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Molecular Biosystems
|
May 10, 2017
GeneSPIDER - gene regulatory network inference benchmarking with controlled network and data properties
Andreas 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 depletion
Etty Grad, Ksenia Zolotarevsky, Haim D Danenberg, et al.
Protein Engineering
|
February 1, 1991
Cassette mutagenesis of Met121 in azurin from Pseudomonas aeruginosa
B G Karlsson, M Nordling, T Pascher, et al.
Bioinformatics (Oxford, England)
|
June 17, 2014
Functional association networks as priors for gene regulatory network inference
Matthew 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 report
Rupali 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 families
C Bjursell, A Erlandson, M Nordling, et al.
Scientific Reports
|
October 3, 2022
Knowledge of the perturbation design is essential for accurate gene regulatory network inference
Deniz 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 Adenomas
M 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 adenomas
M 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 mutation
A Bergman, Z Einbeigi, U Olofsson, et al.
Page
of 7
Search research articles
Search
Showing results (31-40 of 69) with videos related to
Sort By:
Page
of 7
Molecular Biosystems
|
May 10, 2017
GeneSPIDER - gene regulatory network inference benchmarking with controlled network and data properties
Andreas 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 depletion
Etty Grad, Ksenia Zolotarevsky, Haim D Danenberg, et al.
Protein Engineering
|
February 1, 1991
Cassette mutagenesis of Met121 in azurin from Pseudomonas aeruginosa
B G Karlsson, M Nordling, T Pascher, et al.
Bioinformatics (Oxford, England)
|
June 17, 2014
Functional association networks as priors for gene regulatory network inference
Matthew 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 report
Rupali 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 families
C Bjursell, A Erlandson, M Nordling, et al.
Scientific Reports
|
October 3, 2022
Knowledge of the perturbation design is essential for accurate gene regulatory network inference
Deniz 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 Adenomas
M 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 adenomas
M 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 mutation
A Bergman, Z Einbeigi, U Olofsson, et al.
Page
of 7