T Dörk - JoVE Visualize

Showing results (11-20 of 56) with videos related to

Pageof 6

Sort By:

Cytogenetics and Cell Genetics|February 15, 2001

Mutagen sensitivity of human lymphoblastoid cells with a BRCA1 mutation in comparison to ataxia telangiectasia heterozygote cellsG Speit, K Trenz, P Schütz, et al.

Human Genetics|January 1, 1994

Exon 9 of the CFTR gene: splice site haplotypes and cystic fibrosis mutationsT Dörk, R Fislage, T Neumann, et al.

Human Mutation|January 1, 1994

A 32-bp deletion (2991del32) in the cystic fibrosis gene associated with CFTR mRNA reductionT Dörk, K Will, K Grade, et al.

Electrophoresis|October 1, 1995

Analysis of microsatellites by direct blotting electrophoresis and chemiluminescence detectionF Mekus, T Dörk, T Deufel, et al.

Lymphatic Research and Biology|June 23, 2012

Lymphedema of the breast as a symptom of internal diseases or side effect of mTor inhibitorsU Hille, P Soergel, L Makowski, et al.

Human Molecular Genetics|November 1, 1996

Testis-specific protein, Y-encoded (TSPY) expression in testicular tissuesF Schnieders, T Dörk, J Arnemann, et al.

The EMBO Journal|April 4, 2001

Nuclear factor TDP-43 and SR proteins promote in vitro and in vivo CFTR exon 9 skippingE Buratti, T Dörk, E Zuccato, et al.

Strahlentherapie Und Onkologie : Organ Der Deutschen Rontgengesellschaft ... [Et Al]|August 17, 2001

[Bilateral breast carcinoma and local recurrence: prevalence of BRCA-1 and BRCA-2 gene mutations in an unselected patient sample]M Bremer, D Steinmann, T Dörk, et al.

Human Mutation|April 29, 1998

A new missense substitution at a mutational hot spot of the androgen receptor in siblings with complete androgen insensitivity syndromeT Dörk, F Schnieders, S Jakubiczka, et al.

American Journal of Human Genetics|November 1, 1994

Independent origins of cystic fibrosis mutations R334W, R347P, R1162X, and 3849 + 10kbC-->T provide evidence of mutation recurrence in the CFTR geneN Morral, R Llevadot, T Casals, et al.

Pageof 6

Showing results (11-20 of 56) with videos related to

Sort By:

Pageof 6

Cytogenetics and Cell Genetics|February 15, 2001

Mutagen sensitivity of human lymphoblastoid cells with a BRCA1 mutation in comparison to ataxia telangiectasia heterozygote cellsG Speit, K Trenz, P Schütz, et al.

Human Genetics|January 1, 1994

Exon 9 of the CFTR gene: splice site haplotypes and cystic fibrosis mutationsT Dörk, R Fislage, T Neumann, et al.

Human Mutation|January 1, 1994

A 32-bp deletion (2991del32) in the cystic fibrosis gene associated with CFTR mRNA reductionT Dörk, K Will, K Grade, et al.

Electrophoresis|October 1, 1995

Analysis of microsatellites by direct blotting electrophoresis and chemiluminescence detectionF Mekus, T Dörk, T Deufel, et al.

Lymphatic Research and Biology|June 23, 2012

Lymphedema of the breast as a symptom of internal diseases or side effect of mTor inhibitorsU Hille, P Soergel, L Makowski, et al.

Human Molecular Genetics|November 1, 1996

Testis-specific protein, Y-encoded (TSPY) expression in testicular tissuesF Schnieders, T Dörk, J Arnemann, et al.

The EMBO Journal|April 4, 2001

Nuclear factor TDP-43 and SR proteins promote in vitro and in vivo CFTR exon 9 skippingE Buratti, T Dörk, E Zuccato, et al.

Strahlentherapie Und Onkologie : Organ Der Deutschen Rontgengesellschaft ... [Et Al]|August 17, 2001

[Bilateral breast carcinoma and local recurrence: prevalence of BRCA-1 and BRCA-2 gene mutations in an unselected patient sample]M Bremer, D Steinmann, T Dörk, et al.

Human Mutation|April 29, 1998

A new missense substitution at a mutational hot spot of the androgen receptor in siblings with complete androgen insensitivity syndromeT Dörk, F Schnieders, S Jakubiczka, et al.

American Journal of Human Genetics|November 1, 1994

Independent origins of cystic fibrosis mutations R334W, R347P, R1162X, and 3849 + 10kbC-->T provide evidence of mutation recurrence in the CFTR geneN Morral, R Llevadot, T Casals, et al.

Pageof 6