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CH Instruments chi-square or binomial proportion tests
Chi Square Or Binomial Proportion Tests, supplied by CH Instruments, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/binomial+chi-square+test/chi+square+or+binomial+proportion+tests/pmc08841908-149-14-12
Average 90 stars, based on 1 article reviews
chi-square or binomial proportion tests - by Bioz Stars, 2026-10
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Article Title: Low-dose Oral Thimerosal for the Treatment of Oral Herpes: Clinical Trial Results and Improved Outcome After Post-hoc Analysis
Article Snippet: .. Other statistical comparisons of treatment and control data were made using the Chi-square or Binomial Proportion tests. ..



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Atropine but not mecamylamine abolished the depolarizing effects of DAMGO. (A) Application of DAMGO in the presence of a muscarinic receptor antagonist (atropine) produced a reversible hyperpolarization of an LTSI. This effect was reversed after washout. (B) Distribution of changes in the membrane potential induced by DAMGO in eight LTSIs in the presence of atropine. (C) Changes in the firing frequency induced by DAMGO in one spontaneously active LTSI in the presence of atropine. (D) Application of DAMGO in the presence of mecamylamine produced a reversible hyperpolarization of an LTSI. (E) Distribution of changes in the membrane potential induced by DAMGO in 10 LTSIs in the presence of mecamylamine. (F) Another LTSI was reversibly depolarized after DAMGO application in the presence of mecamylamine. This <t>depolarization</t> was associated with increased firing. (G) Distribution of changes in the firing frequency induced by DAMGO in six spontaneously active LTSIs in the presence of mecamylamine. DAMGO significantly increased firing frequency in one LTSI and significantly decreased firing frequency in five LTSIs.
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Atropine but not mecamylamine abolished the depolarizing effects of DAMGO. (A) Application of DAMGO in the presence of a muscarinic receptor antagonist (atropine) produced a reversible hyperpolarization of an LTSI. This effect was reversed after washout. (B) Distribution of changes in the membrane potential induced by DAMGO in eight LTSIs in the presence of atropine. (C) Changes in the firing frequency induced by DAMGO in one spontaneously active LTSI in the presence of atropine. (D) Application of DAMGO in the presence of mecamylamine produced a reversible hyperpolarization of an LTSI. (E) Distribution of changes in the membrane potential induced by DAMGO in 10 LTSIs in the presence of mecamylamine. (F) Another LTSI was reversibly depolarized after DAMGO application in the presence of mecamylamine. This <t>depolarization</t> was associated with increased firing. (G) Distribution of changes in the firing frequency induced by DAMGO in six spontaneously active LTSIs in the presence of mecamylamine. DAMGO significantly increased firing frequency in one LTSI and significantly decreased firing frequency in five LTSIs.
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Atropine but not mecamylamine abolished the depolarizing effects of DAMGO. (A) Application of DAMGO in the presence of a muscarinic receptor antagonist (atropine) produced a reversible hyperpolarization of an LTSI. This effect was reversed after washout. (B) Distribution of changes in the membrane potential induced by DAMGO in eight LTSIs in the presence of atropine. (C) Changes in the firing frequency induced by DAMGO in one spontaneously active LTSI in the presence of atropine. (D) Application of DAMGO in the presence of mecamylamine produced a reversible hyperpolarization of an LTSI. (E) Distribution of changes in the membrane potential induced by DAMGO in 10 LTSIs in the presence of mecamylamine. (F) Another LTSI was reversibly depolarized after DAMGO application in the presence of mecamylamine. This <t>depolarization</t> was associated with increased firing. (G) Distribution of changes in the firing frequency induced by DAMGO in six spontaneously active LTSIs in the presence of mecamylamine. DAMGO significantly increased firing frequency in one LTSI and significantly decreased firing frequency in five LTSIs.
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Atropine but not mecamylamine abolished the depolarizing effects of DAMGO. (A) Application of DAMGO in the presence of a muscarinic receptor antagonist (atropine) produced a reversible hyperpolarization of an LTSI. This effect was reversed after washout. (B) Distribution of changes in the membrane potential induced by DAMGO in eight LTSIs in the presence of atropine. (C) Changes in the firing frequency induced by DAMGO in one spontaneously active LTSI in the presence of atropine. (D) Application of DAMGO in the presence of mecamylamine produced a reversible hyperpolarization of an LTSI. (E) Distribution of changes in the membrane potential induced by DAMGO in 10 LTSIs in the presence of mecamylamine. (F) Another LTSI was reversibly depolarized after DAMGO application in the presence of mecamylamine. This <t>depolarization</t> was associated with increased firing. (G) Distribution of changes in the firing frequency induced by DAMGO in six spontaneously active LTSIs in the presence of mecamylamine. DAMGO significantly increased firing frequency in one LTSI and significantly decreased firing frequency in five LTSIs.
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Atropine but not mecamylamine abolished the depolarizing effects of DAMGO. (A) Application of DAMGO in the presence of a muscarinic receptor antagonist (atropine) produced a reversible hyperpolarization of an LTSI. This effect was reversed after washout. (B) Distribution of changes in the membrane potential induced by DAMGO in eight LTSIs in the presence of atropine. (C) Changes in the firing frequency induced by DAMGO in one spontaneously active LTSI in the presence of atropine. (D) Application of DAMGO in the presence of mecamylamine produced a reversible hyperpolarization of an LTSI. (E) Distribution of changes in the membrane potential induced by DAMGO in 10 LTSIs in the presence of mecamylamine. (F) Another LTSI was reversibly depolarized after DAMGO application in the presence of mecamylamine. This <t>depolarization</t> was associated with increased firing. (G) Distribution of changes in the firing frequency induced by DAMGO in six spontaneously active LTSIs in the presence of mecamylamine. DAMGO significantly increased firing frequency in one LTSI and significantly decreased firing frequency in five LTSIs.
Binomial Chi Squared Test, supplied by CH Instruments, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Atropine but not mecamylamine abolished the depolarizing effects of DAMGO. (A) Application of DAMGO in the presence of a muscarinic receptor antagonist (atropine) produced a reversible hyperpolarization of an LTSI. This effect was reversed after washout. (B) Distribution of changes in the membrane potential induced by DAMGO in eight LTSIs in the presence of atropine. (C) Changes in the firing frequency induced by DAMGO in one spontaneously active LTSI in the presence of atropine. (D) Application of DAMGO in the presence of mecamylamine produced a reversible hyperpolarization of an LTSI. (E) Distribution of changes in the membrane potential induced by DAMGO in 10 LTSIs in the presence of mecamylamine. (F) Another LTSI was reversibly depolarized after DAMGO application in the presence of mecamylamine. This depolarization was associated with increased firing. (G) Distribution of changes in the firing frequency induced by DAMGO in six spontaneously active LTSIs in the presence of mecamylamine. DAMGO significantly increased firing frequency in one LTSI and significantly decreased firing frequency in five LTSIs.

