Sapp P - 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: sapp p. Nature. 1993 Mar 4;362(6415):59-62. doi: 10.1038/362059a0. Nature. 1993. PMID: 8446170

2

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. Among authors: sapp p. Am J Med Genet. 1994 May 15;51(1):61-9. doi: 10.1002/ajmg.1320510114. Am J Med Genet. 1994. PMID: 7913294

3

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. Among authors: sapp p. Hum Mol Genet. 1994 Jun;3(6):981-7. doi: 10.1093/hmg/3.6.981. Hum Mol Genet. 1994. PMID: 7951249

4

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: sapp p. 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.

5

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. Neuromuscul Disord. 1995 Sep;5(5):353-7. doi: 10.1016/0960-8966(95)00007-a. Neuromuscul Disord. 1995. PMID: 7496169

6

Gene linkage in familial amyotrophic lateral sclerosis: a progress report.

Brown RH Jr, Horvitz HR, Rouleau GA, McKenna-Yasek D, Beard C, Sapp P, Haines JL, Gusella JF, Figlewicz DA. Brown RH Jr, et al. Among authors: sapp p. Adv Neurol. 1991;56:215-26. Adv Neurol. 1991. PMID: 1853758 No abstract available.

7

Linkage of a gene causing familial amyotrophic lateral sclerosis to chromosome 21 and evidence of genetic-locus heterogeneity.

Siddique T, Figlewicz DA, Pericak-Vance MA, Haines JL, Rouleau G, Jeffers AJ, Sapp P, Hung WY, Bebout J, McKenna-Yasek D, et al. Siddique T, et al. Among authors: sapp p. N Engl J Med. 1991 May 16;324(20):1381-4. doi: 10.1056/NEJM199105163242001. N Engl J Med. 1991. PMID: 2020294 Free article.

8

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. Among authors: sapp pc. Hum Mol Genet. 1992 Oct;1(7):547. doi: 10.1093/hmg/1.7.547. Hum Mol Genet. 1992. PMID: 1307256 No abstract available.

9

Linkage of familial amyotrophic lateral sclerosis with frontotemporal dementia to chromosome 9q21-q22.

Hosler BA, Siddique T, Sapp PC, Sailor W, Huang MC, Hossain A, Daube JR, Nance M, Fan C, Kaplan J, Hung WY, McKenna-Yasek D, Haines JL, Pericak-Vance MA, Horvitz HR, Brown RH Jr. Hosler BA, et al. Among authors: sapp pc. JAMA. 2000 Oct 4;284(13):1664-9. doi: 10.1001/jama.284.13.1664. JAMA. 2000. PMID: 11015796

10

Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis.

Kwiatkowski TJ Jr, Bosco DA, Leclerc AL, Tamrazian E, Vanderburg CR, Russ C, Davis A, Gilchrist J, Kasarskis EJ, Munsat T, Valdmanis P, Rouleau GA, Hosler BA, Cortelli P, de Jong PJ, Yoshinaga Y, Haines JL, Pericak-Vance MA, Yan J, Ticozzi N, Siddique T, McKenna-Yasek D, Sapp PC, Horvitz HR, Landers JE, Brown RH Jr. Kwiatkowski TJ Jr, et al. Among authors: sapp pc. Science. 2009 Feb 27;323(5918):1205-8. doi: 10.1126/science.1166066. Science. 2009. PMID: 19251627

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