Pages that link to "Q43569750"

The following pages link to The human centromeric survival motor neuron gene (SMN2) rescues embryonic lethality in Smn(-/-) mice and results in a mouse with spinal muscular atrophy (Q43569750):

Displaying 50 items.

• Alternative splicing events are a late feature of pathology in a mouse model of spinal muscular atrophy (Q21144988) (← links)
• WRAP53 is essential for Cajal body formation and for targeting the survival of motor neuron complex to Cajal bodies (Q21145787) (← links)
• Modeling spinal muscular atrophy in Drosophila (Q21562542) (← links)
• Spinal muscular atrophy disrupts the interaction of ZPR1 with the SMN protein (Q24291073) (← links)
• The splicing regulator Sam68 binds to a novel exonic splicing silencer and functions in SMN2 alternative splicing in spinal muscular atrophy (Q24301061) (← links)
• The zinc finger protein ZPR1 is a potential modifier of spinal muscular atrophy. (Q24307665) (← links)
• SMN interacts with a novel family of hnRNP and spliceosomal proteins (Q24535803) (← links)
• Coilin forms the bridge between Cajal bodies and SMN, the spinal muscular atrophy protein (Q24600358) (← links)
• The contribution of mouse models to understanding the pathogenesis of spinal muscular atrophy (Q24604444) (← links)
• Indoprofen upregulates the survival motor neuron protein through a cyclooxygenase-independent mechanism (Q24613087) (← links)
• A SMN missense mutation complements SMN2 restoring snRNPs and rescuing SMA mice (Q24657021) (← links)
• A functional interaction between the survival motor neuron complex and RNA polymerase II (Q24674951) (← links)
• Copy Number Variations in the Survival Motor Neuron Genes: Implications for Spinal Muscular Atrophy and Other Neurodegenerative Diseases (Q26750803) (← links)
• Molecular Mechanisms of Neurodegeneration in Spinal Muscular Atrophy (Q26752798) (← links)
• Spinal muscular atrophy: development and implementation of potential treatments (Q26861377) (← links)
• Stem cell transplantation for motor neuron disease: current approaches and future perspectives (Q26995278) (← links)
• High expression level of Tra2-β1 is responsible for increased SMN2 exon 7 inclusion in the testis of SMA mice (Q27311317) (← links)
• Oxidative Stress Triggers Body-Wide Skipping of Multiple Exons of the Spinal Muscular Atrophy Gene (Q27312184) (← links)
• Skeletal muscle DNA damage precedes spinal motor neuron DNA damage in a mouse model of Spinal Muscular Atrophy (SMA) (Q27312220) (← links)
• Genetic correction of human induced pluripotent stem cells from patients with spinal muscular atrophy (Q27328843) (← links)
• The spinal muscular atrophy disease protein SMN is linked to the Golgi network (Q27329644) (← links)
• A large animal model of spinal muscular atrophy and correction of phenotype (Q27340106) (← links)
• Spinal Muscular Atrophy (Q28080774) (← links)
• The promise and perils of HDAC inhibitors in neurodegeneration (Q28087539) (← links)
• Exclusion of Htra2-beta1, an up-regulator of full-length SMN2 transcript, as a modifying gene for spinal muscular atrophy (Q28142479) (← links)
• An in vivo reporter system for measuring increased inclusion of exon 7 in SMN2 mRNA: potential therapy of SMA (Q28204816) (← links)
• The survival of motor neurons (SMN) protein interacts with the snoRNP proteins fibrillarin and GAR1 (Q28213183) (← links)
• The benzamide M344, a novel histone deacetylase inhibitor, significantly increases SMN2 RNA/protein levels in spinal muscular atrophy cells (Q28242279) (← links)
• Novel aminoglycosides increase SMN levels in spinal muscular atrophy fibroblasts (Q28261807) (← links)
• SAHA ameliorates the SMA phenotype in two mouse models for spinal muscular atrophy (Q28271235) (← links)
• Early heart failure in the SMNDelta7 model of spinal muscular atrophy and correction by postnatal scAAV9-SMN delivery (Q28288188) (← links)
• Trichostatin A increases SMN expression and survival in a mouse model of spinal muscular atrophy (Q28289793) (← links)
• Cardiac defects contribute to the pathology of spinal muscular atrophy models (Q28290032) (← links)
• Doxycycline-controlled splicing modulation by regulated antisense U7 snRNA expression cassettes (Q28290763) (← links)
• Rescue of a severe mouse model for spinal muscular atrophy by U7 snRNA-mediated splicing modulation (Q28300972) (← links)
• Spinal muscular atrophy: SMN2 pre-mRNA splicing corrected by a U7 snRNA derivative carrying a splicing enhancer sequence (Q28302547) (← links)
• Chondrolectin affects cell survival and neuronal outgrowth in in vitro and in vivo models of spinal muscular atrophy (Q28506113) (← links)
• A comparison of three electrophysiological methods for the assessment of disease status in a mild spinal muscular atrophy mouse model (Q28544408) (← links)
• Smn, the spinal muscular atrophy-determining gene product, modulates axon growth and localization of beta-actin mRNA in growth cones of motoneurons (Q28576647) (← links)
• The critical role of membralin in postnatal motor neuron survival and disease (Q28585103) (← links)
• A role for SMN exon 7 splicing in the selective vulnerability of motor neurons in spinal muscular atrophy (Q28586960) (← links)
• Neuron-specific knock-down of SMN1 causes neuron degeneration and death through an apoptotic mechanism (Q28818674) (← links)
• SMN in spinal muscular atrophy and snRNP biogenesis (Q29013847) (← links)
• Induced pluripotent stem cells from a spinal muscular atrophy patient (Q29614340) (← links)
• A genetic approach to access serotonin neurons for in vivo and in vitro studies. (Q30351712) (← links)
• A novel method for oral delivery of drug compounds to the neonatal SMNDelta7 mouse model of spinal muscular atrophy (Q30488346) (← links)
• Effects of 2,4-diaminoquinazoline derivatives on SMN expression and phenotype in a mouse model for spinal muscular atrophy (Q30492560) (← links)
• miRNA malfunction causes spinal motor neuron disease (Q30495998) (← links)
• Postsymptomatic restoration of SMN rescues the disease phenotype in a mouse model of severe spinal muscular atrophy. (Q30503157) (← links)
• Temporal requirement for SMN in motoneuron development. (Q30540382) (← links)