Search Results - "Lohse, Peter"
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1
Pyoderma gangrenosum, acne, and suppurative hidradenitis (PASH)–a new autoinflammatory syndrome distinct from PAPA syndrome
Published in Journal of the American Academy of Dermatology (01-03-2012)“…Background PAPA syndrome is a recently identified hereditary autoinflammatory syndrome clinically characterized by pyogenic arthritis, severe acne, and…”
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2
Linker Unit Modification of Triphenylamine-Based Organic Dyes for Efficient Cobalt Mediated Dye-Sensitized Solar Cells
Published in Journal of physical chemistry. C (17-10-2013)“…Linker unit modification of donor-linker-acceptor-based organic dyes was investigated with respect to the spectral and physicochemical properties of the dyes…”
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3
Immunohistochemistry in the classification of systemic forms of amyloidosis: a systematic investigation of 117 patients
Published in Blood (12-01-2012)“…Amyloidoses are characterized by organ deposition of misfolded proteins. This study evaluated immunohistochemistry as a diagnostic tool for the differentiation…”
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4
Development of a uniform, very aggressive disease phenotype in all homozygous carriers of the NOD2 mutation p.Leu1007fsX1008 with Crohn’s disease and active smoking status resulting in ileal stenosis requiring surgery
Published in PloS one (27-07-2020)“…Background NOD2 variants are the strongest genetic predictors for susceptibility to Crohn's disease (CD). However, the clinical value of NOD2 on an individual…”
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5
Role of the novel Th17 cytokine IL‐17F in inflammatory bowel disease (IBD): Upregulated colonic IL‐17F expression in active Crohn's disease and analysis of the IL17F p.His161Arg polymorphism in IBD
Published in Inflammatory bowel diseases (01-04-2008)“…Background: Interleukin (IL)‐17F, produced in IL‐23R‐expressing Th17 cells, is a novel member of the IL‐17 cytokine family. Given the association of IL23R with…”
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6
Incidence and classification of pediatric diffuse parenchymal lung diseases in Germany
Published in Orphanet journal of rare diseases (12-12-2009)“…Diffuse parenchymal lung diseases (DPLD) in children represent a rare and heterogeneous group of chronic pulmonary disorders. Despite substantial advances in…”
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7
Eosinophils are a major intravascular location for tissue factor storage and exposure
Published in Blood (01-02-2007)“…Blood cell progenitors were scanned for the presence of the coagulation starter protein tissue factor (TF) by immunoelectron microscopy. Thereby, substantial…”
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8
Ultrafast dynamics of the indoline dye D149 on electrodeposited ZnO and sintered ZrO2 and TiO2 thin films
Published in Physical chemistry chemical physics : PCCP (01-01-2012)“…The ultrafast photoinjection and subsequent relaxation steps of the indoline dye D149 were investigated in detail for a mesoporous electrodeposited ZnO thin…”
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9
Combining a Small Hole-Conductor Molecule for Efficient Dye Regeneration and a Hole-Conducting Polymer in a Solid-State Dye-Sensitized Solar Cell
Published in Journal of physical chemistry. C (30-08-2012)“…In dye-sensitized solar cells (DSC) an efficient transfer of holes from the oxidized dye to the contact is necessary, which in solid-state DSC is performed by…”
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10
12′-Apo-β-caroten-12′-al: An Ultrafast "Spy" Molecule for Probing Local Interactions in Ionic Liquids
Published in Angewandte Chemie International Edition (15-03-2010)“…Superquick espionage: Attaching an aldehyde function to a simple carotenoid generates a powerful laser spectroscopy probe for elucidating solvation dynamics…”
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The NOD2 Single Nucleotide Polymorphism rs72796353 (IVS4+10 A>C) Is a Predictor for Perianal Fistulas in Patients with Crohn's Disease in the Absence of Other NOD2 Mutations
Published in PloS one (06-07-2015)“…A previous study suggested an association of the single nucleotide polymorphism (SNP) rs72796353 (IVS4+10 A>C) in the NOD2 gene with susceptibility to Crohn's…”
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12
Characterization of CSF2RA mutation related juvenile pulmonary alveolar proteinosis
Published in Orphanet journal of rare diseases (26-11-2014)“…Juvenile pulmonary alveolar proteinosis (PAP) due to CSF2RA mutations is a rare disorder with only a few cases described worldwide. We identified nine children…”
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13
Treatment of Muckle-Wells syndrome: analysis of two IL-1-blocking regimens
Published in Arthritis research & therapy (01-01-2013)“…Muckle-Wells syndrome (MWS) is an autoinflammatory disease characterized by excessive interleukin-1 (IL-1) release, resulting in recurrent fevers,…”
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14
Homozygosity for a partial deletion of apoprotein A-V signal peptide results in intracellular missorting of the protein and chylomicronemia in a breast-fed infant
Published in Atherosclerosis (01-03-2014)“…Abstract Deficiency of apoprotein A-V (apoA-V) can cause hypertriglyceridemia. In an 11 months old boy presenting with a severe hypertriglyceridemia, a…”
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15
Femtosecond pump-supercontinuum probe and transient lens spectroscopy of adonixanthin
Published in Archives of biochemistry and biophysics (15-03-2009)“…The ultrafast internal conversion (IC) dynamics of adonixanthin in organic solvents were studied by pump-supercontinuum probe (PSCP) and transient lens (TL)…”
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16
Dielectric relaxation and ultrafast transient absorption spectroscopy of [C6mim]+[Tf2N]−/acetonitrile mixtures
Published in Physical chemistry chemical physics : PCCP (14-03-2012)“…Mixtures of the ionic liquid (IL) [C(6)mim](+)[Tf(2)N](-) and acetonitrile have been investigated by a combination of dielectric relaxation spectroscopy (DRS)…”
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17
Antihistamine-resistant Angioedema in Women with Negative Family History: Estrogens and F12 Gene Mutations
Published in The American journal of medicine (01-12-2013)“…Abstract Background In women with sporadic recurrent angioedema with an unknown cause who are unresponsive to antihistamines and have normal C1 inhibitor…”
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18
The NOD2 p.Leu1007fsX1008 mutation (rs2066847) is a stronger predictor of the clinical course of Crohn's disease than the FOXO3A intron variant rs12212067
Published in PloS one (03-11-2014)“…Very recently, a sub-analysis of genome-wide association scans revealed that the non-coding single nucleotide polymorphism (SNP) rs12212067 in the FOXO3A gene…”
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19
The cannabinoid 1 receptor (CNR1) 1359 G/A polymorphism modulates susceptibility to ulcerative colitis and the phenotype in Crohn's disease
Published in PloS one (26-02-2010)“…Recent evidence suggests a crucial role of the endocannabinoid system, including the cannabinoid 1 receptor (CNR1), in intestinal inflammation. We therefore…”
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20
rs1004819 is the main disease-associated IL23R variant in German Crohn's disease patients: combined analysis of IL23R, CARD15, and OCTN1/2 variants
Published in PloS one (05-09-2007)“…The IL23R gene has been identified as a susceptibility gene for inflammatory bowel disease (IBD) in the North American population. The aim of our study was to…”
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