An alternative stochastic model of generation of oligodendrocytes in cell culture

DOI10.1007/S002850100085MaRDI QIDQ1349010zbMATH OpenOpenAlexWikidataFDO

Authors K. M. Boucher, M. Mayer-Proschel, M. Noble, A. V. Zorin, A. Y. Yakovlev

Publication date 21 May 2002

Published in Journal of Mathematical Biology (Search for Journal in Brave)

Full work available at URL https://doi.org/10.1007/s002850100085

zbMATH Keywords

cell proliferationprogenitor cellsoligodendrocytes

Mathematics Subject Classification ID

Applications of statistics to biology and medical sciences; meta analysis (62P10) Applications of branching processes (60J85) Cell biology (92C37)

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Cited in

(14)

• A composite likelihood approach to the analysis of longitudinal clonal data on multitype cellular systems under an age-dependent branching process
• Saddlepoint approximations to the moments of multitype age-dependent branching processes, with applications
• Estimation problems associated with stochastic modeling of proliferation and differentiation of O-2A progenitor cells in vitro
• Stochastic formulations of a clock model for temporally regulated generation of oligodendrocytes in vitro
• Pseudo-likelihood estimation for discretely observed multitype Bellman--Harris branching proc\-esses
• Branching stochastic processes with immigration in analysis of renewing cell populations
• Retinogenesis: stochasticity and the competency model
• Estimating the life-span of oligodendrocytes from clonal data on their development in cell culture
• A random walk model of oligodendrocyte generation in vitro and associated estimation problems
• A stochastic model of temporally regulated generation of oligodendrocytes in cell culture
• On the impact of correlation between collaterally consanguineous cells on lymphocyte population dynamics
• The effect of correlations on the population dynamics of lymphocytes
• Asymptotic behavior of cell populations described by two-type reducible age-dependent branching processes with non-homogeneous immigration
• A Stochastic Model to Analyze Clonal Data on Multi‐Type Cell Populations

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