Smith KD - Search Results

1

A mouse model for X-linked adrenoleukodystrophy.

Lu JF, Lawler AM, Watkins PA, Powers JM, Moser AB, Moser HW, Smith KD. Lu JF, et al. Among authors: smith kd. Proc Natl Acad Sci U S A. 1997 Aug 19;94(17):9366-71. doi: 10.1073/pnas.94.17.9366. Proc Natl Acad Sci U S A. 1997. PMID: 9256488 Free PMC article.

2

Mouse very long-chain acyl-CoA synthetase in X-linked adrenoleukodystrophy.

Heinzer AK, Kemp S, Lu JF, Watkins PA, Smith KD. Heinzer AK, et al. Among authors: smith kd. J Biol Chem. 2002 Aug 9;277(32):28765-73. doi: 10.1074/jbc.M203053200. Epub 2002 Jun 4. J Biol Chem. 2002. PMID: 12048192 Free article.

3

A very long-chain acyl-CoA synthetase-deficient mouse and its relevance to X-linked adrenoleukodystrophy.

Heinzer AK, Watkins PA, Lu JF, Kemp S, Moser AB, Li YY, Mihalik S, Powers JM, Smith KD. Heinzer AK, et al. Among authors: smith kd. Hum Mol Genet. 2003 May 15;12(10):1145-54. doi: 10.1093/hmg/ddg126. Hum Mol Genet. 2003. PMID: 12719378

4

Mouse models and genetic modifiers in X-linked adrenoleukodystrophy.

Heinzer AK, McGuinness MC, Lu JF, Stine OC, Wei H, Van der Vlies M, Dong GX, Powers J, Watkins PA, Smith KD. Heinzer AK, et al. Among authors: smith kd. Adv Exp Med Biol. 2003;544:75-93. doi: 10.1007/978-1-4419-9072-3_12. Adv Exp Med Biol. 2003. PMID: 14713218 Review. No abstract available.

5

X-linked adrenoleukodystrophy: role of very long-chain acyl-CoA synthetases.

Jia Z, Pei Z, Li Y, Wei L, Smith KD, Watkins PA. Jia Z, et al. Among authors: smith kd. Mol Genet Metab. 2004 Sep-Oct;83(1-2):117-27. doi: 10.1016/j.ymgme.2004.06.015. Mol Genet Metab. 2004. PMID: 15464426

6

Gene redundancy and pharmacological gene therapy: implications for X-linked adrenoleukodystrophy.

Kemp S, Wei HM, Lu JF, Braiterman LT, McGuinness MC, Moser AB, Watkins PA, Smith KD. Kemp S, et al. Among authors: smith kd. Nat Med. 1998 Nov;4(11):1261-8. doi: 10.1038/3242. Nat Med. 1998. PMID: 9809549

7

X-linked adrenoleukodystrophy: genes, mutations, and phenotypes.

Smith KD, Kemp S, Braiterman LT, Lu JF, Wei HM, Geraghty M, Stetten G, Bergin JS, Pevsner J, Watkins PA. Smith KD, et al. Neurochem Res. 1999 Apr;24(4):521-35. doi: 10.1023/a:1022535930009. Neurochem Res. 1999. PMID: 10227685 Review.

8

Determination of 30 X-linked adrenoleukodystrophy mutations, including 15 not previously described.

Lachtermacher MB, Seuánez HN, Moser AB, Moser HW, Smith KD. Lachtermacher MB, et al. Among authors: smith kd. Hum Mutat. 2000;15(4):348-53. doi: 10.1002/(SICI)1098-1004(200004)15:4<348::AID-HUMU7>3.0.CO;2-N. Hum Mutat. 2000. PMID: 10737980

9

Adrenoleukodystrophy: incidence, new mutation rate, and results of extended family screening.

Bezman L, Moser AB, Raymond GV, Rinaldo P, Watkins PA, Smith KD, Kass NE, Moser HW. Bezman L, et al. Among authors: smith kd. Ann Neurol. 2001 Apr;49(4):512-7. Ann Neurol. 2001. PMID: 11310629

10

Disruption of a yeast very-long-chain acyl-CoA synthetase gene simulates the cellular phenotype of X-linked adrenoleukodystrophy.

Watkins PA, Lu JF, Braiterman LT, Steinberg SJ, Smith KD. Watkins PA, et al. Among authors: smith kd. Cell Biochem Biophys. 2000;32 Spring:333-7. doi: 10.1385/cbb:32:1-3:333. Cell Biochem Biophys. 2000. PMID: 11330068

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