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1. Correction of ERCC1 deficiency in mice

2. Radically truncated MeCP2 rescues Rett syndrome-like neurological defects

4. Comparative analysis of potential broad spectrum neuronal Cre drivers

8. SALL4 controls cell fate in response to DNA base composition

9. Embryonic lethal phenotype reveals a function of TDG in maintaining epigenetic stability

10. CpG islands influence chromatin structure via the CpG-binding protein Cfp1

11. Neuronal non-CG methylation is an essential target for MeCP2 function

12. SALL4 controls cell fate in response to DNA base composition

16. Neuronal non-CG methylation is an essential target for MeCP2 function

17. SALL4 controls cell fate in response to DNA base composition

21. Affinity for DNA contributes to NLS independent nuclear localization of MeCP2

22. An Orphan CpG Island Drives Expression of a let-7 miRNA Precursor with an Important Role in Mouse Development

23. MeCP2 recognizes cytosine methylated tri-nucleotide and di-nucleotide sequences to tune transcription in the mammalian brain

24. Toxicity of overexpressed MeCP2 is independent of HDAC3 activity

27. A dominant role for the methyl-CpG-binding protein Mbd2 in controlling Th2 induction by dendritic cells

28. Domains of methylated CAC and CG target MeCP2 to tune transcription in the brain

29. Exclusive expression of MeCP2 in the nervous system distinguishes between brain and peripheral Rett syndrome-like phenotypes

30. A dominant role for the methyl-CpG-binding protein Mbd2 in controlling Th2 induction by dendritic cells

32. A single allele of Hdac2 but not Hdac1 is sufficient for normal mouse brain development in the absence of its paralog

33. Rett syndrome mutations abolish the interaction of MeCP2 with the NCoR/SMRT co-repressor

38. Kaiso-Deficient Mice Show Resistance to Intestinal Cancer

47. 53BP1 exchanges slowly at the sites of DNA damage and appears to require RNA for its association with chromatin.

50. Double Replacement Gene Targeting for the Production of a Series of Mouse Strains with Different Prion Protein Gene Alterations

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