المؤلفون: Sinha, B, Köster, D, Ruez, R, Gonnord, P, Bastiani, M, Abankwa, Daniel, Stan, RV, Butler-Browne, G, Vedie, B, Johannes, L, Morone, N, Parton, RG, Raposo, G, Sens, P, Lamaze, C, Nassoy, P

المصدر: Sinha , B , Köster , D , Ruez , R , Gonnord , P , Bastiani , M , Abankwa , D , Stan , RV , Butler-Browne , G , Vedie , B , Johannes , L , Morone , N , Parton , RG , Raposo , G , Sens , P , Lamaze , C & Nassoy , P 2011 , ' Cells Respond to Mechanical Stress by Rapid Disassembly of Caveolae ' , Cell , vol. 144 , no. 3 , pp. 402–413 . https://doi.org/10.1016/j.cell.2010.12.031Test

العلاقة: https://research.abo.fi/en/publications/f3073f46-a134-4a02-8edf-a1512f48e0a4Test

الإتاحة: https://doi.org/10.1016/j.cell.2010.12.031Test
https://research.abo.fi/en/publications/f3073f46-a134-4a02-8edf-a1512f48e0a4Test

المؤلفون: Pinto Mariz, F., Barthélémy, I., Yada, E., Voit, T., Silva-Barbosa, S.D., Savino, W., Butler-Browne, G., Blot, S.

المصدر: Neuromuscular Disorders ; volume 21, issue 9-10, page 656 ; ISSN 0960-8966

مصطلحات موضوعية: Genetics (clinical), Neurology (clinical), Neurology, Pediatrics, Perinatology and Child Health

الإتاحة: https://doi.org/10.1016/j.nmd.2011.06.810Test
https://api.elsevier.com/content/article/PII:S0960896611009990?httpAccept=text/xmlTest
https://api.elsevier.com/content/article/PII:S0960896611009990?httpAccept=text/plainTest

المؤلفون: Castro, F.M.M., Linhares-Lacerda, L., Côrrea-de-Santana, E., Sperandei, S., Ribeiro-Alves, M., Butler-Browne, G., Mouly, V., Silva-Barbosa, S.D., Savino, W.

المصدر: Neuromuscular Disorders ; volume 21, issue 9-10, page 732 ; ISSN 0960-8966

مصطلحات موضوعية: Genetics (clinical), Neurology (clinical), Neurology, Pediatrics, Perinatology and Child Health

الإتاحة: https://doi.org/10.1016/j.nmd.2011.06.1057Test
https://api.elsevier.com/content/article/PII:S0960896611012466?httpAccept=text/xmlTest
https://api.elsevier.com/content/article/PII:S0960896611012466?httpAccept=text/plainTest

المؤلفون: Taylor, L., Zhao, L., Kaminoh, Y., Mamchaoui, K., Mouly, V., Butler-Browne, G., Vulin, A., Wilton, S., Flanigan, K.M.

المصدر: Neuromuscular Disorders ; volume 21, issue 9-10, page 703 ; ISSN 0960-8966

مصطلحات موضوعية: Genetics (clinical), Neurology (clinical), Neurology, Pediatrics, Perinatology and Child Health

الإتاحة: https://doi.org/10.1016/j.nmd.2011.06.963Test
https://api.elsevier.com/content/article/PII:S0960896611011527?httpAccept=text/xmlTest
https://api.elsevier.com/content/article/PII:S0960896611011527?httpAccept=text/plainTest

المؤلفون: Mariz, F. Pinto, Carvalho, L. Rodrigues, Araujo, A.P.Q., de Mello, W., Ribeiro, M.G., Cunha, M.C.S., Riederer, I., Negroni, E., Mouly, V., Voit, T., Desguerre, I., Butler-Browne, G., Savino, W., Silva-Barbosa, S.D.

المصدر: Neuromuscular Disorders ; volume 21, issue 9-10, page 655 ; ISSN 0960-8966

مصطلحات موضوعية: Genetics (clinical), Neurology (clinical), Neurology, Pediatrics, Perinatology and Child Health

الإتاحة: https://doi.org/10.1016/j.nmd.2011.06.807Test
https://api.elsevier.com/content/article/PII:S0960896611009965?httpAccept=text/xmlTest
https://api.elsevier.com/content/article/PII:S0960896611009965?httpAccept=text/plainTest

المؤلفون: Gidaro, T., Mamchaoui, K., Bouazza, B., Perié, S., Svinartchouk, F., Blumen, S., Guily, J.J.S., Butler-Browne, G., Mouly, V., Trollet, C.

