Cells were co-stained with 2B1 and anti-Sm mAb (Y12). The cells shown were extracted from SMN-spot+ CD33++ cells. Data were obtained from two representative individuals; control(C8, 7y; left) and SMA (S7, 5y, right) subjects among the eight examined. The eight-cells were extracted from the SMN spot with the highest intensity. The number in the upper left of the brightfield represents the individual number, depending on the detection order. Images are shown as bright field, nucleus (blue), SMN (green), Sm (red), and merged (yellow).</p
International audienceSpinal muscular atrophy is a neuromuscular disease resulting from mutations in...
Genetic defects leading to the reduction of the survival motor neuron protein (SMN) are a causal fac...
The mechanism underlying selective motor neuron (MN) death remains an essential question in the MN d...
Peripheral blood nuclear cells (PBCs) classified according to types (R2, R3, R4, R5)were analyzed fo...
In total, 40 cells were extracted from the SMN spot with the highest intensity. The numbers at the u...
The analyses of SMN protein expressions. (A) The scatter diagram plotting correlation among the clin...
Spinal muscular atrophy (SMA) is a severe genetic neuromuscular disorder caused by insufficiency of ...
AbstractHomozygous mutations of the telomeric survival motor neurone gene (SMN1) cause spinal muscul...
Spinal muscular atrophy (SMA) is a severe genetic neuromuscular disorder caused by insufficiency of ...
The subcellular localization of the survival motor neuron (SMN) protein, encoded by the spinal muscu...
<div><h3>Objectives</h3><p>Survival Motor Neuron (SMN) protein levels may become key pharmacodynamic...
AbstractThe survival motor neuron (SMN) protein forms cytoplasmic granules when overexpressed. We re...
The survival motor neuron (SMN) gene is the putative disease gene for human spinal muscular atrophy ...
Spinal muscular atrophy (SMA) is a common autosomal recessive neuromuscular disorder which presents ...
Survival motor neuron (SMN) messenger RNA and protein levels in spinal muscular atrophy (SMA) model ...
International audienceSpinal muscular atrophy is a neuromuscular disease resulting from mutations in...
Genetic defects leading to the reduction of the survival motor neuron protein (SMN) are a causal fac...
The mechanism underlying selective motor neuron (MN) death remains an essential question in the MN d...
Peripheral blood nuclear cells (PBCs) classified according to types (R2, R3, R4, R5)were analyzed fo...
In total, 40 cells were extracted from the SMN spot with the highest intensity. The numbers at the u...
The analyses of SMN protein expressions. (A) The scatter diagram plotting correlation among the clin...
Spinal muscular atrophy (SMA) is a severe genetic neuromuscular disorder caused by insufficiency of ...
AbstractHomozygous mutations of the telomeric survival motor neurone gene (SMN1) cause spinal muscul...
Spinal muscular atrophy (SMA) is a severe genetic neuromuscular disorder caused by insufficiency of ...
The subcellular localization of the survival motor neuron (SMN) protein, encoded by the spinal muscu...
<div><h3>Objectives</h3><p>Survival Motor Neuron (SMN) protein levels may become key pharmacodynamic...
AbstractThe survival motor neuron (SMN) protein forms cytoplasmic granules when overexpressed. We re...
The survival motor neuron (SMN) gene is the putative disease gene for human spinal muscular atrophy ...
Spinal muscular atrophy (SMA) is a common autosomal recessive neuromuscular disorder which presents ...
Survival motor neuron (SMN) messenger RNA and protein levels in spinal muscular atrophy (SMA) model ...
International audienceSpinal muscular atrophy is a neuromuscular disease resulting from mutations in...
Genetic defects leading to the reduction of the survival motor neuron protein (SMN) are a causal fac...
The mechanism underlying selective motor neuron (MN) death remains an essential question in the MN d...