Comparative Proteomic Analysis of <i>Brassica napus</i> in Response to Drought Stress by Jin Koh (121651)

“…Functional analysis indicated that the number of proteins associated with metabolism, protein folding and degradation, and signaling decreased, while those related to energy (photosynthesis), protein synthesis, and stress and defense increased in response to drought stress. …”

Table_2_Clostridium cellulovorans Proteomic Responses to Butanol Stress.XLSX by Paolo Costa (1396552)

“…Several additional metabolic adaptations were triggered by butanol exposure such as the up-regulation of V- and F-type ATPases (involved in ATP synthesis/generation of proton motive force), enzymes involved in amino acid (e.g., arginine, lysine, methionine, and branched chain amino acids) biosynthesis and proteins involved in cell envelope re-arrangement (e.g., the products of Clocel_4136, Clocel_4137, Clocel_4144, Clocel_4162 and Clocel_4352, involved in the biosynthesis of saturated fatty acids) and a redistribution of carbon flux through fermentative pathways (acetate and formate yields were increased and decreased, respectively). …”

Table_1_Clostridium cellulovorans Proteomic Responses to Butanol Stress.DOCX by Paolo Costa (1396552)

“…Several additional metabolic adaptations were triggered by butanol exposure such as the up-regulation of V- and F-type ATPases (involved in ATP synthesis/generation of proton motive force), enzymes involved in amino acid (e.g., arginine, lysine, methionine, and branched chain amino acids) biosynthesis and proteins involved in cell envelope re-arrangement (e.g., the products of Clocel_4136, Clocel_4137, Clocel_4144, Clocel_4162 and Clocel_4352, involved in the biosynthesis of saturated fatty acids) and a redistribution of carbon flux through fermentative pathways (acetate and formate yields were increased and decreased, respectively). …”

Table_3_Clostridium cellulovorans Proteomic Responses to Butanol Stress.XLSX by Paolo Costa (1396552)

“…Several additional metabolic adaptations were triggered by butanol exposure such as the up-regulation of V- and F-type ATPases (involved in ATP synthesis/generation of proton motive force), enzymes involved in amino acid (e.g., arginine, lysine, methionine, and branched chain amino acids) biosynthesis and proteins involved in cell envelope re-arrangement (e.g., the products of Clocel_4136, Clocel_4137, Clocel_4144, Clocel_4162 and Clocel_4352, involved in the biosynthesis of saturated fatty acids) and a redistribution of carbon flux through fermentative pathways (acetate and formate yields were increased and decreased, respectively). …”

Table_5_Clostridium cellulovorans Proteomic Responses to Butanol Stress.XLSX by Paolo Costa (1396552)

“…Several additional metabolic adaptations were triggered by butanol exposure such as the up-regulation of V- and F-type ATPases (involved in ATP synthesis/generation of proton motive force), enzymes involved in amino acid (e.g., arginine, lysine, methionine, and branched chain amino acids) biosynthesis and proteins involved in cell envelope re-arrangement (e.g., the products of Clocel_4136, Clocel_4137, Clocel_4144, Clocel_4162 and Clocel_4352, involved in the biosynthesis of saturated fatty acids) and a redistribution of carbon flux through fermentative pathways (acetate and formate yields were increased and decreased, respectively). …”

Table_4_Clostridium cellulovorans Proteomic Responses to Butanol Stress.XLSX by Paolo Costa (1396552)

“…Several additional metabolic adaptations were triggered by butanol exposure such as the up-regulation of V- and F-type ATPases (involved in ATP synthesis/generation of proton motive force), enzymes involved in amino acid (e.g., arginine, lysine, methionine, and branched chain amino acids) biosynthesis and proteins involved in cell envelope re-arrangement (e.g., the products of Clocel_4136, Clocel_4137, Clocel_4144, Clocel_4162 and Clocel_4352, involved in the biosynthesis of saturated fatty acids) and a redistribution of carbon flux through fermentative pathways (acetate and formate yields were increased and decreased, respectively). …”

Image_4_Protein Disulfide Isomerases Regulate IgE-Mediated Mast Cell Responses and Their Inhibition Confers Protective Effects During Food Allergy.tif by Dylan Krajewski (5881880)

“…<p>The thiol isomerase, protein disulfide isomerase (PDI), plays important intracellular roles during protein folding, maintaining cellular function and viability. …”

