Found: 109
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Strain level microbial detection and quantification with applications to single cell metagenomics.
- Published in:
- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-33869-7
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- Article
The landscape of receptor-mediated precision cancer combination therapy via a single-cell perspective.
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- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-29154-2
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- Article
The Genetics of Hypogammaglobulinemia.
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- Current Allergy & Asthma Reports, 2004, v. 4, n. 5, p. 349, doi. 10.1007/s11882-004-0083-4
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- Article
Clinical and Laboratory Features in the Israeli Population with COVID-19 Infection after Pfizer-BioNTech mRNA Booster Vaccination.
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- Vaccines, 2022, v. 10, n. 5, p. 636, doi. 10.3390/vaccines10050636
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- Article
Large-Scale Study of Antibody Titer Decay following BNT162b2 mRNA Vaccine or SARS-CoV-2 Infection.
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- Vaccines, 2022, v. 10, n. 1, p. 64, doi. 10.3390/vaccines10010064
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- Article
Defining and Mapping Mammalian Coat Pattern Genes: Multiple Genomic Regions Implicated in Domestic Cat Stripes and Spots.
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- Genetics, 2010, v. 184, n. 1, p. 267, doi. 10.1534/genetics.109.109629
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- Article
A Domestic cat X Chromosome Linkage Map and the Sex-Linked orange Locus: Mapping of orange, Multiple Origins and Epistasis Over nonagouti.
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- Genetics, 2009, v. 181, n. 4, p. 1415, doi. 10.1534/genetics.108.095240
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- Article
Single-cell resolved ploidy and chromosomal aberrations in nonalcoholic steatohepatitis-(NASH) induced hepatocellular carcinoma and its precursor lesions.
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- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-27173-z
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- Article
Refinement of the gene locus for autosomal recessive juvenile parkinsonism (AR-JP) on chromosome 6q25.2-27 and identification of markers exhibiting linkage disequilibrium.
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- Journal of Human Genetics, 1998, v. 43, n. 1, p. 22, doi. 10.1007/s100380050032
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- Article
Virus Variation Resource - improved response to emergent viral outbreaks.
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- Nucleic Acids Research, 2017, v. 45, n. D1, p. D482, doi. 10.1093/nar/gkw1065
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- Article
Potential non-B DNA regions in the human genome are associated with higher rates of nucleotide mutation and expression variation.
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- Nucleic Acids Research, 2014, v. 42, n. 20, p. 12367, doi. 10.1093/nar/gku921
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- Article
PSI-BLAST pseudocounts and the minimum description length principle.
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- Nucleic Acids Research, 2009, v. 37, n. 3, p. 815, doi. 10.1093/nar/gkn981
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- Article
Retrieval accuracy, statistical significance and compositional similarity in protein sequence database searches.
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- Nucleic Acids Research, 2006, v. 34, n. 20, p. 5966, doi. 10.1093/nar/gkl731
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- Publication type:
- Article
The landscape of receptor-mediated precision cancer combination therapy via a single-cell perspective.
- Published in:
- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-29154-2
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- Publication type:
- Article
Reduced Incidence of Hip Fracture in the Old Order Amish.
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- Journal of Bone & Mineral Research, 2004, v. 19, n. 2, p. 308, doi. 10.1359/JBMR.0301223
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- Article
Autosomal dominant immune dysregulation syndrome in humans with CTLA4 mutations.
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- Nature Medicine, 2014, v. 20, n. 12, p. 1410, doi. 10.1038/nm.3746
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- Article
A novel human primary immunodeficiency syndrome caused by deficiency of the endosomal adaptor protein p14.
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- Nature Medicine, 2007, v. 13, n. 1, p. 38, doi. 10.1038/nm1528
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- Article
JAGN1 deficiency causes aberrant myeloid cell homeostasis and congenital neutropenia.
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- Nature Genetics, 2014, v. 46, n. 9, p. 1021, doi. 10.1038/ng.3069
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- Article
HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease).
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- Nature Genetics, 2007, v. 39, n. 1, p. 86, doi. 10.1038/ng1940
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- Article
Mutant deoxynucleotide carrier is associated with congenital microcephaly.
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- Nature Genetics, 2002, v. 32, n. 1, p. 175, doi. 10.1038/ng948
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- Article
Screening of functional and positional candidate genes in families with common variable immunodeficiency.
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- BMC Immunology, 2008, v. 9, p. 1, doi. 10.1186/1471-2172-9-3
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- Article
Integration of adeno-associated virus (AAV) into the genomes of most Thai and Mongolian liver cancer patients does not induce oncogenesis.
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- BMC Genomics, 2021, v. 22, n. 1, p. 1, doi. 10.1186/s12864-021-08098-9
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- Article
Protein database searches using compositionally adjusted substitution matrices.
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- FEBS Journal, 2005, v. 272, n. 20, p. 5101, doi. 10.1111/j.1742-4658.2005.04945.x
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- Article
Aneuploidy, <italic>TP53</italic> mutation, and amplification of <italic>MYC</italic> correlate with increased intratumor heterogeneity and poor prognosis of breast cancer patients.
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- Genes, Chromosomes & Cancer, 2018, v. 57, n. 4, p. 165, doi. 10.1002/gcc.22515
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- Article
Tumor heterogeneity assessed by sequencing and fluorescence in situ hybridization (FISH) data.
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- Bioinformatics, 2021, v. 37, n. 24, p. 4704, doi. 10.1093/bioinformatics/btab504
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- Article
Four Independent Mutations in the Feline Fibroblast Growth Factor 5 Gene Determine the Long-Haired Phenotype in Domestic Cats.
