Interpreting persistent health problems: The chronic Lyme disease diagnosis. par C. Puppo (14593159)

Sujets: “…diagnostic procedure involved…”

The N-terminus of EDC4 is not required for interaction with DCP1a. par Donald B. Bloch (12423021)

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Interaction between PATL1 and EDC4 requires the presence of the C-terminus of PATL1 and the N-terminus of EDC4. par Donald B. Bloch (12423021)

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NLS-EDC4 localizes to Cajal bodies, and adjacent to PML-nuclear bodies. par Donald B. Bloch (12423021)

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When expressed in HEp-2 cells, GFP-NLS-EDC4 (panel a) localized to Cajal bodies (panels b, c). par Donald B. Bloch (12423021)

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Model of the mammalian mRNA P-body. par Donald B. Bloch (12423021)

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The representations of chronic Lyme disease diagnosis. par C. Puppo (14593159)

Sujets: “…diagnostic procedure involved…”

Schematic of P-body proteins and fragments of proteins that were used in this study. par Donald B. Bloch (12423021)

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Study’s main results. par C. Puppo (14593159)

Sujets: “…diagnostic procedure involved…”

EDC4 interacts with XRN1. par Donald B. Bloch (12423021)

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After depletion of DDX6 and loss of endogenous P bodies, EDC4(630–1437), but not full-length EDC4, was able to localize to cytoplasmic dots. par Donald B. Bloch (12423021)

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After depletion of LSm14a and loss of endogenous P-bodies, GFP-EDC4(630–1437), but not GFP-EDC4, localizes to cytoplasmic dots. par Donald B. Bloch (12423021)

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Endogenous LSm14a and DDX6 did not co-localize with NLS-EDC4 in nuclear dots. par Donald B. Bloch (12423021)

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Co-immunoprecipitation was used to show that the N-terminus of EDC4 is required for interaction with XRN1(1232–1706). par Donald B. Bloch (12423021)

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Characteristics of the study population (n = 24). par C. Puppo (14593159)

Sujets: “…diagnostic procedure involved…”

The experience of uncertainty. par C. Puppo (14593159)

Sujets: “…diagnostic procedure involved…”

Effect of an exogenous nuclear localization sequence (NLS) on the cellular location of P-body components. par Donald B. Bloch (12423021)

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Full-length PATL1 interacts with EDC4. par Donald B. Bloch (12423021)

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EDC4(630–1437) can recruit DCP1a, EDC3 or CCHCR1 to cytoplasmic dots despite depletion of LSm14a and loss of endogenous P-bodes. par Donald B. Bloch (12423021)

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Computational Study Illustrating NCN-Palladium(IV) Involvement in Generating Pd⁰ Species to Facilitate Pd⁰/Pd^II Heck-Type Catalysis with Diphenylio... par Allan J. Canty (1338687)