Literature DB >> 12200622

Motoneuron death in normal and spinal muscular atrophy-affected human fetuses.

Anna Fidziańska1, Janina Rafalowska.   

Abstract

The onset and sequence of motoneuron death in the lumbar part of spinal cord of seven control and five affected fetuses carrying deletion of exon 7 in the SMN gene were studied by light and electron microscopy. Naturally occurring motoneuron death in control fetuses was detected between 8 and 13 weeks of gestation. In affected fetuses motoneuron death was prolonged and also observed at 16 and 20 weeks of gestation. In addition, motoneurons in the affected fetuses displayed nuclear abnormalities as early as 16 weeks of gestation and the changes progressed as the affected fetuses developed and can be considered first signs of motoneuron degeneration.

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Year:  2002        PMID: 12200622     DOI: 10.1007/s00401-002-0566-0

Source DB:  PubMed          Journal:  Acta Neuropathol        ISSN: 0001-6322            Impact factor:   17.088


  7 in total

1.  Onasemnogene abeparvovec for presymptomatic infants with two copies of SMN2 at risk for spinal muscular atrophy type 1: the Phase III SPR1NT trial.

Authors:  Kevin A Strauss; Michelle A Farrar; Francesco Muntoni; Kayoko Saito; Jerry R Mendell; Laurent Servais; Hugh J McMillan; Richard S Finkel; Kathryn J Swoboda; Jennifer M Kwon; Craig M Zaidman; Claudia A Chiriboga; Susan T Iannaccone; Jena M Krueger; Julie A Parsons; Perry B Shieh; Sarah Kavanagh; Sitra Tauscher-Wisniewski; Bryan E McGill; Thomas A Macek
Journal:  Nat Med       Date:  2022-06-17       Impact factor: 87.241

Review 2.  Spinal muscular atrophy: a motor neuron disorder or a multi-organ disease?

Authors:  Monir Shababi; Christian L Lorson; Sabine S Rudnik-Schöneborn
Journal:  J Anat       Date:  2013-07-22       Impact factor: 2.610

3.  Survival motor neuron protein regulates apoptosis in an in vitro model of spinal muscular atrophy.

Authors:  Graham C Parker; Xingli Li; Roumen A Anguelov; Gabor Toth; Adam Cristescu; Gyula Acsadi
Journal:  Neurotox Res       Date:  2008-01       Impact factor: 3.911

Review 4.  The BMP signaling pathway at the Drosophila neuromuscular junction and its links to neurodegenerative diseases.

Authors:  Vafa Bayat; Manish Jaiswal; Hugo J Bellen
Journal:  Curr Opin Neurobiol       Date:  2010-09-09       Impact factor: 6.627

5.  Ultrastructural characterization of peripheral denervation in a mouse model of Type III spinal muscular atrophy.

Authors:  Federica Fulceri; Francesca Biagioni; Fiona Limanaqi; Carla L Busceti; Larisa Ryskalin; Paola Lenzi; Francesco Fornai
Journal:  J Neural Transm (Vienna)       Date:  2021-05-17       Impact factor: 3.575

6.  Modeling the early phenotype at the neuromuscular junction of spinal muscular atrophy using patient-derived iPSCs.

Authors:  Michiko Yoshida; Shiho Kitaoka; Naohiro Egawa; Mayu Yamane; Ryunosuke Ikeda; Kayoko Tsukita; Naoki Amano; Akira Watanabe; Masafumi Morimoto; Jun Takahashi; Hajime Hosoi; Tatsutoshi Nakahata; Haruhisa Inoue; Megumu K Saito
Journal:  Stem Cell Reports       Date:  2015-03-19       Impact factor: 7.765

7.  Functional Abnormalities of Cerebellum and Motor Cortex in Spinal Muscular Atrophy Mice.

Authors:  Arumugarajah Tharaneetharan; Madison Cole; Brandon Norman; Nayeli C Romero; Julian R A Wooltorton; Melissa A Harrington; Jianli Sun
Journal:  Neuroscience       Date:  2020-11-17       Impact factor: 3.590

  7 in total

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