Swanson DA - Search Results

1

PHR1 encodes an abundant, pleckstrin homology domain-containing integral membrane protein in the photoreceptor outer segments.

Xu S, Ladak R, Swanson DA, Soltyk A, Sun H, Ploder L, Vidgen D, Duncan AM, Garami E, Valle D, McInnes RR. Xu S, et al. Among authors: swanson da. J Biol Chem. 1999 Dec 10;274(50):35676-85. doi: 10.1074/jbc.274.50.35676. J Biol Chem. 1999. PMID: 10585447 Free article.

2

A differential hybridization scheme to identify photoreceptor-specific genes.

Swanson DA, Freund CL, Steel JM, Xu S, Ploder L, McInnes RR, Valle D. Swanson DA, et al. Genome Res. 1997 May;7(5):513-21. doi: 10.1101/gr.7.5.513. Genome Res. 1997. PMID: 9149946 Free article.

3

Identification and characterization of the human ortholog of rat STXBP1, a protein implicated in vesicle trafficking and neurotransmitter release.

Swanson DA, Steel JM, Valle D. Swanson DA, et al. Genomics. 1998 Mar 15;48(3):373-6. doi: 10.1006/geno.1997.5202. Genomics. 1998. PMID: 9545644 Free article.

4

Mammalian orthologs of C. elegans unc-119 highly expressed in photoreceptors.

Swanson DA, Chang JT, Campochiaro PA, Zack DJ, Valle D. Swanson DA, et al. Invest Ophthalmol Vis Sci. 1998 Oct;39(11):2085-94. Invest Ophthalmol Vis Sci. 1998. PMID: 9761287

5

A ubiquitin C-terminal hydrolase gene on the proximal short arm of the X chromosome: implications for X-linked retinal disorders.

Swanson DA, Freund CL, Ploder L, McInnes RR, Valle D. Swanson DA, et al. Hum Mol Genet. 1996 Apr;5(4):533-8. doi: 10.1093/hmg/5.4.533. Hum Mol Genet. 1996. PMID: 8845848

6

Expression and processing of human ornithine-delta-aminotransferase in Saccharomyces cerevisiae.

Dougherty KM, Swanson DA, Brody LC, Valle D. Dougherty KM, et al. Among authors: swanson da. Hum Mol Genet. 1993 Nov;2(11):1835-40. doi: 10.1093/hmg/2.11.1835. Hum Mol Genet. 1993. PMID: 8281144

7

Gene order is conserved within the human chromosome 21 linkage group on mouse chromosome 10.

Irving NG, Cabin DE, Swanson DA, Reeves RH. Irving NG, et al. Among authors: swanson da. Genomics. 1994 May 1;21(1):144-9. doi: 10.1006/geno.1994.1236. Genomics. 1994. PMID: 7916323 Free article.

8

A polymorphism, R653Q, in the trifunctional enzyme methylenetetrahydrofolate dehydrogenase/methenyltetrahydrofolate cyclohydrolase/formyltetrahydrofolate synthetase is a maternal genetic risk factor for neural tube defects: report of the Birth Defects Research Group.

Brody LC, Conley M, Cox C, Kirke PN, McKeever MP, Mills JL, Molloy AM, O'Leary VB, Parle-McDermott A, Scott JM, Swanson DA. Brody LC, et al. Among authors: swanson da. Am J Hum Genet. 2002 Nov;71(5):1207-15. doi: 10.1086/344213. Epub 2002 Oct 16. Am J Hum Genet. 2002. PMID: 12384833 Free PMC article.

9

Methionine synthase: high-resolution mapping of the human gene and evaluation as a candidate locus for neural tube defects.

Brody LC, Baker PJ, Chines PS, Musick A, Molloy AM, Swanson DA, Kirke PN, Ghosh S, Scott JM, Mills JL. Brody LC, et al. Among authors: swanson da. Mol Genet Metab. 1999 Aug;67(4):324-33. doi: 10.1006/mgme.1999.2881. Mol Genet Metab. 1999. PMID: 10444343

10

Targeted disruption of the methionine synthase gene in mice.

Swanson DA, Liu ML, Baker PJ, Garrett L, Stitzel M, Wu J, Harris M, Banerjee R, Shane B, Brody LC. Swanson DA, et al. Mol Cell Biol. 2001 Feb;21(4):1058-65. doi: 10.1128/MCB.21.4.1058-1065.2001. Mol Cell Biol. 2001. PMID: 11158293 Free PMC article.

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