Photomicrograph of vaginal smears of the last examined estrous cycle of female Wistar rats (Scale 100 μm). by Ha Thi Nguyen (8937140)

Subjects:

Schematic representation of the role of phenoloxidase enzyme(s) in nutrient cycling. by Benneth O. I. Esiana (11614304)

Perturbation of binucleation decreases yolk protein expression and lipid transport to the germline. by Lotte M. van Rijnberk (3716362)

Mononucleation of the intestine causes an X chromosome specific decrease in expression levels. by Lotte M. van Rijnberk (3716362)

Commute cycling potential in Turku. by Emilia Suomalainen (22614676)

Decreased <i>Bgl-</i>FaNaC expression in the left parietal ganglion following <i>S</i>. <i>mansoni</i> infection. by Laura C. Vicente-Rodríguez (16437803)

“…<p><b>a-c:</b> Decreased <i>Bgl</i>-FaNaC hybridization on the dorsal surface of the left parietal ganglion in infected specimens. …”

nsP4-C483Y or Q192L mutations decrease sensitivity to 4′-FlU. by Peiqi Yin (6533747)

Calculation of chl-a anomalies from <i>in situ</i> analog chl-a values. by Benjamin M. Kraemer (7526225)

ECoG timescales decrease during spatial attention. by Isabel Raposo (21615517)

“…If power was above the threshold (<i>z</i> > 1.96) for a minimum of 10% of the time window (500 ms) after the cue, the channel was considered hemifield-selective. …”

Oxacillin MICs of cycle 50 and cycle 60 VAN-exposed lineages. by Samuel E. Blechman (19506884)

“…All MICs are given in units of μg/ml. Oxacillin MICs increased slightly between (<b>A</b>) cycle 50 and (<b>B</b>) cycle 60 (two-sided Wilcoxon signed-rank test p-value = 0.023).…”

Technoeconomic and Life-Cycle Assessment for Electrocatalytic Production of Furandicarboxylic Acid by Poojan Patel (12134832)

Subjects:

Percentage of exhale flux penetrating through the mask fabric for different values of <i>c</i>_<i>k</i>; a–c and d–f decreasing porosity for outward and inward protection model respectively; <i>k</i>_<i>L</i> is head loss coefficient for inward protection model. by Akshay Anand (118579)

Table_1_Physiology of Highly Radioresistant Escherichia coli After Experimental Evolution for 100 Cycles of Selection.xlsx by Steven T. Bruckbauer (6256799)

“…Utilizing experimental evolution and continuing previous work, we have generated the most IR-resistant Escherichia coli populations developed to date. After 100 cycles of selection, the dose required to kill 99% the four replicate populations (IR9-100, IR10-100, IR11-100, and IR12-100) has increased from 750 Gy to approximately 3,000 Gy. …”

Image_4_Physiology of Highly Radioresistant Escherichia coli After Experimental Evolution for 100 Cycles of Selection.TIF by Steven T. Bruckbauer (6256799)

“…Utilizing experimental evolution and continuing previous work, we have generated the most IR-resistant Escherichia coli populations developed to date. After 100 cycles of selection, the dose required to kill 99% the four replicate populations (IR9-100, IR10-100, IR11-100, and IR12-100) has increased from 750 Gy to approximately 3,000 Gy. …”

Table_3_Physiology of Highly Radioresistant Escherichia coli After Experimental Evolution for 100 Cycles of Selection.xlsx by Steven T. Bruckbauer (6256799)

“…Utilizing experimental evolution and continuing previous work, we have generated the most IR-resistant Escherichia coli populations developed to date. After 100 cycles of selection, the dose required to kill 99% the four replicate populations (IR9-100, IR10-100, IR11-100, and IR12-100) has increased from 750 Gy to approximately 3,000 Gy. …”

Image_3_Physiology of Highly Radioresistant Escherichia coli After Experimental Evolution for 100 Cycles of Selection.TIF by Steven T. Bruckbauer (6256799)

“…Utilizing experimental evolution and continuing previous work, we have generated the most IR-resistant Escherichia coli populations developed to date. After 100 cycles of selection, the dose required to kill 99% the four replicate populations (IR9-100, IR10-100, IR11-100, and IR12-100) has increased from 750 Gy to approximately 3,000 Gy. …”

Image_4_Physiology of Highly Radioresistant Escherichia coli After Experimental Evolution for 100 Cycles of Selection.TIF by Steven T. Bruckbauer (6256799)

“…Utilizing experimental evolution and continuing previous work, we have generated the most IR-resistant Escherichia coli populations developed to date. After 100 cycles of selection, the dose required to kill 99% the four replicate populations (IR9-100, IR10-100, IR11-100, and IR12-100) has increased from 750 Gy to approximately 3,000 Gy. …”

Image_3_Physiology of Highly Radioresistant Escherichia coli After Experimental Evolution for 100 Cycles of Selection.TIF by Steven T. Bruckbauer (6256799)

“…Utilizing experimental evolution and continuing previous work, we have generated the most IR-resistant Escherichia coli populations developed to date. After 100 cycles of selection, the dose required to kill 99% the four replicate populations (IR9-100, IR10-100, IR11-100, and IR12-100) has increased from 750 Gy to approximately 3,000 Gy. …”

Table_3_Physiology of Highly Radioresistant Escherichia coli After Experimental Evolution for 100 Cycles of Selection.xlsx by Steven T. Bruckbauer (6256799)

“…Utilizing experimental evolution and continuing previous work, we have generated the most IR-resistant Escherichia coli populations developed to date. After 100 cycles of selection, the dose required to kill 99% the four replicate populations (IR9-100, IR10-100, IR11-100, and IR12-100) has increased from 750 Gy to approximately 3,000 Gy. …”

Image_2_Physiology of Highly Radioresistant Escherichia coli After Experimental Evolution for 100 Cycles of Selection.TIF by Steven T. Bruckbauer (6256799)

“…Utilizing experimental evolution and continuing previous work, we have generated the most IR-resistant Escherichia coli populations developed to date. After 100 cycles of selection, the dose required to kill 99% the four replicate populations (IR9-100, IR10-100, IR11-100, and IR12-100) has increased from 750 Gy to approximately 3,000 Gy. …”