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The effects of the EW dipeptide optical and chemical isomers on the CFU-S population in intact and irradiated mice.

Deigin VI, Semenets TN, Zamulaeva IA, Maliutina YV, Selivanova EI, Saenko AS, Semina OV. · 2007 · International immunopharmacology

Animal / experimentalEnglish abstractSource linked
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What does this source report?

Optical configuration, peptide linkage and administration before or after irradiation affected colony-forming responses. Normal marrow and injury recovery are different endpoints.

Population and setting
See original report; human, animal and laboratory components must be distinguished.
Evidence type
Animal / experimental
Preparation
Preparation-specific research; no equivalence inferred
Source language
eng
Title provenance
Title as recorded in the linked source or index. A separate original-language title has not been transcribed unless shown above.

What are the limitations?

  • Full methods, preparation identity and risk of bias require appraisal.
  • Related publications may share experiments; source count is not independent-study count.

Publication counts are not counts of independent trials. Reviews, translations and reports sharing participants may overlap. Findings apply to the studied preparation, population and endpoints.

Source access and review scope

Indexed metadata and abstract checked via Europe PMC. Original full methods not reviewed.

Recorded source-check date: 2026-10-02. This date does not imply a completed systematic review.

Open original source or index record ↗

DOI: 10.1016/j.intimp.2006.11.010

Cite and trace this record

Original source: Deigin VI, Semenets TN, Zamulaeva IA, Maliutina YV, Selivanova EI, Saenko AS, Semina OV.. The effects of the EW dipeptide optical and chemical isomers on the CFU-S population in intact and irradiated mice. International immunopharmacology 2007.

Molekul research summary: https://molekul.io/research/gaps-17276896. Cite the original publication for its findings and this page when referring to Molekul’s summary or evidence appraisal.

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