/journal.pone.0131204
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- Publication type:
- Article
DNA Methyltransferase Inhibitor Zebularine Induces Human Cholangiocarcinoma Cell Death through Alteration of DNA Methylation Status.
- Published in:
- PLoS ONE, 2015, v. 10, n. 3, p. 1, doi. 10.1371/journal.pone.0120545
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- Article