BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

81 related articles for article (PubMed ID: 9332670)

  • 1. Genomic structure, sequence, and mapping of human FGF8 with no evidence for its role in craniosynostosis/limb defect syndromes.
    Yoshiura K; Leysens NJ; Chang J; Ward D; Murray JC; Muenke M
    Am J Med Genet; 1997 Oct; 72(3):354-62. PubMed ID: 9332670
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Assignment of FGF8 to human chromosome 10q25-q26: mutations in FGF8 may be responsible for some types of acrocephalosyndactyly linked to this region.
    White RA; Dowler LL; Angeloni SV; Pasztor LM; MacArthur CA
    Genomics; 1995 Nov; 30(1):109-11. PubMed ID: 8595889
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Molecular cloning and characterization of human FGF8 alternative messenger RNA forms.
    Ghosh AK; Shankar DB; Shackleford GM; Wu K; T'Ang A; Miller GJ; Zheng J; Roy-Burman P
    Cell Growth Differ; 1996 Oct; 7(10):1425-34. PubMed ID: 8891346
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Structure and sequence of human FGF8.
    Gemel J; Gorry M; Ehrlich GD; MacArthur CA
    Genomics; 1996 Jul; 35(1):253-7. PubMed ID: 8661131
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A common mutation in the fibroblast growth factor receptor 1 gene in Pfeiffer syndrome.
    Muenke M; Schell U; Hehr A; Robin NH; Losken HW; Schinzel A; Pulleyn LJ; Rutland P; Reardon W; Malcolm S
    Nat Genet; 1994 Nov; 8(3):269-74. PubMed ID: 7874169
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The human FGF-8 gene localizes on chromosome 10q24 and is subjected to induction by androgen in breast cancer cells.
    Payson RA; Wu J; Liu Y; Chiu IM
    Oncogene; 1996 Jul; 13(1):47-53. PubMed ID: 8700553
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Characterisation of the genomic structure of chick Fgf8.
    Haworth KE; Healy C; Sharpe PT
    DNA Seq; 2005 Jun; 16(3):180-6. PubMed ID: 16147873
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Expression of fibroblast growth factors 4, 8, and 10 in limbs, flanks, and blastemas of Ambystoma.
    Christensen RN; Weinstein M; Tassava RA
    Dev Dyn; 2002 Mar; 223(2):193-203. PubMed ID: 11836784
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Integration of proviral sequences, but not at the common integration sites of the FGF8 locus, in an androgen-dependent mouse mammary Shionogi carcinoma.
    Kuriki K; Kamiakito T; Yoshida H; Saito K; Fukayama M; Tanaka A
    Cell Mol Biol (Noisy-le-grand); 2000 Nov; 46(7):1147-56. PubMed ID: 11075944
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Teneurin-2 is expressed in tissues that regulate limb and somite pattern formation and is induced in vitro and in situ by FGF8.
    Tucker RP; Chiquet-Ehrismann R; Chevron MP; Martin D; Hall RJ; Rubin BP
    Dev Dyn; 2001 Jan; 220(1):27-39. PubMed ID: 11146505
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genomic organization and embryonic expression of the mouse fibroblast growth factor 9 gene.
    Colvin JS; Feldman B; Nadeau JH; Goldfarb M; Ornitz DM
    Dev Dyn; 1999 Sep; 216(1):72-88. PubMed ID: 10474167
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Fgf8 signalling from the AER is essential for normal limb development.
    Lewandoski M; Sun X; Martin GR
    Nat Genet; 2000 Dec; 26(4):460-3. PubMed ID: 11101846
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Comparative genomics on FGF8, FGF17, and FGF18 orthologs.
    Katoh M; Katoh M
    Int J Mol Med; 2005 Sep; 16(3):493-6. PubMed ID: 16077960
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Distal limb deficiencies, micrognathia syndrome, and syndromic forms of split hand foot malformation (SHFM) are caused by chromosome 10q genomic rearrangements.
    Dimitrov BI; de Ravel T; Van Driessche J; de Die-Smulders C; Toutain A; Vermeesch JR; Fryns JP; Devriendt K; Debeer P
    J Med Genet; 2010 Feb; 47(2):103-11. PubMed ID: 19584065
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Characterization of the murine Lbx2 promoter, identification of the human homologue, and evaluation as a candidate for Alström syndrome.
    Chen F; Collin GB; Liu KC; Beier DR; Eccles M; Nishina PM; Moshang T; Epstein JA
    Genomics; 2001 Jun; 74(2):219-27. PubMed ID: 11386758
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Regulation of FGF8 expression by the androgen receptor in human prostate cancer.
    Gnanapragasam VJ; Robson CN; Neal DE; Leung HY
    Oncogene; 2002 Aug; 21(33):5069-80. PubMed ID: 12140757
    [TBL] [Abstract][Full Text] [Related]  

  • 17. FGFR2 signaling in normal and limbless chick limb buds.
    Lizarraga G; Ferrari D; Kalinowski M; Ohuchi H; Noji S; Kosher RA; Dealy CN
    Dev Genet; 1999; 25(4):331-8. PubMed ID: 10570465
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Pathogenesis of ectrodactyly in the Dactylaplasia mouse: aberrant cell death of the apical ectodermal ridge.
    Seto ML; Nunes ME; MacArthur CA; Cunningham ML
    Teratology; 1997 Oct; 56(4):262-70. PubMed ID: 9408977
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Sp8 and Sp9, two closely related buttonhead-like transcription factors, regulate Fgf8 expression and limb outgrowth in vertebrate embryos.
    Kawakami Y; Esteban CR; Matsui T; Rodríguez-León J; Kato S; Izpisúa Belmonte JC
    Development; 2004 Oct; 131(19):4763-74. PubMed ID: 15358670
    [TBL] [Abstract][Full Text] [Related]  

  • 20. FGFR2, FGF8, FGF10 and BMP7 as candidate genes for hypospadias.
    Beleza-Meireles A; Lundberg F; Lagerstedt K; Zhou X; Omrani D; Frisén L; Nordenskjöld A
    Eur J Hum Genet; 2007 Apr; 15(4):405-10. PubMed ID: 17264867
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.