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4. Genomic predictors of response to PD-1 inhibition in children with germline DNA replication repair deficiency

6. 1908P Utility of circulating tumor (ct)DNA testing for molecular residual disease (MRD) detection and treatment response monitoring in patients (pts) with renal cell carcinoma (RCC)

7. Colossal magnetoresistance from spin-polarized polarons in an Ising system.

8. Longitudinal Testing of Circulating Tumor DNA in Patients With Metastatic Renal Cell Carcinoma.

9. A simplified approach for efficiency analysis of machine learning algorithms.

10. Early real-world experience monitoring circulating tumor DNA in resected early-stage non-small cell lung cancer.

11. Association of circulating tumor DNA with patient prognosis in surgically resected renal cell carcinoma.

12. Trade-off between training and testing ratio in machine learning for medical image processing.

13. Detection of circulating tumor DNA with ultradeep sequencing of plasma cell-free DNA for monitoring minimal residual disease and early detection of recurrence in early-stage lung cancer.

14. Personalized, tumor-informed, circulating tumor DNA assay for detecting minimal residual disease in non-small cell lung cancer patients receiving curative treatments.

15. Combined Immunotherapy Improves Outcome for Replication-Repair-Deficient (RRD) High-Grade Glioma Failing Anti-PD-1 Monotherapy: A Report from the International RRD Consortium.

16. Efficacy of Nivolumab in Pediatric Cancers with High Mutation Burden and Mismatch Repair Deficiency.

17. ctDNA-based detection of molecular residual disease in stage I-III non-small cell lung cancer patients treated with definitive radiotherapy.

18. Transcriptional immunogenomic analysis reveals distinct immunological clusters in paediatric nervous system tumours.

19. Longitudinal Monitoring of Circulating Tumor DNA to Assess the Efficacy of Immune Checkpoint Inhibitors in Patients With Advanced Genitourinary Malignancies.

20. Circulating tumor DNA-based molecular residual disease detection for treatment monitoring in advanced melanoma patients.

21. Ethical Data Collection for Medical Image Analysis: a Structured Approach.

22. Genomic Microsatellite Signatures Identify Germline Mismatch Repair Deficiency and Risk of Cancer Onset.

23. Feasibility of Longitudinal ctDNA Assessment in Patients with Uterine and Extra-Uterine Leiomyosarcoma.

24. Immune Checkpoint Inhibition as Single Therapy for Synchronous Cancers Exhibiting Hypermutation: An IRRDC Study.

25. Germline Biallelic Mismatch Repair Deficiency in Childhood Glioblastoma and Implications for Clinical Management.

26. Genomic predictors of response to PD-1 inhibition in children with germline DNA replication repair deficiency.

27. Upfront Adjuvant Immunotherapy of Replication Repair-Deficient Pediatric Glioblastoma With Chemoradiation-Sparing Approach.

28. Dual role of allele-specific DNA hypermethylation within the TERT promoter in cancer.

29. Mutations in the RAS/MAPK Pathway Drive Replication Repair-Deficient Hypermutated Tumors and Confer Sensitivity to MEK Inhibition.

30. DNA Polymerase and Mismatch Repair Exert Distinct Microsatellite Instability Signatures in Normal and Malignant Human Cells.

31. Cancers from Novel Pole -Mutant Mouse Models Provide Insights into Polymerase-Mediated Hypermutagenesis and Immune Checkpoint Blockade.

32. B-cell acute lymphoblastic leukemia with high mutation burden presenting in a child with constitutional mismatch repair deficiency.

33. Early Onset Parkinson's disease due to DJ1 mutations: An Indian study.

34. Evidence of mutations in RIC3 acetylcholine receptor chaperone as a novel cause of autosomal-dominant Parkinson's disease with non-motor phenotypes.

35. Discovery of a frameshift mutation in podocalyxin-like (PODXL) gene, coding for a neural adhesion molecule, as causal for autosomal-recessive juvenile Parkinsonism.

36. VPS35 and EIF4G1 mutations are rare in Parkinson's disease among Indians.

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