197 related articles for article (PubMed ID: 32886384)
1. Genotype-Phenotype Correlation of Tracheal Cartilaginous Sleeves and Fgfr2 Mutations in Mice.
Lam AS; Liu CC; Deutsch GH; Rivera J; Perkins JA; Holmes G; Jabs EW; Cunningham ML; Dahl JP
Laryngoscope; 2021 Apr; 131(4):E1349-E1356. PubMed ID: 32886384
[TBL] [Abstract][Full Text] [Related]
2. Beare-Stevenson syndrome: two new patients, including a novel finding of tracheal cartilaginous sleeve.
Wenger TL; Bhoj EJ; Wetmore RF; Mennuti MT; Bartlett SP; Mollen TJ; McDonald-McGinn DM; Zackai EH
Am J Med Genet A; 2015 Apr; 167A(4):852-7. PubMed ID: 25706251
[TBL] [Abstract][Full Text] [Related]
3. Further analysis of the Crouzon mouse: effects of the FGFR2(C342Y) mutation are cranial bone-dependent.
Liu J; Nam HK; Wang E; Hatch NE
Calcif Tissue Int; 2013 May; 92(5):451-66. PubMed ID: 23358860
[TBL] [Abstract][Full Text] [Related]
4. The effect of a Beare-Stevenson syndrome Fgfr2 Y394C mutation on early craniofacial bone volume and relative bone mineral density in mice.
Percival CJ; Wang Y; Zhou X; Jabs EW; Richtsmeier JT
J Anat; 2012 Nov; 221(5):434-42. PubMed ID: 22881429
[TBL] [Abstract][Full Text] [Related]
5. Complex Airway Management in Patients with Tracheal Cartilaginous Sleeves.
Noble AR; Cunningham ML; Lam A; Wenger TL; Sie KC; Perkins JA; Dahl JP
Laryngoscope; 2022 Jan; 132(1):215-221. PubMed ID: 34133757
[TBL] [Abstract][Full Text] [Related]
6. Crouzon syndrome mouse model exhibits cartilage hyperproliferation and defective segmentation in the developing trachea.
Hines EA; Jones MN; Harvey JF; Perlyn C; Ornitz DM; Sun X; Verheyden JM
Sci China Life Sci; 2019 Oct; 62(10):1375-1380. PubMed ID: 31463736
[TBL] [Abstract][Full Text] [Related]
7. The craniofacial phenotype of the Crouzon mouse: analysis of a model for syndromic craniosynostosis using three-dimensional MicroCT.
Perlyn CA; DeLeon VB; Babbs C; Govier D; Burell L; Darvann T; Kreiborg S; Morriss-Kay G
Cleft Palate Craniofac J; 2006 Nov; 43(6):740-8. PubMed ID: 17105336
[TBL] [Abstract][Full Text] [Related]
8. Craniosynostosis-associated Fgfr2(C342Y) mutant bone marrow stromal cells exhibit cell autonomous abnormalities in osteoblast differentiation and bone formation.
Liu J; Kwon TG; Nam HK; Hatch NE
Biomed Res Int; 2013; 2013():292506. PubMed ID: 23762837
[TBL] [Abstract][Full Text] [Related]
9. Hearing loss in syndromic craniosynostoses: otologic manifestations and clinical findings.
Agochukwu NB; Solomon BD; Muenke M
Int J Pediatr Otorhinolaryngol; 2014 Dec; 78(12):2037-47. PubMed ID: 25441602
[TBL] [Abstract][Full Text] [Related]
10. p38 Inhibition ameliorates skin and skull abnormalities in Fgfr2 Beare-Stevenson mice.
