image1_Myostatin Promotes Osteoclastogenesis by Regulating Ccdc50 Gene Expression and RANKL-Induced NF-κB and MAPK Pathways.tif by Xin Zhi (1829224)

“…In RAW264.7 cells and bone marrow monocytes (BMMCs), myostatin activates the expression of the II type receptor ActR II B. Here, we report that myostatin significantly promoted RANKL/M-CSF-induced osteoclastogenesis and activated NF-κB and MAPK pathways in vitro via the Ccdc50 gene. …”

image3_Myostatin Promotes Osteoclastogenesis by Regulating Ccdc50 Gene Expression and RANKL-Induced NF-κB and MAPK Pathways.tif by Xin Zhi (1829224)

“…In RAW264.7 cells and bone marrow monocytes (BMMCs), myostatin activates the expression of the II type receptor ActR II B. Here, we report that myostatin significantly promoted RANKL/M-CSF-induced osteoclastogenesis and activated NF-κB and MAPK pathways in vitro via the Ccdc50 gene. …”

image1_Myostatin Promotes Osteoclastogenesis by Regulating Ccdc50 Gene Expression and RANKL-Induced NF-κB and MAPK Pathways.tif by Xin Zhi (1829224)

“…In RAW264.7 cells and bone marrow monocytes (BMMCs), myostatin activates the expression of the II type receptor ActR II B. Here, we report that myostatin significantly promoted RANKL/M-CSF-induced osteoclastogenesis and activated NF-κB and MAPK pathways in vitro via the Ccdc50 gene. …”

image3_Myostatin Promotes Osteoclastogenesis by Regulating Ccdc50 Gene Expression and RANKL-Induced NF-κB and MAPK Pathways.tif by Xin Zhi (1829224)

“…In RAW264.7 cells and bone marrow monocytes (BMMCs), myostatin activates the expression of the II type receptor ActR II B. Here, we report that myostatin significantly promoted RANKL/M-CSF-induced osteoclastogenesis and activated NF-κB and MAPK pathways in vitro via the Ccdc50 gene. …”

image2_Myostatin Promotes Osteoclastogenesis by Regulating Ccdc50 Gene Expression and RANKL-Induced NF-κB and MAPK Pathways.tif by Xin Zhi (1829224)

“…In RAW264.7 cells and bone marrow monocytes (BMMCs), myostatin activates the expression of the II type receptor ActR II B. Here, we report that myostatin significantly promoted RANKL/M-CSF-induced osteoclastogenesis and activated NF-κB and MAPK pathways in vitro via the Ccdc50 gene. …”

image2_Myostatin Promotes Osteoclastogenesis by Regulating Ccdc50 Gene Expression and RANKL-Induced NF-κB and MAPK Pathways.tif by Xin Zhi (1829224)

“…In RAW264.7 cells and bone marrow monocytes (BMMCs), myostatin activates the expression of the II type receptor ActR II B. Here, we report that myostatin significantly promoted RANKL/M-CSF-induced osteoclastogenesis and activated NF-κB and MAPK pathways in vitro via the Ccdc50 gene. …”

Data_Sheet_1_Characterization of a novel cell wall hydrolase CwlE involved in Bacillus thuringiensis subsp. israelensis mother cell lysis.pdf by Lixin Huang (2852420)

“…The encoded CwlE protein consists of a MurNAc-LAA domain and two highly conserved catalytic residues (E26 and E151). …”

Caveolae/raft-mediated endocytosis is the main route involved in <i>E</i>. <i>granulosus</i> AgB internalization by A549 and RH cells. by Edileuza Danieli da Silva (5176148)

Data for Figs 3–6 and S1–S6 and statistical information for S1–S6 Figs. by Lindsay E. Martin (17377067)

The Role of Oxidoreductases in Determining the Function of the Neisserial Lipid A Phosphoethanolamine Transferase Required for Resistance to Polymyxin by Susannah Piek (629191)

“…LptA decorated one position of the <i>E. coli</i> lipid A headgroups with PEA. …”

Data and statistical information for Figs 7–10 and S7–S10 Figs. by Lindsay E. Martin (17377067)

Efficacy and safety of micafungin versus extensive azoles in the prevention and treatment of invasive fungal infections for neutropenia patients with hematological malignancies: A... by Cho-Hao Lee (4114723)

“…</p><p>Conclusions</p><p>The treatment success rate of MCFG is superior to that of triazoles for the prophylaxis and treatment of IFIs, and correction of the mean patient age demonstrates that efficacy increases as patient age decreases. …”

Over time, the aging-dependent decline in melanization is accelerated by higher temperature. by Lindsay E. Martin (17377067)

The aging-dependent decline in melanization is accelerated by higher temperature. by Lindsay E. Martin (17377067)

Larvae lacking <i>Zip88E</i> have increased susceptibility to high dietary zinc. by Christopher D. Richards (4246669)

“…<i>Zip88E</i>^<i>Δ/Δ</i> flies have a significantly decreased survival rate on 4 and 8 mmol l^-1 ZnCl₂-supplemented media compared to control flies (values are represented as the mean ± SD and compared by multiple unpaired T-test: ***P≤0.001, ****P≤0.0001, n = 3).…”

Representative stromal localization of CS in a cribriform pattern. by Sho Hosokawa (8781551)

Diagrammatic overview of the melanization biochemical cascade and the experimental workflow. by Lindsay E. Martin (17377067)

Summary of the effects of higher temperature, aging, and their interaction on the melanization immune response. by Lindsay E. Martin (17377067)

Principal Components Analyses (PCAs) on the table [degree of niche saturation as a function of mean SST and SST variability] x [6 taxonomic groups]. by Grégory Beaugrand (150537)

Entomopathogenic fungi-derived copper nanoparticles (CuNPs) exhibited minimal toxicity effects against <i>E</i>. <i>eugeniae</i> at 24 and 48h post treatment. by Perumal Vivekanandhan (4863484)