Zobrazeno 1 - 10
of 428
pro vyhledávání: '"Spuler, S"'
Autor:
Fernando, H. J. S., Mann, J., Palma, J. M. L. M., Lundquist, J. K., Barthelmie, R. J., Belo-Pereira, M., Brown, W. O. J., Chow, F. K., Gerz, T., Hocut, C. M., Klein, P. M., Leo, L. S., Matos, J. C., Oncley, S. P., Pryor, S. C., Bariteau, L., Bell, T. M., Bodini, N., Carney, M. B., Courtney, M. S., Creegan, E. D., Dimitrova, R., Gomes, S., Hagen, M., Hyde, J. O., Kigle, S., Krishshnamurthy, R., Lopes, J. C., Mazzaro, L., Neher, J. M. T., Menke, R., Murphy, P., Oswald, L., Otarola-Bustos, S., Pattantyus, A. K., Rodrigues, C. Veiga, Schady, A., Sirin, N., Spuler, S., Svensson, E., Tomaszewski, J., Turner, D. D., van Veen, L., Vasiljević, N., Vasssallo, D., Voss, S., Wildmann, N., Wang, Y.
Publikováno v:
Bulletin of the American Meteorological Society, 2019 May 01. 100(5), 799-820.
Externí odkaz:
https://www.jstor.org/stable/27026719
Publikováno v:
Molecular Therapy - Nucleic Acids. 31:494-511
With thousands of patients worldwide, CAPN3 c.550delA is the most frequent mutation causing severe, progressive, and untreatable limb girdle muscular dystrophy. We aimed to genetically correct this founder mutation in primary human muscle stem cells.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0652db4517ff7458f91fc76ffc4754d7
https://doi.org/10.1016/j.omtn.2023.02.005
https://doi.org/10.1016/j.omtn.2023.02.005
Tissue engineering for the diaphragm and its various therapeutic possibilities - a systematic review
Autor:
Boehm, A.K., Hillebrandt, K.H., Dziodzio, T., Krenzien, F., Neudecker, J., Spuler, S., Pratschke, J., Sauer, I.M., Andreas, M.N.
Diaphragmatic impairments exhibit high morbidity as well as mortality while current treatment options remain unsatisfactory. Tissue engineering (TE) approaches have explored the generation of an optimal biocompatible scaffold for diaphragmatic repair
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=mdc______med::11ff04b4b57da0414ad891f90c43fd17
http://edoc.mdc-berlin.de/21543/1/21543oa.pdf
http://edoc.mdc-berlin.de/21543/1/21543oa.pdf
Akademický článek
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Akademický článek
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K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Mayhew, A. G., James, M. K., Moore, U., Sutherland, H., Jacobs, M., Feng, J., Lowes, L. P., Alfano, L. N., Muni Lofra, R., Rufibach, L. E., Rose, K., Duong, T., Bello, L., Pedrosa-Hernandez, I., Holsten, S., Sakamoto, C., Canal, A., Sanchez-Aguilera Praxedes, N., Thiele, S., Siener, C., Vandevelde, B., Dewolf, B., Maron, E., Gordish-Dressman, H., Hilsden, H., Guglieri, M., Hogrel, J. -Y., Blamire, A. M., Carlier, P. G., Spuler, S., Day, J. W., Jones, K. J., Bharucha-Goebel, D. X., Salort-Campana, E., Pestronk, A., Walter, M. C., Paradas, C., Stojkovic, T., Mori-Yoshimura, M., Bravver, E., Diaz-Manera, J., Pegoraro, E., Mendell, J. R., Jain COS Consortium, Straub, V.
Dysferlinopathy is a muscular dystrophy with a highly variable functional disease progression in which the relationship of function to some patient reported outcome measures (PROMs) has not been previously reported. This analysis aims to identify the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e0372f0afd35e5b3c88a636fb40b4f22
http://hdl.handle.net/11577/3443657
http://hdl.handle.net/11577/3443657
Autor:
Boyer, O., Butler-Browne, G., Chinoy, H., Cossu, G., Galli, F., Lilleker, J.B., Magli, A., Mouly, V., Perlingeiro, R.R., Previtali, S.C., Sampaolesi, M., Smeets, H., Schoewel-Wolf, V., Spuler, S., Torrente, Y., Van Tienen, F.
This article will review myogenic cell transplantation for congenital and acquired diseases of skeletal muscle. There are already a number of excellent reviews on this topic, but they are mostly focused on a specific disease, muscular dystrophies and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=mdc______med::0311d91c6a73006c40c732d64586abe9
http://edoc.mdc-berlin.de/20856/1/20856oa.pdf
http://edoc.mdc-berlin.de/20856/1/20856oa.pdf
Autor:
Escobar, H., Krause, A., Keiper, S., Kieshauer, J., Müthel, S., García de Paredes, M., Metzler, E., Kühn, R., Heyd, F., Spuler, S.
Skeletal muscle can regenerate from muscle stem cells and their myogenic precursor cell progeny, myoblasts. However, precise gene editing in human muscle stem cells for autologous cell replacement therapies of untreatable genetic muscle diseases has
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=mdc______med::d6e3f1d5196bf4ec258e8360ac2f5472
http://edoc.mdc-berlin.de/20178/1/20178oa.pdf
http://edoc.mdc-berlin.de/20178/1/20178oa.pdf
Autor:
Gerhalter, T., Müller, C., Maron, E., Mähler, A., Schütte, T., Boschmann, M., Herzer, R., Spuler, S., Gazzerro, E.
Publikováno v:
In Neuromuscular Disorders October 2022 32 Supplement 1:S58-S58