Beckmann JS - Search Results

1

Human-mouse differences in the embryonic expression patterns of developmental control genes and disease genes.

Fougerousse F, Bullen P, Herasse M, Lindsay S, Richard I, Wilson D, Suel L, Durand M, Robson S, Abitbol M, Beckmann JS, Strachan T. Fougerousse F, et al. Among authors: beckmann js. Hum Mol Genet. 2000 Jan 22;9(2):165-73. doi: 10.1093/hmg/9.2.165. Hum Mol Genet. 2000. PMID: 10607827

2

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

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

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

5

Mapping of the formin gene and exclusion as a candidate gene for the autosomal recessive form of limb-girdle muscular dystrophy.

Richard I, Broux O, Hillaire D, Cherif D, Fougerousse F, Cohen D, Beckmann JS. Richard I, et al. Among authors: beckmann js. Hum Mol Genet. 1992 Nov;1(8):621-4. doi: 10.1093/hmg/1.8.621. Hum Mol Genet. 1992. PMID: 1363783

6

A primary expression map of the chromosome 15q15 region containing the recessive form of limb-girdle muscular dystrophy (LGMD2A) gene.

Chiannilkulchai N, Pasturaud P, Richard I, Auffray C, Beckmann JS. Chiannilkulchai N, et al. Among authors: beckmann js. Hum Mol Genet. 1995 Apr;4(4):717-25. doi: 10.1093/hmg/4.4.717. Hum Mol Genet. 1995. PMID: 7633422

7

Genetic heterogeneity of autosomal recessive limb-girdle muscular dystrophy in a genetic isolate (Amish) and evidence for a new locus.

Allamand V, Broux O, Bourg N, Richard I, Tischfield JA, Hodes ME, Conneally PM, Fardeau M, Jackson CE, Beckmann JS. Allamand V, et al. Among authors: beckmann js. Hum Mol Genet. 1995 Mar;4(3):459-63. doi: 10.1093/hmg/4.3.459. Hum Mol Genet. 1995. PMID: 7795603

8

Dinucleotide repeat at the D15S129 locus.

Richard I, Bourg N, Beckmann JS. Richard I, et al. Among authors: beckmann js. Hum Mol Genet. 1993 Dec;2(12):2199. doi: 10.1093/hmg/2.12.2199-a. Hum Mol Genet. 1993. PMID: 8111397 No abstract available.

9

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.

10

Molecular cloning of mouse canp3, the gene associated with limb-girdle muscular dystrophy 2A in human.

Richard I, Beckmann JS. Richard I, et al. Among authors: beckmann js. Mamm Genome. 1996 May;7(5):377-9. doi: 10.1007/s003359900108. Mamm Genome. 1996. PMID: 8661728 No abstract available.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

409 results

Search Page

Filters