人类生理学/遗传
< 人類生理學
简介[编辑]
DNA[编辑]
基因[编辑]
遗传学[编辑]
转录与转译[编辑]
Inheritance[编辑]
Mechanisms of inheritance[编辑]
单因子遗传[编辑]
多因子遗传[编辑]
性联遗传[编辑]
Exceptions to simple inheritance[编辑]
Polygenic Traits[编辑]
Intermediate Expressions[编辑]
Co-dominance[编辑]
Multiple-Allele Series[编辑]
Modifying and Regulator Genes[编辑]
Incomplete penetrates[编辑]
遗传性基因疾病[编辑]
血色素沉着症(hemochromatosis)[编辑]
血色素沉着症的治疗[编辑]
囊性纤维化(Cystic Fibrosis,CF)[编辑]
囊性纤维化的治疗[编辑]
镰刀型红血球贫血[编辑]
镰刀型红血球贫血的治疗[编辑]
血友病(Hemophilia)[编辑]
血友病的治疗[编辑]
非遗传性基因疾病[编辑]
突变基因[编辑]
基因工程[编辑]
基因治疗[编辑]
Genetic Regulation of Development and Homeostasis[编辑]
词汇表[编辑]
- 等位基因(Allele)
- one member of a pair of genes that occupy a specific position on a specific chromosome
- 体染色体(Autosome)
- chromosome that is not a sex chromosome
- 染色体(Chromosome)
- threadlike strand of DNA and associated proteins in the nucleus of cells that carries the genes and functions in the transmission of heredity information
- 囊性纤维化(Cystic Fibrosis)
- recessive genetic disorder affecting the mucus lining of the lungs, leading to breathing problems and other difficulties
- 胎儿酒精综合症(Fetal Alcohol Syndrome)
- combination of birth defects resulting form high (sometimes low) alcohol consumption by the mother during pregnancy
- 基因(Gene)
- is a segment of nucleic acid that contains the information necessary to produce a functional product, usually a protein.
- 遗传学(Genetics)
- is the science of genes, heredity, and the variation of organisms.
- 基因组(Genome)
- complete set of genetic information of an organism including DNA and RNA
- 基因型(Genotype)
- actual set of genes an organism has. It is the blue print of gentic material.
- 血色病(Hemochromatosis)
- metabolic disorder that causes increased absorption of iron, which is deposited in the body tissues and organs; the iron accumulates in the body where it may become toxic and causes damage
- 血红蛋白(Hemoglobin)
- component of red blood cells that carries oxygen
- 血友病(Hemophilia)
- group of heredity disorders in which affected individuals fail to make
enough of certain proteins needed to form blood clots
- 继承(Inheritance)
- characteristics given to a child by a parent
- 基因修改(Modifying Gene)
- alters how other genes are expressed in the phenotype
Multifactorial Inheritance: trait or disorder determined by multiple genes and/or environmental effects
- 表型(Phenotype)
- organisms physical appearance
- 多基因(Polygenic)
- trait whose expression is influenced by more than one gene
- 调节基因(Regulator Genes)
- initiate or block the expression of other genes.
- 性联(Sex-linked)
- pertaining to a trait of a disorder determined by the sex chromosome in a persons cells or by the genes carried on those chromosomes
- 镰状细胞性贫血(Sickle Cell Anemia)
- recessive disorder in which red blood cells take on an unusual shape, leading to other problems with the blood
- 合成(Synthesize)
- to make using biochemical processes
Unifactorial Inheritance: trait or disorder determined by a single pair of genes
- 合子(Zygote)
- cell formed by the union of male and female gametes. A Zygote is a cell that is the result of fertilization.