Image8_LeishIF3d is a non-canonical cap-binding protein in Leishmania.TIF by Priyanka Bose (7110071)

“…<p>Translation of most cellular mRNAs in eukaryotes proceeds through a cap-dependent pathway, whereby the cap-binding complex, eIF4F, anchors the pre-initiation complex at the 5′ end of mRNAs driving translation initiation. …”

Image1_LeishIF3d is a non-canonical cap-binding protein in Leishmania.TIF by Priyanka Bose (7110071)

“…<p>Translation of most cellular mRNAs in eukaryotes proceeds through a cap-dependent pathway, whereby the cap-binding complex, eIF4F, anchors the pre-initiation complex at the 5′ end of mRNAs driving translation initiation. …”

Restricting the ψ Torsion Angle Has Stereoelectronic Consequences on a Scissile Bond: An Electronic Structure Analysis by Eric R. Strieter (1319670)

Table1_LeishIF3d is a non-canonical cap-binding protein in Leishmania.XLSX by Priyanka Bose (7110071)

“…<p>Translation of most cellular mRNAs in eukaryotes proceeds through a cap-dependent pathway, whereby the cap-binding complex, eIF4F, anchors the pre-initiation complex at the 5′ end of mRNAs driving translation initiation. …”

Table2_LeishIF3d is a non-canonical cap-binding protein in Leishmania.XLSX by Priyanka Bose (7110071)

“…<p>Translation of most cellular mRNAs in eukaryotes proceeds through a cap-dependent pathway, whereby the cap-binding complex, eIF4F, anchors the pre-initiation complex at the 5′ end of mRNAs driving translation initiation. …”

Table3_LeishIF3d is a non-canonical cap-binding protein in Leishmania.XLSX by Priyanka Bose (7110071)

“…<p>Translation of most cellular mRNAs in eukaryotes proceeds through a cap-dependent pathway, whereby the cap-binding complex, eIF4F, anchors the pre-initiation complex at the 5′ end of mRNAs driving translation initiation. …”

Image7_LeishIF3d is a non-canonical cap-binding protein in Leishmania.TIF by Priyanka Bose (7110071)

“…<p>Translation of most cellular mRNAs in eukaryotes proceeds through a cap-dependent pathway, whereby the cap-binding complex, eIF4F, anchors the pre-initiation complex at the 5′ end of mRNAs driving translation initiation. …”

Restricting the ψ Torsion Angle Has Stereoelectronic Consequences on a Scissile Bond: An Electronic Structure Analysis by Eric R. Strieter (1319670)

Image2_LeishIF3d is a non-canonical cap-binding protein in Leishmania.TIF by Priyanka Bose (7110071)

“…<p>Translation of most cellular mRNAs in eukaryotes proceeds through a cap-dependent pathway, whereby the cap-binding complex, eIF4F, anchors the pre-initiation complex at the 5′ end of mRNAs driving translation initiation. …”

Restricting the ψ Torsion Angle Has Stereoelectronic Consequences on a Scissile Bond: An Electronic Structure Analysis by Eric R. Strieter (1319670)

Image6_LeishIF3d is a non-canonical cap-binding protein in Leishmania.TIF by Priyanka Bose (7110071)

“…<p>Translation of most cellular mRNAs in eukaryotes proceeds through a cap-dependent pathway, whereby the cap-binding complex, eIF4F, anchors the pre-initiation complex at the 5′ end of mRNAs driving translation initiation. …”

Image3_LeishIF3d is a non-canonical cap-binding protein in Leishmania.TIF by Priyanka Bose (7110071)

“…<p>Translation of most cellular mRNAs in eukaryotes proceeds through a cap-dependent pathway, whereby the cap-binding complex, eIF4F, anchors the pre-initiation complex at the 5′ end of mRNAs driving translation initiation. …”

Presentation1_LeishIF3d is a non-canonical cap-binding protein in Leishmania.PPTX by Priyanka Bose (7110071)

“…<p>Translation of most cellular mRNAs in eukaryotes proceeds through a cap-dependent pathway, whereby the cap-binding complex, eIF4F, anchors the pre-initiation complex at the 5′ end of mRNAs driving translation initiation. …”

Image4_LeishIF3d is a non-canonical cap-binding protein in Leishmania.TIF by Priyanka Bose (7110071)

“…<p>Translation of most cellular mRNAs in eukaryotes proceeds through a cap-dependent pathway, whereby the cap-binding complex, eIF4F, anchors the pre-initiation complex at the 5′ end of mRNAs driving translation initiation. …”

The Effect of Dosing Regimens on the Antimalarial Efficacy of Dihydroartemisinin-Piperaquine: A Pooled Analysis of Individual Patient Data by The WorldWide Antimalarial Resistance Network (WWARN) DP Study Group (614261)

“…After adjusting for confounding factors, the mg/kg dose of piperaquine was found to be a significant predictor for recrudescence, the risk increasing by 13% (95% CI 5.0%–21%) for every 5 mg/kg decrease in dose; <i>p</i> = 0.002. …”

Radiation increases surface expression of GABA_A Beta 2 containing receptors. by Peter H. Wu (321655)

“…<p>(A) Membrane-impermeable cross-linking studies, performed in dentate slices, revealed a decrease in the intracellular pool of Beta2 subunits without a detectable change in the localization of Beta3 containing receptors. …”

Attenuated LDHA or PDK1 expression increases sensitivity of resistant cell lines to Aβ. by Jordan T. Newington (223389)

“…<b>D</b>) Immunoblots of R2 cell lines (clones 71-23 and 72-5) confirming significantly decreased LDHA expression when compared to a control cell line (SCR) (*P<0.01). …”

Comparison of choroidal thickness in normal eyes and different ocular pathologies in a Brazilian population by Murilo U. Polizelli (10371024)

Data and code from: Ecosystem functional response across precipitation extremes in a sagebrush steppe by Andrew Tredennick (99797)

Effects of TMEM43 on conduction velocity and sodium channel expression. by Vinayakumar Siragam (455948)

“…GAPDH was used as a loading control. Rabbit polyclonal Na_V1.5 antibody specifically detected sodium ion channel (Na_V1.5) expression in all three cell types. …”