Biochemistry, Genetics and Molecular Biology
A J Mouse
11%
Adenylate Cyclase
17%
Agrotis
17%
Allele
24%
Aniridia
34%
ATPase
12%
Autosome
22%
Benzodiazepine
17%
BXD Mouse
21%
Cell Degeneration
17%
Chromosome 12
13%
Chromosome 18 (Human)
17%
Chromosome 4
21%
Chromosome 7
20%
Chromosome Band
17%
Complete Linkage
9%
DBA 2 Mouse
50%
Diazepam
17%
Dystrophin
34%
Essential Thrombocythaemia
17%
Frameshift Mutation
17%
Gene Linkage Disequilibrium
17%
Gene Locus
11%
Genetics
22%
Genomic Imprinting
39%
Heterosis
17%
Heterozygosity
17%
Homeodomain
12%
Inbred Strain
25%
Linkage Analysis
11%
Liquid
17%
Major Gene
21%
Mouse
100%
Mouse Mutant
17%
Multifactorial Inheritance
34%
Neural Tube
17%
Niemann-Pick Disease
17%
NPC1
17%
Open Field Behavior
17%
PAX6
31%
Phylogeny
17%
Porphobilinogen Deaminase
17%
Porphyria
17%
Proto Oncogene
19%
Recombinant Inbred Strain
21%
Single-Strand Conformation Polymorphism
9%
Strain Difference
15%
Voltage-Dependent Calcium Channel
17%
Wilms' Tumor
17%
WT1
14%
Neuroscience
Adenylyl Cyclase
17%
Audiogenic Seizure
17%
Autosome
17%
Balo's Concentric Sclerosis
17%
Behavior Disorder
17%
Behavioral Test
17%
Cell Signaling
8%
Cerebellum
17%
Chromosome 11
11%
Chromosome 12
21%
Chromosome 18q
8%
Chromosome 2
11%
Chromosome 4
55%
Chromosome 7
17%
Chromosome 9
11%
Corneal Dystrophy
17%
Electroretinography
17%
Epigenetic Mechanism
17%
Epileptic Absence
8%
FOSB
17%
Galanin
17%
Gene Locus
17%
Gene Order
17%
Genetic Recombination
8%
Glutamic Acid
17%
Inverse Agonist
17%
Iris
8%
Keratin
17%
Linkage Disequilibrium
17%
Maternal Behavior
17%
Microsatellite
25%
Morphogenesis
17%
Myc
17%
PAX6
34%
Pick's Disease
34%
Proline
17%
Propylthiouracil
17%
Proto Oncogene
17%
Psychosis
17%
Quantitative Trait Locus
17%
Quantitative Trait Locus Mapping
17%
Receptor Trafficking
17%
Sensory Processing
17%
Serine
17%
Somatosensory Cortex
17%
Threonine
17%
Transcription Factor PAX6
25%
Valerian
17%
Vasopressin
8%
Voltage-Dependent Calcium Channel
17%
Keyphrases
Acute Intermittent Porphyria
17%
Adult Tissues
17%
Alimentary Tract
17%
Balo's Concentric Sclerosis
17%
Biomedical Scientists
17%
C57BL
17%
Centromeric Region
17%
Chromosome 18q
17%
Chromosome Bands
17%
Classical Greek
17%
Cysteine-rich Domain
17%
Digraph
17%
Diminutive
17%
Diphthongs
17%
Dystrophin
17%
Fissure
17%
Fukuyama Congenital muscular Dystrophy
17%
Gene Map
17%
Human Adult
17%
Human Bone
17%
Human Chromosome 18
17%
Human Organs
17%
Hypertensive Cardiovascular Disease
17%
Hypertensive Intracerebral Hemorrhage
17%
Insertion mutation
17%
Interconnected Structure
17%
Intramedullary Hemorrhage
17%
Lateral Medullary Syndrome
17%
Latin Language
20%
Less Is More
17%
Ligature
17%
Linkage Analysis
17%
Modern Biology
17%
Mouse Mus musculus
17%
N-methyl-D-aspartate Receptor (NMDAR)
17%
Niemann-Pick Type
17%
Nulligravid
17%
Organology
17%
PAX6 mutation
17%
Physiologist
17%
Plasticity Mechanisms
17%
Porphobilinogen Deaminase
17%
Prolegomena
17%
Protestant
17%
Purkinje Cell Degeneration
17%
Recombinant Inbred Strains
34%
Signaling Pathway
17%
Special Functions
17%
Two-locus Model
17%
Vowels
17%
