A Chromatin-Dependent Role of the Fragile X Mental Retardation Protein FMRP in the DNA Damage Response, Cell, vol.157, issue.4, pp.869-81, 2014. ,
DOI : 10.1016/j.cell.2014.03.040
Synaptic Signaling by All-Trans Retinoic Acid in Homeostatic Synaptic Plasticity, Neuron, vol.60, issue.2, pp.60-308, 2008. ,
DOI : 10.1016/j.neuron.2008.08.012
URL : http://doi.org/10.1016/j.neuron.2008.08.012
FMR1 protein: conserved RNP family domains and selective RNA binding, Science, vol.262, issue.5133, pp.563-566, 1993. ,
DOI : 10.1126/science.7692601
Human and murine FMR-1: alternative splicing and translational initiation downstream of the CGG???repeat, Nature Genetics, vol.157, issue.3, pp.244-251, 1993. ,
DOI : 10.1006/abio.1987.9999
Functional Assembly of AMPA and Kainate Receptors Is Mediated by Several Discrete Protein-Protein Interactions, Neuron, vol.31, issue.1, pp.103-113, 2001. ,
DOI : 10.1016/S0896-6273(01)00333-6
Understanding fragile X syndrome: insights from animal models, Cytogenetic and Genome Research, vol.100, issue.1-4, pp.111-123, 2003. ,
DOI : 10.1159/000072845
Fmr1 knockout mice: A model to study Fragile X mental retardation, Cell, vol.78, pp.23-33, 1994. ,
82-FIP, a novel FMRP (Fragile X Mental Retardation Protein) interacting protein, shows a cell cycle-dependent intracellular localization, Human Molecular Genetics, vol.12, issue.14, pp.1689-1698, 2003. ,
DOI : 10.1093/hmg/ddg181
URL : https://academic.oup.com/hmg/article-pdf/12/14/1689/1563429/ddg181.pdf
The mGluR theory of fragile X mental retardation, Trends in Neurosciences, vol.27, issue.7, pp.370-77, 2004. ,
DOI : 10.1016/j.tins.2004.04.009
Redistribution of transcription start sites within the FMR1 promoter region with expansion of the downstream CGG-repeat element, Human Molecular Genetics, vol.13, issue.5, pp.543-592, 2004. ,
DOI : 10.1093/hmg/ddh053
A pilot open label, single dose trial of fenobam in adults with fragile X syndrome, Journal of Medical Genetics, vol.46, issue.4, pp.266-271, 2009. ,
DOI : 10.1136/jmg.2008.063701
Long-lasting potentiation of synaptic transmission in the dentate area of the anaesthetized rabbit following stimulation of the perforant path, The Journal of Physiology, vol.232, issue.2, pp.331-56, 1973. ,
DOI : 10.1113/jphysiol.1973.sp010273
Microarray Identification of FMRP-Associated Brain mRNAs and Altered mRNA Translational Profiles in Fragile X Syndrome, Cell, vol.107, issue.4, pp.477-487, 2001. ,
DOI : 10.1016/S0092-8674(01)00568-2
Sp1 and AP2 transcription factors are required for the human fragile mental retardation promoter activity in SK-N-SH neuronal cells, Neuroscience Letters, vol.276, issue.3, pp.149-152, 1999. ,
DOI : 10.1016/S0304-3940(99)00798-3
Identification of small molecules rescuing fragile X syndrome phenotypes in Drosophila, Nature Chemical Biology, vol.143, issue.4, pp.256-263, 2008. ,
DOI : 10.1038/nchembio.78
Upstream stimulatory factors are mediators of Ca2þ-responsive transcription in neurons, J Neurosci, vol.23, pp.2572-2581, 2003. ,
Prolonged Epileptiform Discharges Induced by Altered Group I Metabotropic Glutamate Receptor-Mediated Synaptic Responses in Hippocampal Slices of a Fragile X Mouse Model, Journal of Neuroscience, vol.25, issue.35, pp.8048-8055, 2005. ,
DOI : 10.1523/JNEUROSCI.1777-05.2005
Role of gene regulation in song circuit development and song learning, Journal of Neurobiology, vol.273, issue.5, pp.549-71, 1997. ,
DOI : 10.1093/icb/31.2.318
