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B Wieringa

Showing results (161-170 of 173) with videos related to

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The New England Journal of Medicine|February 18, 1993
Brief report: reverse mutation in myotonic dystrophyH G Brunner, G Jansen, W Nillesen, et al.
Atherosclerosis|November 1, 1994
Diet-induced hypercholesterolemia and atherosclerosis in heterozygous apolipoprotein E-deficient miceJ H van Ree, W J van den Broek, V E Dahlmans, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 8, 2001
Adenylate kinase phosphotransfer communicates cellular energetic signals to ATP-sensitive potassium channelsA J Carrasco, P P Dzeja, A E Alekseev, et al.
American Journal of Human Genetics|November 1, 1993
Influence of sex of the transmitting parent as well as of parental allele size on the CTG expansion in myotonic dystrophy (DM)H G Brunner, H T Brüggenwirth, W Nillesen, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 1, 1989
Chromosomal jumping from the DXS165 locus allows molecular characterization of four microdeletions and a de novo chromosome X/13 translocation associated with choroideremiaF P Cremers, D J van de Pol, B Wieringa, et al.
Journal of Neurochemistry|September 3, 2004
Cerebral creatine kinase deficiency influences metabolite levels and morphology in the mouse brain: a quantitative in vivo 1H and 31P magnetic resonance studyH J A in 't Zandt, W K J Renema, F Streijger, et al.
Brain : a Journal of Neurology|October 1, 1991
Myotonic dystrophy. Predictive value of normal results on clinical examinationH G Brunner, H J Smeets, W Nillesen, et al.
American Journal of Human Genetics|June 1, 1992
Detection and characterization of point mutations in the choroideremia candidate gene by PCR-SSCP analysis and direct DNA sequencingJ A van den Hurk, T J van de Pol, C M Molloy, et al.
The Journal of Physiology|November 7, 2012
Disturbed energy metabolism and muscular dystrophy caused by pure creatine deficiency are reversible by creatine intakeC I Nabuurs, C U Choe, A Veltien, et al.
Cell|April 4, 1997
Altered Ca2+ responses in muscles with combined mitochondrial and cytosolic creatine kinase deficienciesK Steeghs, A Benders, F Oerlemans, et al.
Pageof 18

Showing results (161-170 of 173) with videos related to

Sort By:
Pageof 18
The New England Journal of Medicine|February 18, 1993
Brief report: reverse mutation in myotonic dystrophyH G Brunner, G Jansen, W Nillesen, et al.
Atherosclerosis|November 1, 1994
Diet-induced hypercholesterolemia and atherosclerosis in heterozygous apolipoprotein E-deficient miceJ H van Ree, W J van den Broek, V E Dahlmans, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 8, 2001
Adenylate kinase phosphotransfer communicates cellular energetic signals to ATP-sensitive potassium channelsA J Carrasco, P P Dzeja, A E Alekseev, et al.
American Journal of Human Genetics|November 1, 1993
Influence of sex of the transmitting parent as well as of parental allele size on the CTG expansion in myotonic dystrophy (DM)H G Brunner, H T Brüggenwirth, W Nillesen, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 1, 1989
Chromosomal jumping from the DXS165 locus allows molecular characterization of four microdeletions and a de novo chromosome X/13 translocation associated with choroideremiaF P Cremers, D J van de Pol, B Wieringa, et al.
Journal of Neurochemistry|September 3, 2004
Cerebral creatine kinase deficiency influences metabolite levels and morphology in the mouse brain: a quantitative in vivo 1H and 31P magnetic resonance studyH J A in 't Zandt, W K J Renema, F Streijger, et al.
Brain : a Journal of Neurology|October 1, 1991
Myotonic dystrophy. Predictive value of normal results on clinical examinationH G Brunner, H J Smeets, W Nillesen, et al.
American Journal of Human Genetics|June 1, 1992
Detection and characterization of point mutations in the choroideremia candidate gene by PCR-SSCP analysis and direct DNA sequencingJ A van den Hurk, T J van de Pol, C M Molloy, et al.
The Journal of Physiology|November 7, 2012
Disturbed energy metabolism and muscular dystrophy caused by pure creatine deficiency are reversible by creatine intakeC I Nabuurs, C U Choe, A Veltien, et al.
Cell|April 4, 1997
Altered Ca2+ responses in muscles with combined mitochondrial and cytosolic creatine kinase deficienciesK Steeghs, A Benders, F Oerlemans, et al.
Pageof 18