Sutcliffe JS - Search Results

1

Characterization of a highly polymorphic dinucleotide repeat 150 KB proximal to the fragile X site.

Riggins GJ, Sherman SL, Oostra BA, Sutcliffe JS, Feitell D, Nelson DL, van Oost BA, Smits AP, Ramos FJ, Pfendner E, et al. Riggins GJ, et al. Among authors: sutcliffe js. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):237-43. doi: 10.1002/ajmg.1320430138. Am J Med Genet. 1992. PMID: 1605197

2

DNA methylation represses FMR-1 transcription in fragile X syndrome.

Sutcliffe JS, Nelson DL, Zhang F, Pieretti M, Caskey CT, Saxe D, Warren ST. Sutcliffe JS, et al. Hum Mol Genet. 1992 Sep;1(6):397-400. doi: 10.1093/hmg/1.6.397. Hum Mol Genet. 1992. PMID: 1301913

3

PCR amplification and analysis of yeast artificial chromosomes.

Sutcliffe JS, Zhang F, Caskey CT, Nelson DL, Warren ST. Sutcliffe JS, et al. Genomics. 1992 Aug;13(4):1303-6. doi: 10.1016/0888-7543(92)90051-s. Genomics. 1992. PMID: 1380485

4

Strategy for molecular cloning of the fragile X site DNA.

Warren ST, Zhang FP, Sutcliffe JS, Peters JF. Warren ST, et al. Among authors: sutcliffe js. Am J Med Genet. 1988 May-Jun;30(1-2):613-23. doi: 10.1002/ajmg.1320300162. Am J Med Genet. 1988. PMID: 3177473

5

Human and murine FMR-1: alternative splicing and translational initiation downstream of the CGG-repeat.

Ashley CT, Sutcliffe JS, Kunst CB, Leiner HA, Eichler EE, Nelson DL, Warren ST. Ashley CT, et al. Among authors: sutcliffe js. Nat Genet. 1993 Jul;4(3):244-51. doi: 10.1038/ng0793-244. Nat Genet. 1993. PMID: 8358432

6

Tissue specific expression of FMR-1 provides evidence for a functional role in fragile X syndrome.

Hinds HL, Ashley CT, Sutcliffe JS, Nelson DL, Warren ST, Housman DE, Schalling M. Hinds HL, et al. Among authors: sutcliffe js. Nat Genet. 1993 Jan;3(1):36-43. doi: 10.1038/ng0193-36. Nat Genet. 1993. PMID: 8490651

7

Variation of the CGG repeat at the fragile X site results in genetic instability: resolution of the Sherman paradox.

Fu YH, Kuhl DP, Pizzuti A, Pieretti M, Sutcliffe JS, Richards S, Verkerk AJ, Holden JJ, Fenwick RG Jr, Warren ST, et al. Fu YH, et al. Among authors: sutcliffe js. Cell. 1991 Dec 20;67(6):1047-58. doi: 10.1016/0092-8674(91)90283-5. Cell. 1991. PMID: 1760838

8

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome.

Verkerk AJ, Pieretti M, Sutcliffe JS, Fu YH, Kuhl DP, Pizzuti A, Reiner O, Richards S, Victoria MF, Zhang FP, et al. Verkerk AJ, et al. Among authors: sutcliffe js. Cell. 1991 May 31;65(5):905-14. doi: 10.1016/0092-8674(91)90397-h. Cell. 1991. PMID: 1710175

9

Imprinted expression of the murine Angelman syndrome gene, Ube3a, in hippocampal and Purkinje neurons.

Albrecht U, Sutcliffe JS, Cattanach BM, Beechey CV, Armstrong D, Eichele G, Beaudet AL. Albrecht U, et al. Among authors: sutcliffe js. Nat Genet. 1997 Sep;17(1):75-8. doi: 10.1038/ng0997-75. Nat Genet. 1997. PMID: 9288101

10

Validation studies of SNRPN methylation as a diagnostic test for Prader-Willi syndrome.

Kubota T, Sutcliffe JS, Aradhya S, Gillessen-Kaesbach G, Christian SL, Horsthemke B, Beaudet AL, Ledbetter DH. Kubota T, et al. Among authors: sutcliffe js. Am J Med Genet. 1996 Dec 2;66(1):77-80. doi: 10.1002/(SICI)1096-8628(19961202)66:1<77::AID-AJMG18>3.0.CO;2-N. Am J Med Genet. 1996. PMID: 8957518

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