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7
Dysferlinopathy (LGMD2B) a 23-year follow-up study of 10 patients homozygous for the same frameshifting dysferlin mutations.pdf
Dysferlinopathy (LGMD2B) a 23-year follow-up study of 10 patients homozygous for the same frameshifting dysferlin mutations
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62
Dysferlinopathy的临床、病理及分子生物学研究.pdf
Dysferlinopathy的临床、病理及分子生物学研究Dysferlinopathy的临床、病理及分子生物学研究Dysferlinopathy的临床、病理及分子生物学研究
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37
systemic delivery of dysferlin overlap vectors provides long-term functional improvement for dysferlinopathy.[2017][hum gene ther][10.1089hum.2017..pdf
systemic delivery of dysferlin overlap vectors provides long-term functional improvement for dysferlinopathy.[2017][hum gene ther][10.1089hum.2017.
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58
DYSFERLINOPATHY分子免疫病理学研究.pdf
DYSFERLINOPATHY分子免疫病理学研究免疫,研究,分子病理学,病理学,分子病理,免疫病理学,免疫分子,分子免疫学
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12
genetic profile for suspected dysferlinopathy identified by targeted next-generation sequencing.因涉嫌dysferlinopathy基因档案被针对下一代测序.pdf
genetic profile for suspected dysferlinopathy identified by targeted next-generation sequencing.因涉嫌dysferlinopathy基因档案被针对下一代测序
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11
lack of correlation between outcomes of membrane repair assay and correction of dystrophic changes in experimental therapeutic strategy in dysferlinopathy.pdf
lack of correlation between outcomes of membrane repair assay and correction of dystrophic changes in experimental therapeutic strategy in dysferlinopathy
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9
Muscle hypertrophy induced by myostatin inhibition accelerates degeneration in dysferlinopathy.pdf
Muscle hypertrophy induced by myostatin inhibition accelerates degeneration in dysferlinopathy
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3
lgmd phenotype due to a new gene and dysferlinopathy investigated by next-generation sequencing.lgmd表型由于新基因和dysferlinopathy调查下.pdf
lgmd phenotype due to a new gene and dysferlinopathy investigated by next-generation sequencing.lgmd表型由于新基因和dysferlinopathy调查下
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9
gene co-expression network analysis of dysferlinopathy_altered cellular processes and functional prediction of tor1aip1,a novel muscular dystrophy g.pdf
gene co-expression network analysis of dysferlinopathy_altered cellular processes and functional prediction of tor1aip1,a novel muscular dystrophy g
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