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Species-Dependent Posttranscriptional Regulation of NOS1 by FMRP in the Developing Cerebral Cortex.
Kwan KY, Lam MM, Johnson MB, Dube U, Shim S, Rašin MR, Sousa AM, Fertuzinhos S, Chen JG, Arellano JI, Chan DW, Pletikos M, Vasung L, Rowitch DH, Huang EJ, Schwartz ML, Willemsen R, Oostra BA, Rakic P, Heffer M, Kostović I, Judaš M, Sestan N.
Cell. 2012 May 11;149(4):899-911
22579290
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Depression and anxiety symptoms among women who carry the FMR1 premutation: Impact of raising a child with fragile X syndrome is moderated by CRHR1 polymorphisms.
Hunter JE, Leslie M, Novak G, Hamilton D, Shubeck L, Charen K, Abramowitz A, Epstein MP, Lori A, Binder E, Cubells JF, Sherman SL.
Am J Med Genet B Neuropsychiatr Genet. 2012 May 9. doi: 10.1002/ajmg.b.32061. [Epub ahead of print
22573456
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MicroRNA-277 Modulates the Neurodegeneration Caused by Fragile X Premutation rCGG Repeats.
Tan H, Poidevin M, Li H, Chen D, Jin P.
PLoS Genet. 2012 May;8(5):e1002681. Epub 2012 May 3
22570635
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Spontaneous expression of FRA16B in a non-consanguineous couple experiencing multiple fetal losses.
Aswini S, Jegatheesan T, Chandra N.
J Obstet Gynaecol Res. 2012 May 8. doi: 10.1111/j.1447-0756.2012.01850.x. [Epub ahead of print
22564372
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Finiteness Marking in Boys with Fragile X Syndrome.
Sterling AM, Rice ML, Warren SF.
J Speech Lang Hear Res. 2012 May 4. [Epub ahead of print
22562829
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De novo microduplication of the FMR1 gene in a patient with developmental delay, epilepsy and hyperactivity.
Vengoechea J, Parikh AS, Zhang S, Tassone F.
Eur J Hum Genet. 2012 May 2. doi: 10.1038/ejhg.2012.78. [Epub ahead of print
22549406
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Evidence for a fragile x mental retardation protein-mediated translational switch in metabotropic glutamate receptor-triggered arc translation and long-term depression.
Niere F, Wilkerson JR, Huber KM.
J Neurosci. 2012 Apr 25;32(17):5924-36
22539853
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Negative Allosteric Modulation of the mGluR5 Receptor Reduces Repetitive Behaviors and Rescues Social Deficits in Mouse Models of Autism.
Silverman JL, Smith DG, Rizzo SJ, Karras MN, Turner SM, Tolu SS, Bryce DK, Smith DL, Fonseca K, Ring RH, Crawley JN.
Sci Transl Med. 2012 Apr 25;4(131):131ra51
22539775
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A 'learning platform' approach to outcome measurement in fragile X syndrome: a preliminary psychometric study.
Hall SS, Hammond JL, Hirt M, Reiss AL.
J Intellect Disabil Res. 2012 Apr 25. doi: 10.1111/j.1365-2788.2012.01560.x. [Epub ahead of print
22533667
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Systematic mapping of Fragile X granules in the developing mouse brain reveals a potential role for presynaptic FMRP in sensorimotor functions.
Akins MR, Leblanc HF, Stackpole EE, Chyung E, Fallon JR.
J Comp Neurol. 2012 Apr 23. doi: 10.1002/cne.23123. [Epub ahead of print
22522693
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The trouble with spines in fragile X syndrome: density, maturity and plasticity.
He CX, Portera-Cailliau C.
Neuroscience. 2012 Apr 20. [Epub ahead of print
22522472
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Does attention constrain developmental trajectories in fragile x syndrome? A 3-year prospective longitudinal study.
Cornish K, Cole V, Longhi E, Karmiloff-Smith A, Scerif G.
Am J Intellect Dev Disabil. 2012 Mar;117(2):103-20
22515826
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Heart activity and autistic behavior in infants and toddlers with fragile x syndrome.
Roberts JE, Tonnsen B, Robinson A, Shinkareva SV.
Am J Intellect Dev Disabil. 2012 Mar;117(2):90-102
22515825
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Fragile X Protein is required for inhibition of insulin signaling and regulates glial-dependent neuroblast reactivation in the developing brain.
Callan MA, Clements N, Ahrendt N, Zarnescu DC.
Brain Res. 2012 Mar 27. [Epub ahead of print
22513101
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Chronic Pharmacological mGlu5 Inhibition Corrects Fragile X in Adult Mice.
Michalon A, Sidorov M, Ballard TM, Ozmen L, Spooren W, Wettstein JG, Jaeschke G, Bear MF, Lindemann L.
Neuron. 2012 Apr 12;74(1):49-56
22500629
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Fragile X Syndrome Therapeutics S(C)TEP through the Developmental Window.
Bhattacharya A, Klann E.
Neuron. 2012 Apr 12;74(1):1-3
22500622
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AGG interruptions within the maternal FMR1 gene reduce the risk of offspring with fragile X syndrome.
Yrigollen CM, Durbin-Johnson B, Gane L, Nelson DL, Hagerman R, Hagerman PJ, Tassone F.
Genet Med. 2012 Apr 12. doi: 10.1038/gim.2012.34. [Epub ahead of print
22498846
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Severe phenotype in MPS II patients associated with a large deletion including contiguous genes.
Brusius-Facchin AC, De Souza CF, Schwartz IV, Riegel M, Melaragno MI, Correia P, Moraes LM, Llerena J Jr, Giugliani R, Leistner-Segal S.
Am J Med Genet A. 2012 May;158A(5):1055-9. doi: 10.1002/ajmg.a.35271. Epub 2012 Apr 10
22492741
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Fragile X syndrome: mechanistic insights and therapeutic avenues regarding the role of potassium channels.
Lee HY, Jan LY.
Curr Opin Neurobiol. 2012 Apr 5. [Epub ahead of print
22483378
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Fragile X and X-linked intellectual disability: four decades of discovery.
Lubs HA, Stevenson RE, Schwartz CE.
Am J Hum Genet. 2012 Apr 6;90(4):579-90
22482801
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