自然科学 SAT - 解剖学と遺伝学
ここでは、SAT で合格するために必要な「脾臓」、「動脈」、「一倍体」など、解剖学や遺伝学に関連する英単語を学びます。
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a sack of tissue that is attached to the large intestine and is surgically removed if infected

虫垂

relating to the intestines, which are part of the digestive system responsible for absorbing nutrients and removing waste from the body

腸の, 腸管の

the front part of the brain involved in higher cognition and executive functions

前頭前皮質, 前頭皮質

(anatomy) a bone of the shoulder girdle that connects the breastbone to the shoulder bone

鎖骨

(anatomy) a spiral cavity in the inner ear that contains sensory organs which send nerve signals to the brain in response to vibrations

蝸牛

a place in the body where two bones meet, enabling one of them to bend or move around

関節, ジョイント

the row of small bones that are joined together down the center of the back of the body

脊椎, 背骨

(anatomy) a system of interconnected organs or tissues that perform a particular task in the body

経路, トラクト

a small, butterfly-shaped gland located at the base of the neck, responsible for producing hormones that regulate metabolism and other bodily functions

甲状腺, サトウグループ

the bone that forms the ankle joint with the tibia and fibula, supporting the body's weight and allowing movement of the foot

距骨

relating to processes and behaviors involved in the creation of offspring within a species

生殖的, 生殖に関する

(anatomy) connected with the sensory part of the eye that sends signals to the brain, called retina

網膜の, 網膜に関する

a very small threadlike structure in a living organism that carries the genes and genetic information

染色体

the genetic makeup of an organism, determined by the combination of genes inherited from its parents

遺伝子型

the observable physical and behavioral characteristics of an organism, resulting from the interaction of its genotype (genetic makeup) with the environment

表現型

one of two or more alternative forms of a gene that arise by mutation and are found at the same place on a chromosome

アレル

(of a gene or trait) showing its specific appearance only when an individual inherits it from both parents

劣性の, 劣性遺伝の

(of genes) causing a person to inherit a particular physical feature, even if it is only present in one parent's genome

優性の, ドミナント

the process by which information from a gene is used to synthesize functional gene products, such as proteins, which can influence an organism's traits

遺伝子発現, 遺伝子の発現

to alter or change the genetic makeup of an organism through genetic engineering techniques

修正する, 変更する

(biology) a change in the structure of the genes of an individual that causes them to develop different physical features

突然変異, 遺伝子の変化

to receive traits or attributes from a previous generation through genetic inheritance

相続する, 遺伝する

(of an organism) having genetic material from another species that has been artificially introduced into its genome

トランスジェニック, 遺伝子組み換え

a specialist in or student of the branch of biology that deals with how individual features and different characteristics are passed through genes

遺伝学者, 遺伝子専門家

a visual display of an individual's chromosomes, used for genetic analysis and identifying abnormalities

核型

the practice of improving the genetic quality of a human population through selective breeding and other methods

優生学

a genetic condition in which an individual has three copies of a chromosome instead of the usual two

トリソミー, 21番染色体のトリソミー

the region of a chromosome where the two sister chromatids are joined and where the spindle fibers attach during cell division

セントロメア

a DNA sequence that has the same order of nucleotides on each side of the complementary DNA strands

回文

the branch of genetics that studies the structure and function of chromosomes using microscopic and molecular techniques

細胞遺伝学

any chromosome that is not involved in determining sex, present in pairs in both males and females, and carrying most of an individual's genetic information

常染色体, 常染色体

the process of introducing foreign DNA or RNA into eukaryotic cells to study gene function or manipulate gene expression

トランスフェクション

a cell or organism containing a single set of unpaired chromosomes, typically denoted as n, representing half the genetic material of a diploid cell

単相染色体

