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A gene for type I hair keratin was lost in the human lineage. Keratins are a major component of hairs. Humans still have nine functional type I hair keratin genes, but the loss of that particular gene may have caused the thinning of human body hair.
In humans, the SRY gene is located on short (p) arm of the Y chromosome at position 11.2. Sex-determining region Y protein (SRY), or testis-determining factor (TDF), is a DNA-binding protein (also known as gene-regulatory protein/transcription factor) encoded by the SRY gene that is responsible for the initiation of male sex determination in therian mammals (placentals and marsupials). [5]
In humans, the MSTN gene is located on the long (q) arm of chromosome 2 at position 32.2. [5] Myostatin (also known as growth differentiation factor 8, abbreviated GDF8) is a protein that in humans is encoded by the MSTN gene. [6] Myostatin is a myokine that is produced and released by myocytes and acts on muscle cells to inhibit muscle growth. [7]
The frequency of stereotypic behaviours, such as hair-pulling, have been reduced in captive primates using enrichment activities including placing food articles in holes made in a tree, which encourages the monkeys to spend time extracting these objects as opposed to engaging in behaviours such as hair-pulling. [5]
Results from the human and chimpanzee genome analyses should help in understanding some human diseases. Humans appear to have lost a functional Caspase 12 gene, which in other primates codes for an enzyme that may protect against Alzheimer's disease. Human and chimpanzee genomes. M stands for Mitochondrial DNA
In humans, the vermiform appendix is sometimes called a vestigial structure as it has lost much of its ancestral digestive function.. Vestigiality is the retention, during the process of evolution, of genetically determined structures or attributes that have lost some or all of the ancestral function in a given species. [1]
Humans are the only primate species that have undergone significant hair loss. The hairlessness of humans compared to related species may be due to loss of functionality in the pseudogene KRTHAP1 (which helps produce keratin) [16] Although the researchers dated the mutation to 240 000 ya, both the Altai Neandertal and Denisovan peoples ...
Expression of some of the gap genes in bands in the Drosophila early embryo. A gap gene is a type of gene involved in the development of the segmented embryos of some arthropods. Gap genes are defined by the effect of a mutation in that gene, which causes the loss of contiguous body segments, resembling a gap in the normal body plan. Each gap ...