List of works - Amy E Merrill

A phylogenetically conserved cis-regulatory module in the Msx2 promoter is sufficient for BMP-dependent transcription in murine and Drosophila embryos

scientific journal article

A requirement for Fgfr2 in middle ear development

scientific article published on 04 October 2018

Bent bone dysplasia syndrome reveals nucleolar activity for FGFR2 in ribosomal DNA transcription

scientific article

Bent bone dysplasia-FGFR2 type, a distinct skeletal disorder, has deficient canonical FGF signaling

scientific article published in March 2012

Cell mixing at a neural crest-mesoderm boundary and deficient ephrin-Eph signaling in the pathogenesis of craniosynostosis

scientific article

Clinical and radiographic delineation of Bent Bone Dysplasia-FGFR2 type or Bent Bone Dysplasia with Distinctive Clavicles and Angel-shaped Phalanges.

scientific article published on 30 May 2016

FGF signaling patterns cell fate at the interface between tendon and bone

scientific article published on 02 August 2019

FGFR2 mutations in bent bone dysplasia syndrome activate nucleolar stress and perturb cell fate determination.

scientific article published on 8 June 2017

Modeling craniofacial and skeletal congenital birth defects to advance therapies.

scientific article published on 26 June 2016

Msx2 and Twist cooperatively control the development of the neural crest-derived skeletogenic mesenchyme of the murine skull vault.

scientific article published in December 2003

Msx2 is an immediate downstream effector of Pax3 in the development of the murine cardiac neural crest.

scientific article

Mutations in the Gene Encoding the RER Protein FKBP65 Cause Autosomal-Recessive Osteogenesis Imperfecta.

scientific article

Mutations in the gene encoding the RER protein FKBP65 cause autosomal-recessive osteogenesis imperfecta

scientific article

Nuclear FGFR2 regulates musculoskeletal integration within the developing limb

scientific article published on 28 January 2019

Ribosome biogenesis in skeletal development and the pathogenesis of skeletal disorders

scientific article

Ribosome biogenesis is dynamically regulated during osteoblast differentiation

scientific article published on 12 November 2016

Signaling Pathways in Craniofacial Development: Insights from Rare Skeletal Disorders

scientific article published on 23 October 2015

Signaling networks in joint development

scientific article published on 18 November 2016

TGFβ and BMP Dependent Cell Fate Changes Due to Loss of Filamin B Produces Disc Degeneration and Progressive Vertebral Fusions

scientific article

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

scientific article published on 22 July 2016

List of works by Amy E Merrill

A phylogenetically conserved cis-regulatory module in the Msx2 promoter is sufficient for BMP-dependent transcription in murine and Drosophila embryos

A requirement for Fgfr2 in middle ear development

Bent bone dysplasia syndrome reveals nucleolar activity for FGFR2 in ribosomal DNA transcription

Bent bone dysplasia-FGFR2 type, a distinct skeletal disorder, has deficient canonical FGF signaling

Cell mixing at a neural crest-mesoderm boundary and deficient ephrin-Eph signaling in the pathogenesis of craniosynostosis

Clinical and radiographic delineation of Bent Bone Dysplasia-FGFR2 type or Bent Bone Dysplasia with Distinctive Clavicles and Angel-shaped Phalanges.

FGF signaling patterns cell fate at the interface between tendon and bone

FGFR2 mutations in bent bone dysplasia syndrome activate nucleolar stress and perturb cell fate determination.

Modeling craniofacial and skeletal congenital birth defects to advance therapies.

Msx2 and Twist cooperatively control the development of the neural crest-derived skeletogenic mesenchyme of the murine skull vault.

Msx2 is an immediate downstream effector of Pax3 in the development of the murine cardiac neural crest.

Mutations in the Gene Encoding the RER Protein FKBP65 Cause Autosomal-Recessive Osteogenesis Imperfecta.

Mutations in the gene encoding the RER protein FKBP65 cause autosomal-recessive osteogenesis imperfecta

Nuclear FGFR2 regulates musculoskeletal integration within the developing limb

Ribosome biogenesis in skeletal development and the pathogenesis of skeletal disorders

Ribosome biogenesis is dynamically regulated during osteoblast differentiation

Signaling Pathways in Craniofacial Development: Insights from Rare Skeletal Disorders

Signaling networks in joint development

TGFβ and BMP Dependent Cell Fate Changes Due to Loss of Filamin B Produces Disc Degeneration and Progressive Vertebral Fusions

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