Mosaic FMR1 deletion causes Fragile X syndrome and can lead to molecular misdiagnosis: A case report and review of the literature, Am J Med Genet A, vol.146, pp.1358-1367, 2008. ,
Fragile X mental retardation protein has a unique, evolutionarily conserved neuronal function not shared with FXR1P or FXR2P, Disease Models & Mechanisms, vol.3, issue.7-8, pp.471-485, 2010. ,
DOI : 10.1242/dmm.004598
URL : http://dmm.biologists.org/content/dmm/3/7-8/471.full.pdf
Identification of Novel FMR1 Variants by Massively Parallel Sequencing in Developmentally Delayed Males American journal of medical genetics, Part A, vol.152, issue.10, pp.2512-2532, 2010. ,
Antagonism between bicuculline and GABA in the cat brain, Brain Research, vol.33, issue.1, pp.57-73, 1971. ,
DOI : 10.1016/0006-8993(71)90305-2
Advanced transfection with Lipofectamine 2000 reagent: primary neurons, siRNA, and high-throughput applications, Methods, vol.33, issue.2, pp.95-103, 2004. ,
DOI : 10.1016/j.ymeth.2003.11.023
Fragile X Mental Retardation Protein Targets G Quartet mRNAs Important for Neuronal Function, Cell, vol.107, issue.4, pp.489-499, 2001. ,
DOI : 10.1016/S0092-8674(01)00566-9
URL : http://doi.org/10.1016/s0092-8674(01)00566-9
FMRP Stalls Ribosomal Translocation on mRNAs Linked to Synaptic Function and Autism, Cell, vol.146, issue.2, pp.247-261, 2011. ,
DOI : 10.1016/j.cell.2011.06.013
URL : http://doi.org/10.1016/j.cell.2011.06.013
A point mutation in the FMR-1 gene associated with fragile X mental retardation, Nature Genetics, vol.101, issue.1, pp.31-35, 1993. ,
DOI : 10.1016/0092-8674(91)90125-I
NMDA Receptor Activation Dephosphorylates AMPA Receptor Glutamate Receptor 1 Subunits at Threonine 840, Journal of Neuroscience, vol.27, issue.48, pp.13210-13221, 2007. ,
DOI : 10.1523/JNEUROSCI.3056-07.2007
URL : http://www.jneurosci.org/content/jneuro/27/48/13210.full.pdf
Generation and Characterization of Fmr1 Knockout Zebrafish, PLoS ONE, vol.4, issue.11, p.7910, 2009. ,
DOI : 10.1371/journal.pone.0007910.g002
The FMR???1 protein is cytoplasmic, most abundant in neurons and appears normal in carriers of a fragile X premutation, Nature Genetics, vol.11, issue.4, pp.335-340, 1993. ,
DOI : 10.1016/0022-1759(80)90146-5
A Direct Role for FMRP in Activity-Dependent Dendritic mRNA Transport Links Filopodial-Spine Morphogenesis to Fragile X Syndrome, Developmental Cell, vol.14, issue.6, pp.926-939, 2008. ,
DOI : 10.1016/j.devcel.2008.04.003
The fragile X mental retardation protein is a ribonucleoprotein containing both nuclear localization and nuclear export signals, Human Molecular Genetics, vol.5, issue.8, pp.1083-91, 1996. ,
DOI : 10.1093/hmg/5.8.1083
Characterization of Fxr1 in Danio rerio; a simple vertebrate model to study costamere development, Journal of Experimental Biology, vol.207, issue.19, pp.3329-3338, 2004. ,
DOI : 10.1242/jeb.01146
Fragile X protein controls the efficacy of mRNA transport in Drosophila neurons, Molecular and Cellular Neuroscience, vol.39, issue.2, pp.170-179, 2008. ,
DOI : 10.1016/j.mcn.2008.06.012
Fragile X mental retardation protein: Nucleocytoplasmic shuttling and association with somatodendritic ribosomes, J Neurosci, vol.17, pp.1539-1547, 1997. ,
The FMRP regulon: from targets to disease convergence, Frontiers in Neuroscience, vol.7, p.191, 2013. ,
DOI : 10.3389/fnins.2013.00191
Expansion of an FMR1 Grey-Zone Allele to a Full Mutation in Two Generations, The Journal of Molecular Diagnostics, vol.11, issue.4, pp.306-310, 2009. ,
DOI : 10.2353/jmoldx.2009.080174
