Lewis C - Search Results

1

Molecular characterization of CTNS deletions in nephropathic cystinosis: development of a PCR-based detection assay.

Forestier L, Jean G, Attard M, Cherqui S, Lewis C, van't Hoff W, Broyer M, Town M, Antignac C. Forestier L, et al. Among authors: lewis c. Am J Hum Genet. 1999 Aug;65(2):353-9. doi: 10.1086/302509. Am J Hum Genet. 1999. PMID: 10417278 Free PMC article.

2

DNA variation in a 5-Mb region of the X chromosome and estimates of sex-specific/type-specific mutation rates.

Anagnostopoulos T, Green PM, Rowley G, Lewis CM, Giannelli F. Anagnostopoulos T, et al. Among authors: lewis cm. Am J Hum Genet. 1999 Feb;64(2):508-17. doi: 10.1086/302250. Am J Hum Genet. 1999. PMID: 9973287 Free PMC article.

3

Mutation rates in humans. I. Overall and sex-specific rates obtained from a population study of hemophilia B.

Green PM, Saad S, Lewis CM, Giannelli F. Green PM, et al. Among authors: lewis cm. Am J Hum Genet. 1999 Dec;65(6):1572-9. doi: 10.1086/302651. Am J Hum Genet. 1999. PMID: 10577910 Free PMC article.

4

Stability and haplotype analysis of the FRAXE region.

Murray A, Ennis S, Youings SA, Sharrock AJ, Lewis C, Pound MC, Macpherson JN, Dennis NR, Morton NE, Jacobs PA. Murray A, et al. Among authors: lewis c. Eur J Hum Genet. 2000 Aug;8(8):583-9. doi: 10.1038/sj.ejhg.5200504. Eur J Hum Genet. 2000. PMID: 10951520

5

The number of loci needed for ELOD calculations.

Lewis CM, Cannings C. Lewis CM, et al. Ann Hum Genet. 1992 Jan;56(1):59-69. doi: 10.1111/j.1469-1809.1992.tb01129.x. Ann Hum Genet. 1992. PMID: 1586133

6

Linkage studies in dominant optic atrophy, Kjer type: possible evidence for heterogeneity.

Seller MJ, Behnam JT, Lewis CM, Johnston RL, Burdon MA, Spalton DJ. Seller MJ, et al. Among authors: lewis cm. J Med Genet. 1997 Dec;34(12):967-72. doi: 10.1136/jmg.34.12.967. J Med Genet. 1997. PMID: 9429135 Free PMC article.

7

FRAXA and FRAXE: the results of a five year survey.

Youings SA, Murray A, Dennis N, Ennis S, Lewis C, McKechnie N, Pound M, Sharrock A, Jacobs P. Youings SA, et al. Among authors: lewis c. J Med Genet. 2000 Jun;37(6):415-21. doi: 10.1136/jmg.37.6.415. J Med Genet. 2000. PMID: 10851251 Free PMC article.

8

The cystic fibrosis delta F508 gene mutation and cancer.

Padua RA, Warren N, Grimshaw D, Smith M, Lewis C, Whittaker J, Laidler P, Wright P, Douglas-Jones A, Fenaux P, Sharma A, Horgan K, West R. Padua RA, et al. Among authors: lewis c. Hum Mutat. 1997;10(1):45-8. doi: 10.1002/(SICI)1098-1004(1997)10:1<45::AID-HUMU6>3.0.CO;2-L. Hum Mutat. 1997. PMID: 9222759

9

Repurposing the Antihypertensive Agent Hydralazine As an Inhibitor of the Base Excision Repair Enzyme APE1.

Islam T, Nunna V, Liyanarachchi DP, Melton D, Lewis CD, Gates KS. Islam T, et al. Among authors: lewis cd. Chem Res Toxicol. 2024 Dec 24. doi: 10.1021/acs.chemrestox.4c00445. Online ahead of print. Chem Res Toxicol. 2024. PMID: 39718352

10

Quantitative profiling of human translation initiation reveals elements that potently regulate endogenous and therapeutically modified mRNAs.

Lewis CJT, Xie LH, Bhandarkar SM, Jin D, Abdallah K, Draycott AS, Chen Y, Thoreen CC, Gilbert WV. Lewis CJT, et al. Mol Cell. 2024 Dec 12:S1097-2765(24)00955-9. doi: 10.1016/j.molcel.2024.11.030. Online ahead of print. Mol Cell. 2024. PMID: 39706187

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