Tandem Imaging of Breath Ethanol and Acetaldehyde Based on Multiwavelength Enzymatic Biofluorometry by Kenta Iitani (4175995)

“…Reduction of AcH by ADH_RD consumed NADH, leading to a decrease in blue fluorescence (ex. 340 nm, fl. 490 nm). …”

Tandem Imaging of Breath Ethanol and Acetaldehyde Based on Multiwavelength Enzymatic Biofluorometry by Kenta Iitani (4175995)

“…Reduction of AcH by ADH_RD consumed NADH, leading to a decrease in blue fluorescence (ex. 340 nm, fl. 490 nm). …”

Tandem Imaging of Breath Ethanol and Acetaldehyde Based on Multiwavelength Enzymatic Biofluorometry by Kenta Iitani (4175995)

“…Reduction of AcH by ADH_RD consumed NADH, leading to a decrease in blue fluorescence (ex. 340 nm, fl. 490 nm). …”

Tandem Imaging of Breath Ethanol and Acetaldehyde Based on Multiwavelength Enzymatic Biofluorometry by Kenta Iitani (4175995)

“…Reduction of AcH by ADH_RD consumed NADH, leading to a decrease in blue fluorescence (ex. 340 nm, fl. 490 nm). …”

Tandem Imaging of Breath Ethanol and Acetaldehyde Based on Multiwavelength Enzymatic Biofluorometry by Kenta Iitani (4175995)

“…Reduction of AcH by ADH_RD consumed NADH, leading to a decrease in blue fluorescence (ex. 340 nm, fl. 490 nm). …”

The Cellular and Molecular Basis of Bitter Tastant-Induced Bronchodilation by Cheng-Hai Zhang (385288)

“…Interestingly, they increase global intracellular [Ca²⁺]_i, although to a much lower level than bronchoconstrictors. We show that these Ca²⁺ changes in cells at rest are mediated via activation of the canonical bitter taste signaling cascade (i.e., TAS2R-gustducin-phospholipase Cβ [PLCβ]- inositol 1,4,5-triphosphate receptor [IP3R]), and are not sufficient to impact airway contractility. …”

Tandem Imaging of Breath Ethanol and Acetaldehyde Based on Multiwavelength Enzymatic Biofluorometry by Kenta Iitani (4175995)

“…Reduction of AcH by ADH_RD consumed NADH, leading to a decrease in blue fluorescence (ex. 340 nm, fl. 490 nm). …”

Tandem Imaging of Breath Ethanol and Acetaldehyde Based on Multiwavelength Enzymatic Biofluorometry by Kenta Iitani (4175995)

“…Reduction of AcH by ADH_RD consumed NADH, leading to a decrease in blue fluorescence (ex. 340 nm, fl. 490 nm). …”

Minimum number of receptors required for stable binding and the influence of receptor diffusion on binding. by Oliwia M. Szklarczyk (485214)

“…(<b>B</b>) The mean number of stably bound receptors decreases with decreasing diffusivity of the receptors. …”

Table_1_Meta-Analysis of Dyslipidemia Management for the Prevention of Ischemic Stroke Recurrence in China.DOCX by Kang-Ning Chen (9659927)

“…</p><p>Conclusions: Effective lipid-lowering therapy could decrease the blood LDL-C level, which had a protective effect against stroke recurrence. …”

Race and Neighborhood-Related Disparities Spanning the COVID-19 Pandemic: Trajectories of Combined Glycemic Control and Body Mass Index in Youth with Diabetes by Mary Ellen Vajravelu (14205766)

Comparison of the fraction of positive relations for different behavioral updating. by Xiaochen He (455300)

“…<p>The simulation is carried out 10 times on a random network consisting of 100 nodes with average network connectivity 〈<i>k</i>〉 = 4. …”

Enhanced megakaryopoiesis and thrombopoieisis after DT-mediated MK ablation. by Catherine Angénieux (145933)

“…(<b>A</b>) PLT counts of saline- and DT-treated mice (n = 5 and 20, respectively) were measured on day 7 and 8. …”

Enols of Substituted Cyanomalonamides by Ahmad Basheer (1914646)

“…Similar tendency for either the CC/C−C or the C−O/CO bonds was observed. This is ascribed to a hydrogen shift between two regioisomeric enols in an asymmetric double-well potential, which becomes faster at a higher temperature. …”

Enols of Substituted Cyanomalonamides by Ahmad Basheer (1914646)

“…Similar tendency for either the CC/C−C or the C−O/CO bonds was observed. This is ascribed to a hydrogen shift between two regioisomeric enols in an asymmetric double-well potential, which becomes faster at a higher temperature. …”

Enols of Substituted Cyanomalonamides by Ahmad Basheer (1914646)

“…Similar tendency for either the CC/C−C or the C−O/CO bonds was observed. This is ascribed to a hydrogen shift between two regioisomeric enols in an asymmetric double-well potential, which becomes faster at a higher temperature. …”

Enols of Substituted Cyanomalonamides by Ahmad Basheer (1914646)

“…Similar tendency for either the CC/C−C or the C−O/CO bonds was observed. This is ascribed to a hydrogen shift between two regioisomeric enols in an asymmetric double-well potential, which becomes faster at a higher temperature. …”

Enols of Substituted Cyanomalonamides by Ahmad Basheer (1914646)

“…Similar tendency for either the CC/C−C or the C−O/CO bonds was observed. This is ascribed to a hydrogen shift between two regioisomeric enols in an asymmetric double-well potential, which becomes faster at a higher temperature. …”

Enols of Substituted Cyanomalonamides by Ahmad Basheer (1914646)

“…Similar tendency for either the CC/C−C or the C−O/CO bonds was observed. This is ascribed to a hydrogen shift between two regioisomeric enols in an asymmetric double-well potential, which becomes faster at a higher temperature. …”

Enols of Substituted Cyanomalonamides by Ahmad Basheer (1914646)

“…Similar tendency for either the CC/C−C or the C−O/CO bonds was observed. This is ascribed to a hydrogen shift between two regioisomeric enols in an asymmetric double-well potential, which becomes faster at a higher temperature. …”