These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

112 related articles for article (PubMed ID: 11328652)

  • 1. Cloning and sequencing of the rabbit FGFR2 cDNA.
    Yang ZW; Mooney MP; Ferrell RE
    DNA Seq; 2000; 11(5):439-46. PubMed ID: 11328652
    [No Abstract]   [Full Text] [Related]  

  • 2. Constitutive receptor activation by Crouzon syndrome mutations in fibroblast growth factor receptor (FGFR)2 and FGFR2/Neu chimeras.
    Galvin BD; Hart KC; Meyer AN; Webster MK; Donoghue DJ
    Proc Natl Acad Sci U S A; 1996 Jul; 93(15):7894-9. PubMed ID: 8755573
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Re: Sequence analysis of fibroblast growth factor receptor 2 (FGFR2) in Japanese patients with craniosynostosis. Sakai et al. J Craniofac. Surg. 2001, 12: 580-585.
    Warren SM; Longaker MT
    J Craniofac Surg; 2002 Jul; 13(4):597-9. PubMed ID: 12140430
    [No Abstract]   [Full Text] [Related]  

  • 4. Unclassifiable craniosynostosis phenotypes, FGFR2 Trp290 mutations, acanthosis nigricans, and unpaired cysteine mutations.
    Cohen MM
    Am J Med Genet; 2002 Nov; 113(1):1-3. PubMed ID: 12400057
    [No Abstract]   [Full Text] [Related]  

  • 5. Mutations in fibroblast growth factor receptor 2 and fibroblast growth factor receptor 3 genes associated with human gastric and colorectal cancers.
    Jang JH; Shin KH; Park JG
    Cancer Res; 2001 May; 61(9):3541-3. PubMed ID: 11325814
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Craniosynostosis with tracheal sleeve: a patient with Pfeiffer syndrome, tracheal sleeve and additional malformations in whom an FGFR2 mutation was found.
    Zackai EH; McDonald-McGinn DM; Stolle C; Huff DS
    Clin Dysmorphol; 2003 Jul; 12(3):209. PubMed ID: 14564165
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Cloning and interspecies comparisons of three newt (Notophthalmus viridescens) fibroblast growth factor receptor sequences.
    Poulin ML; Botelho MJ; Chiu IM
    Mol Cell Biochem; 1997 Oct; 175(1-2):11-9. PubMed ID: 9350028
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Novel FGFR2 mutations in Crouzon and Jackson-Weiss syndromes show allelic heterogeneity and phenotypic variability.
    Park WJ; Meyers GA; Li X; Theda C; Day D; Orlow SJ; Jones MC; Jabs EW
    Hum Mol Genet; 1995 Jul; 4(7):1229-33. PubMed ID: 8528214
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Further evidence that fibroblast growth factor receptor 2 mutations cause Antley-Bixler syndrome.
    Tsai FJ; Wu JY; Yang CF; Tsai CH
    Acta Paediatr; 2001 May; 90(5):595-7. PubMed ID: 11430730
    [No Abstract]   [Full Text] [Related]  

  • 10. The mutations in FGFR2-associated craniosynostoses are clustered in five structural elements of immunoglobulin-like domain III of the receptor.
    Steinberger D; Vriend G; Mulliken JB; Müller U
    Hum Genet; 1998 Feb; 102(2):145-50. PubMed ID: 9521581
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Lumpers, splitters, and FGFRs.
    Winter RM; Reardon W
    Am J Med Genet; 1996 Jun; 63(3):501-2. PubMed ID: 8737660
    [No Abstract]   [Full Text] [Related]  

  • 12. 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]  

  • 13. Jackson-Weiss and Crouzon syndromes are allelic with mutations in fibroblast growth factor receptor 2.
    Jabs EW; Li X; Scott AF; Meyers G; Chen W; Eccles M; Mao JI; Charnas LR; Jackson CE; Jaye M
    Nat Genet; 1994 Nov; 8(3):275-9. PubMed ID: 7874170
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Not Antley-Bixler syndrome.
    Gripp KW; Zackai EH; Cohen MM
    Am J Med Genet; 1999 Mar; 83(1):65-8. PubMed ID: 10076887
    [No Abstract]   [Full Text] [Related]  

  • 15. A novel mutation, Ala315Ser, in FGFR2: a gene-environment interaction leading to craniosynostosis?
    Johnson D; Wall SA; Mann S; Wilkie AO
    Eur J Hum Genet; 2000 Aug; 8(8):571-7. PubMed ID: 10951518
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Patient described by Chun et al. may not present Antley-Bixler syndrome.
    Gorlin RJ
    Am J Med Genet; 1999 Mar; 83(1):64. PubMed ID: 10076886
    [No Abstract]   [Full Text] [Related]  

  • 17. Craniosynostosis: genes and mechanisms.
    Wilkie AO
    Hum Mol Genet; 1997; 6(10):1647-56. PubMed ID: 9300656
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Analysis of patients with craniosynostosis syndromes for a pro246Arg mutation of FGFR4.
    Gaudenz K; Roessler E; Vainikka S; Alitalo K; Muenke M
    Mol Genet Metab; 1998 May; 64(1):76-9. PubMed ID: 9682222
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [From gene to disease; craniosynostosis syndromes due to FGFR2-mutation].
    van Ravenswaaij-Arts CM; van den Ouweland AM; Hoogeboom AJ; Herbergs J; Pals G
    Ned Tijdschr Geneeskd; 2002 Jan; 146(2):63-6. PubMed ID: 11820058
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Novel SNP at the common primer site of exon IIIa of FGFR2 gene causes error in molecular diagnosis of craniosynostosis syndrome.
    Wong LJ; Chen TJ; Dai P; Bird L; Muenke M
    Am J Med Genet; 2001 Aug; 102(3):282-5. PubMed ID: 11484208
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.