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Menstrual disorders in adolescence: a marker for hyperandrogenaemia and increased metabolic risks in later life? Finnish general population-based birth cohort study

Human reproduction (Oxford), 2012-11, Vol.27 (11), p.3279-3286

2012

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ENDOGENOUS BMP-4 AND BMP-7 GENE EXPRESSION IN CD-1 MOUSE DURING CHONDROGENESIS INDUCED BY BOVINE BONE MORPHOGENETIC PROTEIN IMPLANTATION

Journal of musculoskeletal research, 2000-09, Vol.4 (3), p.161-168

2000

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Osteoinductivity of partially purified native ostrich ( Struthio camelus) bone morphogenetic protein: Comparison with mammalian species

Life sciences (1973), 2005-09, Vol.77 (19), p.2425-2437

2005

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Mutations in the AIRE Gene: Effects on Subcellular Location and Transactivation Function of the Autoimmune Polyendocrinopathy-Candidiasis–Ectodermal Dystrophy Protein

American journal of human genetics, 2000-02, Vol.66 (2), p.378-392

2000

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Biofuel developments in Sweden and the Netherlands Protection and socio-technical change in a long-term perspective

Renewable & sustainable energy reviews, 2009-08, Vol.13 (6-7), p.1406-1417

2009

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APECED‐causing mutations in AIRE reveal the functional domains of the protein

Human mutation, 2004-03, Vol.23 (3), p.245-257

2004

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Subcellular Location and Expression Pattern of Autoimmune Regulator (Aire), the Mouse Orthologue for Human Gene Defective in Autoimmune Polyendocrinopathy Candidiasis Ectodermal Dystrophy (APECED)

The journal of histochemistry and cytochemistry, 2001-02, Vol.49 (2), p.197-208

2001

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AIRE mutations and human leukocyte antigen genotypes as determinants of the autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy phenotype

The journal of clinical endocrinology and metabolism, 2002-06, Vol.87 (6), p.2568

2002

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Localization of the APECED Protein in Distinct Nuclear Structures

Human molecular genetics, 1999-02, Vol.8 (2), p.259-266

1999

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Functional analysis of SAND mutations in AIRE supports dominant inheritance of the G228W mutation

Human mutation, 2005-10, Vol.26 (4), p.322-331

2005

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Binding of a new Ca2+ sensitizer, levosimendan, to recombinant human cardiac troponin C. A molecular modelling, fluorescence probe, and proton nuclear magnetic resonance study

The Journal of biological chemistry, 1994-11, Vol.269 (46), p.28584-28590

1994

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Monogenic autoimmune diseases — lessons of self-tolerance

Current Opinion in Immunology, 2005-12, Vol.17 (6), p.609-615

2005

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The TRIM37 Gene Encodes a Peroxisomal RING-B-Box-Coiled-Coil Protein: Classification of Mulibrey Nanism as a New Peroxisomal Disorder

American journal of human genetics, 2002-05, Vol.70 (5), p.1215-1228

2002

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Aire deficient mice do not develop the same profile of tissue-specific autoantibodies as APECED patients

Journal of autoimmunity, 2006-09, Vol.27 (2), p.96-104

2006

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Triallelic patterns in STR loci used for paternity analysis: Evidence for a duplication in chromosome 2 containing the TPOX STR locus

Forensic science international, 2006-12, Vol.164 (1), p.3-9

2006

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Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED) in the Irish population

Journal of Pediatric Endocrinology and Metabolism, 2006-11, Vol.19 (11), p.1343

2006

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Genotypes of catechol- O-methyltransferase and response to levodopa treatment in patients with Parkinson's disease

Neuroscience letters, 2001-02, Vol.298 (2), p.131-134

2001

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Genomic organization of the human catechol O‐methyltransferase gene and its expression from two distinct promoters

European journal of biochemistry, 1994-08, Vol.223 (3), p.1049-1059

1994

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Childcare and eldercare policies in Sweden

