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Neural crest stem cells： discovery, properties and potential for therapy

Cell research, 2012-02, Vol.22 (2), p.288-304

2012

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Prevention of Treacher Collins syndrome craniofacial anomalies in mouse models via maternal antioxidant supplementation

Nature communications, 2016-01, Vol.7 (1), p.10328-10328, Article 10328

2016

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Mutations in Hcfc1 and Ronin result in an inborn error of cobalamin metabolism and ribosomopathy

Nature communications, 2022-01, Vol.13 (1), p.134-134, Article 134

2022

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The Roles of RNA Polymerase I and III Subunits Polr1c and Polr1d in Craniofacial Development and in Zebrafish Models of Treacher Collins Syndrome

PLoS genetics, 2016-07, Vol.12 (7), p.e1006187-e1006187

2016

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Dynamic regulation and requirement for ribosomal RNA transcription during mammalian development

Proceedings of the National Academy of Sciences - PNAS, 2022-08, Vol.119 (31), p.e2116974119-e2116974119

2022

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Nr6a1 controls Hox expression dynamics and is a master regulator of vertebrate trunk development

Nature communications, 2022-12, Vol.13 (1), p.7766-7766

2022

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Foxc2 is required for proper cardiac neural crest cell migration, outflow tract septation, and ventricle expansion

Developmental dynamics, 2018-12, Vol.247 (12), p.1286-1296

2018

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PAR-6 is required for junction formation but not apicobasal polarization in C. elegans embryonic epithelial cells

Development (Cambridge), 2007-04, Vol.134 (7), p.1259-1268

2007

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PAR-3 mediates the initial clustering and apical localization of junction and polarity proteins during C. elegans intestinal epithelial cell polarization

Development (Cambridge), 2010-06, Vol.137 (11), p.1833-1842

2010

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Ronin (Thap11) is Implicated in a New Cobalamin Deficiency Syndrome Impacting the Central Nervous System

The FASEB journal, 2017-04, Vol.31 (S1)

2017

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A New Role of Ronin (Thap11) in the Neural Crest and Craniofacial Development in the Mouse

The FASEB journal, 2017-04, Vol.31 (S1)

2017

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Mouse models to study the pathophysiology of combined methylmalonic acidemia and homocystinuria, cblC type

Developmental biology, 2020-12, Vol.468 (1-2), p.1-13

2020

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The Craniofacial‐specific Role of the Ribosomal Gene Polr1c and its Role in Treacher Collins Syndrome

The FASEB journal, 2015-04, Vol.29 (S1)

2015

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Mouse Models of Rare Craniofacial Disorders

Current topics in developmental biology, 2015, Vol.115, p.413

2015

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Genetic dissection of Treacher Collins Syndrome: Polr1c and Polr1d

The FASEB journal, 2013-04, Vol.27 (S1)

2013

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Orphan Nuclear Receptor, GCNF, Is Required for Early Neural Crest Cell Induction and Survival

The FASEB journal, 2017-04, Vol.31 (S1)

2017

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Ronin (Thap11) Deficiency Results in a Disease Impacting both Vitamin B12 Metabolism and Ribosome Biogenesis

The FASEB journal, 2019-04, Vol.33 (S1), p.449.2-449.2

2019

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Ronin (Thap11) Deficiency Results in a Disease Impacting both Vitamin B 12 Metabolism and Ribosome Biogenesis

The FASEB journal, 2019-04, Vol.33 (S1)

2019

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CblX is a New Cobalamin Syndrome Affecting Craniofacial Development

The FASEB journal, 2020-04, Vol.34 (S1), p.1-1

2020

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MBTPS1/SKI-1/S1P proprotein convertase is required for ECM signaling and axial elongation during somitogenesis and vertebral development

Human molecular genetics, 2015-05, Vol.24 (10), p.2884-2898

2015

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Germ cell nuclear factor (Gcnf/Nr6a1) plays a novel role in neural crest cell induction

The FASEB journal, 2013-04, Vol.27 (S1)

2013

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PAR-3 mediates the initial clustering and apical localization of junction and polarity proteins during C. elegans intestinal epithelial cell polarization

Journal of cell science, 2010-06, Vol.123 (11), p.e1-e1

2010

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Understanding neural crest cell development using Gcnf−/− mutant mice as a model system

Developmental biology, 2011-08, Vol.356 (1), p.185-185

2011

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MBTPS1/SKI-1/S1P proprotein convertase is required for ECM signaling and axial elongation during somitogenesis and vertebral development super()

Human molecular genetics, 2015-05, Vol.24 (10), p.2884-2898

2015

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Establishment of apicobasal polarity and junction formation by the PAR proteins in the Caenorhabditis elegans embryonic epithelial cells

Achilleos, Annita

2010

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Neural crest stem cells： discovery, properties and potential for therapy

Prevention of Treacher Collins syndrome craniofacial anomalies in mouse models via maternal antioxidant supplementation

Mutations in Hcfc1 and Ronin result in an inborn error of cobalamin metabolism and ribosomopathy

The Roles of RNA Polymerase I and III Subunits Polr1c and Polr1d in Craniofacial Development and in Zebrafish Models of Treacher Collins Syndrome

Dynamic regulation and requirement for ribosomal RNA transcription during mammalian development

Nr6a1 controls Hox expression dynamics and is a master regulator of vertebrate trunk development

Foxc2 is required for proper cardiac neural crest cell migration, outflow tract septation, and ventricle expansion

PAR-6 is required for junction formation but not apicobasal polarization in C. elegans embryonic epithelial cells

PAR-3 mediates the initial clustering and apical localization of junction and polarity proteins during C. elegans intestinal epithelial cell polarization

Ronin (Thap11) is Implicated in a New Cobalamin Deficiency Syndrome Impacting the Central Nervous System

A New Role of Ronin (Thap11) in the Neural Crest and Craniofacial Development in the Mouse

Mouse models to study the pathophysiology of combined methylmalonic acidemia and homocystinuria, cblC type

The Craniofacial‐specific Role of the Ribosomal Gene Polr1c and its Role in Treacher Collins Syndrome

Mouse Models of Rare Craniofacial Disorders

Genetic dissection of Treacher Collins Syndrome: Polr1c and Polr1d

Orphan Nuclear Receptor, GCNF, Is Required for Early Neural Crest Cell Induction and Survival

Ronin (Thap11) Deficiency Results in a Disease Impacting both Vitamin B12 Metabolism and Ribosome Biogenesis

Ronin (Thap11) Deficiency Results in a Disease Impacting both Vitamin B 12 Metabolism and Ribosome Biogenesis

CblX is a New Cobalamin Syndrome Affecting Craniofacial Development

MBTPS1/SKI-1/S1P proprotein convertase is required for ECM signaling and axial elongation during somitogenesis and vertebral development

Germ cell nuclear factor (Gcnf/Nr6a1) plays a novel role in neural crest cell induction

PAR-3 mediates the initial clustering and apical localization of junction and polarity proteins during C. elegans intestinal epithelial cell polarization

Understanding neural crest cell development using Gcnf−/− mutant mice as a model system

MBTPS1/SKI-1/S1P proprotein convertase is required for ECM signaling and axial elongation during somitogenesis and vertebral development super()

Establishment of apicobasal polarity and junction formation by the PAR proteins in the Caenorhabditis elegans embryonic epithelial cells

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