Homologous chromosome - Search results - Wiki Homologous Chromosome
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A pair of homologous chromosomes, or homologs, are a set of one maternal and one paternal chromosome that pair up with each other inside a cell during... |
Meiosis (redirect from Tetrad (chromosomal formation)) Chi (Χ)) between the homologous chromosomes. In most organisms, these links can help direct each pair of homologous chromosomes to segregate away from... |
Chromosomal crossover, or crossing over, is the exchange of genetic material during sexual reproduction between two homologous chromosomes' non-sister... |
Ploidy (redirect from Chromosome number) number of maternal and paternal chromosome copies, respectively, in each homologous chromosome pair, which chromosomes naturally exist as. Somatic cells... |
Chromosome segregation is the process in eukaryotes by which two sister chromatids formed as a consequence of DNA replication, or paired homologous chromosomes... |
by facilitating chromosomal crossover, in which regions of similar but not identical DNA are exchanged between homologous chromosomes. This creates new... |
Prophase (section Condensation of chromosomes) paternally derived non-sister chromatids of homologous chromosome pairs.: 98 The paired homologous chromosome bound by the synaptonemal complex are referred... |
Genetic recombination (section Chromosomal crossover) alleles whose loci are on different but homologous chromosomes (random orientation of pairs of homologous chromosomes in meiosis I); & (2) intrachromosomal... |
pairs of chromosomes, a total of 46 chromosomes. The first 22 pairs are called autosomes. Autosomes are homologous chromosomes i.e. chromosomes which contain... |
Sister chromatids (redirect from Sister chromosome) corresponding sections of the homologous chromatids with which they are paired during meiosis. Homologous chromosomes might or might not be the same... |
is a chromosome abnormality caused by exchange of parts between non-homologous chromosomes. Two detached fragments of two different chromosomes are switched... |
Bivalent (genetics) (redirect from Bivalent chromosome) bivalent is one pair of chromosomes (homologous chromosomes) in a tetrad. A tetrad is the association of a pair of homologous chromosomes (4 sister chromatids)... |
Synapsis (section Chromosome silencing) of two chromosomes that occurs during meiosis. It allows matching-up of homologous pairs prior to their segregation, and possible chromosomal crossover... |
recombination between repetitive sequences, or through chromosomal breakage followed by non-homologous end joining. Inversions are of two types: paracentric... |
according to the 2nd Mendelian rule (“Law of Segregation of genes“) homologous chromosomes are randomly distributed among daughter nuclei, there are various... |
Nondisjunction (redirect from Chromosomal nondisjunction) Nondisjunction is the failure of homologous chromosomes or sister chromatids to separate properly during cell division (mitosis/meiosis). There are three... |
Sequence homology (redirect from Homologous gene) whose relationship was completely homologous in an ancestral species. In allopolyploids, the homologous chromosomes within each parental sub-genome should... |
Polyploidy (section Homoeologous chromosomes) pair of (homologous) chromosomes. Most species whose cells have nuclei (eukaryotes) are diploid, meaning they have two complete sets of chromosomes, one from... |
strands derived from different sources, such as from different homologous chromosomes or even from different organisms. One such example is the heteroduplex... |
Chromatid (category Chromosomes) confused with the ploidy of an organism, which is the number of homologous versions of a chromosome. Chromatids may be sister or non-sister chromatids. A sister... |