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Year | Number of Results |
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2021 | 1 |
2022 | 2 |
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2024 | 0 |
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Schwann cells are axo-protective after injury irrespective of myelination status in mouse Schwann cell-neuron cocultures.
J Cell Sci. 2023 Sep 15;136(18):jcs261557. doi: 10.1242/jcs.261557. Epub 2023 Sep 20.
J Cell Sci. 2023.
PMID: 37642648
Free PMC article.
Expanding SPTAN1 monoallelic variant associated disorders: From epileptic encephalopathy to pure spastic paraplegia and ataxia.
Morsy H, Benkirane M, Cali E, Rocca C, Zhelcheska K, Cipriani V, Galanaki E, Maroofian R, Efthymiou S, Murphy D, O'Driscoll M, Suri M, Banka S, Clayton-Smith J, Wright T, Redman M, Bassetti JA, Nizon M, Cogne B, Jamra RA, Bartolomaeus T, Heruth M, Krey I, Gburek-Augustat J, Wieczorek D, Gattermann F, Mcentagart M, Goldenberg A, Guyant-Marechal L, Garcia-Moreno H, Giunti P, Chabrol B, Bacrot S, Buissonnière R, Magry V, Gowda VK, Srinivasan VM, Melegh B, Szabó A, Sümegi K, Cossée M, Ziff M, Butterfield R, Hunt D, Bird-Lieberman G, Hanna M, Koenig M, Stankewich M, Vandrovcova J, Houlden H; Genomics England Research Consortium.
Morsy H, et al.
Genet Med. 2023 Jan;25(1):76-89. doi: 10.1016/j.gim.2022.09.013. Epub 2022 Nov 4.
Genet Med. 2023.
PMID: 36331550
Free PMC article.
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Natural variants of human SARM1 cause both intrinsic and dominant loss-of-function influencing axon survival.
Ademi M, Yang X, Coleman MP, Gilley J.
Ademi M, et al.
Sci Rep. 2022 Aug 16;12(1):13846. doi: 10.1038/s41598-022-18052-8.
Sci Rep. 2022.
PMID: 35974060
Free PMC article.
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Enrichment of SARM1 alleles encoding variants with constitutively hyperactive NADase in patients with ALS and other motor nerve disorders.
Gilley J, Jackson O, Pipis M, Estiar MA, Al-Chalabi A, Danzi MC, van Eijk KR, Goutman SA, Harms MB, Houlden H, Iacoangeli A, Kaye J, Lima L; Queen Square Genomics; Ravits J, Rouleau GA, Schüle R, Xu J, Züchner S, Cooper-Knock J, Gan-Or Z, Reilly MM, Coleman MP.
Gilley J, et al.
Elife. 2021 Nov 19;10:e70905. doi: 10.7554/eLife.70905.
Elife. 2021.
PMID: 34796871
Free PMC article.
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