Effects of GCGR interactor overexpression on glucagon-induced cAMP accumulation in primary mouse hepatocytes, CHO cells expressing GCGR and HepG2 stably expressing GCGR. by Junfeng Han (755026)

“…Each sample was analyzed in triplicate. C) Overexpression of YWHAB significantly decreased glucagon-induced cAMP accumulation in CHO cells expressing GCGR (*p<0.05 when compared to the pcDNA3.1 control group, N = 3); Overexpression of LDLR and TMED2 significantly increased glucagon-induced cAMP accumulation in CHO cells expressing GCGR (*p<0.05, N = 3), 0.1 nM glucagon. …”

Expression of the LMP1 protein is sufficient to inhibit eIF2α phosphorylation and inhibit ATF4 and CHOP expression in uninfected NOKs. by Deo R. Singh (4784112)

Higher frequency (50 Hz) conduction is associated with shortening of stationary, and an increase in distance between stationary mitochondria. by Marija Sajic (332611)

“…(C). Frequency distribution of length of stationary mitochondria between groups showed a significantly lower number of long mitochondria (i.e., 4 µm) and higher number of short (i.e., 2 µm) in axons conducting at high frequency, than in sham-stimulated axons. …”

DataSheet_2_Light activation of the dopaminergic system occurs after eye-opening in the mouse retina.xlsx by Vrinda Jain (15429665)

Changes in decadal precipitation and JULES inundation between 1990–1999 and 2089–2098. by Nic Gedney (19762301)

The impact of PdcB phase variation on toxin production is unclear. by Leila M. Reyes Ruiz (6690206)

Phase variation of PdcB modulates c-di-GMP at the population and single-cell levels. by Leila M. Reyes Ruiz (6690206)

Method for the Large-Scale Synthesis of Multifunctional 1,4-Dihydro-pyrrolo[3,2‑<i>b</i>]pyrroles by Mariusz Tasior (1457731)

“…The conditions identified (first step: toluene/AcOH = 1:1, 1 h, 50 °C; second step: toluene/AcOH = 1:1, Fe­(ClO₄)₃·H₂O, 16 h, 50 °C) resulted in the formation of tetraarylpyrrolo­[3,2-<i>b</i>]­pyrroles in a 6–69% yield. …”

Method for the Large-Scale Synthesis of Multifunctional 1,4-Dihydro-pyrrolo[3,2‑<i>b</i>]pyrroles by Mariusz Tasior (1457731)

“…The conditions identified (first step: toluene/AcOH = 1:1, 1 h, 50 °C; second step: toluene/AcOH = 1:1, Fe­(ClO₄)₃·H₂O, 16 h, 50 °C) resulted in the formation of tetraarylpyrrolo­[3,2-<i>b</i>]­pyrroles in a 6–69% yield. …”

Effects of overexpression of selected GCGR interactors on glucose production in primary mouse hepatocytes. by Junfeng Han (755026)

“…Results are presented as mean ± S.E. of three independent experiments. C) Overexpression of CAV1 and GALK1 increased glucose production significantly at basal level (*p< 0.05, **p<0.01 vs cells transfected with pcDNA3.1); D) Overexpression of LDLR and TMED2 increased 100 nM glucagon-stimulated glucose production while YWHAB decreased glucagon-stimulated glucose production significantly (*p< 0.05,**p<0.01 vs cells transfected with pcDNA3.1, N = 3 per group).…”

Transgenerational alteration and inheritance of DNA methylation patterns in 20 randomly chosen S1 plants derived from a Hg²⁺(50 µm)-stressed S0 individual. by Xiufang Ou (136093)

Unambiguous Identification of Möbius Aromaticity for <i>meso</i>-Aryl-Substituted [28]Hexaphyrins(1.1.1.1.1.1) by Jeyaraman Sankar (1607209)

“…In the solid state, [28]hexaphyrins(1.1.1.1.1.1) take either planar or Möbius-twisted conformations, depending upon the <i>meso</i>-aryl substituents and crystallization conditions, indicating a small energy difference between the two conformers. Importantly, when the temperature is decreased to −100 °C in THF, these rapid interconversions among Möbius conformations are frozen, allowing the detection of a single [28]hexaphyrin(1.1.1.1.1.1) species having a Möbius conformation. …”

Unambiguous Identification of Möbius Aromaticity for <i>meso</i>-Aryl-Substituted [28]Hexaphyrins(1.1.1.1.1.1) by Jeyaraman Sankar (1607209)

