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The histone methyltransferase Wolf-Hirschhorn syndrome candidate 1-like 1 (WHSC1L1) is involved in human carcinogenesis.
- Published in:
- Genes, Chromosomes & Cancer, 2013, v. 52, n. 2, p. 126, doi. 10.1002/gcc.22012
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- Article
Sudden death in a case of megalencephaly capillary malformation associated with a de novo mutation in AKT3.
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- Child's Nervous System, 2015, v. 31, n. 3, p. 465, doi. 10.1007/s00381-014-2589-y
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- Article
Estimating transcription factor bindability on DNA.
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- Bioinformatics, 1999, v. 15, n. 7, p. 622, doi. 10.1093/bioinformatics/15.7.622
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- Article
Bigram-PGK: phosphoglycerylation prediction using the technique of bigram probabilities of position specific scoring matrix.
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- BMC Molecular & Cell Biology, 2019, p. 1, doi. 10.1186/s12860-019-0240-1
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- Article
A replication study confirmed the EDAR gene to be a major contributor to population differentiation regarding head hair thickness in Asia.
- Published in:
- Human Genetics, 2008, v. 124, n. 2, p. 179, doi. 10.1007/s00439-008-0537-1
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- Article
Calbindin 1, fibroblast growth factor 20, and α-synuclein in sporadic Parkinson’s disease.
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- Human Genetics, 2008, v. 124, n. 1, p. 89, doi. 10.1007/s00439-008-0525-5
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- Article
Polymorphisms in the 3′ UTR in the neurocalcin δ gene affect mRNA stability, and confer susceptibility to diabetic nephropathy.
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- Human Genetics, 2007, v. 122, n. 3/4, p. 397, doi. 10.1007/s00439-007-0414-3
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- Article
Performance comparison of four commercial human whole-exome capture platforms.
- Published in:
- Scientific Reports, 2015, p. 12742, doi. 10.1038/srep12742
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- Article
A combination of targeted enrichment methodologies for whole-exome sequencing reveals novel pathogenic mutations.
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- Scientific Reports, 2015, p. 9331, doi. 10.1038/srep09331
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- Article
A practical method to detect SNVs and indels from whole genome and exome sequencing data.
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- Scientific Reports, 2013, p. 1, doi. 10.1038/srep02161
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- Article
KIF1A mutation in a patient with progressive neurodegeneration.
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- Journal of Human Genetics, 2014, v. 59, n. 11, p. 639, doi. 10.1038/jhg.2014.80
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- Article
Identification of membrane-type matrix metalloproteinase-1 as a target of the β-catenin/Tcf4 complex in human colorectal cancers.
- Published in:
- Oncogene, 2002, v. 21, n. 38, p. 5861, doi. 10.1038/sj.onc.1205755
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- Article
Molecular diagnosis of colorectal tumors by expression profiles of 50 genes expressed differentially in adenomas and carcinomas.
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- Oncogene, 2002, v. 21, n. 26, p. 4120, doi. 10.1038/sj.onc.1205518
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- Article
Identification of AXUD1, a novel human gene induced by AXIN1 and its reduced expression in human carcinomas of the lung, liver, colon and kidney.
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- Oncogene, 2001, v. 20, n. 36, p. 5062, doi. 10.1038/sj.onc.1204603
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- Article
hzAnalyzer: detection, quantification, and visualization of contiguous homozygosity in high-density genotyping datasets.
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- Genome Biology, 2011, v. 12, n. 3, p. 1, doi. 10.1186/gb-2011-12-3-r21
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- Article
Arete - candidate gene prioritization using biological network topology with additional evidence types.
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- BioData Mining, 2017, v. 10, p. 1, doi. 10.1186/s13040-017-0141-9
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- Article
Improving succinylation prediction accuracy by incorporating the secondary structure via helix, strand and coil, and evolutionary information from profile bigrams.
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- PLoS ONE, 2018, v. 13, n. 2, p. 1, doi. 10.1371/journal.pone.0191900
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- Article
Gene masking - a technique to improve accuracy for cancer classification with high dimensionality in microarray data.
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- BMC Medical Genomics, 2016, v. 9, p. 261, doi. 10.1186/s12920-016-0233-2
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- Article
Effects of clovamide and its related compounds on the aggregations of amyloid polypeptides.
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- Journal of Natural Medicines, 2021, v. 75, n. 2, p. 299, doi. 10.1007/s11418-020-01467-w
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- Article
Association of solute carrier family 12 (sodium/chloride) member 3 with diabetic nephropathy, identified by genome-wide analyses of single nucleotide polymorphisms.
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- 2003
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- Publication type:
- journal 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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- Article
Pathway analysis of genome-wide data improves arfarin dose prediction.
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- BMC Genomics, 2013, v. 14, n. Suppl 3, p. 1, doi. 10.1186/1471-2164-14-S3-S11
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- Publication type:
- Article
Forecasting the spread of COVID-19 using LSTM network.
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- BMC Bioinformatics, 2021, v. 22, n. 1, p. 1, doi. 10.1186/s12859-021-04224-2
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- Article
SPECTRA: a tool for enhanced brain wave signal recognition.
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- BMC Bioinformatics, 2021, v. 22, n. 6, p. 1, doi. 10.1186/s12859-021-04091-x
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- Article
SumSec: Accurate Prediction of Sumoylation Sites Using Predicted Secondary Structure.
