• Shuffle
    Toggle On
    Toggle Off
  • Alphabetize
    Toggle On
    Toggle Off
  • Front First
    Toggle On
    Toggle Off
  • Both Sides
    Toggle On
    Toggle Off
  • Read
    Toggle On
    Toggle Off
Reading...
Front

Card Range To Study

through

image

Play button

image

Play button

image

Progress

1/85

Click to flip

Use LEFT and RIGHT arrow keys to navigate between flashcards;

Use UP and DOWN arrow keys to flip the card;

H to show hint;

A reads text to speech;

85 Cards in this Set

  • Front
  • Back
forebrain
prosencephalon- the frontal division of the neural tube, containing the cerebral hemispheres, the thalamus and the hypothalamus
proencephalon
telencephalon and diencephalon
midbrain
mesencephalon- the middle division of the brain
hindbrain
rhombencephalon- the rear division of the brain; in the mature vertebrate, the hindbrain contains the cerebellum, pons, and medulla
rhombencephalon
cosisting of the metencephalon and the myelencephalon
development of the nervous system six stages
1. Neurogenesis, 2. cell migration 3. differentiation 4. synaptogenesis 5. Neuronal cell death 6. synapse rearrangement
zygote
the fertilized egg
ectoderm
the outer cellular layer of the developing fetus, giving rise to the skin and the nervous system
neuronal groove
in the developing embryo, the groove btw. the neural folds.
neural tube
an embryonic struc. w. subdivisions that correspond to the future forebrain, midbrain, and hindbrain.
embryo
the earliest stage in a developing animal
fetus
a developing individual after the embryo stage
neurogenesis
the mitotic division of nonneuronal cells to produce neurons
cell migration
the massive movements of nerve cells or their precursors to establish distinct nerve cell populations (nuclei in the CNS, layers of the cerebral cortex and so on)
differentiation
____ of cells into distinctive types of neurons or glial cells
synaptogenesis
the establishment of synaptic connections as axons and dendrites grow
neuronal cell death
the selective death of many nerve cells
synapse rearrangement
the loss of some synapses and development of others, to refine sysnaptic connections
mitosis
the process of division of somatic cells that involves duplication of DNA
ventricular zone
also called ependymal layer. A region lining the cerebral ventricles that displays mitosis, providing neurons early in development and glial cells throughout life.
cell--cell interactions
the general process during development in which one cell affects the differentiation of other, usually neighboring cells
cell migration
the movement of cells from site of origin to final location
radial glial cells
glial cells that form early in development, spanning the width of the emerging cerebral hemispheres , and guide migrating neurons.
cell adhesion molecule (CAM)
a protein found on the surface of a cell that guides cell migration and/or axonal pathfinding
retrograde degeneration
destruction of the nerve cell body following injury to its axon
anterograde degeneration
also called wallerian degeneration- the loss of the distal portion of an axon resulting from injury to the axon
notochord
a midline struc. arising early in the embryonic development of vertebrates
induction
the process by which one set of cells influences the fate of neighboring cells usually by secreting a chem. factor that changes gene expression in the target cells.
regulation
an adaptive response to early injury, as when developing individuals conpensate for missing or injured cells
stem cell
a cell that is undifferentiated and therefore can take on the fate of any cell that a donor organism can produce
process outgrowth
the extensive growth of axons and dnedrites
synaptogenesis
the establishment of synaptic connections as axons and dendrites grow.
growth cone
the growing tip of an axon or a dendirte
filopodia
very fine, tubular outgrowths from the growth cone.
lamellipodia
sheetlike extensions of a growth cone
chemoattractants
compounds that attract particular classes of growth cones.
chemorepellants
compounds that repel particular classes of growth cones.
death gene
a gene that is expressed only when a cell becomes committed to natural cell death (apoptosis)
caspases
a family of proteins that regulate cell death
diablo
a protein released by mitochondria in response to high calcium levels, that activates apoptosis
inhibitor of apoptosis proteins (IAPs)
a family of proteins that inhibit caspases and thereby stave off apoptosis
Bcl-2
a family of proteins that regulate apoptosis by preventing diablo release from mitochondria
neurotrophic factor (trophic factor)
a target dervived chemical that acts as if it feeds certain neurons to help them survive.
nerve growth factor (NGF)
a susbstance that markedly affects the growth of neurons in spinal ganglia and in the ganglia of the sympathetic nervous system.
