Institute for Clinical Neurobiology
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Specific interaction of Smn, the spinal muscular atrophy determining gene product, with hnRNP-R and gry-rbp/hnRNP-Q: a role for Smn in RNA processing in motor axons?
Human molecular genetics Jan, 2002 | Pubmed ID: 11773003
Gene targeting of Gemin2 in mice reveals a correlation between defects in the biogenesis of U snRNPs and motoneuron cell death.
Proceedings of the National Academy of Sciences of the United States of America Jul, 2002 | Pubmed ID: 12091709
A new gene family (FAM9) of low-copy repeats in Xp22.3 expressed exclusively in testis: implications for recombinations in this region.
Genomics Sep, 2002 | Pubmed ID: 12213195
Missense mutation in the tubulin-specific chaperone E (Tbce) gene in the mouse mutant progressive motor neuronopathy, a model of human motoneuron disease.
The Journal of cell biology Nov, 2002 | Pubmed ID: 12446740
A transgene carrying an A2G missense mutation in the SMN gene modulates phenotypic severity in mice with severe (type I) spinal muscular atrophy.
The Journal of cell biology Jan, 2003 | Pubmed ID: 12515823
Smn, the spinal muscular atrophy-determining gene product, modulates axon growth and localization of beta-actin mRNA in growth cones of motoneurons.
The Journal of cell biology Nov, 2003 | Pubmed ID: 14623865
Axonal defects in mouse models of motoneuron disease.
Journal of neurobiology Feb, 2004 | Pubmed ID: 14704958
Characterization of Ighmbp2 in motor neurons and implications for the pathomechanism in a mouse model of human spinal muscular atrophy with respiratory distress type 1 (SMARD1).
Human molecular genetics Sep, 2004 | Pubmed ID: 15269181
Bag1 is essential for differentiation and survival of hematopoietic and neuronal cells.
Nature neuroscience Sep, 2005 | Pubmed ID: 16116448
Distinct and overlapping alterations in motor and sensory neurons in a mouse model of spinal muscular atrophy.
Human molecular genetics Feb, 2006 | Pubmed ID: 16396995
Large-scale pathways-based association study in amyotrophic lateral sclerosis.
Brain : a journal of neurology Sep, 2007 | Pubmed ID: 17439985
Defective Ca2+ channel clustering in axon terminals disturbs excitability in motoneurons in spinal muscular atrophy.
The Journal of cell biology Oct, 2007 | Pubmed ID: 17923533
Adenosine receptor A2A-R contributes to motoneuron survival by transactivating the tyrosine kinase receptor TrkB.
Proceedings of the National Academy of Sciences of the United States of America Oct, 2007 | Pubmed ID: 17940030
Clinical variability in distal spinal muscular atrophy type 1 (DSMA1): determination of steady-state IGHMBP2 protein levels in five patients with infantile and juvenile disease.
Journal of molecular medicine (Berlin, Germany) Jan, 2009 | Pubmed ID: 18802676
IGHMBP2 is a ribosome-associated helicase inactive in the neuromuscular disorder distal SMA type 1 (DSMA1).
Human molecular genetics Apr, 2009 | Pubmed ID: 19158098
Valproic acid blocks excitability in SMA type I mouse motor neurons.
Neurobiology of disease Dec, 2009 | Pubmed ID: 19733665
Ciliary neurotrophic factor-induced sprouting preserves motor function in a mouse model of mild spinal muscular atrophy.
Human molecular genetics Mar, 2010 | Pubmed ID: 20022887
Isolation and enrichment of embryonic mouse motoneurons from the lumbar spinal cord of individual mouse embryos.
Nature protocols , 2010 | Pubmed ID: 20057379
Neuromuscular defects and breathing disorders in a new mouse model of spinal muscular atrophy.
Neurobiology of disease Apr, 2010 | Pubmed ID: 20085811
Stiff person syndrome-associated autoantibodies to amphiphysin mediate reduced GABAergic inhibition.
Brain : a journal of neurology Nov, 2010 | Pubmed ID: 20884644
Isolation and characterization of neural stem cells from the neonatal rat cochlear nucleus.
Cell and tissue research Mar, 2011 | Pubmed ID: 21258945
Growth behavior of cochlear nucleus neuronal cells on semiconductor substrates.
Journal of biomedical materials research. Part A May, 2011 | Pubmed ID: 21370446
The spinal muscular atrophy disease protein SMN is linked to the Rho-kinase pathway via profilin.
Human molecular genetics Dec, 2011 | Pubmed ID: 21920940
Therapeutic effects of PEGylated insulin-like growth factor I in the pmn mouse model of motoneuron disease.
Experimental neurology Dec, 2011 | Pubmed ID: 21963648
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