Found: 16
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CCL2 enhances pluripotency of human induced pluripotent stem cells by activating hypoxia related genes.
- Published in:
- Scientific Reports, 2014, p. 1, doi. 10.1038/srep05228
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- Publication type:
- Article
Common and Rare Genetic Variants That Could Contribute to Severe Otitis Media in an Australian Aboriginal Population.
- Published in:
- Clinical Infectious Diseases, 2021, v. 73, n. 10, p. 1860, doi. 10.1093/cid/ciab216
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- Publication type:
- Article
Analysis of the complement and molecular evolution of tRNA genes in cow.
- Published in:
- BMC Genomics, 2009, v. 10, p. 1, doi. 10.1186/1471-2164-10-188
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- Publication type:
- Article
Site-specific DICER and DROSHA RNA products control the DNA-damage response.
- Published in:
- Nature, 2012, v. 488, n. 7410, p. 231, doi. 10.1038/nature11179
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- Publication type:
- Article
A novel, homozygous mutation in <italic>desert hedgehog</italic> (<italic>DHH</italic>) in a 46, XY patient with dysgenetic testes presenting with primary amenorrhoea: a case report.
- Published in:
- 2018
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- Publication type:
- Case Study
Short stature and hypoparathyroidism in a child with Kenny-Caffey syndrome type 2 due to a novel mutation in FAM111A gene.
- Published in:
- International Journal of Pediatric Endocrinology, 2017, v. 2017, p. 1, doi. 10.1186/s13633-016-0041-7
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- Publication type:
- Article
Identification of Anchor Genes during Kidney Development Defines Ontological Relationships, Molecular Subcompartments and Regulatory Pathways.
- Published in:
- PLoS ONE, 2011, v. 6, n. 2, p. 1, doi. 10.1371/journal.pone.0017286
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- Publication type:
- Article
A Genome Wide Survey of SNP Variation Reveals the Genetic Structure of Sheep Breeds.
- Published in:
- PLoS ONE, 2009, v. 4, n. 3, p. 1, doi. 10.1371/journal.pone.0004668
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- Publication type:
- Article
High expression of insulin receptor on tumour-associated blood vessels in invasive bladder cancer predicts poor overall and progression-free survival.
- Published in:
- Journal of Pathology, 2017, v. 242, n. 2, p. 193, doi. 10.1002/path.4892
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- Publication type:
- Article
The rare and undiagnosed diseases diagnostic service - application of massively parallel sequencing in a state-wide clinical service.
- Published in:
- 2016
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- Publication type:
- journal article
A flexible computational pipeline for research analyses of unsolved clinical exome cases.
- Published in:
- NPJ Genomic Medicine, 2020, v. 5, n. 1, p. 1, doi. 10.1038/s41525-020-00161-w
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- Publication type:
- Article
The bone marrow microenvironment of pre-B acute lymphoblastic leukemia at single-cell resolution.
- Published in:
- Scientific Reports, 2020, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41598-020-76157-4
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- Publication type:
- Article
Suppression of artifacts and barcode bias in high-throughput transcriptome analyses utilizing template switching.
- Published in:
- Nucleic Acids Research, 2013, v. 41, n. 3, p. e44, doi. 10.1093/nar/gks1128
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- Publication type:
- Article
RNA-MATE: a recursive mapping strategy for high-throughput RNA-sequencing data.
- Published in:
- Bioinformatics, 2009, v. 25, n. 19, p. 2615, doi. 10.1093/bioinformatics/btp459
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- Publication type:
- Article
piRNAs warrant investigation in Rett Syndrome: An omics perspective.
- Published in:
- Disease Markers, 2012, v. 33, n. 5, p. 261, doi. 10.1155/2012/396737
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- Publication type:
- Article
A human minisatellite hosts an alternative transcription start site for NPRL3 driving its expression in a repeat number‐dependent manner.
- Published in:
- Human Mutation, 2020, v. 41, n. 4, p. 807, doi. 10.1002/humu.23974
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- Publication type:
- Article