Signaling Mechanisms Linking Neuronal Activity to Gene Expression and Plasticity of the Nervous System, Annual Review of Neuroscience, vol.31, issue.1, pp.563-590, 2008. ,
DOI : 10.1146/annurev.neuro.31.060407.125631
Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox, Cell, vol.67, issue.6, pp.1047-56, 1991. ,
DOI : 10.1016/0092-8674(91)90283-5
Long-Term Rearrangements of Hippocampal Mossy Fiber Terminal Connectivity in the Adult Regulated by Experience, Neuron, vol.50, issue.5, pp.749-763, 2006. ,
DOI : 10.1016/j.neuron.2006.04.026
Sequence of abnormal dendritic spine development in primary somatosensory cortex of a mouse model of the fragile X mental retardation syndrome, American Journal of Medical Genetics Part A, vol.38, issue.2, pp.155-160, 2005. ,
DOI : 10.1002/ajmg.a.30709
Diseases of Unstable Repeat Expansion: Mechanisms and Common Principles, Nature Reviews Genetics, vol.101, issue.10, pp.743-755, 2005. ,
DOI : 10.1016/S0092-8674(00)80623-6
Preparation of organotypic hippocampal slice cultures for long-term live imaging, Nature Protocols, vol.124, issue.3, pp.1165-71, 2006. ,
DOI : 10.1038/nprot.2006.168
Synaptic regulation of protein synthesis and the fragile X protein, Proceedings of the National Academy of Sciences, vol.94, issue.10, pp.7101-7107, 2001. ,
DOI : 10.1073/pnas.94.10.5401
Effect of folic acid treatment in the fragile X syndrome, Clinical Genetics, vol.5, issue.5, pp.463-467, 1985. ,
DOI : 10.1111/j.1399-0004.1985.tb00196.x
Fragile X syndrome: from gene discovery to therapy, Frontiers in Bioscience, vol.16, issue.1, pp.1211-1243, 2011. ,
DOI : 10.2741/3785
Molecular architecture and dynamics of the neuronal cytoskeleton, pp.5-74, 1991. ,
Tissue specific expression of FMR???1 provides evidence for a functional role in fragile X syndrome, Nature Genetics, vol.28, issue.1, pp.36-43, 1993. ,
DOI : 10.1016/0006-3223(90)90652-I
Analysis of neocortex in three males with the fragile X syndrome, American Journal of Medical Genetics, vol.38, issue.3, pp.289-294, 1991. ,
DOI : 10.1001/archneur.1980.00500610029003
Sp1 transcription factor binds DNA and activates transcription even when the binding site is CpG methylated., Genes & Development, vol.2, issue.9, pp.1127-1162, 1988. ,
DOI : 10.1101/gad.2.9.1127
Role for Rapid Dendritic Protein Synthesis in Hippocampal mGluR-Dependent Long-Term Depression, Science, vol.288, issue.5469, pp.1254-1256, 2000. ,
DOI : 10.1126/science.288.5469.1254
Altered synaptic plasticity in a mouse model of fragile X mental retardation, Proceedings of the National Academy of Sciences, vol.79, issue.2, pp.7746-7750, 2002. ,
DOI : 10.1515/REVNEURO.2001.12.2.121
In Vitro DNA Methylation Inhibits FMR-1 Promoter, Biochemical and Biophysical Research Communications, vol.193, issue.1, pp.324-329, 1993. ,
DOI : 10.1006/bbrc.1993.1627
Dendritic spine and dendritic field characteristics of layer V pyramidal neurons in the visual cortex of fragile-X knockout mice, American Journal of Medical Genetics, vol.38, issue.2, pp.140-146, 2002. ,
DOI : 10.1002/ajmg.10500
Understanding the molecular basis of fragile X syndrome, Human Molecular Genetics, vol.9, issue.6, pp.901-908, 2003. ,
DOI : 10.1093/hmg/9.6.901
Biochemical and genetic interaction between the fragile X mental retardation protein and the microRNA pathway, Nature Neuroscience, vol.7, issue.2, pp.113-117, 2004. ,
DOI : 10.1038/nn1174
Synaptic Activity and the Construction of Cortical Circuits, Science, vol.274, issue.5290, pp.1133-1138, 1996. ,
