The Leri-Weill and Turner syndrome homeobox gene SHOX encodes a cell-type specific transcriptional activator

Human Molecular Genetics

Volumn 10, Issue 26, 2001, Pages 3083-3091

  Rao, Ercole ^a   Blaschke, Rüdiger J ^a   Marchini, Antonio ^a   Niesler, Beate ^a   Burnett, Michael ^a   Rappold, Gudrun A ^a  

^a UNIVERSITY OF HEIDELBERG   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL CELL; ARTICLE; CARBOXY TERMINAL SEQUENCE; CELL CULTURE; CELL LINE; CELL NUCLEUS; CELL SPECIFICITY; CELL TYPE; CELLULAR DISTRIBUTION; CONTROLLED STUDY; DYSCHONDROSTEOSIS; GENE ACTIVATION; GENE CONSTRUCT; GENETIC TRANSCRIPTION; GENETIC TRANSFECTION; HOMEOBOX; HUMAN; HUMAN CELL; MODEL; MODULATION; NONHUMAN; OSTEOBLAST; PHENOTYPE; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN LOCALIZATION; QUANTITATIVE TRAIT LOCUS; REPORTER GENE; SHORT STATURE; SKELETON MALFORMATION; TRANSACTIVATION; TURNER SYNDROME;

ANIMALIA;

EID: 0035894660     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/10.26.3083     Document Type: Article

References (24)

1. Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome
2. PHOG, a candidate gene for involvement in the short stature of Turner syndrome
3. SHOX mutations in dyschondrosteosis (Leri-Weill syndrome)
4. Mutation and deletion of the pseudoautosomal gene SHOX cause Leri-Weill dyschondrosteosis
5. Phenotypic variation and genetic heterogeneity in Leri-Weill syndrome
6. Vertebrate aristaless-related genes
7. Orthopedia, a novel homeobox-containing gene expressed in the developing CNS of both mouse and Drosophila
8. The short stature homeobox gene SHOX is involved in skeletal abnormalities in Turner syndrome
9. Cooperative dimerization of paired class homeodomains on DNA
10. High resolution crystal structure of a paired (Pax) class cooperative homeodomain dimer on DNA
11. Regulation of transcription factor localization: Fine-tuning of gene expression
12. Alx-4, a transcriptional activator whose expression is restricted to sites of epithelial-mesenchymal interactions
13. Multiple signals converging on NF-κB
14. SHOT, a SHOX-related homeobox gene, is implicated in craniofacial, brain, heart and limb development
15. The recessive phenotype displayed by a dominant negative microphthalmia-associated transcription factor mutant is a result of impaired nucleation potential
16. Nuclear targeting sequences-a consensus?
17. Human CART1, a paired-class homeodomain protein, activates transcription through palindromic binding sites
18. Physical and genetic interactions between Alx4 and Cart1
19. Direct regulation of rhodopsin 1 by Pax-6/eyeless in Drosophila: Evidence for a conserved function in photoreceptors
20. Allosteric effects of Pit-1 DNA sites on long-term repression in cell type specification
21. The control of trunk Hox specificity and activity by Extradenticle
22. The nuclear hormone receptor Ftz-F1 is a cofactor for the Drosophila homeodomain protein Ftz
23. Regulation of the HNF-1 homeodomain proteins by DCoH
24. Developmental role of transcription factor isoforms generated by alternative splicing