Rene C, Parks R
Sci Rep. 2025; 15(1):5674.
PMID: 39955442
PMC: 11830090.
DOI: 10.1038/s41598-025-90083-3.
Morrey J, Siddharthan V, Wang H, Oliveira A, Susuki K, Kaundal R
Sci Rep. 2025; 15(1):2926.
PMID: 39848964
PMC: 11757732.
DOI: 10.1038/s41598-025-86475-0.
Zhang W, Yin Y, Yang D, Liu M, Ye C, Yan R
Front Pharmacol. 2025; 15():1475884.
PMID: 39840097
PMC: 11747325.
DOI: 10.3389/fphar.2024.1475884.
Davie J, Sattarifard H, Sudhakar S, Roberts C, Beacon T, Muker I
Subcell Biochem. 2025; 108():1-49.
PMID: 39820859
DOI: 10.1007/978-3-031-75980-2_1.
Allison R, Mangione C, Suneja M, Gawrys J, Melvin B, Belous N
Mol Ther. 2024; 33(2):734-751.
PMID: 39673131
PMC: 11853362.
DOI: 10.1016/j.ymthe.2024.12.016.
Analysis of the serum proteome profile of wild stump-tailed macaques () seropositive for Zika virus antibodies in Thailand.
Ruengket P, Roytrakul S, Tongthainan D, Boonnak K, Taruyanon K, Sangkharak B
Front Vet Sci. 2024; 11:1463160.
PMID: 39600882
PMC: 11588686.
DOI: 10.3389/fvets.2024.1463160.
SMN Deficiency Induces an Early Non-Atrophic Myopathy with Alterations in the Contractile and Excitatory Coupling Machinery of Skeletal Myofibers in the SMN∆7 Mouse Model of Spinal Muscular Atrophy.
Berciano M, Gatius A, Puente-Bedia A, Rufino-Gomez A, Tarabal O, Rodriguez-Rey J
Int J Mol Sci. 2024; 25(22).
PMID: 39596480
PMC: 11595111.
DOI: 10.3390/ijms252212415.
MicroRNAs as Biomarkers in Spinal Muscular Atrophy.
Barbo M, Glavac D, Jezernik G, Ravnik-Glavac M
Biomedicines. 2024; 12(11).
PMID: 39594995
PMC: 11592373.
DOI: 10.3390/biomedicines12112428.
Evaluating the clinical efficacy of a long-read sequencing-based approach for carrier screening of spinal muscular atrophy.
Long J, Cui D, Yu C, Meng W
Hum Genomics. 2024; 18(1):110.
PMID: 39343938
PMC: 11440943.
DOI: 10.1186/s40246-024-00676-8.
Recent Progress in Gene-Targeting Therapies for Spinal Muscular Atrophy: Promises and Challenges.
Haque U, Yokota T
Genes (Basel). 2024; 15(8).
PMID: 39202360
PMC: 11353366.
DOI: 10.3390/genes15080999.
The Impact of Comorbidities and Motor Impairment on the Quality of Life of Patients with Spinal Muscular Atrophy: A Case-Control Study.
Blauciak M, Ubysz J, Pokryszko-Dragan A, Koszewicz M
J Clin Med. 2024; 13(14).
PMID: 39064224
PMC: 11277901.
DOI: 10.3390/jcm13144184.
Rare Variants of the Gene Detected during Neonatal Screening.
Akhkiamova M, Polyakov A, Marakhonov A, Voronin S, Saifullina E, Vafina Z
Genes (Basel). 2024; 15(7).
PMID: 39062735
PMC: 11275604.
DOI: 10.3390/genes15070956.
Therapeutic strategy for spinal muscular atrophy by combining gene supplementation and genome editing.
Hatanaka F, Suzuki K, Shojima K, Yu J, Takahashi Y, Sakamoto A
Nat Commun. 2024; 15(1):6191.
PMID: 39048567
PMC: 11269569.
DOI: 10.1038/s41467-024-50095-5.
Truncated variants of MAGEL2 are involved in the etiologies of the Schaaf-Yang and Prader-Willi syndromes.
Heimdorfer D, Vorleuter A, Eschlbock A, Spathopoulou A, Suarez-Cubero M, Farhan H
Am J Hum Genet. 2024; 111(7):1383-1404.
PMID: 38908375
PMC: 11267527.
DOI: 10.1016/j.ajhg.2024.05.023.
Disrupted individual-level morphological brain network in spinal muscular atrophy types 2 and 3.
Li Y, Nie H, Xiang P, Shen W, Yan M, Yan C
CNS Neurosci Ther. 2024; 30(6):e14804.
PMID: 38887183
PMC: 11183166.
DOI: 10.1111/cns.14804.
Beyond Contractures in Spinal Muscular Atrophy: Identifying Lower-Limb Joint Hypermobility.
Harding E, Kanner C, Pasternak A, Glanzman A, Dunaway Young S, Rao A
J Clin Med. 2024; 13(9).
PMID: 38731167
PMC: 11084694.
DOI: 10.3390/jcm13092634.
bootGSEA: a bootstrap and rank aggregation pipeline for multi-study and multi-omics enrichment analyses.
Kumar S, Tapken I, Kuhn D, Claus P, Jung K
Front Bioinform. 2024; 4:1380928.
PMID: 38633435
PMC: 11021641.
DOI: 10.3389/fbinf.2024.1380928.
Real-World Safety Data of the Orphan Drug Onasemnogene Abeparvovec (Zolgensma) for the SMA Rare Disease: A Pharmacovigilance Study Based on the EMA Adverse Event Reporting System.
Ruggiero R, Balzano N, Nicoletti M, Mauro G, Fraenza F, Campitiello M
Pharmaceuticals (Basel). 2024; 17(3).
PMID: 38543180
PMC: 10974574.
DOI: 10.3390/ph17030394.
No significant sex differences in incidence or phenotype for the SMNΔ7 mouse model of spinal muscular atrophy.
Cottam N, Harrington M, Schork P, Sun J
Neuromuscul Disord. 2024; 37:13-22.
PMID: 38493520
PMC: 11031329.
DOI: 10.1016/j.nmd.2024.03.002.
Modeling Spinal Muscular Atrophy in Zebrafish: Current Advances and Future Perspectives.
Gonzalez D, Vasquez-Doorman C, Luna A, Allende M
Int J Mol Sci. 2024; 25(4).
PMID: 38396640
PMC: 10888324.
DOI: 10.3390/ijms25041962.