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2,478 results for “nasal”

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zenodo40/100

Fig. 13 in Comparative Morphology Of The Internal Nasal Skeleton Of Adult Marsupials Based On X-Ray Computed Tomography

Fig. 13. Coronal CT images showing the morphology of the caudodorsal portion of caudal nasoturbinal (caudal to nasoturbinal division around endoturbinal I; char. 10). (A) caudodorsal portion is unfolded (ch. 10.0), Dromiciops gliroides, C245 (FMNH 127463), scale bar equals 1 mm; (B) caudodorsal portion curls (char. 10.1), Phalanger orientalis, C250 (AMNH 157211), scale bar equals 5 mm. Abbreviations: Ecto, ectoturbinal; Endo, endoturbinal; ONS, ossified nasal septum; SER, sphenethmoid recess.

opencc-by-4.0Jan 2012View details →
zenodo40/100

Fig. 8. Schematic diagram showing a in Comparative Morphology Of The Internal Nasal Skeleton Of Adult Marsupials Based On X-Ray Computed Tomography

Fig. 8. Schematic diagram showing a dorsal view of the paries nasi of the chondrocranium of a marsupial. Rostral is to the left. Figure modeled after Smith and Rossie (2006: fig. 8.4). Abbreviations: EC, ectoturbinal; EN, endoturbinal.

opencc-by-4.0Jan 2012View details →
zenodo40/100

Fig. 28 in Comparative Morphology Of The Internal Nasal Skeleton Of Adult Marsupials Based On X-Ray Computed Tomography

Fig. 28. Coronal CT images showing the complexity of the rostral portion of the maxilloturbinal in marsupials (char. 1). (A) arborlike maxilloturbinal (char. 1.0), Dasyurus hallucatus, C208 (TMM M-6921); (B) simple maxilloturbinal (char. 1.1), Isoodon macrourus, C150 (TMM M-6922); (C) curled lamella (char. 1.1), Phascolarctos cinereus, C129 (TMM M-2946). All scale bars equal 5 mm. Abbreviations: Endo, endoturbinal; ONS, ossified nasal septum.

opencc-by-4.0Jan 2012View details →
zenodo40/100

Fig. 16 in Comparative Morphology Of The Internal Nasal Skeleton Of Adult Marsupials Based On X-Ray Computed Tomography

Fig. 16. Coronal CT images showing the caudalmost extent of ventral attachment of nasoturbinal (char. 13). (A) attachment is rostral to caudal terminus of maxilloturbinal (char. 13.0), Petauroides volans, C450 (AMNH 150055); (B) attachment is at coronal level of caudal terminus of maxilloturbinal (char. 13.1), Trichosurus vulpecula, C212 (TMM M-849); (C) attachment is caudal to caudal terminus of maxilloturbinal (char. 13.2), Isoodon macrourus, C374 (TMM M-6922). All scale bars equal 5 mm. Abbreviations: Ecto, ectoturbinal; Endo, endoturbinal; ONS, ossified nasal septum; PTL, posterior transverse lamina.

opencc-by-4.0Jan 2012View details →
zenodo40/100

Fig. 12 in Comparative Morphology Of The Internal Nasal Skeleton Of Adult Marsupials Based On X-Ray Computed Tomography

Fig. 12. Coronal CT images showing the morphology of the caudal nasoturbinal (char. 7). (A) caudal nasoturbinal is unbranched (char. 7.0), Dromiciops gliroides, C230 (FMNH 127463); (B) caudal nasoturbinal has at least one branch (char. 7.1), Caenolestes fuliginosus, C389 (KU 124015). Both scale bars equal 1 mm. Abbreviations: Ecto, ectoturbinal; Endo, endoturbinal; ONS, ossified nasal septum.

opencc-by-4.0Jan 2012View details →
zenodo40/100

Fig. 27 in Comparative Morphology Of The Internal Nasal Skeleton Of Adult Marsupials Based On X-Ray Computed Tomography

Fig. 27. Coronal CT images showing the morphology of the maxillary recess (char. 26). (A) caudal portion of recess is medially enclosed by posterior transverse lamina (char. 26.0), Dasyurus hallucatus, C330 (TMM M-6921), scale bar equals 5 mm; (B) uncinate process of the caudal nasoturbinal also contributes to the medial wall of the recess (char. 26.1), Monodelphis domestica, C190 (TMM M-7599), scale bar equals 1 mm. Abbreviation: Ecto, ectoturbinal; Endo, endoturbinal; ONS, ossified nasal septum; NPM, nasopharyngeal meatus; PTL, posterior transverse lamina; SER, sphenethmoid recess.