DOI : 10.1126/science.274.5290.1133
Molecular phenotype of Fragile X syndrome: FMRP, FXRPs, and protein targets, Microscopy Research and Technique, vol.84, issue.3, pp.135-144, 2002. ,
DOI : 10.1002/(SICI)1096-8628(19990528)84:3<268::AID-AJMG20>3.0.CO;2-#
A heterogeneous set of FMR1 proteins is widely distributed in mouse tissues and is modulated in cell culture, Human Molecular Genetics, vol.4, issue.5, pp.783-789, 1995. ,
DOI : 10.1093/hmg/4.5.783
Novel isoforms of the fragile X related protein FXR1P are expressed during myogenesis, Human Molecular Genetics, vol.7, issue.13, pp.2121-2149, 1998. ,
DOI : 10.1093/hmg/7.13.2121
Biology of the fragile X mental retardation protein, an RNA-binding protein, Biochemistry and Cell Biology, vol.77, issue.4, pp.331-342, 1999. ,
DOI : 10.1139/o99-035
RNA and protein synthesis in relation to neural function. A study of the neurobiological activity of actinomycin D in cat spinal cord, Trans Am Neurol Assoc, vol.92, pp.250-252, 1967. ,
Interaction of the Transcription Factors USF1, USF2, and ??-Pal/Nrf-1 with the FMR1 Promoter, Journal of Biological Chemistry, vol.269, issue.6, pp.4357-64, 2001. ,
DOI : 10.1093/hmg/8.12.2317
Species-Dependent Posttranscriptional Regulation of NOS1 by FMRP in the Developing Cerebral Cortex, Cell, vol.149, issue.4, pp.899-911, 2012. ,
DOI : 10.1016/j.cell.2012.02.060
Potential therapeutic interventions for fragile X syndrome, Trends in Molecular Medicine, vol.16, issue.11, pp.16-516, 2010. ,
DOI : 10.1016/j.molmed.2010.08.005
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2981507
AFQ056, a new mGluR5 antagonist for treatment of fragile X syndrome, Neurobiology of Disease, vol.42, issue.3, pp.311-317, 2011. ,
DOI : 10.1016/j.nbd.2011.01.022
Regulating fragile X gene transcription in the brain and beyond, Journal of Cellular Physiology, vol.381, issue.2, pp.170-75, 2005. ,
DOI : 10.1128/MCB.10.11.5883
CTEP: A Novel, Potent, Long-Acting, and Orally Bioavailable Metabotropic Glutamate Receptor 5 Inhibitor, Journal of Pharmacology and Experimental Therapeutics, vol.339, issue.2, pp.474-486, 2011. ,
DOI : 10.1124/jpet.111.185660
URL : http://jpet.aspetjournals.org/content/jpet/339/2/474.full.pdf
Tdrd3 is a novel stress granule-associated protein interacting with the Fragile-X syndrome protein FMRP, Human Molecular Genetics, vol.17, issue.20, pp.3236-3246, 2008. ,
DOI : 10.1093/hmg/ddn219
A marker X chromosome, Am J Hum Genet, vol.3, pp.231-275, 1969. ,
Intragenic loss of function mutations demonstrate the primary role of FMR1 in fragile X syndrome, Nature Genetics, vol.2, issue.4, pp.483-488, 1995. ,
DOI : 10.1016/0092-8674(94)90232-1
A PEDIGREE OF MENTAL DEFECT SHOWING SEX-LINKAGE, Journal of Neurology, Neurosurgery & Psychiatry, vol.6, issue.3-4, pp.154-157, 1943. ,
DOI : 10.1136/jnnp.6.3-4.154
Instability of a 550-base pair DNA segment and abnormal methylation in Fragile X syndrome, Science, vol.252, pp.1097-1102, 1991. ,
The C Terminus of Fragile X Mental Retardation Protein Interacts with the Multi-domain Ran-binding Protein in the Microtubule-organising Centre, Journal of Molecular Biology, vol.343, issue.1, pp.43-53, 2004. ,
DOI : 10.1016/j.jmb.2004.08.024
RNA Cargoes Associating with FMRP Reveal Deficits in Cellular Functioning in Fmr1 Null Mice, Neuron, vol.37, issue.3, pp.417-431, 2003. ,
DOI : 10.1016/S0896-6273(03)00034-5
Audiogenic Seizures Susceptibility in Transgenic Mice with Fragile X Syndrome, Epilepsia, vol.17, issue.1, pp.19-23, 2000. ,
