Search Results - "Pytte J"

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  1. 1

    Phosphorothioate antisense oligonucleotide induced innate immune activation is attenuated by tryptophan oxidation products.

    Authors: Pytte J Saldana L Zhang W et al.

    Source: Nucleic acids research [Nucleic Acids Res] 2026 Apr 13; Vol. 54 (7).

    Publication Type: Journal Article

    Journal Info: Publisher: Oxford University Press Country of Publication: England NLM ID: 0411011 Publication Model: Print Cited Medium: Internet ISSN: 1362-4962 (Electronic) Linking ISSN: 03051048 NLM ISO Abbreviation: Nucleic Acids Res Subsets: MEDLINE

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  2. 2

    Splice-modulating antisense oligonucleotides targeting a pathogenic intronic variant in adult polyglucosan body disease correct mis-splicing and restore enzyme activity in patient cells.

    Authors: Thomas R Miyoshi E Akman HO et al.

    Source: Nucleic acids research [Nucleic Acids Res] 2025 Jul 08; Vol. 53 (13).

    Publication Type: Journal Article

    Journal Info: Publisher: Oxford University Press Country of Publication: England NLM ID: 0411011 Publication Model: Print Cited Medium: Internet ISSN: 1362-4962 (Electronic) Linking ISSN: 03051048 NLM ISO Abbreviation: Nucleic Acids Res Subsets: MEDLINE

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  3. 3

    Bridging the gap: Short structural variants in the genetics of anorexia nervosa.

    Authors: Berthold N Pytte J Bulik CM et al.

    Source: The International journal of eating disorders [Int J Eat Disord] 2022 Jun; Vol. 55 (6), pp. 747-753. Date of Electronic Publication: 2022 Apr 26.

    Publication Type: Journal Article; Research Support, Non-U.S. Gov't

    Journal Info: Publisher: Wiley Country of Publication: United States NLM ID: 8111226 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1098-108X (Electronic) Linking ISSN: 02763478 NLM ISO Abbreviation: Int J Eat Disord Subsets: MEDLINE

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  4. 4

    Structural Variants May Be a Source of Missing Heritability in sALS.

    Authors: Theunissen F Flynn LL Anderton RS et al.

    Source: Frontiers in neuroscience [Front Neurosci] 2020 Jan 31; Vol. 14, pp. 47. Date of Electronic Publication: 2020 Jan 31 (Print Publication: 2020).

    Publication Type: Journal Article

    Journal Info: Publisher: Frontiers Research Foundation Country of Publication: Switzerland NLM ID: 101478481 Publication Model: eCollection Cited Medium: Print ISSN: 1662-4548 (Print) Linking ISSN: 1662453X NLM ISO Abbreviation: Front Neurosci Subsets: PubMed not MEDLINE

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  5. 5

    Disease-modifying effects of an SCAF4 structural variant in a predominantly SOD1 ALS cohort.

    Authors: Pytte J Flynn LL Anderton RS et al.

    Source: Neurology. Genetics [Neurol Genet] 2020 Jul 01; Vol. 6 (4), pp. e470. Date of Electronic Publication: 2020 Jul 01 (Print Publication: 2020).

    Publication Type: Journal Article

    Journal Info: Publisher: Published for the American Academy of Neurology by Wolters Kluwer Country of Publication: United States NLM ID: 101671068 Publication Model: eCollection Cited Medium: Print ISSN: 2376-7839 (Print) Linking ISSN: 23767839 NLM ISO Abbreviation: Neurol Genet Subsets: PubMed not MEDLINE

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  6. 6

    Association of a structural variant within the SQSTM1 gene with amyotrophic lateral sclerosis.

    Authors: Pytte J Anderton RS Flynn LL et al.

    Source: Neurology. Genetics [Neurol Genet] 2020 Feb 27; Vol. 6 (2), pp. e406. Date of Electronic Publication: 2020 Feb 27 (Print Publication: 2020).

    Publication Type: Journal Article

    Journal Info: Publisher: Published for the American Academy of Neurology by Wolters Kluwer Country of Publication: United States NLM ID: 101671068 Publication Model: eCollection Cited Medium: Print ISSN: 2376-7839 (Print) Linking ISSN: 23767839 NLM ISO Abbreviation: Neurol Genet Subsets: PubMed not MEDLINE

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