Biochemistry, Genetics and Molecular Biology
Chromosome Instability
100%
Aneuploidy
98%
Cancer Cell
67%
Genome Instability
47%
P53
42%
Whole Genome Sequencing
39%
Genetics
32%
Karyotype
31%
Spindle Checkpoint
29%
Centrosome
26%
Carcinogenesis
26%
Haplotype
24%
Sister Chromatid Exchange
24%
DNA Replication
21%
Mouse
21%
Cisplatin
20%
Human Genome
20%
Gene Expression Profiling
18%
Drive
18%
DNA Damage
17%
S Phase
17%
BRCA2
16%
Eicosanoid Receptor
16%
DNA Template
14%
Mouse Model
14%
RNA Sequence
14%
Chromosome 12
14%
Polyploid
14%
Genetic Variation
13%
Ploidy
13%
Hepatocyte
12%
Gene Amplification
12%
Sister Chromatid
12%
Gene Dosage
12%
Chromosome Size
12%
B Cell
12%
TRAIL
12%
Caspase 8
11%
Wild Type
11%
Promoter Region
11%
Gene Fusion
11%
Chromothripsis
11%
Drug Resistance
11%
DNA Repair
11%
Dynamics
10%
P21
10%
Cell Death
10%
BRCA1
10%
Homologous Recombination
10%
Signal Transduction
9%
Medicine and Dentistry
Neoplasm
25%
Non Small Cell Lung Cancer
22%
Ovarian Cancer
21%
Circulating Tumor Cell
20%
Tumor Cell
18%
Chromosomal Instability
17%
Cancer Cell
16%
DNA Replication
12%
Organoid
12%
Leukapheresis
11%
Stromal Cell
11%
Glycosidase
11%
DNA Mismatch Repair
11%
Diagnosis
10%
Malignant Neoplasm
10%
Cell Line
9%
Ganglioneuroblastoma
9%
Genomic Instability
8%
Cancer Model
7%
Very Late Activation Antigen 4
7%
In Vitro
7%
Ex Vivo
6%
Epithelial Cell
6%
Treatment Response
6%
Very Late Activation Antigen 5
6%
Colorectal Cancer
5%
Caspase 8
5%
Death Receptor
5%
Cytotoxic T-Cell
5%
Stroma
5%
DNA Sequence
5%
Beta1 Integrin
5%
S Phase
5%
Embryo Development
5%
Fallopian Tube
5%
Poly(adenosine Diphosphate Ribose)
5%
Xenograft
5%
Downregulation
5%
Aurora A Kinase
5%
Karyotype Evolution
5%
Drug Resistance
5%
Colon Carcinoma Cell Line
5%
Double Stranded DNA
5%
Cytokinesis
5%
Cell DNA
5%
DNA Damage Response
5%
DNA Damage
5%
Immune Checkpoint Blockade
5%
Uterine Cancer
5%
PARP Inhibitor
5%
Keyphrases
Aneuploidy
25%
Chromosomal Instability
22%
Genomic Instability
18%
Strand-seq
13%
Structural Variation
12%
Stromal Cells
11%
Sister Chromatid Exchange
11%
Non-small Cell Lung Cancer (NSCLC)
11%
Yeast Cells
11%
Circulating Tumor Cells
11%
Human Bone Marrow
11%
Endometrial Cancer
11%
Mismatch Repair
11%
Diagnostic Leukapheresis
11%
Double-strand Breaks
8%
Cancer Cells
8%
VLA-4
7%
Copy number Variation
7%
Single-cell Whole-genome Sequencing
7%
Chromosome Size
7%
Structural Variants
7%
Sigma Phase
6%
Single-cell RNA Sequencing (scRNA-seq)
6%
Centrosome Amplification
6%
PIDDosome
6%
Centrosome
6%
VLA-5
6%
Tumor Cells
6%
Tumor
5%
Metastatic Pheochromocytoma/paraganglioma
5%
Fallopian Tube Epithelial Cells
5%
PARG Inhibitor
5%
Lung Repair
5%
Lymphocyte Apoptosis
5%
FRTL-5 Cells
5%
Gene Copy number
5%
Inhalable
5%
Chromosome Segregation Errors
5%
Restoration of Parts
5%
Neurodegenerative Diseases
5%
Living Biobank
5%
Early Stress
5%
Cyclin E1
5%
Bayesian Inversion
5%
Inversion Genotyping
5%
Gene Amplification
5%
Endotoxin
5%
Genome Stability
5%
Leukemic Cells
5%
Human Genome
5%
