Two EcoRI RFLPs at the GLUT2 locus

Por Vilhelmsdotter, S., Luthman, H.
Publicado em 1990

High efficiency polyoma DNA transfection of chloroquine treated cells.

Por Luthman, H, Magnusson, G
Publicado em 1983

Inhibition of polyoma DNA synthesis by base pair substitutions at the replication origin.

Por Luthman, H, Osterlund, M, Magnusson, G
Publicado em 1984

Regulation of human insulin receptor RNA splicing in vivo.

Por Norgren, S, Zierath, J, Wedell, A, Wallberg-Henriksson, H, Luthman, H
Publicado em 1994

Haplotypes of the steroid 21-hydroxylase gene region encoding mild steroid 21-hydroxylase deficiency.

Por Haglund-Stengler, B, Martin Ritzén, E, Gustafsson, J, Luthman, H
Publicado em 1991

Steroid 21-hydroxylase deficiency: three additional mutated alleles and establishment of phenotype-genotype relationships of common mutations.

Por Wedell, A, Ritzén, E M, Haglund-Stengler, B, Luthman, H
Publicado em 1992

Human insulin receptor RFLPs detected by HindIII and DraI.

Por Sten-Linder, M, Stern, I, Bell, G I, Luthman, H
Publicado em 1989

DraI and PstI RFLPs in the tyrosine hydroxylase (TH) and insulin gene (INS) region of chromosome 11.

Por Sten-Linder, M, Granqvist, M, Stern, I, Bell, G I, Luthman, H
Publicado em 1989

Quantitative determination of mdr1 gene expression in leukaemic cells from patients with acute leukaemia.

Por Gruber, A., Vitols, S., Norgren, S., Areström, I., Peterson, C., Björkholm, M., Reizenstein, P., Luthman, H.
Publicado em 1992

Epigenetic regulation of PPARGC1A in human type 2 diabetic islets and effect on insulin secretion

Por Ling, C., Del Guerra, S., Lupi, R., Rönn, T., Granhall, C., Luthman, H., Masiello, P., Marchetti, P., Groop, L., Del Prato, S.
Publicado em 2008

Genetic and functional evaluation of an interleukin-12 polymorphism (IDDM18) in families with type 1 diabetes

Por Bergholdt, R, Ghandil, P, Johannesen, J, Kristiansen, O, Kockum, I, Luthman, H, Ronningen, K, Nerup, J, Julier, C, Pociot, F
Publicado em 2004

21-hydroxylase autoantibodies in adult patients with endocrine autoimmune diseases are highly specific for Addison's disease

Por FALORNI, A, LAURETI, S, NIKOSHKOV, A, PICCHIO, M L, HALLENGREN, B, VANDEWALLE, C L, GORUS, F K, TORTOIOLI, C, LUTHMAN, H, BRUNETTI, P, SANTEUSANIO, F
Publicado em 1997