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B Wieringa

Showing results (41-50 of 173) with videos related to

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FEBS Letters|October 20, 1999
Identification and molecular characterization of BP75, a novel bromodomain-containing proteinE Cuppen, M van Ham, B Pepers, et al.
Experimental Physiology|May 1, 1995
The effects of MM-creatine kinase deficiency on sustained force production of mouse fast skeletal muscleA de Haan, J C Koudijs, R A Wevers, et al.
Journal of Microscopy|March 3, 2009
Advantages of indium-tin oxide-coated glass slides in correlative scanning electron microscopy applications of uncoated cultured cellsH Pluk, D J Stokes, B Lich, et al.
Nederlands Tijdschrift Voor Geneeskunde|November 27, 1993
[An unstable mutation as cause of myotonic dystrophy]H G Brunner, C J Höweler, H J Smeets, et al.
Clinical Genetics|May 1, 1985
Complex glycerol kinase deficiency syndrome explained as X-chromosomal deletionB Wieringa, T Hustinx, J Scheres, et al.
Human Genetics|October 1, 1989
Use of variable simple sequence motifs as genetic markers: application to study of myotonic dystrophyH J Smeets, H G Brunner, H H Ropers, et al.
Advances in Neurology|January 1, 1988
Genetic and physical demarcation of the locus for dystrophia myotonicaB Wieringa, H Brunner, T Hulsebos, et al.
NMR in Biomedicine|October 12, 1999
Effects of ischemia on skeletal muscle energy metabolism in mice lacking creatine kinase monitored by in vivo 31P nuclear magnetic resonance spectroscopyH J in 't Zandt, F Oerlemans, B Wieringa, et al.
Journal of Applied Physiology (Bethesda, Md. : 1985)|March 10, 2000
Myofibrillar or mitochondrial creatine kinase deficiency alone does not impair mouse diaphragm isotonic functionJ F Watchko, M J Daood, B Wieringa, et al.
Muscle & Nerve|August 9, 2001
Changes in glycolytic network and mitochondrial design in creatine kinase-deficient musclesA J de Groof, F T Oerlemans, C R Jost, et al.
Pageof 18

Showing results (41-50 of 173) with videos related to

Sort By:
Pageof 18
FEBS Letters|October 20, 1999
Identification and molecular characterization of BP75, a novel bromodomain-containing proteinE Cuppen, M van Ham, B Pepers, et al.
Experimental Physiology|May 1, 1995
The effects of MM-creatine kinase deficiency on sustained force production of mouse fast skeletal muscleA de Haan, J C Koudijs, R A Wevers, et al.
Journal of Microscopy|March 3, 2009
Advantages of indium-tin oxide-coated glass slides in correlative scanning electron microscopy applications of uncoated cultured cellsH Pluk, D J Stokes, B Lich, et al.
Nederlands Tijdschrift Voor Geneeskunde|November 27, 1993
[An unstable mutation as cause of myotonic dystrophy]H G Brunner, C J Höweler, H J Smeets, et al.
Clinical Genetics|May 1, 1985
Complex glycerol kinase deficiency syndrome explained as X-chromosomal deletionB Wieringa, T Hustinx, J Scheres, et al.
Human Genetics|October 1, 1989
Use of variable simple sequence motifs as genetic markers: application to study of myotonic dystrophyH J Smeets, H G Brunner, H H Ropers, et al.
Advances in Neurology|January 1, 1988
Genetic and physical demarcation of the locus for dystrophia myotonicaB Wieringa, H Brunner, T Hulsebos, et al.
NMR in Biomedicine|October 12, 1999
Effects of ischemia on skeletal muscle energy metabolism in mice lacking creatine kinase monitored by in vivo 31P nuclear magnetic resonance spectroscopyH J in 't Zandt, F Oerlemans, B Wieringa, et al.
Journal of Applied Physiology (Bethesda, Md. : 1985)|March 10, 2000
Myofibrillar or mitochondrial creatine kinase deficiency alone does not impair mouse diaphragm isotonic functionJ F Watchko, M J Daood, B Wieringa, et al.
Muscle & Nerve|August 9, 2001
Changes in glycolytic network and mitochondrial design in creatine kinase-deficient musclesA J de Groof, F T Oerlemans, C R Jost, et al.
Pageof 18