“…In the solid state, [28]hexaphyrins(1.1.1.1.1.1) take either planar or Möbius-twisted conformations, depending upon the <i>meso</i>-aryl substituents and crystallization conditions, indicating a small energy difference between the two conformers. Importantly, when the temperature is decreased to −100 °C in THF, these rapid interconversions among Möbius conformations are frozen, allowing the detection of a single [28]hexaphyrin(1.1.1.1.1.1) species having a Möbius conformation. …”

Unambiguous Identification of Möbius Aromaticity for <i>meso</i>-Aryl-Substituted [28]Hexaphyrins(1.1.1.1.1.1) by Jeyaraman Sankar (1607209)

“…In the solid state, [28]hexaphyrins(1.1.1.1.1.1) take either planar or Möbius-twisted conformations, depending upon the <i>meso</i>-aryl substituents and crystallization conditions, indicating a small energy difference between the two conformers. Importantly, when the temperature is decreased to −100 °C in THF, these rapid interconversions among Möbius conformations are frozen, allowing the detection of a single [28]hexaphyrin(1.1.1.1.1.1) species having a Möbius conformation. …”

Unambiguous Identification of Möbius Aromaticity for <i>meso</i>-Aryl-Substituted [28]Hexaphyrins(1.1.1.1.1.1) by Jeyaraman Sankar (1607209)

“…In the solid state, [28]hexaphyrins(1.1.1.1.1.1) take either planar or Möbius-twisted conformations, depending upon the <i>meso</i>-aryl substituents and crystallization conditions, indicating a small energy difference between the two conformers. Importantly, when the temperature is decreased to −100 °C in THF, these rapid interconversions among Möbius conformations are frozen, allowing the detection of a single [28]hexaphyrin(1.1.1.1.1.1) species having a Möbius conformation. …”

Unambiguous Identification of Möbius Aromaticity for <i>meso</i>-Aryl-Substituted [28]Hexaphyrins(1.1.1.1.1.1) by Jeyaraman Sankar (1607209)

“…In the solid state, [28]hexaphyrins(1.1.1.1.1.1) take either planar or Möbius-twisted conformations, depending upon the <i>meso</i>-aryl substituents and crystallization conditions, indicating a small energy difference between the two conformers. Importantly, when the temperature is decreased to −100 °C in THF, these rapid interconversions among Möbius conformations are frozen, allowing the detection of a single [28]hexaphyrin(1.1.1.1.1.1) species having a Möbius conformation. …”

Unambiguous Identification of Möbius Aromaticity for <i>meso</i>-Aryl-Substituted [28]Hexaphyrins(1.1.1.1.1.1) by Jeyaraman Sankar (1607209)

“…In the solid state, [28]hexaphyrins(1.1.1.1.1.1) take either planar or Möbius-twisted conformations, depending upon the <i>meso</i>-aryl substituents and crystallization conditions, indicating a small energy difference between the two conformers. Importantly, when the temperature is decreased to −100 °C in THF, these rapid interconversions among Möbius conformations are frozen, allowing the detection of a single [28]hexaphyrin(1.1.1.1.1.1) species having a Möbius conformation. …”

Unambiguous Identification of Möbius Aromaticity for <i>meso</i>-Aryl-Substituted [28]Hexaphyrins(1.1.1.1.1.1) by Jeyaraman Sankar (1607209)

“…In the solid state, [28]hexaphyrins(1.1.1.1.1.1) take either planar or Möbius-twisted conformations, depending upon the <i>meso</i>-aryl substituents and crystallization conditions, indicating a small energy difference between the two conformers. Importantly, when the temperature is decreased to −100 °C in THF, these rapid interconversions among Möbius conformations are frozen, allowing the detection of a single [28]hexaphyrin(1.1.1.1.1.1) species having a Möbius conformation. …”

Unambiguous Identification of Möbius Aromaticity for <i>meso</i>-Aryl-Substituted [28]Hexaphyrins(1.1.1.1.1.1) by Jeyaraman Sankar (1607209)

“…In the solid state, [28]hexaphyrins(1.1.1.1.1.1) take either planar or Möbius-twisted conformations, depending upon the <i>meso</i>-aryl substituents and crystallization conditions, indicating a small energy difference between the two conformers. Importantly, when the temperature is decreased to −100 °C in THF, these rapid interconversions among Möbius conformations are frozen, allowing the detection of a single [28]hexaphyrin(1.1.1.1.1.1) species having a Möbius conformation. …”

Details of statistical analyses applied related to Figs 2 and S1. by Eudald Pascual-Carreras (12115380)