Effect of prevention of procollagen triple-helix formation on proline 3-hydroxylation in freshly isolated chick-embryo tendon cells.

Por Majamaa, K
Publicado em 1981

Labelling of prolyl hydroxylase tetrameric subunits in freshly isolated chick-embryo tendon cells and in certain chick-embryo tissues in vivo.

Por Majamaa, K, Oikarinen, J
Publicado em 1982

Detection of meningeal fibrosis after subarachnoid haemorrhage by assaying procollagen propeptides in cerebrospinal fluid

Por Sajanti, J., Majamaa, K.
Publicado em 1999

High concentrations of procollagen propeptides in chronic subdural haematoma and effusion

Por Sajanti, J, Majamaa, K
Publicado em 2003

Prolyl 3-hydroxylase and 4-hydroxylase activities in certain rat and chick-embryo tissues and age-related changes in their activities in the rat.

Por Tryggvason, K, Majamaa, K, Kivirikko, K I
Publicado em 1979

Regulation of proline 3-hydroxylation and prolyl 3-hydroxylase and 4-hydroxylase activities in transformed cells.

Por Majamaa, K, Myllylä, R, Alitalo, K, Vaheri, A
Publicado em 1982

Familial aggregation of Parkinson's disease in a Finnish population

Por Autere, J., Moilanen, J., Myllyla, V., Majamaa, K.
Publicado em 2000

Partial purification and characterization of chick-embryo prolyl 3-hydroxylase.

Por Tryggvason, K, Majamaa, K, Risteli, J, Kivirikko, K I
Publicado em 1979

Increased risk of sensorineural hearing loss and migraine in patients with a rare mitochondrial DNA variant 4336A>G in tRNA(Gln)

Por Finnila, S., Autere, J., Lehtovirta, M., Hartikainen, P., Mannermaa, A., Soininen, H., Majamaa, K.
Publicado em 2001

APP locus duplication in a Finnish family with dementia and intracerebral haemorrhage

Por Rovelet‐Lecrux, A, Frebourg, T, Tuominen, H, Majamaa, K, Campion, D, Remes, A M
Publicado em 2007

Analysis of mitochondrial DNA sequences in patients with isolated or combined oxidative phosphorylation system deficiency

Por Hinttala, R, Smeets, R, Moilanen, J S, Ugalde, C, Uusimaa, J, Smeitink, J A M, Majamaa, K
Publicado em 2006

Genetics of early onset Parkinson’s disease in Finland: exome sequencing and genome-wide association study

Por Siitonen, A, Nalls, MA, Hernández, D, Gibbs, JR, Ding, J, Ylikotila, P, Edsall, C, Singleton, A, Majamaa, K
Publicado no Neurobiol Aging (2017)

Differences between collagen hydroxylases and 2-oxoglutarate dehydrogenase in their inhibition by structural analogues of 2-oxoglutarate.

Por Majamaa, K, Turpeenniemi-Hujanen, T M, Latipää, P, Günzler, V, Hanauske-Abel, H M, Hassinen, I E, Kivirikko, K I
Publicado em 1985

Epidemiology of the mitochondrial DNA 8344A>G mutation for the myoclonus epilepsy and ragged red fibres (MERRF) syndrome

Por Remes, A, Karppa, M, Rusanen, H, Majamaa, K, Hassinen, I, Moilanen, J, Uimonen, S, Sorri, M, Salmela, P, Karvonen, S, Karvonen, S
Publicado em 2003

No association of the mitochondrial DNA A12308G polymorphism with increased risk of stroke in patients with the A3243G mutation

Por Deschauer, M, Chinnery, P, Schaefer, A, Turnbull, D, Taylor, R, Zierz, S, Shanske, S, DiMauro, S, Majamaa, K, Wilichowski, E, Thorburn, D
Publicado em 2004

Epidemiology of A3243G, the mutation for mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes: prevalence of the mutation in an adult population.

Por Majamaa, K, Moilanen, J S, Uimonen, S, Remes, A M, Salmela, P I, Kärppä, M, Majamaa-Voltti, K A, Rusanen, H, Sorri, M, Peuhkurinen, K J, Hassinen, I E
Publicado em 1998