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相关概念视频

Comparing Copy Number Variations and SNPs02:26

Comparing Copy Number Variations and SNPs

17.7K
Sequencing of the human genome has opened up several best-kept secrets of the genome. Scientists have identified thousands of genome variations that exist within a population. These variations can be a single nucleotide or a larger chromosomal variation.
Copy number variations or CNVs are the structural variations that cover more than 1kb of DNA sequence. The single nucleotide polymorphism (SNP), on the other hand, is a single nucleotide change or a point mutation that is found in more than 1%...
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Histone Variants at the Centromere02:30

Histone Variants at the Centromere

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Histone variants are the histone proteins with structural and sequence variations. These variants may be regarded as “mutant” forms that replace their canonical histone counterparts in the nucleosomes. Specific post-translational modifications on the histone variants enable further chromatin complexity and regulate tissue-specific gene expression. The most common histone variants are from histone H2A, H2B, and linker histone H1 families. However, several variants of histone H3...
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Incomplete Dominance01:43

Incomplete Dominance

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Gregor Mendel's work (1822 - 1884) was primarily focused on pea plants. Through his initial experiments, he determined that every gene in a diploid cell has two variants called alleles inherited from each parent. He suggested that amongst these two alleles, one allele is dominant in character and the other recessive. The combination of alleles determines the phenotype of a gene in an organism.
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Pathophysiology of Heart Failure01:17

Pathophysiology of Heart Failure

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Heart failure (HF) is a progressive syndrome involving ventricles that leads to inadequate cardiac output. It can be classified based on location and output or ejection fraction. Ejection fraction (EF) is an essential measurement in the diagnosis and surveillance of HF. Reduced EF corresponds to systolic heart failure (HFrEF). However, HF with preserved ejection fraction (HFpEF) is becoming increasingly prevalent. Also known as diastolic HF, this form of HF is related to aging. The...
1.6K
Genetic Variation01:25

Genetic Variation

281
Genetic variation is the diversity in DNA sequences found among individuals of the same species. This diversity is crucial for a species' survival because it helps organisms adapt to environmental changes. Genetic variation begins with fertilization, where an egg and sperm cell merge. Each of these cells carries 23 chromosomes, up to 46 in the fertilized egg. Chromosomes are long DNA strands that contain genes, the basic units of heredity.
Genes exist in different versions called alleles,...
281
Genetic Lingo01:11

Genetic Lingo

102.7K
Overview
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相关实验视频

Updated: Jun 29, 2025

Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
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在HCM中ATTR基因变异

Anthony J Kanelidis1, Jeremy A Slivnick1, Rachel Campagna1

  • 1University of Chicago Medicine, Chicago, Illinois, USA.

JACC. Case reports
|March 29, 2024
PubMed
概括

过度缩性心肌病变 (HCM) 通常是遗传的. 然而,TTR基因变异导致心脏粉症可以模仿HCM,突出显示一个未被认可的诊断重叠.

科学领域:

  • 心脏病学 心脏病学
  • 遗传学 是一个遗传学.
  • 分子生物学分子生物学

背景情况:

  • 增高性心肌病变 (HCM) 是最常见的遗传性心脏病,影响200人中的1人到500人中的1人.
  • 心脏 Amyloidosis 涉及错误折叠的 transthyretin (TTR) 蛋白在心肌中的沉积,导致心肌病变.
  • 氨基粉症可以是获得的或遗传的,呈现诊断挑战.
关键词:
这种基因是TTR基因.心脏氨基粉症的发生.遗传学 遗传学 遗传学 是一个过度缩性心肌病变性心脏病.透性心肌病 - 透性心肌病

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