Journal: Frontiers in Cellular Neuroscience

Article Title: Dichotomous Effects of Mu Opioid Receptor Activation on Striatal Low-Threshold Spike Interneurons

doi: 10.3389/fncel.2017.00385

Figure Lengend Snippet: Atropine but not mecamylamine abolished the depolarizing effects of DAMGO. (A) Application of DAMGO in the presence of a muscarinic receptor antagonist (atropine) produced a reversible hyperpolarization of an LTSI. This effect was reversed after washout. (B) Distribution of changes in the membrane potential induced by DAMGO in eight LTSIs in the presence of atropine. (C) Changes in the firing frequency induced by DAMGO in one spontaneously active LTSI in the presence of atropine. (D) Application of DAMGO in the presence of mecamylamine produced a reversible hyperpolarization of an LTSI. (E) Distribution of changes in the membrane potential induced by DAMGO in 10 LTSIs in the presence of mecamylamine. (F) Another LTSI was reversibly depolarized after DAMGO application in the presence of mecamylamine. This depolarization was associated with increased firing. (G) Distribution of changes in the firing frequency induced by DAMGO in six spontaneously active LTSIs in the presence of mecamylamine. DAMGO significantly increased firing frequency in one LTSI and significantly decreased firing frequency in five LTSIs.

Article Snippet: The proportion of depolarization caused by DAMGO in the presence of TTX (66.7%) was significantly larger than that observed in control solution (15.38%; p = 0.007; N-1 Chi-squared test for binomial distributions).

Techniques: Produced, Membrane