|
MeSH term |
Japanese |
Link |
S H M T 2 |
|
Open Reading Frames
|
オープンリーディングフレーム
|
|
|
|
Gene Library
|
遺伝子ライブラリー
|
|
|
|
Base Sequence
|
塩基配列
|
|
|
|
Chromosomes, Human, 21-22 and Y
|
ヒト第21-22およびY染色体
|
|
|
|
Dominance, Cerebral
|
大脳半球優位性
|
|
|
|
Transplantation Immunology
|
移植免疫
|
|
|
|
Gene Expression Regulation, Enzymologic
|
酵素遺伝子発現調節
|
|
|
|
Substrate Specificity
|
基質特異性
|
|
|
|
Environment
|
環境
|
|
|
|
Maternal-Fetal Exchange
|
母体胎児間物質交換
|
|
|
|
Protein Conformation
|
蛋白質高次構造
|
|
|
|
Chromosomes, Human, Pair 20
|
ヒト第20染色体
|
|
|
|
Polymorphism, Single Nucleotide
|
一塩基多型
|
|
|
|
Fluorescence
|
蛍光
|
|
|
|
Antibody Formation
|
抗体産生
|
|
|
|
Alleles
|
対立遺伝子
|
|
|
|
Protein Sorting Signals
|
蛋白質ソーティングシグナル
|
|
|
|
Algorithms
|
アルゴリズム
|
|
|
|
Chromosomes, Human, Pair 12
|
ヒト第12染色体
|
|
|
|
Sequence Homology, Amino Acid
|
アミノ酸配列相同性
|
|
|
|
Kinetics
|
運動力学
|
|
|
|
Chromosomes, Human, Pair 17
|
ヒト第17染色体
|
|
|
|
Nucleic Acid Conformation
|
核酸高次構造
|
|
|
|
Amino Acid Sequence
|
アミノ酸配列
|
|
|
|
Promoter Regions, Genetic
|
プロモーター領域
|
|
|
|
Genotype
|
遺伝子型
|
|
|
|
Polymorphism, Genetic
|
遺伝子多型
|
|
|
|
Protein Binding
|
蛋白質結合
|
|
|
|
Catalysis
|
触媒作用
|
|
|
|
Polymorphism, Single-Stranded Conformational
|
PCR-SSCP法
|
|
|
|
Dimerization
|
二量化
|
|
|
|
Sensitivity and Specificity
|
感度と特異度
|
|
|
|
Alternative Splicing
|
選択的スプライシング
|
|
|
|
Sequence Deletion
|
配列欠失
|
|
|
|
Sequence Homology, Nucleic Acid
|
核酸配列相同性
|
|
|
|
Genetic Variation
|
遺伝的多様性
|
|
|
|
Lymphocyte Activation
|
リンパ球活性化
|
|
|
|
Tissue Distribution
|
組織内分布
|
|
|
|
Cell Survival
|
細胞生存
|
|
|
|
Pregnancy
|
妊娠
|
|
|
|
Gene Frequency
|
遺伝子頻度
|
|
|
|
Gene Expression Regulation, Neoplastic
|
腫瘍遺伝子発現調節
|
|
|
|
Genetic Predisposition to Disease
|
遺伝的素因(疾患)
|
|
|
|
Dose-Response Relationship, Drug
|
薬物用量効果相互関係
|
|
|
|
Binding Sites
|
結合部位
|
|
|
|
Transcription, Genetic
|
転写
|
|
|
|
Gene Expression
|
遺伝子発現
|
|
|
|
Phosphorylation
|
リン酸化
|
|
|
|
Transfection
|
トランスフェクション
|
|
|
|
Mutation
|
変異
|
|
|