Suppressed expression of <i>CDS1</i> and <i>CDS2</i> resulted in the defective embryonic development. by Xin-Qiao Du (13150022)

Image_2_SIRT1 haplo-insufficiency results in reduced cortical bone thickness, increased porosity and decreased estrogen receptor alpha in bone in adult 129/Sv female mice.tif by Hanna Artsi (777390)

“…</p>Discussion<p>These findings demonstrate that 50% reduction in SIRT1 is sufficient to induce the hallmarks of skeletal aging namely, decreased cortical thickness and increased porosity in female mice, highlighting the role of SIRT1 as a regulator of cortical bone quantity and quality. …”

Image_1_SIRT1 haplo-insufficiency results in reduced cortical bone thickness, increased porosity and decreased estrogen receptor alpha in bone in adult 129/Sv female mice.tif by Hanna Artsi (777390)

“…</p>Discussion<p>These findings demonstrate that 50% reduction in SIRT1 is sufficient to induce the hallmarks of skeletal aging namely, decreased cortical thickness and increased porosity in female mice, highlighting the role of SIRT1 as a regulator of cortical bone quantity and quality. …”

Optimal strategies for high <i>v</i>_<i>R</i> = 1.1386 and <i>T</i>_<i>R</i> = 0.1: (10% of population tested daily). by Mackenzie Dalton (14093874)

Ecdysone response genes are expressed in the ovary of <i>R</i>. <i>prolixus</i> adult females. by Samiha Benrabaa (14817602)

Temporal transcript expression of ecdysone response genes in ovaries. by Samiha Benrabaa (14817602)

Protein kinase substrate identification on functional protein arrays-5 by Lihao Meng (43762)

IRE1 depletion increases chromosome instability. by Iratxe Zuazo-Gaztelu (21071939)

Data_Sheet_1_Changes at a Critical Branchpoint in the Anthocyanin Biosynthetic Pathway Underlie the Blue to Orange Flower Color Transition in Lysimachia arvensis.zip by Mercedes Sánchez-Cabrera (10176290)

“…In particular, F3′5′H and DFR, two genes at a critical branchpoint in the ABP for determining flower color, showed differential expression. …”

Charge Distribution in Cationic Molybdenum Imido Alkylidene <i>N</i>‑Heterocyclic Carbene Complexes: A Combined X‑ray, XAS, XES, DFT, Mössbauer, and Catalysis Approach by Mathis Benedikter (9726148)

“…The binding situation in the corresponding cationic complexes Mo­(<i>N</i>-2,6-Me₂C₆H₃)­(CHCMe₂Ph)­(NHC)­(OC­(CF₃)₃)⁺ B­(Ar^F)₄^– (NHC = IMes (<b>1</b>), IMesCl₂ (<b>2</b>), IMesMe₂ (<b>3</b>), and IMesH₂ (<b>4</b>) was compared to that of the analogous neutral Schrock catalyst Mo­(<i>N</i>-2,6-Me₂C₆H₃)­(CHCMe₂Ph)­((OC­(CF₃)₃))₂ (<b>5</b>). Single-crystal X-ray data were used as a starting point for the optimization of the geometries of the catalysts at the PBE0-D3BJ/def2-SVP level of theory; the obtained data were compared to those obtained from X-ray absorption (XAS) and emission spectroscopy (XES). …”

Charge Distribution in Cationic Molybdenum Imido Alkylidene <i>N</i>‑Heterocyclic Carbene Complexes: A Combined X‑ray, XAS, XES, DFT, Mössbauer, and Catalysis Approach by Mathis Benedikter (9726148)

“…The binding situation in the corresponding cationic complexes Mo­(<i>N</i>-2,6-Me₂C₆H₃)­(CHCMe₂Ph)­(NHC)­(OC­(CF₃)₃)⁺ B­(Ar^F)₄^– (NHC = IMes (<b>1</b>), IMesCl₂ (<b>2</b>), IMesMe₂ (<b>3</b>), and IMesH₂ (<b>4</b>) was compared to that of the analogous neutral Schrock catalyst Mo­(<i>N</i>-2,6-Me₂C₆H₃)­(CHCMe₂Ph)­((OC­(CF₃)₃))₂ (<b>5</b>). Single-crystal X-ray data were used as a starting point for the optimization of the geometries of the catalysts at the PBE0-D3BJ/def2-SVP level of theory; the obtained data were compared to those obtained from X-ray absorption (XAS) and emission spectroscopy (XES). …”

Charge Distribution in Cationic Molybdenum Imido Alkylidene <i>N</i>‑Heterocyclic Carbene Complexes: A Combined X‑ray, XAS, XES, DFT, Mössbauer, and Catalysis Approach by Mathis Benedikter (9726148)

