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K Oexle

Showing results (1-10 of 18) with videos related to

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Journal of Theoretical Biology|June 6, 1998
Telomere length distribution and Southern blot analysisK Oexle
Neuropediatrics|August 25, 2001
Cause of progression in Duchenne muscular dystrophy: impaired differentiation more probable than replicative agingK Oexle, A Kohlschütter
Human Molecular Genetics|June 1, 1997
Advanced telomere shortening in respiratory chain disordersK Oexle, A Zwirner
Der Nervenarzt|June 26, 2015
[Genetics of dementia]J Diehl-Schmid, K Oexle
Pediatric Research|August 1, 1997
Examination of telomere lengths in muscle tissue casts doubt on replicative aging as cause of progression in Duchenne muscular dystrophyK Oexle, A Zwirner, K Freudenberg, et al.
Journal of Inherited Metabolic Disease|December 20, 2008
Three-generational alkaptonuria in a non-consanguineous familyK Oexle, K Engel, S Tinschert, et al.
Brain Research|February 26, 1996
NADH in the pyramidal cell layer of hippocampal regions CA1 and CA3 upon selective inhibition and uncoupling of oxidative phosphorylationM W Riepe, K Schmalzigaug, F Fink, et al.
European Journal of Pediatrics|May 1, 1992
Intracranial chordoma in a neonateK Oexle, O Dammann, B Bechmann, et al.
Neuromuscular Disorders : NMD|May 1, 1997
Congenital myopathy with excess of thin myofilamentsH H Goebel, J R Anderson, C Hübner, et al.
Human Molecular Genetics|July 1, 1996
A cysteine 3340 substitution in the dystroglycan-binding domain of dystrophin associated with Duchenne muscular dystrophy, mental retardation and absence of the ERG b-waveU Lenk, K Oexle, T Voit, et al.
Pageof 2

Showing results (1-10 of 18) with videos related to

Sort By:
Pageof 2
Journal of Theoretical Biology|June 6, 1998
Telomere length distribution and Southern blot analysisK Oexle
Neuropediatrics|August 25, 2001
Cause of progression in Duchenne muscular dystrophy: impaired differentiation more probable than replicative agingK Oexle, A Kohlschütter
Human Molecular Genetics|June 1, 1997
Advanced telomere shortening in respiratory chain disordersK Oexle, A Zwirner
Der Nervenarzt|June 26, 2015
[Genetics of dementia]J Diehl-Schmid, K Oexle
Pediatric Research|August 1, 1997
Examination of telomere lengths in muscle tissue casts doubt on replicative aging as cause of progression in Duchenne muscular dystrophyK Oexle, A Zwirner, K Freudenberg, et al.
Journal of Inherited Metabolic Disease|December 20, 2008
Three-generational alkaptonuria in a non-consanguineous familyK Oexle, K Engel, S Tinschert, et al.
Brain Research|February 26, 1996
NADH in the pyramidal cell layer of hippocampal regions CA1 and CA3 upon selective inhibition and uncoupling of oxidative phosphorylationM W Riepe, K Schmalzigaug, F Fink, et al.
European Journal of Pediatrics|May 1, 1992
Intracranial chordoma in a neonateK Oexle, O Dammann, B Bechmann, et al.
Neuromuscular Disorders : NMD|May 1, 1997
Congenital myopathy with excess of thin myofilamentsH H Goebel, J R Anderson, C Hübner, et al.
Human Molecular Genetics|July 1, 1996
A cysteine 3340 substitution in the dystroglycan-binding domain of dystrophin associated with Duchenne muscular dystrophy, mental retardation and absence of the ERG b-waveU Lenk, K Oexle, T Voit, et al.
Pageof 2