Characterisation of the transcriptome of the spinal cord and quadriceps of delta 7 mice treated with haloperidol (NIH BioProject Accession number: PRJNA1251322) and hiPSC-motoneurons derived from pati

Zenodo2026-03-11 更新20

dataset documenting article "Circulating MyomiRs as Potential Biomarkers to Monitor Response to Nusinersen in Pediatric SMA Patients"

生物标志物

脊髓性肌萎缩症

Raw data obtained by Real time PCR performed to assess the expression of muscle-specific miRNAs, miR206, miR-133a, miR-133b, miR-1, in serum of 21 infantile SMA patients at baseline and after 6 months

NIAID Data Ecosystem90

Suppression of NCALD protects against spinal muscular atrophy by restoring impaired endocytosis. Homo sapiens

脊髓性肌萎缩症

内吞作用机制

Spinal muscular atrophy (SMA) is a common genetic motor neuron (MN) disease caused by low levels of the ubiquitously expressed housekeeping survival motor neuron (SMN) protein, whereas concomitant ove

NIAID Data Ecosystem30

Electrophysiologic assessment of SMA type 2 and 3 patients.

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