Craigen WJ - Search Results

1

An integrated approach for classifying mitochondrial DNA variants: one clinical diagnostic laboratory's experience.

Wang J, Schmitt ES, Landsverk ML, Zhang VW, Li FY, Graham BH, Craigen WJ, Wong LJ. Wang J, et al. Among authors: craigen wj. Genet Med. 2012 Jun;14(6):620-6. doi: 10.1038/gim.2012.4. Epub 2012 Mar 8. Genet Med. 2012. PMID: 22402757 Free 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

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.

4

The physiological properties of a novel family of VDAC-like proteins from Drosophila melanogaster.

Komarov AG, Graham BH, Craigen WJ, Colombini M. Komarov AG, et al. Among authors: craigen wj. Biophys J. 2004 Jan;86(1 Pt 1):152-62. doi: 10.1016/S0006-3495(04)74093-X. Biophys J. 2004. PMID: 14695259 Free PMC article.

5

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.

6

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

7

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

8

Increased MECP2 gene copy number as the result of genomic duplication in neurodevelopmentally delayed males.

del Gaudio D, Fang P, Scaglia F, Ward PA, Craigen WJ, Glaze DG, Neul JL, Patel A, Lee JA, Irons M, Berry SA, Pursley AA, Grebe TA, Freedenberg D, Martin RA, Hsich GE, Khera JR, Friedman NR, Zoghbi HY, Eng CM, Lupski JR, Beaudet AL, Cheung SW, Roa BB. del Gaudio D, et al. Among authors: craigen wj. Genet Med. 2006 Dec;8(12):784-92. doi: 10.1097/01.gim.0000250502.28516.3c. Genet Med. 2006. PMID: 17172942 Free article.

9

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

10

Clinical and molecular features of mitochondrial DNA depletion due to mutations in deoxyguanosine kinase.

Dimmock DP, Zhang Q, Dionisi-Vici C, Carrozzo R, Shieh J, Tang LY, Truong C, Schmitt E, Sifry-Platt M, Lucioli S, Santorelli FM, Ficicioglu CH, Rodriguez M, Wierenga K, Enns GM, Longo N, Lipson MH, Vallance H, Craigen WJ, Scaglia F, Wong LJ. Dimmock DP, et al. Among authors: craigen wj. Hum Mutat. 2008 Feb;29(2):330-1. doi: 10.1002/humu.9519. Hum Mutat. 2008. PMID: 18205204

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