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2013
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2024
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Predicting PD-L1 expression on human cancer cells using next-generation sequencing information in computational simulation models.
Not available
S-EPMC5394567
|
biostudies-literature
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CTLA4 blockade abrogates KEAP1/STK11-related resistance to PD-(L)1 inhibitors.
Not available
S-EPMC11560846
|
biostudies-literature
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The tale of TILs in breast cancer: A report from The International Immuno-Oncology Biomarker Working Group.
Not available
S-EPMC8636568
|
biostudies-literature
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Study of the doubly charmed tetraquark [Formula: see text].
Not available
S-EPMC9203551
|
biostudies-literature
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Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction.
Not available
S-EPMC4319990
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biostudies-literature
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Exome sequencing and genome-wide linkage analysis in 17 families illustrate the complex contribution of TTN truncating variants to dilated cardiomyopathy.
Not available
S-EPMC3815606
|
biostudies-literature
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Rare loss of function variants in candidate genes and risk of colorectal cancer.
Not available
S-EPMC6283057
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biostudies-literature
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Quantifying rare, deleterious variation in 12 human cytochrome P450 drug-metabolism genes in a large-scale exome dataset.
Not available
S-EPMC3959810
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biostudies-literature
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TGFB2 mutations cause familial thoracic aortic aneurysms and dissections associated with mild systemic features of Marfan syndrome.
Not available
S-EPMC4033668
|
biostudies-literature
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Common and rare von Willebrand factor (VWF) coding variants, VWF levels, and factor VIII levels in African Americans: the NHLBI Exome Sequencing Project.
Not available
S-EPMC3724194
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biostudies-literature
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