Kass SU - Search Results

1

Nucleosome assembly on methylated CGG triplet repeats in the fragile X mental retardation gene 1 promoter.

Godde JS, Kass SU, Hirst MC, Wolffe AP. Godde JS, et al. Among authors: kass su. J Biol Chem. 1996 Oct 4;271(40):24325-8. doi: 10.1074/jbc.271.40.24325. J Biol Chem. 1996. PMID: 8798682 Free article.

2

How does DNA methylation repress transcription?

Kass SU, Pruss D, Wolffe AP. Kass SU, et al. Trends Genet. 1997 Nov;13(11):444-9. doi: 10.1016/s0168-9525(97)01268-7. Trends Genet. 1997. PMID: 9385841 Review.

3

DNA methylation directs a time-dependent repression of transcription initiation.

Kass SU, Landsberger N, Wolffe AP. Kass SU, et al. Curr Biol. 1997 Mar 1;7(3):157-65. doi: 10.1016/s0960-9822(97)70086-1. Curr Biol. 1997. PMID: 9395433 Free article.

4

DNA methylation, nucleosomes and the inheritance of chromatin structure and function.

Kass SU, Wolffe AP. Kass SU, et al. Novartis Found Symp. 1998;214:22-35; discussion 36-50. doi: 10.1002/9780470515501.ch3. Novartis Found Symp. 1998. PMID: 9601010 Review.

5

Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription.

Jones PL, Veenstra GJ, Wade PA, Vermaak D, Kass SU, Landsberger N, Strouboulis J, Wolffe AP. Jones PL, et al. Among authors: kass su. Nat Genet. 1998 Jun;19(2):187-91. doi: 10.1038/561. Nat Genet. 1998. PMID: 9620779

6

A gene defect that causes conduction system disease and dilated cardiomyopathy maps to chromosome 1p1-1q1.

Kass S, MacRae C, Graber HL, Sparks EA, McNamara D, Boudoulas H, Basson CT, Baker PB 3rd, Cody RJ, Fishman MC, et al. Kass S, et al. Nat Genet. 1994 Aug;7(4):546-51. doi: 10.1038/ng0894-546. Nat Genet. 1994. PMID: 7951328

7

Familial Hypertrophic cardiomyopathy with Wolff-Parkinson-White syndrome maps to a locus on chromosome 7q3.

MacRae CA, Ghaisas N, Kass S, Donnelly S, Basson CT, Watkins HC, Anan R, Thierfelder LH, McGarry K, Rowland E, et al. MacRae CA, et al. J Clin Invest. 1995 Sep;96(3):1216-20. doi: 10.1172/JCI118154. J Clin Invest. 1995. PMID: 7657794 Free PMC article.

8

A molecular basis for familial hypertrophic cardiomyopathy: an alpha/beta cardiac myosin heavy chain hybrid gene.

Tanigawa G, Jarcho JA, Kass S, Solomon SD, Vosberg HP, Seidman JG, Seidman CE. Tanigawa G, et al. Cell. 1990 Sep 7;62(5):991-8. doi: 10.1016/0092-8674(90)90273-h. Cell. 1990. PMID: 2144212

9

A molecular basis for familial hypertrophic cardiomyopathy: a beta cardiac myosin heavy chain gene missense mutation.

Geisterfer-Lowrance AA, Kass S, Tanigawa G, Vosberg HP, McKenna W, Seidman CE, Seidman JG. Geisterfer-Lowrance AA, et al. Cell. 1990 Sep 7;62(5):999-1006. doi: 10.1016/0092-8674(90)90274-i. Cell. 1990. PMID: 1975517

10

Gene expression profiles highlight adaptive brain mechanisms in corticotropin releasing factor overexpressing mice.

Peeters PJ, Fierens FL, van den Wyngaert I, Goehlmann HW, Swagemakers SM, Kass SU, Langlois X, Pullan S, Stenzel-Poore MP, Steckler T. Peeters PJ, et al. Among authors: kass su. Brain Res Mol Brain Res. 2004 Oct 22;129(1-2):135-50. doi: 10.1016/j.molbrainres.2004.06.038. Brain Res Mol Brain Res. 2004. PMID: 15469890

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