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Items: 1 to 20 of 492

1.
Multiscale mechanical characterisation of the craniofacial system under external forces
Marius Didziokas, Dominic Jones, Ali Alazmani, Miranda Steacy, Erwin Pauws, Mehran Moazen
Biomech Model Mechanobiol. 2024; 23(2): 675–685. Published online 2024 Jan 13. doi: 10.1007/s10237-023-01799-y
PMCID:
PMC10963580
AbstractArticlePDF–3.6M
2.
Role of Fibroblast Growth Factor Receptor 2 (FGFR2) in Corneal Stromal Thinning
Roy Joseph, Akosua Boateng, Om P. Srivastava, Roswell R. Pfister
Invest Ophthalmol Vis Sci. 2023 Sep; 64(12): 40. Published online 2023 Sep 26. doi: 10.1167/iovs.64.12.40
PMCID:
PMC10541240
AbstractArticlePDF–3.2M
3.
Spontaneous acinar and ductal regrowth after meibomian gland atrophy induced by deletion of FGFR2 in a mouse model
Xiaowei Yang, Xingwu Zhong, Andrew JW. Huang, Lixing W. Reneker
Ocul Surf. Author manuscript; available in PMC 2023 Jul 3.
Published in final edited form as: Ocul Surf. 2022 Oct; 26: 300–309. Published online 2021 Nov 16. doi: 10.1016/j.jtos.2021.11.005
PMCID:
PMC10317283
AbstractArticlePDF–3.5M
4.
Neonatal loss of FGFR2 in astroglial cells affects locomotion, sociability, working memory, and glia-neuron interactions in mice
Hanna E. Stevens, Soraya Scuderi, Sarah C. Collica, Simone Tomasi, Tamas L. Horvath, Flora M. Vaccarino
Transl Psychiatry. 2023; 13: 89. Published online 2023 Mar 11. doi: 10.1038/s41398-023-02372-y
PMCID:
PMC10008554
AbstractArticlePDF–2.0M
5.
A dysmorphic mouse model reveals developmental interactions of chondrocranium and dermatocranium
Susan M Motch Perrine, M Kathleen Pitirri, Emily L Durham, Mizuho Kawasaki, Hao Zheng, Danny Z Chen, Kazuhiko Kawasaki, Joan T Richtsmeier
eLife. 2022; 11: e76653. Published online 2022 Jun 15. doi: 10.7554/eLife.76653
PMCID:
PMC9259032
AbstractArticlePDF–11M
6.
Mechanical loading of cranial joints minimizes the craniofacial phenotype in Crouzon syndrome
Mehran Moazen, Mahbubeh Hejazi, Dawn Savery, Dominic Jones, Arsalan Marghoub, Ali Alazmani, Erwin Pauws
Sci Rep. 2022; 12: 9693. Published online 2022 Jun 11. doi: 10.1038/s41598-022-13807-9
PMCID:
PMC9188582
AbstractArticlePDF–4.6M
7.
Septal chondrocyte hypertrophy contributes to midface deformity in a mouse model of Apert syndrome
Bong-Soo Kim, Hye-Rim Shin, Hyun-Jung Kim, Heein Yoon, Young-Dan Cho, Kang-Young Choi, Je-Yong Choi, Woo-Jin Kim, Hyun-Mo Ryoo
Sci Rep. 2021; 11: 7979. Published online 2021 Apr 12. doi: 10.1038/s41598-021-87260-5
PMCID:
PMC8041873
AbstractArticlePDF–7.0M
8.
Genotype-phenotype correlation of tracheal cartilaginous sleeves and Fgfr2 mutations in mice
Austin S Lam, C Carrie Liu, Gail H Deutsch, Joshua Rivera, Jonathan A Perkins, Greg Holmes, Ethylin Wang Jabs, Michael L Cunningham, John P Dahl
Laryngoscope. Author manuscript; available in PMC 2022 Apr 1.
Published in final edited form as: Laryngoscope. 2021 Apr; 131(4): E1349–E1356. Published online 2020 Sep 4. doi: 10.1002/lary.29060
PMCID:
PMC7930142
AbstractArticlePDF–1.4M
9.
Viral delivery of tissue nonspecific alkaline phosphatase diminishes craniosynostosis in one of two FGFR2C342Y/+ mouse models of Crouzon syndrome
Hwa Kyung Nam, Iva Vesela, Sara Dean Schutte, Nan E. Hatch
PLoS One. 2020; 15(5): e0234073. Published online 2020 May 29. doi: 10.1371/journal.pone.0234073
PMCID:
PMC7259715
AbstractArticlePDF–1.7M
10.
FGFR2 Is Required for AEC2 Homeostasis and Survival after Bleomycin-induced Lung Injury
Samuel J. Dorry, Brandon O. Ansbro, David M. Ornitz, Gökhan M. Mutlu, Robert D. Guzy
Am J Respir Cell Mol Biol. 2020 May; 62(5): 608–621. doi: 10.1165/rcmb.2019-0079OC
PMCID:
PMC7193788
AbstractArticlePDF–3.5M
11.