opencc-by-4.0Jan 2012View details →
zenodo40/100

Biomarker Signatures of Quality for Engineering Nasal Chondrocyte-Derived Cartilage

<p>Data underlying the figures in the publication &ldquo;Biomarker Signatures of Quality for Engineering Nasal Chondrocyte-Derived Cartilage&rdquo;, published in <em>Front Bioeng Biotechnol., </em><strong>2020</strong>, 8: 283. (DOI: 10.3389/fbioe.2020.00283).</p> <p>Table of contents:</p> <p><strong>1. biochem_summary</strong>; Biochemistry data and MBS of pellets made from NC and PC mixtures in the titration experiment.</p> <p><strong>2. dirty-clean-biochem</strong>; Biochemistry data and MBS of pellets made from passage 2 cells from dirty/clean biopsies.</p> <p><strong>3. identity_all</strong>; All passage 1 and passage 2 cells of type pure NC and pure PC from the titration and dirty/clean datasets. All PCR data included.</p> <p><strong>4. identity_titration</strong>; Passage 1 and 2 and pellets made from pure NC and PC populations in the titration experiment. All PCR data included. Average (avg) refers to the average of the biologicsl replicates (which are already the average of the experimental replicates of Data 5).</p> <p><strong>5. identity_titration_avg</strong>; Passage 1 and 2 and pellets made from pure NC and PC populations in the titration experiment. All PCR data included. All experimental replicate information is included (which are the average of the technical replicates).</p> <p><strong>6. PCR_cells_summary</strong>; For the purity and potency assays, mixtures of increasing NC to PC cell ratios were created. The PCR data from those mixtures are here for passage 2 and for the pure populations as passage 1.</p> <p><strong>7. PCR_pellet_summary</strong>; For the purity and potency assays, mixtures of increasing NC to PC cell ratios were created. PCR data from engineered pellets are here included.</p> <p><strong>8. PCRdirty-clean</strong>; PCR data of cells obtained from dirty/clean biopsies at passage 0,1, and 2.</p> <p><strong>9. PCRsummary_all</strong>; Combined Data 5, 7, and 8.</p> <p><strong>10. Proliferation_TOT</strong>; Proliferation rates of cells from clean and dirty biopsies.&nbsp;</p>

opencc-by-4.0Sep 2021View details →
dryad40/100

Proteomic and metabolomic analysis of COVID-19 nasal swabs

<p>The epithelial barrier's primary role is to protect against entry of foreign and pathogenic elements. Global and targeted approaches were applied to nasal swabs from healthy and COVID-19-confirmed cases within 24 hours post-positive-confirmation and at 3 weeks post-infection to observe changes in proteome and metabolome.</p> <p>We found that the tryptophan/kynurenine metabolism pathway is a pinch-point regulator of canonical and non-canonical transcription activation, macrophage release of cytokines and significant changes in the immune and metabolic status with increasing severity and disease course.</p>

opencc-zeroFeb 2023View details →
zenodo40/100

Automatic speech recognition datasets for Gronings, Nasal, and Besemah

<p>Automatic speech recognition datasets for Gronings, Nasal, and Besemah for experiments reported in Bartelds, San,&nbsp;McDonnell,&nbsp;Jurafsky and&nbsp;Wieling (2023).&nbsp;<em>Making More of Little Data: Improving Low-Resource Automatic Speech Recognition Using Data Augmentation</em>. ACL 2023.</p> <p>Model training code available at:&nbsp;https://github.com/Bartelds/asr-augmentation</p>

opencc-by-4.0May 2023View details →
ClinicalTrials.gov40/100

Dupilumab in Japanese Patients With Chronic Rhinosinusitis With Nasal Polyp (SINUS-M52)

ClinicalTrials.gov study NCT05049122. IPD Sharing: YES. Countries: 1. Publications: 1.

controlledIPD-YESFeb 2026View details →
ClinicalTrials.gov40/100

Examining Changes in Nasal IL-1 During Acute Asthma Exacerbation in Adolescents

ClinicalTrials.gov study NCT04748055. IPD Sharing: YES. Countries: 1. Publications: 1.

