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  2. Neoteny - Wikipedia

    en.wikipedia.org/wiki/Neoteny

    Axolotl and olm are perennibranchiate salamander species which retain their juvenile aquatic form throughout adulthood, examples of full neoteny. Gills are a common juvenile characteristic in amphibians which are kept after maturation; examples are the tiger salamander and rough-skinned newt, both of which retain gills into adulthood. [33]

  3. Nucleic acid notation - Wikipedia

    en.wikipedia.org/wiki/Nucleic_acid_notation

    One example of an ambigraphic nucleic acid notation is AmbiScript, a rationally designed nucleic acid notations that combined many of the visual and functional features of its predecessors. [11] Its notation also uses spatially offset characters to facilitate the visual review and analysis of genetic data.

  4. Human genome - Wikipedia

    en.wikipedia.org/wiki/Human_genome

    The human genome is a complete set of nucleic acid sequences for humans, encoded as the DNA within each of the 24 distinct chromosomes in the cell nucleus. A small DNA molecule is found within individual mitochondria.

  5. Nucleic acid - Wikipedia

    en.wikipedia.org/wiki/Nucleic_acid

    Deoxyribonucleic acid (DNA) is a nucleic acid containing the genetic instructions used in the development and functioning of all known living organisms. The chemical DNA was discovered in 1869, but its role in genetic inheritance was not demonstrated until 1943. The DNA segments that carry this genetic information are called genes.

  6. DNA annotation - Wikipedia

    en.wikipedia.org/wiki/DNA_annotation

    In molecular biology and genetics, DNA annotation or genome annotation is the process of describing the structure and function of the components of a genome, [2] by analyzing and interpreting them in order to extract their biological significance and understand the biological processes in which they participate. [3]

  7. Genetic disorder - Wikipedia

    en.wikipedia.org/wiki/Genetic_disorder

    A chromosomal disorder is a missing, extra, or irregular portion of chromosomal DNA. [33] It can be from an atypical number of chromosomes or a structural abnormality in one or more chromosomes. An example of these disorders is Trisomy 21 (the most common form of Down syndrome), in which there is an extra copy of chromosome 21 in all cells. [34]

  8. Genetic marker - Wikipedia

    en.wikipedia.org/wiki/Genetic_marker

    Genetic markers can be used to study the relationship between an inherited disease and its genetic cause (for example, a particular mutation of a gene that results in a defective protein). It is known that pieces of DNA that lie near each other on a chromosome tend to be inherited together.

  9. Nucleic acid structure - Wikipedia

    en.wikipedia.org/wiki/Nucleic_acid_structure

    In DNA double helix, the two strands of DNA are held together by hydrogen bonds. The nucleotides on one strand base pairs with the nucleotide on the other strand. The secondary structure is responsible for the shape that the nucleic acid assumes. The bases in the DNA are classified as purines and pyrimidines. The purines are adenine and guanine ...