Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

T Martinsson

Showing results (101-110 of 146) with videos related to

Pageof 15
Sort By:
Proceedings of the National Academy of Sciences of the United States of America|January 11, 2000
Autosomal dominant myopathy: missense mutation (Glu-706 --> Lys) in the myosin heavy chain IIa geneT Martinsson, A Oldfors, N Darin, et al.
Allergy|February 15, 2007
Inverse relation between nasal fluid Clara Cell Protein 16 levels and symptoms and signs of rhinitis in allergen-challenged patients with intermittent allergic rhinitisM Benson, M Fransson, T Martinsson, et al.
Glycoconjugate Journal|February 1, 1997
Structural and immunochemical identification of Le(a), Le(b), H type 1, and related glycolipids in small intestinal mucosa of a group O Le(a-b-) nonsecretorS Henry, P A Jovall, S Ghardashkhani, et al.
Acta Paediatrica (Oslo, Norway : 1992)|September 15, 1998
Failure of short-term mannose therapy of patients with carbohydrate-deficient glycoprotein syndrome type 1AS Kjaergaard, B Kristiansson, H Stibler, et al.
Genomics|December 1, 1991
Genomic organization and chromosomal localization of the human CTP synthetase gene (CTPS)M Yamauchi, N Yamauchi, G Phear, et al.
Neurology|March 13, 2002
Myosin heavy chain IIa gene mutation E706K is pathogenic and its expression increases with ageH Tajsharghi, L-E Thornell, N Darin, et al.
Genes, Chromosomes & Cancer|November 1, 1989
Neuroblastoma consensus deletion maps to 1p36.1-2A Weith, T Martinsson, C Cziepluch, et al.
The British Journal of Dermatology|February 21, 1998
Genetic counselling in psoriasis: empirical data on psoriasis among first-degree relatives of 3095 psoriatic probandsG Swanbeck, A Inerot, T Martinsson, et al.
The Journal of Investigative Dermatology|November 5, 1997
Significantly earlier age at onset for the HLA-Cw6-positive than for the Cw6-negative psoriatic siblingC Enerbäck, T Martinsson, A Inerot, et al.
Genomics|February 1, 1997
Fine mapping of the gene for carbohydrate-deficient glycoprotein syndrome, type I (CDG1): linkage disequilibrium and founder effect in Scandinavian familiesC Bjursell, H Stibler, J Wahlström, et al.
Pageof 15

Showing results (101-110 of 146) with videos related to

Sort By:
Pageof 15
Proceedings of the National Academy of Sciences of the United States of America|January 11, 2000
Autosomal dominant myopathy: missense mutation (Glu-706 --> Lys) in the myosin heavy chain IIa geneT Martinsson, A Oldfors, N Darin, et al.
Allergy|February 15, 2007
Inverse relation between nasal fluid Clara Cell Protein 16 levels and symptoms and signs of rhinitis in allergen-challenged patients with intermittent allergic rhinitisM Benson, M Fransson, T Martinsson, et al.
Glycoconjugate Journal|February 1, 1997
Structural and immunochemical identification of Le(a), Le(b), H type 1, and related glycolipids in small intestinal mucosa of a group O Le(a-b-) nonsecretorS Henry, P A Jovall, S Ghardashkhani, et al.
Acta Paediatrica (Oslo, Norway : 1992)|September 15, 1998
Failure of short-term mannose therapy of patients with carbohydrate-deficient glycoprotein syndrome type 1AS Kjaergaard, B Kristiansson, H Stibler, et al.
Genomics|December 1, 1991
Genomic organization and chromosomal localization of the human CTP synthetase gene (CTPS)M Yamauchi, N Yamauchi, G Phear, et al.
Neurology|March 13, 2002
Myosin heavy chain IIa gene mutation E706K is pathogenic and its expression increases with ageH Tajsharghi, L-E Thornell, N Darin, et al.
Genes, Chromosomes & Cancer|November 1, 1989
Neuroblastoma consensus deletion maps to 1p36.1-2A Weith, T Martinsson, C Cziepluch, et al.
The British Journal of Dermatology|February 21, 1998
Genetic counselling in psoriasis: empirical data on psoriasis among first-degree relatives of 3095 psoriatic probandsG Swanbeck, A Inerot, T Martinsson, et al.
The Journal of Investigative Dermatology|November 5, 1997
Significantly earlier age at onset for the HLA-Cw6-positive than for the Cw6-negative psoriatic siblingC Enerbäck, T Martinsson, A Inerot, et al.
Genomics|February 1, 1997
Fine mapping of the gene for carbohydrate-deficient glycoprotein syndrome, type I (CDG1): linkage disequilibrium and founder effect in Scandinavian familiesC Bjursell, H Stibler, J Wahlström, et al.
Pageof 15