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Developmental and genetic perspectives on Pierre Robin sequence

American journal of medical genetics. Part C, Seminars in medical genetics, 2013-11, Vol.163C (4), p.295-305

2013

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Co-option of the cardiac transcription factor Nkx2.5 during development of the emu wing

Nature communications, 2017-07, Vol.8 (1), p.132-12, Article 132

2017

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Cauli: a mouse strain with an Ift140 mutation that results in a skeletal ciliopathy modelling Jeune syndrome

PLoS genetics, 2013-08, Vol.9 (8), p.e1003746-e1003746

2013

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Sox10 overexpression induces neural crest‐like cells from all dorsoventral levels of the neural tube but inhibits differentiation

Developmental dynamics, 2005-06, Vol.233 (2), p.430-444

2005

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Twist2 contributes to termination of limb bud outgrowth and patterning through direct regulation of Grem1

Developmental biology, 2012-10, Vol.370 (1), p.145-153

2012

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avian Z-linked gene DMRT1 is required for male sex determination in the chicken

Nature (London), 2009-09, Vol.461 (7261), p.267-271

2009

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Global comparative transcriptome analysis of cartilage formation in vivo

BMC developmental biology, 2009-03, Vol.9 (1), p.20-20, Article 20

2009

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YPEL1 overexpression in early avian craniofacial mesenchyme causes mandibular dysmorphogenesis by up‐regulating apoptosis

Developmental dynamics, 2015-08, Vol.244 (8), p.1022-1030

2015

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Limb patterning genes and heterochronic development of the emu wing bud

EvoDevo, 2016-12, Vol.7 (1), p.26-26, Article 26

2016

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Deficiency of the Wnt receptor Ryk causes multiple cardiac and outflow tract defects

Growth factors (Chur, Switzerland), 2018-03, Vol.36 (1-2), p.58-68

2018

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bfb, a novel ENU-induced blebs mutant resulting from a missense mutation in Fras1

PloS one, 2013-10, Vol.8 (10), p.e76342

2013

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Best Practices for the Diagnosis and Evaluation of Infants With Robin Sequence: A Clinical Consensus Report

JAMA pediatrics, 2016-09, Vol.170 (9), p.894

2016

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The RCAS retroviral expression system in the study of skeletal development

Developmental dynamics, 2009-04, Vol.238 (4), p.797-811

2009

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Role of Dlx genes in craniofacial morphogenesis: Dlx2 influences skeletal patterning by inducing ectomesenchymal aggregation in ovo

Evolution & development, 2010-09, Vol.12 (5), p.459-473

2010

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Frontonasal Dysplasia: Towards an Understanding of Molecular and Developmental Aetiology

Molecular syndromology, 2016-11, Vol.7 (6), p.312-321

2016

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The ontogeny of Robin sequence

American journal of medical genetics. Part A, 2018-06, Vol.176 (6), p.1349-1368

2018

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Proteomic profiling of facial development in chick embryos

Proteomics (Weinheim), 2005-07, Vol.5 (10), p.2542-2550

2005

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Rare syndromes of the head and face-Pierre Robin sequence

Wiley interdisciplinary reviews. Developmental biology, 2013-05, Vol.2 (3), p.369-377

2013

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Clinical and Molecular Characterisation of Children with Pierre Robin Sequence and Additional Anomalies

Molecular syndromology, 2016-11, Vol.7 (6), p.322-328

2016

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Olfr603, an orphan olfactory receptor, is expressed in multiple specific embryonic tissues

Gene Expression Patterns, 2015-09, Vol.19 (1-2), p.30-35

2015

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Phenotypic variability of distal 22q11.2 copy number abnormalities

American journal of medical genetics. Part A, 2011-07, Vol.155A (7), p.1623-1633

2011

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CXCL14 expression during chick embryonic development

The International journal of developmental biology, 2011, Vol.55 (3), p.335-340

2011

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Isolation and embryonic expression of avian ADAM 12 and ADAM 19

Gene Expression Patterns, 2004-11, Vol.5 (1), p.75-79

2004

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Ryk-deficient mice exhibit craniofacial defects associated with perturbed Eph receptor crosstalk

Nature genetics, 2000-08, Vol.25 (4), p.414-418

2000

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Developmental and genetic perspectives on Pierre Robin sequence

Co-option of the cardiac transcription factor Nkx2.5 during development of the emu wing

Cauli: a mouse strain with an Ift140 mutation that results in a skeletal ciliopathy modelling Jeune syndrome

Sox10 overexpression induces neural crest‐like cells from all dorsoventral levels of the neural tube but inhibits differentiation

Twist2 contributes to termination of limb bud outgrowth and patterning through direct regulation of Grem1

avian Z-linked gene DMRT1 is required for male sex determination in the chicken

Global comparative transcriptome analysis of cartilage formation in vivo

YPEL1 overexpression in early avian craniofacial mesenchyme causes mandibular dysmorphogenesis by up‐regulating apoptosis

Limb patterning genes and heterochronic development of the emu wing bud

Deficiency of the Wnt receptor Ryk causes multiple cardiac and outflow tract defects

bfb, a novel ENU-induced blebs mutant resulting from a missense mutation in Fras1

Best Practices for the Diagnosis and Evaluation of Infants With Robin Sequence: A Clinical Consensus Report

The RCAS retroviral expression system in the study of skeletal development

Role of Dlx genes in craniofacial morphogenesis: Dlx2 influences skeletal patterning by inducing ectomesenchymal aggregation in ovo

Monoallelic BMP2 Variants Predicted to Result in Haploinsufficiency Cause Craniofacial, Skeletal, and Cardiac Features Overlapping Those of 20p12 Deletions

Frontonasal Dysplasia: Towards an Understanding of Molecular and Developmental Aetiology

The ontogeny of Robin sequence

Proteomic profiling of facial development in chick embryos

Rare syndromes of the head and face-Pierre Robin sequence

Clinical and Molecular Characterisation of Children with Pierre Robin Sequence and Additional Anomalies

Olfr603, an orphan olfactory receptor, is expressed in multiple specific embryonic tissues

Phenotypic variability of distal 22q11.2 copy number abnormalities

CXCL14 expression during chick embryonic development

Isolation and embryonic expression of avian ADAM 12 and ADAM 19

Ryk-deficient mice exhibit craniofacial defects associated with perturbed Eph receptor crosstalk

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