Amy E. Merrill

发表

Development and maintenance of tendons and ligaments.

J. Crump, Lauren Bobzin, Ryan R. Roberts, 2021, Development.

Ciliary abnormalities due to defects in the retrograde transport protein DYNC2H1 in short-rib polydactyly syndrome.

S. Nelson, B. Merriman, D. Rimoin, 2009, American journal of human genetics.

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

K. Lyons, A. Wilkie, D. Pilz, 2006, Human molecular genetics.

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

P. Trainor, Kristin E Noack Watt, C. Neben, 2016, PLoS genetics.

Mesenchyme-dependent BMP signaling directs the timing of mandibular osteogenesis

B. Eames, R. Schneider, Amy E. Merrill, 2008, Development.

MusMorph, a database of standardized mouse morphology data for morphometric meta-analyses

B. Hallgrímsson, A. Visel, J. Cheverud, 2022, Scientific data.

Msx genes in organogenesis and human disease">Msx genes in organogenesis and human disease

R. Maxson, Amy E. Merrill, M. Ishii, 2003 .

tp53-dependent and independent signaling underlies the pathogenesis and possible prevention of Acrofacial Dysostosis–Cincinnati type

P. Trainor, C. Neben, Amy E. Merrill, 2018, Human molecular genetics.

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

P. Byers, Brendan H. Lee, D. Eyre, 2010, American journal of human genetics.

Summary Msx 2 and Twist cooperatively control the development of the neural crest-derived skeletogenic mesenchyme of the murine skull vault

D. Rice, H. Sucov, I. Gitelman, 2003 .

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

D. Rice, H. Sucov, I. Gitelman, 2003, Development.

Msx2 is a target of Pax3

R. Maas, H. Sucov, R. Maxson, 2001 .

The neural crest, a migratory cell population originating in the dorsal neural tube, is required for the development of the mammalian heart. The cardiac subpopulation of the neural crest emerges from rhombomeres

R. Maas, H. Sucov, R. Maxson, 2001 .

Nuclear FGFR2 regulates musculoskeletal integration within the developing limb

Ryan R. Roberts, Amy E. Merrill, Joanna E Salva, 2019, Developmental dynamics : an official publication of the American Association of Anatomists.

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

D. Krakow, J. Rice, C. Neben, 2014, Human molecular genetics.

Prmt1 regulates craniofacial bone formation upstream of Msx1

Jian Xu, T. Ho, Y. Chai, 2018, Mechanisms of Development.

Nuclear Fibroblast Growth Factor Receptor Signaling in Skeletal Development and Disease

Creighton T Tuzon, Amy E. Merrill, C. Tuzon, 2019, Current Osteoporosis Reports.

Ribosome biogenesis in skeletal development and the pathogenesis of skeletal disorders.

P. Trainor, Amy E. Merrill, 2014, Biochimica et biophysica acta.

Signaling networks in joint development

Amy E. Merrill, Joanna E Salva, 2017, Developmental dynamics : an official publication of the American Association of Anatomists.

Signaling Pathways in Craniofacial Development: Insights from Rare Skeletal Disorders.

C. Neben, Amy E. Merrill, 2015, Current topics in developmental biology.

MusMorph, a database of standardized mouse morphology data for morphometric meta-analyses

Nathan M. Young, B. Hallgrímsson, A. Visel, 2021, Scientific Data.

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

R. Schweitzer, Creighton T Tuzon, Lauren Bobzin, 2019, Development.

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

K. Lyons, D. Krakow, J. Zieba, 2016, PLoS genetics.

Title TGF beta and BMP Dependent Cell Fate Changes Due to Loss of Filamin B Produces Disc Degeneration and Progressive Vertebral Fusions Permalink

K. Lyons, D. Krakow, J. Zieba, 2016 .

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

R. Maas, H. Sucov, R. Maxson, 2002, Development.

The developing mouse coronal suture at single-cell resolution

N. Ashley, S. Twigg, A. Wilkie, 2021, Nature Communications.

Modeling craniofacial and skeletal congenital birth defects to advance therapies.

O. Klein, K. Dipple, C. Neben, 2016, Human molecular genetics.

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

F. Lay, C. Neben, Creighton T Tuzon, 2017, Human molecular genetics.

Ribosome biogenesis is dynamically regulated during osteoblast differentiation.

F. Lay, C. Neben, Creighton T Tuzon, 2017, Gene.

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

A. Elliott, W. Wilcox, D. Krakow, 2016, American journal of medical genetics. Part A.

A requirement for Fgfr2 in middle ear development

Lauren Bobzin, Ryan R. Roberts, Amy E. Merrill, 2018, Genesis.

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

K. Lyons, D. Chitayat, C. Curry, 2012, American journal of human genetics.

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

K. Lyons, S. E. Yi, N. Wu, 2004, Development.

Nuclear receptor Nr5a2 promotes diverse connective tissue fates in the jaw.

A. Tucker, Lindsey A Barske, Ryan R. Roberts, 2023, Developmental cell.

Ciliary abnormalities due to defects in the retrograde transport protein DYNC2H1 in short-rib polydactyly syndrome.

S. Nelson, B. Merriman, D. Rimoin, 2009, American journal of human genetics.

Fibroblast growth factor 2.

Amy E. Merrill, Audrey Nickle, Sebastian Ko, 2023, Differentiation; research in biological diversity.