A. Iitiä

发表

Detection of human immunodeficiency virus type 1 by using the polymerase chain reaction and a time-resolved fluorescence-based hybridization assay

Å. Frostell, P. Dahlén, M. Kwiatkowski, 1991, Journal of clinical microbiology.

Triple-label hybridization assay for type-1 diabetes-related HLA alleles.

J. Ilonen, H. Reijonen, T. Lövgren, 1995, BioTechniques.

Robust nonradioactive oligonucleotide ligation assay to detect a common point mutation in the CYP2D6 gene causing abnormal drug metabolism.

M. Hørder, O. Blaabjerg, N. E. Petersen, 1995, Clinical chemistry.

Rapid HLA-DQB1 Genotyping for Four Alleles in the Assessment of Risk for IDDM in the Finnish Population

J. Ilonen, M. Knip, H. Reijonen, 1996, Diabetes Care.

Time-resolved fluorometry in the genetic diagnosis of familial defective apolipoprotein B-100.

M. Eriksson, B. Angelin, O. Wiklund, 1994, Journal of lipid research.

Simultaneous detection of two cystic fibrosis alleles using dual-label time-resolved fluorometry.

H. Siitari, A. Iitiä, L. Liukkonen, 1992, Molecular and cellular probes.

Detection of amplified HTLV-I/-II viral sequences using time-resolved fluorometry.

H. Siitari, P. Dahlén, M. Nunn, 1992, Analytical biochemistry.

15 – Detection of Lanthanide Chelates by Time-Resolved Fluorescence

T. Lövgren, A. Iitiä, T. Lövgren, 1995 .

Detection of Philadelphia chromosome using PCR and europium-labeled DNA probes.

H. Siitari, P. Dahlén, J. Eskola, 1994, Clinical biochemistry.

Population screening for the common G985 mutation causing medium-chain acyl-CoA dehydrogenase deficiency with Eu-labeled oligonucleotides and the DELFIA system.

A Green, R. Pollitt, A. Green, 1997, Clinical chemistry.

The frequency of an inactivating point mutation (566C-->T) of the human follicle-stimulating hormone receptor gene in four populations using allele-specific hybridization and time-resolved fluorometry.

A. de la Chapelle, K. Aittomäki, I. Huhtaniemi, 1998, The Journal of clinical endocrinology and metabolism.

Sensitive bioaffinity assays with individual microparticles and time-resolved fluorometry.

K. Pettersson, T. Lövgren, H. Hakala, 1997, Clinical Chemistry.

Simple triple-label detection of seven cystic fibrosis mutations by time-resolved fluorometry.

T. Lövgren, T. Torresani, A. Iitiä, 1997, Clinical chemistry.

Europium-labeled oligonucleotide hybridization probes: preparation and properties.

T. Lövgren, H. Siitari, P. Hurskainen, 1994, Bioconjugate chemistry.

The use of europium (Eu3+) labelled primers in PCR amplification of specific target DNA.

P. Hurskainen, P. Dahlén, M. Kwiatkowski, 1991, Molecular and cellular probes.

Quantitative reverse transcription-PCR assay with an internal standard for the detection of prostate-specific antigen mRNA.

H. Lilja, M. Karp, T. Lövgren, 1999, Clinical chemistry.

C-terminal truncations of a thermostable Bacillus stearothermophilus alpha-amylase.

M. Vihinen, P. Mäntsälä, I. Suominen, 1994, Protein engineering.

Detection of a point mutation using short oligonucleotide probes in allele-specific hybridization.

M. Mikola, N. Gregersen, T. Lövgren, 1994, BioTechniques.

Time‐resolved fluorometry in the diagnosis of Leber hereditary optic neuroretinopathy

K. Huoponen, M. Savontaus, H. Siitari, 1994, Human mutation.

Detection of mutation delta F508 in the cystic fibrosis gene using allele-specific PCR primers and time-resolved fluorometry.

J. Vuust, H. Siitari, E. Høgdall, 1992, PCR methods and applications.

Determination of a common genetic variant of luteinizing hormone using DNA hybridization and immunoassays

S. Easteal, I. Huhtaniemi, K. Pettersson, 1998, Clinical endocrinology.