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M Marcelis

Showing results (191-200 of 223) with videos related to

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Human Molecular Genetics|August 12, 2011
Repetitive disruptions of the nuclear envelope invoke temporary loss of cellular compartmentalization in laminopathiesWinnok H De Vos, Frederik Houben, Miriam Kamps, et al.
Nanoscale|April 27, 2013
Cytotoxicity of surface-functionalized silicon and germanium nanoparticles: the dominant role of surface chargesSourav Bhattacharjee, Ivonne M C M Rietjens, Mani P Singh, et al.
Human Molecular Genetics|July 11, 2006
Compound heterozygosity for mutations in LMNA causes a progeria syndrome without prelamin A accumulationValerie L R M Verstraeten, Jos L V Broers, Maurice A M van Steensel, et al.
Birth Defects Research|November 12, 2020
Maternal risk associated with the VACTERL association: A case-control studyRomy van de Putte, Hermien E K de Walle, Kirsten J M van Hooijdonk, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|May 21, 2014
No major role for periconceptional folic acid use and its interaction with the MTHFR C677T polymorphism in the etiology of congenital anorectal malformationsCharlotte H W Wijers, Ivo de Blaauw, Nadine Zwink, et al.
Nature Food|April 28, 2023
Current status and future challenges in implementing and upscaling vertical farming systemsS H van Delden, M SharathKumar, M Butturini, et al.
Journal of Cellular and Molecular Medicine|February 18, 2009
The R439C mutation in LMNA causes lamin oligomerization and susceptibility to oxidative stressValerie L R M Verstraeten, Sandrine Caputo, Maurice A M van Steensel, et al.
Pediatric Surgery International|August 24, 2010
Research perspectives in the etiology of congenital anorectal malformations using data of the International Consortium on Anorectal Malformations: evidence for risk factors across different populationsCharlotte H W Wijers, Ivo de Blaauw, Carlo L M Marcelis, et al.
European Journal of Human Genetics : EJHG|April 4, 2013
De novo microduplications at 1q41, 2q37.3, and 8q24.3 in patients with VATER/VACTERL associationAlina Hilger, Charlotte Schramm, Tracie Pennimpede, et al.
BJOG : an International Journal of Obstetrics and Gynaecology|April 12, 2013
Anorectal malformations and pregnancy-related disorders: a registry-based case-control study in 17 European regionsC H W Wijers, I A L M van Rooij, M K Bakker, et al.
Pageof 23

Showing results (191-200 of 223) with videos related to

Sort By:
Pageof 23
Human Molecular Genetics|August 12, 2011
Repetitive disruptions of the nuclear envelope invoke temporary loss of cellular compartmentalization in laminopathiesWinnok H De Vos, Frederik Houben, Miriam Kamps, et al.
Nanoscale|April 27, 2013
Cytotoxicity of surface-functionalized silicon and germanium nanoparticles: the dominant role of surface chargesSourav Bhattacharjee, Ivonne M C M Rietjens, Mani P Singh, et al.
Human Molecular Genetics|July 11, 2006
Compound heterozygosity for mutations in LMNA causes a progeria syndrome without prelamin A accumulationValerie L R M Verstraeten, Jos L V Broers, Maurice A M van Steensel, et al.
Birth Defects Research|November 12, 2020
Maternal risk associated with the VACTERL association: A case-control studyRomy van de Putte, Hermien E K de Walle, Kirsten J M van Hooijdonk, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|May 21, 2014
No major role for periconceptional folic acid use and its interaction with the MTHFR C677T polymorphism in the etiology of congenital anorectal malformationsCharlotte H W Wijers, Ivo de Blaauw, Nadine Zwink, et al.
Nature Food|April 28, 2023
Current status and future challenges in implementing and upscaling vertical farming systemsS H van Delden, M SharathKumar, M Butturini, et al.
Journal of Cellular and Molecular Medicine|February 18, 2009
The R439C mutation in LMNA causes lamin oligomerization and susceptibility to oxidative stressValerie L R M Verstraeten, Sandrine Caputo, Maurice A M van Steensel, et al.
Pediatric Surgery International|August 24, 2010
Research perspectives in the etiology of congenital anorectal malformations using data of the International Consortium on Anorectal Malformations: evidence for risk factors across different populationsCharlotte H W Wijers, Ivo de Blaauw, Carlo L M Marcelis, et al.
European Journal of Human Genetics : EJHG|April 4, 2013
De novo microduplications at 1q41, 2q37.3, and 8q24.3 in patients with VATER/VACTERL associationAlina Hilger, Charlotte Schramm, Tracie Pennimpede, et al.
BJOG : an International Journal of Obstetrics and Gynaecology|April 12, 2013
Anorectal malformations and pregnancy-related disorders: a registry-based case-control study in 17 European regionsC H W Wijers, I A L M van Rooij, M K Bakker, et al.
Pageof 23