Literature DB >> 12138998

Spinal muscular atrophy.

Carmen Cifuentes-Diaz1, Tony Frugier, Judith Melki.   

Abstract

Spinal muscular atrophies (SMA) are characterized by degeneration of lower motor neurons associated with muscle paralysis and atrophy. Childhood SMA is a common recessive autosomal disorder and represents one of the most common genetic causes of death in childhood. The pathophysiology remains unknown, and no curative treatment is available so far. The last 10 years have seen major advances in the field of SMA, which are starting points towards understanding the SMA pathogenesis and developing therapeutic strategies for this devastating neurodegenerative disease.

Entities:  

Mesh:

Substances:

Year:  2002        PMID: 12138998     DOI: 10.1053/spen.2002.33801

Source DB:  PubMed          Journal:  Semin Pediatr Neurol        ISSN: 1071-9091            Impact factor:   1.636


  12 in total

1.  The survival of motor neurons protein determines the capacity for snRNP assembly: biochemical deficiency in spinal muscular atrophy.

Authors:  Lili Wan; Daniel J Battle; Jeongsik Yong; Amelie K Gubitz; Stephen J Kolb; Jin Wang; Gideon Dreyfuss
Journal:  Mol Cell Biol       Date:  2005-07       Impact factor: 4.272

2.  Lymphotropic Herpesvirus saimiri uses the SMN complex to assemble Sm cores on its small RNAs.

Authors:  Tracey J Golembe; Jeongsik Yong; Daniel J Battle; Wenqin Feng; Lili Wan; Gideon Dreyfuss
Journal:  Mol Cell Biol       Date:  2005-01       Impact factor: 4.272

3.  Specific sequence features, recognized by the SMN complex, identify snRNAs and determine their fate as snRNPs.

Authors:  Tracey J Golembe; Jeongsik Yong; Gideon Dreyfuss
Journal:  Mol Cell Biol       Date:  2005-12       Impact factor: 4.272

4.  Reduced levels of survival motor neuron protein leads to aberrant motoneuron growth in a Xenopus model of muscular atrophy.

Authors:  Qods Ymlahi-Ouazzani; Odile J Bronchain; Elodie Paillard; Chantal Ballagny; Albert Chesneau; Aurélie Jadaud; André Mazabraud; Nicolas Pollet
Journal:  Neurogenetics       Date:  2009-06-11       Impact factor: 2.660

5.  U1 snRNP protects pre-mRNAs from premature cleavage and polyadenylation.

Authors:  Daisuke Kaida; Michael G Berg; Ihab Younis; Mumtaz Kasim; Larry N Singh; Lili Wan; Gideon Dreyfuss
Journal:  Nature       Date:  2010-09-29       Impact factor: 49.962

6.  Dysregulation of synaptogenesis genes antecedes motor neuron pathology in spinal muscular atrophy.

Authors:  Zhenxi Zhang; Anna Maria Pinto; Lili Wan; Wei Wang; Michael G Berg; Isabela Oliva; Larry N Singh; Christopher Dengler; Zhi Wei; Gideon Dreyfuss
Journal:  Proc Natl Acad Sci U S A       Date:  2013-11-04       Impact factor: 11.205

7.  Using General Anesthesia plus Muscle Relaxant in a Patient with Spinal Muscular Atrophy Type IV: A Case Report.

Authors:  Xiu-Fen Liu; Dong-Xin Wang; Daqing Ma
Journal:  Case Rep Anesthesiol       Date:  2011-10-19

8.  Inactivation of the SMN complex by oxidative stress.

Authors:  Lili Wan; Elizabeth Ottinger; Sungchan Cho; Gideon Dreyfuss
Journal:  Mol Cell       Date:  2008-07-25       Impact factor: 19.328

9.  Drug treatment for spinal muscular atrophy type I.

Authors:  Renske I Wadman; W Ludo van der Pol; Wendy Mj Bosboom; Fay-Lynn Asselman; Leonard H van den Berg; Susan T Iannaccone; Alexander Fje Vrancken
Journal:  Cochrane Database Syst Rev       Date:  2019-12-11

10.  SMN deficiency causes tissue-specific perturbations in the repertoire of snRNAs and widespread defects in splicing.

Authors:  Zhenxi Zhang; Francesco Lotti; Kimberly Dittmar; Ihab Younis; Lili Wan; Mumtaz Kasim; Gideon Dreyfuss
Journal:  Cell       Date:  2008-05-16       Impact factor: 41.582

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.