21 results on '"Kimmerling, Robert J"'
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2. Mutation and cell state compatibility is required and targetable in Ph+ acute lymphoblastic leukemia minimal residual disease
3. A pipeline for malignancy and therapy agnostic assessment of cancer drug response using cell mass measurements
4. Cellular Mass Response to Therapy Correlates With Clinical Response for a Range of Malignancies
5. Mass measurements during lymphocytic leukemia cell polyploidization decouple cell cycle- and cell size-dependent growth
6. Linking single-cell measurements of mass, growth rate, and gene expression
7. Microfluidic active loading of single cells enables analysis of complex clinical specimens
8. Mass measurements of polyploid lymphocytes reveal that growth is not size limited but depends strongly on cell cycle
9. Rapid and high-precision sizing of single particles using parallel suspended microchannel resonator arrays and deconvolution
10. Quantification of somatic mutation flow across individual cell division events by lineage sequencing
11. Trisomy of a Down Syndrome Critical Region Globally Amplifies Transcription via HMGN1 Overexpression
12. Linking single-cell measurements of mass, growth rate, and gene expression
13. Determining therapeutic susceptibility in multiple myeloma by single-cell mass accumulation
14. Microfluidic platform for characterizing TCR–pMHC interactions
15. Drug sensitivity of single cancer cells is predicted by changes in mass accumulation rate
16. High-throughput measurement of single-cell growth rates using serial microfluidic mass sensor arrays
17. Biophysical changes reduce energetic demand in growth factor–deprived lymphocytes
18. A microfluidic platform enabling single-cell RNA-seq of multigenerational lineages
19. Linking Biophysical and Transcriptional Profiles of In Vivo-Treated Human Leukemias on a Single-Cell Level Uniquely Resolves Subpopulations of Response
20. Biophysical changes reduce energetic demand in growth factor--deprived lymphocytes.
21. Mutation and cell state compatibility is required and targetable in Ph+ acute lymphoblastic leukemia minimal residual disease.
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