DOI : 10.1128/MCB.16.7.3825
URL : http://onlinelibrary.wiley.com/doi/10.1111/j.1528-1157.2000.tb01499.x/pdf
The Fragile X Syndrome Protein Represses Activity-Dependent Translation through CYFIP1, a New 4E-BP, Cell, vol.134, issue.6, pp.1042-1054, 2008. ,
DOI : 10.1016/j.cell.2008.07.031
The Unstable Repeats???Three Evolving Faces of Neurological Disease, Neuron, vol.77, issue.5, pp.825-843, 2013. ,
DOI : 10.1016/j.neuron.2013.02.022
The role of GABA in the pathophysiology and treatment of anxiety disorders, Psychopharmacol Bull, vol.37, issue.4, pp.133-179, 2003. ,
Tetrodotoxin (TTX) as a Therapeutic Agent for Pain, Marine Drugs, vol.18, issue.12, pp.281-305, 2012. ,
DOI : 10.3747/co.v18i3.732
URL : http://www.mdpi.com/1660-3397/10/2/281/pdf
Biolistic transfection of neuronal cultures using a hand-held gene gun, Nature Protocols, vol.16, issue.2, pp.977-81, 2006. ,
DOI : 10.1073/pnas.0404712102
Absence of expression of the FMR-1 gene in fragile X syndrome, Cell, vol.66, issue.4, pp.817-822, 1991. ,
DOI : 10.1016/0092-8674(91)90125-I
Fragile X syndrome: a preclinical review on metabotropic glutamate receptor 5 (mGluR5) antagonists and drug development, Psychopharmacology, vol.107, issue.6, pp.1217-1243, 2013. ,
DOI : 10.1016/S0092-8674(01)00589-X
Mechanism of transcriptional activation by Sp1: Evidence for coactivators, Cell, vol.61, issue.7, pp.1187-1197, 1990. ,
DOI : 10.1016/0092-8674(90)90683-6
Role of microRNA Pathway in Mental Retardation, The Scientific World JOURNAL, vol.7, pp.146-54, 2007. ,
DOI : 10.1100/tsw.2007.208
Pharmacology of catamenial epilepsy, Methods and Findings in Experimental and Clinical Pharmacology, vol.26, issue.7, pp.547-61, 2004. ,
DOI : 10.1358/mf.2004.26.7.863737
A highly conserved protein family interacting with the fragile X mental retardation protein (FMRP) and displaying selective interactions with FMRP-related proteins FXR1P and FXR2P, Proceedings of the National Academy of Sciences, vol.10, issue.4, pp.8844-8849, 2001. ,
DOI : 10.1093/hmg/10.4.329
Glycine-induced changes in synaptic efficacy in hippocampal slices involve changes in AMPA receptors, Brain Research, vol.627, issue.2, pp.261-267, 1993. ,
DOI : 10.1016/0006-8993(93)90329-L
Fragile X mental retardation protein is required for chemically-induced long-term potentiation of the hippocampus in adult mice, Journal of Neurochemistry, vol.25, issue.3, pp.635-681, 2009. ,
DOI : 10.1126/science.288.5469.1254
Next-generation DNA sequencing, Nature Biotechnology, vol.105, issue.10, pp.1135-1180, 2008. ,
DOI : 10.1101/gr.8.3.175
Rapid Spine Delivery and Redistribution of AMPA Receptors After Synaptic NMDA Receptor Activation, Science, vol.284, issue.5421, pp.1811-1816, 1999. ,
DOI : 10.1126/science.284.5421.1811
Identification of a Signaling Pathway Involved in Calcium Regulation of BDNF Expression, Neuron, vol.20, issue.4, pp.727-740, 1998. ,
DOI : 10.1016/S0896-6273(00)81011-9
The protein product of the fragile X gene, FMR1, has characteristics of an RNA-binding protein, Cell, vol.74, issue.2, pp.291-298, 1993. ,
DOI : 10.1016/0092-8674(93)90420-U
Occupancy and synergistic activation of the FMR1 promoter by Nrf-1 and Sp1 in vivo, Human Molecular Genetics, vol.13, issue.15, pp.1611-1632, 2004. ,
DOI : 10.1093/hmg/ddh172
Fragile sites on human chromosomes: demonstration of their dependence on the type of tissue culture medium, Science, vol.197, issue.4300, pp.265-266, 1977. ,
DOI : 10.1126/science.877551
