Craigen WJ - Search Results

1

Recurrent ACADVL molecular findings in individuals with a positive newborn screen for very long chain acyl-coA dehydrogenase (VLCAD) deficiency in the United States.

Miller MJ, Burrage LC, Gibson JB, Strenk ME, Lose EJ, Bick DP, Elsea SH, Sutton VR, Sun Q, Graham BH, Craigen WJ, Zhang VW, Wong LJ. Miller MJ, et al. Among authors: craigen wj. Mol Genet Metab. 2015 Nov;116(3):139-45. doi: 10.1016/j.ymgme.2015.08.011. Epub 2015 Sep 2. Mol Genet Metab. 2015. PMID: 26385305 Free PMC article.

2

Postpartum coma and death due to carbamoyl-phosphate synthetase I deficiency.

Wong LJ, Craigen WJ, O'Brien WE. Wong LJ, et al. Among authors: craigen wj. Ann Intern Med. 1994 Feb 1;120(3):216-7. doi: 10.7326/0003-4819-120-3-199402010-00007. Ann Intern Med. 1994. PMID: 8273985 No abstract available.

3

Regional localization of the mouse argininosuccinate lyase gene to chromosome 5.

Sutton VR, Pan Y, Craigen WJ. Sutton VR, et al. Among authors: craigen wj. Mamm Genome. 1997;8(11):871. doi: 10.1007/s003359900600. Mamm Genome. 1997. PMID: 9337408 No abstract available.

4

The tissue-specific, alternatively spliced single ATG exon of the type 3 voltage-dependent anion channel gene does not create a truncated protein isoform in vivo.

Decker WK, Craigen WJ. Decker WK, et al. Among authors: craigen wj. Mol Genet Metab. 2000 May;70(1):69-74. doi: 10.1006/mgme.2000.2987. Mol Genet Metab. 2000. PMID: 10833333

5

Noninvasive, in vivo approaches to evaluating behavior and exercise physiology in mouse models of mitochondrial disease.

Graham BH, David Sweatt J, Craigen WJ. Graham BH, et al. Among authors: craigen wj. Methods. 2002 Apr;26(4):364-70. doi: 10.1016/S1046-2023(02)00043-9. Methods. 2002. PMID: 12054928 Review.

6

A mouse model of argininosuccinic aciduria: biochemical characterization.

Reid Sutton V, Pan Y, Davis EC, Craigen WJ. Reid Sutton V, et al. Among authors: craigen wj. Mol Genet Metab. 2003 Jan;78(1):11-6. doi: 10.1016/s1096-7192(02)00206-8. Mol Genet Metab. 2003. PMID: 12559843

7

Genetic approaches to analyzing mitochondrial outer membrane permeability.

Graham BH, Craigen WJ. Graham BH, et al. Among authors: craigen wj. Curr Top Dev Biol. 2004;59:87-118. doi: 10.1016/S0070-2153(04)59004-X. Curr Top Dev Biol. 2004. PMID: 14975248 Review. No abstract available.

8

Clinical spectrum, morbidity, and mortality in 113 pediatric patients with mitochondrial disease.

Scaglia F, Towbin JA, Craigen WJ, Belmont JW, Smith EO, Neish SR, Ware SM, Hunter JV, Fernbach SD, Vladutiu GD, Wong LJ, Vogel H. Scaglia F, et al. Among authors: craigen wj. Pediatrics. 2004 Oct;114(4):925-31. doi: 10.1542/peds.2004-0718. Pediatrics. 2004. PMID: 15466086

9

Mitochondrial voltage-dependent anion channel gene family in Drosophila melanogaster: complex patterns of evolution, genomic organization, and developmental expression.

Graham BH, Craigen WJ. Graham BH, et al. Among authors: craigen wj. Mol Genet Metab. 2005 Aug;85(4):308-17. doi: 10.1016/j.ymgme.2005.03.009. Mol Genet Metab. 2005. PMID: 15886041

10

Mutations in the MPV17 gene are responsible for rapidly progressive liver failure in infancy.

Wong LJ, Brunetti-Pierri N, Zhang Q, Yazigi N, Bove KE, Dahms BB, Puchowicz MA, Gonzalez-Gomez I, Schmitt ES, Truong CK, Hoppel CL, Chou PC, Wang J, Baldwin EE, Adams D, Leslie N, Boles RG, Kerr DS, Craigen WJ. Wong LJ, et al. Among authors: craigen wj. Hepatology. 2007 Oct;46(4):1218-27. doi: 10.1002/hep.21799. Hepatology. 2007. PMID: 17694548

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