Related references
Note: Only part of the references are listed.Drosophila SMN complex proteins Gemin2, Gemin3, and Gemin5 are components of U bodies
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EXPERIMENTAL CELL RESEARCH (2010)
SMN deficiency disrupts brain development in a mouse model of severe spinal muscular atrophy
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HUMAN MOLECULAR GENETICS (2010)
Drosophila type II neuroblast lineages keep Prospero levels low to generate large clones that contribute to the adult brain central complex
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DEVELOPMENT (2009)
The spinal muscular atrophy protein SMN affects Drosophila germline nuclear organization through the U body-P body pathway
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DEVELOPMENTAL BIOLOGY (2009)
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MOLECULAR BIOLOGY OF THE CELL (2009)
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MOLECULAR BIOLOGY OF THE CELL (2009)
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NATURE REVIEWS NEUROSCIENCE (2009)
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PLOS ONE (2009)
Alternative Splicing Events Are a Late Feature of Pathology in a Mouse Model of Spinal Muscular Atrophy
Dirk Baeumer et al.
PLOS GENETICS (2009)
Congenital heart defects in spinal muscular atrophy type I: A clinical report of two siblings and a review of the literature
Leonie A. Menke et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2008)
Temporal transcription factors and their targets schedule the end of neural proliferation in Drosophila
Cedric Maurange et al.
CELL (2008)
Tissue-specific splicing factor gene expression signatures
Ana Rita Grosso et al.
NUCLEIC ACIDS RESEARCH (2008)
Modeling Spinal Muscular Atrophy in Drosophila
Howard Chia-Hao Chang et al.
PLOS ONE (2008)
Evolution of an RNP assembly system:: A minimal SMN complex facilitates formation of UsnRNPs in Drosophila melanogaster
Matthias Kroiss et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2008)
A Motor Function for the DEAD-Box RNA Helicase, Gemin3, in Drosophila
Ruben J. Cauchi et al.
PLOS GENETICS (2008)
Congenital heart disease is a feature of severe infantile spinal muscular atrophy
S. Rudnik-Schoeneborn et al.
JOURNAL OF MEDICAL GENETICS (2008)
Molecular mechanisms of spinal muscular atrophy
Charlotte J. Sumner
JOURNAL OF CHILD NEUROLOGY (2007)
U bodies are cytoplasmic structures that contain uridine-rich small nuclear ribonucleoproteins and associate with P bodies
Ji-Long Liu et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2007)
Male and female Drosophila germline stem cells:: Two versions of immortality
Margaret T. Fuller et al.
SCIENCE (2007)
A Drosophila melanogaster model of spinal muscular atrophy reveals a function for SMN in striated muscle
T. K. Rajendra et al.
JOURNAL OF CELL BIOLOGY (2007)
Neonatal spinal muscular atrophy type I with bone fractures and heart defect
Eve Vaidla et al.
JOURNAL OF CHILD NEUROLOGY (2007)
Prospero acts as a binary switch between self-renewal and differentiation in Drosophila neural stem cells
Semil P. Choksi et al.
DEVELOPMENTAL CELL (2006)
The Drosophila melanogaster Cajal body
JL Liu et al.
JOURNAL OF CELL BIOLOGY (2006)
The activity of the spinal muscular atrophy protein is regulated during development and cellular differentiation
F Gabanella et al.
HUMAN MOLECULAR GENETICS (2005)
Regulation of post-embryonic neuroblasts by Drosophila Grainyhead
MS Almeida et al.
MECHANISMS OF DEVELOPMENT (2005)
Reduced U snRNP assembly causes motor axon degeneration in an animal model for spinal muscular atrophy
C Winkler et al.
GENES & DEVELOPMENT (2005)
Neonatal spinal muscular atrophy with multiple contractures, bone fractures, respiratory insufficiency and 5q13 deletion
MA García-Cabezas et al.
ACTA NEUROPATHOLOGICA (2004)
rigor mortis encodes a novel nuclear receptor interacting protein required for ecdysone signaling during Drosophila larval development
J Gates et al.
DEVELOPMENT (2004)
Smn, the spinal muscular atrophy-determining gene product, modulates axon growth and localization of β-actin mRNA in growth cones of motoneurons
W Rossoll et al.
JOURNAL OF CELL BIOLOGY (2003)
Neuromuscular defects in a Drosophila survival motor neuron gene mutant
YB Chan et al.
HUMAN MOLECULAR GENETICS (2003)
Classical infantile spinal muscular atrophy with SMN deficiency causes sensory neuronopathy
S Rudnik-Schöneborn et al.
NEUROLOGY (2003)
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?
W Rossoll et al.
HUMAN MOLECULAR GENETICS (2002)
Mosaic analysis with a repressible cell marker (MARCM) for Drosophila neural development
TM Lee et al.
TRENDS IN NEUROSCIENCES (2001)
Disruption of SMN function by ectopic expression of the human SMN gene in Drosophila
I Miguel-Aliaga et al.
FEBS LETTERS (2000)
An exonic enhancer is required for inclusion of an essential exon in the SMA-determining gene SMN
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HUMAN MOLECULAR GENETICS (2000)