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相关概念视频

Disorders of Leukocytes01:27

Disorders of Leukocytes

Leukocyte disorders can lead to either leukopenia, characterized by an abnormally low leukocyte count, or leukocytosis, marked by a very high leukocyte number.
Leukopenia may result from bone marrow disorders, autoimmune diseases, and infectious diseases. For example, conditions such as multiple myeloma and aplastic anemia can impair the bone marrow's ability to produce adequate leukocytes. Similarly, autoimmune diseases like lupus and viral infections such as HIV can prompt the immune system...
Overview of Protein Metabolism01:21

Overview of Protein Metabolism

Proteins are broken down into amino acids during digestion. Unlike fats and carbohydrates, which are stored for later use, proteins are not. Instead, amino acids are either used to produce ATP through oxidation or contribute to the creation of new proteins for the growth and repair of the body. Any surplus amino acids from the diet are converted into glucose or triglycerides rather than excreted.
Amino acids play various roles in the body once they are absorbed into cells. They are restructured...
Overview of Lipid Metabolism01:24

Overview of Lipid Metabolism

Lipid metabolism is a crucial process in the human body that involves the synthesis and degradation of lipids. This process is essential for energy production, cell membrane formation, and hormone production, among other functions.
Lipolysis: The Breakdown of Lipids:
Lipolysis is the process of breaking down lipids, particularly triglycerides, into glycerol and fatty acids. This process typically occurs in the adipose tissue and is triggered by various hormones, including glucagon and...
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...
Diabetic Retinopathy01:27

Diabetic Retinopathy

DefinitionDiabetic retinopathy is a microvascular complication of diabetes affecting the retinal blood vessels.Risk FactorsDiabetic retinopathy is present in almost all individuals with type 1 diabetes and more than 60% of those with type 2 diabetes after two decades of disease.The risk increases with poor glycemic control, hypertension, dyslipidemia, smoking, pregnancy, and puberty.Although cataracts and glaucoma are also more frequent in people with diabetes, retinopathy remains the leading...
Jaundice01:25

Jaundice

Jaundice, or icterus, is the yellow discoloration of the skin, sclerae, and mucous membranes. It happens when plasma bilirubin levels rise above 2.5-3 mg/dL, leading to bilirubin deposition in tissue.Bilirubin is a byproduct of hemoglobin degradation. In macrophages, hemoglobin breaks down into globin and heme. Globin is converted into amino acids, while heme is turned into biliverdin by heme oxygenase, which is then reduced to unconjugated bilirubin by biliverdin reductase.Unconjugated...

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Cell-free Biochemical Fluorometric Enzymatic Assay for High-throughput Measurement of Lipid Peroxidation in High Density Lipoprotein
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高血和高蛋白血:一种新的代谢障碍.

Barry Sampson1, Magne K Fagerhol, Cord Sunderkötter

  • 1Department of Clinical Chemistry, Charing Cross Hospital, W6 8RF, London, UK. b.sampson@ic.ac.uk

Lancet (London, England)
|December 14, 2002
PubMed
概括

一种以复发性感染和炎症为特征的新疾病与高血calprotectin和高血症有关. 这种情况涉及代谢和S100A8/S100A9蛋白质的失调.

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Isolation of Primary Mouse Hepatocytes for Nascent Protein Synthesis Analysis by Non-radioactive L-azidohomoalanine Labeling Method
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Isolation and Analysis of Plasma Lipoproteins by Ultracentrifugation
06:47

Isolation and Analysis of Plasma Lipoproteins by Ultracentrifugation

Published on: January 28, 2021

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Cell-free Biochemical Fluorometric Enzymatic Assay for High-throughput Measurement of Lipid Peroxidation in High Density Lipoprotein
07:29

Cell-free Biochemical Fluorometric Enzymatic Assay for High-throughput Measurement of Lipid Peroxidation in High Density Lipoprotein

Published on: October 12, 2017

Isolation of Primary Mouse Hepatocytes for Nascent Protein Synthesis Analysis by Non-radioactive L-azidohomoalanine Labeling Method
08:04

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Isolation and Analysis of Plasma Lipoproteins by Ultracentrifugation
06:47

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Published on: January 28, 2021

科学领域:

  • 免疫学 免疫学 免疫学
  • 代谢障碍 代谢障碍 代谢障碍
  • 遗传学 是一个遗传学.

背景情况:

  • 蛋白,S100A8和S100A9的复合体,是细胞中关键的和结合蛋白.
  • 一种新的综合征呈现出由于血calprotectin升高而导致的复发性感染,炎症和高血.

研究的目的:

  • 描述一种与高血calprotectin和高血症相关的新综合征.
  • 研究失调的代谢和蛋白质复合体形成的潜在机制.

主要方法:

  • 用ELISA和原子吸收光谱法测量的血calprotectin和水平.
  • 使用尺寸排除染色学和电泳学分化蛋白质.
  • 通过MALDI-TOFMS识别蛋白质.

主要成果:

  • 五名患者表现出高血 (77-200μmol/L) 和显著增加的血calprotectin (1.4-6.5g/L).
  • 临床特征包括经常性感染,肝炎,贫血,全身炎症,在某些情况下,皮肤炎症或严重的生长失败.
  • 发现和calprotectin在高分子量分数 (100-300 kDa) 中与正常的S100A8和S100A9子单元相关.

结论:

  • 一种新型疾病是由代谢失调和S100A8/S100A9蛋白质在血中的积累来定义的.
  • 这种情况凸显了S100蛋白家族在人类疾病中的失调的病理作用.