Parvalbumin (PVALB) ELISA Kits

Human Parvalbumin (PVALB) interaction partners

1. Our data support the hypothesis that the loss of PVALB (show MB ELISA Kits) plays a role in the pathogenesis of thyroid tumors.

2. This study showed that the density of parvalbumin was significantly diminished in the basolateral complex in patients with Parkinson Disease.

3. excitatory synapse density is lower selectively on parvalbumin interneurons in schizophrenia and predicts the activity-dependent down-regulation of parvalbumin and GAD67 (show GAD1 ELISA Kits)

4. Increased numbers of PVALB (show MB ELISA Kits) neurons and fiber labeling in focal cortical dysplasia compared to nondysplastic epileptic temporal neocortex and postmortem controls may be related to cortical malformation.

5. TRPV1 (show TRPV1 ELISA Kits)-, TRPV2 (show TRPV2 ELISA Kits)-, P2X3-, and parvalbumin-immunoreactivity neurons in the human nodose ganglion innervate the pharynx and epiglottis through the pharyngeal branch and superior laryngeal nerve

6. This study demonistrated that differentially expressed in PV neurons in subjects with schizophrenia, including genes associated with WNT (wingless-type), NOTCH, and PGE2 (prostaglandin E2) signaling.

7. This study showed that the parvalbumin basket cell inputs in the dorsolateral prefrontal cortex were lower in patient with schizophrenia.

8. mRNA labeling at the single cell level shows a significant decrease in parvalbumin expression in Parkinson's (PD) cases; however, neuronal density of parvalbumin-positive neurons was not significantly different between PD patients and controls.

9. A subpopulation of projection neurons containing calcium-binding protein parvalbumin (PV) is identified in a precise mapping of the GABAergic cortical distribution.

10. Parvalbumin neurons decrease the drive of the input to the visual cortex in contrast sensitivity.

Mouse (Murine) Parvalbumin (PVALB) interaction partners

1. HIV-1 Tat (show TAT ELISA Kits) causes cognitive deficits and selective loss of parvalbumin, somatostatin (show SST ELISA Kits), and neuronal nitric oxide synthase (show NOS1 ELISA Kits) expressing hippocampal CA1 (show CA1 ELISA Kits) interneuron subpopulations.

2. "reduction of PV(+) neurons" was in all cases, i.e., in PV+/-, Shank1 (show SHANK1 ELISA Kits)-/- and Shank3B (show SHANK3 ELISA Kits)-/- mice, was due to a reduction in Pvalb mRNA and PV protein

3. The calcium-binding protein parvalbumin (PV) is a crucial marker in defining the most predominant interneuron subtype within the cerebral cortex.

4. dysfunction of parvalbumin positive interneurons signaling in the prefrontal cortex (PFC (show CFP ELISA Kits)) specifically produces deficits in the cognitive domain, but does not give rise to PFC (show CFP ELISA Kits)-dependent correlates of negative or positive symptoms.

5. Thus PV+ GP neurons are synaptically positioned to directly coordinate activity between BG input nuclei, the striatum and STN, and thalamic-output from the SNr.

6. The PTEN autism spectrum disorder alleles are hypomorphic in regulating cell size and the parvalbumin/somatostatin ratio in comparison to WT PTEN.

7. These findings confirm that fate determination of cortical interneurons subgroups is crucially influenced by Shh (show SHH ELISA Kits) signaling, and provide a system for the further study of interneuron fate and function.

8. Parvalbumin and Npas1 neurons have different topologies within the basal ganglia.

9. Nearly all parvalbumin interneurons express Lynx1 did not detect Lypd6 in this population. Conversely, in somatostatin interneurons Lypd6 was found in a subset localized to deep cortical layers but no somatostatin neurons show detectable levels of Lynx1.

10. There was a significant correlation between Y-maze performance and PV expression in the dorsal hippocampus in WT mice, but no such correlation in BDNF (show BDNF ELISA Kits)+/- mice.

Rabbit Parvalbumin (PVALB) interaction partners

1. Calbindin (show CALB1 ELISA Kits) and parvalbumin show complementary patterns of expression, but some temporary differences in their time course appear.

2. findings indicate that spinal transection affects nNOS (show NOS1 ELISA Kits) and parvalbumin in different neuronal circuits