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Developmental increase of total cell numbers in the murine cerebellum

https://doi.org/10.1080/14734220601169699
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1001/archneur.1985.04060040016006openalex-snapshot
The Cerebellum and Neural Control
inferredcites →https://doi.org/10.1002/(sici)1096-9861(19970915)386:1<2::aid-cne2>3.0.co;2-6openalex-snapshot
Quantification without pontification: Choosing a method for counting objects in sectioned tissues
inferredcites →https://doi.org/10.1002/cne.902740202openalex-snapshot
Quantitative study of granule and Purkinje cells in the cerebellar cortex of the rat
inferredcites →https://doi.org/10.1002/glia.440070406openalex-snapshot
Development and differentiation of glial precursor cells in the rat cerebellum
inferredcites →https://doi.org/10.1002/jnr.10655openalex-snapshot
Developmental and cell type‐specific expression of the neuronal marker NeuN in the murine cerebellum
inferredcites →https://doi.org/10.1007/bf00223234openalex-snapshot
Cell number and cell density in the cerebellar cortex of man and some other mammals
inferredcites →https://doi.org/10.1007/bf00297482openalex-snapshot
Proliferation of bergmann-glia in the developing rat cerebellum
inferredcites →https://doi.org/10.1016/0165-3806(83)90119-0openalex-snapshot
Direct correlation between Purkinje and granule cell number in the cerebella of lurcher chimeras and wild-type mice
inferredcites →https://doi.org/10.1016/0165-5728(81)90023-0openalex-snapshot
Characterization of isolated mouse cerebellar cell populations in vitro
inferredcites →https://doi.org/10.1016/0165-5728(81)90024-2openalex-snapshot
Developmental expression of cell type-specific markers in mouse cerebellar cells in vitro
inferredcites →https://doi.org/10.1016/j.devbrainres.2004.03.011openalex-snapshot
Morphological development and maturation of the GABAergic synapses in the mouse cerebellar granular layer
inferredcites →https://doi.org/10.1016/j.jtbi.2006.05.030openalex-snapshot
A continuum approach to modelling cell–cell adhesion
inferredcites →https://doi.org/10.1016/j.neuroscience.2006.03.070openalex-snapshot
Stereological estimation of Purkinje neuron number in C57BL/6 mice and its relation to associative learning
inferredcites →https://doi.org/10.1016/j.tins.2004.02.007openalex-snapshot
Interneuron Diversity series: Circuit complexity and axon wiring economy of cortical interneurons
inferredcites →https://doi.org/10.1016/s0925-4773(01)00471-3openalex-snapshot
Cell type specific expression of vascular endothelial growth factor and angiopoietin-1 and -2 suggests an important role of astrocytes in cerebellar vascularization
inferredcites →https://doi.org/10.1038/35098076openalex-snapshot
A general model for ontogenetic growth
inferredcites →https://doi.org/10.1046/j.1365-2818.2002.01054.xopenalex-snapshot
The smooth fractionator
inferredcites →https://doi.org/10.1046/j.1460-9568.2003.02698.xopenalex-snapshot
Subtype switching of vesicular glutamate transporters at parallel fibre–Purkinje cell synapses in developing mouse cerebellum
inferredcites →https://doi.org/10.1046/j.1469-7580.2000.19640501.xopenalex-snapshot
Evolution of the basal ganglia: new perspectives through a comparative approach
inferredcites →https://doi.org/10.1073/pnas.0408145102openalex-snapshot
Big brains, enhanced cognition, and response of birds to novel environments
inferredcites →https://doi.org/10.1073/pnas.0604911103openalex-snapshot
Cellular scaling rules for rodent brains
inferredcites →https://doi.org/10.1073/pnas.0605843103openalex-snapshot
Evolution of increased glia–neuron ratios in the human frontal cortex
inferredcites →https://doi.org/10.1073/pnas.87.14.5568openalex-snapshot
Learning causes synaptogenesis, whereas motor activity causes angiogenesis, in cerebellar cortex of adult rats.
inferredcites →https://doi.org/10.1073/pnas.93.7.3083openalex-snapshot
Evolution of GABAergic circuitry in the mammalian medial geniculate body.
