|
MeSH term |
Japanese |
Link |
01 |
|
Chromosomes, Human, X
|
ヒトX染色体
|
|
|
|
Heterozygote
|
ヘテロ接合体
|
|
|
|
Phenotype
|
表現型
|
|
|
|
X Chromosome
|
X染色体
|
|
|
|
Body Patterning
|
ボディパターニング
|
|
|
|
Morphogenesis
|
形態形成
|
|
|
|
Genetic Linkage
|
連鎖(遺伝学)
|
|
|
|
Luteal Phase
|
黄体期
|
|
|
|
Signal Transduction
|
シグナルトランスダクション
|
|
|
|
Dosage Compensation, Genetic
|
遺伝子量補正
|
|
|
|
Mosaicism
|
モザイク現象
|
|
|
|
Sequence Homology, Amino Acid
|
アミノ酸配列相同性
|
|
|
|
Genes, Regulator
|
調節遺伝子
|
|
|
|
Bone Development
|
骨発育
|
|
|
|
Chromosomes, Artificial, Yeast
|
酵母人工染色体
|
|
|
|
Cell Compartmentation
|
細胞内区画化
|
|
|
|
Germ-Line Mutation
|
生殖細胞系変異
|
|
|
|
Cell Lineage
|
細胞系譜
|
|
|
|
Embryonic and Fetal Development
|
胚と胎児の成長
|
|
|
|
Protein Transport
|
蛋白質輸送
|
|
|
|
Protein Processing, Post-Translational
|
翻訳後蛋白質プロセシング
|
|
|
|
Mutation
|
変異
|
|
|
|
Neovascularization, Physiologic
|
生理的血管新生
|
|
|
|
Amino Acid Sequence
|
アミノ酸配列
|
|
|
|
Mutation, Missense
|
ミスセンス変異
|
|
|
|
Base Sequence
|
塩基配列
|
|
|
|
Multigene Family
|
多重遺伝子族
|
|
|
|
Cell Adhesion
|
細胞接着
|
|
|
|
Sequence Deletion
|
配列欠失
|
|
|
|
Phosphorylation
|
リン酸化
|
|
|
|
Gene Deletion
|
遺伝子欠失
|
|
|
|
Haplotypes
|
ハプロタイプ
|
|
|
|
Genetic Markers
|
遺伝子マーカー
|
|
|
|
Cell Movement
|
細胞運動
|
|
|
|
Genetic Predisposition to Disease
|
遺伝的素因(疾患)
|
|
|
|
Gene Expression Regulation, Developmental
|
発生遺伝子発現調節
|
|
|
|
Gene Expression Regulation, Neoplastic
|
腫瘍遺伝子発現調節
|
|
|
|
Protein Structure, Tertiary
|
蛋白質三次構造
|
|
|
|
Enzyme Activation
|
酵素活性化
|
|
|
|
Exons
|
エクソン
|
|
|
|
Protein Binding
|
蛋白質結合
|
|
|
|
Cell Differentiation
|
細胞分化
|
|
|
|
Transfection
|
トランスフェクション
|
|
|
|
Immunohistochemistry
|
免疫組織化学
|
|
|