Biochemistry, Genetics and Molecular Biology
T Cell
100%
B Cell
81%
Allele
32%
BCL6
28%
Missense Mutation
28%
Fluorescence in Situ Hybridization
26%
P53
24%
Progeny
23%
Chromosomal Translocation
19%
Methylation
19%
Linkage Analysis
19%
Promoter Region
19%
Carcinogenesis
19%
Chromosomal Rearrangement
17%
Polymerase Chain Reaction
17%
Gene Linkage
17%
Kinase
16%
Phosphotransferase
16%
Cosmid
15%
Loss of Heterozygosity
15%
Exon
13%
Receptor Gene
13%
Cytogenetics
12%
Germ Cell
12%
Single-Nucleotide Polymorphism
11%
Genotyping
11%
Anticipation
11%
Gene Rearrangement
11%
Transcriptome
11%
Comparative Genomic Hybridization
11%
Gene Function
11%
Cerebriform Nuclei
11%
Stakeholder Engagement
11%
Breed
11%
Myeloid
11%
Major Histocompatibility Complex
11%
Somatic Hypermutation
11%
in Situ Hybridization
11%
Genetic Epidemiology
11%
Chromosomal Abnormalities
11%
Gene Dosage
11%
Genetic Susceptibility
11%
Somatic Mutation
10%
Epigenetics
9%
CpG Island
9%
Tumor Suppressor Gene
9%
Amino Acid Substitution
9%
Reciprocal Chromosome Translocation
8%
Wild Type
8%
Codon
8%
Medicine and Dentistry
B-Cell Chronic Lymphocytic Leukemia
69%
Prolymphocytic Leukemia
31%
Diseases
28%
Disease Predisposition
25%
Ataxia Telangiectasia
15%
T Cell
14%
Pleiotropy
14%
Genetic Susceptibility
11%
Leukemia Cell
11%
Familial Disease
11%
B Lymphocyte
11%
Heart Failure
11%
Chronic Myelogenous Leukemia
11%
Insulin Resistance
11%
Health Care Cost
11%
Patient Care
11%
Somatic Hypermutation
11%
Birth Order
11%
Human Genome
11%
Cooperation
11%
Biomedical Research
11%
Analytic Method
11%
Sezary Cell
11%
Impaired Glucose Tolerance
11%
Acute Lymphoblastic Leukemia
9%
Blast Cell Crisis
7%
Leukemia
7%
Carcinogenesis
6%
Allele
6%
Neoplasm
6%
Malignant Neoplasm
6%
Hematologic Malignancy
6%
Child
5%
Translating (Language)
5%
