O'Brien WE - Search Results

1

Double-blind therapeutic trial in Angelman syndrome using betaine and folic acid.

Peters SU, Bird LM, Kimonis V, Glaze DG, Shinawi LM, Bichell TJ, Barbieri-Welge R, Nespeca M, Anselm I, Waisbren S, Sanborn E, Sun Q, O'Brien WE, Beaudet AL, Bacino CA. Peters SU, et al. Among authors: o brien we. Am J Med Genet A. 2010 Aug;152A(8):1994-2001. doi: 10.1002/ajmg.a.33509. Am J Med Genet A. 2010. PMID: 20635355 Free PMC article. Clinical Trial.

2

A study of the treatment of Rett syndrome with folate and betaine.

Glaze DG, Percy AK, Motil KJ, Lane JB, Isaacs JS, Schultz RJ, Barrish JO, Neul JL, O'Brien WE, Smith EO. Glaze DG, et al. Among authors: o brien we. J Child Neurol. 2009 May;24(5):551-6. doi: 10.1177/0883073808327827. Epub 2009 Feb 18. J Child Neurol. 2009. PMID: 19225139 Free PMC article. Clinical Trial.

3

Diagnosis of creatine metabolism disorders by determining creatine and guanidinoacetate in plasma and urine.

Sun Q, O'Brien WE. Sun Q, et al. Among authors: o brien we. Methods Mol Biol. 2010;603:175-85. doi: 10.1007/978-1-60761-459-3_17. Methods Mol Biol. 2010. PMID: 20077070

4

Extensive DNA polymorphism at the factor XIIIa (F13A) locus and linkage to HLA.

Zoghbi HY, Daiger SP, McCall A, O'Brien WE, Beaudet AL. Zoghbi HY, et al. Am J Hum Genet. 1988 Jun;42(6):877-83. Am J Hum Genet. 1988. PMID: 2897163 Free PMC article.

5

Generation of a mouse model for citrullinemia by targeted disruption of the argininosuccinate synthetase gene.

Patejunas G, Bradley A, Beaudet AL, O'Brien WE. Patejunas G, et al. Somat Cell Mol Genet. 1994 Jan;20(1):55-60. doi: 10.1007/BF02257486. Somat Cell Mol Genet. 1994. PMID: 8197477

6

Nucleotide sequence of the cDNA from the mouse leukocyte adhesion protein CD18.

Wilson RW, O'Brien WE, Beaudet AL. Wilson RW, et al. Nucleic Acids Res. 1989 Jul 11;17(13):5397. doi: 10.1093/nar/17.13.5397. Nucleic Acids Res. 1989. PMID: 2569711 Free PMC article. No abstract available.

7

Prenatal diagnosis of cystic fibrosis by using linked DNA markers in 138 pregnancies at 1-in-4 risk.

Feldman GL, Lewiston N, Fernbach SD, O'Brien WE, Williamson R, Wainwright BJ, Beaudet AL. Feldman GL, et al. Am J Med Genet. 1989 Jun;33(2):238-41. doi: 10.1002/ajmg.1320330219. Am J Med Genet. 1989. PMID: 2569827

8

Nucleotide sequence of the cDNA for murine intercellular adhesion molecule-1 (ICAM-1).

Ballantyne CM, O'Brien WE, Beaudet AL. Ballantyne CM, et al. Nucleic Acids Res. 1989 Jul 25;17(14):5853. doi: 10.1093/nar/17.14.5853. Nucleic Acids Res. 1989. PMID: 2762164 Free PMC article. No abstract available.

9

Uniparental disomy as a mechanism for human genetic disease.

Spence JE, Perciaccante RG, Greig GM, Willard HF, Ledbetter DH, Hejtmancik JF, Pollack MS, O'Brien WE, Beaudet AL. Spence JE, et al. Am J Hum Genet. 1988 Feb;42(2):217-26. Am J Hum Genet. 1988. PMID: 2893543 Free PMC article.

10

Linkage disequilibrium, cystic fibrosis, and genetic counseling.

Beaudet AL, Feldman GL, Fernbach SD, Buffone GJ, O'Brien WE. Beaudet AL, et al. Am J Hum Genet. 1989 Mar;44(3):319-26. Am J Hum Genet. 1989. PMID: 2916578 Free PMC article.

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