Selective vulnerability in neuronal populations in nmd/SMARD1 mice-Reference-Cited by-同舟云学术

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Selective vulnerability in neuronal populations in nmd/SMARD1 mice

Published:2017-12-20 Issue:4 Volume:27 Page:679-690
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Villalón Eric¹²,Shababi Monir¹²,Kline Rachel¹²,Lorson Zachary C¹²,Florea Kyra M¹²,Lorson Christian L¹²

Affiliation:

1. Department of Veterinary Pathobiology, Christopher S. Bond Life Sciences Center, University of Missouri, Columbia, MO 65211, USA

2. Department of Veterinary Pathobiology, College of Veterinary Medicine, University of Missouri, Columbia, MO 65211, USA

Funder

National Institutes of Health

Publisher

Oxford University Press (OUP)

Subject

Genetics(clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/27/4/679/24325943/ddx434.pdf

Reference62 articles.

1. The natural course of infantile spinal muscular atrophy with respiratory distress type 1 (SMARD1);Eckart;Pediatrics,2012

2. Mutations in the gene encoding immunoglobulin mu-binding protein 2 cause spinal muscular atrophy with respiratory distress type 1;Grohmann;Nat. Genet,2001

3. Diaphragmatic spinal muscular atrophy with respiratory distress is heterogeneous, and one form is linked to chromosome 11q13-q21;Grohmann;Am. J. Hum. Genet,1999

4. The wide spectrum of clinical phenotypes of spinal muscular atrophy with respiratory distress type 1: a systematic review;Porro;J. Neurol. Sci,2014

5. Infantile spinal muscular atrophy with respiratory distress type 1 (SMARD1);Grohmann;Ann. Neurol,2003

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1. Clinically relevant mouse models of severe spinal muscular atrophy with respiratory distress type 1;Human Molecular Genetics;2024-08-12

2. The molecular mechanisms that underlie IGHMBP2‐related diseases;Neuropathology and Applied Neurobiology;2024-08

3. Disease Mechanisms and Therapeutic Approaches in SMARD1—Insights from Animal Models and Cell Models;Biomedicines;2024-04-11

4. ABT1 modifies SMARD1 pathology via interactions with IGHMBP2 and stimulation of ATPase and helicase activity;JCI Insight;2023-01-24

5. Functional regeneration of the murine neuromuscular synapse relies on long-lasting morphological adaptations;BMC Biology;2022-07-08

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