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Human genome
The human genome consists of 23 chromosome and the small mitochondrial DNA. 22 of the 23 chromosomes are autosomal chromosome pairs and the last one being a gender-determining pair. In total, the human genome contains the sequences of the 3 billion chemical base pairs that make up human DNA and approximately 20,000-25,000 genes. By understanding human genome, scientists are able to develop new medical applications that can significantly advance the state of health care.
Contributors in Human genome
Human genome
dysphagia
Medical; Human genome
1) Difficulty in swallowing which may result from neuromuscular disorder or mechanical obstruction. Dysphagia is classified into two distinct types: oropharyngeal dysphagia due to malfunction of the ...
epistasis
Medical; Human genome
1) One gene interferes with or prevents the expression of another gene located at a different locus. 2) Epistasis is a circumstance where the expression of one gene is affected by the expression of ...
endoplasmic reticulum
Medical; Human genome
A system of interconnected vesicular and lamellar cytoplasmic membranes that functions especially in the transport of materials within the cell and that is studded with ribosomes in some places.
fundus
Medical; Human genome
The larger part of a hollow organ that is farthest away from the organ's opening. The bladder, gallbladder, stomach, uterus, eye, and cavity of the middle ear all have a fundus.
gallbladder
Medical; Human genome
A membranous muscular sac in which bile from the liver is stored--called also cholecyst.
genetic discrimination
Medical; Human genome
Genetic discrimination is prejudice directed against people who have or may have a genetic disease. Genetic discrimination can involve being denied employment or health insurance. In a healthcare ...
flow cytometry
Medical; Human genome
1) Flow cytometry is a technique for counting, examining and sorting microscopic particles suspended in a stream of fluid. (from Wikipedia) 2) A technique for identifying and sorting cells and ...
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