Results 211 to 220 of about 55,907 (261)
Loss of SMN Impairs Osteoblast-Osteoclast Coupling via IGF1-Akt-OPG Axis in Spinal Muscular Atrophy. [PDF]
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Experimental Cell Research, 2004
The survival of motor neurons (SMN) protein is the product of the disease-determining gene of the neurodegenerative disorder spinal muscular atrophy (SMA). SMN is part of a stable multiprotein complex that is found in all metazoan cells in the cytoplasm and in nuclear Gems.
Gideon Dreyfuss
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The survival of motor neurons (SMN) protein is the product of the disease-determining gene of the neurodegenerative disorder spinal muscular atrophy (SMA). SMN is part of a stable multiprotein complex that is found in all metazoan cells in the cytoplasm and in nuclear Gems.
Gideon Dreyfuss
exaly +3 more sources
2021
Charinus caribensis (Quintero, 1986) Figs 12, 17–19; Table 1 Tricharinus caribensis Quintero, 1986: 209, 211–212, figs 18–21, 27–28 Tricharinus caribensis – Weygoldt 1994: 244; 2000a: 25, 43, 129. — Ávila Calvo & Armas 1997: 31. — Weygoldt et al. 2002: 295. — Armas 2004: 38. Charinus caribensis – Harvey 2002b: 455; 2003: 5. — Armas 2004: 38; 2006b: 226,
Miranda, Gustavo Silva de +3 more
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Charinus caribensis (Quintero, 1986) Figs 12, 17–19; Table 1 Tricharinus caribensis Quintero, 1986: 209, 211–212, figs 18–21, 27–28 Tricharinus caribensis – Weygoldt 1994: 244; 2000a: 25, 43, 129. — Ávila Calvo & Armas 1997: 31. — Weygoldt et al. 2002: 295. — Armas 2004: 38. Charinus caribensis – Harvey 2002b: 455; 2003: 5. — Armas 2004: 38; 2006b: 226,
Miranda, Gustavo Silva de +3 more
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Optimization of SMN Trans-Splicing Through the Analysis of SMN Introns
Journal of Molecular Neuroscience, 2011Spinal muscular atrophy (SMA), a neurodegenerative disease, is the leading genetic cause of infantile death and is caused by the loss of survival motor neuron 1 (SMN1). Humans carry a duplicated copy gene, SMN2, which produces very low levels of functional protein due to an alternative splicing event.
Monir, Shababi, Christian L, Lorson
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Neurology, 2008
Spinal muscular atrophy (SMA) is the most common fatal genetic disorder of infancy with an estimated population carrier frequency of 1:37, an autosomal recessive pattern of inheritance, and an estimated incidence of 1:6,000 to 1:10,000 live births.1 The genomic region on 5q11-q13, in which the causative survival of motor neuron (SMN) gene was ...
Carsten G. Bönnemann +1 more
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Spinal muscular atrophy (SMA) is the most common fatal genetic disorder of infancy with an estimated population carrier frequency of 1:37, an autosomal recessive pattern of inheritance, and an estimated incidence of 1:6,000 to 1:10,000 live births.1 The genomic region on 5q11-q13, in which the causative survival of motor neuron (SMN) gene was ...
Carsten G. Bönnemann +1 more
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Journal of Magnetism and Magnetic Materials, 1979
Abstract Specific heat results for SmN give clear evidence of magnetic order at 18.2 K. Susceptibility results are less convincing, but indicate an ordering temperature in the range 13–15 K. In neutron diffraction experiments, we have found no evidence of magnetic order at temperatures above 1.6 K.
R.M. Moon, W.C. Koehler
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Abstract Specific heat results for SmN give clear evidence of magnetic order at 18.2 K. Susceptibility results are less convincing, but indicate an ordering temperature in the range 13–15 K. In neutron diffraction experiments, we have found no evidence of magnetic order at temperatures above 1.6 K.
R.M. Moon, W.C. Koehler
openaire +1 more source