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  2. Neurogenetics - Wikipedia

    en.wikipedia.org/wiki/Neurogenetics

    Human karyogram. Neurogenetics studies the role of genetics in the development and function of the nervous system.It considers neural characteristics as phenotypes (i.e. manifestations, measurable or not, of the genetic make-up of an individual), and is mainly based on the observation that the nervous systems of individuals, even of those belonging to the same species, may not be identical.

  3. Development of the nervous system in humans - Wikipedia

    en.wikipedia.org/wiki/Development_of_the_nervous...

    The development of the nervous system in humans, or neural development, or neurodevelopment involves the studies of embryology, developmental biology, and neuroscience.These describe the cellular and molecular mechanisms by which the complex nervous system forms in humans, develops during prenatal development, and continues to develop postnatally.

  4. Evolution of the brain - Wikipedia

    en.wikipedia.org/wiki/Evolution_of_the_brain

    Genes involved in the neuro-development and in neuron physiology are extremely conserved between mammalian species (94% of genes expressed in common between humans and chimpanzees, 75% between humans and mice), compared to other organs. Therefore, few genes account for species differences in the human brain development and function. [15]

  5. Trinucleotide repeat expansion - Wikipedia

    en.wikipedia.org/wiki/Trinucleotide_repeat_expansion

    Trinucleotide repeat expansion, is a DNA mutation that is responsible for causing any type of disorder classified as a trinucleotide repeat disorder. These disorders are progressive and affect the sequences of the human genome, frequently within the nervous system.

  6. Ribose-5-phosphate isomerase deficiency - Wikipedia

    en.wikipedia.org/wiki/Ribose-5-phosphate_isomer...

    Ribose-5-phosphate isomerase deficiency (RPID) is a rare human disorder caused by mutations in ribose-5-phosphate isomerase, an enzyme of the pentose phosphate pathway.With only four known cases – all diagnosed between 1984 and 2019 – RPI deficiency is the second rarest disease, with Fields condition being the rarest, affecting two known individuals, Catherine and Kirstie Fields.

  7. Behavior mutation - Wikipedia

    en.wikipedia.org/wiki/Behavior_mutation

    For example, when individuals suffer from a mutation that causes them to have low levels of serotonin, there is an observed increase in impulsivity and depression [8] With neurotransmitters playing a central role in the development of aggressive behaviour, it follows that many of the gene mutations that have been implicated with aggressive ...

  8. Development of the nervous system - Wikipedia

    en.wikipedia.org/wiki/Development_of_the_nervous...

    This process is known as neurulation. [8] When the tube is closed at both ends it is filled with embryonic cerebrospinal fluid. [9] As the embryo develops, the anterior part of the neural tube expands and forms three primary brain vesicles, which become the forebrain (prosencephalon), midbrain (mesencephalon), and hindbrain (rhombencephalon).

  9. Developmental plasticity - Wikipedia

    en.wikipedia.org/wiki/Developmental_plasticity

    Developmental plasticity is a general term referring to changes in neural connections during development as a result of environmental interactions as well as neural changes induced by learning. [1] Much like neuroplasticity , or brain plasticity, developmental plasticity is specific to the change in neurons and synaptic connections as a ...