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What does Gemütlichkeit literally translate as?

What does literally translate as?

The adjective“gemütlich” means ‘cosy/comfortable’, and by adding “keit” onto the end it becomes a noun meaning “the feeling of comfort/cosiness”. Interestingly, the noun Gemüt in gemütlich is also quite difficult to accurately translate: broadly speaking, it refers to mood and feeling.

How can you use it in a sentence?

Using the adjective, you can say “So gemütlich wie Zuhause wird es nie hier“, meaning something like „It will never be as cosy/comfortable here as it is at home”.

What is the nearest English equivalent?

It translates to “cosiness” or “comfort”, but those words aren’t adequate because they are too simple for the concept of Gemütlichkeit .

Sind deutsche Weihnachtsmärkte gemütlich? Are German Christmas markets gemütlich? Photo by Adelina Horn on flickr.com

Interesting facts:

Gemütlichkeit Days

Fremdscham: Second-hand embarassment

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Sadistic pleasure, sadism

Drachenfutter: Doghouse key (related to being ‘in the doghouse’), peace offering

Please feel free to add any more. Until next time!

Also – hooray for Germany in the football!!

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About the Author: Constanze

Servus! I'm Constanze. I'm half English and half German. I write here because I'm passionate about my languages and my roots. I also work as a translator group fitness instructor.

Years ago I learned a German nursery rhyme called “Hänchen klein” and there was a part that said “Stock und Hut steht ihn gut / ist gar wohl gemüt.” I never understood what gemüt meant, and my German teacher did a poor job explain it. I’ve been hung up on it for years but this finally explains it; it makes so much sense now! Thank you!


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I think I remember that song from my own childhood!! I’m so glad that my post helped you to understand that word a little better. Thank you for your comment.

Jens Tröger:

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What's This Home Worth?
Sell with Long Foster
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Listing Updated 7/6/2018 10:25 PM
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Status: Closed
MLS#: 329431
Type: Residential - Single Family-Detached
Style: Victorian
County: Pulaski

Large Victorian style home with large rooms and abundant square footage. Hard wood floors throughout. This could be an Investment opportunity. This home has a lot of potential and could be beautiful if properly restored.

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Research Article
Dentin reactions to caries are misinterpreted by histological “gold standards” [version 1; referees: 1 approved, 2 approved with reservations]
Priscila Florentino Silva, Danilo Augusto de Holanda Ferreira, Kássia Regina Simões Meira, Franklin Delano Soares Forte, Ana Maria Barros Chaves, Hermès Leather Bogue Oxfords Buy Cheap Sneakernews Free Shipping Manchester Great Sale Free Shipping With Credit Card Clearance Authentic B9Phu5R
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Kássia Regina Simões Meira, Franklin Delano Soares Forte, Ana Maria Barros Chaves, Frederico Barbosa de Sousa
PUBLISHED 16 一月 2014
Department of Morphology, Health Science Center, Federal University of Paraiba, Cidade Universitária, Paraiba, 58051-900, João Pessoa, Brazil Laboratory of Microscopy and Biological Image, Health Sciences Center, Federal University of Paraiba, Cidade Universitária, Paraiba, 58051-900, João Pessoa, Brazil Department of Clinical and Social Dentistry, Health Sciences Center, Federal University of Paraiba, Cidade Universitária, Paraiba, 58051-900, João Pessoa, Brazil


Dentin reactions to caries, crucial for pathogenesis and for the determination of the severity of caries lesions, are believed to be reasonably detected by stereomicroscopy (SM) and polarized light microscopy in quinoline (PLMQ), but accuracies are not available. Here, stereomicroscopy of wet (SW) and dry (SD) ground sections of natural occlusal caries lesions resulted in moderate (0.7, for normal dentin) and low accuracies (< 0.6, for carious and sclerotic dentin) as validated by contrast-corrected microradiography. Accuracies of PLMQ were moderate for both normal (0.71) and carious dentin (0.71). The hypothesis that detection of dentin reactions by SM and PLMQ would be influenced by the contrast quality of micrographic images was rejected. Dentin reactions were scored by SW, SD, PLMQ, and three types of microradiographic images with varying contrast qualities and each technique was compared against the one that resulted in the highest number of scores for each dentin reaction. Large differences resulted, mainly related to the detection of sclerotic dentin by both SW and SD, and normal and carious dentin by PLMQ. It is concluded that contrast-corrected microradiography should be preferred as the gold standard and SM and PLMQ should be avoided, but the relationship of PLMQ with dentin mineralization deserves further investigation.


sclerotic dentin, dentin, dental caries, histopathology, diagnosis, stereomicroscopy, microradiography

Corresponding Author(s)
Frederico Barbosa de Sousa ( [email protected] )
Grant information: The first author received a master degree scholarship from CNPq (Brazilian Ministry of Science, Innovation and Technology).


