VDR regulates TRPV5 expression. by YongMing Chen (5104925)

“…<p>(A) RT-PCR and (B) WB were performed to examine the expression of TRPV5 following VDR overexpression or knockdown in caki-1 cells. …”

Sensitivity/specificity v.s. threshold parameter. by Lei Nie (556344)

Cobalamin status in autism and schizophrenia. by Yiting Zhang (391974)

Enumeration and characterization of 5$t-expressing CTCs. by Steven R. Pirie-Shepherd (2224690)

“…<p><b>A</b>- Characterized control cell lines representing high (H226), moderate (H1975), low (H2122) and negative (H460) 5T4 staining were prepared and spiked into healthy human blood samples as described in materials and methods. …”

Results of a field experiment testing the response of lobsters aggregated in dens to the introduction of a healthy or clinically infected lobster. by Mark J. Butler IV (419498)

Glycocalyx of BAEC monolayers cultured in 5 by Sandra V. Lopez-Quintero (486268)

“…Only the mean fluorescence representative of Heparan Sulfate was significantly decreased to 55.5±11% in HG (p = 0.023). In addition, the contents of the core proteins Syndecan-1 and Glypican-1 were determined by western blot and consistenly showed that neither high glucose nor Mannitol had an effect on these components. …”

Video_5_Contribution of 5-HT2 Receptors to the Control of the Spinal Locomotor System in Intact Rats.WMV by Henryk Majczyński (830716)

“…Little is known about the role of 5-HT receptors in the control of voluntary locomotion, so we administered inverse agonists of 5-HT₂ (Cyproheptadine; Cypr), 5-HT_2A neutral antagonist (Volinanserin; Volin), 5-HT_2C neutral antagonist (SB 242084), and 5-HT_2B/2C inverse agonist (SB 206553) receptors intrathecally in intact rats and monitored their effects on unrestrained locomotion. …”

Redox and methylation metabolite and cobalamin status in GCLM KO mice. by Yiting Zhang (391974)

Force–displacement curves of M5. by Yukun Hu (427264)

Expression of Fbln5 in targeted mice. by Kathleen Chin (275937)

“…<b>E.</b> Effect of Fbln5 cKO on spontaneous development of prolapse as a function of age. …”

C-terminal, low complexity regions of Pbp1 mediate its interaction with Puf3. by Floortje van de Poll (15810877)

“…Transcript levels are shown in <a href="http://www.plosgenetics.org/article/info:doi/10.1371/journal.pgen.1010774#pgen.1010774.s005" target="_blank">S5 Fig</a>. …”

OmpA Binding Mediates the Effect of Antimicrobial Peptide LL-37 on <i>Acinetobacter baumannii</i> by Ming-Feng Lin (768243)

“…The bacteria-killing effect of LL-37 on <i>A</i>. <i>baumannii</i> was more efficient compared to other AMPs, including human ß–defensin 3 (hBD3) and histatin 5 (Hst5). …”

Five models of human dietary protein resources at Kosenivka using the software FRUITS, v. 3.1 [108]. by Katharina Fuchs (551018)

“…<p>1: Proportions of cereal grain protein (C) and animal meat (A) in the diet of humans from Kosenivka reconstructed from mean δ¹³C and δ¹⁵N values and SEM (<a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0289769#pone.0289769.t004" target="_blank">Table 4</a>). 2: Proportion of cereals calculated for the human mean (h, n = 3) as in model 1 and for individuals 5–7, arranged by decreasing δ¹⁵N in cranial bone collagen. 3: As model 2 but for the proportion of animal meat. 4, 5: Results for food source inputs to the human diet considering either δ¹³C (4) or δ¹⁵N (5) as a single fraction in the FRUITS model (see <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0289769#pone.0289769.s004" target="_blank">S2 Table</a>). …”

Raw, uncropped blots for Fig 5. by Seung Ah Choi (755291)

Expression of <i>Nars2</i> in mouse inner ear and brain. by Mariella Simon (711384)

Age-related differences in ingroup bias and learning mechanisms among Chinese individuals. by Ziyan Guo (7021535)

“…<p><b>A</b> Pre-test stage: the interaction effect between age and dividers’ group reveals a decrease in punishing unfair ingroup dividers (blue) with increasing age (<i>b</i> = -0.03, <i>SE</i> = 0.02, <i>z</i> = -2.05, <i>p</i> = .040), while punishment rates for outgroup dividers (purple) remain unchanged (<i>b</i> = -0.01, <i>SE</i> = 0.02, <i>z</i> = -0.34, <i>p</i> = .734). …”

Effects of evodiamine (EVO) on the cell cycle distribution and apoptosis rate of the H446 and H1688 SCLC cells. by Chunshu Fang (675298)

Systemic role of the peripheral 5HT. by Igor Erjavec (2265613)

“…Changes in the serum Ca²⁺ level, influenced by PTH from parathyroid glands and by 1,25(OH)₂D₃ from the kidney, impact the platelet 5HTT activity, with a bidirectional effect on PSL (green-red arrow). …”

Effects of glycosylation on V1V2 peptide region in the context of the BG505 Env trimeric spike. by Jianhui Tian (383833)

“…Computed secondary structure percentage for amino acid stretches that contain glycans adjacent to Cysteins (HXB2 numbering): 131–157 (analogous to the V1V2 peptide), 385–418 and 296–331. It further demonstrates, in the context of Env trimer, that glycosylation decreases the amount of alpha-helix, beta strands, bridge and turns in these regions.…”

Table 3_Genetic association of ACE2 rs2285666 (C>T) and rs2106809 (A>G) and susceptibility to SARS-CoV-2 infection among the Ghanaian population.docx by Alexander Owusu Boakye (13716966)

“…Among females, those with the T allele of ACE2 rs2285666 had a 38% decreased susceptibility to SARS-CoV-2 infection under the dominant [adjusted odds ratio (aOR) = 0.62; 95%CI = 0.45–0.85, P = 0.003] and heterozygous advantage models (aOR = 0.62; 95%CI = 0.45–0.86, P = 0.004), after adjusting for confounders, but not thee recessive model (aOR = 0.41; 95%CI = 0.03–5.22, P = 0.490). …”