Fast quantification of nucleic acid hybrids by affinity-based hybrid collection.

Por Syvänen, A C, Laaksonen, M, Söderlund, H
Publicado em 1986

A complex of single-strand binding protein and M13 DNA as hybridization probe.

Por Syvänen, A C, Alanen, M, Söderlund, H
Publicado em 1985

Identification of individuals by analysis of biallelic DNA markers, using PCR and solid-phase minisequencing.

Por Syvänen, A C, Sajantila, A, Lukka, M
Publicado em 1993

Quantification of polymerase chain reaction products by affinity-based hybrid collection.

Por Syvänen, A C, Bengtström, M, Tenhunen, J, Söderlund, H
Publicado em 1988

Time-resolved fluorometry: a sensitive method to quantify DNA-hybrids.

Por Syvänen, A C, Tchen, P, Ranki, M, Söderlund, H
Publicado em 1986

Unexpectedly high allelic diversity at the KIT locus causing dominant white color in the domestic pig.

Por Pielberg, G, Olsson, C, Syvänen, A C, Andersson, L
Publicado em 2002

Recurrence of Marfan syndrome as a result of parental germ-line mosaicism for an FBN1 mutation.

Por Rantamäki, T, Kaitila, I, Syvänen, A C, Lukka, M, Peltonen, L
Publicado em 1999

Cytomegalovirus in urine: detection of viral DNA by sandwich hybridization.

Por Virtanen, M, Syvänen, A C, Oram, J, Söderlund, H, Ranki, M
Publicado em 1984

A chimeric disposition of the elongation factor genes in Rickettsia prowazekii.

Por Syvänen, A C, Amiri, H, Jamal, A, Andersson, S G, Kurland, C G
Publicado em 1996

Structural analysis of the regulatory elements of the type-II procollagen gene. Conservation of promoter and first intron sequences between human and mouse.

Por Vikkula, M, Metsäranta, M, Syvänen, A C, Ala-Kokko, L, Vuorio, E, Peltonen, L
Publicado em 1992

Spectrum of mutations in aspartylglucosaminuria.

Por Ikonen, E, Aula, P, Grön, K, Tollersrud, O, Halila, R, Manninen, T, Syvänen, A C, Peltonen, L
Publicado em 1991

Aspartylglucosaminuria: cDNA encoding human aspartylglucosaminidase and the missense mutation causing the disease.

Por Ikonen, E, Baumann, M, Grön, K, Syvänen, A C, Enomaa, N, Halila, R, Aula, P, Peltonen, L
Publicado em 1991

Rapid diagnostic test for the major mutation underlying Batten disease.

Por Järvelä, I, Mitchison, H M, Munroe, P B, O'Rawe, A M, Mole, S E, Syvänen, A C
Publicado em 1996

The familial hypercholesterolemia (FH)-North Karelia mutation of the low density lipoprotein receptor gene deletes seven nucleotides of exon 6 and is a common cause of FH in Finlan...

Por Koivisto, U M, Turtola, H, Aalto-Setälä, K, Top, B, Frants, R R, Kovanen, P T, Syvänen, A C, Kontula, K
Publicado em 1992

Comparison of methods for pharmacogenomics: SNaPshot, SNPstream UHT, Nanogen, and RFLP

Por Alnæs, GIG, Johansen, FE, Nordgard, SH, Hihn, B, Edvardsen, H, Hilden, VI, Lønning, PE, Syvänen, A-C, Børresen-Dale, A-L, Kristensen, VN
Publicado no Breast Cancer Res (2005)

Digital gene expression profiling of primary acute lymphoblastic leukemia cells

Por Nordlund, J, Kiialainen, A, Karlberg, O, Berglund, E C, Göransson-Kultima, H, Sønderkær, M, Nielsen, K L, Gustafsson, M G, Behrendtz, M, Forestier, E, Perkkiö, M, Söderhäll, S, Lönnerholm, G, Syvänen, A-C
Publicado em 2012

Interferon regulatory factor 5 (IRF5) gene variants are associated with multiple sclerosis in three distinct populations

Por Kristjansdottir, G, Sandling, J K, Bonetti, A, Roos, I M, Milani, L, Wang, C, Gustafsdottir, S M, Sigurdsson, S, Lundmark, A, Tienari, P J, Koivisto, K, Elovaara, I, Pirttilä, T, Reunanen, M, Peltonen, L, Saarela, J, Hillert, J, Olsson, T, Landegren, U, Alcina, A, Fernández, O, Leyva, L, Guerrero, M, Lucas, M, Izquierdo, G, Matesanz, F, Syvänen, A-C
Publicado em 2008