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The Journal of Clinical Investigation
|
April 29, 1998
Drug export activity of the human canalicular multispecific organic anion transporter in polarized kidney MDCK cells expressing cMOAT (MRP2) cDNA
R Evers, M Kool, L van Deemter, et al.
Cancer Research
|
November 1, 1988
Genes amplified and overexpressed in human multidrug-resistant cell lines
A M Van der Bliek, F Baas, T Van der Velde-Koerts, et al.
European Journal of Human Genetics : EJHG
|
May 5, 2019
Informing relatives at risk of inherited cardiac conditions: experiences and attitudes of healthcare professionals and counselees
Lieke M van den Heuvel, Mette J Huisinga, Yvonne M Hoedemaekers, et al.
Hepatology (Baltimore, Md.)
|
June 1, 1997
A mutation in the human canalicular multispecific organic anion transporter gene causes the Dubin-Johnson syndrome
C C Paulusma, M Kool, P J Bosma, et al.
Human Molecular Genetics
|
October 1, 1993
Cloning the breakpoint cluster region of the inv(16) in acute nonlymphocytic leukemia M4 Eo
J G Dauwerse, J W Wessels, R H Giles, et al.
Neurology
|
March 29, 2001
Homozygous deletion of the survival motor neuron 2 gene is a prognostic factor in sporadic ALS
J H Veldink, L H van den Berg, J M Cobben, et al.
NPJ Digital Medicine
|
February 27, 2021
Automatic multilabel detection of ICD10 codes in Dutch cardiology discharge letters using neural networks
Arjan Sammani, Ayoub Bagheri, Peter G M van der Heijden, et al.
Journal of the Neurological Sciences
|
May 1, 1995
Differential diagnosis in spinal and bulbar muscular atrophy clinical and molecular aspects
G J Jöbsis, E S Louwerse, M de Visser, et al.
European Journal of Heart Failure
|
March 3, 2015
A systematic analysis of genetic dilated cardiomyopathy reveals numerous ubiquitously expressed and muscle-specific genes
Magdalena Harakalova, Gijs Kummeling, Arjan Sammani, et al.
Human Genetics
|
February 1, 1994
Evidence for genetic heterogeneity underlying hereditary neuropathy with liability to pressure palsies
E C Mariman, A A Gabreëls-Festen, S E van Beersum, et al.
Page
of 25
Search research articles
Search
Showing results (141-150 of 245) with videos related to
Sort By:
Page
of 25
The Journal of Clinical Investigation
|
April 29, 1998
Drug export activity of the human canalicular multispecific organic anion transporter in polarized kidney MDCK cells expressing cMOAT (MRP2) cDNA
R Evers, M Kool, L van Deemter, et al.
Cancer Research
|
November 1, 1988
Genes amplified and overexpressed in human multidrug-resistant cell lines
A M Van der Bliek, F Baas, T Van der Velde-Koerts, et al.
European Journal of Human Genetics : EJHG
|
May 5, 2019
Informing relatives at risk of inherited cardiac conditions: experiences and attitudes of healthcare professionals and counselees
Lieke M van den Heuvel, Mette J Huisinga, Yvonne M Hoedemaekers, et al.
Hepatology (Baltimore, Md.)
|
June 1, 1997
A mutation in the human canalicular multispecific organic anion transporter gene causes the Dubin-Johnson syndrome
C C Paulusma, M Kool, P J Bosma, et al.
Human Molecular Genetics
|
October 1, 1993
Cloning the breakpoint cluster region of the inv(16) in acute nonlymphocytic leukemia M4 Eo
J G Dauwerse, J W Wessels, R H Giles, et al.
Neurology
|
March 29, 2001
Homozygous deletion of the survival motor neuron 2 gene is a prognostic factor in sporadic ALS
J H Veldink, L H van den Berg, J M Cobben, et al.
NPJ Digital Medicine
|
February 27, 2021
Automatic multilabel detection of ICD10 codes in Dutch cardiology discharge letters using neural networks
Arjan Sammani, Ayoub Bagheri, Peter G M van der Heijden, et al.
Journal of the Neurological Sciences
|
May 1, 1995
Differential diagnosis in spinal and bulbar muscular atrophy clinical and molecular aspects
G J Jöbsis, E S Louwerse, M de Visser, et al.
European Journal of Heart Failure
|
March 3, 2015
A systematic analysis of genetic dilated cardiomyopathy reveals numerous ubiquitously expressed and muscle-specific genes
Magdalena Harakalova, Gijs Kummeling, Arjan Sammani, et al.
Human Genetics
|
February 1, 1994
Evidence for genetic heterogeneity underlying hereditary neuropathy with liability to pressure palsies
E C Mariman, A A Gabreëls-Festen, S E van Beersum, et al.
Page
of 25