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1. Exploratory analysis of the cervix tumoral HPV antigen-specific T-cell repertoire during chemoradiation and after brachytherapy

2. Tumor-resident Lactobacillus iners confer chemoradiation resistance through lactate-induced metabolic rewiring

3. Circulating neutrophils and tumor-associated myeloid cells function as a powerful biomarker for response to chemoradiation in locally advanced cervical cancer

4. Metagenomes of rectal swabs in larger, advanced stage cervical cancers have enhanced mucus degrading functionalities and distinct taxonomic structure

6. Microbial Diversity and Composition Is Associated with Patient-Reported Toxicity during Chemoradiation Therapy for Cervical Cancer

7. Exploratory analysis of the cervix tumoral HPV antigen-specific T-cell repertoire during chemoradiation and after brachytherapy

9. Gut microbiome diversity is an independent predictor of survival in cervical cancer patients receiving chemoradiation

11. Supplemental Tables from Expansion of Candidate HPV-Specific T Cells in the Tumor Microenvironment during Chemoradiotherapy Is Prognostic in HPV16+ Cancers

12. Data from Expansion of Candidate HPV-Specific T Cells in the Tumor Microenvironment during Chemoradiotherapy Is Prognostic in HPV16+ Cancers

13. Supplemental Table Legends from Expansion of Candidate HPV-Specific T Cells in the Tumor Microenvironment during Chemoradiotherapy Is Prognostic in HPV16+ Cancers

14. Supplementary Data from Expansion of Candidate HPV-Specific T Cells in the Tumor Microenvironment during Chemoradiotherapy Is Prognostic in HPV16+ Cancers

15. Cervicovaginal Microbiota Profiles in Precancerous Lesions and Cervical Cancer among Ethiopian Women

16. Immune environment and antigen specificity of the T cell receptor repertoire of malignant ascites in ovarian cancer

17. 674 IMMUNOCERV, an ongoing phase II trial combining PDS0101, an HPV-specific T cell immunotherapy, with chemotherapy and radiation for treatment of locally advanced cervical cancers

18. Cancer-associated Lactobacillus iners are genetically distinct and associated with chemoradiation resistance in cervical cancer

19. Additional file 1 of Metagenomes of rectal swabs in larger, advanced stage cervical cancers have enhanced mucus degrading functionalities and distinct taxonomic structure

20. Expansion of Candidate HPV-Specific T Cells in the Tumor Microenvironment during Chemoradiotherapy Is Prognostic in HPV16+ Cancers

21. Tumor-Resident  Lactobacillus iners Confers Chemoradiation Resistance in Cervical Cancer Patients Through Acquired Metabolic Functions

22. Diversity and composition of gut microbiome of cervical cancer patients: Do results of 16S rRNA sequencing and whole genome sequencing approaches align?

23. Candidate HPV-Specific T-Cells Expand in the Tumor Microenvironment During Chemoradiotherapy

24. A prospective study of the adaptive changes in the gut microbiome during standard-of-care chemoradiotherapy for gynecologic cancers

25. Diversity and Composition of Gut Microbiome of Cervical Cancer Patients by 16S rRNA and Whole-metagenome Sequencing

26. Gut microbiome diversity is an independent predictor of survival in cervical cancer patients receiving chemoradiation

27. Gut microbiome diversity as an independent predictor of survival in cervical cancer patients receiving chemoradiation.

28. Adaptive changes in the gut microbiome during standard-of-care chemoradiotherapy for gynecologic cancers

29. Dynamic evolution of cervical cancer mutations during chemoradiation using novel sampling approach

30. Expansion of Candidate HPV-Specific T Cells in the Tumor Microenvironment during Chemoradiotherapy Is Prognostic in HPV16 + Cancers.

31. Longitudinal characterization of the tumoral microbiome during radiotherapy in HPV-associated oropharynx cancer.

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