Talbot K - Search Results

1

Correction of amyotrophic lateral sclerosis related phenotypes in induced pluripotent stem cell-derived motor neurons carrying a hexanucleotide expansion mutation in C9orf72 by CRISPR/Cas9 genome editing using homology-directed repair.

Ababneh NA, Scaber J, Flynn R, Douglas A, Barbagallo P, Candalija A, Turner MR, Sims D, Dafinca R, Cowley SA, Talbot K. Ababneh NA, et al. Among authors: talbot k. Hum Mol Genet. 2020 Aug 3;29(13):2200-2217. doi: 10.1093/hmg/ddaa106. Hum Mol Genet. 2020. PMID: 32504093 Free PMC article.

2

Deletions in the survival motor neuron gene on 5q13 in autosomal recessive spinal muscular atrophy.

Rodrigues NR, Owen N, Talbot K, Ignatius J, Dubowitz V, Davies KE. Rodrigues NR, et al. Among authors: talbot k. Hum Mol Genet. 1995 Apr;4(4):631-4. doi: 10.1093/hmg/4.4.631. Hum Mol Genet. 1995. PMID: 7633412

3

Characterization of a gene encoding survival motor neuron (SMN)-related protein, a constituent of the spliceosome complex.

Talbot K, Miguel-Aliaga I, Mohaghegh P, Ponting CP, Davies KE. Talbot K, et al. Hum Mol Genet. 1998 Dec;7(13):2149-56. doi: 10.1093/hmg/7.13.2149. Hum Mol Genet. 1998. PMID: 9817934

4

A mutation in the small heat-shock protein HSPB1 leading to distal hereditary motor neuronopathy disrupts neurofilament assembly and the axonal transport of specific cellular cargoes.

Ackerley S, James PA, Kalli A, French S, Davies KE, Talbot K. Ackerley S, et al. Among authors: talbot k. Hum Mol Genet. 2006 Jan 15;15(2):347-54. doi: 10.1093/hmg/ddi452. Epub 2005 Dec 20. Hum Mol Genet. 2006. PMID: 16368711

5

Recent advances in the genetics of amyotrophic lateral sclerosis and frontotemporal dementia: common pathways in neurodegenerative disease.

Talbot K, Ansorge O. Talbot K, et al. Hum Mol Genet. 2006 Oct 15;15 Spec No 2:R182-7. doi: 10.1093/hmg/ddl202. Hum Mol Genet. 2006. PMID: 16987882 Review.

6

Genetics of sporadic amyotrophic lateral sclerosis.

Schymick JC, Talbot K, Traynor BJ. Schymick JC, et al. Among authors: talbot k. Hum Mol Genet. 2007 Oct 15;16 Spec No. 2:R233-42. doi: 10.1093/hmg/ddm215. Hum Mol Genet. 2007. PMID: 17911166 Review.

7

A case of celiac disease mimicking amyotrophic lateral sclerosis.

Turner MR, Chohan G, Quaghebeur G, Greenhall RC, Hadjivassiliou M, Talbot K. Turner MR, et al. Among authors: talbot k. Nat Clin Pract Neurol. 2007 Oct;3(10):581-4. doi: 10.1038/ncpneuro0631. Nat Clin Pract Neurol. 2007. PMID: 17914346

8

TDP-43 expression in mouse models of amyotrophic lateral sclerosis and spinal muscular atrophy.

Turner BJ, Bäumer D, Parkinson NJ, Scaber J, Ansorge O, Talbot K. Turner BJ, et al. Among authors: talbot k. BMC Neurosci. 2008 Oct 28;9:104. doi: 10.1186/1471-2202-9-104. BMC Neurosci. 2008. PMID: 18957104 Free PMC article.

9

Biomarkers in amyotrophic lateral sclerosis.

Turner MR, Kiernan MC, Leigh PN, Talbot K. Turner MR, et al. Among authors: talbot k. Lancet Neurol. 2009 Jan;8(1):94-109. doi: 10.1016/S1474-4422(08)70293-X. Lancet Neurol. 2009. PMID: 19081518 Review.

10

Functional vitamin B12 deficiency.

Turner MR, Talbot K. Turner MR, et al. Among authors: talbot k. Pract Neurol. 2009 Feb;9(1):37-41. doi: 10.1136/jnnp.2008.161968. Pract Neurol. 2009. PMID: 19151237

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