|
MeSH term |
Japanese |
Link |
01 |
|
|
Ion Channel Gating
|
イオンチャンネルゲート機構
|
|
|
|
|
Chromosomes, Human, Pair 12
|
ヒト第12染色体
|
|
|
|
|
Biophysics
|
生物物理学
|
|
|
|
|
Alu Elements
|
Alu配列
|
|
|
|
|
Birth Weight
|
出生体重
|
|
|
|
|
Codon, Terminator
|
終止コドン
|
|
|
|
|
Blood Pressure
|
血圧
|
|
|
|
|
Ion Transport
|
イオン輸送
|
|
|
|
|
Base Sequence
|
塩基配列
|
|
|
|
|
Mutagenesis, Insertional
|
挿入型変異誘発
|
|
|
|
|
Cell Membrane Permeability
|
細胞膜透過性
|
|
|
|
|
Biological Transport, Active
|
能動輸送
|
|
|
|
|
Cosmids
|
コスミド
|
|
|
|
|
Genetic Linkage
|
連鎖(遺伝学)
|
|
|
|
|
Chromosomes
|
染色体
|
|
|
|
|
Mutation
|
変異
|
|
|
|
|
Genes, Recessive
|
劣性遺伝子
|
|
|
|
|
Electrophysiology
|
電気生理学
|
|
|
|
|
Membrane Potentials
|
膜電位
|
|
|
|
|
Exons
|
エクソン
|
|
|
|
|
Repetitive Sequences, Nucleic Acid
|
核酸反復配列
|
|
|
|
|
Polymorphism, Single-Stranded Conformational
|
PCR-SSCP法
|
|
|
|
|
Cohort Studies
|
コホート研究
|
|
|
|
|
Polymorphism, Genetic
|
遺伝子多型
|
|
|
|
|
Gene Library
|
遺伝子ライブラリー
|
|
|
|
|
Alternative Splicing
|
選択的スプライシング
|
|
|
|
|
Sequence Homology, Amino Acid
|
アミノ酸配列相同性
|
|
|
|
|
Sequence Deletion
|
配列欠失
|
|
|
|
|
Age Factors
|
年齢因子
|
|
|
|
|
Genetic Markers
|
遺伝子マーカー
|
|
|
|
|
Structure-Activity Relationship
|
構造活性相関
|
|
|
|
|
Genetic Variation
|
遺伝的多様性
|
|
|
|
|
Gene Expression
|
遺伝子発現
|
|
|
|
|
Sequence Homology, Nucleic Acid
|
核酸配列相同性
|
|
|
|
|
Introns
|
イントロン
|
|
|
|
|
Genetic Predisposition to Disease
|
遺伝的素因(疾患)
|
|
|
|
|
Gene Expression Regulation, Developmental
|
発生遺伝子発現調節
|
|
|
|
|
Case-Control Studies
|
症例対照研究
|
|
|
|
|
Amino Acid Sequence
|
アミノ酸配列
|
|
|
|
|
Tissue Distribution
|
組織内分布
|
|
|
|
|
Genes
|
遺伝子
|
|
|
|
|
Alleles
|
対立遺伝子
|
|
|
|
|
Promoter Regions, Genetic
|
プロモーター領域
|
|
|
|
|
Protein Binding
|
蛋白質結合
|
|
|
|
|
Phosphorylation
|
リン酸化
|
|
|
|
|
Gene Expression Regulation
|
遺伝子発現調節
|
|
|
