Literature DB >> 22909818

Down syndrome DSCR1 causes spine pathology via the Fragile X-related protein FMRP.

Francesco Roselli1.   

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Year:  2012        PMID: 22909818      PMCID: PMC3442279          DOI: 10.1038/emboj.2012.239

Source DB:  PubMed          Journal:  EMBO J        ISSN: 0261-4189            Impact factor:   11.598


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  10 in total

1.  Over-expression of RCAN1 causes Down syndrome-like hippocampal deficits that alter learning and memory.

Authors:  Katherine R Martin; Alicia Corlett; Daphne Dubach; Tomris Mustafa; Harold A Coleman; Helena C Parkington; Tobias D Merson; James A Bourne; Sílvia Porta; Maria L Arbonés; David I Finkelstein; Melanie A Pritchard
Journal:  Hum Mol Genet       Date:  2012-04-17       Impact factor: 6.150

2.  Reversible inhibition of PSD-95 mRNA translation by miR-125a, FMRP phosphorylation, and mGluR signaling.

Authors:  Ravi S Muddashetty; Vijayalaxmi C Nalavadi; Christina Gross; Xiaodi Yao; Lei Xing; Oskar Laur; Stephen T Warren; Gary J Bassell
Journal:  Mol Cell       Date:  2011-06-10       Impact factor: 17.970

3.  Hypersensitivity to mGluR5 and ERK1/2 leads to excessive protein synthesis in the hippocampus of a mouse model of fragile X syndrome.

Authors:  Emily K Osterweil; Dilja D Krueger; Kimberly Reinhold; Mark F Bear
Journal:  J Neurosci       Date:  2010-11-17       Impact factor: 6.167

4.  Reversal of learning deficits in a Tsc2+/- mouse model of tuberous sclerosis.

Authors:  Dan Ehninger; Sangyeul Han; Carrie Shilyansky; Yu Zhou; Weidong Li; David J Kwiatkowski; Vijaya Ramesh; Alcino J Silva
Journal:  Nat Med       Date:  2008-06-22       Impact factor: 53.440

5.  DSCR1 interacts with FMRP and is required for spine morphogenesis and local protein synthesis.

Authors:  Wei Wang; John Z Zhu; Karen T Chang; Kyung-Tai Min
Journal:  EMBO J       Date:  2012-08-03       Impact factor: 11.598

Review 6.  Molecular genetic analysis of Down syndrome.

Authors:  David Patterson
Journal:  Hum Genet       Date:  2009-06-13       Impact factor: 4.132

7.  Chronic pharmacological mGlu5 inhibition corrects fragile X in adult mice.

Authors:  Aubin Michalon; Michael Sidorov; Theresa M Ballard; Laurence Ozmen; Will Spooren; Joseph G Wettstein; Georg Jaeschke; Mark F Bear; Lothar Lindemann
Journal:  Neuron       Date:  2012-04-12       Impact factor: 17.173

8.  Disrupted Homer scaffolds mediate abnormal mGluR5 function in a mouse model of fragile X syndrome.

Authors:  Jennifer A Ronesi; Katie A Collins; Seth A Hays; Nien-Pei Tsai; Weirui Guo; Shari G Birnbaum; Jia-Hua Hu; Paul F Worley; Jay R Gibson; Kimberly M Huber
Journal:  Nat Neurosci       Date:  2012-01-22       Impact factor: 24.884

9.  Mutations causing syndromic autism define an axis of synaptic pathophysiology.

Authors:  Benjamin D Auerbach; Emily K Osterweil; Mark F Bear
Journal:  Nature       Date:  2011-11-23       Impact factor: 49.962

10.  Defining mechanisms of actin polymerization and depolymerization during dendritic spine morphogenesis.

Authors:  Pirta Hotulainen; Olaya Llano; Sergei Smirnov; Kimmo Tanhuanpää; Jan Faix; Claudio Rivera; Pekka Lappalainen
Journal:  J Cell Biol       Date:  2009-04-20       Impact factor: 10.539

  10 in total
  3 in total

1.  The effect of early life status epilepticus on ultrasonic vocalizations in mice.

Authors:  Conner D Reynolds; Gregory Smith; Taylor Jefferson; Joaquin N Lugo
Journal:  Epilepsia       Date:  2016-07-05       Impact factor: 5.864

2.  DAP5 increases axonal outgrowth of hippocampal neurons by enhancing the cap-independent translation of DSCR1.4 mRNA.

Authors:  Ji-Young Seo; Youngseob Jung; Do-Yeon Kim; Hye Guk Ryu; Juhyun Lee; Sung Wook Kim; Kyong-Tai Kim
Journal:  Cell Death Dis       Date:  2019-01-18       Impact factor: 8.469

3.  Association Between DSCR1 Variations and Congenital Heart Disease Susceptibility.

Authors:  Ren Yu Guo; Xiao Feng Li; Song Bai; Jian Guo; Nan Ding; Zhong Zhi Li
Journal:  Med Sci Monit       Date:  2015-11-16
  3 in total

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