The Sandwich Generation, 2017, p.242-261

2017

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Functional consequences of amyloidosis mutation for gelsolin polypeptide — analysis of gelsolin-actin interaction and gelsolin processing in gelsolin knock-out fibroblasts

FEBS letters, 1999-07, Vol.454 (3), p.233-239

1999

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Cloning and characterization of human placental catechol-O-methyltransferase cDNA

DNA and cell biology, 1991-04, Vol.10 (3), p.181

1991

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Production of human UDP-glucuronosyltransferases 1A6 and 1A9 using the Semliki Forest virus expression system

Life sciences (1973), 2000-10, Vol.67 (20), p.2473-2484

2000

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The autoimmune regulator: a key toward understanding the molecular pathogenesis of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy

The Keio Journal of Medicine, 2001, Vol.50(4), pp.225-239

2001

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A unique cap(m 7GpppXm)-dependent influenza virion endonuclease cleaves capped RNAs to generate the primers that initiate viral RNA transcription

Cell, 1981-03, Vol.23 (3), p.847-858

1981

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Molecular cloning and characterization of rat liver catechol- O-methyltransferase

Gene, 1990, Vol.93 (2), p.241-247

1990

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Molecular Sequence Data
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Menstrual disorders in adolescence: a marker for hyperandrogenaemia and increased metabolic risks in later life? Finnish general population-based birth cohort study

ENDOGENOUS BMP-4 AND BMP-7 GENE EXPRESSION IN CD-1 MOUSE DURING CHONDROGENESIS INDUCED BY BOVINE BONE MORPHOGENETIC PROTEIN IMPLANTATION

Osteoinductivity of partially purified native ostrich ( Struthio camelus) bone morphogenetic protein: Comparison with mammalian species

Mutations in the AIRE Gene: Effects on Subcellular Location and Transactivation Function of the Autoimmune Polyendocrinopathy-Candidiasis–Ectodermal Dystrophy Protein

Biofuel developments in Sweden and the Netherlands Protection and socio-technical change in a long-term perspective

APECED‐causing mutations in AIRE reveal the functional domains of the protein

Subcellular Location and Expression Pattern of Autoimmune Regulator (Aire), the Mouse Orthologue for Human Gene Defective in Autoimmune Polyendocrinopathy Candidiasis Ectodermal Dystrophy (APECED)

AIRE mutations and human leukocyte antigen genotypes as determinants of the autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy phenotype

Localization of the APECED Protein in Distinct Nuclear Structures

Functional analysis of SAND mutations in AIRE supports dominant inheritance of the G228W mutation

Binding of a new Ca2+ sensitizer, levosimendan, to recombinant human cardiac troponin C. A molecular modelling, fluorescence probe, and proton nuclear magnetic resonance study

Monogenic autoimmune diseases — lessons of self-tolerance

The TRIM37 Gene Encodes a Peroxisomal RING-B-Box-Coiled-Coil Protein: Classification of Mulibrey Nanism as a New Peroxisomal Disorder

Aire deficient mice do not develop the same profile of tissue-specific autoantibodies as APECED patients

Triallelic patterns in STR loci used for paternity analysis: Evidence for a duplication in chromosome 2 containing the TPOX STR locus

Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED) in the Irish population

Genotypes of catechol- O-methyltransferase and response to levodopa treatment in patients with Parkinson's disease

Genomic organization of the human catechol O‐methyltransferase gene and its expression from two distinct promoters

Childcare and eldercare policies in Sweden

Functional consequences of amyloidosis mutation for gelsolin polypeptide — analysis of gelsolin-actin interaction and gelsolin processing in gelsolin knock-out fibroblasts

Cloning and characterization of human placental catechol-O-methyltransferase cDNA

Production of human UDP-glucuronosyltransferases 1A6 and 1A9 using the Semliki Forest virus expression system

The autoimmune regulator: a key toward understanding the molecular pathogenesis of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy

A unique cap(m 7GpppXm)-dependent influenza virion endonuclease cleaves capped RNAs to generate the primers that initiate viral RNA transcription

Molecular cloning and characterization of rat liver catechol- O-methyltransferase

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