Search research articles
Contact Us
Filters
Showing results (101-110 of 245) with videos related to
Page
of 25
Sort By:
Cell
|
March 16, 2004
Complete polarization of single intestinal epithelial cells upon activation of LKB1 by STRAD
Annette F Baas, Jeroen Kuipers, Nicole N van der Wel, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 15, 1995
Role of glutathione in the export of compounds from cells by the multidrug-resistance-associated protein
G J Zaman, J Lankelma, O van Tellingen, et al.
Annals of Neurology
|
October 1, 1996
Clinically distinct codon 69 mutations in major myelin protein zero in demyelinating neuropathies
P H Meijerink, J E Hoogendijk, A A Gabreëls-Festen, et al.
Origins of Life and Evolution of the Biosphere : the Journal of the International Society for the Study of the Origin of Life
|
January 1, 1985
Photochemical reactions in interstellar grains photolysis of CO, NH3, and H2O
V K Agarwal, W Schutte, J M Greenberg, et al.
Nature Genetics
|
September 1, 1996
Type VI collagen mutations in Bethlem myopathy, an autosomal dominant myopathy with contractures
G J Jöbsis, H Keizers, J P Vreijling, et al.
The British Journal of Surgery
|
April 10, 2016
Quality of life from a randomized trial of open and endovascular repair for abdominal aortic aneurysm
J L de Bruin, R H H Groenwold, A F Baas, et al.
The EMBO Journal
|
November 1, 1987
The human mdr3 gene encodes a novel P-glycoprotein homologue and gives rise to alternatively spliced mRNAs in liver
A M Van der Bliek, F Baas, T Ten Houte de Lange, et al.
Stroke
|
April 24, 2004
Plasminogen activator inhibitor-1 4G allele in the 4G/5G promoter polymorphism increases the occurrence of cerebral ischemia after aneurysmal subarachnoid hemorrhage
M D I Vergouwen, C J M Frijns, Y B W E M Roos, et al.
Human Molecular Genetics
|
May 18, 2000
Identification of mutations in the gene encoding lamins A/C in autosomal dominant limb girdle muscular dystrophy with atrioventricular conduction disturbances (LGMD1B)
A Muchir, G Bonne, A J van der Kooi, et al.
Nucleic Acids Research
|
April 25, 1983
The human thyroglobulin gene contains two 15-17 kb introns near its 3'-end
G J van Ommen, A C Arnberg, F Baas, et al.
Page
of 25
Search research articles
Search
Showing results (101-110 of 245) with videos related to
Sort By:
Page
of 25
Cell
|
March 16, 2004
Complete polarization of single intestinal epithelial cells upon activation of LKB1 by STRAD
Annette F Baas, Jeroen Kuipers, Nicole N van der Wel, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 15, 1995
Role of glutathione in the export of compounds from cells by the multidrug-resistance-associated protein
G J Zaman, J Lankelma, O van Tellingen, et al.
Annals of Neurology
|
October 1, 1996
Clinically distinct codon 69 mutations in major myelin protein zero in demyelinating neuropathies
P H Meijerink, J E Hoogendijk, A A Gabreëls-Festen, et al.
Origins of Life and Evolution of the Biosphere : the Journal of the International Society for the Study of the Origin of Life
|
January 1, 1985
Photochemical reactions in interstellar grains photolysis of CO, NH3, and H2O
V K Agarwal, W Schutte, J M Greenberg, et al.
Nature Genetics
|
September 1, 1996
Type VI collagen mutations in Bethlem myopathy, an autosomal dominant myopathy with contractures
G J Jöbsis, H Keizers, J P Vreijling, et al.
The British Journal of Surgery
|
April 10, 2016
Quality of life from a randomized trial of open and endovascular repair for abdominal aortic aneurysm
J L de Bruin, R H H Groenwold, A F Baas, et al.
The EMBO Journal
|
November 1, 1987
The human mdr3 gene encodes a novel P-glycoprotein homologue and gives rise to alternatively spliced mRNAs in liver
A M Van der Bliek, F Baas, T Ten Houte de Lange, et al.
Stroke
|
April 24, 2004
Plasminogen activator inhibitor-1 4G allele in the 4G/5G promoter polymorphism increases the occurrence of cerebral ischemia after aneurysmal subarachnoid hemorrhage
M D I Vergouwen, C J M Frijns, Y B W E M Roos, et al.
Human Molecular Genetics
|
May 18, 2000
Identification of mutations in the gene encoding lamins A/C in autosomal dominant limb girdle muscular dystrophy with atrioventricular conduction disturbances (LGMD1B)
A Muchir, G Bonne, A J van der Kooi, et al.
Nucleic Acids Research
|
April 25, 1983
The human thyroglobulin gene contains two 15-17 kb introns near its 3'-end
G J van Ommen, A C Arnberg, F Baas, et al.
Page
of 25