Gusella JF - Search Results

1

Prevalence of Huntington's disease gene CAG repeat alleles in sporadic amyotrophic lateral sclerosis patients.

Ramos EM, Keagle P, Gillis T, Lowe P, Mysore JS, Leclerc AL, Ratti A, Ticozzi N, Gellera C, Gusella JF, Silani V, Alonso I, Brown RH Jr, MacDonald ME, Landers JE. Ramos EM, et al. Among authors: gusella jf. Amyotroph Lateral Scler. 2012 May;13(3):265-9. doi: 10.3109/17482968.2011.653573. Epub 2012 Mar 13. Amyotroph Lateral Scler. 2012. PMID: 22409360

2

Assay by polymerase chain reaction (PCR) of multi-allele polymorphisms in the Huntington's disease region of chromosome 4.

Allitto BA, McClatchey AI, Barnes G, Altherr M, Wasmuth J, Frischauf AM, MacDonald ME, Gusella J. Allitto BA, et al. Mol Cell Probes. 1992 Dec;6(6):513-20. doi: 10.1016/0890-8508(92)90048-3. Mol Cell Probes. 1992. PMID: 1480191

3

Trinucleotide repeat length and progression of illness in Huntington's disease.

Kieburtz K, MacDonald M, Shih C, Feigin A, Steinberg K, Bordwell K, Zimmerman C, Srinidhi J, Sotack J, Gusella J, et al. Kieburtz K, et al. J Med Genet. 1994 Nov;31(11):872-4. doi: 10.1136/jmg.31.11.872. J Med Genet. 1994. PMID: 7853373 Free PMC article.

4

Mapping of a human A2a adenosine receptor (ADORA2) to chromosome 22.

MacCollin M, Peterfreund R, MacDonald M, Fink JS, Gusella J. MacCollin M, et al. Genomics. 1994 Mar 15;20(2):332-3. doi: 10.1006/geno.1994.1181. Genomics. 1994. PMID: 8020991 No abstract available.

5

Distribution of trinucleotide repeat sequences across a 2 Mbp region containing the Huntington's disease gene.

Hummerich H, Baxendale S, Mott R, Kirby SF, MacDonald ME, Gusella J, Lehrach H, Bates GP. Hummerich H, et al. Hum Mol Genet. 1994 Jan;3(1):73-8. doi: 10.1093/hmg/3.1.73. Hum Mol Genet. 1994. PMID: 8162055

6

Structure and expression of the Huntington's disease gene: evidence against simple inactivation due to an expanded CAG repeat.

Ambrose CM, Duyao MP, Barnes G, Bates GP, Lin CS, Srinidhi J, Baxendale S, Hummerich H, Lehrach H, Altherr M, Wasmuth J, Buckler A, Church D, Housman D, Berks M, Micklem G, Durbin R, Dodge A, Read A, Gusella J, MacDonald ME. Ambrose CM, et al. Somat Cell Mol Genet. 1994 Jan;20(1):27-38. doi: 10.1007/BF02257483. Somat Cell Mol Genet. 1994. PMID: 8197474

7

No post-genetics era in human disease research.

Gusella J, MacDonald M. Gusella J, et al. Nat Rev Genet. 2002 Jan;3(1):72-9. doi: 10.1038/nrg706. Nat Rev Genet. 2002. PMID: 11823793 Review.

8

Early phenotypes that presage late-onset neurodegenerative disease allow testing of modifiers in Hdh CAG knock-in mice.

Wheeler VC, Gutekunst CA, Vrbanac V, Lebel LA, Schilling G, Hersch S, Friedlander RM, Gusella JF, Vonsattel JP, Borchelt DR, MacDonald ME. Wheeler VC, et al. Among authors: gusella jf. Hum Mol Genet. 2002 Mar 15;11(6):633-40. doi: 10.1093/hmg/11.6.633. Hum Mol Genet. 2002. PMID: 11912178

9

Identification of a presymptomatic molecular phenotype in Hdh CAG knock-in mice.

Fossale E, Wheeler VC, Vrbanac V, Lebel LA, Teed A, Mysore JS, Gusella JF, MacDonald ME, Persichetti F. Fossale E, et al. Among authors: gusella jf. Hum Mol Genet. 2002 Sep 15;11(19):2233-41. doi: 10.1093/hmg/11.19.2233. Hum Mol Genet. 2002. PMID: 12217951

10

Specific progressive cAMP reduction implicates energy deficit in presymptomatic Huntington's disease knock-in mice.

Gines S, Seong IS, Fossale E, Ivanova E, Trettel F, Gusella JF, Wheeler VC, Persichetti F, MacDonald ME. Gines S, et al. Among authors: gusella jf. Hum Mol Genet. 2003 Mar 1;12(5):497-508. doi: 10.1093/hmg/ddg046. Hum Mol Genet. 2003. PMID: 12588797

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