La Spada AR - Search Results

1

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.

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

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.

5

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.

6

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.

7

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.

8

Gene expression analysis reveals early dysregulation of disease pathways and links Chmp7 to pathogenesis of spinal and bulbar muscular atrophy.

Malik B, Devine H, Patani R, La Spada AR, Hanna MG, Greensmith L. Malik B, et al. Among authors: la spada ar. Sci Rep. 2019 Mar 5;9(1):3539. doi: 10.1038/s41598-019-40118-3. Sci Rep. 2019. PMID: 30837566 Free PMC article.

9

Deterioration of muscle force and contractile characteristics are early pathological events in spinal and bulbar muscular atrophy mice.

Gray AL, Annan L, Dick JRT, La Spada AR, Hanna MG, Greensmith L, Malik B. Gray AL, et al. Among authors: la spada ar. Dis Model Mech. 2020 May 26;13(5):dmm042424. doi: 10.1242/dmm.042424. Dis Model Mech. 2020. PMID: 32152060 Free PMC article.

10

A candidate gene for X-linked spinal muscular atrophy.

Fischbeck KH, Souders D, La Spada A. Fischbeck KH, et al. Adv Neurol. 1991;56:209-13. Adv Neurol. 1991. PMID: 1853757 No abstract available.

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