brain-derived neurotrophic factor (BDNF)
a protein purified from the brains of animals that can keep some classes of neurons alive
neurotrophin
a chemical that prevents neurons from ddying
synapse rearrangement
also called synaptic remodeling. The loss of some synapses and the development of others; a refinement of synaptic connections that is often seen in development.
chemoaffinity hypothesis
the notion that each cell has a chemical identity that directs it to synapse on he proper target cell during development
multiple sclerosis
disorder characterized by widespread degeneration of myelin
genotype or genome
all the genetic info that one specific individual has inherited
phenotype
the sum of an individual's physical characteristics at one particular time
mutation
a change in the nucleotide sequence of a gene as a result of unfaithful replication
mutant
an animal carrying a gene that differs from the norm or from the alleles carried by its parents
identifiable neurons
neurons that are large and similar from one individual to the next, enabling investigators to recognize them and give them names.
site directed mutagenesis
a technique in molecular biology that changes the sequence of nucleotides in an existing gene.
knockout organism
an individual in which a particular gene has been disabled by an experimenter
transgenic
referring to an animal in which a new or altered gene has bee deliberately introduced into the genome.
amblyopia
reduced visual acuity that is not caused by optical or retinal impairments
binocular deprivation
depriving both eyes of form vision, as by sealing the eyelids
sensitive period
the period during development in which an organism can be permanently altered by a particular experience or treatment
monocular deprivation
depriving one eye of light
ocular dominance histogram
a graph that portrays the strength of response of a brain neuron to stimuli presented to either the left eye or the right eye
Hebbian synapse
a synapse that is strengthened when it successfully drives the postsynaptic cell.
hypoxia
a transient lack of oxygen
phenylketonuria (PKU)
an inherited disorder of protein metabolism in which the absence of an enzyme leads to a toxic buildup of certain compounds, causing mental retardation
down syndrome
mental retardation that is associated with an extra copy of chromosome 21
fragile X syndrome
a condition that is a frequent cause of inherited mental retardation; produced by a fragile site on the X chromosome that seems prone to braking because the DNA there is unstable
trinucleotide repeat
repetition of the same three nucleotides within a gene, which can lead to dysfunction, as in the cases of Huntington's disease and fragile X Syndrome
behavioral teratology
thestudy of impairments in behavior that are produced by embryonic or fetal exposure to toxic substances
fetal alcohol syndrome (FAS)
a disorder including mental retardation and characteristic facial anomalies that affects children exposed to alcohol (through maternal ingestion) during fetal development
attention deficit hyperactivity disorder (ADHD)
syndrome of distractability, impulsiveness, and hyperactivity which, in children, interferes with school performance.
autism
a disorder arising during childhood, characterized by social withdrawal and perseverative (such as by continually nodding the head or making stereotyped finger movements)behavior
perseverate
to continue to show a behavior repeatedly
asperger's syndrome
sometimes called high-functioning autism. A syndrome characterized by difficulties in social cognitive processing; usually accompanied by strong language skills.
Alzheimer's disease
a form of dementia that may appear in middle age but is more frequent among the aged
dementia
drastic failure of cognitive ability, including memory failure and loss of orientation
senile dementia
a neurological disorder of the aged that is characterized by progressive behavioral deterioration, including personality change and profound intellectual decline. It includes, but is not limited to, alzheimer's disease.
senile plaques (amyloid plaques)
small areas of the brain that have abnormal cellular and chemical patterns. senile plaques corelate with senile dementia
beta amyloid
a protein that accumulates in senile plaques in alzheimers disease
neurofibrillary tangle
an abnormal whorl of neurofilaments within nerve cells.
tau
a protein associated with neurofibrillary tangles in alzheimer's disease
amyloid precursor protein (APP)
a protein that, when cleaved by several enzymes, produces beta amyloid.
beta-secretase
an enzyme that cleaves amyloid precursor protein, forming beta amyloid, which can lead to alzheimer's disease.
presenilin
an enzyme that cleaves amyloid precursor protein, forming beta-amyloid, which can lead to alzheimer's disease
apolipoprotein E (ApoE)
a protein that may help break down amyloid.