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M Duno

Showing results (1-10 of 24) with videos related to

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Annals of Human Genetics|June 15, 2007
Leukocyte cDNA analysis of NSD1 derived from confirmed Sotos syndrome patientsM Duno, F Skovby, M Schwartz
Neuromuscular Disorders : NMD|September 4, 2012
Becker muscular dystrophy with widespread muscle hypertrophy and a non-sense mutation of exon 2N Witting, M Duno, J Vissing
Molecular and Cellular Biology|January 12, 2001
Molecular dissection of interactions between Rad51 and members of the recombination-repair groupL Krejci, J Damborsky, B Thomsen, et al.
Molecular Biology Reports|August 12, 2000
Homomeric interaction of the mouse Rad52 proteinL Krejci, B Thomsen, M Duno, et al.
Journal of Medical Genetics|September 1, 2010
Mutations in PCDH21 cause autosomal recessive cone-rod dystrophyE Ostergaard, M Batbayli, M Duno, et al.
Spinal Cord|October 16, 2013
Hereditary spastic paraplegia is not associated with C9ORF72 repeat expansions in a Danish cohortT T Nielsen, K Svenstrup, M Duno, et al.
Journal of Inherited Metabolic Disease|March 6, 2007
Xanthurenic aciduria due to a mutation in KYNU encoding kynureninaseM Christensen, M Duno, A M Lund, et al.
Mitochondrion|February 5, 2013
Muscle regeneration in mitochondrial myopathiesT O Krag, S Hauerslev, T D Jeppesen, et al.
Journal of Neurology|February 22, 2012
Endocrine function in 97 patients with myotonic dystrophy type 1M C Ørngreen, P Arlien-Søborg, M Duno, et al.
British Journal of Cancer|March 6, 2015
Mitochondrial dysfunction and risk of cancerM Lund, M Melbye, L J Diaz, et al.
Pageof 3

Showing results (1-10 of 24) with videos related to

Sort By:
Pageof 3
Annals of Human Genetics|June 15, 2007
Leukocyte cDNA analysis of NSD1 derived from confirmed Sotos syndrome patientsM Duno, F Skovby, M Schwartz
Neuromuscular Disorders : NMD|September 4, 2012
Becker muscular dystrophy with widespread muscle hypertrophy and a non-sense mutation of exon 2N Witting, M Duno, J Vissing
Molecular and Cellular Biology|January 12, 2001
Molecular dissection of interactions between Rad51 and members of the recombination-repair groupL Krejci, J Damborsky, B Thomsen, et al.
Molecular Biology Reports|August 12, 2000
Homomeric interaction of the mouse Rad52 proteinL Krejci, B Thomsen, M Duno, et al.
Journal of Medical Genetics|September 1, 2010
Mutations in PCDH21 cause autosomal recessive cone-rod dystrophyE Ostergaard, M Batbayli, M Duno, et al.
Spinal Cord|October 16, 2013
Hereditary spastic paraplegia is not associated with C9ORF72 repeat expansions in a Danish cohortT T Nielsen, K Svenstrup, M Duno, et al.
Journal of Inherited Metabolic Disease|March 6, 2007
Xanthurenic aciduria due to a mutation in KYNU encoding kynureninaseM Christensen, M Duno, A M Lund, et al.
Mitochondrion|February 5, 2013
Muscle regeneration in mitochondrial myopathiesT O Krag, S Hauerslev, T D Jeppesen, et al.
Journal of Neurology|February 22, 2012
Endocrine function in 97 patients with myotonic dystrophy type 1M C Ørngreen, P Arlien-Søborg, M Duno, et al.
British Journal of Cancer|March 6, 2015
Mitochondrial dysfunction and risk of cancerM Lund, M Melbye, L J Diaz, et al.
Pageof 3