Spuler S - Search Results

1

MyoMiner: explore gene co-expression in normal and pathological muscle.

Malatras A, Michalopoulos I, Duguez S, Butler-Browne G, Spuler S, Duddy WJ. Malatras A, et al. Among authors: spuler s. BMC Med Genomics. 2020 May 11;13(1):67. doi: 10.1186/s12920-020-0712-3. BMC Med Genomics. 2020. PMID: 32393257 Free PMC article.

2

Immortalized pathological human myoblasts: towards a universal tool for the study of neuromuscular disorders.

Mamchaoui K, Trollet C, Bigot A, Negroni E, Chaouch S, Wolff A, Kandalla PK, Marie S, Di Santo J, St Guily JL, Muntoni F, Kim J, Philippi S, Spuler S, Levy N, Blumen SC, Voit T, Wright WE, Aamiri A, Butler-Browne G, Mouly V. Mamchaoui K, et al. Among authors: spuler s. Skelet Muscle. 2011 Nov 1;1:34. doi: 10.1186/2044-5040-1-34. Skelet Muscle. 2011. PMID: 22040608 Free PMC article.

3

Inflammation-induced acute phase response in skeletal muscle and critical illness myopathy.

Langhans C, Weber-Carstens S, Schmidt F, Hamati J, Kny M, Zhu X, Wollersheim T, Koch S, Krebs M, Schulz H, Lodka D, Saar K, Labeit S, Spies C, Hubner N, Spranger J, Spuler S, Boschmann M, Dittmar G, Butler-Browne G, Mouly V, Fielitz J. Langhans C, et al. Among authors: spuler s. PLoS One. 2014 Mar 20;9(3):e92048. doi: 10.1371/journal.pone.0092048. eCollection 2014. PLoS One. 2014. PMID: 24651840 Free PMC article.

4

Myogenic Cell Transplantation in Genetic and Acquired Diseases of Skeletal Muscle.

Boyer O, Butler-Browne G, Chinoy H, Cossu G, Galli F, Lilleker JB, Magli A, Mouly V, Perlingeiro RCR, Previtali SC, Sampaolesi M, Smeets H, Schoewel-Wolf V, Spuler S, Torrente Y, Van Tienen F; Study Group. Boyer O, et al. Among authors: spuler s. Front Genet. 2021 Aug 2;12:702547. doi: 10.3389/fgene.2021.702547. eCollection 2021. Front Genet. 2021. PMID: 34408774 Free PMC article. Review.

5

Delay in diagnosis of muscle disorders depends on the subspecialty of the initially consulted physician.

Spuler S, Stroux A, Kuschel F, Kuhlmey A, Kendel F. Spuler S, et al. BMC Health Serv Res. 2011 May 4;11:91. doi: 10.1186/1472-6963-11-91. BMC Health Serv Res. 2011. PMID: 21542919 Free PMC article.

6

Altered expression of cyclin A 1 in muscle of patients with facioscapulohumeral muscle dystrophy (FSHD-1).

Pakula A, Schneider J, Janke J, Zacharias U, Schulz H, Hübner N, Mähler A, Spuler A, Spuler S, Carlier P, Boschmann M. Pakula A, et al. Among authors: spuler a, spuler s. PLoS One. 2013 Sep 3;8(9):e73573. doi: 10.1371/journal.pone.0073573. eCollection 2013. PLoS One. 2013. PMID: 24019929 Free PMC article.

7

Single-nucleus transcriptomics reveals functional compartmentalization in syncytial skeletal muscle cells.

Kim M, Franke V, Brandt B, Lowenstein ED, Schöwel V, Spuler S, Akalin A, Birchmeier C. Kim M, et al. Among authors: spuler s. Nat Commun. 2020 Dec 11;11(1):6375. doi: 10.1038/s41467-020-20064-9. Nat Commun. 2020. PMID: 33311457 Free PMC article.

8

Base editing repairs an SGCA mutation in human primary muscle stem cells.

Escobar H, Krause A, Keiper S, Kieshauer J, Müthel S, de Paredes MG, Metzler E, Kühn R, Heyd F, Spuler S. Escobar H, et al. Among authors: spuler s. JCI Insight. 2021 May 24;6(10):e145994. doi: 10.1172/jci.insight.145994. JCI Insight. 2021. PMID: 33848270 Free PMC article.

9

LMNA Co-Regulated Gene Expression as a Suitable Readout after Precise Gene Correction.

Wang H, Krause A, Escobar H, Müthel S, Metzler E, Spuler S. Wang H, et al. Among authors: spuler s. Int J Mol Sci. 2022 Dec 8;23(24):15525. doi: 10.3390/ijms232415525. Int J Mol Sci. 2022. PMID: 36555163 Free PMC article.

10

Gene-editing in patient and humanized-mice primary muscle stem cells rescues dysferlin expression in dysferlin-deficient muscular dystrophy.

Escobar H, Di Francescantonio S, Smirnova J, Graf R, Müthel S, Marg A, Zhogov A, Krishna S, Metzler E, Petkova M, Daumke O, Kühn R, Spuler S. Escobar H, et al. Among authors: spuler s. Nat Commun. 2025 Jan 2;16(1):120. doi: 10.1038/s41467-024-55086-0. Nat Commun. 2025. PMID: 39747848 Free PMC article.

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