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- Journal of Heredity, 2007, v. 98, n. 6, p. 555, doi. 10.1093/jhered/esm072
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- Article
Mutation in CEP290 Discovered for Cat Model of Human Retinal Degeneration.
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- Journal of Heredity, 2007, v. 98, n. 3, p. 211, doi. 10.1093/jhered/esm019
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- Article
Outcome differences by sex in oncology clinical trials.
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- Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-46945-x
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- Article
Genome-wide DNA methylation profiling of HPV-negative leukoplakia and gingivobuccal complex cancers.
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- Clinical Epigenetics, 2023, v. 15, n. 1, p. 1, doi. 10.1186/s13148-023-01510-z
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- Article
An Integrative CGH, MSI and Candidate Genes Methylation Analysis of Colorectal Tumors.
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- PLoS ONE, 2014, v. 9, n. 1, p. 1, doi. 10.1371/journal.pone.0082185
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- Article
Living the Good Life? Mortality and Hospital Utilization Patterns in the Old Order Amish.
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- PLoS ONE, 2012, v. 7, n. 12, p. 1, doi. 10.1371/journal.pone.0051560
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- Article
Genomic Aberrations in an African American Colorectal Cancer Cohort Reveals a MSI-Specific Profile and Chromosome X Amplification in Male Patients.
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- PLoS ONE, 2012, v. 7, n. 8, p. 1, doi. 10.1371/journal.pone.0040392
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- Article
Case-Control Study of Vitamin D, dickkopf homolog 1 (DKK1) Gene Methylation, VDR Gene Polymorphism and the Risk of Colon Adenoma in African Americans.
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- PLoS ONE, 2011, v. 6, n. 10, p. 1, doi. 10.1371/journal.pone.0025314
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- Article
Genomic Profiling of Advanced-Stage Oral Cancers Reveals Chromosome 11q Alterations as Markers of Poor Clinical Outcome.
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- PLoS ONE, 2011, v. 6, n. 2, p. 1, doi. 10.1371/journal.pone.0017250
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- Article
Distinct Genetic Alterations in Colorectal Cancer.
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- PLoS ONE, 2010, v. 5, n. 1, p. 1, doi. 10.1371/journal.pone.0008879
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- Article
Characterization of Oncology Clinical Trials Using Germline Genetic Data.
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- JAMA Network Open, 2022, v. 5, n. 11, p. e2242370, doi. 10.1001/jamanetworkopen.2022.42370
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- Article
Linkage analysis of a large African family segregating stuttering suggests polygenic inheritance.
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- Human Genetics, 2013, v. 132, n. 4, p. 385, doi. 10.1007/s00439-012-1252-5
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- Article
Genetic alterations in caspase-10 may be causative or protective in autoimmune lymphoproliferative syndrome.
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- Human Genetics, 2006, v. 119, n. 3, p. 284, doi. 10.1007/s00439-006-0138-9
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- Article
Analysis of families with common variable immunodeficiency (CVID) and IgA deficiency suggests linkage of CVID to chromosome 16q.
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- Human Genetics, 2006, v. 118, n. 6, p. 725, doi. 10.1007/s00439-005-0101-1
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- Article
A genome-wide scan for primary open-angle glaucoma (POAG): the Barbados Family Study of Open-Angle Glaucoma.
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- Human Genetics, 2003, v. 112, n. 5/6, p. 600, doi. 10.1007/s00439-003-0910-z
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- Article
Identification of drugs associated with reduced severity of COVID-19 – a casecontrol study in a large population.
- Published in:
- eLife, 2021, p. 1, doi. 10.7554/eLife.68165
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- Article
Pan-Cancer Analysis of Patient Tumor Single-Cell Transcriptomes Identifies Promising Selective and Safe Chimeric Antigen Receptor Targets in Head and Neck Cancer.
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- Cancers, 2023, v. 15, n. 19, p. 4885, doi. 10.3390/cancers15194885
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- Article
Sex Biases in Cancer and Autoimmune Disease Incidence Are Strongly Positively Correlated with Mitochondrial Gene Expression across Human Tissues.
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- Cancers, 2022, v. 14, n. 23, p. 5885, doi. 10.3390/cancers14235885
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On the statistical properties of family-based association tests in datasets containing both pedigrees and unrelated case-control samples.
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- European Journal of Human Genetics, 2012, v. 20, n. 2, p. 217, doi. 10.1038/ejhg.2011.173
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- Article
Linkage of autosomal-dominant common variable immunodeficiency to chromosome 4q.
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- European Journal of Human Genetics, 2006, v. 14, n. 7, p. 867, doi. 10.1038/sj.ejhg.5201634
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- Article
Evaluating annotations of an Agilent expression chip suggests that many features cannot be interpreted.
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- BMC Genomics, 2009, v. 10, p. 566, doi. 10.1186/1471-2164-10-566
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- Article
A Calculator for COVID-19 Severity Prediction Based on Patient Risk Factors and Number of Vaccines Received.
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- Microorganisms, 2022, v. 10, n. 6, p. 1238, doi. 10.3390/microorganisms10061238
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- Article
Glucose-6-phosphate dehydrogenase deficiency and long-term risk of immune-related disorders.
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- Frontiers in Immunology, 2023, p. 1, doi. 10.3389/fimmu.2023.1232560
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- Article
Improving the accuracy of PSI-BLAST protein database searches with composition-based statistics and other refinements.
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- Nucleic Acids Research, 2001, v. 29, n. 14, p. 2994, doi. 10.1093/nar/29.14.2994
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- Article
Protein sequence similarity searches using patterns as seeds.
- Published in:
- Nucleic Acids Research, 1998, v. 26, n. 17, p. 3986, doi. 10.1093/nar/26.17.3986
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- Article