|
MeSH term |
Japanese |
Link |
01 |
|
|
X Chromosome
|
X染色体
|
|
|
|
|
Sex Determination Processes
|
性決定(遺伝学)
|
|
|
|
|
Chromosomes, Human, X
|
ヒトX染色体
|
|
|
|
|
DNA Transposable Elements
|
挿入配列因子
|
|
|
|
|
Genes, Recessive
|
劣性遺伝子
|
|
|
|
|
Embryonic Development
|
胚発生
|
|
|
|
|
Chromatin
|
クロマチン
|
|
|
|
|
Mutagenesis, Insertional
|
挿入型変異誘発
|
|
|
|
|
Genes, Regulator
|
調節遺伝子
|
|
|
|
|
Open Reading Frames
|
オープンリーディングフレーム
|
|
|
|
|
3' Untranslated Regions
|
3'非翻訳領域
|
|
|
|
|
Biological Evolution
|
進化
|
|
|
|
|
Conserved Sequence
|
保存配列
|
|
|
|
|
Chromosomes, Artificial, Yeast
|
酵母人工染色体
|
|
|
|
|
Gene Expression Regulation, Developmental
|
発生遺伝子発現調節
|
|
|
|
|
Chromosome Inversion
|
染色体逆位
|
|
|
|
|
Base Sequence
|
塩基配列
|
|
|
|
|
Sequence Deletion
|
配列欠失
|
|
|
|
|
Intraocular Pressure
|
眼圧
|
|
|
|
|
Genetic Linkage
|
連鎖(遺伝学)
|
|
|
|
|
Point Mutation
|
点変異
|
|
|
|
|
Sex Chromosome Aberrations
|
性染色体異常
|
|
|
|
|
Sequence Homology, Amino Acid
|
アミノ酸配列相同性
|
|
|
|
|
Gene Expression Regulation
|
遺伝子発現調節
|
|
|
|
|
Chromosomes, Human, Pair 13
|
ヒト第13染色体
|
|
|
|
|
Mutation
|
変異
|
|
|
|
|
Chromosomes, Human, Pair 3
|
ヒト第3染色体
|
|
|
|
|
Amino Acid Sequence
|
アミノ酸配列
|
|
|
|
|
Chromosomes, Human, Pair 2
|
ヒト第2染色体
|
|
|
|
|
Chromosome Aberrations
|
染色体異常
|
|
|
|
|
Alleles
|
対立遺伝子
|
|
|
|
|
Genetic Predisposition to Disease
|
遺伝的素因(疾患)
|
|
|
|
|
Genetic Markers
|
遺伝子マーカー
|
|
|
