Trends in Pharmacological Sciences, Journal Year: 2019, Volume and Issue: 40(2), P. 128 - 141
Published: Jan. 3, 2019
Language: Английский
Trends in Pharmacological Sciences, Journal Year: 2019, Volume and Issue: 40(2), P. 128 - 141
Published: Jan. 3, 2019
Language: Английский
Nature, Journal Year: 2017, Volume and Issue: 547(7664), P. 453 - 457
Published: July 1, 2017
Language: Английский
Citations
1565Experimental & Molecular Medicine, Journal Year: 2018, Volume and Issue: 50(8), P. 1 - 14
Published: Aug. 1, 2018
Rapid progress in the development of next-generation sequencing (NGS) technologies recent years has provided many valuable insights into complex biological systems, ranging from cancer genomics to diverse microbial communities. NGS-based for genomics, transcriptomics, and epigenomics are now increasingly focused on characterization individual cells. These single-cell analyses will allow researchers uncover new potentially unexpected discoveries relative traditional profiling methods that assess bulk populations. Single-cell RNA (scRNA-seq), example, can reveal rare cell populations, regulatory relationships between genes, track trajectories distinct lineages development. In this review, we focus technical challenges isolation library preparation computational analysis pipelines available analyzing scRNA-seq data. Further improvements at level molecular biology bioinformatics tools greatly facilitate both basic science medical applications these technologies. Showing which genes expressed, or switched on, cells may help first signs disease. Each an organism contains same genetic information, but type behavior depend expressed. Previously, could only sequence batches, averaging results, technological expressed cell, known as (scRNA-seq). Ji Hyun Lee (Kyung Hee University, Seoul) Duhee Bang Byungjin Hwang (Yonsei have reviewed strategies analyze large quantities data produced. They conclude impact science, illuminating drug resistance revealing pathways differentiation during
Language: Английский
Citations
1555Nature, Journal Year: 2017, Volume and Issue: 551(7679), P. 247 - 250
Published: Oct. 31, 2017
Language: Английский
Citations
1352Nature Cell Biology, Journal Year: 2018, Volume and Issue: 20(8), P. 888 - 899
Published: July 19, 2018
Language: Английский
Citations
828Cancer Cell, Journal Year: 2018, Volume and Issue: 33(5), P. 890 - 904.e5
Published: April 12, 2018
Language: Английский
Citations
800Cancer Cell, Journal Year: 2020, Volume and Issue: 37(4), P. 471 - 484
Published: April 1, 2020
Language: Английский
Citations
725Nature Methods, Journal Year: 2018, Volume and Issue: 15(7), P. 539 - 542
Published: June 22, 2018
Language: Английский
Citations
695Cell, Journal Year: 2018, Volume and Issue: 174(4), P. 843 - 855.e19
Published: July 13, 2018
Language: Английский
Citations
637International Journal of Molecular Sciences, Journal Year: 2020, Volume and Issue: 21(3), P. 1102 - 1102
Published: Feb. 7, 2020
Mitogen-activated protein kinase (MAPK) pathways represent ubiquitous signal transduction that regulate all aspects of life and are frequently altered in disease. Here, we focus on the role MAPK modulating drug sensitivity resistance cancer. We briefly discuss new findings extracellular signaling-regulated (ERK) pathway, but mainly mechanisms how stress activated pathways, such as p38 Jun N-terminal kinases (JNK), impact response cancer cells to chemotherapies targeted therapies. In this context, also metabolic epigenetic aberrations therapeutic opportunities arising from these changes.
Language: Английский
Citations
637Nature Reviews Drug Discovery, Journal Year: 2019, Volume and Issue: 19(1), P. 39 - 56
Published: Oct. 10, 2019
Language: Английский
Citations
603