controlledIPD-YESFeb 2026View details →
dryad40/100

Proteomic and metabolomic analysis of COVID-19 nasal swabs

Open the record for dataset details and reuse information.

publicFeb 2023View details →
dryad36/100

Anatomy of the nasal and auditory regions of the fossil lagomorph Palaeolagus haydeni: systematic and evolutionary implications

<p>Palaeolagus, a late Eocene to early Miocene North American lagomorph genus, represented by numerous and well-preserved specimens, has been long considered a basal leporid, although it is currently understood as a stem lagomorph. Based on micro-computed tomography (μCT) data and 3D reconstructions, here we present the first description of intracranial structures of the nasal and auditory regions of a complete skull of Palaeolagus haydeni from the early Oligocene of Nebraska. Although Palaeolagus haydeni shows a puzzling mixture of extant leporid and ochotonid characters, it helps to polarize and re-evaluate already known lagomorph intracranial characters based on outgroup comparison with Rodentia and Scandentia. Common derived features of Palaeolagus haydeni and extant Lagomorpha are the dendritic maxilloturbinal and the excavated nasoturbinal that contacts the lamina semicircularis. Generally, Palaeolagus haydeni and Leporidae have several characters in common, some of which are certainly plesiomorphic (e.g., thin wall of bulla tympani and flat conic cochlea). Palaeolagus haydeni resembles Leporidae in having an interturbinal between the two frontoturbinals, and three ethmoturbinals plus one interturbinal between ethmoturbinal I and II. Now, this should also be regarded as a plesiomorphic grundplan pattern for Leporidae whereas ochotonids are derived from the lagomorph grundplan as concerns the number of frontoturbinals. Concerning the middle ear, Palaeolagus haydeni significantly contributes to the polarization of the anterior anchoring of the malleus in extant lagomorphs. Palaeolagus haydeni resembles the pattern observed in early ontogenetic stages of Ochotonidae, i.e., the attachment of the malleus to the ectotympanic via a short processus anterior. The patterns in adult ochotonids and leporids now can be regarded as two different and apomorphic character states. Autapomorphic characters of Palaeolagus haydeni are the reduced frontoturbinal 2 and the additional anterolaterally oriented process of the lamina semicircularis. Interestingly, among the investigated intracranial structures the loss of the secondary crus commune is the only apomorphic grundplan character of crown Lagomorpha.</p> <p> </p>

opencc-zeroJun 2021View details →
zenodo36/100

Evaluation of comparative Efficacy of two routes of administration of Carathmus Tinctorius (Medicated Enema and Nasal Administration) as an Adjuvant Therapy with Standard Care With Physiotherapy in the Rehabilitation of Thrombolytic Stroke (Pakshaghat): A Randomized Controlled Trial Protocol

Open the record for dataset details and reuse information.

opencc-by-4.0Apr 2024View details →
zenodo36/100

Infant RSV immunoprophylaxis changes nasal epithelial DNAmethylation at 6 years of age

<p>Respiratory syncytial virus (RSV) infection has been associated with childhood wheeze and asthma, and potential mechanisms include persistent epigenetic effects.&nbsp;In the randomized, placebo-controlled MAKI trial (ISRCTN registry, number ISRCTN73641710), preterm infants randomly received RSV immunoprophylaxis with palivizumab or placebo during their first RSV season.&nbsp;DNA methylation in cells obtained by nasal brushes at age 6 was measured by Illumina MethylationEPIC array.</p> <p>This dataset contains summary statistics for the methylome-wide association study using DNAm data collected from 274 Children at age 6.</p> <p>The corresponding paper can be found here:&nbsp;https://pubmed.ncbi.nlm.nih.gov/34473906/.</p> <p>Upload of this dataset was completed by The EWAS Catalog team. The data can be queried along with hundreds of other EWAS at ewascatalog.org. To upload your EWAS summary statistics and have a Zenodo DOI generated for you go to ewascatalog.org/upload.</p>

opencc-by-4.0Jan 2022View details →
zenodo36/100

Supplemental Figures - Detection of SARS-CoV-2-Specific Secretory IgA and Neutralizing Antibodies in the Nasal Secretions of Exposed Seronegative Individuals