Differential expression of FMR1, FXR1 and FXR2 proteins in human brain and testis, Human Molecular Genetics, vol.6, issue.8, pp.1315-1322, 1997. ,
DOI : 10.1093/hmg/6.8.1315
Altered maturation of the primary somatosensory cortex in a mouse model of fragile X syndrome, Human Molecular Genetics, vol.21, issue.10, pp.2143-2156, 2012. ,
DOI : 10.1093/hmg/dds030
Expression of three zebrafish orthologs of human FMR1-related genes and their phylogenetic relationships, Development Genes and Evolution, vol.14, issue.11, pp.567-574, 2004. ,
DOI : 10.1007/s00427-004-0438-9
Characterization and localization of the FMR-1 gene product associated with fragile X syndrome, Nature, vol.363, issue.6431, pp.722-724, 1993. ,
DOI : 10.1038/363722a0
Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome, Cell, vol.65, issue.5, pp.905-914, 1991. ,
DOI : 10.1016/0092-8674(91)90397-H
La depression synaptique à long terme: un mécanisme pour la mémoire et l'apprentissage au niveau du cervelet, Médecine sciences, pp.437-441, 2003. ,
Characterization of dFMR1, a Drosophila melanogaster Homolog of the Fragile X Mental Retardation Protein, Molecular and Cellular Biology, vol.20, issue.22, pp.8536-8547, 2000. ,
DOI : 10.1128/MCB.20.22.8536-8547.2000
Isolation of the human chromosomal band Xq28 within somatic cell hybrids by fragile X site breakage., Proceedings of the National Academy of Sciences, vol.87, issue.10, 1990. ,
DOI : 10.1073/pnas.87.10.3856
Metabotropic glutamate receptors trigger postsynaptic protein synthesis., Proc. Natl. Acad. Sci. USA 99, pp.1639-1644, 1993. ,
DOI : 10.1073/pnas.90.15.7168
URL : https://www.ncbi.nlm.nih.gov/pmc/articles/PMC47097/pdf
Calcium regulation of neuronal gene expression, Proc. Natl. Acad. Sci. USA 98, pp.11024-11031, 2001. ,
DOI : 10.1016/S0896-6273(00)81011-9
Preparation of Gene Gun Bullets and Biolistic Transfection of Neurons in Slice Culture, Journal of Visualized Experiments, vol.experiments, issue.12, pp.3-6, 2008. ,
DOI : 10.3791/675
A new function for the fragile X mental retardation protein in regulation of PSD-95 mRNA stability, Nature Neuroscience, vol.165, issue.5, pp.578-587, 2007. ,
DOI : 10.1016/j.schres.2005.07.003
The Fragile X Syndrome Protein FMRP Associates with BC1 RNA and Regulates the Translation of Specific mRNAs at Synapses, Cell, vol.112, issue.3, pp.317-327, 2003. ,
DOI : 10.1016/S0092-8674(03)00079-5
Whole-brain expression analysis of FMRP in adult monkey and its relationship to cognitive deficits in fragile X syndrome, Brain Research, vol.1264, pp.76-84, 2009. ,
DOI : 10.1016/j.brainres.2009.01.059
The Fragile X mental retardation syndrome protein interacts with novel homologs FXR1 and FXR2, EMBO J, vol.14, pp.5358-5366, 1995. ,
Mice deficient for BMP2 are nonviable and have defects in amnion/chorion and cardiac development, Development, vol.122, pp.2977-2986, 1996. ,
Drosophila Fragile X-Related Gene Regulates the MAP1B Homolog Futsch to Control Synaptic Structure and Function, Cell, vol.107, issue.5, pp.591-603, 2001. ,
DOI : 10.1016/S0092-8674(01)00589-X
URL : http://doi.org/10.1016/s0092-8674(01)00589-x
The Drosophila fragile X-related gene regulates axoneme differentiation during spermatogenesis, Developmental Biology, vol.270, issue.2, pp.290-307, 2004. ,
DOI : 10.1016/j.ydbio.2004.02.010
URL : http://doi.org/10.1016/j.ydbio.2004.02.010
SnapShot: Ca2+-Dependent Transcription in Neurons, Cell, vol.134, issue.6, 2008. ,
DOI : 10.1016/j.cell.2008.09.010
URL : http://doi.org/10.1016/j.cell.2008.09.010