Lincoln RR - Search Results

1

Linkage analysis of candidate myelin genes in familial multiple sclerosis.

Seboun E, Oksenberg JR, Rombos A, Usuku K, Goodkin DE, Lincoln RR, Wong M, Pham-Dinh D, Boesplug-Tanguy O, Carsique R, Fitoussi R, Gartioux C, Reyes C, Ribierre F, Faure S, Fizames C, Gyapay G, Weissenbach J, Dautigny A, Rimmler JB, Garcia ME, Pericak-Vance MA, Haines JL, Hauser SL. Seboun E, et al. Among authors: lincoln rr. Neurogenetics. 1999 Sep;2(3):155-62. doi: 10.1007/s100480050076. Neurogenetics. 1999. PMID: 10541588

2

Cytokine accumulations in CSF of multiple sclerosis patients: frequent detection of interleukin-1 and tumor necrosis factor but not interleukin-6.

Hauser SL, Doolittle TH, Lincoln R, Brown RH, Dinarello CA. Hauser SL, et al. Neurology. 1990 Nov;40(11):1735-9. doi: 10.1212/wnl.40.11.1735. Neurology. 1990. PMID: 2234430

3

Elevated mast cell tryptase in cerebrospinal fluid of multiple sclerosis patients.

Rozniecki JJ, Hauser SL, Stein M, Lincoln R, Theoharides TC. Rozniecki JJ, et al. Ann Neurol. 1995 Jan;37(1):63-6. doi: 10.1002/ana.410370112. Ann Neurol. 1995. PMID: 7818259

4

Unusual organization of the human T-cell receptor beta-chain gene complex is linked to recombination hotspots.

Seboun E, Houghton L, Hatem CJ Jr, Lincoln R, Hauser SL. Seboun E, et al. Proc Natl Acad Sci U S A. 1993 Jun 1;90(11):5026-9. doi: 10.1073/pnas.90.11.5026. Proc Natl Acad Sci U S A. 1993. PMID: 8099448 Free PMC article.

5

Segregation of immunoglobulin heavy chain constant region genes in multiple sclerosis sibling pairs.

Yu JS, Pandey JP, Massacesi L, Lincoln R, Usuku K, Seboun E, Hauser SL. Yu JS, et al. J Neuroimmunol. 1993 Jan;42(1):113-6. doi: 10.1016/0165-5728(93)90218-n. J Neuroimmunol. 1993. PMID: 8423203 No abstract available.

6

A complete genomic screen for multiple sclerosis underscores a role for the major histocompatability complex. The Multiple Sclerosis Genetics Group.

Haines JL, Ter-Minassian M, Bazyk A, Gusella JF, Kim DJ, Terwedow H, Pericak-Vance MA, Rimmler JB, Haynes CS, Roses AD, Lee A, Shaner B, Menold M, Seboun E, Fitoussi RP, Gartioux C, Reyes C, Ribierre F, Gyapay G, Weissenbach J, Hauser SL, Goodkin DE, Lincoln R, Usuku K, Oksenberg JR, et al. Haines JL, et al. Nat Genet. 1996 Aug;13(4):469-71. doi: 10.1038/ng0896-469. Nat Genet. 1996. PMID: 8696344

7

Tumor necrosis factor (TNF) microsatellite haplotypes in relation to extended haplotypes, susceptibility to diseases associated with the major histocompatibility complex and TNF secretion.

Garcia-Merino A, Alper CA, Usuku K, Marcus-Bagley D, Lincoln R, Awdeh Z, Yunis EJ, Eisenbarth GS, Brink SJ, Hauser SL. Garcia-Merino A, et al. Hum Immunol. 1996 Sep 15;50(1):11-21. doi: 10.1016/0198-8859(96)00064-x. Hum Immunol. 1996. PMID: 8872171

8

Linkage of the MHC to familial multiple sclerosis suggests genetic heterogeneity. The Multiple Sclerosis Genetics Group.

Haines JL, Terwedow HA, Burgess K, Pericak-Vance MA, Rimmler JB, Martin ER, Oksenberg JR, Lincoln R, Zhang DY, Banatao DR, Gatto N, Goodkin DE, Hauser SL. Haines JL, et al. Hum Mol Genet. 1998 Aug;7(8):1229-34. doi: 10.1093/hmg/7.8.1229. Hum Mol Genet. 1998. PMID: 9668163

9

Interaction between HLA-DR2 and abnormal brain MRI in optic neuritis and early MS. Optic Neuritis Study Group.

Hauser SL, Oksenberg JR, Lincoln R, Garovoy J, Beck RW, Cole SR, Moke PS, Kip KE, Gal RL, Long DT. Hauser SL, et al. Neurology. 2000 May 9;54(9):1859-61. doi: 10.1212/wnl.54.9.1859. Neurology. 2000. PMID: 10802800

10

CC-chemokine receptor 5 polymorphism and age of onset in familial multiple sclerosis. Multiple Sclerosis Genetics Group.

Barcellos LF, Schito AM, Rimmler JB, Vittinghoff E, Shih A, Lincoln R, Callier S, Elkins MK, Goodkin DE, Haines JL, Pericak-Vance MA, Hauser SL, Oksenberg JR. Barcellos LF, et al. Immunogenetics. 2000 Apr;51(4-5):281-8. doi: 10.1007/s002510050621. Immunogenetics. 2000. PMID: 10803840

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