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Volumn 78, Issue 1, 2006, Pages 167-170

Transactivation function of an ∼800-bp evolutionarily conserved sequence at the SHOX 3′ region: Implication for the downstream enhancer

Author keywords

[No Author keywords available]

Indexed keywords

3' UNTRANSLATED REGION; ENHANCER REGION; GENE; GENE FUNCTION; GENE SEQUENCE; GENETIC CONSERVATION; LETTER; PRIORITY JOURNAL; SEQUENCE ANALYSIS; SHOX GENE; TRANSACTIVATION; BINDING SITE; BIOLOGY; CHONDRODYSPLASIA; COMPARATIVE STUDY; FLUORESCENCE IN SITU HYBRIDIZATION; GENETIC POLYMORPHISM; GENETICS; GENOTYPE; HUMAN; JAPAN; MOLECULAR GENETICS; MUTATION; NOTE; NUCLEOTIDE SEQUENCE; PEDIGREE;

EID: 29244486467     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/499254     Document Type: Letter
Times cited : (61)

References (9)
  • 2
    • 0346220283 scopus 로고    scopus 로고
    • Transcriptional and translational regulation of the Leri-Weill and Turner syndrome homeobox gene SHOX
    • Blaschke RJ, Topfer C, Marchini A, Steinbeisser H, Janssen JW, Rappold GA (2003) Transcriptional and translational regulation of the Leri-Weill and Turner syndrome homeobox gene SHOX. J Biol Chem 278:47820-47826
    • (2003) J Biol Chem , vol.278 , pp. 47820-47826
    • Blaschke, R.J.1    Topfer, C.2    Marchini, A.3    Steinbeisser, H.4    Janssen, J.W.5    Rappold, G.A.6
  • 5
    • 23344443566 scopus 로고    scopus 로고
    • Microdeletion in the SHOX 3′ region associated with skeletal phenotypes of Langer mesomelic dysplasia in a 45,X/46,X,r(X) infant and Leri-Weill dyschondrosteosis in her 46,XX mother: Implication for the SHOX enhancer
    • Fukami M, Okuyama T, Yamamori S, Nishimura G, Ogata T (2005) Microdeletion in the SHOX 3′ region associated with skeletal phenotypes of Langer mesomelic dysplasia in a 45,X/46,X,r(X) infant and Leri-Weill dyschondrosteosis in her 46,XX mother: implication for the SHOX enhancer. Am J Med Genet A 137:72-76
    • (2005) Am J Med Genet A , vol.137 , pp. 72-76
    • Fukami, M.1    Okuyama, T.2    Yamamori, S.3    Nishimura, G.4    Ogata, T.5
  • 7
    • 0035894660 scopus 로고    scopus 로고
    • The Leri-Weill and Turner syndrome homeobox gene SHOX encodes a cell-type specific transcriptional activator
    • Rao E, Blaschke RJ, Marchini A, Niesler B, Burnett M, Rappold GA (2001) The Leri-Weill and Turner syndrome homeobox gene SHOX encodes a cell-type specific transcriptional activator. Hum Mol Genet 10:3083-3091
    • (2001) Hum Mol Genet , vol.10 , pp. 3083-3091
    • Rao, E.1    Blaschke, R.J.2    Marchini, A.3    Niesler, B.4    Burnett, M.5    Rappold, G.A.6
  • 9
    • 0032902095 scopus 로고    scopus 로고
    • Hox genes in digit development and evolution
    • Zákány J, Duboule D (1999) Hox genes in digit development and evolution. Cell Tissue Res 296:19-25
    • (1999) Cell Tissue Res , vol.296 , pp. 19-25
    • Zákány, J.1    Duboule, D.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.