Mechanism of skull suture maintenance and interdigitation

T Miura, CA Perlyn, M Kinboshi, N Ogihara… - Journal of …, 2009 - Wiley Online Library
Skull sutures serve as growth centers whose function involves multiple molecular pathways.
During periods of brain growth the sutures remain thin and straight, later developing …

Cranial shape and size variation in human evolution: structural and functional perspectives

E Bruner - Child's Nervous System, 2007 - Springer
A glimpse into modern paleoanthropology In the last decades, paleoanthropology has been
deeply modified, changing from a descriptive and historical science to a more quantitative …

[HTML][HTML] Inactivation of Msx1 and Msx2 in neural crest reveals an unexpected role in suppressing heterotopic bone formation in the head

PG Roybal, NL Wu, J Sun, M Ting, CA Schafer… - Developmental …, 2010 - Elsevier
In an effort to understand the morphogenetic forces that shape the bones of the skull, we
inactivated Msx1 and Msx2 conditionally in neural crest. We show that Wnt1-Cre inactivation …

Cranial sutures work collectively to distribute strain throughout the reptile skull

N Curtis, MEH Jones, SE Evans… - Journal of the …, 2013 - royalsocietypublishing.org
The skull is composed of many bones that come together at sutures. These sutures are
important sites of growth, and as growth ceases some become fused while others remain …

[HTML][HTML] Jagged1 functions downstream of Twist1 in the specification of the coronal suture and the formation of a boundary between osteogenic and non-osteogenic …

HY Yen, MC Ting, RE Maxson - Developmental biology, 2010 - Elsevier
The Notch pathway is crucial for a wide variety of developmental processes including the
formation of tissue boundaries. That it may function in calvarial suture development and …

A tale of two cities: The genetic mechanisms governing calvarial bone development

JW Ferguson, RP Atit - genesis, 2019 - Wiley Online Library
The skull bones must grow in a coordinated, three‐dimensional manner to coalesce and
form the head and face. Mammalian skull bones have a dual embryonic origin from cranial …

Expanding the mutation spectrum in 182 Spanish probands with craniosynostosis: identification and characterization of novel TCF12 variants

B Paumard-Hernández, J Berges-Soria… - European Journal of …, 2015 - nature.com
Craniosynostosis, caused by the premature fusion of one or more of the cranial sutures, can
be classified into non-syndromic or syndromic and by which sutures are affected. Clinical …

[HTML][HTML] A combined series of Fgf9 and Fgf18 mutant alleles identifies unique and redundant roles in skeletal development

IH Hung, GC Schoenwolf, M Lewandoski… - Developmental …, 2016 - Elsevier
Fibroblast growth factor (FGF) signaling is a critical regulator of skeletal development. Fgf9
and Fgf18 are the only FGF ligands with identified functions in embryonic bone growth. Mice …

Predicting skull loading: applying multibody dynamics analysis to a macaque skull

N Curtis, K Kupczik, P O'higgins… - … Record: Advances in …, 2008 - Wiley Online Library
Evaluating stress and strain fields in anatomical structures is a way to test hypotheses that
relate specific features of facial and skeletal morphology to mechanical loading. Engineering …

Activation of p38 MAPK pathway in the skull abnormalities of Apert syndrome Fgfr2+P253R mice

Y Wang, M Sun, VL Uhlhorn, X Zhou, I Peter… - BMC developmental …, 2010 - Springer
Background Apert syndrome is characterized by craniosynostosis and limb abnormalities
and is primarily caused by FGFR2+/P253R and+/S252W mutations. The former mutation is …