Wang Y; Zhou X; Oberoi K; Phelps R; Couwenhoven R; Sun M; Rezza A; Holmes G; Percival CJ; Friedenthal J; Krejci P; Richtsmeier JT; Huso DL; Rendl M; Jabs EW
J Clin Invest; 2012 Jun; 122(6):2153-64. PubMed ID: 22585574
[TBL] [Abstract][Full Text] [Related]
11. Overexpression of
Lee KKL; Peskett E; Quinn CM; Aiello R; Adeeva L; Moulding DA; Stanier P; Pauws E
Dis Model Mech; 2018 Nov; 11(11):. PubMed ID: 30266836
[TBL] [Abstract][Full Text] [Related]
12. Activation of p38 MAPK pathway in the skull abnormalities of Apert syndrome Fgfr2(+P253R) mice.
Wang Y; Sun M; Uhlhorn VL; Zhou X; Peter I; Martinez-Abadias N; Hill CA; Percival CJ; Richtsmeier JT; Huso DL; Jabs EW
BMC Dev Biol; 2010 Feb; 10():22. PubMed ID: 20175913
[TBL] [Abstract][Full Text] [Related]
13. Dura in the pathogenesis of syndromic craniosynostosis: fibroblast growth factor receptor 2 mutations in dural cells promote osteogenic proliferation and differentiation of osteoblasts.
Ang BU; Spivak RM; Nah HD; Kirschner RE
J Craniofac Surg; 2010 Mar; 21(2):462-7. PubMed ID: 20489451
[TBL] [Abstract][Full Text] [Related]
14. Midface and upper airway dysgenesis in FGFR2-related craniosynostosis involves multiple tissue-specific and cell cycle effects.
Holmes G; O'Rourke C; Motch Perrine SM; Lu N; van Bakel H; Richtsmeier JT; Jabs EW
Development; 2018 Oct; 145(19):. PubMed ID: 30228104
[TBL] [Abstract][Full Text] [Related]
15. Tracheal cartilaginous sleeves in children with syndromic craniosynostosis.
Wenger TL; Dahl J; Bhoj EJ; Rosen A; McDonald-McGinn D; Zackai E; Jacobs I; Heike CL; Hing A; Santani A; Inglis AF; Sie KC; Cunningham M; Perkins J
Genet Med; 2017 Jan; 19(1):62-68. PubMed ID: 27228464
[TBL] [Abstract][Full Text] [Related]
16. Synchondrosis fusion contributes to the progression of postnatal craniofacial dysmorphology in syndromic craniosynostosis.
Hoshino Y; Takechi M; Moazen M; Steacy M; Koyabu D; Furutera T; Ninomiya Y; Nuri T; Pauws E; Iseki S
J Anat; 2023 Mar; 242(3):387-401. PubMed ID: 36394990
[TBL] [Abstract][Full Text] [Related]
17. Genetic background dependent modifiers of craniosynostosis severity.
Dudakovic A; Nam HK; Wijnen AJV; Hatch NE
J Struct Biol; 2020 Dec; 212(3):107629. PubMed ID: 32976998
[TBL] [Abstract][Full Text] [Related]
18. Description of a new mutation and characterization of FGFR1, FGFR2, and FGFR3 mutations among Brazilian patients with syndromic craniosynostoses.
Passos-Bueno MR; Sertié AL; Richieri-Costa A; Alonso LG; Zatz M; Alonso N; Brunoni D; Ribeiro SF
Am J Med Genet; 1998 Jul; 78(3):237-41. PubMed ID: 9677057
[TBL] [Abstract][Full Text] [Related]
19. Mandibular dysmorphology due to abnormal embryonic osteogenesis in FGFR2-related craniosynostosis mice.
Motch Perrine SM; Wu M; Stephens NB; Kriti D; van Bakel H; Jabs EW; Richtsmeier JT
Dis Model Mech; 2019 May; 12(5):. PubMed ID: 31064775
[TBL] [Abstract][Full Text] [Related]
20. A Case of Beare-Stevenson Syndrome with Unusual Manifestations.
Ron N; Leung S; Carney E; Gerber A; David KL
Am J Case Rep; 2016 Apr; 17():254-8. PubMed ID: 27079505
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
