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1 h a dry macula ("D") and immediate preceding visits ("D-1") were analyzed with an automated optical coherence tomography-
4 Extracts from single alpha and beta cells were analyzed with CE-ESI-MS to obtain qualitative informatio
5 l contributions of autoregulatory segment to cMLCK activity were analyzed with chimeras of skMLCK and cMLCK.
6 Once extracted, the cellular contents were analyzed with conventional methods, including fluorescen
9 Longer-term mortality before repair and reintervention were analyzed with Cox proportional hazards regression.
13 type and functionality of antigen-specific effector T cells were analyzed with flow cytometry after polyclonal and pathog
14 ls from children and adults with EoE, and healthy controls, were analyzed with flow cytometry regarding levels of CD23, C
18 eceptor p75(NTR), and the proneurotrophin receptor sortilin were analyzed with immunohistochemistry in a cohort of thyroi
25 ntake with children's BMI trajectories and body composition were analyzed with multivariable linear mixed and regression
26 ry outcomes of survival and need for extracorporeal support were analyzed with multivariable logistic regression.
27 e mean deviation (MD) and pattern standard deviation (PSD), were analyzed with multivariable regression models.
28 ere iontophoretically filled with Lucifer yellow and spines were analyzed with NeuronStudio software.
30 Gene expression and protein expression were analyzed with quantitative polymerase chain reaction and
32 and influx rate constant (Ki) values for [(18)F]fluorodopa were analyzed with region-of-interest and whole-brain voxel-b
34 largest NOTES registry worldwide-the German NOTES registry-were analyzed with respect to demographic data, procedural da
36 CLCuD infested asymptomatic and symptomatic plants were analyzed with RNA-seq using an Illumina HiSeq.
37 Multiple localized pressure measurements were analyzed with spatially-matched histochemical images of
41 ) of the German High-Grade Non-Hodgkin Lymphoma Study Group were analyzed with the Lymph2Cx assay for COO classification,
50 tes (1-7 per patient) and single-nucleotide variants (SNVs) were analyzed, with reference to the index patient's isolate.
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