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24 results on '"Higgs DR"'

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1. Suppression of the alternative lengthening of telomere pathway by the chromatin remodelling factor ATRX.

2. ATRX Plays a Key Role in Maintaining Silencing at Interstitial Heterochromatic Loci and Imprinted Genes.

3. ATRX dysfunction induces replication defects in primary mouse cells.

4. The chromatin remodeller ATRX: a repeat offender in human disease.

5. Functional significance of mutations in the Snf2 domain of ATRX.

6. Combinatorial readout of histone H3 modifications specifies localization of ATRX to heterochromatin.

7. ATRX: taming tandem repeats.

8. ATR-X syndrome protein targets tandem repeats and influences allele-specific expression in a size-dependent manner.

9. Neuronal death resulting from targeted disruption of the Snf2 protein ATRX is mediated by p53.

10. Structural consequences of disease-causing mutations in the ATRX-DNMT3-DNMT3L (ADD) domain of the chromatin-associated protein ATRX.

11. A novel mutation in the last exon of ATRX in a patient with alpha-thalassemia myelodysplastic syndrome.

12. Loss of Atrx affects trophoblast development and the pattern of X-inactivation in extraembryonic tissues.

13. The chromatin-remodeling protein ATRX is critical for neuronal survival during corticogenesis.

14. Acquired somatic ATRX mutations in myelodysplastic syndrome associated with alpha thalassemia (ATMDS) convey a more severe hematologic phenotype than germline ATRX mutations.

15. A conserved truncated isoform of the ATR-X syndrome protein lacking the SWI/SNF-homology domain.

16. Identification of acquired somatic mutations in the gene encoding chromatin-remodeling factor ATRX in the alpha-thalassemia myelodysplasia syndrome (ATMDS).

17. Molecular-clinical spectrum of the ATR-X syndrome.

18. Mutations in ATRX, encoding a SWI/SNF-like protein, cause diverse changes in the pattern of DNA methylation.

19. A nonsense mutation of the ATRX gene causing mild mental retardation and epilepsy.

20. Localization of a putative transcriptional regulator (ATRX) at pericentromeric heterochromatin and the short arms of acrocentric chromosomes.

21. Mutations in transcriptional regulator ATRX establish the functional significance of a PHD-like domain.

22. ATRX encodes a novel member of the SNF2 family of proteins: mutations point to a common mechanism underlying the ATR-X syndrome.

23. Mutations in a putative global transcriptional regulator cause X-linked mental retardation with alpha-thalassemia (ATR-X syndrome).

24. The chromatin remodeller ATRX facilitates diverse nuclear processes, in a stochastic manner, in both heterochromatin and euchromatin

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