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11 merged results for "Bernard F. and Alva B. Gimbel Foundation, Inc."

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  1. Untitled

    Author unknown · 2023

    uncertain Transparent signal score 50/100 · policy 1.0.0

    Found in doab · no DOI

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    • cautionMetadata completeness: 4 of 6 scored descriptive metadata groups are present; missing fields increase uncertainty. Source: Normalized work metadata; license: Caller-provided; provenance license not supplied to scorer
  2. Diagnostic capabilities of nanopore long-read sequencing in muscular dystrophy.

    Bruels CC, Littel HR, Daugherty AL, Stafki S · 2022 · Ann Clin Transl Neurol

    limited evidence Transparent signal score 45/100 · policy 1.0.0

    Found in europe-pmc · DOI 10.1002/acn3.51612

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    • supportingOpen access status: Normalized open-access status: open. Source: Normalized work metadata; license: Caller-provided; provenance license not supplied to scorer
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    • not scoredPublication version: A publication version was supplied but is not scored. Source: Normalized work metadata; license: Caller-provided; provenance license not supplied to scorer
    • cautionMetadata completeness: 5 of 6 scored descriptive metadata groups are present; missing fields increase uncertainty. Source: Normalized work metadata; license: Caller-provided; provenance license not supplied to scorer
  3. Variants in DTNA cause a mild, dominantly inherited muscular dystrophy.

    Nascimento A, Bruels CC, Donkervoort S, Foley AR · 2023 · Acta Neuropathol

    limited evidence Transparent signal score 43/100 · policy 1.0.0

    Found in europe-pmc · DOI 10.1007/s00401-023-02551-7

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    • cautionMetadata completeness: 5 of 6 scored descriptive metadata groups are present; missing fields increase uncertainty. Source: Normalized work metadata; license: Caller-provided; provenance license not supplied to scorer
  4. Mutations in the satellite cell gene MEGF10 cause a recessive congenital myopathy with minicores.

    Boyden SE, Mahoney LJ, Kawahara G, Myers JA · 2012 · Neurogenetics

    limited evidence Transparent signal score 45/100 · policy 1.0.0

    Found in europe-pmc · DOI 10.1007/s10048-012-0315-z

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    • supportingOpen access status: Normalized open-access status: open. Source: Normalized work metadata; license: Caller-provided; provenance license not supplied to scorer
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    • cautionMetadata completeness: 5 of 6 scored descriptive metadata groups are present; missing fields increase uncertainty. Source: Normalized work metadata; license: Caller-provided; provenance license not supplied to scorer
  5. MicroRNA-199a is induced in dystrophic muscle and affects WNT signaling, cell proliferation, and myogenic differentiation.

    Alexander MS, Kawahara G, Motohashi N, Casar JC · 2013 · Cell Death Differ

    limited evidence Transparent signal score 43/100 · policy 1.0.0

    Found in europe-pmc · DOI 10.1038/cdd.2013.62

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    • cautionMetadata completeness: 5 of 6 scored descriptive metadata groups are present; missing fields increase uncertainty. Source: Normalized work metadata; license: Caller-provided; provenance license not supplied to scorer
  6. Dystrophin is a tumor suppressor in human cancers with myogenic programs.

    Wang Y, Marino-Enriquez A, Bennett RR, Zhu M · 2014 · Nat Genet

    limited evidence Transparent signal score 45/100 · policy 1.0.0

    Found in europe-pmc · DOI 10.1038/ng.2974

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    • cautionMetadata completeness: 5 of 6 scored descriptive metadata groups are present; missing fields increase uncertainty. Source: Normalized work metadata; license: Caller-provided; provenance license not supplied to scorer
  7. Conditional Dmd ablation in muscle and brain causes profound effects on muscle function and neurobehavior.

    Karuppasamy M, English KG, Conner JR, Rorrer SN · 2025 · Commun Biol

    limited evidence Transparent signal score 45/100 · policy 1.0.0

    Found in europe-pmc · DOI 10.1038/s42003-025-09128-y

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    • cautionMetadata completeness: 5 of 6 scored descriptive metadata groups are present; missing fields increase uncertainty. Source: Normalized work metadata; license: Caller-provided; provenance license not supplied to scorer
  8. Repression of phosphatidylinositol transfer protein α ameliorates the pathology of Duchenne muscular dystrophy.

    Vieira NM, Spinazzola JM, Alexander MS, Moreira YB · 2017 · Proc Natl Acad Sci U S A

    limited evidence Transparent signal score 43/100 · policy 1.0.0

    Found in europe-pmc · DOI 10.1073/pnas.1703556114

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    • cautionMetadata completeness: 5 of 6 scored descriptive metadata groups are present; missing fields increase uncertainty. Source: Normalized work metadata; license: Caller-provided; provenance license not supplied to scorer
  9. Muscle-specific increased expression of <i>JAG1</i> improves the skeletal muscle phenotype in dystrophin-deficient mice.

    de Souza Leite F, Lambert MR, Zhang TY, Conner JR · 2025 · Proc Natl Acad Sci U S A

    limited evidence Transparent signal score 45/100 · policy 1.0.0

    Found in europe-pmc · DOI 10.1073/pnas.2506437122

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    • supportingOpen access status: Normalized open-access status: open. Source: Normalized work metadata; license: Caller-provided; provenance license not supplied to scorer
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    • cautionMetadata completeness: 5 of 6 scored descriptive metadata groups are present; missing fields increase uncertainty. Source: Normalized work metadata; license: Caller-provided; provenance license not supplied to scorer
  10. A limb-girdle muscular dystrophy 2I model of muscular dystrophy identifies corrective drug compounds for dystroglycanopathies.

    Serafini PR, Feyder MJ, Hightower RM, Garcia-Perez D · 2018 · JCI Insight

    limited evidence Transparent signal score 43/100 · policy 1.0.0

    Found in europe-pmc · DOI 10.1172/jci.insight.120493

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    • cautionMetadata completeness: 5 of 6 scored descriptive metadata groups are present; missing fields increase uncertainty. Source: Normalized work metadata; license: Caller-provided; provenance license not supplied to scorer
  11. Skeletal Muscle MicroRNAs: Their Diagnostic and Therapeutic Potential in Human Muscle Diseases.

    Alexander MS, Kunkel LM. · 2015 · J Neuromuscul Dis

    limited evidence Transparent signal score 45/100 · policy 1.0.0

    Found in europe-pmc · DOI 10.3233/jnd-140058

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    • cautionMetadata completeness: 5 of 6 scored descriptive metadata groups are present; missing fields increase uncertainty. Source: Normalized work metadata; license: Caller-provided; provenance license not supplied to scorer