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Published in 2018 at "International Journal of Cancer"
DOI: 10.1002/ijc.31351
Abstract: Emerging evidence indicates that germline variations may interact with somatic events in carcinogenesis. However, the germline–somatic interaction in lung cancer remains largely unknown. We investigated whether lung cancer driver genes (CDGs) were more likely to…
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Keywords:
susceptibility;
analysis;
lung cancer;
cancer ... See more keywords
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Published in 2020 at "Nature Medicine"
DOI: 10.1038/s41591-020-0839-y
Abstract: PD-1 blockade has transformed the management of advanced clear cell renal cell carcinoma (ccRCC), but the drivers and resistors of the PD-1 response remain incompletely elucidated. Here, we analyzed 592 tumors from patients with advanced…
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Keywords:
renal cell;
response;
infiltration;
blockade ... See more keywords
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Published in 2019 at "Annals of Oncology"
DOI: 10.1093/annonc/mdz431.012
Abstract: Abstract Background Perturbations in key driver genes or recurrently somatic mutated genes, as well as altered signaling pathways underlying pancreatic cancer have been largely discovered with the help of massive parallel sequencing. However, to date,…
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Keywords:
clinical features;
whole exome;
pancreatic cancer;
cancer ... See more keywords
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Published in 2021 at "GigaScience"
DOI: 10.1093/gigascience/giab036
Abstract: Abstract Background Multi-region sequencing (MRS) has been widely used to analyze intra-tumor heterogeneity (ITH) and cancer evolution. However, comprehensive analysis of mutational data from MRS is still challenging, necessitating complicated integration of a plethora of…
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Keywords:
meskit;
cancer;
cancer evolution;
somatic alterations ... See more keywords
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Published in 2020 at "Cancer Science"
DOI: 10.1111/cas.14630
Abstract: Copy number variation (CNV) is a polymorphism in the human genome involving DNA fragments larger than 1 kb. Copy number variation sites provide hotspots of somatic alterations in cancers. Herein, we examined somatic alterations at…
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Keywords:
copy number;
number variation;
breast;
number ... See more keywords
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Published in 2019 at "Blood"
DOI: 10.1182/blood-2019-128570
Abstract: Somatic alterations including single nucleotide variants (SNVs), copy number alterations (CNAs) and structural variants (SVs) are an important component and the hallmark of Multiple Myeloma (MM) with certain alterations having clinical implications. Recently, the chronological…
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Keywords:
iqr;
consultancy;
mgus smm;
smm ... See more keywords
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Published in 2018 at "Journal of Clinical Oncology"
DOI: 10.1200/jco.2018.36.15_suppl.3592
Abstract: 3592Background: Right-sided (RCC) and left-sided colon cancers (LCC) have different clinical/biological characteristics. Comprehensive genomic analysis (Whole exome/genome, Copy number, RNA, MicroR...
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Keywords:
left sided;
right versus;
versus left;
alterations right ... See more keywords
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Published in 2021 at "Cancers"
DOI: 10.3390/cancers13163947
Abstract: Simple Summary For patients whose prostate cancer spreads beyond the confines of the prostate, treatment options continue to increase. However, we are missing the information that is needed to choose for each patient the best…
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Keywords:
androgen;
treatment;
prostate cancer;
cancer ... See more keywords