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F Baas

Showing results (101-110 of 245) with videos related to

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Cell|March 16, 2004
Complete polarization of single intestinal epithelial cells upon activation of LKB1 by STRADAnnette 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 proteinG 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 neuropathiesP 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 H2OV 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 contracturesG 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 aneurysmJ 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 liverA 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 hemorrhageM 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'-endG J van Ommen, A C Arnberg, F Baas, et al.
Pageof 25

Showing results (101-110 of 245) with videos related to

Sort By:
Pageof 25
Cell|March 16, 2004
Complete polarization of single intestinal epithelial cells upon activation of LKB1 by STRADAnnette 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 proteinG 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 neuropathiesP 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 H2OV 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 contracturesG 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 aneurysmJ 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 liverA 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 hemorrhageM 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'-endG J van Ommen, A C Arnberg, F Baas, et al.
Pageof 25