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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
Cis configuration
Medical; Human genome
1) Term which indicates that an individual who is heterozygous at two neighbouring loci has the two mutations in question on the same chromosome. 3) characterised by having certain atoms or groups ...
Conductive hearing loss
Medical; Human genome
10 Involves lesions of the external and middle ear resulting in malconduction of airborne sound. 2) Hearing loss due to interference with the mechanical reception or amplification of sound to the ...
Chimerism
Medical; Human genome
The occurrence in an individual of two or more cell populations of different chromosomal constitutions, derived from different individuals. This contrasts with mosaicism in which the different cell ...
Central nervous system
Medical; Human genome
1) The main information-processing organs of the nervous system, consisting of the brain, spinal cord, and meninges. 2) The brain and spinal cord.
Collecting tubule
Medical; Human genome
A nonsecretory tubule that receives urine from several nephrons and discharges it into the pelvis of the kidney—called also collecting duct.
Chylomicrons
Medical; Human genome
A class of lipoproteins that carry dietary cholesterol and triglycerides from the small intestines to the tissues.
Conservative change
Medical; Human genome
An amino acid change that does not affect significantly the function of the protein.
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