Titan cells generation <i>in vitro</i> is impacted by various environmental conditions. by Benjamin Hommel (523072)

“…<p>(<b>A</b>) The sequence of media used at steps 2 and 3 of the protocol was crucial for titan cells generation: yeasts cultured in Yeast Peptone Dextrose (YPD) and transferred to minimal medium (MM) produced significantly more titan cells (cells >10μm, dotted grey line) than yeasts cultured in MM or YPD and transferred in MM or YPD, respectively; (<b>B</b>) Exposure to d light at step 3 had a positive impact on titan cells generation compared to incubation in the dark; (<b>C</b>) Raising the incubation temperature to 37°C at step 3 decreased titan cells formation compared to 30°C; (<b>D</b>) Modification of the initial pH of the MM used at step 3 impacted titan cells formation with pH 5.5 being optimal while a more acidic (pH = 4), a neutral (pH = 7) or an alkaline (pH = 8.5) pH inhibited titan cells formation; (<b>E</b>) The impact of hypoxia was tested by physical (closed cap) and by chemical (COCl₂ in MM at 1 nM) method and compared to normoxia (21% oxygen). …”

Change in log10 concentration (CFU/mL) from pre-UV disinfection (N0), immediately after UV disinfection (Nt), and after 24 hour repair incubations for dark (diamond, solid lines) a... by Daniel Ma (12698752)

Enrichment in genes with concordant responses vs. non-concordant responses between the survival profiling and transcriptome profiling experiments. by Alexandra Ketcham (492291)

Titan cells generation is dependent on various genes and requires signaling through the Gpr/PKA/Rim101 pathway <i>in vitro</i>. by Benjamin Hommel (523072)

“…Rim101 (<b>C</b>) and <i>GPR4</i> and <i>GPR5</i> and <i>CAC1</i> <b>(D)</b> are required for titan cells generation <i>in vitro</i> in H99 and KN99α. …”

LRIG1 and CDK6 expression in the lateral ventricular wall cells by Hyung-song Nam (8914220)

“…Although the <i>Cdk6</i> mRNA decreases significantly in the neuroblasts, the DCX+ neuroblasts still show a lot of td-sfGFP immunoreactivity.…”

Host survival and pathogen load during <i>Listeria monocytogenes</i> infection. by Adam Bajgar (730380)

Over-expression of DYRK1A increases HBV RNA levels in HBV-infected dHepaRG cells. by Florentin Pastor (19852287)

Comparison of the histopathological changes after KA/E2 treatment in WT and TLR2 KO mice. by Mi-Kyung Park (56053)

Collapse occurs through attrition of dVL cells. by Christine M. Tait (8648631)

Casein kinase 1 inhibitor partly mimics <i>CSNK1G2</i> effect on PI3K/AKT/mTOR/S6K and ERK signaling in breast cancer cells. by Anh Thu Nguyen Hoang (10661003)

S1 Dataset - by Pamela Bakkabulindi (12914980)

“…Strengthening immunization data quality and its use for improving immunization program performance are critical steps toward improving coverage and equity of immunization programs. …”

S2 Fig - by Octavio A. C. Talyuli (4285141)

Multiple trauma and hemorrhagic shock induce a transcriptional immune response. by Marc-Alexander Oestreich (13961375)

Activation of the AMPK/mTOR signaling pathway correlates with curcumin-activated autophagy to restore D-gal-induced tight junction damage in SCs. by Chen Xue (699418)

Survival data for E. coli K-12 represented as change in log₁₀ concentration (CFU/mL) from pre-UV disinfection (N0), immediately after UV disinfection (Nt), and after 24... by Daniel Ma (12698752)

Apical polarity proteins and tight junctions are reduced on delaminating VL cells. by Christine M. Tait (8648631)

S1 Data - by Fitriani Yustikasari Lubis (17610540)

“…<div><p>The Indonesian government implemented a large-scale social restriction policy as part of the efforts to tackle the COVID-19 pandemic. …”

Effect of <i>CSNK1G2</i> on TAM-mediated PI3K/AKT/mTOR/S6K gene expression in human breast cancer cells. by Anh Thu Nguyen Hoang (10661003)

HPx1 expression is controlled by dietary heme and the E75 transcription factor. by Octavio A. C. Talyuli (4285141)

Table_1_Effect of COVID-19 vaccine on blood glucose metrics in Arabic people with type 1 diabetes.docx by Ebaa Al-Ozairi (5956982)