Vicki L McGovern
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Explore the profile of Vicki L McGovern including associated specialties, affiliations and a list of published articles.
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31
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1633
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Recent Articles
1.
Foust K, Wang X, McGovern V, Braun L, Bevan A, Haidet A, et al.
Nat Biotechnol
. 2022 Oct;
40(11):1692.
PMID: 36203015
No abstract available.
2.
Thomsen G, Burghes A, Hsieh C, Do J, Chu B, Perry S, et al.
Nat Med
. 2021 Oct;
27(10):1701-1711.
PMID: 34608334
Spinal muscular atrophy type 1 (SMA1) is a debilitating neurodegenerative disease resulting from survival motor neuron 1 gene (SMN1) deletion/mutation. Onasemnogene abeparvovec (formerly AVXS-101) is a gene therapy that restores...
3.
Blatnik 3rd A, McGovern V, Burghes A
Int J Mol Sci
. 2021 Aug;
22(16).
PMID: 34445199
Proximal spinal muscular atrophy (SMA) is an autosomal recessive neurodegenerative disorder characterized by motor neuron loss and subsequent atrophy of skeletal muscle. SMA is caused by deficiency of the essential...
4.
Kray K, McGovern V, Chugh D, Arnold W, Burghes A
Neurobiol Dis
. 2021 Aug;
159:105488.
PMID: 34425216
Spinal muscular atrophy (SMA) is an autosomal recessive disease characterized by survival motor neuron (SMN) protein deficiency which results in motor neuron loss and muscle atrophy. SMA is caused by...
5.
McGovern V, Kray K, Arnold W, Duque S, Iyer C, Massoni-Laporte A, et al.
Hum Mol Genet
. 2020 Oct;
29(21):3493-3503.
PMID: 33084884
Spinal muscular atrophy is caused by reduced levels of SMN resulting from the loss of SMN1 and reliance on SMN2 for the production of SMN. Loss of SMN entirely is...
6.
Blatnik A, McGovern V, Le T, Iyer C, Kaspar B, Burghes A
Hum Mol Genet
. 2020 Oct;
29(21):3477-3492.
PMID: 33075805
Spinal muscular atrophy (SMA) is caused by mutation or deletion of survival motor neuron 1 (SMN1) and retention of SMN2 leading to SMN protein deficiency. We developed an immortalized mouse...
7.
Ruhno C, McGovern V, Avenarius M, Snyder P, Prior T, Nery F, et al.
Hum Genet
. 2019 Feb;
138(3):241-256.
PMID: 30788592
Spinal muscular atrophy (SMA) is a progressive motor neuron disease caused by loss or mutation of the survival motor neuron 1 (SMN1) gene and retention of SMN2. We performed targeted...
8.
Iyer C, Corlett K, Massoni-Laporte A, Duque S, Madabusi N, Tisdale S, et al.
Hum Mol Genet
. 2018 Jul;
27(19):3404-3416.
PMID: 29982416
Spinal muscular atrophy (SMA) is caused by reduced levels of full-length SMN (FL-SMN). In SMA patients with one or two copies of the Survival Motor Neuron 2 (SMN2) gene there...
9.
Kolb S, Coffey C, Yankey J, Krosschell K, Arnold W, Rutkove S, et al.
Ann Neurol
. 2017 Nov;
82(6):883-891.
PMID: 29149772
Objective: Infantile-onset spinal muscular atrophy (SMA) is the most common genetic cause of infant mortality, typically resulting in death preceding age 2. Clinical trials in this population require an understanding...
10.
Iyer C, Wang X, Renusch S, Duque S, Wehr A, Mo X, et al.
J Neuromuscul Dis
. 2017 Mar;
4(1):59-66.
PMID: 28269795
Background: Spinal Muscular Atrophy (SMA) is an autosomal recessive motor neuron disease that results in loss of spinal motor neurons, muscular weakness and, in severe cases, respiratory failure and death....