Soussi-Yanicostas N - Search Results

1

Distinct contractile protein profile in congenital myotonic dystrophy and X-linked myotubular myopathy.

Soussi-Yanicostas N, Chevallay M, Laurent-Winter C, Tomé FM, Fardeau M, Butler-Browne GS. Soussi-Yanicostas N, et al. Neuromuscul Disord. 1991;1(2):103-11. doi: 10.1016/0960-8966(91)90057-y. Neuromuscul Disord. 1991. PMID: 1822780

2

Transition of myosin isozymes during development of human masseter muscle. Persistence of developmental isoforms during postnatal stage.

Soussi-Yanicostas N, Barbet JP, Laurent-Winter C, Barton P, Butler-Browne GS. Soussi-Yanicostas N, et al. Development. 1990 Feb;108(2):239-49. doi: 10.1242/dev.108.2.239. Development. 1990. PMID: 2140978

3

Transcription of the embryonic myosin light chain gene is restricted to type II muscle fibers in human adult masseter.

Soussi-Yanicostas N, Butler-Browne GS. Soussi-Yanicostas N, et al. Dev Biol. 1991 Oct;147(2):374-80. doi: 10.1016/0012-1606(91)90295-e. Dev Biol. 1991. PMID: 1717324

4

Modification in the expression and localization of contractile and cytoskeletal proteins in Schwartz-Jampel syndrome.

Soussi-Yanicostas N, Ben Hamida C, Butler-Browne GS, Hentati F, Bejaoui K, Ben Hamida M. Soussi-Yanicostas N, et al. J Neurol Sci. 1991 Jul;104(1):64-73. doi: 10.1016/0022-510x(91)90217-u. J Neurol Sci. 1991. PMID: 1919599

5

Biphasic expression of slow myosin light chains and slow tropomyosin isoforms during the development of the human quadriceps muscle.

Laurent-Winter C, Soussi-Yanicostas N, Butler-Browne GS. Laurent-Winter C, et al. FEBS Lett. 1991 Mar 25;280(2):292-6. doi: 10.1016/0014-5793(91)80315-t. FEBS Lett. 1991. PMID: 2013326 Free article.

6

Evolution of muscle specific proteins in Werdnig-Hoffman's disease.

Soussi-Yanicostas N, Ben Hamida C, Bejaoui K, Hentati F, Ben Hamida M, Butler-Browne GS. Soussi-Yanicostas N, et al. J Neurol Sci. 1992 May;109(1):111-20. doi: 10.1016/0022-510x(92)90103-r. J Neurol Sci. 1992. PMID: 1387678

7

Expression of myosin isoforms and of desmin, vimentin and titin in Tunisian Duchenne-like autosomal recessive muscular dystrophy.

Hamida CB, Soussi-Yanicostas N, Bejaoui K, Butler-Browne GS, Hentati F, Ben Hamida M. Hamida CB, et al. J Neurol Sci. 1994 May;123(1-2):114-21. doi: 10.1016/0022-510x(94)90212-7. J Neurol Sci. 1994. PMID: 8064303

8

Biochemical and immunocytochemical analysis in chronic proximal spinal muscular atrophy.

Ben Hamida C, Soussi-Yanicostas N, Butler-Browne GS, Bejaoui K, Hentati F, Ben Hamida M. Ben Hamida C, et al. Muscle Nerve. 1994 Apr;17(4):400-10. doi: 10.1002/mus.880170407. Muscle Nerve. 1994. PMID: 8170486

9

The human embryonic myosin alkali light chain gene: use of alternative promoters and 3' non-coding regions.

Rotter M, Zimmerman K, Poustka A, Soussi-Yanicostas N, Starzinski-Powitz A. Rotter M, et al. Nucleic Acids Res. 1991 Apr 11;19(7):1497-504. doi: 10.1093/nar/19.7.1497. Nucleic Acids Res. 1991. PMID: 2027757 Free PMC article.

10

Anosmin-1 is a regionally restricted component of basement membranes and interstitial matrices during organogenesis: implications for the developmental anomalies of X chromosome-linked Kallmann syndrome.

Hardelin JP, Julliard AK, Moniot B, Soussi-Yanicostas N, Verney C, Schwanzel-Fukuda M, Ayer-Le Lievre C, Petit C. Hardelin JP, et al. Dev Dyn. 1999 May;215(1):26-44. doi: 10.1002/(SICI)1097-0177(199905)215:1<26::AID-DVDY4>3.0.CO;2-D. Dev Dyn. 1999. PMID: 10340754 Free article.

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