BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

271 related articles for article (PubMed ID: 8106171)

  • 1. A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis.
    Jabs EW; Müller U; Li X; Ma L; Luo W; Haworth IS; Klisak I; Sparkes R; Warman ML; Mulliken JB
    Cell; 1993 Nov; 75(3):443-50. PubMed ID: 8106171
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Msx2 gene dosage influences the number of proliferative osteogenic cells in growth centers of the developing murine skull: a possible mechanism for MSX2-mediated craniosynostosis in humans.
    Liu YH; Tang Z; Kundu RK; Wu L; Luo W; Zhu D; Sangiorgi F; Snead ML; Maxson RE
    Dev Biol; 1999 Jan; 205(2):260-74. PubMed ID: 9917362
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The molecular basis of Boston-type craniosynostosis: the Pro148-->His mutation in the N-terminal arm of the MSX2 homeodomain stabilizes DNA binding without altering nucleotide sequence preferences.
    Ma L; Golden S; Wu L; Maxson R
    Hum Mol Genet; 1996 Dec; 5(12):1915-20. PubMed ID: 8968743
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Premature suture closure and ectopic cranial bone in mice expressing Msx2 transgenes in the developing skull.
    Liu YH; Kundu R; Wu L; Luo W; Ignelzi MA; Snead ML; Maxson RE
    Proc Natl Acad Sci U S A; 1995 Jun; 92(13):6137-41. PubMed ID: 7597092
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Identification of mutations in the MSX2 homeobox gene in families affected with foramina parietalia permagna.
    Wuyts W; Reardon W; Preis S; Homfray T; Rasore-Quartino A; Christians H; Willems PJ; Van Hul W
    Hum Mol Genet; 2000 May; 9(8):1251-5. PubMed ID: 10767351
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Boston type craniosynostosis: report of a second mutation in MSX2.
    Florisson JM; Verkerk AJ; Huigh D; Hoogeboom AJ; Swagemakers S; Kremer A; Heijsman D; Lequin MH; Mathijssen IM; van der Spek PJ
    Am J Med Genet A; 2013 Oct; 161A(10):2626-33. PubMed ID: 23949913
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Functional haploinsufficiency of the human homeobox gene MSX2 causes defects in skull ossification.
    Wilkie AO; Tang Z; Elanko N; Walsh S; Twigg SR; Hurst JA; Wall SA; Chrzanowska KH; Maxson RE
    Nat Genet; 2000 Apr; 24(4):387-90. PubMed ID: 10742103
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Fibroblast growth factors lead to increased Msx2 expression and fusion in calvarial sutures.
    Ignelzi MA; Wang W; Young AT
    J Bone Miner Res; 2003 Apr; 18(4):751-9. PubMed ID: 12674336
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Evidence for locus heterogeneity in acrocephalosyndactyly: a refined localization for the Saethre-Chotzen syndrome locus on distal chromosome 7p--and exclusion of Jackson-Weiss syndrome from craniosynostosis loci on 7p and 5q.
    van Herwerden L; Rose CS; Reardon W; Brueton LA; Weissenbach J; Malcolm S; Winter RM
    Am J Hum Genet; 1994 Apr; 54(4):669-74. PubMed ID: 8128964
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The canine homeobox gene MSX2: sequence, chromosome assignment and genetic analysis in dogs of different breeds.
    Haworth K; Breen M; Binns M; Hopkinson DA; Edwards YH
    Anim Genet; 2001 Feb; 32(1):32-6. PubMed ID: 11419342
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Miz1, a novel zinc finger transcription factor that interacts with Msx2 and enhances its affinity for DNA.
    Wu L; Wu H; Ma L; Sangiorgi F; Wu N; Bell JR; Lyons GE; Maxson R
    Mech Dev; 1997 Jul; 65(1-2):3-17. PubMed ID: 9256341
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Balanced translocation in a patient with craniosynostosis disrupts the SOX6 gene and an evolutionarily conserved non-transcribed region.
    Tagariello A; Heller R; Greven A; Kalscheuer VM; Molter T; Rauch A; Kress W; Winterpacht A
    J Med Genet; 2006 Jun; 43(6):534-40. PubMed ID: 16258006
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The mapping of a gene for craniosynostosis: evidence for linkage of the Saethre-Chotzen syndrome to distal chromosome 7p.
    Brueton LA; van Herwerden L; Chotai KA; Winter RM
    J Med Genet; 1992 Oct; 29(10):681-5. PubMed ID: 1433226
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Assignment of a gene locus involved in craniosynostosis to chromosome 5qter.
    Müller U; Warman ML; Mulliken JB; Weber JL
    Hum Mol Genet; 1993 Feb; 2(2):119-22. PubMed ID: 8499900
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Second family with the Boston-type craniosynostosis syndrome: novel mutation and expansion of the clinical spectrum.
    Janssen A; Hosen MJ; Jeannin P; Coucke PJ; De Paepe A; Vanakker OM
    Am J Med Genet A; 2013 Sep; 161A(9):2352-7. PubMed ID: 23918290
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Craniosynostosis suggestive of Saethre-Chotzen syndrome: clinical description of a large kindred and exclusion of candidate regions on 7p.
    von Gernet S; Schuffenhauer S; Golla A; Lichtner P; Balg S; Mühlbauer W; Murken J; Fairley J; Meitinger T
    Am J Med Genet; 1996 May; 63(1):177-84. PubMed ID: 8723106
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Identical mutations in three different fibroblast growth factor receptor genes in autosomal dominant craniosynostosis syndromes.
    Bellus GA; Gaudenz K; Zackai EH; Clarke LA; Szabo J; Francomano CA; Muenke M
    Nat Genet; 1996 Oct; 14(2):174-6. PubMed ID: 8841188
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) essential for maintenance of the photoreceptor.
    Freund CL; Gregory-Evans CY; Furukawa T; Papaioannou M; Looser J; Ploder L; Bellingham J; Ng D; Herbrick JA; Duncan A; Scherer SW; Tsui LC; Loutradis-Anagnostou A; Jacobson SG; Cepko CL; Bhattacharya SS; McInnes RR
    Cell; 1997 Nov; 91(4):543-53. PubMed ID: 9390563
    [TBL] [Abstract][Full Text] [Related]  

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

  • 20. Craniosynostosis in a patient with 2q37.3 deletion 5q34 duplication: association of extra copy of MSX2 with craniosynostosis.
    Kariminejad A; Kariminejad R; Tzschach A; Ullmann R; Ahmed A; Asghari-Roodsari A; Salehpour S; Afroozan F; Ropers HH; Kariminejad MH
    Am J Med Genet A; 2009 Jul; 149A(7):1544-9. PubMed ID: 19533795
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.