المصدر: Neuromuscular Disorders ; volume 21, issue 9-10, page 674 ; ISSN 0960-8966

مصطلحات موضوعية: Genetics (clinical), Neurology (clinical), Neurology, Pediatrics, Perinatology and Child Health

الإتاحة: https://doi.org/10.1016/j.nmd.2011.06.867Test
https://api.elsevier.com/content/article/PII:S096089661101056X?httpAccept=text/xmlTest
https://api.elsevier.com/content/article/PII:S096089661101056X?httpAccept=text/plainTest

المؤلفون: Corrêa-de-Santana, E., Linhares-Lacerda, L., Ribeiro-Alves, M., Sperandei, S., Monteiro-de-Castro, F.M., Butler-Browne, G., Mouly, V., Savino, W.

المصدر: Neuromuscular Disorders ; volume 21, issue 9-10, page 747-748 ; ISSN 0960-8966

مصطلحات موضوعية: Genetics (clinical), Neurology (clinical), Neurology, Pediatrics, Perinatology and Child Health

الإتاحة: https://doi.org/10.1016/j.nmd.2011.06.1107Test
https://api.elsevier.com/content/article/PII:S096089661101296X?httpAccept=text/xmlTest
https://api.elsevier.com/content/article/PII:S096089661101296X?httpAccept=text/plainTest

المؤلفون: Riederer, I., Negroni, E., Bencze, M., Wolf, A., Di Santo, J.P., Silva-Barbosa, S.D., Butler-Browne, G., Savino, W., Mouly, V.

المصدر: Neuromuscular Disorders ; volume 21, issue 9-10, page 714 ; ISSN 0960-8966

مصطلحات موضوعية: Genetics (clinical), Neurology (clinical), Neurology, Pediatrics, Perinatology and Child Health

الإتاحة: https://doi.org/10.1016/j.nmd.2011.06.998Test
https://api.elsevier.com/content/article/PII:S0960896611011874?httpAccept=text/xmlTest
https://api.elsevier.com/content/article/PII:S0960896611011874?httpAccept=text/plainTest

المؤلفون: Berghella L., De Angelis L., Coletta M., Berarducci B., Sonnino C., Salvatori G., Anthonissen C., Cooper R., Butler-Browne G. S., Mouly V., Ferrari G., Mavilio F., Cossu G.

المساهمون: Berghella, L., De Angelis, L., Coletta, M., Berarducci, B., Sonnino, C., Salvatori, G., Anthonissen, C., Cooper, R., Butler-Browne, G. S., Mouly, V., Ferrari, G., Mavilio, F., Cossu, G.

العلاقة: info:eu-repo/semantics/altIdentifier/wos/WOS:000081361800003; volume:10; issue:10; firstpage:1607; lastpage:1617; journal:HUMAN GENE THERAPY; http://hdl.handle.net/11380/1248044Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-0033166880

الإتاحة: https://doi.org/10.1089/10430349950017617Test
http://hdl.handle.net/11380/1248044Test

المؤلفون: Trollet, C., Anvar, S.Y., Venema, A., Hargreaves, I.P., Foster, Keith, Vignaud, A., Ferry, A., Negroni, E, Hourde, C., Baraibar, M.A., t'Hoen, P.A.C., Davies, J.E., Rubinsztein, D.C., Heales, S.J., Mouly, V., van der Maarel, S.M., Butler-Browne, G., Raz, V., Dickson, G.

العلاقة: Trollet, C., Anvar, S.Y., Venema, A., Hargreaves, I.P., Foster, K. , Vignaud, A., Ferry, A., Negroni, E., Hourde, C., Baraibar, M.A., t'Hoen, P.A.C., Davies, J.E., Rubinsztein, D.C., Heales, S.J., Mouly, V., van der Maarel, S.M., Butler-Browne, G., Raz, V. and Dickson, G. (2010) Molecular and phenotypic characterization of a mouse model of oculopharyngeal muscular dystrophy reveals severe muscular atrophy restricted to fast glycolytic fibres. Human Molecular Genetics, 19 (11). pp. 2191-2207. ISSN 1460-2083 doi: https://doi.org/10.1093/hmg/ddq098Test

الإتاحة: https://doi.org/10.1093/hmg/ddq098Test
https://centaur.reading.ac.uk/32371Test/
http://hmg.oxfordjournals.org/content/19/11/2191.full.pdf+htmlTest