Fougerousse F - Search Results

1

Molecular tools for the study of titin's differential expression.

Centner T, Fougerousse F, Freiburg A, Witt C, Beckmann JS, Granzier H, Trombitás K, Gregorio CC, Labeit S. Centner T, et al. Among authors: fougerousse f. Adv Exp Med Biol. 2000;481:35-49; discussion 50-2. doi: 10.1007/978-1-4615-4267-4_3. Adv Exp Med Biol. 2000. PMID: 10987065 Review.

2

Series of exon-skipping events in the elastic spring region of titin as the structural basis for myofibrillar elastic diversity.

Freiburg A, Trombitas K, Hell W, Cazorla O, Fougerousse F, Centner T, Kolmerer B, Witt C, Beckmann JS, Gregorio CC, Granzier H, Labeit S. Freiburg A, et al. Among authors: fougerousse f. Circ Res. 2000 Jun 9;86(11):1114-21. doi: 10.1161/01.res.86.11.1114. Circ Res. 2000. PMID: 10850961 Free article.

3

Calpain3 expression during human cardiogenesis.

Fougerousse F, Anderson LV, Delezoide AL, Suel L, Durand M, Beckmann JS. Fougerousse F, et al. Neuromuscul Disord. 2000 Jun;10(4-5):251-6. doi: 10.1016/s0960-8966(99)00107-8. Neuromuscul Disord. 2000. PMID: 10838251

4

Expression and functional characteristics of calpain 3 isoforms generated through tissue-specific transcriptional and posttranscriptional events.

Herasse M, Ono Y, Fougerousse F, Kimura E, Stockholm D, Beley C, Montarras D, Pinset C, Sorimachi H, Suzuki K, Beckmann JS, Richard I. Herasse M, et al. Among authors: fougerousse f. Mol Cell Biol. 1999 Jun;19(6):4047-55. doi: 10.1128/MCB.19.6.4047. Mol Cell Biol. 1999. PMID: 10330145 Free PMC article.

5

Expression of genes (CAPN3, SGCA, SGCB, and TTN) involved in progressive muscular dystrophies during early human development.

Fougerousse F, Durand M, Suel L, Pourquié O, Delezoide AL, Romero NB, Abitbol M, Beckmann JS. Fougerousse F, et al. Genomics. 1998 Mar 1;48(2):145-56. doi: 10.1006/geno.1997.5160. Genomics. 1998. PMID: 9521867

6

Cardiac myosin binding protein C gene is specifically expressed in heart during murine and human development.

Fougerousse F, Delezoide AL, Fiszman MY, Schwartz K, Beckmann JS, Carrier L. Fougerousse F, et al. Circ Res. 1998 Jan 9-23;82(1):130-3. doi: 10.1161/01.res.82.1.130. Circ Res. 1998. PMID: 9440712

7

Developmental expression of myotilin, a gene mutated in limb-girdle muscular dystrophy type 1A.

Mologni L, Salmikangas P, Fougerousse F, Beckmann JS, Carpén O. Mologni L, et al. Among authors: fougerousse f. Mech Dev. 2001 May;103(1-2):121-5. doi: 10.1016/s0925-4773(01)00325-2. Mech Dev. 2001. PMID: 11335118 Free article.

8

Sequential expression of genes involved in muscular dystrophies during human development.

Durand M, Suel L, Barbet JP, Beckmann JS, Fougerousse F. Durand M, et al. Among authors: fougerousse f. Morphologie. 2002 Jun;86(273):9-12. Morphologie. 2002. PMID: 12224393

9

Dinucleotide repeat polymorphism at the locus D15S222.

Fougerousse F, Pasturaud P, Beckmann JS. Fougerousse F, et al. Hum Mol Genet. 1993 Dec;2(12):2200. doi: 10.1093/hmg/2.12.2200. Hum Mol Genet. 1993. PMID: 8111400 No abstract available.

10

Dysferlin is a plasma membrane protein and is expressed early in human development.

Anderson LV, Davison K, Moss JA, Young C, Cullen MJ, Walsh J, Johnson MA, Bashir R, Britton S, Keers S, Argov Z, Mahjneh I, Fougerousse F, Beckmann JS, Bushby KM. Anderson LV, et al. Among authors: fougerousse f. Hum Mol Genet. 1999 May;8(5):855-61. doi: 10.1093/hmg/8.5.855. Hum Mol Genet. 1999. PMID: 10196375

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