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Recurrent exon-deleting activating mutations in AHR act as drivers of urinary tract cancer.
- Published in:
- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-14256-0
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- Article
Common anti-cancer therapies induce somatic mutations in stem cells of healthy tissue.
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- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-33663-5
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- Publication type:
- Article
Machine learning-based tissue of origin classification for cancer of unknown primary diagnostics using genome-wide mutation features.
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- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-31666-w
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- Article
Pluripotency in the light of the developmental hourglass.
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- Biological Reviews, 2015, v. 90, n. 2, p. 428, doi. 10.1111/brv.12117
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- Article
Feasibility of whole‐genome sequencing‐based tumor diagnostics in routine pathology practice.
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- Journal of Pathology, 2022, v. 258, n. 2, p. 179, doi. 10.1002/path.5988
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- Article
Precancerous liver diseases do not cause increased mutagenesis in liver stem cells.
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- Communications Biology, 2021, v. 4, n. 1, p. 1, doi. 10.1038/s42003-021-02839-y
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- Article
Mlh1 Deficiency in Zebrafish Results in Male Sterility and Aneuploid as Well as Triploid Progeny in Females.
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- Genetics, 2007, v. 175, n. 4, p. 1561, doi. 10.1534/genetics.106.068171
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- Article
Identification of a Rat Model for Usher Syndrome Type 1B by N-Ethyl-N-nitrosourea Mutagenesis-Driven Forward Genetics.
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- Genetics, 2005, v. 170, n. 4, p. 1887, doi. 10.1534/genetics.105.044222
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- Article
The G-Protein Beta-Subunit GPB-2 in Caenorhabditis elegans Regulates the...
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- Genetics, 2001, v. 158, n. 1, p. 221, doi. 10.1093/genetics/158.1.221
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- Article
The genome-wide mutational consequences of DNA hypomethylation.
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- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-33932-3
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- Article
Genome-wide analysis reveals NRP1 as a direct HIF1α-E2F7 target in the regulation of motorneuron guidance in vivo.
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- Nucleic Acids Research, 2016, v. 44, n. 8, p. 3549, doi. 10.1093/nar/gkv1471
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- Article
E2F7 represses a network of oscillating cell cycle genes to control S-phase progression.
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- Nucleic Acids Research, 2012, v. 40, n. 8, p. 3511, doi. 10.1093/nar/gkr1203
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- Article
Integrated genome-wide analysis of transcription factor occupancy, RNA polymerase II binding and steady-state RNA levels identify differentially regulated functional gene classes.
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- Nucleic Acids Research, 2012, v. 40, n. 1, p. 148, doi. 10.1093/nar/gkr720
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- Publication type:
- Article
Accurate SNP and mutation detection by targeted custom microarray-based genomic enrichment of short-fragment sequencing libraries.
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- Nucleic Acids Research, 2010, v. 38, n. 10, p. e116, doi. 10.1093/nar/gkq072
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- Article
Alkylation damage causes MMR-dependent chromosomal instability in vertebrate embryos.
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- Nucleic Acids Research, 2008, v. 36, n. 12, p. 4047, doi. 10.1093/nar/gkn341
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- Article
Mouse microRNA profiles determined with a new and sensitive cloning method.
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- Nucleic Acids Research, 2006, v. 34, n. 17, p. e115, doi. 10.1093/nar/gkl653
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- Article
The genomic landscape of 85 advanced neuroendocrine neoplasms reveals subtype-heterogeneity and potential therapeutic targets.
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- Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-021-24812-3
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- Publication type:
- Article
Learning mutational signatures and their multidimensional genomic properties with TensorSignatures.
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- Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-021-23551-9
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- Article
Author Correction: Whole genome sequencing of metastatic colorectal cancer reveals prior treatment effects and specific metastasis features.
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- 2021
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- Correction Notice
Expanding the spectrum of phenotypes associated with germline PIGA mutations: A child with developmental delay, accelerated linear growth, facial dysmorphisms, elevated alkaline phosphatase, and progressive CNS abnormalities.
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- American Journal of Medical Genetics. Part A, 2014, v. 164A, n. 1, p. 29, doi. 10.1002/ajmg.a.36184
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- Article
Tubuloids derived from human adult kidney and urine for personalized disease modeling.
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- Nature Biotechnology, 2019, v. 37, n. 3, p. 303, doi. 10.1038/s41587-019-0048-8
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- Article
Toward effective software solutions for big biology.
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- Nature Biotechnology, 2015, v. 33, n. 7, p. 686, doi. 10.1038/nbt.3240
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- Article
SNP and haplotype mapping for genetic analysis in the rat.
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- Nature Genetics, 2008, v. 40, n. 5, p. 560, doi. 10.1038/ng.124
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- Article
Distribution and functional impact of DNA copy number variation in the rat.
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- Nature Genetics, 2008, v. 40, n. 5, p. 538, doi. 10.1038/ng.141
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- Article
Progress and prospects in rat genetics: a community view.
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- Nature Genetics, 2008, v. 40, n. 5, p. 516, doi. 10.1038/ng.147
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- Article
Diversity of microRNAs in human and chimpanzee brain.
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- Nature Genetics, 2006, v. 38, n. 12, p. 1375, doi. 10.1038/ng1914
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- Article
Approaches to microRNA discovery.
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- Nature Genetics, 2006, v. 38, p. S2, doi. 10.1038/ng1794
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- Article
The microRNA-producing enzyme Dicer1 is essential for zebrafish development.
