Lennon G - Search Results

1

Mutations in the Cacnl1a4 calcium channel gene are associated with seizures, cerebellar degeneration, and ataxia in tottering and leaner mutant mice.

Doyle J, Ren X, Lennon G, Stubbs L. Doyle J, et al. Among authors: lennon g. Mamm Genome. 1997 Feb;8(2):113-20. doi: 10.1007/s003359900369. Mamm Genome. 1997. PMID: 9060410

2

Report an abstracts of the third international workshop on human chromosome 19 mapping 1996.

Mohrenweiser H, Olsen A, Archibald A, Beattie C, Burmeister M, Lamerdin J, Lennon G, Stewart E, Stubbs L, Weber JL, Johnson K. Mohrenweiser H, et al. Among authors: lennon g. Cytogenet Cell Genet. 1996;74(3):161-86. doi: 10.1159/000134408. Cytogenet Cell Genet. 1996. PMID: 8941368 No abstract available.

3

Characterization of the human neurocan gene, CSPG3.

Prange CK, Pennacchio LA, Lieuallen K, Fan W, Lennon GG. Prange CK, et al. Among authors: lennon gg. Gene. 1998 Oct 23;221(2):199-205. doi: 10.1016/s0378-1119(98)00455-7. Gene. 1998. PMID: 9795216

4

Six transcripts map within 200 kilobases of the myotonic dystrophy expanded repeat.

Alwazzan M, Hamshere MG, Lennon GG, Brook JD. Alwazzan M, et al. Among authors: lennon gg. Mamm Genome. 1998 Jun;9(6):485-7. doi: 10.1007/s003359900804. Mamm Genome. 1998. PMID: 9585442 No abstract available.

5

Hybridization fingerprinting of high-density cDNA-library arrays with cDNA pools derived from whole tissues.

Gress TM, Hoheisel JD, Lennon GG, Zehetner G, Lehrach H. Gress TM, et al. Among authors: lennon gg. Mamm Genome. 1992;3(11):609-19. doi: 10.1007/BF00352477. Mamm Genome. 1992. PMID: 1450511

6

Large-scale concatenation cDNA sequencing.

Yu W, Andersson B, Worley KC, Muzny DM, Ding Y, Liu W, Ricafrente JY, Wentland MA, Lennon G, Gibbs RA. Yu W, et al. Among authors: lennon g. Genome Res. 1997 Apr;7(4):353-8. doi: 10.1101/gr.7.4.353. Genome Res. 1997. PMID: 9110174 Free PMC article.

7

Human endopeptidase 24.15 (THOP1) is localized on chromosome 19p13.3 and is excluded from the linkage region for late-onset Alzheimer disease.

Torres MP, Prange C, Lennon G. Torres MP, et al. Among authors: lennon g. Genomics. 1998 Oct 15;53(2):239-40. doi: 10.1006/geno.1998.5487. Genomics. 1998. PMID: 9790774

8

Normalization and subtraction: two approaches to facilitate gene discovery.

Bonaldo MF, Lennon G, Soares MB. Bonaldo MF, et al. Among authors: lennon g. Genome Res. 1996 Sep;6(9):791-806. doi: 10.1101/gr.6.9.791. Genome Res. 1996. PMID: 8889548 Free article.

9

An integrated metric physical map of human chromosome 19.

Ashworth LK, Batzer MA, Brandriff B, Branscomb E, de Jong P, Garcia E, Garnes JA, Gordon LA, Lamerdin JE, Lennon G, Mohrenweiser H, Olsen AS, Slezak T, Carrano AV. Ashworth LK, et al. Among authors: lennon g. Nat Genet. 1995 Dec;11(4):422-7. doi: 10.1038/ng1295-422. Nat Genet. 1995. PMID: 7493023

10

An STS from a cDNA located in the myotonic dystrophy region (DM) on human chromosome 19q13.3.

Lennon GG, Lamerdin J, Lieuallen K, Amemiya C, Aslanidis C, de Jong PJ, Carrano AV. Lennon GG, et al. Hum Mol Genet. 1992 Jun;1(3):217. doi: 10.1093/hmg/1.3.217. Hum Mol Genet. 1992. PMID: 1303190 No abstract available.

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