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Hamilton Institute
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The Branching Point in Erythro-Myeloid Differentiation.
Cell Dec, 2015 | Pubmed ID: 26687356
Inferring average generation via division-linked labeling.
Journal of mathematical biology Aug, 2016 | Pubmed ID: 26733310
Site-specific recombinatorics: in situ cellular barcoding with the Cre Lox system.
BMC systems biology Jun, 2016 | Pubmed ID: 27363727
Retracing the in vivo haematopoietic tree using single-cell methods.
FEBS letters Nov, 2016 | Pubmed ID: 27404207
Exploring STR signal in the single- and multicopy number regimes: Deductions from an in silico model of the entire DNA laboratory process.
Electrophoresis Mar, 2017 | Pubmed ID: 27981603
Production of high-fidelity electropherograms results in improved and consistent DNA interpretation: Standardizing the forensic validation process.
Forensic science international. Genetics Nov, 2017 | Pubmed ID: 28950155
A large-scale dataset of single and mixed-source short tandem repeat profiles to inform human identification strategies: PROVEDIt.
Forensic science international. Genetics Jan, 2018 | Pubmed ID: 29091906
Proliferation dynamics of acute myeloid leukaemia and haematopoietic progenitors competing for bone marrow space.
Nature communications Feb, 2018 | Pubmed ID: 29410432
Multiplexed Division Tracking Dyes for Proliferation-Based Clonal Lineage Tracing.
Journal of immunology (Baltimore, Md. : 1950) Aug, 2018 | Pubmed ID: 29914887
Stochastically Timed Competition Between Division and Differentiation Fates Regulates the Transition From B Lymphoblast to Plasma Cell.
Frontiers in immunology , 2018 | Pubmed ID: 30250473
Sample path properties of the average generation of a Bellman-Harris process.
Journal of mathematical biology Jul, 2019 | Pubmed ID: 31069504
A large-scale validation of NOCIt's a posteriori probability of the number of contributors and its integration into forensic interpretation pipelines.
Forensic science international. Genetics Jul, 2020 | Pubmed ID: 32339916
Manipulating niche composition limits damage to haematopoietic stem cells during Plasmodium infection.
Nature cell biology Dec, 2020 | Pubmed ID: 33230302
Towards developing forensically relevant single-cell pipelines by incorporating direct-to-PCR extraction: compatibility, signal quality, and allele detection.
International journal of legal medicine May, 2021 | Pubmed ID: 33484330
HSPCs display within-family homogeneity in differentiation and proliferation despite population heterogeneity.
eLife May, 2021 | Pubmed ID: 34002698
The a posteriori probability of the number of contributors when conditioned on an assumed contributor.
Forensic science international. Genetics Sep, 2021 | Pubmed ID: 34284325
High-quality data from a forensically relevant single-cell pipeline enabled by low PBS and proteinase K concentrations.
Journal of forensic sciences Mar, 2022 | Pubmed ID: 34936089
Corrigendum to "The a posteriori probability of the number of contributors when conditioned on an assumed contributor" [Forensic Sci. Int. Genet. 54 (2021) 102563].
Forensic science international. Genetics May, 2022 | Pubmed ID: 35168909
Replicative history marks transcriptional and functional disparity in the CD8 T cell memory pool.
Nature immunology May, 2022 | Pubmed ID: 35393592
Author Correction: Replicative history marks transcriptional and functional disparity in the CD8 T cell memory pool.
Nature immunology Jul, 2022 | Pubmed ID: 35606445
Cyton2: A Model of Immune Cell Population Dynamics That Includes Familial Instructional Inheritance.
Frontiers in bioinformatics , 2021 | Pubmed ID: 36303793
Evidentiary evaluation of single cells renders highly informative forensic comparisons across multifarious admixtures.
Forensic science international. Genetics Mar, 2023 | Pubmed ID: 36934551
Maynooth University
Alessandro Donada1,
Tamar Tak1,
Giulio Prevedello1,2,3,4,
Idan Milo1,
Ken R. Duffy2,
Leïla Perié1
1Quantitative Immuno-hematology, CNRS UMR168, Institut Curie,
2Hamilton Institute, Maynooth University,
3, Institut Curie, PSL Research University, CNRS UMR 3348, Orsay,
4, Université Paris-Sud, Université Paris-Saclay, CNRS UMR 3348, Orsay
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