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资源简介：
SMN protein in human muscle.
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创建时间：
2011-08-31
相关数据集
Additional file 12 of Long-term nusinersen treatment across a wide spectrum of spinal muscular atrophy severity: a real-world experience
Additional file 12: Changes in the RULM score versus baseline for ambulant and non-ambulant patients and comparison the results.
DataCite Commons2024-08-14 更新110
Motor function in SMA type 2 and 3 patients.
Motor function in SMA type 2 and 3 patients.
NIAID Data Ecosystem70
Suppression of NCALD protects against spinal muscular atrophy by restoring impaired endocytosis. Homo sapiens
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
dataset documenting article "Circulating MyomiRs as Potential Biomarkers to Monitor Response to Nusinersen in Pediatric SMA Patients"
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
Comparison of mean and median survival time of SMN mice injected with PMO(-10-34) or Scramble.
Comparison of mean and median survival time of SMN mice injected with PMO(-10-34) or Scramble.
NIAID Data Ecosystem60
