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International Journal of Cancer
|
March 3, 1995
Mechanisms of MRP over-expression in four human lung-cancer cell lines and analysis of the MRP amplicon
E W Eijdems, M De Haas, J M Coco-Martin, et al.
American Journal of Human Genetics
|
June 1, 2000
N-myc downstream-regulated gene 1 is mutated in hereditary motor and sensory neuropathy-Lom
L Kalaydjieva, D Gresham, R Gooding, et al.
Human Genetics
|
December 1, 1991
The duplication in Charcot-Marie-Tooth disease type 1a spans at least 1100 kb on chromosome 17p11.2
J E Hoogendijk, G W Hensels, I Zorn, et al.
Human Molecular Genetics
|
May 1, 1995
High-resolution DNA Fiber-FISH for genomic DNA mapping and colour bar-coding of large genes
R J Florijn, L A Bonden, H Vrolijk, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
September 13, 1994
The human multidrug resistance-associated protein MRP is a plasma membrane drug-efflux pump
G J Zaman, M J Flens, M R van Leusden, et al.
The Journal of Infection
|
May 11, 2018
Variation in coagulation and fibrinolysis genes evaluated for their contribution to cerebrovascular complications in adults with bacterial meningitis in the Netherlands
A T Kloek, H N Khan, M Valls Seron, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
April 1, 1997
Autosomal dominant cerebellar ataxia with retinal degeneration (ADCA II): clinical and neuropathological findings in two pedigrees and genetic linkage to 3p12-p21.1
G J Jöbsis, J W Weber, P G Barth, et al.
Cancer Research
|
April 15, 1993
Analysis of the expression of MRP, the gene for a new putative transmembrane drug transporter, in human multidrug resistant lung cancer cell lines
G J Zaman, C H Versantvoort, J J Smit, et al.
Cell Death and Differentiation
|
January 22, 2011
Endoplasmic reticulum stress activates autophagy but not the proteasome in neuronal cells: implications for Alzheimer's disease
D A T Nijholt, T R de Graaf, E S van Haastert, et al.
Lancet (London, England)
|
May 2, 1992
De-novo mutation in hereditary motor and sensory neuropathy type I
J E Hoogendijk, G W Hensels, A A Gabreëls-Festen, et al.
Page
of 25
Search research articles
Search
Showing results (151-160 of 245) with videos related to
Sort By:
Page
of 25
International Journal of Cancer
|
March 3, 1995
Mechanisms of MRP over-expression in four human lung-cancer cell lines and analysis of the MRP amplicon
E W Eijdems, M De Haas, J M Coco-Martin, et al.
American Journal of Human Genetics
|
June 1, 2000
N-myc downstream-regulated gene 1 is mutated in hereditary motor and sensory neuropathy-Lom
L Kalaydjieva, D Gresham, R Gooding, et al.
Human Genetics
|
December 1, 1991
The duplication in Charcot-Marie-Tooth disease type 1a spans at least 1100 kb on chromosome 17p11.2
J E Hoogendijk, G W Hensels, I Zorn, et al.
Human Molecular Genetics
|
May 1, 1995
High-resolution DNA Fiber-FISH for genomic DNA mapping and colour bar-coding of large genes
R J Florijn, L A Bonden, H Vrolijk, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
September 13, 1994
The human multidrug resistance-associated protein MRP is a plasma membrane drug-efflux pump
G J Zaman, M J Flens, M R van Leusden, et al.
The Journal of Infection
|
May 11, 2018
Variation in coagulation and fibrinolysis genes evaluated for their contribution to cerebrovascular complications in adults with bacterial meningitis in the Netherlands
A T Kloek, H N Khan, M Valls Seron, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
April 1, 1997
Autosomal dominant cerebellar ataxia with retinal degeneration (ADCA II): clinical and neuropathological findings in two pedigrees and genetic linkage to 3p12-p21.1
G J Jöbsis, J W Weber, P G Barth, et al.
Cancer Research
|
April 15, 1993
Analysis of the expression of MRP, the gene for a new putative transmembrane drug transporter, in human multidrug resistant lung cancer cell lines
G J Zaman, C H Versantvoort, J J Smit, et al.
Cell Death and Differentiation
|
January 22, 2011
Endoplasmic reticulum stress activates autophagy but not the proteasome in neuronal cells: implications for Alzheimer's disease
D A T Nijholt, T R de Graaf, E S van Haastert, et al.
Lancet (London, England)
|
May 2, 1992
De-novo mutation in hereditary motor and sensory neuropathy type I
J E Hoogendijk, G W Hensels, A A Gabreëls-Festen, et al.
Page
of 25