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P Molenaar

Showing results (71-80 of 77) with videos related to

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Neurology|February 19, 2024
Brody Disease, an Early-Onset Myopathy With Delayed Relaxation and Abnormal Gait: A Case Series of 9 ChildrenJamie I Verhoeven, Jasper Kramer, Juergen Seeger, et al.
Biochemistry and Biophysics Reports|April 6, 2026
Sarco/endoplasmatic reticulum calcium ATPase activity in healthy muscle and Brody diseaseJ P Molenaar, M M Snoeck, S Treves, et al.
Journal of Molecular and Cellular Cardiology|January 25, 2011
Molecular architecture of the human specialised atrioventricular conduction axisI D Greener, O Monfredi, S Inada, et al.
American Journal of Human Genetics|July 5, 2016
Mutations in Complex I Assembly Factor TMEM126B Result in Muscle Weakness and Isolated Complex I DeficiencyLaura Sánchez-Caballero, Benedetta Ruzzenente, Lucas Bianchi, et al.
The Journal of Pharmacology and Experimental Therapeutics|June 17, 1998
The contribution of classical (beta1/2-) and atypical beta-adrenoceptors to the stimulation of human white adipocyte lipolysis and right atrial appendage contraction by novel beta3-adrenoceptor agonists of differing selectivitiesM V Sennitt, A J Kaumann, P Molenaar, et al.
Brain : a Journal of Neurology|February 11, 2020
Clinical, morphological and genetic characterization of Brody disease: an international study of 40 patientsJoery P Molenaar, Jamie I Verhoeven, Richard J Rodenburg, et al.
The Journal of Clinical Investigation|November 1, 2019
KBTBD13 is an actin-binding protein that modulates muscle kineticsJosine M de Winter, Joery P Molenaar, Michaela Yuen, et al.
Pageof 8

Showing results (71-80 of 77) with videos related to

Sort By:
Pageof 8
You have reached the last page of results.This site can display upto 77 results.
Neurology|February 19, 2024
Brody Disease, an Early-Onset Myopathy With Delayed Relaxation and Abnormal Gait: A Case Series of 9 ChildrenJamie I Verhoeven, Jasper Kramer, Juergen Seeger, et al.
Biochemistry and Biophysics Reports|April 6, 2026
Sarco/endoplasmatic reticulum calcium ATPase activity in healthy muscle and Brody diseaseJ P Molenaar, M M Snoeck, S Treves, et al.
Journal of Molecular and Cellular Cardiology|January 25, 2011
Molecular architecture of the human specialised atrioventricular conduction axisI D Greener, O Monfredi, S Inada, et al.
American Journal of Human Genetics|July 5, 2016
Mutations in Complex I Assembly Factor TMEM126B Result in Muscle Weakness and Isolated Complex I DeficiencyLaura Sánchez-Caballero, Benedetta Ruzzenente, Lucas Bianchi, et al.
The Journal of Pharmacology and Experimental Therapeutics|June 17, 1998
The contribution of classical (beta1/2-) and atypical beta-adrenoceptors to the stimulation of human white adipocyte lipolysis and right atrial appendage contraction by novel beta3-adrenoceptor agonists of differing selectivitiesM V Sennitt, A J Kaumann, P Molenaar, et al.
Brain : a Journal of Neurology|February 11, 2020
Clinical, morphological and genetic characterization of Brody disease: an international study of 40 patientsJoery P Molenaar, Jamie I Verhoeven, Richard J Rodenburg, et al.
The Journal of Clinical Investigation|November 1, 2019
KBTBD13 is an actin-binding protein that modulates muscle kineticsJosine M de Winter, Joery P Molenaar, Michaela Yuen, et al.
Pageof 8