2021
Loss of Cxcr4 in Endometriosis Reduces Proliferation and Lesion Number while Increasing Intraepithelial Lymphocyte Infiltration
Tal A, Tal R, Kliman HJ, Taylor HS. Loss of Cxcr4 in Endometriosis Reduces Proliferation and Lesion Number while Increasing Intraepithelial Lymphocyte Infiltration. American Journal Of Pathology 2021, 191: 1292-1302. PMID: 33964217, PMCID: PMC8261475, DOI: 10.1016/j.ajpath.2021.04.011.Peer-Reviewed Original ResearchMeSH KeywordsAnimalsCell ProliferationEndometriosisEpithelial CellsFemaleIntraepithelial LymphocytesMiceReceptors, CXCR4ConceptsEndometriosis lesionsEpithelial compartmentLesion numberDisruption of CXCR4Intraepithelial lymphocyte infiltrationAdult female miceLoss of CXCR4CXCL12-CXCR4 axisTotal lesion areaProgesterone receptor promoterEndometriosis inductionLymphocyte infiltrationCXCR4 expressionFemale miceHost miceControl lesionsProestrus stageEpithelial proliferationImmune evasionCXCR4LesionsTherapeutic potentialLesion areaReduces ProliferationEpithelial cells
2001
Maternal Hoxa10 is required for pinopod formation in the development of mouse uterine receptivity to embryo implantation
Bagot C, Kliman H, Taylor H. Maternal Hoxa10 is required for pinopod formation in the development of mouse uterine receptivity to embryo implantation. Developmental Dynamics 2001, 222: 538-544. PMID: 11747087, DOI: 10.1002/dvdy.1209.Peer-Reviewed Original ResearchConceptsEndometrial receptivityPinopod formationBlastocyst implantationHOXA10 expressionEndometrial stromal cell proliferationUterine endometrial epithelial cellsAdult female miceState of receptivityExpression of HOXA10Endometrial epithelial cellsStromal cell proliferationTime of implantationHOXA10 antisenseAdult reproductive tractEndometrial developmentGenitourinary tractFemale miceUterine receptivityMouse uterusUterusReproductive tractEpithelial cellsCell proliferationCellular proliferationHOXA10