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    Methods in molecular biology (Clifton, N.J.)

    Methods in molecular biology (Clifton, N.J.)

    JournalISSN 1064-3745eISSN 1940-6029

    年发文量

    研究主题

    论文(76734)

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    1Unwinding Quadruplex Structures with RNA Helicases
    John C. Marecki,Jun Gao,Kevin D. Raney
    2026
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    2Correction To: Live-Cell Imaging of Mrna Using a Pepper RNA Tag
    Jiahui Wu, Samie R. Jaffrey
    2026
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    3DNA/RNA Heteroduplex Oligonucleotide for Highly Efficient Gene Silencing
    Rintaro Iwata Hara,Kotaro Yoshioka
    2026引用:1
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    4A Flow Cytometric Method of Determining CD71+ Erythroid Cells in Neonatal Whole Blood.
    Wenhui Li, William O Scott, Dominique Paz, Rebecca C Hale, Connie M Arthur

    The neonatal immune system exhibits a unique composition and function, rendering neonates particularly susceptible to infections and inflammatory conditions such as necrotizing enterocolitis (NEC). A distinct feature of neonatal immunity is the abundance of CD71+ erythroid cells (CECs), which are significantly more prevalent in neonates than in adults and possess immunosuppressive properties that can modulate neonatal immune responses. However, their quantification and functional analysis have been challenging given the small volume of blood typically available for assessment.. In this study, we present a comprehensive 24-color flow cytometry panel optimized to detect and quantify CD71+CD235a+ cells in minimal volumes of neonatal whole blood. This panel enables precise enumeration of CECs and detailed characterization of other key immune cell subsets, including T cells, monocytes, and natural killer cells. Additionally, our method allows for the functional assessment of CECs, such as evaluating Arginase 2 levels, to better understand their immunomodulatory roles. This approach provides a robust tool for dissecting the neonatal immune landscape and offers valuable insights into how CECs may impact other immune populations. Ultimately, this approach lays the groundwork for further research into the mechanisms behind neonatal vulnerability to infections and inflammation, potentially guiding the development of targeted therapeutic strategies.

    2026
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    5EMEM and DMEM As an Alternative Media for Leptospiral Culture, Diagnostic, and Pathogenesis Studies.
    Camila Hamond,Elsio A Wunder

    Leptospires require specific conditions and nutrition to survive and thrive, essential for its ability to multiply or adapt to in vitro culture. This constraint on laboratory cultures limits the applicability of in vitro studies to the understanding of even simple pathogenic processes and diagnostics. Culture of leptospires in a laboratory setting using DMEM and EMEM media, common for culture of mammalian cells, is an alternative that mimics host environmental conditions, less complex, with high performance, and lower cost, which are imperative characteristics to improve routine laboratory activities and studies of leptospirosis.

    2026
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    高被引作者

    作者引用发文
    Helen Skaletsky201621
    S Rozen201621
    Stephen Burgess1664718
    George Davey Smith1041131
    Jack Bowden860212
    Philip C. Haycock83803
    Feng Zhang79642
    Le Cong79081
    Amos Bairoch78514
    Denis F. Hochstrasser754613

    高产作者

    作者引用发文
    Robert C. Elston3422126
    Joan E. Bailey-Wilson1641115
    Paul C Guest296892
    Peter Kraft356683
    Andrew Morris260283
    Robert Hoffman78974
    John Blangero244770
    Shelley Bull54369
    Terri Hagan Beaty268066
    Heather J. Cordell133766

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