Chimpanzee neonatal brain size: Implications for brain growth in Homo erectus

2006 ◽  
Vol 51 (2) ◽  
pp. 207-212 ◽  
Author(s):  
J DESILVA ◽  
J LESNIK
2015 ◽  
Vol 81 ◽  
pp. 41-47 ◽  
Author(s):  
Zachary Cofran ◽  
Jeremy M. DeSilva
Keyword(s):  

2001 ◽  
Vol 24 (2) ◽  
pp. 278-279 ◽  
Author(s):  
Francisco Aboitiz

Finlay et al. address the importance of developmental constraints in brain size evolution. I discuss some aspects of this view such as the relation of brain size with processing capacity. In particular, I argue that in human evolution there must have been specific selection for increased processing capacity, and as a consequence for increased brain size.


1993 ◽  
Vol 72 (1) ◽  
pp. 85-97 ◽  
Author(s):  
Charles R. Goodlett ◽  
Jonathan T. Leo ◽  
James P. O'Callaghan ◽  
Jolonda C. Mahoney ◽  
James R. West

Nature ◽  
2004 ◽  
Vol 431 (7006) ◽  
pp. 299-302 ◽  
Author(s):  
H. Coqueugniot ◽  
J.-J. Hublin ◽  
F. Veillon ◽  
F. Houët ◽  
T. Jacob

2000 ◽  
Vol 22 (5) ◽  
pp. 695-701 ◽  
Author(s):  
Jennifer D. Thomas ◽  
Megan E. Garrison ◽  
Craig J. Slawecki ◽  
Cindy L. Ehlers ◽  
Edward P. Riley

2021 ◽  
Vol 35 (23-24) ◽  
pp. 1551-1578
Author(s):  
Thao P. Phan ◽  
Andrew J. Holland

Primary microcephaly is a brain growth disorder characterized by a severe reduction of brain size and thinning of the cerebral cortex. Many primary microcephaly mutations occur in genes that encode centrosome proteins, highlighting an important role for centrosomes in cortical development. Centrosomes are microtubule organizing centers that participate in several processes, including controlling polarity, catalyzing spindle assembly in mitosis, and building primary cilia. Understanding which of these processes are altered and how these disruptions contribute to microcephaly pathogenesis is a central unresolved question. In this review, we revisit the different models that have been proposed to explain how centrosome dysfunction impairs cortical development. We review the evidence supporting a unified model in which centrosome defects reduce cell proliferation in the developing cortex by prolonging mitosis and activating a mitotic surveillance pathway. Finally, we also extend our discussion to centrosome-independent microcephaly mutations, such as those involved in DNA replication and repair.


2006 ◽  
Vol 29 (1) ◽  
pp. 19-20 ◽  
Author(s):  
Juan Pascual-Leone

Using neoPiagetian theory of mental attention (or working memory), I task-analyze two complex performances of great apes and one symbolic performance (funeral burials) of early Homo sapiens. Relating results to brain size growth data, I derive estimates of mental attention for great apes, Homo erectus, Neanderthals, and modern Homo sapiens, and use children's cognitive development as reference. This heuristic model seems consistent with research.


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