Search research articles
Contact Us
Filters
Showing results (191-200 of 223) with videos related to
Page
of 23
Sort By:
Human Molecular Genetics
|
August 12, 2011
Repetitive disruptions of the nuclear envelope invoke temporary loss of cellular compartmentalization in laminopathies
Winnok 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 charges
Sourav 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 accumulation
Valerie 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 study
Romy 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 malformations
Charlotte 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 systems
S 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 stress
Valerie 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 populations
Charlotte 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 association
Alina 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 regions
C H W Wijers, I A L M van Rooij, M K Bakker, et al.
Page
of 23
Search research articles
Search
Showing results (191-200 of 223) with videos related to
Sort By:
Page
of 23
Human Molecular Genetics
|
August 12, 2011
Repetitive disruptions of the nuclear envelope invoke temporary loss of cellular compartmentalization in laminopathies
Winnok 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 charges
Sourav 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 accumulation
Valerie 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 study
Romy 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 malformations
Charlotte 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 systems
S 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 stress
Valerie 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 populations
Charlotte 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 association
Alina 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 regions
C H W Wijers, I A L M van Rooij, M K Bakker, et al.
Page
of 23