O'Regan JP - Search Results

1

Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis.

Rosen DR, Siddique T, Patterson D, Figlewicz DA, Sapp P, Hentati A, Donaldson D, Goto J, O'Regan JP, Deng HX, et al. Rosen DR, et al. Among authors: o regan jp. Nature. 1993 Mar 4;362(6415):59-62. doi: 10.1038/362059a0. Nature. 1993. PMID: 8446170

2

Identification of three novel mutations in the gene for Cu/Zn superoxide dismutase in patients with familial amyotrophic lateral sclerosis.

Sapp PC, Rosen DR, Hosler BA, Esteban J, McKenna-Yasek D, O'Regan JP, Horvitz HR, Brown RH Jr. Sapp PC, et al. Among authors: o regan jp. Neuromuscul Disord. 1995 Sep;5(5):353-7. doi: 10.1016/0960-8966(95)00007-a. Neuromuscul Disord. 1995. PMID: 7496169

3

Identification of two novel mutations and a new polymorphism in the gene for Cu/Zn superoxide dismutase in patients with amyotrophic lateral sclerosis.

Esteban J, Rosen DR, Bowling AC, Sapp P, McKenna-Yasek D, O'Regan JP, Beal MF, Horvitz HR, Brown RH Jr. Esteban J, et al. Among authors: o regan jp. Hum Mol Genet. 1994 Jun;3(6):997-8. doi: 10.1093/hmg/3.6.997. Hum Mol Genet. 1994. PMID: 7951252 No abstract available.

4

Genetic linkage analysis of familial amyotrophic lateral sclerosis using human chromosome 21 microsatellite DNA markers.

Rosen DR, Sapp P, O'Regan J, McKenna-Yasek D, Schlumpf KS, Haines JL, Gusella JF, Horvitz HR, Brown RH Jr. Rosen DR, et al. Am J Med Genet. 1994 May 15;51(1):61-9. doi: 10.1002/ajmg.1320510114. Am J Med Genet. 1994. PMID: 7913294

5

A frequent ala 4 to val superoxide dismutase-1 mutation is associated with a rapidly progressive familial amyotrophic lateral sclerosis.

Rosen DR, Bowling AC, Patterson D, Usdin TB, Sapp P, Mezey E, McKenna-Yasek D, O'Regan J, Rahmani Z, Ferrante RJ, et al. Rosen DR, et al. Hum Mol Genet. 1994 Jun;3(6):981-7. doi: 10.1093/hmg/3.6.981. Hum Mol Genet. 1994. PMID: 7951249

6

Dinucleotide repeat polymorphisms (D21S223 and D21S224) at 21q22.1.

Rosen DR, Sapp PC, O'Regan J, Horvitz HR, Donaldson DH, Nussbaum C, Gusella JF, Haines JL, Pestka S, Jung V, et al. Rosen DR, et al. Hum Mol Genet. 1992 Oct;1(7):547. doi: 10.1093/hmg/1.7.547. Hum Mol Genet. 1992. PMID: 1307256 No abstract available.

7

Genetic and physical mapping of the GLUR5 glutamate receptor gene on human chromosome 21.

Gregor P, Gaston SM, Yang X, O'Regan JP, Rosen DR, Tanzi RE, Patterson D, Haines JL, Horvitz HR, Uhl GR, et al. Gregor P, et al. Among authors: o regan jp. Hum Genet. 1994 Nov;94(5):565-70. doi: 10.1007/BF00211029. Hum Genet. 1994. PMID: 7959697

8

Two independent dinucleotide repeat polymorphisms at the D21S235 locus (21q22.1).

Donaldson DH, Rosen DR, O'Regan J, Sapp PC, Horvitz HR, Gusella JF, Haines JL, Pestka S, Jung V, Nusbaum C, et al. Donaldson DH, et al. Hum Mol Genet. 1992 Nov;1(8):651. doi: 10.1093/hmg/1.8.651. Hum Mol Genet. 1992. PMID: 1301176 No abstract available.

9

Snoring, sleepiness and the obstructive sleep apnea syndrome.

Walsh JK, Ulett GA, Schweitzer PK, O'Regan JP. Walsh JK, et al. Among authors: o regan jp. Mo Med. 1982 Jan;79(1):21-3, 26. Mo Med. 1982. PMID: 7054652 No abstract available.

10

Diabetes and appendicectomy: testing a hypothesis.

Corridan JP, O'Regan JP, O'Sullivan DJ. Corridan JP, et al. Among authors: o regan jp. Br Med J. 1977 Apr 30;1(6069):1135. doi: 10.1136/bmj.1.6069.1135. Br Med J. 1977. PMID: 861501 Free PMC article. No abstract available.

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