Driscoll DJ - Search Results

1

High plasma neurotensin levels in children with Prader-Willi syndrome.

Butler MG, Nelson TA, Driscoll DJ, Manzardo AM. Butler MG, et al. Among authors: driscoll dj. Am J Med Genet A. 2015 Aug;167A(8):1773-8. doi: 10.1002/ajmg.a.37103. Epub 2015 Apr 5. Am J Med Genet A. 2015. PMID: 25847417 Free PMC article.

2

A DNA methylation imprint, determined by the sex of the parent, distinguishes the Angelman and Prader-Willi syndromes.

Driscoll DJ, Waters MF, Williams CA, Zori RT, Glenn CC, Avidano KM, Nicholls RD. Driscoll DJ, et al. Genomics. 1992 Aug;13(4):917-24. doi: 10.1016/0888-7543(92)90001-9. Genomics. 1992. PMID: 1505981

3

Modification of 15q11-q13 DNA methylation imprints in unique Angelman and Prader-Willi patients.

Glenn CC, Nicholls RD, Robinson WP, Saitoh S, Niikawa N, Schinzel A, Horsthemke B, Driscoll DJ. Glenn CC, et al. Among authors: driscoll dj. Hum Mol Genet. 1993 Sep;2(9):1377-82. doi: 10.1093/hmg/2.9.1377. Hum Mol Genet. 1993. PMID: 8242060 Free article.

4

Difference in methylation patterns within the D15S9 region of chromosome 15q11-13 in first cousins with Angelman syndrome and Prader-Willi syndrome.

Clayton-Smith J, Driscoll DJ, Waters MF, Webb T, Andrews T, Malcolm S, Pembrey ME, Nicholls RD. Clayton-Smith J, et al. Among authors: driscoll dj. Am J Med Genet. 1993 Oct 1;47(5):683-6. doi: 10.1002/ajmg.1320470519. Am J Med Genet. 1993. PMID: 8266996

5

Gene structure, DNA methylation, and imprinted expression of the human SNRPN gene.

Glenn CC, Saitoh S, Jong MT, Filbrandt MM, Surti U, Driscoll DJ, Nicholls RD. Glenn CC, et al. Among authors: driscoll dj. Am J Hum Genet. 1996 Feb;58(2):335-46. Am J Hum Genet. 1996. PMID: 8571960 Free PMC article.

6

DNA methylation patterns in human tissues of uniparental origin using a zinc-finger gene (ZNF127) from the Angelman/Prader-Willi region.

Mowery-Rushton PA, Driscoll DJ, Nicholls RD, Locker J, Surti U. Mowery-Rushton PA, et al. Among authors: driscoll dj. Am J Med Genet. 1996 Jan 11;61(2):140-6. doi: 10.1002/(SICI)1096-8628(19960111)61:2<140::AID-AJMG7>3.0.CO;2-0. Am J Med Genet. 1996. PMID: 8669440

7

Distinct 15q genotypes in Russell-Silver and ring 15 syndromes.

Rogan PK, Seip JR, Driscoll DJ, Papenhausen PR, Johnson VP, Raskin S, Woodward AL, Butler MG. Rogan PK, et al. Among authors: driscoll dj. Am J Med Genet. 1996 Mar 1;62(1):10-5. doi: 10.1002/(SICI)1096-8628(19960301)62:1<10::AID-AJMG3>3.0.CO;2-#. Am J Med Genet. 1996. PMID: 8779316 Free PMC article.

8

Clinical spectrum and molecular diagnosis of Angelman and Prader-Willi syndrome patients with an imprinting mutation.

Saitoh S, Buiting K, Cassidy SB, Conroy JM, Driscoll DJ, Gabriel JM, Gillessen-Kaesbach G, Glenn CC, Greenswag LR, Horsthemke B, Kondo I, Kuwajima K, Niikawa N, Rogan PK, Schwartz S, Seip J, Williams CA, Nicholls RD. Saitoh S, et al. Among authors: driscoll dj. Am J Med Genet. 1997 Jan 20;68(2):195-206. Am J Med Genet. 1997. PMID: 9028458

9

Genomic imprinting: potential function and mechanisms revealed by the Prader-Willi and Angelman syndromes.

Glenn CC, Driscoll DJ, Yang TP, Nicholls RD. Glenn CC, et al. Among authors: driscoll dj. Mol Hum Reprod. 1997 Apr;3(4):321-32. doi: 10.1093/molehr/3.4.321. Mol Hum Reprod. 1997. PMID: 9237260 Review.

10

Imprinting-mutation mechanisms in Prader-Willi syndrome.

Ohta T, Gray TA, Rogan PK, Buiting K, Gabriel JM, Saitoh S, Muralidhar B, Bilienska B, Krajewska-Walasek M, Driscoll DJ, Horsthemke B, Butler MG, Nicholls RD. Ohta T, et al. Among authors: driscoll dj. Am J Hum Genet. 1999 Feb;64(2):397-413. doi: 10.1086/302233. Am J Hum Genet. 1999. PMID: 9973278 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

385 results

Search Page

Filters