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- Molecules, 2018, v. 23, n. 12, p. 3260, doi. 10.3390/molecules23123260
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- Article
Integrative immunogenomic analysis of gastric cancer dictates novel immunological classification and the functional status of tumor‐infiltrating cells.
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- Clinical & Translational Immunology, 2020, v. 9, n. 10, p. 1, doi. 10.1002/cti2.1194
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- Article
Brain wave classification using long short-term memory network based OPTICAL predictor.
- Published in:
- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-45605-1
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- Article
PhoglyStruct: Prediction of phosphoglycerylated lysine residues using structural properties of amino acids.
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- Scientific Reports, 2018, v. 8, n. 1, p. 1, doi. 10.1038/s41598-018-36203-8
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- Publication type:
- Article
Gene expression dataset for whole cochlea of Macaca fascicularis.
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- Scientific Reports, 2018, v. 8, n. 1, p. 1, doi. 10.1038/s41598-018-33985-9
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- Article
Genetic differences in the two main groups of the Japanese population based on autosomal SNPs and haplotypes.
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- Journal of Human Genetics, 2012, v. 57, n. 5, p. 326, doi. 10.1038/jhg.2012.26
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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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- Article
Common variants on 14q32 and 13q12 are associated with DLBCL susceptibility.
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- Journal of Human Genetics, 2011, v. 56, n. 6, p. 436, doi. 10.1038/jhg.2011.35
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- Article
SNPs on chromosome 5p15.3 associated with myocardial infarction in Japanese population.
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- Journal of Human Genetics, 2011, v. 56, n. 1, p. 47, doi. 10.1038/jhg.2010.141
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- Article
Making a haplotype catalog with estimated frequencies based on SNP homozygotes.
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- Journal of Human Genetics, 2010, v. 55, n. 8, p. 500, doi. 10.1038/jhg.2010.56
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- Article
FGFR2 is associated with hair thickness in Asian populations.
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- Journal of Human Genetics, 2009, v. 54, n. 8, p. 461, doi. 10.1038/jhg.2009.61
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- Article
Combinational effect of genes for the renin–angiotensin system in conferring susceptibility to diabetic nephropathy.
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- Journal of Human Genetics, 2007, v. 52, n. 2, p. 143, doi. 10.1007/s10038-006-0090-5
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- Article
A genomewide linkage analysis of Kawasaki disease: evidence for linkage to chromosome 12.
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- Journal of Human Genetics, 2007, v. 52, n. 2, p. 179, doi. 10.1007/s10038-006-0092-3
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- Article
Association study of COL9A2 with lumbar disc disease in the Japanese population.
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- Journal of Human Genetics, 2006, v. 51, n. 12, p. 1063, doi. 10.1007/s10038-006-0062-9
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- Article
Genetic variations in the gene encoding TFAP2B are associated with type 2 diabetes mellitus.
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- Journal of Human Genetics, 2005, v. 50, n. 6, p. 283, doi. 10.1007/s10038-005-0253-9
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- Article
Association of a single-nucleotide polymorphism in the immunoglobulin µ-binding protein 2 gene with immunoglobulin A nephropathy.
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- Journal of Human Genetics, 2005, v. 50, n. 1, p. 30, doi. 10.1007/s10038-004-0214-8
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- Publication type:
- Article
Association of single-nucleotide polymorphisms in the polymeric immunoglobulin receptor gene with immunoglobulin A nephropathy (IgAN) in Japanese patients.
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- Journal of Human Genetics, 2003, v. 48, n. 6, p. 293, doi. 10.1007/s10038-003-0027-1
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- Article
Expression profiles of two types of human knee-joint cartilage.
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- Journal of Human Genetics, 2003, v. 48, n. 4, p. 177, doi. 10.1007/s10038-003-0004-8
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- Article
Genome-wide association study identifies three novel loci for type 2 diabetes.
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- Human Molecular Genetics, 2014, v. 23, n. 1, p. 239
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- Publication type:
- Article
A single-nucleotide polymorphism in ANK1 is associated with susceptibility to type 2 diabetes in Japanese populations.
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- Human Molecular Genetics, 2012, v. 21, n. 13, p. 3042
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- Article
IRX4 at 5p15 suppresses prostate cancer growth through the interaction with vitamin D receptor, conferring prostate cancer susceptibility.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 9, p. 2076, doi. 10.1093/hmg/dds025
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- Article
A genome-wide association study identifies locus at 10q22 associated with clinical outcomes of adjuvant tamoxifen therapy for breast cancer patients in Japanese.
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- Human Molecular Genetics, 2012, v. 21, n. 7, p. 1665, doi. 10.1093/hmg/ddr597
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- Article
A genome-wide association study of chronic hepatitis B identified novel risk locus in a Japanese population.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 19, p. 3884, doi. 10.1093/hmg/ddr301
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- Article
A functional variant in ZNF512B is associated with susceptibility to amyotrophic lateral sclerosis in Japanese.
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- Human Molecular Genetics, 2011, v. 20, n. 18, p. 3684, doi. 10.1093/hmg/ddr268
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- Article
Genome-wide association study for C-reactive protein levels identified pleiotropic associations in the IL6 locus.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 6, p. 1224, doi. 10.1093/hmg/ddq551
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- Article
Population-genetic nature of copy number variations in the human genome.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. 5, p. 761, doi. 10.1093/hmg/ddp541
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- Article