Search Results - "Parzer, M."
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High solubility of Al and enhanced thermoelectric performance due to resonant states in Fe2VAlx
Published in Applied physics letters (14-02-2022)“…Recently, n-type Fe2VAl-based full-Heusler systems, exhibiting high thermoelectric power factors, have sparked new interest in this material class for…”
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2
Free fatty acids trigger apoptosis and inhibit cell cycle progression in human vascular endothelial cells
Published in The FASEB journal (01-01-2004)“…ABSTRACT Plasma free fatty acid (FFA) concentrations are increased in states of insulin resistance and impair endothelial function. Because the underlying…”
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3
Duplications of the Functional CYP21A2 Gene Are Primarily Restricted to Q318X Alleles: Evidence for a Founder Effect
Published in The journal of clinical endocrinology and metabolism (01-10-2009)“…Context: Rare haplotypes with Q318X mutations and duplicated CYP21A2 genes have been reported to occur in different populations to a varying extent…”
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4
Carrier Frequency of Congenital Adrenal Hyperplasia (21-Hydroxylase Deficiency) in a Middle European Population
Published in The journal of clinical endocrinology and metabolism (01-02-2005)“…Based on newborn screening data, the carrier frequency of congenital adrenal hyperplasia (CAH) in the general population has been estimated to be 1:55. The…”
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5
Reduction of both number and proliferative activity of human endothelial progenitor cells in obesity
Published in International Journal of Obesity (01-04-2010)“…Objective: Circulating endothelial progenitor cells (EPCs), responsible for neoangiogenesis and vascular repair, negatively correlate with vascular dysfunction…”
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6
Fasting and postprandial liver glycogen content in patients with type 1 diabetes mellitus after successful pancreas-kidney transplantation with systemic venous insulin delivery
Published in Clinical endocrinology (Oxford) (01-02-2014)“…Background In patients with type 1 diabetes mellitus (T1DM), insulin is usually replaced systemically (subcutaneously) and not via the physiological portal…”
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Polymorphisms in Exon 13 and Intron 14 of the RET Protooncogene: Genetic Modifiers of Medullary Thyroid Carcinoma?
Published in The journal of clinical endocrinology and metabolism (01-11-2005)“…Context: Single-nucleotide polymorphisms (SNPs) of the RET protooncogene (RET) could modify disease susceptibility and clinical phenotype in patients with…”
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8
High-glucose-triggered apoptosis in cultured endothelial cells
Published in Diabetes (New York, N.Y.) (01-11-1995)“…High ambient glucose concentration, linked to vascular complications in diabetes in vivo, modulates mRNA expression of fibronectin, collagen, tissue-type…”
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Fatty acids induce apoptosis in human smooth muscle cells depending on chain length, saturation, and duration of exposure
Published in Atherosclerosis (01-02-2009)“…Abstract Objective Plasma free fatty acid (FFA) concentrations are increased in states of insulin resistance. Therefore, this study evaluated apoptosis and…”
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10
Modulation by leptin of proliferation and apoptosis in vascular endothelial cells
Published in International Journal of Obesity (01-04-2002)“…AIM: Plasma leptin concentrations not only correlate with body fat mass, but also with the degree of hypertensive retinopathy. The present study was designed…”
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11
Mutational spectrum of steroid 21-hydroxylase and the genotype-phenotype association in Middle European patients with congenital adrenal hyperplasia
Published in European journal of endocrinology (01-07-2005)“…Objective: To analyze the mutational spectrum of steroid 21-hydroxylase (CYP21) and the genotype– phenotype correlation in patients with congenital adrenal…”
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12
Different mechanisms of saturated versus polyunsaturated FFA-induced apoptosis in human endothelial cells
Published in Journal of lipid research (01-12-2008)“…Apoptosis and underlying mechanisms were evaluated in human umbilical vein endothelial cells (HUVECs), in target tissues of late diabetic vascular…”
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13
Insulin does not regulate glucose transport and metabolism in human endothelium
Published in European journal of clinical investigation (01-08-2007)“…Background Although endothelial cells express insulin receptors, it is controversially discussed whether the endothelium represents an insulin‐responsive…”
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14
Evaluation of MEN1 risk in individuals bearing R171Q. R171Q - single nucleotide polymorphism (SNP) or not SNP - that is the question
Published in Clinical endocrinology (Oxford) (01-08-2011)Get full text
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15
Acute effects of hydrocortisone on the metabolic response to a glucose load: increase in the first-phase insulin secretion
Published in European journal of endocrinology (01-08-2010)“…Background and aimSeveral basic science studies support the existence of non-genomic glucocorticoid signaling in pancreas, liver, and adipocytes, but its…”
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16
Predisposition for de Novo Gene Aberrations in the Offspring of Mothers with a Duplicated CYP21A2 Gene
Published in The journal of clinical endocrinology and metabolism (01-03-2007)“…Context: Although CYP21A2 de novo mutations are assumed to account for 1 to 2% of congenital adrenal hyperplasia (CAH) alleles and CYP21 genotyping has been…”
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17
Diabetic LDL Triggers Apoptosis in Vascular Endothelial Cells
Published in Diabetes (New York, N.Y.) (01-05-2003)“…Diabetic LDL Triggers Apoptosis in Vascular Endothelial Cells Michaela Artwohl 1 , Wolfgang F. Graier 2 , Michael Roden 1 , Martin Bischof 1 , Angelika…”
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Thiazolidinediones inhibit apoptosis and heat shock protein 60 expression in human vascular endothelial cells
Published in Thrombosis and haemostasis (01-05-2005)“…This study evaluated direct effects of peroxisome proliferatoractivated receptor gamma(PPARgamma) agonists, including thiazolidinediones (TZDs), on vascular…”
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Increased prevalence of heterozygous 21-OH germline mutations in patients with adrenal incidentalomas
Published in Clinical endocrinology (Oxford) (01-06-2002)“…Summary objective As a result of the widespread use and the enhanced quality of high‐resolution radiological techniques [computed tomography (CT), magnetic…”
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Mutational spectrum of the steroid 21-hydroxylase gene in Austria : Identification of a novel missense mutation
Published in The journal of clinical endocrinology and metabolism (01-10-2001)“…This study attempted an analysis of the mutational spectrum of 21-hydroxylase deficiency in 79 unrelated Austrian patients with classical and nonclassical…”
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