Beckmann JS - 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: beckmann js. 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: beckmann js. 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. Among authors: beckmann js. Neuromuscul Disord. 2000 Jun;10(4-5):251-6. doi: 10.1016/s0960-8966(99)00107-8. Neuromuscul Disord. 2000. PMID: 10838251

4

Secondary calpain3 deficiency in 2q-linked muscular dystrophy: titin is the candidate gene.

Haravuori H, Vihola A, Straub V, Auranen M, Richard I, Marchand S, Voit T, Labeit S, Somer H, Peltonen L, Beckmann JS, Udd B. Haravuori H, et al. Among authors: beckmann js. Neurology. 2001 Apr 10;56(7):869-77. doi: 10.1212/wnl.56.7.869. Neurology. 2001. PMID: 11294923

5

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: beckmann js. 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.

6

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. Among authors: beckmann js. Genomics. 1998 Mar 1;48(2):145-56. doi: 10.1006/geno.1997.5160. Genomics. 1998. PMID: 9521867

7

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. Among authors: beckmann js. Circ Res. 1998 Jan 9-23;82(1):130-3. doi: 10.1161/01.res.82.1.130. Circ Res. 1998. PMID: 9440712 Free article.

8

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: beckmann js. Mech Dev. 2001 May;103(1-2):121-5. doi: 10.1016/s0925-4773(01)00325-2. Mech Dev. 2001. PMID: 11335118 Free article.

9

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: beckmann js. Morphologie. 2002 Jun;86(273):9-12. Morphologie. 2002. PMID: 12224393

10

Dinucleotide repeat polymorphism at the locus D15S222.

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

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