Familial osteorthorsisPALOTIE, A.Biomedicine & pharmacotherapy. 1990, Vol 44, Num 6, pp 339-340, issn 0753-3322, 2 p.Article

A DEFECT IN THE STRUCTURE OF TYPE I PROCOLLAGEN IN A PATIENT WHO HAD OSTEOGENESIS IMPERFECTA: EXCESS MANNOSE IN THE COOH-TERMINAL PROPEPTIDEPELTONEN L; PALOTIE A; PROCKOP DJ et al.1980; PROC. NATL. ACAD. SCI. U.S.A., BIOL. SCI.; USA; DA. 1980; VOL. 77; NO 10; PP. 6179-6183; BIBL. 29 REF.Article

Development of molecular genetic methods for monitoring myeloid malignanciesPALOTIE, A; SYVÄNEN, A.-C.Scandinavian journal of clinical & laboratory investigation. Supplement. 1993, Vol 53, Num 213, pp 29-38, issn 0085-591XArticle

THERMAL STABILITY OF TYPE 1 AND TYPE II PROCOLLAGENS FROM NORMAL HUMAN FIBROBLASTS AND FROM A PATIENT WITH OSTEOGENESIS IMPERFECTAPELTONEN L; PALOTIE A; HAYASHI T et al.1980; PROC. NATION. ACAD. SCI.; USA; DA. 1980; VOL. 77; NO 1 PART. 1; PP. 162-166; BIBL. 24 REF.Article

Diagnosis of pancreatic lesions using fine needle aspiration cytology : detection of K-ras point mutations using solid phase minisequencingIHALAINEN, J; TAAVITSAINEN, M; SALMIVAARA, T et al.Journal of clinical pathology. 1994, Vol 47, Num 12, pp 1082-1084, issn 0021-9746Article

DNA-polymorphism of type I collagen gene detected with Bgl II in the genetically isolated Finnish populationAHTI, H; PALOTIE, A; PELTONEN, L et al.Human genetics. 1987, Vol 75, Num 1, pp 79-80, issn 0340-6717Article

Effect of the structural components of basement membranes on the attachment of teratocarcinoma-derived endodermal cellsPALOTIE, A; PELTONEN, L; RISTELI, L et al.Experimental cell research. 1983, Vol 144, Num 1, pp 31-37, issn 0014-4827Article

Components of subendothelial aorta basement membrane Immunohistochemical localization and role in cell attachmentPALOTIE, A; TRYGGVASON, K; PELTONEN, L et al.Laboratory investigation. 1983, Vol 49, Num 3, pp 362-370, issn 0023-6837Article

Hypoparathyroidism in a patient with long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency caused by the G1528C mutationTYNI, T; RAPOLA, J; PALOTIE, A et al.The Journal of pediatrics. 1997, Vol 131, Num 5, pp 766-768, issn 0022-3476Article

Visual mapping by high resolution FISHHEISKANEN, M; PELTONEN, L; PALOTIE, A et al.Trends in genetics (Regular ed.). 1996, Vol 12, Num 10, pp 379-382, issn 0168-9525Article

Regulation of sex hormone-binding globulin production by isoflavonoids and patterns of isoflavonoid conjugation in HepG2 cell culturesLOUKOVAARA, M; CARSON, M; PALOTIE, A et al.Steroids. 1995, Vol 60, Num 9, pp 656-661, issn 0039-128XArticle

RFLP analysis of three different types of acute intermittent porphyriaKAUPPINEN, R; PELTONEN, L; PALOTIE, A et al.Human genetics. 1990, Vol 85, Num 2, pp 160-164, issn 0340-6717Article

High-resolution Fluorescence In Situ Hybridization : A New Approach in Genome MappingPALOTIE, A; HEISKANEN, M; LAAN, M et al.Annals of medicine (Helsinki). 1996, Vol 28, Num 2, pp 101-106, issn 0785-3890Article

Head to tail organization of the human COL6A1 and COL6A2 genes by fiber-FISHHEISKANEN, M; SAITTA, B; PALOTIE, A et al.Genomics (San Diego, Calif.). 1995, Vol 29, Num 3, pp 801-803, issn 0888-7543Article

Characterization of a novel gene, PNUTL2, on human chromosome 17q22-q23 and its exclusion as the Meckel syndrome genePAAVOLA, P; HORELLI-KUITUNEN, N; PALOTIE, A et al.Genomics (San Diego, Calif.). 1999, Vol 55, Num 1, pp 122-125, issn 0888-7543Article

Polymorphic restriction sites of type II collagen gene: their location and frequencies in the finnish populationVAÏSÄNEN, P; ELIMA, K; PALOTIE, A et al.Human heredity. 1988, Vol 38, Num 2, pp 65-71, issn 0001-5652Article

Collagen biosynthesis in systemic scleroderma: regulation of posttranslational modifications and synthesis of procollagen in cultured fibroblastsPELTONEN, L; PALOTIE, A; MYLLYLA, R et al.Journal of investigative dermatology. 1985, Vol 84, Num 1, pp 14-18, issn 0022-202XArticle

Interstitial deletion of bands 11q21→22.3 in a three-year-old girl defined using fluorescence in situ hybridization on metaphase chromosomesHORELLI-KUITUNEN, N; GAHMBERG, N; EEVA, M et al.American journal of medical genetics. 1999, Vol 86, Num 5, pp 416-419, issn 0148-7299Article

Assignment of laminin alpha 2-chain gene (Lama2) to mouse chromosome 10A4-B1 by fluorescence in situ hybridizationSALLINEN, R; KUANG, W; ENGVALL, E et al.Cytogenetics and cell genetics. 1999, Vol 87, Num 3-4, pp 195-196, issn 0301-0171Article

Deficiency in the A-subunit of coagulation factor XIII : two novel point mutations demonstrate different effects on transcript levelsMIKKOLA, H; SYRJÄLÄ, M; VESA RASI et al.Blood. 1994, Vol 84, Num 2, pp 517-525, issn 0006-4971Article

Hypermethylation of the calcitonin gene in the myelodysplastic syndromesJARKKO IHALAINEN; SEPPO PAKKALA; SAVOLAINEN, E.-R et al.Leukemia. 1993, Vol 7, Num 2, pp 263-267, issn 0887-6924Article

Exclusion map of Salla disease : attempts to localize the disease gene using a computer programHAATAJA, L; SCHLEUTKER, J; RENLUND, M et al.Human genetics. 1992, Vol 88, Num 3, pp 298-300, issn 0340-6717Article

Assignment of the locus for a new lethal neonatal metabolic syndrome to 2q33-37VISAPÄÄ, I; FELLMAN, V; VARILO, T et al.American journal of human genetics. 1998, Vol 63, Num 5, pp 1396-1403, issn 0002-9297Article

A colorimetric minisequencing assay for the mutation in codon 506 of the coagulation factor V geneSITBON, G; HURTIG, M; PALOTIE, A et al.Thrombosis and haemostasis. 1997, Vol 77, Num 4, pp 701-703, issn 0340-6245Article

The order and transcriptional orientation of the human COL13A1 and P4HA genes on chromosome 10 long arm determined by high-resolution FISHHORELLI-KUITUNEN, N; KVIST, A.-P; HELAAKOSKI, T et al.Genomics (San Diego, Calif.). 1997, Vol 46, Num 2, pp 299-302, issn 0888-7543Article