Primary abstract and byline: Regina Bruggisser, Katrin von Daeniken, Gernot Jundt, Willi Schaffner and Heide Tullberg-Reinert. Planta Medica 68(5), 445–448 (May 2002), DOI 10.1055/s-2002-32073. Cell number assessed by crystal violet declined while MTT formazan increased under kaempferol treatment. Cell-free tests showed direct reduction with kaempferol, resveratrol and selected extracts. These observations motivate chemical and optical controls; they do not make every positive assay signal a cell count.

Additional verified locator: final two sentences of the primary abstract, PMID 12058323. Washing kaempferol-treated MCF7 and HS578 cells before adding MTT significantly reduced direct dye reduction. The comparison supports chemical interference under those assay conditions; it does not show that washing eliminates all interference or reverses prior biological exposure. pubmed.ncbi.nlm.nih.gov/12058323/?dopt=Abstract

Primary source: www.urmc.rochester.edu/labs/mosmann

Verified locator: Official laboratory homepage names Tim R. Mosmann and directly lists the 1983 assay with PMID 6606682. Lab Members www.urmc.rochester.edu/labs/mosmann/lab-members names Tim R. Mosmann, describes cytokine/T-cell research and explicitly identifies the Tim Mosmann portrait link www.urmc.rochester.edu/neuroscience/_shared/img/faculty/TimMosmann.jpg . No expansion of R. or birth date.

Primary source: www.sigmaaldrich.com/deepweb/assets/sigmaaldrich/product/documents/191/466/11465007001.pdf

Verified locator: Manufacturer instructions, version 20, content version December 2020. Printed p. 3 names the MTT bromide reagent; §3.1 and Fig. 4 on printed p. 9 show yellow tetrazolium reduction to purple formazan, solubilization and multiwell optical measurement. Publisher-hosted document retains Roche kit branding.

T. Mosmann, Journal of Immunological Methods 65(1–2), 55–63 (16 December 1983), DOI 10.1016/0022-1759(83)90303-4. Primary Abstract: a tetrazolium-based colorimetric method detects living mammalian cells, with signal depending on cellular activation, and is read using a multiwell scanning spectrophotometer. Exact initial-only byline retained.

Verified author linkage: the official Rochester Mosmann laboratory homepage www.urmc.rochester.edu/labs/mosmann names Tim R. Mosmann and directly lists this 1983 paper with PMID 6606682 in Selected Publications. The Lab Members page independently names Tim R. Mosmann. Preserve the paper’s literal T. Mosmann byline and original source title; the canonical person/Work now use Tim R. Mosmann, with both old IDs retained as aliases. R. remains unexpanded.

PNAS105(40),15346–15351(2008); DOI10.1073/pnas.0706805105. Original author-hosted paper biodynamics.ucsd.edu/wp-content/uploads/pubs/pdfs/Volfson08.pdf; Abstract and Figure1: growing E.coli in a microfluidic chemostat, cell alignment and expansion flow. Full primary byline Dmitri Volfson verified.

Science249(4975),1431–1433(1990); DOI10.1126/science.1698311. Abstract: LPS/LBP recognition and anti-CD14 blockade of LPS-induced TNF-alpha synthesis in whole blood. Initial-only S.D.Wright retained.

Journal of Cell Biology124(1994),677–688; DOI10.1083/jcb.124.5.677. Primary abstract and Figures5–7: J-774 macrophage latex-bead phagosomes isolated on sucrose gradients, pulse/chase analysis and changes in membrane markers. Initial-only author form retained; full name not inferred from secondary indexes.

Nature309(1984),30–33; DOI10.1038/309030a0. Primary abstract: L-arginyl-glycyl-L-aspartyl-L-serine tetrapeptide accounts for measured attachment activity. Both original initial-only author forms retained. No coating protocol or peptide-control concentration inferred.

Journal of Experimental Medicine152(1),20–30(1980); abstract: erythrocyte membrane gp205, C3-convertase decay and C3b-inactivator-assisted cleavage; receptor identification across blood-cell classes.

Blood74(7),2527–2534(1989). Abstract: two-color immunofluorescence/flow cytometry, CD14/CD16 coexpression, approximately13percent of CD14-defined monocytes in reported samples; morphology and functional comparisons.

By S. D. Wright and S. C. Silverstein. Nature 309, 359–361 (May 1984), DOI doi.org/10.1038/309359a0

Original abstract: protein access beneath macrophages on glass versus ligand-coated glass; access by molecular mass200000 in the former condition and exclusion even at50000 in the latter. Byline remains initial-only; a functional contact seal is supported without asserting that every molecule is impermeable.

By S. D. Wright and S. C. Silverstein. Journal of Experimental Medicine158(6),2016–2023(1December1983). DOI doi.org/10.1084/jem.158.6.2016

Abstract and Figure1: ligand-coated surfaces, cultured monocytes and fibronectin; complement-receptor-associated phagocytosis can be separated from hydrogen-peroxide release. C3bi is the historical spelling used by the paper.

Journal of Cell Biology111(1990),3129–3139; DOI10.1083/jcb.111.6.3129. Original full byline verifies Michael S.Diamond. Abstract and reciprocal-binding assays: purified proteins, engineered cells and antibody blocking establish Mac-1/ICAM-1 interaction; stimulated neutrophil/endothelial conjugates examined. Slash in source title must become hyphen in magic-link argument.

Cell51(1987),813–819; DOI10.1016/0092-8674(87)90104-8. Full primary publisher byline verifies Steven D.Marlin and Timothy A.Springer. Abstract: purified ICAM-1 in supported lipid membranes; LFA-1-positive/negative cell comparison and antibody blocking. Existing T.A.Springer author/Work by records refer to this collaborator; do not create a duplicate full-name article.

Journal of Experimental Medicine 156, 1000–1009 (1982), DOI 10.1084/jem.156.4.1000. Abstract: antibody inhibition of C3bi-dependent rosetting, comparison with C3b and Fc-receptor functions.

Nature 341, 619–624 (1989), DOI 10.1038/341619a0. Abstract: antigen-receptor cross-linking causes rapid, transient increase in LFA-1/ICAM-mediated adhesion.

Science 303, 1532–1535 (2004), DOI 10.1126/science.1092385. Abstract: activated neutrophils release chromatin and granule proteins forming bacteria-binding extracellular fibers.

PNAS 68, 3092–3096 (1971), DOI 10.1073/pnas.68.12.3092. Abstract: isolated sea-urchin sperm axonemes, limited trypsin digestion and ATP-induced separation/sliding of tubules.

Circulation Research79(3),581–589 (1996), DOI10.1161/01.res.79.3.581. Primary indexed abstract: bright-field and fluorescence microscopy of hamster cremaster capillaries, distinct tracer/blood-cell domains and light-dye perturbation. Direct PubMed page returned an incomplete response; indexed primary abstract inspected. Initials retained as published.

PNAS 75(10), 5071–5075 (1978), DOI 10.1073/pnas.75.10.5071. Indexed title spelling monlayers retained. Primary archive pmc.ncbi.nlm.nih.gov/articles/PMC336265/ ; author-institution record vivo.weill.cornell.edu/display/pubid283416 . Abstract and electron-microscopic observations: polarized budding in epithelial monolayers.