Integration of Brain and Skull in Prenatal Mouse Models of Apert and Crouzon Syndromes
Susan M. Motch Perrine, Tim Stecko, Thomas Neuberger, Ethylin W. Jabs, Timothy M. Ryan, Joan T. Richtsmeier
Front Hum Neurosci. 2017; 11: 369. Published online 2017 Jul 25. doi: 10.3389/fnhum.2017.00369
PMCID:
PMC5525342
AbstractArticlePDF–4.4M
12.
Fibroblast Growth Factor Receptor 2 (FGFR2) Is Required for Meibomian Gland Homeostasis in the Adult Mouse
Lixing W. Reneker, Lanlan Wang, Rebecca T. Irlmeier, Andrew J. W. Huang
Invest Ophthalmol Vis Sci. 2017 May; 58(5): 2638–2646. doi: 10.1167/iovs.16-21204
PMCID:
PMC5444547
AbstractArticlePDF–1.4M
13.
Cell and Tissue Scale Forces Coregulate Fgfr2-Dependent Tetrads and Rosettes in the Mouse Embryo
Jun Wen, Hirotaka Tao, Kimberly Lau, Haijiao Liu, Craig A. Simmons, Yu Sun, Sevan Hopyan
Biophys J. 2017 May 23; 112(10): 2209–2218. Published online 2017 May 23. doi: 10.1016/j.bpj.2017.04.024
PMCID:
PMC5444237
AbstractArticlePDF–3.3M
14.
Deformed Skull Morphology Is Caused by the Combined Effects of the Maldevelopment of Calvarias, Cranial Base and Brain in FGFR2-P253R Mice Mimicking Human Apert Syndrome
Fengtao Luo, Yangli Xie, Wei Xu, Junlan Huang, Siru Zhou, Zuqiang Wang, Xiaoqing Luo, Mi Liu, Lin Chen, Xiaolan Du
Int J Biol Sci. 2017; 13(1): 32–45. Published online 2017 Jan 1. doi: 10.7150/ijbs.16287
PMCID:
PMC5264259
AbstractArticlePDF–2.5M
15.
Mechanical Properties of Calvarial Bones in a Mouse Model for Craniosynostosis
Mehran Moazen, Emma Peskett, Christian Babbs, Erwin Pauws, Michael J. Fagan
PLoS One. 2015; 10(5): e0125757. Published online 2015 May 12. doi: 10.1371/journal.pone.0125757
PMCID:
PMC4429024
AbstractArticlePDF–5.6M
16.
Inhibited Wnt Signaling Causes Age-Dependent Abnormalities in the Bone Matrix Mineralization in the Apert Syndrome FGFR2S252W/+ Mice
Li Zhang, Peng Chen, Lin Chen, Tujun Weng, Shichang Zhang, Xia Zhou, Bo Zhang, Luchuan Liu
PLoS One. 2015; 10(2): e112716. Published online 2015 Feb 18. doi: 10.1371/journal.pone.0112716
PMCID:
PMC4333342
AbstractArticlePDF–10M
17.
Craniofacial divergence by distinct prenatal growth patterns in Fgfr2 mutant mice
Susan M Motch Perrine, Theodore M Cole, III, Neus Martínez-Abadías, Kristina Aldridge, Ethylin Wang Jabs, Joan T Richtsmeier
BMC Dev Biol. 2014; 14: 8. Published online 2014 Feb 28. doi: 10.1186/1471-213X-14-8
PMCID:
PMC4101838
AbstractArticlePDF–3.0M
18.
Therapeutic Effect of Nanogel-Based Delivery of Soluble FGFR2 with S252W Mutation on Craniosynostosis
Masako Yokota, Yukiho Kobayashi, Jumpei Morita, Hiroyuki Suzuki, Yoshihide Hashimoto, Yoshihiro Sasaki, Kazunari Akiyoshi, Keiji Moriyama
PLoS One. 2014; 9(7): e101693. Published online 2014 Jul 8. doi: 10.1371/journal.pone.0101693
PMCID:
PMC4086955
AbstractArticlePDF–3.2M
19.
Embryonic Craniofacial Bone Volume and Bone Mineral Density in Fgfr2+/P253R and Nonmutant Mice
Christopher J. Percival, Yuan Huang, Ethylin Wang Jabs, Runze Li, Joan T. Richtsmeier
Dev Dyn. Author manuscript; available in PMC 2014 Apr 24.
Published in final edited form as: Dev Dyn. 2014 Apr; 243(4): 541–551. Published online 2014 Feb 7. doi: 10.1002/dvdy.24095
PMCID:
PMC3998671
AbstractArticlePDF–1.6M
20.
A Ser252Trp Mutation in Fibroblast Growth Factor Receptor 2 (FGFR2) Mimicking Human Apert Syndrome Reveals an Essential Role for FGF Signaling in the Regulation of Endochondral Bone Formation
Peng Chen, Li Zhang, Tujun Weng, Shichang Zhang, Shijin Sun, Mingtao Chang, Yang Li, Bo Zhang, Lianyang Zhang
PLoS One. 2014; 9(1): e87311. Published online 2014 Jan 28. doi: 10.1371/journal.pone.0087311
PMCID:
PMC3904987
AbstractArticlePDF–6.8M

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