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- Nature Genetics, 2003, v. 35, n. 3, p. 217, doi. 10.1038/ng1251
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- Article
Mutation discovery by targeted genomic enrichment of multiplexed barcoded samples.
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- Nature Methods, 2010, v. 7, n. 11, p. 913, doi. 10.1038/nmeth.1516
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- Article
Limitations and possibilities of small RNA digital gene expression profiling.
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- 2009
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- Publication type:
- Letter
A novel Dock8 gene mutation confers diabetogenic susceptibility in the LEW.1AR1/Ztm- iddm rat, an animal model of human type 1 diabetes.
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- Diabetologia, 2015, v. 58, n. 12, p. 2800, doi. 10.1007/s00125-015-3757-7
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- Article
VIRUSBreakend: Viral Integration Recognition Using Single Breakends.
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- Bioinformatics, 2021, v. 37, n. 19, p. 3115, doi. 10.1093/bioinformatics/btab343
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- Article
Generation and characterization of rat liver stem cell lines and their engraftment in a rat model of liver failure.
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- Scientific Reports, 2016, p. 22154, doi. 10.1038/srep22154
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- Article
GRIDSS2: comprehensive characterisation of somatic structural variation using single breakend variants and structural variant phasing.
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- Genome Biology, 2021, v. 22, p. 1, doi. 10.1186/s13059-021-02423-x
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- Article
Lack of Major Genome Instability in Tumors of p53 Null Rats.
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- PLoS ONE, 2015, v. 10, n. 3, p. 1, doi. 10.1371/journal.pone.0122066
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- Article
Genetic Etiology of Renal Agenesis: Fine Mapping of Renag1 and Identification of Kit as the Candidate Functional Gene.
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- PLoS ONE, 2015, v. 10, n. 2, p. 1, doi. 10.1371/journal.pone.0118147
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- Article
<i>Pmch</i>-Deficiency in Rats Is Associated with Normal Adipocyte Differentiation and Lower Sympathetic Adipose Drive.
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- PLoS ONE, 2013, v. 8, n. 3, p. 1, doi. 10.1371/journal.pone.0060214
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- Article
A Deep Sequencing Approach to Uncover the miRNOME in the Human Heart.
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- PLoS ONE, 2013, v. 8, n. 2, p. 1, doi. 10.1371/journal.pone.0057800
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- Publication type:
- Article
miR-127 Protects Proximal Tubule Cells against Ischemia/Reperfusion: Identification of Kinesin Family Member 3B as miR-127 Target.
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- PLoS ONE, 2012, v. 7, n. 9, p. 1, doi. 10.1371/journal.pone.0044305
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- Article
A Functional Screen Identifies Specific MicroRNAs Capable of Inhibiting Human Melanoma Cell Viability.
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- PLoS ONE, 2012, v. 7, n. 8, p. 1, doi. 10.1371/journal.pone.0043569
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- Article
The ter Mutation in the Rat Dnd1 Gene Initiates Gonadal Teratomas and Infertility in Both Genders.
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- PLoS ONE, 2012, v. 7, n. 5, p. 1, doi. 10.1371/journal.pone.0038001
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- Article
Chronic Loss of Melanin-Concentrating Hormone Affects Motivational Aspects of Feeding in the Rat.
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- PLoS ONE, 2011, v. 6, n. 5, p. 1, doi. 10.1371/journal.pone.0019600
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- Article
An ENU-Mutagenesis Screen in the Mouse: Identification of Novel Developmental Gene Functions.
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- PLoS ONE, 2011, v. 6, n. 4, p. 1, doi. 10.1371/journal.pone.0019357
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- Article
A Mutation in Myo15 Leads to Usher-Like Symptoms in LEW/Ztm-ci2 Rats.
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- PLoS ONE, 2011, v. 6, n. 3, p. 1, doi. 10.1371/journal.pone.0015669
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- Publication type:
- Article
Efficient Double Fragmentation ChIP-seq Provides Nucleotide Resolution Protein-DNA Binding Profiles.
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- PLoS ONE, 2010, v. 5, n. 11, p. 1, doi. 10.1371/journal.pone.0015092
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- Publication type:
- Article
Study protocol of the GLOW study: maximising treatment options for recurrent glioblastoma patients by whole genome sequencing-based diagnostics—a prospective multicenter cohort study.
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- BMC Medical Genomics, 2022, v. 15, n. 1, p. 1, doi. 10.1186/s12920-022-01343-4
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- Publication type:
- Article
Multi-omic analysis identifies hypoalbuminemia as independent biomarker of poor outcome upon PD-1 blockade in metastatic melanoma.
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- Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-61150-y
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- Article
The genomic landscape of metastatic castration-resistant prostate cancers reveals multiple distinct genotypes with potential clinical impact.
- Published in:
- Nature Communications, 2019, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41467-019-13084-7
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- Article
5-Fluorouracil treatment induces characteristic T>G mutations in human cancer.
- Published in:
- Nature Communications, 2019, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41467-019-12594-8
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- Publication type:
- Article
Genomic Alterations Associated with Estrogen Receptor Pathway Activity in Metastatic Breast Cancer Have a Differential Impact on Downstream ER Signaling.
- Published in:
- Cancers, 2023, v. 15, n. 17, p. 4416, doi. 10.3390/cancers15174416
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- Article