Dentin reactions to caries are crucial for the pathogenesis and severity determination of caries lesions. Since caries is mainly a demineralization process, the high ratio of X-ray absorbance between calcium and the chemical elements of the organic content, and the fact that the density of the mineral content is higher (more than 2 times) than that of the organic content, radiography with microscopic resolution (microradiography, MR) is considered as a highly reliable gold standard for detecting variations in dentin mineral content. Also widely accepted as gold standards for dentin reactions are stereomicroscopy (SM; commonly referred as histology) and (to a lesser extent) polarized light microscopy with quinoline as the immersion medium (PLMQ). The acceptance of SW, the currently most used “gold standard”, is based on studies reporting opaque and translucent dentin under SM related to radiolucent and radiopaque dentin, respectively. It is lacking, however, accuracy in numbers. To our knowledge, data regarding the accuracy of SM are available from only one study that included unerupted teeth and no data on translucent/sclerotic dentin. In addition, early studies with MR reported cases classified as translucent dentin by transmitted light microscopy (where the interaction of light with dentin is similar to that under SM) that were then classified as demineralized dentin by the use of MR.

Currently the only evidence for the detection of dentin reactions by PLMQ is only qualitative. Thus, research into the accuracy of SM and PLMQ is needed. Regarding the use of MR as a gold standard, it must be considered that images of microradiographic plates taken using transmitted light microscopy are commonly biased by the effect of heterogeneous illumination, which is inversely proportional to the objective magnification. Heterogeneous illumination is expected to influence judgment of brightness (a procedure required for diagnosis from MR images), possibly including bias when other techniques are validated using MR.

The aim of this study was three fold: to test the accuracy of both SM and PLMQ in detecting dentin reactions to natural caries; to test the hypothesis that elements of accuracy are influenced by the quality of the microradiographic image contrast; and to test the hypothesis that SM, PLMQ and MR (regardless of image contrast quality) detect dentin reactions equally.

Diagnosis of occlusal caries lesions using ICDAS II

Forty three erupted third molars with various stages of natural occlusal caries were collected from volunteers who signed consent terms (as approved by the Ethical Committee of the Federal University of Paraiba; certificate of ethical appreciation number 4125.0.000.126-10). All teeth were gently cleaned with 1% hypochlorite solution (Vetec, Brazil), mounted in a wax base and surrounded by a rubber dam isolator prior to analysis of their occlusal surfaces using the ICDAS II scoring system. Before obtaining final ICDAS scores for analysis, examiners were calibrated using a sub-set of the whole sample. Thirty occlusal sites were scored by two calibrated examiners (Kappa’s intra-examiner’s scores of 0.9 and 0.89, and 0.85 for inter-examiner agreement), with a one week interval, in order to test intra- and inter-examiner reproducibilities. Final scores were those obtained by a consensus between examiners. In nine teeth, two sites on the occlusal surface were selected, yielding a total of 52 occlusal caries lesions.

Ground section preparation

All teeth were cut longitudinally to their crowns (through their occlusal surfaces) using a diamond disc mounted (Kavo Sorensen, Brazil) in a low-speed handpiece under water irrigation, so that a section of the selected site with a given IDCAS score was obtained. All cuts were then ground using a customized metallic (brass) lapping jip and silicon carbide paper (granulations of 240–1200) under water irrigation to achieve a final thickness of ~100 ± 20 μm. Prepared ground sections (n = 52) were kept in a 0.02% sodium azide aqueous solution until examination.

Calibration of examiners of ground sections and selection of histological sites

At each ground section, histological sites (area of ~150 μm × 150 μm) presenting suggestive signs of normal, carious, or sclerotic dentin were selected. All examinations of ground sections (SM of wet and dry samples, three types of MR images, and PLMQ) were performed by the same two examiners, whose intra and inter-examiner reproducibilities were determined (using Kappa’s statistics) from their scores of all histological sites (of all samples) from each technique obtained with a one week interval. Examiners agreed on the final scores by consulting with each other.

Histological sites were selected from the outer half of the dentin layer, including the area adjacent to the deepest enamel lesion; at least one dentin reaction type per sample was included where possible. Cases were included in the sample when two sites had the same type of dentin reaction detected by SM, while showing different types of dentin reactions when detected using MR. Thus, up to 6 histological sites were selected per sample, yielding a total sample size of 168 sites.

Stereomicroscopy (SM)

SM (10× magnification) with reflected light was used to analyze ground sections under two conditions: wet (SW) and dried (SD; after exposure to 25ºC and 50% relative humidity for 2 hours). Temperature and relative humidity were measured just adjacent to the samples. Digital photomicrographs (digital camera Nikon D80) of wet and dried samples were obtained. Dentin reactions were scored as normal, carious discolored (white/yellow/brown), and translucent (“sclerotic”).

Microradiography (MR)

All samples were mounted in a microradiographic plate (resolution of 2000 lines/mm; AGHD plates, Microchrome Technology, San Jose, USA) and exposed to X-rays in a PCBA Inspector (tungsten anode filtered with a 0.25 mm-thick beryllium window, GE, Germany) for 25 minutes using 40 keV and 0.25 mA. Digital photomicrographs of the microradiographic plate were obtained in a transmitted light microscope (2× objective) under different conditions:

Condition 1: using the condenser aligned according to the principles of Kohler illumination for low magnification objectives;

Condition 2: no condenser and using a light shaping filter (Luminit, USA) above the field diaphragm.

