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M Nordling

Showing results (31-40 of 69) with videos related to

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Molecular Biosystems|May 10, 2017
GeneSPIDER - gene regulatory network inference benchmarking with controlled network and data propertiesAndreas Tjärnberg, Daniel C Morgan, Matthew Studham, et al.
Drug Delivery and Translational Research|June 29, 2017
The role of monocyte subpopulations in vascular injury following partial and transient depletionEtty Grad, Ksenia Zolotarevsky, Haim D Danenberg, et al.
Protein Engineering|February 1, 1991
Cassette mutagenesis of Met121 in azurin from Pseudomonas aeruginosaB G Karlsson, M Nordling, T Pascher, et al.
Bioinformatics (Oxford, England)|June 17, 2014
Functional association networks as priors for gene regulatory network inferenceMatthew E Studham, Andreas Tjärnberg, Torbjörn E M Nordling, et al.
Acta Ophthalmologica|February 21, 2018
Potential link between sporadic cerebral amyloid angiopathy and vision loss: a case reportRupali Vohra, Tina D Hjortshøj, Mette M Nordling, et al.
Human Mutation|November 3, 2000
PMM2 mutation spectrum, including 10 novel mutations, in a large CDG type 1A family material with a focus on Scandinavian familiesC Bjursell, A Erlandson, M Nordling, et al.
Scientific Reports|October 3, 2022
Knowledge of the perturbation design is essential for accurate gene regulatory network inferenceDeniz Seçilmiş, Thomas Hillerton, Andreas Tjärnberg, et al.
Scandinavian Journal of Gastroenterology|April 27, 2017
Effects on Cell Proliferation, Activator Protein-1 and Genotoxicity by Fecal Water from Patients with Colorectal AdenomasM M Nordling, B Glinghammar, P C Karlsson, et al.
Scandinavian Journal of Gastroenterology|June 11, 2003
Effects on cell proliferation, activator protein-1 and genotoxicity by fecal water from patients with colorectal adenomasM M Nordling, B Glinghammar, P C Karlsson, et al.
European Journal of Human Genetics : EJHG|January 10, 2002
The western Swedish BRCA1 founder mutation 3171ins5; a 3.7 cM conserved haplotype of today is a reminiscence of a 1500-year-old mutationA Bergman, Z Einbeigi, U Olofsson, et al.
Pageof 7

Showing results (31-40 of 69) with videos related to

Sort By:
Pageof 7
Molecular Biosystems|May 10, 2017
GeneSPIDER - gene regulatory network inference benchmarking with controlled network and data propertiesAndreas Tjärnberg, Daniel C Morgan, Matthew Studham, et al.
Drug Delivery and Translational Research|June 29, 2017
The role of monocyte subpopulations in vascular injury following partial and transient depletionEtty Grad, Ksenia Zolotarevsky, Haim D Danenberg, et al.
Protein Engineering|February 1, 1991
Cassette mutagenesis of Met121 in azurin from Pseudomonas aeruginosaB G Karlsson, M Nordling, T Pascher, et al.
Bioinformatics (Oxford, England)|June 17, 2014
Functional association networks as priors for gene regulatory network inferenceMatthew E Studham, Andreas Tjärnberg, Torbjörn E M Nordling, et al.
Acta Ophthalmologica|February 21, 2018
Potential link between sporadic cerebral amyloid angiopathy and vision loss: a case reportRupali Vohra, Tina D Hjortshøj, Mette M Nordling, et al.
Human Mutation|November 3, 2000
PMM2 mutation spectrum, including 10 novel mutations, in a large CDG type 1A family material with a focus on Scandinavian familiesC Bjursell, A Erlandson, M Nordling, et al.
Scientific Reports|October 3, 2022
Knowledge of the perturbation design is essential for accurate gene regulatory network inferenceDeniz Seçilmiş, Thomas Hillerton, Andreas Tjärnberg, et al.
Scandinavian Journal of Gastroenterology|April 27, 2017
Effects on Cell Proliferation, Activator Protein-1 and Genotoxicity by Fecal Water from Patients with Colorectal AdenomasM M Nordling, B Glinghammar, P C Karlsson, et al.
Scandinavian Journal of Gastroenterology|June 11, 2003
Effects on cell proliferation, activator protein-1 and genotoxicity by fecal water from patients with colorectal adenomasM M Nordling, B Glinghammar, P C Karlsson, et al.
European Journal of Human Genetics : EJHG|January 10, 2002
The western Swedish BRCA1 founder mutation 3171ins5; a 3.7 cM conserved haplotype of today is a reminiscence of a 1500-year-old mutationA Bergman, Z Einbeigi, U Olofsson, et al.
Pageof 7