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Amy E. Merrill
Amy E. Merrill
在 usc.edu 的电子邮件经过验证 - 首页
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Mutations in the gene encoding the RER protein FKBP65 cause autosomal-recessive osteogenesis imperfecta
Y Alanay, H Avaygan, N Camacho, GE Utine, K Boduroglu, D Aktas, ...
The American Journal of Human Genetics 86 (4), 551-559, 2010
3652010
Cell mixing at a neural crest-mesoderm boundary and deficient ephrin-Eph signaling in the pathogenesis of craniosynostosis
AE Merrill, EG Bochukova, SM Brugger, M Ishii, DT Pilz, SA Wall, ...
Human molecular genetics 15 (8), 1319-1328, 2006
2382006
Msx2 and Twist cooperatively control the development of the neural crest-derived skeletogenic mesenchyme of the murine skull vault
M Ishii, AE Merrill, YS Chan, I Gitelman, DPC Rice, HM Sucov, ...
Oxford University Press for The Company of Biologists Limited 130 (24), 6131 …, 2003
2222003
A phylogenetically conserved cis-regulatory module in the Msx2promoter is sufficient for BMP-dependent transcription in murine and Drosophila embryos
SM Brugger, AE Merrill, J Torres-Vazquez, N Wu, MC Ting, JYM Cho, ...
Oxford University Press for The Company of Biologists Limited 131 (20), 5153 …, 2004
1572004
Ciliary abnormalities due to defects in the retrograde transport protein DYNC2H1 in short-rib polydactyly syndrome
AE Merrill, B Merriman, C Farrington-Rock, N Camacho, ET Sebald, ...
The American Journal of Human Genetics 84 (4), 542-549, 2009
1552009
Msx2 is an immediate downstream effector of Pax3 in the development of the murine cardiac neural crest
SJ Kwang, SM Brugger, A Lazik, AE Merrill, LY Wu, YH Liu, M Ishii, ...
Oxford University Press for The Company of Biologists Limited 129 (2), 527-538, 2002
1182002
Ribosome biogenesis in skeletal development and the pathogenesis of skeletal disorders
PA Trainor, AE Merrill
Biochimica et Biophysica Acta (BBA)-Molecular Basis of Disease 1842 (6), 769-778, 2014
1102014
The roles of RNA polymerase I and III subunits Polr1c and Polr1d in craniofacial development and in zebrafish models of Treacher Collins syndrome
KE Noack Watt, A Achilleos, CL Neben, AE Merrill, PA Trainor
PLoS genetics 12 (7), e1006187, 2016
1042016
Bent bone dysplasia-FGFR2 type, a distinct skeletal disorder, has deficient canonical FGF signaling
AE Merrill, A Sarukhanov, P Krejci, B Idoni, N Camacho, KD Estrada, ...
The American Journal of Human Genetics 90 (3), 550-557, 2012
802012
Mesenchyme-dependent BMP signaling directs the timing of mandibular osteogenesis
AE Merrill, BF Eames, SJ Weston, T Heath, RA Schneider
Oxford University Press for The Company of Biologists Limited 135 (7), 1223-1234, 2008
772008
The developing mouse coronal suture at single-cell resolution
DJT Farmer, H Mlcochova, Y Zhou, N Koelling, G Wang, N Ashley, ...
Nature Communications 12 (1), 4797, 2021
622021
TGFβ and BMP dependent cell fate changes due to loss of filamin B produces disc degeneration and progressive vertebral fusions
J Zieba, KN Forlenza, JS Khatra, A Sarukhanov, I Duran, D Rigueur, ...
PLoS genetics 12 (3), e1005936, 2016
522016
Bent bone dysplasia syndrome reveals nucleolar activity for FGFR2 in ribosomal DNA transcription
CL Neben, B Idoni, JE Salva, CT Tuzon, JC Rice, D Krakow, AE Merrill
Human Molecular Genetics 23 (21), 5659-5671, 2014
452014
Development and maintenance of tendons and ligaments
L Bobzin, RR Roberts, HJ Chen, JG Crump, AE Merrill
Development 148 (8), dev186916, 2021
372021
Signaling networks in joint development
JE Salva, AE Merrill
Developmental Dynamics 246 (4), 262-274, 2017
322017
FGF signaling patterns cell fate at the interface between tendon and bone
RR Roberts, L Bobzin, CS Teng, D Pal, CT Tuzon, R Schweitzer, ...
Development 146 (15), dev170241, 2019
292019
tp53-dependent and independent signaling underlies the pathogenesis and possible prevention of Acrofacial Dysostosis–Cincinnati type
KEN Watt, CL Neben, S Hall, AE Merrill, PA Trainor
Human Molecular Genetics 27 (15), 2628-2643, 2018
272018
Nuclear fibroblast growth factor receptor signaling in skeletal development and disease
CT Tuzon, D Rigueur, AE Merrill
Current osteoporosis reports 17, 138-146, 2019
262019
Signaling pathways in craniofacial development: insights from rare skeletal disorders
CL Neben, AE Merrill
Current topics in developmental biology 115, 493-542, 2015
232015
FGFR2 mutations in bent bone dysplasia syndrome activate nucleolar stress and perturb cell fate determination
CL Neben, CT Tuzon, X Mao, FD Lay, AE Merrill
Human Molecular Genetics 26 (17), 3253-3270, 2017
172017
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