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