“…The binding situation in the corresponding cationic complexes Mo­(<i>N</i>-2,6-Me₂C₆H₃)­(CHCMe₂Ph)­(NHC)­(OC­(CF₃)₃)⁺ B­(Ar^F)₄^– (NHC = IMes (<b>1</b>), IMesCl₂ (<b>2</b>), IMesMe₂ (<b>3</b>), and IMesH₂ (<b>4</b>) was compared to that of the analogous neutral Schrock catalyst Mo­(<i>N</i>-2,6-Me₂C₆H₃)­(CHCMe₂Ph)­((OC­(CF₃)₃))₂ (<b>5</b>). Single-crystal X-ray data were used as a starting point for the optimization of the geometries of the catalysts at the PBE0-D3BJ/def2-SVP level of theory; the obtained data were compared to those obtained from X-ray absorption (XAS) and emission spectroscopy (XES). …”

Charge Distribution in Cationic Molybdenum Imido Alkylidene <i>N</i>‑Heterocyclic Carbene Complexes: A Combined X‑ray, XAS, XES, DFT, Mössbauer, and Catalysis Approach by Mathis Benedikter (9726148)

“…The binding situation in the corresponding cationic complexes Mo­(<i>N</i>-2,6-Me₂C₆H₃)­(CHCMe₂Ph)­(NHC)­(OC­(CF₃)₃)⁺ B­(Ar^F)₄^– (NHC = IMes (<b>1</b>), IMesCl₂ (<b>2</b>), IMesMe₂ (<b>3</b>), and IMesH₂ (<b>4</b>) was compared to that of the analogous neutral Schrock catalyst Mo­(<i>N</i>-2,6-Me₂C₆H₃)­(CHCMe₂Ph)­((OC­(CF₃)₃))₂ (<b>5</b>). Single-crystal X-ray data were used as a starting point for the optimization of the geometries of the catalysts at the PBE0-D3BJ/def2-SVP level of theory; the obtained data were compared to those obtained from X-ray absorption (XAS) and emission spectroscopy (XES). …”

Charge Distribution in Cationic Molybdenum Imido Alkylidene <i>N</i>‑Heterocyclic Carbene Complexes: A Combined X‑ray, XAS, XES, DFT, Mössbauer, and Catalysis Approach by Mathis Benedikter (9726148)

“…The binding situation in the corresponding cationic complexes Mo­(<i>N</i>-2,6-Me₂C₆H₃)­(CHCMe₂Ph)­(NHC)­(OC­(CF₃)₃)⁺ B­(Ar^F)₄^– (NHC = IMes (<b>1</b>), IMesCl₂ (<b>2</b>), IMesMe₂ (<b>3</b>), and IMesH₂ (<b>4</b>) was compared to that of the analogous neutral Schrock catalyst Mo­(<i>N</i>-2,6-Me₂C₆H₃)­(CHCMe₂Ph)­((OC­(CF₃)₃))₂ (<b>5</b>). Single-crystal X-ray data were used as a starting point for the optimization of the geometries of the catalysts at the PBE0-D3BJ/def2-SVP level of theory; the obtained data were compared to those obtained from X-ray absorption (XAS) and emission spectroscopy (XES). …”

Charge Distribution in Cationic Molybdenum Imido Alkylidene <i>N</i>‑Heterocyclic Carbene Complexes: A Combined X‑ray, XAS, XES, DFT, Mössbauer, and Catalysis Approach by Mathis Benedikter (9726148)

“…The binding situation in the corresponding cationic complexes Mo­(<i>N</i>-2,6-Me₂C₆H₃)­(CHCMe₂Ph)­(NHC)­(OC­(CF₃)₃)⁺ B­(Ar^F)₄^– (NHC = IMes (<b>1</b>), IMesCl₂ (<b>2</b>), IMesMe₂ (<b>3</b>), and IMesH₂ (<b>4</b>) was compared to that of the analogous neutral Schrock catalyst Mo­(<i>N</i>-2,6-Me₂C₆H₃)­(CHCMe₂Ph)­((OC­(CF₃)₃))₂ (<b>5</b>). Single-crystal X-ray data were used as a starting point for the optimization of the geometries of the catalysts at the PBE0-D3BJ/def2-SVP level of theory; the obtained data were compared to those obtained from X-ray absorption (XAS) and emission spectroscopy (XES). …”

Prorenin increases M1 phenotype (CD86-positive) switching in primary microglial cells. by Li Hu (326656)

PEDV does not induce macropinocytosis in Vero cells. by Xiongnan Chen (13307178)

A Ligand-Based Drug Design. Discovery of 4‑Trifluoromethyl-7,8-pyranocoumarin as a Selective Inhibitor of Human Cytochrome P450 1A2 by Jiawang Liu (1330971)

“…With a 5 min preincubation in the presence of NADPH, 0.01 μM 7,8-furanoflavone completely inactivates P450 1A2 but does not influence the activities of P450s 1A1 and 1B1. …”

Changes in the SF change rate every 5 s in Experiment 1. by Hiroaki Furukawa (14341649)

“…Compared to no footsteps condition (NF), the step frequency seems to decrease in the +5 bpm (A) and -5 bpm (B) footsteps condition but there were no significant differences between these conditions.…”

Immunohistochemistry (IMH) and hybridization (ISH) of synovial tissues for BMP-5 by Carsten P Bramlage (18991)