Search Results - "Pulkkinen, Leena"
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Gene expression of peripheral blood mononuclear cells as a tool in dietary intervention studies: What do we know so far?
Published in Molecular nutrition & food research (01-07-2012)“…Peripheral blood mononuclear cells (PBMCs) generally refer to monocytes and lymphocytes, representing cells of the innate and adaptive immune systems. PBMCs…”
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DNA methylation in obesity and type 2 diabetes
Published in Annals of medicine (Helsinki) (01-05-2014)“…To elucidate the mechanisms related to the development of type 2 diabetes (T2D) and other degenerative diseases at a molecular level, a better understanding of…”
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Association of ADIPOQ gene variants with body weight, type 2 diabetes and serum adiponectin concentrations: the Finnish Diabetes Prevention Study
Published in BMC genetics (10-01-2011)“…Adiponectin, secreted mainly by mature adipocytes, is a protein with insulin-sensitising and anti-atherogenic effects. Human adiponectin is encoded by the…”
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Targeted Ablation of the Abcc6 Gene Results in Ectopic Mineralization of Connective Tissues
Published in Molecular and Cellular Biology (01-09-2005)“…Article Usage Stats Services MCB Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley…”
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Mutation analysis and molecular genetics of epidermolysis bullosa
Published in Matrix biology (01-02-1999)“…Cutaneous basement membrane zone (BMZ) consists of a number of attachment structures that are critical for stable association of the epidermis to the…”
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Tissue-Specific Expression of the ABCC6 Gene
Published in Journal of investigative dermatology (01-11-2005)“…The ABCC6 gene encodes MRP6, a member of the multidrug resistance-associated protein (MRP) family. Interest in ABCC6/MRP6 derives, in part, from the fact that…”
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Molecular genetics of pseudoxanthoma elasticum: a metabolic disorder at the environment–genome interface?
Published in Trends in molecular medicine (2001)“…Pseudoxanthoma elasticum (PXE) is a relatively rare heritable disorder affecting the skin, eyes and cardiovascular system, with considerable morbidity and…”
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Variation in the UCP2 and UCP3 genes associates with abdominal obesity and serum lipids: the Finnish Diabetes Prevention Study
Published in BMC medical genetics (21-09-2009)“…We explored the associations of three variants in the uncoupling protein 2 (UCP2) gene, one variant in the UCP2-UCP3 intergenic region and five variants in the…”
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Association of ADIPOR2 gene variants with cardiovascular disease and type 2 diabetes risk in individuals with impaired glucose tolerance: the Finnish Diabetes Prevention Study
Published in Cardiovascular diabetology (24-09-2011)“…Adiponectin is an adipokine with insulin-sensitising and anti-atherogenic effects. Two receptors for adiponectin, ADIPOR1 and ADIPOR2, have been characterized…”
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Variations in the ghrelin receptor gene associate with obesity and glucose metabolism in individuals with impaired glucose tolerance
Published in PloS one (13-08-2008)“…Ghrelin may influence the development of obesity through its role in the control of energy balance, food intake, and regulation of body weight. The effects of…”
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Targeted Inactivation of Murine Laminin γ2-Chain Gene Recapitulates Human Junctional Epidermolysis Bullosa
Published in Journal of investigative dermatology (01-10-2003)“…Junctional forms of epidermolysis bullosa (JEB) are associated with mutations in six distinct genes expressed in the cutaneous basement membrane zone; these…”
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Laminin 5 mutations in junctional epidermolysis bullosa: molecular basis of Herlitz vs non-Herlitz phenotypes
Published in Human genetics (01-01-2002)“…Junctional epidermolysis bullosa (JEB) is a group of heritable blistering diseases in which tissue separation occurs within the lamina lucida of the cutaneous…”
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Revertant Mosaicism in Epidermolysis Bullosa Caused by Mitotic Gene Conversion
Published in Cell (21-02-1997)“…Mitotic gene conversion acting as reverse mutation has not been previously demonstrated in human. We report here that the revertant mosaicism of a compound…”
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Compound Heterozygosity for a Recurrent 16.5-kb Alu-Mediated Deletion Mutation and Single-Base-Pair Substitutions in the ABCC6 Gene Results in Pseudoxanthoma Elasticum
Published in American journal of human genetics (01-03-2001)“…Pseudoxanthoma elasticum (PXE) is a systemic heritable disorder affecting the elastic structures in the skin, eyes, and cardiovascular system, with…”
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Identification of ABCC6 pseudogenes on human chromosome 16p : implications for mutation detection in pseudoxanthoma elasticum
Published in Human genetics (01-09-2001)“…Pseudoxanthoma elasticum (PXE), a heritable disorder affecting the skin, eyes, and the cardiovascular system, has recently been linked to mutations in the…”
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Prenatal diagnosis for Epidermolysis bullosa: a study of 144 consecutive pregnancies at risk
Published in Prenatal diagnosis (01-06-2003)“…Epidermolysis bullosa (EB) is a group of inherited disorders characterized by increased skin fragility, resulting in blisters and erosions after minor trauma…”
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Gene Expression of FTO in Human Subcutaneous Adipose Tissue, Peripheral Blood Mononuclear Cells and Adipocyte Cell Line
Published in Journal of nutrigenetics and nutrigenomics (01-01-2010)“…Background/Aims: The common polymorphism rs9939609 of the fat mass and obesity-associated gene (FTO) is strongly associated with obesity, but the biological…”
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Herlitz's junctional epidermolysis bullosa is linked to mutations in the gene (LAMC2) for the γ2 subunit of nicein/kalinin (LAMININ-5)
Published in Nature genetics (01-03-1994)Get full text
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Mutations in the γ2 chain gene (LAMC2) of kalinin/laminin 5 in the junctional forms of epidermolysis bullosa
Published in Nature genetics (01-03-1994)Get full text
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Ghrelin in Diabetes and Metabolic Syndrome
Published in International journal of peptides (01-01-2010)“…Metabolic syndrome is a cluster of related risk factors for cardiovascular disease, type 2 diabetes and liver disease. Obesity, which has become a global…”
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