<p>Figure S1: Flow diagram of exposed seronegative cohort.</p> <p>Figure S2: SARS-CoV-2-specific neutralization activity at Days 1 and 8 relative to enrollment in exposed seronegative nasal SIgA positive and infected participants. NPS SARS-CoV-2-specific neutralization activity is shown for exposed seronegative and infected participants with normalized OD490 at Day 1 and Day 8, respectively. Sample sizes (N) are indicated in parentheses. Wilcoxon signed-rank tests were used to determine if the median SARS-CoV-2 nasal SIgA neutralization activity differed significantly. A two-tailed p &lt; 0.05 was considered significant.</p>

opencc-by-4.0May 2024View details →
zenodo36/100

Text-fig. 4. Rib fragment inserted in the nasal cavity of canid skull fragment (10). in Consumption Of Canid Meat At The Gravettian Předmostí Site, The Czech Republic

Text-fig. 4. Rib fragment inserted in the nasal cavity of canid skull fragment (10).

opencc-by-4.0Dec 2017View details →
dryad36/100

MicroCT scan of the nasal airway of a domestic short hair cat

<p>The peripheral structures of mammalian sensory organs often serve to support their functionality, such as alignment of hair cells to the mechanical properties of the inner ear. Here, we examined the structure-function relationship for mammalian olfaction by creating an anatomically accurate computational nasal model for the domestic cat (<em>Felis catus</em>) based on high resolution microCT and sequential histological sections. Our results showed a distinct separation of respiratory and olfactory flow regimes, featuring a high-speed dorsal medial stream that increases odor delivery speed and efficiency to the ethmoid olfactory region without compromising the filtration and conditioning purpose of the nose. These results corroborated previous findings in other mammalian species, which implicates a common theme to deal with the physical size limitation of the head that confines the nasal airway from increasing in length infinitely as a straight tube. We thus hypothesized that these ethmoid olfactory channels function as parallel coiled chromatograph channels, and further showed that the theoretical plate number, a widely-used indicator of gas chromatograph efficiency, is more than 100 times higher in the cat nose than an "amphibian-like" straight channel fitting the similar skull space, at restful breathing state. The parallel feature also reduces airflow speed within each coil, which is critical to achieving the high plate number, while feeding collectively from the high-speed dorsal medial stream so that total odor sampling speed is not sacrificed. The occurrence of ethmoid turbinates is an important step in the evolution of mammalian species that correlates to their expansive olfactory function and brain development. Our findings reveal novel mechanisms on how such structure may facilitate better olfactory performance, furthering our understanding of the successful adaptation of mammalian species, including <em>F. catus</em>, a popular pet, to diverse environments.</p>

opencc-zeroMay 2023View details →
zenodo36/100

The Path from Nasal Tissue to Nasal Mucosa on Chip Part 2- Advanced Microfluidic Nasal In Vitro Model for Drug Absorption Testing

<p><strong>Abstract: </strong>The nasal mucosa, being accessible and highly vascularized, opens up new opportunities for the systemic administration of drugs. However, due to several protective functions like the mucociliary clearance, this physiological barrier is a difficult obstacle for drug candidates to overcome. For this reason, effective testing procedures are required in the preclinical phase of pharmaceutical development. Based on a recently reported immortalized porcine nasal epithelial cell line, we developed a test platform based on a tissue-compatible microfluidic chip. A biomimetic glass chip equipped with a controlled bidirectional airflow to induce a physiologically relevant wall shear stress on the epithelial cell layer was microfabricated. By developing a membrane transfer technique, the epithelial cell layer could be pre-cultivated in a static holder prior to cultivation in the microfluidic environment. The dynamic cultivation within the chip showed a homogenous distribution of the mucus film on top of the cell layer and a significant increase of cilia formation compared to static cultivation condition. In addition, the recording of the ciliary transport mechanism by micro particle image velocimetry was successful. Using FITC-dextran&nbsp;4000 as an example, it was shown that this nasal mucosa on a chip is suitable for permeation studies. The obtained permeation coefficient was in the range of values determined by means of other established in vitro and in vivo models. The novel nasal mucosa on chip can in future be automated and used as a substitute for animal testing.</p>

opencc-by-4.0Aug 2023View details →
ClinicalTrials.gov36/100

Comparing Nasal Suction Devices in Children With Bronchiolitis: A Pilot Study

ClinicalTrials.gov study NCT02219334. IPD Sharing: NO. Countries: 1. Publications: 11.

closedIPD-NOFeb 2026View details →

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electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
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The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.

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behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

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