Click the Why column to see why an item matched the search.
| Match | Type | Why |
|---|
| Miller, Jeffrey | Person |
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| Zhou, Lan | Person |
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| Association of Duchenne muscular dystrophy with autism spectrum disorder. | Academic Article |
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| CCR2 deficiency does not provide sustained improvement of muscular dystrophy in mdx5cv mice. | Academic Article |
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| Diagnosis of occult muscular dystrophy: importance of the "chance" finding of elevated serum aminotransferase activities. | Academic Article |
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| Effects of AFO use on walking in boys with Duchenne muscular dystrophy: a pilot study. | Academic Article |
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| Erythrocyte deformation in human muscular dystrophy. | Academic Article |
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| HnRNP A1 and A/B interaction with PABPN1 in oculopharyngeal muscular dystrophy. | Academic Article |
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| Identification and Function of Fibrocytes in Skeletal Muscle Injury Repair and Muscular Dystrophy. | Academic Article |
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| Inhibition of apoptosis improves outcome in a model of congenital muscular dystrophy. | Academic Article |
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| Knockdown of col22a1 gene in zebrafish induces a muscular dystrophy by disruption of the myotendinous junction. | Academic Article |
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| Lymphocyte capping in carriers of Duchenne muscular dystrophy. | Academic Article |
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| Muscular dystrophy in PTFR/cavin-1 null mice. | Academic Article |
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| Myogenic Akt signaling upregulates the utrophin-glycoprotein complex and promotes sarcolemma stability in muscular dystrophy. | Academic Article |
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| Myogenic enhancers regulate expression of the facioscapulohumeral muscular dystrophy-associated DUX4 gene. | Academic Article |
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