Illustration of the change of depth coordinates of the second data set of upper arm flexion in light clothing. af Vytautas Abromavičius (22008573)

Illustration of the variation of the depth coordinates in the first test of the upper arm flexion of the first data set. af Vytautas Abromavičius (22008573)

Illustration of the result of the 3D human skeleton for flexion of the upper arm in the first data set. af Vytautas Abromavičius (22008573)

Illustration of the 3D human skeleton result of flexion of the upper arm in the second data set. af Vytautas Abromavičius (22008573)

Group mean values and variance components of the median inclination of the upper right arm and trunk according to inclinometry and observation. af Svend Erik Mathiassen (10321072)

Fag: “...observation strategies involving...”

Light-Armed Nitric Oxide-Releasing Micromotor <i>In Vivo</i> af Tiange Zhang (7284944)

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Difference in odds of attaining BP control and normal BMI between treatment arms. af Grace Wambura Mbuthia (6019439)

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Mean difference in diopters and axis between refractive error measured by face-to-face (f2f) optometrist and the tele-refraction arm (trained technician with remote optometrist). af Neha Kapur (18874640)

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Reengagement program outcome: proportion returned to care among all identified as LTFU (in intervention study arms). LTFU, lost to follow-up. af Ali Mirzazadeh (2170738)

ECDFs of the European (^____) and Non-European (——) meta-arms, with respect to the PLVs. af Massimo Attanasio (267727)

RBS1, an RNA Binding Protein, Interacts with SPIN1 and Is Involved in Flowering Time Control in Rice af Yuhui Cai (517102)

Anti-plasmid defense in hypervirulent <i>Klebsiella pneumoniae</i> involves Type I-like and Type IV restriction modification systems af Guodong Oo (13405763)

“...Collectively, our study provides the first report on the susceptibility of hvKp strains to plasmid transfer and evidence of unusual RM systems restricting plasmid acquisition. It reveals an arms race between plasmids evolving to bypass RM systems and host strains developing new defenses. ...”

Synthesis, Spectroscopic, and Structural Studies on Transition Metal Complexes Involving Homoleptic Tripodal Selenoether and Telluroether Coordination af William Levason (1275612)

“...The thioether complex (C₁₈H₃₆F₆O₆RuS₈, <i>a</i> = 8.658(3) Å, <i>b</i> = 11.533(3) Å, <i>c</i> = 8.659(2) Å, <i>α</i> = 108.33(2)°, <i>β</i> = 91.53(3)°, <i>γ</i> = 106.01(2)°, triclinic, <i>P</i>1̄, <i>Z</i> = 1) is isostructural with its selenoether analogue, involving two facially coordinated trithioether ligands in the syn configuration. ...”

Supplementary Material for: Acquired Generalized Lipodystrophy with Extensive Autoimmune Involvement: A Case Report and Review of the Literature af figshare admin karger (2628495)

Parasites promote the evolution of host complexity. af Luis Zaman (386870)

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Frozen and replayed parasite genotypes fail to recapitulate the level of complexity seen in the coevolution treatment. af Luis Zaman (386870)

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Proportion of point mutations that switch functions without changing the number of tasks performed in paired genotypes, where each pair includes hosts from the coevolution and evol... af Luis Zaman (386870)

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Effect of coevolution on coalescence times in host phylogenies. af Luis Zaman (386870)

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Proportion of point mutations in host genomes that switch functions without changing the number of functions performed. af Luis Zaman (386870)

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Effects of parasites on the host's adaptive landscape. af Luis Zaman (386870)

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