The possible scores for dentin reactions using MR were: normal dentin, demineralized (radiolucent) dentin, and hypermineralized (highly radiopaque; sclerotic) dentin. Digital images were analysed (using the freeware program ImageJ, NIH, USA) with the following contrast conditions:

Image obtained with aligned condenser, without any adjustment of brightness and contrast from ImageJ, and no light shaping filter (NFNBC image);

Image obtained with aligned condenser, no light shaping filter, but with adjustment of brightness and contrast from ImageJ (NFBC image);

Image obtained without a condenser, with both a light shaping filter and adjustment of brightness and contrast from ImageJ (FBC image).

Such conditions created an ordinary scale of heterogeneous illumination of the field of view. Images without light shaping filter (NF) and FBC images presented a Gaussian normalized light intensity (R = 0.87 for both) across the field of view with heights of 0.13 and 0.05 (lower heterogeneity), respectively. Brightness and contrast adjustment (according to a consensus from both examiners) allowed this difference to be easily detected by the naked eye.

Polarized light microscopy in quinoline (PLMQ)

Ground sections were dried at room temperature for 24 hours, immersed in quinoline (Vetec, Brazil) for 24 hours, and then were positioned with the dentin tubules at – 45º on the stage of a polarizing microscope (Axioskop, Carl Zeiss, Germany) equipped with a Red I filter, 2× objective, and digital camera (Nikon D80, Japan). Dentin reactions were scored as either negatively (carious) or positively birefringent (normal). Since the technique of PLMQ is not intended to diagnosis dentin sclerosis, no diagnosis of sclerotic dentin was attempted. Color digital images were split into color channels using ImageJ, resulting in a sharp demarcation of negatively and positively birefringent areas.

We tested the accuracies of the SW, SD, and PLMQ techniques for detecting dentin reactions using the FBC MR image as the gold standard in all cases. Total positive (TP), total negative (TN), false positive (FP), and false negative values (FN) were obtained and used to calculate accuracy (AC) from:

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Nishii, Kenichiro; Brodin, Erik; Renshaw, Taylor; Weesner, Rachael; Moran, Emma; Soker, Shay; Sparks, Jessica L


The role of fluid stresses in activating the hepatic stem/progenitor cell regenerative response is not well understood. This study hypothesized that immediate early genes (IEGs) with known links to liver regeneration will be upregulated in liver progenitor cells (LPCs) exposed to in vitro shear stresses on the order of those produced from elevated interstitial flow after partial hepatectomy. The objectives were: (1) to develop a shear flow chamber for application of fluid stress to LPCs in 3D culture; and (2) to determine the effects of fluid stress on IEG expression in LPCs. Two hours of shear stress exposure at ∼4 dyn/cm 2 was applied to LPCs embedded individually or as 3D spheroids within a hyaluronic acid/collagen I hydrogel. Results were compared against static controls. Quantitative reverse transcriptase polymerase chain reaction was used to evaluate the effect of experimental treatments on gene expression. Twenty-nine genes were analyzed, including IEGs and other genes linked to liver regeneration . Four IEGs (CFOS, IP10, MKP1, ALB) and three other regeneration -related genes (WNT, VEGF, EpCAM) were significantly upregulated in LPCs in response to fluid mechanical stress. LPCs maintained an early to intermediate stage of differentiation in spheroid culture in the absence of the hydrogel, and addition of the gel initiated cholangiocyte differentiation programs which were abrogated by the onset of flow. Collectively the flow-upregulated genes fit the pattern of an LPC-mediated proliferative/regenerative response. These results suggest that fluid stresses are potentially important regulators of the LPC-mediated regeneration response in liver . © 2017 Wiley Periodicals, Inc.

Effect of Resorbable Collagen Plug on Bone Regeneration in Rat Critical-Size Defect Model.

Liu, Weiqing; Kang, Ning; Dong, Yuliang; Guo, Yuchen; Zhao, Dan; Zhang, Shiwen; Zhou, Liyan; Seriwatanachai, Dutmanee; Liang, Xing; Yuan, Quan

The purpose of this investigation was to examine the effect of resorbable collagen plug (RCP) on bone regeneration in rat calvarial critical-size defects. About 5-mm-diameter calvarial defects were created in forty 12-week-old male Sprague-Dawley rats and implanted with or without RCP. Animals were killed at 1, 2, 4, and 8 weeks postoperatively. After being killed, specimens were collected and subjected to micro-computed tomography (μCT) and histological analysis. The μCT showed a significant increase of newly formed bone volume/tissue volume in RCP-implanted defect compared with controls at all designated time points. After 8 weeks, the defects implanted with RCP displayed almost complete closure. Hematoxylin and eosin staining of the decalcified sections confirmed these observations and evidenced active bone regeneration in the RCP group. In addition, Masson's trichrome staining demonstrated that RCP implantation accelerated the process of collagen maturation. The RCP enhances bone regeneration in rat critical-size cranial defects, which suggest it might be a desired material for bone defect repair.

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