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A Deisseroth

Showing results (91-100 of 101) with videos related to

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Annals of Oncology : Official Journal of the European Society for Medical Oncology|January 1, 1997
Long-range amplification of genomic DNA detects the t(2;5)(p23;q35) in anaplastic large-cell lymphoma, but not in other non-Hodgkin's lymphomas, Hodgkin's disease, or lymphomatoid papulosisA H Sarris, R Luthra, V Papadimitracopoulou, et al.
The Cancer Journal From Scientific American|June 10, 1998
Molecular therapy for cancerA Deisseroth, D Guo, T Wang, et al.
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing|November 30, 2016
EMPOWERING MULTI-COHORT GENE EXPRESSION ANALYSIS TO INCREASE REPRODUCIBILITYWinston A Haynes, Francesco Vallania, Charles Liu, et al.
Cancer Treatment Reports|December 1, 1982
Phase I trial of Staphylococcus aureus Cowan I immunoperfusionG Messerschmidt, C Bowles, D Dean, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 31, 2019
AVADA: toward automated pathogenic variant evidence retrieval directly from the full-text literatureJohannes Birgmeier, Cole A Deisseroth, Laura E Hayward, et al.
Bone Marrow Transplantation|April 1, 1999
A phase I study of paclitaxel for mobilization of peripheral blood progenitor cellsB A Burtness, A Psyrri, M Rose, et al.
Blood|December 1, 1995
CD8-depleted donor lymphocyte infusion as treatment for relapsed chronic myelogenous leukemia after allogeneic bone marrow transplantationS Giralt, J Hester, Y Huh, et al.
Annals of Neurology|March 27, 2022
An Integrated Phenotypic and Genotypic Approach Reveals a High-Risk Subtype Association for EBF3 Missense Variants Affecting the Zinc Finger DomainCole A Deisseroth, Vanesa C Lerma, Christina L Magyar, et al.
Science Translational Medicine|May 22, 2020
AMELIE speeds Mendelian diagnosis by matching patient phenotype and genotype to primary literatureJohannes Birgmeier, Maximilian Haeussler, Cole A Deisseroth, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 6, 2018
ClinPhen extracts and prioritizes patient phenotypes directly from medical records to expedite genetic disease diagnosisCole A Deisseroth, Johannes Birgmeier, Ethan E Bodle, et al.
Pageof 11

Showing results (91-100 of 101) with videos related to

Sort By:
Pageof 11
Annals of Oncology : Official Journal of the European Society for Medical Oncology|January 1, 1997
Long-range amplification of genomic DNA detects the t(2;5)(p23;q35) in anaplastic large-cell lymphoma, but not in other non-Hodgkin's lymphomas, Hodgkin's disease, or lymphomatoid papulosisA H Sarris, R Luthra, V Papadimitracopoulou, et al.
The Cancer Journal From Scientific American|June 10, 1998
Molecular therapy for cancerA Deisseroth, D Guo, T Wang, et al.
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing|November 30, 2016
EMPOWERING MULTI-COHORT GENE EXPRESSION ANALYSIS TO INCREASE REPRODUCIBILITYWinston A Haynes, Francesco Vallania, Charles Liu, et al.
Cancer Treatment Reports|December 1, 1982
Phase I trial of Staphylococcus aureus Cowan I immunoperfusionG Messerschmidt, C Bowles, D Dean, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 31, 2019
AVADA: toward automated pathogenic variant evidence retrieval directly from the full-text literatureJohannes Birgmeier, Cole A Deisseroth, Laura E Hayward, et al.
Bone Marrow Transplantation|April 1, 1999
A phase I study of paclitaxel for mobilization of peripheral blood progenitor cellsB A Burtness, A Psyrri, M Rose, et al.
Blood|December 1, 1995
CD8-depleted donor lymphocyte infusion as treatment for relapsed chronic myelogenous leukemia after allogeneic bone marrow transplantationS Giralt, J Hester, Y Huh, et al.
Annals of Neurology|March 27, 2022
An Integrated Phenotypic and Genotypic Approach Reveals a High-Risk Subtype Association for EBF3 Missense Variants Affecting the Zinc Finger DomainCole A Deisseroth, Vanesa C Lerma, Christina L Magyar, et al.
Science Translational Medicine|May 22, 2020
AMELIE speeds Mendelian diagnosis by matching patient phenotype and genotype to primary literatureJohannes Birgmeier, Maximilian Haeussler, Cole A Deisseroth, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 6, 2018
ClinPhen extracts and prioritizes patient phenotypes directly from medical records to expedite genetic disease diagnosisCole A Deisseroth, Johannes Birgmeier, Ethan E Bodle, et al.
Pageof 11