Sibylle Jablonka

Institute for Clinical Neurobiology, University of Wuerzburg

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JoVE Journal Publications

ArticleTotal : 1	Year
Publication title Cited by 21	2011

Other Publications

Article	Year
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\| PubMed ID: 11773003	2002
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\| PubMed ID: 12091709	2002
A new gene family (FAM9) of low-copy repeats in Xp22.3 expressed exclusively in testis: implications for recombinations in this region. Genomics\| PubMed ID: 12213195	2002
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\| PubMed ID: 12446740	2002
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\| PubMed ID: 12515823	2003
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\| PubMed ID: 14623865	2003
Axonal defects in mouse models of motoneuron disease. Journal of neurobiology\| PubMed ID: 14704958	2004
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\| PubMed ID: 15269181	2004
Bag1 is essential for differentiation and survival of hematopoietic and neuronal cells. Nature neuroscience\| PubMed ID: 16116448	2005
Distinct and overlapping alterations in motor and sensory neurons in a mouse model of spinal muscular atrophy. Human molecular genetics\| PubMed ID: 16396995	2006
Large-scale pathways-based association study in amyotrophic lateral sclerosis. Brain : a journal of neurology\| PubMed ID: 17439985	2007
Defective Ca2+ channel clustering in axon terminals disturbs excitability in motoneurons in spinal muscular atrophy. The Journal of cell biology\| PubMed ID: 17923533	2007
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\| PubMed ID: 17940030	2007
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)\| PubMed ID: 18802676	2009
IGHMBP2 is a ribosome-associated helicase inactive in the neuromuscular disorder distal SMA type 1 (DSMA1). Human molecular genetics\| PubMed ID: 19158098	2009
Valproic acid blocks excitability in SMA type I mouse motor neurons. Neurobiology of disease\| PubMed ID: 19733665	2009
Ciliary neurotrophic factor-induced sprouting preserves motor function in a mouse model of mild spinal muscular atrophy. Human molecular genetics\| PubMed ID: 20022887	2010
Isolation and enrichment of embryonic mouse motoneurons from the lumbar spinal cord of individual mouse embryos. Nature protocols\| PubMed ID: 20057379	2010
Neuromuscular defects and breathing disorders in a new mouse model of spinal muscular atrophy. Neurobiology of disease\| PubMed ID: 20085811	2010
Stiff person syndrome-associated autoantibodies to amphiphysin mediate reduced GABAergic inhibition. Brain : a journal of neurology\| PubMed ID: 20884644	2010
Isolation and characterization of neural stem cells from the neonatal rat cochlear nucleus. Cell and tissue research\| PubMed ID: 21258945	2011
Growth behavior of cochlear nucleus neuronal cells on semiconductor substrates. Journal of biomedical materials research. Part A\| PubMed ID: 21370446	2011
The spinal muscular atrophy disease protein SMN is linked to the Rho-kinase pathway via profilin. Human molecular genetics\| PubMed ID: 21920940	2011
Therapeutic effects of PEGylated insulin-like growth factor I in the pmn mouse model of motoneuron disease. Experimental neurology\| PubMed ID: 21963648	2011