Image_3_Protein Disulfide Isomerases Regulate IgE-Mediated Mast Cell Responses and Their Inhibition Confers Protective Effects During Food Allergy.tif by Dylan Krajewski (5881880)

“…<p>The thiol isomerase, protein disulfide isomerase (PDI), plays important intracellular roles during protein folding, maintaining cellular function and viability. …”

Image_1_Protein Disulfide Isomerases Regulate IgE-Mediated Mast Cell Responses and Their Inhibition Confers Protective Effects During Food Allergy.tif by Dylan Krajewski (5881880)

“…<p>The thiol isomerase, protein disulfide isomerase (PDI), plays important intracellular roles during protein folding, maintaining cellular function and viability. …”

Image_2_Protein Disulfide Isomerases Regulate IgE-Mediated Mast Cell Responses and Their Inhibition Confers Protective Effects During Food Allergy.tif by Dylan Krajewski (5881880)

“…<p>The thiol isomerase, protein disulfide isomerase (PDI), plays important intracellular roles during protein folding, maintaining cellular function and viability. …”

Power-law product rule for integration of two input signals in an FCD system, where both inputs bind the same receptor with different number of sites. by Yuval Hart (384894)

“…<p>(A) Let L₁ have one binding site, and L₂ have two sites. …”

DataSheet_1_Network Biology Identifies Novel Regulators of CFTR Trafficking and Membrane Stability.pdf by Cláudia Almeida Loureiro (6796022)

“…Although small-molecule compounds have been identified and commercialized that can correct its folding or gating, an efficient retention of F508del CFTR at the PM has not yet been explored pharmacologically despite being recognized as a crucial factor for improving functional rescue of chloride transport. …”

Table_2_Network Biology Identifies Novel Regulators of CFTR Trafficking and Membrane Stability.xlsx by Cláudia Almeida Loureiro (6796022)

“…Although small-molecule compounds have been identified and commercialized that can correct its folding or gating, an efficient retention of F508del CFTR at the PM has not yet been explored pharmacologically despite being recognized as a crucial factor for improving functional rescue of chloride transport. …”

Table_1_Network Biology Identifies Novel Regulators of CFTR Trafficking and Membrane Stability.xlsx by Cláudia Almeida Loureiro (6796022)

“…Although small-molecule compounds have been identified and commercialized that can correct its folding or gating, an efficient retention of F508del CFTR at the PM has not yet been explored pharmacologically despite being recognized as a crucial factor for improving functional rescue of chloride transport. …”

Sensory setae, epidermal glands and VNC structure in PS 2 of <i>Pseudopallene</i> sp. by Georg Brenneis (552078)

“…<b>A</b>: Walking leg segment 1 to anal tubercle, ventral view. …”

Proteome dynamics of cold-acclimating <i>Rhododendron</i> species contrasting in their freezing tolerance and thermonasty behavior by Jose V. Die (460385)

“…<div><p>To gain a better understanding of cold acclimation in rhododendron and in woody perennials in general, we used the 2D-DIGE technique to analyze the rhododendron proteome during the seasonal development of freezing tolerance. …”

Table1_Cryo-EM Structure and Activator Screening of Human Tryptophan Hydroxylase 2.docx by Kongfu Zhu (13247319)

“…Here, we solved the 3.0 Å cryo-EM structure of the TPH2 tetramer. Then, based on the structure, we conducted allosteric site prediction and small-molecule activator screening to the obtained cavity. …”

Image2_Cryo-EM Structure and Activator Screening of Human Tryptophan Hydroxylase 2.TIF by Kongfu Zhu (13247319)

“…Here, we solved the 3.0 Å cryo-EM structure of the TPH2 tetramer. Then, based on the structure, we conducted allosteric site prediction and small-molecule activator screening to the obtained cavity. …”

Image1_Cryo-EM Structure and Activator Screening of Human Tryptophan Hydroxylase 2.TIF by Kongfu Zhu (13247319)

“…Here, we solved the 3.0 Å cryo-EM structure of the TPH2 tetramer. Then, based on the structure, we conducted allosteric site prediction and small-molecule activator screening to the obtained cavity. …”

Image3_Cryo-EM Structure and Activator Screening of Human Tryptophan Hydroxylase 2.TIF by Kongfu Zhu (13247319)

“…Here, we solved the 3.0 Å cryo-EM structure of the TPH2 tetramer. Then, based on the structure, we conducted allosteric site prediction and small-molecule activator screening to the obtained cavity. …”