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M Stumm

Showing results (51-60 of 57) with videos related to

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The Journal of Cell Biology|July 29, 1998
Bassoon, a novel zinc-finger CAG/glutamine-repeat protein selectively localized at the active zone of presynaptic nerve terminalsS tom Dieck, L Sanmartí-Vila, K Langnaese, et al.
Cytogenetic and Genome Research|April 18, 2009
10p11.2 to 10q11.2 is a yet unreported region leading to unbalanced chromosomal abnormalities without phenotypic consequencesT Liehr, M Stumm, R D Wegner, et al.
Molecular Cell|January 10, 2002
DNA ligase IV mutations identified in patients exhibiting developmental delay and immunodeficiencyM O'Driscoll, K M Cerosaletti, P M Girard, et al.
Cell|May 20, 1998
Nibrin, a novel DNA double-strand break repair protein, is mutated in Nijmegen breakage syndromeR Varon, C Vissinga, M Platzer, et al.
Journal of Molecular Medicine (Berlin, Germany)|August 23, 2000
Mutations of the gene encoding the transmembrane transporter protein ABC-C6 cause pseudoxanthoma elasticumB Struk, L Cai, S Zäch, et al.
International Journal of Molecular Medicine|May 10, 2007
Forty-eight new cases with infertility due to balanced chromosomal rearrangements: detailed molecular cytogenetic analysis of the 90 involved breakpointsM Manvelyan, I Schreyer, I Höls-Herpertz, et al.
Journal of Molecular Medicine (Berlin, Germany)|April 12, 2000
A 500-kb region on chromosome 16p13.1 contains the pseudoxanthoma elasticum locus: high-resolution mapping and genomic structureL Cai, B Struk, M D Adams, et al.
Pageof 6

Showing results (51-60 of 57) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 57 results.
The Journal of Cell Biology|July 29, 1998
Bassoon, a novel zinc-finger CAG/glutamine-repeat protein selectively localized at the active zone of presynaptic nerve terminalsS tom Dieck, L Sanmartí-Vila, K Langnaese, et al.
Cytogenetic and Genome Research|April 18, 2009
10p11.2 to 10q11.2 is a yet unreported region leading to unbalanced chromosomal abnormalities without phenotypic consequencesT Liehr, M Stumm, R D Wegner, et al.
Molecular Cell|January 10, 2002
DNA ligase IV mutations identified in patients exhibiting developmental delay and immunodeficiencyM O'Driscoll, K M Cerosaletti, P M Girard, et al.
Cell|May 20, 1998
Nibrin, a novel DNA double-strand break repair protein, is mutated in Nijmegen breakage syndromeR Varon, C Vissinga, M Platzer, et al.
Journal of Molecular Medicine (Berlin, Germany)|August 23, 2000
Mutations of the gene encoding the transmembrane transporter protein ABC-C6 cause pseudoxanthoma elasticumB Struk, L Cai, S Zäch, et al.
International Journal of Molecular Medicine|May 10, 2007
Forty-eight new cases with infertility due to balanced chromosomal rearrangements: detailed molecular cytogenetic analysis of the 90 involved breakpointsM Manvelyan, I Schreyer, I Höls-Herpertz, et al.
Journal of Molecular Medicine (Berlin, Germany)|April 12, 2000
A 500-kb region on chromosome 16p13.1 contains the pseudoxanthoma elasticum locus: high-resolution mapping and genomic structureL Cai, B Struk, M D Adams, et al.
Pageof 6