Search research articles
Contact Us
Filters
Showing results (111-120 of 245) with videos related to
Page
of 25
Sort By:
Cancer Research
|
August 15, 1997
Analysis of expression of cMOAT (MRP2), MRP3, MRP4, and MRP5, homologues of the multidrug resistance-associated protein gene (MRP1), in human cancer cell lines
M Kool, M de Haas, G L Scheffer, et al.
Stem Cell Research
|
April 18, 2025
Generation of induced pluripotent stem cell lines from five individuals from two families carrying a pathogenic Dutch MYBPC3 founder variant with variable degrees of hypertrophic cardiomyopathy
Floor W van den Dolder, Vincent A J Warnaar, Yeszamin L Onderwater, et al.
The EMBO Journal
|
October 1, 2003
MO25alpha/beta interact with STRADalpha/beta enhancing their ability to bind, activate and localize LKB1 in the cytoplasm
Jérôme Boudeau, Annette F Baas, Maria Deak, et al.
Neuromuscular Disorders : NMD
|
January 22, 2002
Two amino-acid substitutions in the myelin protein zero gene of a case of Charcot-Marie-Tooth disease associated with light-near dissociation
H M E Bienfait, F Baas, A A W M Gabreëls-Festen, et al.
Human Molecular Genetics
|
July 27, 2001
Antisense-induced exon skipping restores dystrophin expression in DMD patient derived muscle cells
J C van Deutekom, M Bremmer-Bout, A A Janson, et al.
Neuroscience
|
May 6, 2014
SGCZ mutations are unlikely to be associated with myoclonus dystonia
K J Peall, K Ritz, A J Waite, et al.
Neurology
|
November 15, 2006
Distal myoclonus and late onset in a large Dutch family with myoclonus-dystonia
E M J Foncke, M C F Gerrits, F van Ruissen, et al.
British Journal of Cancer
|
August 1, 1995
Altered MRP is associated with multidrug resistance and reduced drug accumulation in human SW-1573 cells
E W Eijdems, G J Zaman, M de Haas, et al.
Neuromuscular Disorders : NMD
|
July 23, 1998
Genetic heterogeneity in Miyoshi-type distal muscular dystrophy
W H Linssen, M de Visser, N C Notermans, et al.
Neurology
|
August 23, 2000
14-3-3 testing in diagnosing Creutzfeldt-Jakob disease: a prospective study in 112 patients
A W Lemstra, M T van Meegen, J P Vreyling, et al.
Page
of 25
Search research articles
Search
Showing results (111-120 of 245) with videos related to
Sort By:
Page
of 25
Cancer Research
|
August 15, 1997
Analysis of expression of cMOAT (MRP2), MRP3, MRP4, and MRP5, homologues of the multidrug resistance-associated protein gene (MRP1), in human cancer cell lines
M Kool, M de Haas, G L Scheffer, et al.
Stem Cell Research
|
April 18, 2025
Generation of induced pluripotent stem cell lines from five individuals from two families carrying a pathogenic Dutch MYBPC3 founder variant with variable degrees of hypertrophic cardiomyopathy
Floor W van den Dolder, Vincent A J Warnaar, Yeszamin L Onderwater, et al.
The EMBO Journal
|
October 1, 2003
MO25alpha/beta interact with STRADalpha/beta enhancing their ability to bind, activate and localize LKB1 in the cytoplasm
Jérôme Boudeau, Annette F Baas, Maria Deak, et al.
Neuromuscular Disorders : NMD
|
January 22, 2002
Two amino-acid substitutions in the myelin protein zero gene of a case of Charcot-Marie-Tooth disease associated with light-near dissociation
H M E Bienfait, F Baas, A A W M Gabreëls-Festen, et al.
Human Molecular Genetics
|
July 27, 2001
Antisense-induced exon skipping restores dystrophin expression in DMD patient derived muscle cells
J C van Deutekom, M Bremmer-Bout, A A Janson, et al.
Neuroscience
|
May 6, 2014
SGCZ mutations are unlikely to be associated with myoclonus dystonia
K J Peall, K Ritz, A J Waite, et al.
Neurology
|
November 15, 2006
Distal myoclonus and late onset in a large Dutch family with myoclonus-dystonia
E M J Foncke, M C F Gerrits, F van Ruissen, et al.
British Journal of Cancer
|
August 1, 1995
Altered MRP is associated with multidrug resistance and reduced drug accumulation in human SW-1573 cells
E W Eijdems, G J Zaman, M de Haas, et al.
Neuromuscular Disorders : NMD
|
July 23, 1998
Genetic heterogeneity in Miyoshi-type distal muscular dystrophy
W H Linssen, M de Visser, N C Notermans, et al.
Neurology
|
August 23, 2000
14-3-3 testing in diagnosing Creutzfeldt-Jakob disease: a prospective study in 112 patients
A W Lemstra, M T van Meegen, J P Vreyling, et al.
Page
of 25