Mechanism of skull suture maintenance and interdigitation
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 …
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 …
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
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 …
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
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 …
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 …
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 …
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 …
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 …
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
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 …
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 …
and is primarily caused by FGFR2+/P253R and+/S252W mutations. The former mutation is …