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K Forsman-Semb

Showing results (1-10 of 11) with videos related to

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Investigative Ophthalmology & Visual Science|April 2, 1999
Bothnia dystrophy caused by mutations in the cellular retinaldehyde-binding protein gene (RLBP1) on chromosome 15q26M S Burstedt, O Sandgren, G Holmgren, et al.
The EMBO Journal|April 4, 2000
Regulatory cross-talk between adhesin operons in Escherichia coli: inhibition of type 1 fimbriae expression by the PapB proteinY Xia, D Gally, K Forsman-Semb, et al.
Free Radical Biology & Medicine|October 24, 2003
Overexpression of Prdx6 reduces H2O2 but does not prevent diet-induced atherosclerosis in the aortic rootS A Phelan, X Wang, P Wallbrandt, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|February 15, 2001
Ocular phenotype of bothnia dystrophy, an autosomal recessive retinitis pigmentosa associated with an R234W mutation in the RLBP1 geneM S Burstedt, K Forsman-Semb, I Golovleva, et al.
Journal of Neurochemistry|December 3, 1999
Genomic organization of human DLG4, the gene encoding postsynaptic density 95D G Stathakis, N Udar, O Sandgren, et al.
Journal of Dental Research|May 31, 2001
Cloning and characterization of the mouse and human enamelin genesJ C Hu, C H Zhang, Y Yang, et al.
Neurology|December 11, 2002
Identification of a susceptibility locus for migraine with and without aura on 6p12.2-p21.1A Carlsson, L Forsgren, P-O Nylander, et al.
The European Respiratory Journal|October 4, 2011
Total desmosines in plasma and urine correlate with lung functionC A Lindberg, G Engström, M Gerhardsson de Verdier, et al.
European Journal of Oral Sciences|May 2, 2001
Human ameloblastin gene: genomic organization and mutation analysis in amelogenesis imperfecta patientsC K Mårdh, B Bäckman, D Simmons, et al.
Ophthalmic Genetics|January 3, 2001
Autosomal dominant cone-rod dystrophy due to a missense mutation (R838C) in the guanylate cyclase 2D gene (GUCY2D) with preserved rod function in one branch of the familyM Van Ghelue, H L Eriksen, V Ponjavic, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Investigative Ophthalmology & Visual Science|April 2, 1999
Bothnia dystrophy caused by mutations in the cellular retinaldehyde-binding protein gene (RLBP1) on chromosome 15q26M S Burstedt, O Sandgren, G Holmgren, et al.
The EMBO Journal|April 4, 2000
Regulatory cross-talk between adhesin operons in Escherichia coli: inhibition of type 1 fimbriae expression by the PapB proteinY Xia, D Gally, K Forsman-Semb, et al.
Free Radical Biology & Medicine|October 24, 2003
Overexpression of Prdx6 reduces H2O2 but does not prevent diet-induced atherosclerosis in the aortic rootS A Phelan, X Wang, P Wallbrandt, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|February 15, 2001
Ocular phenotype of bothnia dystrophy, an autosomal recessive retinitis pigmentosa associated with an R234W mutation in the RLBP1 geneM S Burstedt, K Forsman-Semb, I Golovleva, et al.
Journal of Neurochemistry|December 3, 1999
Genomic organization of human DLG4, the gene encoding postsynaptic density 95D G Stathakis, N Udar, O Sandgren, et al.
Journal of Dental Research|May 31, 2001
Cloning and characterization of the mouse and human enamelin genesJ C Hu, C H Zhang, Y Yang, et al.
Neurology|December 11, 2002
Identification of a susceptibility locus for migraine with and without aura on 6p12.2-p21.1A Carlsson, L Forsgren, P-O Nylander, et al.
The European Respiratory Journal|October 4, 2011
Total desmosines in plasma and urine correlate with lung functionC A Lindberg, G Engström, M Gerhardsson de Verdier, et al.
European Journal of Oral Sciences|May 2, 2001
Human ameloblastin gene: genomic organization and mutation analysis in amelogenesis imperfecta patientsC K Mårdh, B Bäckman, D Simmons, et al.
Ophthalmic Genetics|January 3, 2001
Autosomal dominant cone-rod dystrophy due to a missense mutation (R838C) in the guanylate cyclase 2D gene (GUCY2D) with preserved rod function in one branch of the familyM Van Ghelue, H L Eriksen, V Ponjavic, et al.
Pageof 2