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GENETIC BURDEN 27 Apr 2012 | 01:00 am
GENETIC BURDEN The mutation, GENETIC BURDEN The human genetic burden is a term set by the sum of man's harmful genes, genes that have lost their normal function by mutation. Recessive disease genes s...
Specific gene 26 Apr 2012 | 12:45 am
Specific gene Properties not related to their specific DNA gene. Many functional "anonymous" genes are found in the sequence database that ORFer (open reading frames, an open reading frame), which p...
What is human genome 25 Apr 2012 | 12:51 am
Human genome and Genki Arteta Since the X chromosome in males alone, all the condition of sex-linked inheritance is due to genes on the same chromosome. In the 1930s it was found that color-blindness...
CHROMOSOMAL 24 Apr 2012 | 12:31 am
CHROMOSOMAL Chromosomes can be studying in the cells during division, for example. In bone marrow cells or cultured cells, most commonly in white blood cells that are stimulated to divide. At the app...
Human population genetics 23 Apr 2012 | 12:25 am
Human population genetics POPULATION GENETICS, EVOLUTION, HISTORY OF RESEARCH Population genetics study is based on that in different population's maps the frequency of various inherited properties,...
MULTIFACTORIAL GENETIC DISEASE 22 Apr 2012 | 12:15 am
MULTIFACTORIAL GENETIC DISEASE When you find irregular familial occurrence of a qualitative trait, the reason usually a combination of several single gene variations and environmental factors. Such p...
Mitochondrial diseases 21 Apr 2012 | 12:12 am
MITOCHONDRIAL DISEASES The 16 569 base pair's long mitochondrial genomes found in several hundred mitochondria per cell and is transmitted through the egg cell plasma of the fertilized egg. Nothing c...
Triplet diseases 20 Apr 2012 | 12:03 am
TRIPLET DISEASES The most single gensykdommer cause that a gene has been changed in a simple way (replacement of one base to another, loss of or deposit of an extra base, etc.) then inherited in its ...
Genetic diseases in humans 18 Apr 2012 | 11:43 pm
Genetic diseases in humans ENKELTGEN DISEASE Referee Extremely short finger was the first property that was proven to have Mendelian inheritance in man (1903). Some other examples of autosomal domin...
Conserved sequences 17 Apr 2012 | 11:37 pm
Conserved sequences Non-coding DNA, highly conserved unique sequences (HCS) Of recent date is the discovery that in the non-coding DNA is stretches of unique DNA sequences that are considerably conse...
