Image1_Hyperactive KRAS/MAPK signaling disrupts normal lymphatic vessel architecture and function.JPEG by Lorenzo M. Fernandes (17038200)

Image3_Hyperactive KRAS/MAPK signaling disrupts normal lymphatic vessel architecture and function.JPEG by Lorenzo M. Fernandes (17038200)

Image2_Hyperactive KRAS/MAPK signaling disrupts normal lymphatic vessel architecture and function.JPEG by Lorenzo M. Fernandes (17038200)

Image4_Hyperactive KRAS/MAPK signaling disrupts normal lymphatic vessel architecture and function.JPEG by Lorenzo M. Fernandes (17038200)

Image4_Hyperactive KRAS/MAPK signaling disrupts normal lymphatic vessel architecture and function.JPEG by Lorenzo M. Fernandes (17038200)

Image5_Hyperactive KRAS/MAPK signaling disrupts normal lymphatic vessel architecture and function.JPEG by Lorenzo M. Fernandes (17038200)

Image1_Hyperactive KRAS/MAPK signaling disrupts normal lymphatic vessel architecture and function.JPEG by Lorenzo M. Fernandes (17038200)

Image3_Hyperactive KRAS/MAPK signaling disrupts normal lymphatic vessel architecture and function.JPEG by Lorenzo M. Fernandes (17038200)

Image5_Hyperactive KRAS/MAPK signaling disrupts normal lymphatic vessel architecture and function.JPEG by Lorenzo M. Fernandes (17038200)

Image2_Hyperactive KRAS/MAPK signaling disrupts normal lymphatic vessel architecture and function.JPEG by Lorenzo M. Fernandes (17038200)

Orientation- and size-dependent room-temperature plasticity in ZrC crystals by S. Kiani (692469)

“…For both the orientations, yield strengths increase with decreasing crystal size. ZrC(111) is found to be up to 10× softer than ZrC(100). …”

Specific amino acids are over-represented at position 2 in <i>S</i>. <i>cerevisiae</i> proteome. by Salomé Nashed (16839488)

“…Table (right) recapitulates quantitative values calculated to identify significant amino acid usage biases at position 2: position2/mean log2Ratio, HGT score obtained from hypergeometric tests, and aspecificity scores (see <a href="http://www.plosgenetics.org/article/info:doi/10.1371/journal.pgen.1010848#sec012" target="_blank">Methods</a>). …”

DataSheet_1_Effects of osteoblast-derived extracellular vesicles on aggressiveness, redox status and mitochondrial bioenergetics of MNNG/HOS osteosarcoma cells.pdf by Marco Ponzetti (14216126)

“…In summary, our findings suggest that OB-EVs could serve as important means through which TME and osteosarcoma core cross-communicate. …”

Effects of Innexin knockdown with RNAi on the strength of the JON-GF connection. by Adeline P. Pézier (2600692)

“…For full genotypes see <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0152211#pone.0152211.s004" target="_blank">S1 Table</a>.…”

Table_3_Identifying Temporally Regulated Root Nodulation Biomarkers Using Time Series Gene Co-Expression Network Analysis.xlsx by William L. Poehlman (7598351)

Image_2_Identifying Temporally Regulated Root Nodulation Biomarkers Using Time Series Gene Co-Expression Network Analysis.tif by William L. Poehlman (7598351)

Table_1_Identifying Temporally Regulated Root Nodulation Biomarkers Using Time Series Gene Co-Expression Network Analysis.xlsx by William L. Poehlman (7598351)

Table_4_Identifying Temporally Regulated Root Nodulation Biomarkers Using Time Series Gene Co-Expression Network Analysis.xlsx by William L. Poehlman (7598351)

<i>Wolbachia</i>-mediated virus blocking in mosquito cells is dependent on XRN1-mediated viral RNA degradation and influenced by viral replication rate by Saijo Thomas (204009)

Image_1_Identifying Temporally Regulated Root Nodulation Biomarkers Using Time Series Gene Co-Expression Network Analysis.tif by William L. Poehlman (7598351)