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Peter Hackman

Showing results (1-10 of 82) with videos related to

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Duodecim; Laaketieteellinen Aikakauskirja|September 2, 2005
[The kinase domain of titin controls muscle gene expression and protein turnover]Peter Hackman, Anna Vihola, Bjarne Udd
Neuromuscular Disorders : NMD|December 3, 2015
Targeted next-generation sequencing assay for detection of mutations in primary myopathiesAnni Evilä, Meharji Arumilli, Bjarne Udd, et al.
Neuromuscular Disorders : NMD|February 19, 2017
219th ENMC International Workshop Titinopathies International database of titin mutations and phenotypes, Heemskerk, The Netherlands, 29 April-1 May 2016Peter Hackman, Bjarne Udd, Carsten G Bönnemann, et al.
Analytical Biochemistry|April 12, 2003
Touch-down method for high-performance sequencing of polymerase chain reaction productsSylvie Marchand, Philippe Hajdari, Peter Hackman, et al.
Journal of Neuromuscular Diseases|March 17, 2020
Is Gene-Size an Issue for the Diagnosis of Skeletal Muscle Disorders?Marco Savarese, Salla Välipakka, Mridul Johari, et al.
Journal of Neuromuscular Diseases|November 18, 2016
Increasing Role of Titin Mutations in Neuromuscular DisordersMarco Savarese, Jaakko Sarparanta, Anna Vihola, et al.
European Journal of Neurology|January 24, 2023
Long-term favorable prognosis in late onset dominant distal titinopathy: Tibial muscular dystrophyVictoria Lillback, Marco Savarese, Niina Sandholm, et al.
BMC Genomics|May 14, 2026
Poly(A)+ selection limits detection of long and alternatively spliced transcripts compared with rRNA depletion in RNA-SequencingSwethaa Natraj Gayathri, Victoria Lillback, Bjarne Udd, et al.
BMC Medical Genetics|April 13, 2017
SIRT6 polymorphism rs117385980 is associated with longevity and healthy aging in Finnish menKatariina Hirvonen, Hannele Laivuori, Jari Lahti, et al.
European Journal of Human Genetics : EJHG|April 27, 2012
Autosomal dominant late-onset spinal motor neuronopathy is linked to a new locus on chromosome 22q11.2-q13.2Sini Penttilä, Manu Jokela, Peter Hackman, et al.
Pageof 9

Showing results (1-10 of 82) with videos related to

Sort By:
Pageof 9
Duodecim; Laaketieteellinen Aikakauskirja|September 2, 2005
[The kinase domain of titin controls muscle gene expression and protein turnover]Peter Hackman, Anna Vihola, Bjarne Udd
Neuromuscular Disorders : NMD|December 3, 2015
Targeted next-generation sequencing assay for detection of mutations in primary myopathiesAnni Evilä, Meharji Arumilli, Bjarne Udd, et al.
Neuromuscular Disorders : NMD|February 19, 2017
219th ENMC International Workshop Titinopathies International database of titin mutations and phenotypes, Heemskerk, The Netherlands, 29 April-1 May 2016Peter Hackman, Bjarne Udd, Carsten G Bönnemann, et al.
Analytical Biochemistry|April 12, 2003
Touch-down method for high-performance sequencing of polymerase chain reaction productsSylvie Marchand, Philippe Hajdari, Peter Hackman, et al.
Journal of Neuromuscular Diseases|March 17, 2020
Is Gene-Size an Issue for the Diagnosis of Skeletal Muscle Disorders?Marco Savarese, Salla Välipakka, Mridul Johari, et al.
Journal of Neuromuscular Diseases|November 18, 2016
Increasing Role of Titin Mutations in Neuromuscular DisordersMarco Savarese, Jaakko Sarparanta, Anna Vihola, et al.
European Journal of Neurology|January 24, 2023
Long-term favorable prognosis in late onset dominant distal titinopathy: Tibial muscular dystrophyVictoria Lillback, Marco Savarese, Niina Sandholm, et al.
BMC Genomics|May 14, 2026
Poly(A)+ selection limits detection of long and alternatively spliced transcripts compared with rRNA depletion in RNA-SequencingSwethaa Natraj Gayathri, Victoria Lillback, Bjarne Udd, et al.
BMC Medical Genetics|April 13, 2017
SIRT6 polymorphism rs117385980 is associated with longevity and healthy aging in Finnish menKatariina Hirvonen, Hannele Laivuori, Jari Lahti, et al.
European Journal of Human Genetics : EJHG|April 27, 2012
Autosomal dominant late-onset spinal motor neuronopathy is linked to a new locus on chromosome 22q11.2-q13.2Sini Penttilä, Manu Jokela, Peter Hackman, et al.
Pageof 9