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G Tromp

Showing results (51-60 of 80) with videos related to

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The Journal of Biological Chemistry|March 15, 1986
Use of R-loop mapping for the assessment of human collagen mutationsW de Wett, M Sippola, G Tromp, et al.
Matrix Biology : Journal of the International Society for Matrix Biology|June 18, 1999
Analysis of coding sequences for tissue inhibitor of metalloproteinases 1 (TIMP1) and 2 (TIMP2) in patients with aneurysmsX Wang, G Tromp, C W Cole, et al.
The Journal of Biological Chemistry|September 15, 1995
Quantitative polymerase chain reaction of lysyl oxidase mRNA in malignantly transformed human cell lines demonstrates that their low lysyl oxidase activity is due to low quantities of its mRNA and low levels of transcription of the respective geneE R Hämäläinen, R Kemppainen, H Kuivaniemi, et al.
Lancet (London, England)|February 8, 1997
Familial intracranial aneurysmsA Ronkainen, J Hernesniemi, M Puranen, et al.
Neurology|August 3, 1999
Founder mutations and the high prevalence of myotonia congenita in northern FinlandH Papponen, T Toppinen, P Baumann, et al.
The Biochemical Journal|August 1, 1988
Structure of a full-length cDNA clone for the prepro alpha 1(I) chain of human type I procollagenG Tromp, H Kuivaniemi, A Stacey, et al.
Matrix Biology : Journal of the International Society for Matrix Biology|December 24, 1997
Synthesis and conformational properties of a recombinant C-propeptide of human type III procollagenK Zafarullah, E M Brown, H Kuivaniemi, et al.
European Journal of Clinical Microbiology & Infectious Diseases : Official Publication of the European Society of Clinical Microbiology|August 16, 2011
Presence of Borrelia burgdorferi sensu lato antibodies in the serum of patients with abdominal aortic aneurysmsI Hinterseher, G Gäbel, F Corvinus, et al.
American Journal of Medical Genetics|May 15, 1993
Single base mutation that substitutes glutamic acid for glycine 1021 in the COL3A1 gene and causes Ehlers-Danlos syndrome type IVP Narcisi, Y Wu, G Tromp, et al.
Human Mutation|January 1, 1997
Two new recurrent nucleotide mutations in the COL1A1 gene in four patients with osteogenesis imperfecta: about one-fifth are recurrentJ Körkkö, H Kuivaniemi, P Paassilta, et al.
Pageof 8

Showing results (51-60 of 80) with videos related to

Sort By:
Pageof 8
The Journal of Biological Chemistry|March 15, 1986
Use of R-loop mapping for the assessment of human collagen mutationsW de Wett, M Sippola, G Tromp, et al.
Matrix Biology : Journal of the International Society for Matrix Biology|June 18, 1999
Analysis of coding sequences for tissue inhibitor of metalloproteinases 1 (TIMP1) and 2 (TIMP2) in patients with aneurysmsX Wang, G Tromp, C W Cole, et al.
The Journal of Biological Chemistry|September 15, 1995
Quantitative polymerase chain reaction of lysyl oxidase mRNA in malignantly transformed human cell lines demonstrates that their low lysyl oxidase activity is due to low quantities of its mRNA and low levels of transcription of the respective geneE R Hämäläinen, R Kemppainen, H Kuivaniemi, et al.
Lancet (London, England)|February 8, 1997
Familial intracranial aneurysmsA Ronkainen, J Hernesniemi, M Puranen, et al.
Neurology|August 3, 1999
Founder mutations and the high prevalence of myotonia congenita in northern FinlandH Papponen, T Toppinen, P Baumann, et al.
The Biochemical Journal|August 1, 1988
Structure of a full-length cDNA clone for the prepro alpha 1(I) chain of human type I procollagenG Tromp, H Kuivaniemi, A Stacey, et al.
Matrix Biology : Journal of the International Society for Matrix Biology|December 24, 1997
Synthesis and conformational properties of a recombinant C-propeptide of human type III procollagenK Zafarullah, E M Brown, H Kuivaniemi, et al.
European Journal of Clinical Microbiology & Infectious Diseases : Official Publication of the European Society of Clinical Microbiology|August 16, 2011
Presence of Borrelia burgdorferi sensu lato antibodies in the serum of patients with abdominal aortic aneurysmsI Hinterseher, G Gäbel, F Corvinus, et al.
American Journal of Medical Genetics|May 15, 1993
Single base mutation that substitutes glutamic acid for glycine 1021 in the COL3A1 gene and causes Ehlers-Danlos syndrome type IVP Narcisi, Y Wu, G Tromp, et al.
Human Mutation|January 1, 1997
Two new recurrent nucleotide mutations in the COL1A1 gene in four patients with osteogenesis imperfecta: about one-fifth are recurrentJ Körkkö, H Kuivaniemi, P Paassilta, et al.
Pageof 8