BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

187 related articles for article (PubMed ID: 35651944)

  • 1. Meckel's Cartilage in Mandibular Development and Dysmorphogenesis.
    Pitirri MK; Durham EL; Romano NA; Santos JI; Coupe AP; Zheng H; Chen DZ; Kawasaki K; Jabs EW; Richtsmeier JT; Wu M; Motch Perrine SM
    Front Genet; 2022; 13():871927. PubMed ID: 35651944
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. A dysmorphic mouse model reveals developmental interactions of chondrocranium and dermatocranium.
    Motch Perrine SM; Pitirri MK; Durham EL; Kawasaki M; Zheng H; Chen DZ; Kawasaki K; Richtsmeier JT
    Elife; 2022 Jun; 11():. PubMed ID: 35704354
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. A gain-of-function mutation of Fgfr2c demonstrates the roles of this receptor variant in osteogenesis.
    Eswarakumar VP; Horowitz MC; Locklin R; Morriss-Kay GM; Lonai P
    Proc Natl Acad Sci U S A; 2004 Aug; 101(34):12555-60. PubMed ID: 15316116
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Integration of Brain and Skull in Prenatal Mouse Models of Apert and Crouzon Syndromes.
    Motch Perrine SM; Stecko T; Neuberger T; Jabs EW; Ryan TM; Richtsmeier JT
    Front Hum Neurosci; 2017; 11():369. PubMed ID: 28790902
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Tissue-specific responses to aberrant FGF signaling in complex head phenotypes.
    Martínez-Abadías N; Motch SM; Pankratz TL; Wang Y; Aldridge K; Jabs EW; Richtsmeier JT
    Dev Dyn; 2013 Jan; 242(1):80-94. PubMed ID: 23172727
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Extensive phenotyping of the orofacial and dental complex in Crouzon syndrome.
    Khominsky A; Yong R; Ranjitkar S; Townsend G; Anderson PJ
    Arch Oral Biol; 2018 Feb; 86():123-130. PubMed ID: 29223639
    [TBL] [Abstract][Full Text] [Related]  

  • 11. FGFR2 mutation in 46,XY sex reversal with craniosynostosis.
    Bagheri-Fam S; Ono M; Li L; Zhao L; Ryan J; Lai R; Katsura Y; Rossello FJ; Koopman P; Scherer G; Bartsch O; Eswarakumar JV; Harley VR
    Hum Mol Genet; 2015 Dec; 24(23):6699-710. PubMed ID: 26362256
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Analysis of the
    Peskett E; Kumar S; Baird W; Jaiswal J; Li M; Patel P; Britto JA; Pauws E
    Biol Open; 2017 Feb; 6(2):223-231. PubMed ID: 28069589
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Computational mouse atlases and their application to automatic assessment of craniofacial dysmorphology caused by the Crouzon mutation Fgfr2(C342Y).
    Olafsdóttir H; Darvann TA; Hermann NV; Oubel E; Ersbøll BK; Frangi AF; Larsen P; Perlyn CA; Morriss-Kay GM; Kreiborg S
    J Anat; 2007 Jul; 211(1):37-52. PubMed ID: 17553099
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Tissue-specific expression of Fgfr2b and Fgfr2c isoforms, Fgf10 and Fgf9 in the developing chick mandible.
    Havens BA; Rodgers B; Mina M
    Arch Oral Biol; 2006 Feb; 51(2):134-45. PubMed ID: 16105644
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Altered mandibular development precedes the time of palate closure in mice homozygous for disproportionate micromelia: an oral clefting model supporting the Pierre-Robin sequence.
    Ricks JE; Ryder VM; Bridgewater LC; Schaalje B; Seegmiller RE
    Teratology; 2002 Mar; 65(3):116-20. PubMed ID: 11877774
    [TBL] [Abstract][Full Text] [Related]  

  • 17. FGFR2c-mediated ERK-MAPK activity regulates coronal suture development.
    Pfaff MJ; Xue K; Li L; Horowitz MC; Steinbacher DM; Eswarakumar JVP
    Dev Biol; 2016 Jul; 415(2):242-250. PubMed ID: 27034231
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Roles of FGFR3 during morphogenesis of Meckel's cartilage and mandibular bones.
    Havens BA; Velonis D; Kronenberg MS; Lichtler AC; Oliver B; Mina M
    Dev Biol; 2008 Apr; 316(2):336-49. PubMed ID: 18339367
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Meckel's cartilage differentiation is dependent on hedgehog signaling.
    Melnick M; Witcher D; Bringas P; Carlsson P; Jaskoll T
    Cells Tissues Organs; 2005; 179(4):146-57. PubMed ID: 16046861
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 10.