Found: 16
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Genetic interaction mapping and exon-resolution functional genomics with a hybrid Cas9–Cas12a platform.
- Published in:
- Nature Biotechnology, 2020, v. 38, n. 5, p. 638, doi. 10.1038/s41587-020-0437-z
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- Article
Germ-line DNA copy number variation frequencies in a large North American population.
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- Human Genetics, 2007, v. 122, n. 3/4, p. 345, doi. 10.1007/s00439-007-0404-5
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- Article
Comparison of Affymetrix Gene Array with the Exon Array shows potential application for detection of transcript isoform variation.
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- BMC Genomics, 2009, v. 10, p. 519, doi. 10.1186/1471-2164-10-519
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- Article
Engineering of a miniaturized, robotic clinical laboratory.
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- Bioengineering & Translational Medicine, 2018, v. 3, n. 1, p. 58, doi. 10.1002/btm2.10084
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- Article
A Newly Synthesized Tris(crown ether) Ionophore for Assisted Ion Transfer at NanoITIES Electrodes.
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- ChemElectroChem, 2020, v. 7, n. 4, p. 967, doi. 10.1002/celc.201901997
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- Article
Macropinocytosis Exploitation by Cancers and Cancer Therapeutics.
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- Frontiers in Physiology, 2016, p. 1, doi. 10.3389/fphys.2016.00381
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- Article
Transfusion-Transmitted Cache Valley Virus Infection in a Kidney Transplant Recipient With Meningoencephalitis.
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- Clinical Infectious Diseases, 2023, v. 76, n. 3, p. e1320, doi. 10.1093/cid/ciac566
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- Article
Encapsulated relapsed FLT3+AML (myeloid sarcoma) and Hürthle cell adenoma presenting in composite: Unlikely partners.
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- American Journal of Hematology, 2016, v. 91, n. 12, p. E505, doi. 10.1002/ajh.24558
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- Article
Identifying human pre-mRNA cleavage and polyadenylation factors by genome-wide CRISPR screens using a dual fluorescence readthrough reporter.
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- Nucleic Acids Research, 2024, v. 52, n. 8, p. 4483, doi. 10.1093/nar/gkae240
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- Article
QAPA: a new method for the systematic analysis of alternative polyadenylation from RNA-seq data.
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- Genome Biology, 2018, v. 19, p. 1, doi. 10.1186/s13059-018-1414-4
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- Article
Novel Mutations in SCO1 as a Cause of Fatal Infantile Encephalopathy and Lactic Acidosis.
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- Human Mutation, 2013, v. 34, n. 10, p. 1366, doi. 10.1002/humu.22385
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- Article
Unexpected allelic heterogeneity and spectrum of mutations in Fowler syndrome revealed by next-generation exome sequencing.
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- Human Mutation, 2010, v. 31, n. 8, p. 918, doi. 10.1002/humu.21293
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- Article
A Case of Tick-Borne Paralysis in a Traveling Patient.
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- Case Reports in Neurological Medicine, 2019, p. 1, doi. 10.1155/2019/3934696
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- Article
The RNA-binding protein SERBP1 functions as a novel oncogenic factor in glioblastoma by bridging cancer metabolism and epigenetic regulation.
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- Genome Biology, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s13059-020-02115-y
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- Article
Methicillin‐resistant Staphylococcus aureus and Pseudomonas aeruginosa community acquired pneumonia: Prevalence and locally derived risk factors in a single hospital system.
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- Journal of the American College of Emergency Physicians Open, 2023, v. 4, n. 6, p. 1, doi. 10.1002/emp2.13061
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- Article
Differential contribution of transcriptomic regulatory layers in the definition of neuronal identity.
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- Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-020-20483-8
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- Article