Lovett M - Search Results

1

The EXT2 multiple exostoses gene defines a family of putative tumour suppressor genes.

Stickens D, Clines G, Burbee D, Ramos P, Thomas S, Hogue D, Hecht JT, Lovett M, Evans GA. Stickens D, et al. Among authors: lovett m. Nat Genet. 1996 Sep;14(1):25-32. doi: 10.1038/ng0996-25. Nat Genet. 1996. PMID: 8782816

2

Diminished levels of the putative tumor suppressor proteins EXT1 and EXT2 in exostosis chondrocytes.

Bernard MA, Hall CE, Hogue DA, Cole WG, Scott A, Snuggs MB, Clines GA, Lüdecke HJ, Lovett M, Van Winkle WB, Hecht JT. Bernard MA, et al. Among authors: lovett m. Cell Motil Cytoskeleton. 2001 Feb;48(2):149-62. doi: 10.1002/1097-0169(200102)48:2<149::AID-CM1005>3.0.CO;2-3. Cell Motil Cytoskeleton. 2001. PMID: 11169766

3

Identification and localization of the gene for EXTL, a third member of the multiple exostoses gene family.

Wise CA, Clines GA, Massa H, Trask BJ, Lovett M. Wise CA, et al. Among authors: lovett m. Genome Res. 1997 Jan;7(1):10-6. doi: 10.1101/gr.7.1.10. Genome Res. 1997. PMID: 9037597 Free article.

4

The structure of the human multiple exostoses 2 gene and characterization of homologs in mouse and Caenorhabditis elegans.

Clines GA, Ashley JA, Shah S, Lovett M. Clines GA, et al. Among authors: lovett m. Genome Res. 1997 Apr;7(4):359-67. doi: 10.1101/gr.7.4.359. Genome Res. 1997. PMID: 9110175 Free PMC article.

5

Human chromosome-specific cDNA libraries: new tools for gene identification and genome annotation.

Del Mastro RG, Wang L, Simmons AD, Gallardo TD, Clines GA, Ashley JA, Hilliard CJ, Wasmuth JJ, McPherson JD, Lovett M. Del Mastro RG, et al. Among authors: lovett m. Genome Res. 1995 Sep;5(2):185-94. doi: 10.1101/gr.5.2.185. Genome Res. 1995. PMID: 9132272 Free article.

6

A direct interaction between EXT proteins and glycosyltransferases is defective in hereditary multiple exostoses.

Simmons AD, Musy MM, Lopes CS, Hwang LY, Yang YP, Lovett M. Simmons AD, et al. Among authors: lovett m. Hum Mol Genet. 1999 Nov;8(12):2155-64. doi: 10.1093/hmg/8.12.2155. Hum Mol Genet. 1999. PMID: 10545594

7

Identification of the Finnish founder mutation for diastrophic dysplasia (DTD).

Hästbacka J, Kerrebrock A, Mokkala K, Clines G, Lovett M, Kaitila I, de la Chapelle A, Lander ES. Hästbacka J, et al. Among authors: lovett m. Eur J Hum Genet. 1999 Sep;7(6):664-70. doi: 10.1038/sj.ejhg.5200361. Eur J Hum Genet. 1999. PMID: 10482955

8

Five novel genes from the cri-du-chat critical region isolated by direct selection.

Simmons AD, Goodart SA, Gallardo TD, Overhauser J, Lovett M. Simmons AD, et al. Among authors: lovett m. Hum Mol Genet. 1995 Feb;4(2):295-302. doi: 10.1093/hmg/4.2.295. Hum Mol Genet. 1995. PMID: 7757083

9

A single ataxia telangiectasia gene with a product similar to PI-3 kinase.

Savitsky K, Bar-Shira A, Gilad S, Rotman G, Ziv Y, Vanagaite L, Tagle DA, Smith S, Uziel T, Sfez S, Ashkenazi M, Pecker I, Frydman M, Harnik R, Patanjali SR, Simmons A, Clines GA, Sartiel A, Gatti RA, Chessa L, Sanal O, Lavin MF, Jaspers NG, Taylor AM, Arlett CF, Miki T, Weissman SM, Lovett M, Collins FS, Shiloh Y. Savitsky K, et al. Among authors: lovett m. Science. 1995 Jun 23;268(5218):1749-53. doi: 10.1126/science.7792600. Science. 1995. PMID: 7792600

10

Fishing for complements: finding genes by direct selection.

Lovett M. Lovett M. Trends Genet. 1994 Oct;10(10):352-7. doi: 10.1016/0168-9525(94)90131-7. Trends Genet. 1994. PMID: 7985239 Review.

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