La Spada AR - Search Results

1

Absence of disturbed axonal transport in spinal and bulbar muscular atrophy.

Malik B, Nirmalananthan N, Bilsland LG, La Spada AR, Hanna MG, Schiavo G, Gallo JM, Greensmith L. Malik B, et al. Among authors: la spada ar. Hum Mol Genet. 2011 May 1;20(9):1776-86. doi: 10.1093/hmg/ddr061. Epub 2011 Feb 11. Hum Mol Genet. 2011. PMID: 21317158 Free PMC article.

2

Meiotic stability and genotype-phenotype correlation of the trinucleotide repeat in X-linked spinal and bulbar muscular atrophy.

La Spada AR, Roling DB, Harding AE, Warner CL, Spiegel R, Hausmanowa-Petrusewicz I, Yee WC, Fischbeck KH. La Spada AR, et al. Nat Genet. 1992 Dec;2(4):301-4. doi: 10.1038/ng1292-301. Nat Genet. 1992. PMID: 1303283

3

Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy.

La Spada AR, Wilson EM, Lubahn DB, Harding AE, Fischbeck KH. La Spada AR, et al. Nature. 1991 Jul 4;352(6330):77-9. doi: 10.1038/352077a0. Nature. 1991. PMID: 2062380

4

Androgen receptor YAC transgenic mice carrying CAG 45 alleles show trinucleotide repeat instability.

La Spada AR, Peterson KR, Meadows SA, McClain ME, Jeng G, Chmelar RS, Haugen HA, Chen K, Singer MJ, Moore D, Trask BJ, Fischbeck KH, Clegg CH, McKnight GS. La Spada AR, et al. Hum Mol Genet. 1998 Jun;7(6):959-67. doi: 10.1093/hmg/7.6.959. Hum Mol Genet. 1998. PMID: 9580659

5

Loss of endogenous androgen receptor protein accelerates motor neuron degeneration and accentuates androgen insensitivity in a mouse model of X-linked spinal and bulbar muscular atrophy.

Thomas PS Jr, Fraley GS, Damian V, Woodke LB, Zapata F, Sopher BL, Plymate SR, La Spada AR. Thomas PS Jr, et al. Among authors: la spada ar. Hum Mol Genet. 2006 Jul 15;15(14):2225-38. doi: 10.1093/hmg/ddl148. Epub 2006 Jun 13. Hum Mol Genet. 2006. PMID: 16772330

6

FUS is not dysregulated by the spinal bulbar muscular atrophy androgen receptor polyglutamine repeat expansion.

Fratta P, Malik B, Gray A, La Spada AR, Hanna MG, Fisher EM, Greensmith L. Fratta P, et al. Among authors: la spada ar. Neurobiol Aging. 2013 May;34(5):1516.e17-9. doi: 10.1016/j.neurobiolaging.2012.09.008. Epub 2012 Oct 9. Neurobiol Aging. 2013. PMID: 23062703 Free article.

7

Reduction of mutant ataxin-7 expression restores motor function and prevents cerebellar synaptic reorganization in a conditional mouse model of SCA7.

Furrer SA, Waldherr SM, Mohanachandran MS, Baughn TD, Nguyen KT, Sopher BL, Damian VA, Garden GA, La Spada AR. Furrer SA, et al. Among authors: la spada ar. Hum Mol Genet. 2013 Mar 1;22(5):890-903. doi: 10.1093/hmg/dds495. Epub 2012 Nov 29. Hum Mol Genet. 2013. PMID: 23197655 Free PMC article.

8

Co-induction of the heat shock response ameliorates disease progression in a mouse model of human spinal and bulbar muscular atrophy: implications for therapy.

Malik B, Nirmalananthan N, Gray AL, La Spada AR, Hanna MG, Greensmith L. Malik B, et al. Among authors: la spada ar. Brain. 2013 Mar;136(Pt 3):926-43. doi: 10.1093/brain/aws343. Epub 2013 Feb 7. Brain. 2013. PMID: 23393146 Free PMC article.

9

Endoplasmic reticulum stress in spinal and bulbar muscular atrophy: a potential target for therapy.

Montague K, Malik B, Gray AL, La Spada AR, Hanna MG, Szabadkai G, Greensmith L. Montague K, et al. Among authors: la spada ar. Brain. 2014 Jul;137(Pt 7):1894-906. doi: 10.1093/brain/awu114. Epub 2014 Jun 4. Brain. 2014. PMID: 24898351 Free PMC article.

10

Senataxin mutations elicit motor neuron degeneration phenotypes and yield TDP-43 mislocalization in ALS4 mice and human patients.

Bennett CL, Dastidar SG, Ling SC, Malik B, Ashe T, Wadhwa M, Miller DB, Lee C, Mitchell MB, van Es MA, Grunseich C, Chen Y, Sopher BL, Greensmith L, Cleveland DW, La Spada AR. Bennett CL, et al. Among authors: la spada ar. Acta Neuropathol. 2018 Sep;136(3):425-443. doi: 10.1007/s00401-018-1852-9. Epub 2018 May 3. Acta Neuropathol. 2018. PMID: 29725819 Free PMC article.

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