Jackson CE - Search Results

1

Genetic heterogeneity in hereditary haemorrhagic telangiectasia: possible correlation with clinical phenotype.

McAllister KA, Lennon F, Bowles-Biesecker B, McKinnon WC, Helmbold EA, Markel DS, Jackson CE, Guttmacher AE, Pericak-Vance MA, Marchuk DA. McAllister KA, et al. Among authors: jackson ce. J Med Genet. 1994 Dec;31(12):927-32. doi: 10.1136/jmg.31.12.927. J Med Genet. 1994. PMID: 7891374 Free PMC article.

2

The activin receptor-like kinase 1 gene: genomic structure and mutations in hereditary hemorrhagic telangiectasia type 2.

Berg JN, Gallione CJ, Stenzel TT, Johnson DW, Allen WP, Schwartz CE, Jackson CE, Porteous ME, Marchuk DA. Berg JN, et al. Among authors: jackson ce. Am J Hum Genet. 1997 Jul;61(1):60-7. doi: 10.1086/513903. Am J Hum Genet. 1997. PMID: 9245985 Free PMC article.

3

Mutation and expression analysis of the endoglin gene in hereditary hemorrhagic telangiectasia reveals null alleles.

Gallione CJ, Klaus DJ, Yeh EY, Stenzel TT, Xue Y, Anthony KB, McAllister KA, Baldwin MA, Berg JN, Lux A, Smith JD, Vary CP, Craigen WJ, Westermann CJ, Warner ML, Miller YE, Jackson CE, Guttmacher AE, Marchuk DA. Gallione CJ, et al. Among authors: jackson ce. Hum Mutat. 1998;11(4):286-94. doi: 10.1002/(SICI)1098-1004(1998)11:4<286::AID-HUMU6>3.0.CO;2-B. Hum Mutat. 1998. PMID: 9554745

4

Endoglin, a TGF-beta binding protein of endothelial cells, is the gene for hereditary haemorrhagic telangiectasia type 1.

McAllister KA, Grogg KM, Johnson DW, Gallione CJ, Baldwin MA, Jackson CE, Helmbold EA, Markel DS, McKinnon WC, Murrell J, et al. McAllister KA, et al. Among authors: jackson ce. Nat Genet. 1994 Dec;8(4):345-51. doi: 10.1038/ng1294-345. Nat Genet. 1994. PMID: 7894484

5

Mutations in the activin receptor-like kinase 1 gene in hereditary haemorrhagic telangiectasia type 2.

Johnson DW, Berg JN, Baldwin MA, Gallione CJ, Marondel I, Yoon SJ, Stenzel TT, Speer M, Pericak-Vance MA, Diamond A, Guttmacher AE, Jackson CE, Attisano L, Kucherlapati R, Porteous ME, Marchuk DA. Johnson DW, et al. Among authors: jackson ce. Nat Genet. 1996 Jun;13(2):189-95. doi: 10.1038/ng0696-189. Nat Genet. 1996. PMID: 8640225

6

A second locus for hereditary hemorrhagic telangiectasia maps to chromosome 12.

Johnson DW, Berg JN, Gallione CJ, McAllister KA, Warner JP, Helmbold EA, Markel DS, Jackson CE, Porteous ME, Marchuk DA. Johnson DW, et al. Among authors: jackson ce. Genome Res. 1995 Aug;5(1):21-8. doi: 10.1101/gr.5.1.21. Genome Res. 1995. PMID: 8717052 Free article.

7

Combinatorial Mismatch Scan (CMS) for loci associated with dementia in the Amish.

McCauley JL, Hahs DW, Jiang L, Scott WK, Welsh-Bohmer KA, Jackson CE, Vance JM, Pericak-Vance MA, Haines JL. McCauley JL, et al. Among authors: jackson ce. BMC Med Genet. 2006 Mar 3;7:19. doi: 10.1186/1471-2350-7-19. BMC Med Genet. 2006. PMID: 16515697 Free PMC article.

8

An autosomal genomic screen for dementia in an extended Amish family.

Ashley-Koch AE, Shao Y, Rimmler JB, Gaskell PC, Welsh-Bohmer KA, Jackson CE, Scott WK, Haines JL, Pericak-Vance MA. Ashley-Koch AE, et al. Among authors: jackson ce. Neurosci Lett. 2005 May 13;379(3):199-204. doi: 10.1016/j.neulet.2004.12.065. Neurosci Lett. 2005. PMID: 15843063

9

A genome-wide linkage analysis of dementia in the Amish.

Hahs DW, McCauley JL, Crunk AE, McFarland LL, Gaskell PC, Jiang L, Slifer SH, Vance JM, Scott WK, Welsh-Bohmer KA, Johnson SR, Jackson CE, Pericak-Vance MA, Haines JL. Hahs DW, et al. Among authors: jackson ce. Am J Med Genet B Neuropsychiatr Genet. 2006 Mar 5;141B(2):160-6. doi: 10.1002/ajmg.b.30257. Am J Med Genet B Neuropsychiatr Genet. 2006. PMID: 16389594 Free PMC article.

10

Successful aging shows linkage to chromosomes 6, 7, and 14 in the Amish.

Edwards DR, Gilbert JR, Jiang L, Gallins PJ, Caywood L, Creason M, Fuzzell D, Knebusch C, Jackson CE, Pericak-Vance MA, Haines JL, Scott WK. Edwards DR, et al. Among authors: jackson ce. Ann Hum Genet. 2011 Jul;75(4):516-28. doi: 10.1111/j.1469-1809.2011.00658.x. Ann Hum Genet. 2011. PMID: 21668908 Free PMC article.

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