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相关概念视频

Multiple Allele Traits01:49

Multiple Allele Traits

The Concept of Multiple Allelism
Sex-linked Disorders01:43

Sex-linked Disorders

Like autosomes, sex chromosomes contain a variety of genes necessary for normal body function. When a mutation in one of these genes results in biological deficits, the disorder is considered sex-linked.
Lethal Alleles02:41

Lethal Alleles

Agouti: A Lethal Allele
Lucien Cuénot discovered lethal alleles in 1905 while studying the inheritance of coat color in mice. The agouti gene is responsible for the color of the coat in mice. This gene codes for an agouti-signaling protein, which is responsible for melanin distribution in mammals. The wild-type allele gives rise to gray-brown coat color in mice, while the mutant allele gives rise to yellow coat color. In addition to coat color, the agouti gene is associated with the yellow...
Sex Linked Disorders01:43

Sex Linked Disorders

Like autosomes, sex chromosomes contain a variety of genes necessary for normal body function. When a mutation in one of these genes results in biological deficits, the disorder is considered sex-linked.
Inborn Errors of Metabolism01:20

Inborn Errors of Metabolism

Phenylketonuria (PKU) is a protein metabolism disorder characterized by high blood levels of the amino acid phenylalanine. This results from a mutation in the gene responsible for phenylalanine hydroxylase, an enzyme that converts phenylalanine into tyrosine. When this enzyme is deficient, phenylalanine builds up in the blood, leading to symptoms such as vomiting, rashes, seizures, growth deficiency, and severe mental retardation. An early diagnosis and a diet restricting phenylalanine intake...
Amebiasis01:28

Amebiasis

Entamoeba histolytica, a protozoan parasite, is responsible for intestinal and extraintestinal amebiasis. Though a significant proportion of infections remain asymptomatic, approximately 50 million individuals annually are estimated to present with clinical disease, resulting in up to 100,000 deaths globally. The disease burden is disproportionately high in regions with lower socioeconomic status, such as parts of India, Africa, Mexico, and Latin America.Etiology and TransmissionThe infective...

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Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association·1990

相关实验视频

Updated: Jun 21, 2026

An Allele-specific Gene Expression Assay to Test the Functional Basis of Genetic Associations
10:17

An Allele-specific Gene Expression Assay to Test the Functional Basis of Genetic Associations

Published on: November 3, 2010

在阿尔法-萨拉塞米亚中发生的血球蛋白H和巴特血球蛋白:一个家庭有2个可能的同性恋病例与G-6-PD缺陷.

P W HELLEMAN, K PUNT, M C VERLOOP

    Nature
    |March 7, 1964
    PubMed
    概括

    No abstract available in PubMed .

    关键词:
    贫血,低染色体的贫血血液蛋白质的电泳过程孩子是一个孩子.遗传学,人类葡萄糖酸盐 - 药物生成缺陷血球蛋白,不正常的情况萨拉塞米亚症 (thalassemia) 是一种疾病.

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    Personalized Peptide Arrays for Detection of HLA Alloantibodies in Organ Transplantation
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    Personalized Peptide Arrays for Detection of HLA Alloantibodies in Organ Transplantation

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    Genetic Analysis of Hereditary Transthyretin Ala97Ser Related Amyloidosis

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    相关实验视频

    Last Updated: Jun 21, 2026

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    10:17

    An Allele-specific Gene Expression Assay to Test the Functional Basis of Genetic Associations

    Published on: November 3, 2010

    Personalized Peptide Arrays for Detection of HLA Alloantibodies in Organ Transplantation
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    Personalized Peptide Arrays for Detection of HLA Alloantibodies in Organ Transplantation

    Published on: September 6, 2017

    Genetic Analysis of Hereditary Transthyretin Ala97Ser Related Amyloidosis
    06:33

    Genetic Analysis of Hereditary Transthyretin Ala97Ser Related Amyloidosis

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