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  2. Medium spiny neuron - Wikipedia

    en.wikipedia.org/wiki/Medium_spiny_neuron

    Medium spiny neurons have two primary phenotypes (characteristic types): D1-type MSNs of the direct pathway and D2-type MSNs of the indirect pathway. [ 2 ] [ 3 ] [ 4 ] Most striatal MSNs contain only D1-type or D2-type dopamine receptors , but a subpopulation of MSNs exhibit both phenotypes.

  3. Hypertonia - Wikipedia

    en.wikipedia.org/wiki/Hypertonia

    Hypertonia is a term sometimes used synonymously with spasticity and rigidity in the literature surrounding damage to the central nervous system, namely upper motor neuron lesions. [1] Impaired ability of damaged motor neurons to regulate descending pathways gives rise to disordered spinal reflexes , increased excitability of muscle spindles ...

  4. D1–D2 dopamine receptor heteromer - Wikipedia

    en.wikipedia.org/wiki/D1–D2_dopamine_receptor...

    D 1 and D 2 receptors interact primarily through discrete amino acids in the cytoplasmic regions of each receptor, with no involvement of transmembrane parts. The intracellular loop 3 of the D 2 receptor contains two adjacent arginine residues, while the carboxyl tail of the D 1 receptor possesses two adjacent glutamic acid residues.

  5. Nigrostriatal pathway - Wikipedia

    en.wikipedia.org/wiki/Nigrostriatal_pathway

    The substantia nigra is located in the ventral midbrain of each hemisphere. It has two distinct parts, the pars compacta (SNc) and the pars reticulata (SNr). The pars compacta contains dopaminergic neurons from the A9 cell group that forms the nigrostriatal pathway that, by supplying dopamine to the striatum, relays information to the basal ganglia.

  6. Upper motor neuron lesion - Wikipedia

    en.wikipedia.org/wiki/Upper_motor_neuron_lesion

    In Babinski's sign, there is dorsiflexion of the big toe and abduction of the other toes. Physiologically, it is normally present in infants from birth to 12 months. The presence of the Babinski sign after 12 months is the sign of a non-specific upper motor neuron lesion. Increased deep tendon reflex (DTR) Pronator drift [3]

  7. Dopamine receptor D1 - Wikipedia

    en.wikipedia.org/wiki/Dopamine_receptor_D1

    DRD1 Available structures PDB Ortholog search: PDBe RCSB List of PDB id codes 1OZ5 Identifiers Aliases DRD1, dopamine receptor D1, DADR, DRD1A External IDs OMIM: 126449 ; MGI: 99578 ; HomoloGene: 30992 ; GeneCards: DRD1 ; OMA: DRD1 - orthologs Gene location (Human) Chr. Chromosome 5 (human) Band 5q35.2 Start 175,440,036 bp End 175,444,182 bp Gene location (Mouse) Chr. Chromosome 13 (mouse ...

  8. D1-like receptor - Wikipedia

    en.wikipedia.org/wiki/D1-like_receptor

    The D 1-like receptors are a subfamily of dopamine receptors that bind the endogenous neurotransmitter dopamine. [1] The D 1-like subfamily consists of two G protein–coupled receptors that are coupled to G s and mediate excitatory neurotransmission, of which include D 1 and D 5. [2]

  9. Parkinsonian gait - Wikipedia

    en.wikipedia.org/wiki/Parkinsonian_gait

    Parkinsonian gait (or festinating gait, from Latin festinare [to hurry]) is the type of gait exhibited by patients with Parkinson's disease (PD). [2] It is often described by people with Parkinson's as feeling like being stuck in place, when initiating a step or turning, and can increase the risk of falling. [3]