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The evolution of human artistic creativity

Journal of anatomy, 2010-02, Vol.216 (2), p.158-176

Morriss‐Kay, Gillian M.

2010

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Growth of the normal skull vault and its alteration in craniosynostosis: insights from human genetics and experimental studies

Journal of anatomy, 2005-11, Vol.207 (5), p.637-653

2005

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Mechanism of skull suture maintenance and interdigitation

Journal of anatomy, 2009-12, Vol.215 (6), p.642-655

2009

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Mutations of Ephrin-B1 (EFNB1), a Marker of Tissue Boundary Formation, Cause Craniofrontonasal Syndrome

Proceedings of the National Academy of Sciences - PNAS, 2004-06, Vol.101 (23), p.8652-8657

2004

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A Gain-of-Function Mutation of Fgfr2c Demonstrates the Roles of This Receptor Variant in Osteogenesis

Proceedings of the National Academy of Sciences - PNAS, 2004-08, Vol.101 (34), p.12555-12560

2004

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Genetics of craniofacial development and malformation

Nature reviews. Genetics, 2001-06, Vol.2 (6), p.458-468

2001

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The IIIc alternative of Fgfr2 is a positive regulator of bone formation

Development (Cambridge), 2002-08, Vol.129 (16), p.3783-3793

2002

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Alx4 and Msx2 play phenotypically similar and additive roles in skull vault differentiation

Journal of anatomy, 2004-06, Vol.204 (6), p.487-499

2004

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Derivation of the mammalian skull vault

Journal of anatomy, 2001-07, Vol.199 (1‐2), p.143-151

MORRISS‐KAY, GILLIAN M.

2001

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Haploinsufficiency of the human homeobox gene ALX4 causes skull ossification defects

Nature genetics, 2001-01, Vol.27 (1), p.17-18

2001

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Tissue Origins and Interactions in the Mammalian Skull Vault

Developmental biology, 2002-01, Vol.241 (1), p.106-116

2002

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Developmental mechanisms underlying polydactyly in the mouse mutant Doublefoot

Journal of anatomy, 2003-01, Vol.202 (1), p.21-26

2003

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Skeletal analysis of the Fgfr3(P244R) mouse, a genetic model for the Muenke craniosynostosis syndrome

Developmental dynamics, 2009-02, Vol.238 (2), p.331-342

2009

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Nprl3 is required for normal development of the cardiovascular system

Mammalian genome, 2012-08, Vol.23 (7-8), p.404-415

2012

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Functional anatomy of the human brain

Journal of anatomy, 2004-12, Vol.205 (6), p.415-415

2004

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CD34 expression patterns during early mouse development are related to modes of blood vessel formation and reveal additional sites of hematopoiesis

Blood, 1997-09, Vol.90 (6), p.2300-2311

1997

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Craniofacial defects in AP-2 null mutant mice

BioEssays, 1996-10, Vol.18 (10), p.785-788

Morriss-Kay, Gillian M.

1996

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Treatment of mice with retinoids in vivo and in vitro

Methods in molecular biology (Clifton, N.J.), 2008, Vol.461, p.31

Morriss-Kay, Gillian M

2008

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Computational mouse atlases and their application to automatic assessment of craniofacial dysmorphology caused by the Crouzon mutation Fgfr2(C342Y)

Journal of anatomy, 2007-07, Vol.211 (1), p.37-52

2007

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Skeletal analysis of the Fgfr3P244R mouse, a genetic model for the Muenke craniosynostosis syndrome

Developmental dynamics, 2009-02, Vol.238 (2), p.331-342

2009

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Functional anatomy of the brain

Journal of anatomy, 2005-07, Vol.207 (1), p.1-2

2005

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Computational mouse atlases and their application to automatic assessment of craniofacial dysmorphology caused by the Crouzon mutation Fgfr2C342Y

Journal of anatomy, 2007-07, Vol.211 (1), p.37-52

2007

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Retinoic acid specifically downregulates Fgf4 and inhibits posterior cell proliferation in the developing mouse autopod

Journal of anatomy, 2001-05, Vol.198 (5), p.561-568

2001

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Apoptotic cell death in neuronal differentiation of P19 EC cells: Cell death follows reentry into S phase

Journal of cellular physiology, 1997-07, Vol.172 (1), p.25-35

1997

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Derivation of the mammalian skull vault

American journal of anatomy, 2001-08, Vol.199 (1-2), p.143-151

MORRISS-KAY, GILLIAN M.

2001

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The evolution of human artistic creativity

Growth of the normal skull vault and its alteration in craniosynostosis: insights from human genetics and experimental studies

Mechanism of skull suture maintenance and interdigitation

Mutations of Ephrin-B1 (EFNB1), a Marker of Tissue Boundary Formation, Cause Craniofrontonasal Syndrome

A Gain-of-Function Mutation of Fgfr2c Demonstrates the Roles of This Receptor Variant in Osteogenesis

Genetics of craniofacial development and malformation

The IIIc alternative of Fgfr2 is a positive regulator of bone formation

Alx4 and Msx2 play phenotypically similar and additive roles in skull vault differentiation

Derivation of the mammalian skull vault

Haploinsufficiency of the human homeobox gene ALX4 causes skull ossification defects

Tissue Origins and Interactions in the Mammalian Skull Vault

Developmental mechanisms underlying polydactyly in the mouse mutant Doublefoot

Skeletal analysis of the Fgfr3(P244R) mouse, a genetic model for the Muenke craniosynostosis syndrome

Nprl3 is required for normal development of the cardiovascular system

Functional anatomy of the human brain

CD34 expression patterns during early mouse development are related to modes of blood vessel formation and reveal additional sites of hematopoiesis

Craniofacial defects in AP-2 null mutant mice

Treatment of mice with retinoids in vivo and in vitro

Computational mouse atlases and their application to automatic assessment of craniofacial dysmorphology caused by the Crouzon mutation Fgfr2(C342Y)

Skeletal analysis of the Fgfr3P244R mouse, a genetic model for the Muenke craniosynostosis syndrome

Functional anatomy of the brain

Computational mouse atlases and their application to automatic assessment of craniofacial dysmorphology caused by the Crouzon mutation Fgfr2C342Y

Retinoic acid specifically downregulates Fgf4 and inhibits posterior cell proliferation in the developing mouse autopod

Apoptotic cell death in neuronal differentiation of P19 EC cells: Cell death follows reentry into S phase

Derivation of the mammalian skull vault

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