inferredcites →https://doi.org/10.1083/jcb.32.2.277openalex-snapshot
QUANTITATIVE ANALYSIS OF CELL PROLIFERATION AND DIFFERENTIATION IN THE CORTEX OF THE POSTNATAL MOUSE CEREBELLUM
inferredcites →https://doi.org/10.1093/cercor/10.2.127openalex-snapshot
Theoretical Neuroanatomy: Relating Anatomical and Functional Connectivity in Graphs and Cortical Connection Matrices
inferredcites →https://doi.org/10.1093/cercor/13.6.541openalex-snapshot
Developmental and Evolutionary Adaptations of Cortical Radial Glia
inferredcites →https://doi.org/10.1111/j.1365-2818.1986.tb02764.xopenalex-snapshot
Stereology of arbitrary particles*
inferredcites →https://doi.org/10.1111/j.1460-9568.2006.04915.xopenalex-snapshot
Postnatal development of the murine cerebellar cortex: formation and early dispersal of basket, stellate and Golgi neurons
inferredcites →https://doi.org/10.1128/aem.56.6.1875-1881.1990openalex-snapshot
Modeling of the Bacterial Growth Curve
inferredcites →https://doi.org/10.1146/annurev.ne.11.030188.002231openalex-snapshot
The Control Of Neuron Number
inferredcites →https://doi.org/10.1159/000452856openalex-snapshot
Cellular Scaling Rules for the Brains of Marsupials: Not as “Primitive” as Expected
inferredcites →https://doi.org/10.1242/dev.102.2.409openalex-snapshot
Development of macroglial cells in rat cerebellum II. An in situ immunohistochemical study of oligodendroglial lineage from precursor to mature myelinating cell
inferredcites →https://doi.org/10.1371/journal.pbio.0020369openalex-snapshot
Motifs in Brain Networks
inferredcites →https://doi.org/10.1523/jneurosci.02-10-01494.1982openalex-snapshot
Cerebellar Purkinje cells are descended from a small number of progenitors committed during early development: quantitative analysis of lurcher chimeric mice
inferredcites →https://doi.org/10.1523/jneurosci.09-10-03454.1989openalex-snapshot
Numerical matching between granule and Purkinje cells in lurcher chimeric mice: a hypothesis for the trophic rescue of granule cells from target-related cell death
inferredcites →https://doi.org/10.1523/jneurosci.1610-06.2006openalex-snapshot
Unipolar Brush Cells of the Cerebellum Are Produced in the Rhombic Lip and Migrate through Developing White Matter
inferredcites →https://doi.org/10.1523/jneurosci.4526-04.2005openalex-snapshot
Isotropic Fractionator: A Simple, Rapid Method for the Quantification of Total Cell and Neuron Numbers in the Brain
inferredcites →https://doi.org/10.2527/2000.7871816xopenalex-snapshot
A generalized Michaelis-Menten equation for the analysis of growth.
inferredcites →https://doi.org/10.7551/mitpress/5817.001.0001openalex-snapshot
Recollections of My Life

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4608450openalex-extracted
inferred← citeshttps://doi.org/10.1002/glia.22683openalex-snapshot
The glia/neuron ratio: How it varies uniformly across brain structures and species and what that means for brain physiology and evolution
inferred← citeshttps://doi.org/10.1007/s00418-023-02251-zopenalex-snapshot
Revisiting the development of cerebellar inhibitory interneurons in the light of single-cell genetic analyses
inferred← citeshttps://doi.org/10.1007/s12311-008-0063-7openalex-snapshot
The Cerebellum, Cerebellar Disorders, and Cerebellar Research—Two Centuries of Discoveries
inferred← citeshttps://doi.org/10.1007/s12311-008-0079-zopenalex-snapshot
Development of Cerebellar GABAergic Interneurons: Origin and Shaping of the “Minibrain” Local Connections
inferred← citeshttps://doi.org/10.1016/b978-0-12-814407-7.00025-0openalex-snapshot
The impact of different modes of neuronal migration on brain evolution
inferred← citeshttps://doi.org/10.1016/j.asd.2023.101329openalex-snapshot
Brain Size Scaling Through Development in the Whitelined Sphinx Moth (Hyles Lineata) Shows Mass and Cell Number Comparable to Flies, Bees, and Wasps
inferred← citeshttps://doi.org/10.1016/j.jneumeth.2017.05.025openalex-snapshot
Comparison of estimates of neuronal number obtained using the isotropic fractionator method and unbiased stereology in day old chicks (Gallus domesticus)
inferred← citeshttps://doi.org/10.1086/721766openalex-snapshot
The Adaptive Potential of Nonheritable Somatic Mutations
inferred← citeshttps://doi.org/10.1101/2021.04.30.442123openalex-snapshot
The adaptive potential of non-heritable somatic mutations
inferred← citeshttps://doi.org/10.1155/2011/516942openalex-snapshot
3D Winding Number: Theory and Application to Medical Imaging
inferred← citeshttps://doi.org/10.1159/000327319openalex-snapshot
Variability in Neuron Densities across the Cortical Sheet in Primates
inferred← citeshttps://doi.org/10.1186/1750-1326-7-58openalex-snapshot
The isotropic fractionator provides evidence for differential loss of hippocampal neurons in two mouse models of Alzheimer's disease
inferred← citeshttps://doi.org/10.13041/jpvm.2019.43.2.47openalex-snapshot
Expression of vascular endothelial growth factor and Its receptors in 35-day-old murine cerebellum under chronic hypoxia
inferred← citeshttps://doi.org/10.3389/fnana.2012.00027openalex-snapshot
Use of flow cytometry for high-throughput cell population estimates in brain tissue
inferred← citeshttps://doi.org/10.3389/neuro.05.005.2010openalex-snapshot
A rapid and reliable method of counting neurons and other cells in brain tissue: a comparison of flow cytometry and manual counting methods
inferred← citeshttps://doi.org/10.7554/elife.68045openalex-snapshot
Maturation of Purkinje cell firing properties relies on neurogenesis of excitatory neurons
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