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6,234 results for “phenotypes”
Genetic and phenotypic differences between sexes in congenital hypogonadotropic hopogonadism(CHH):large cohort analysis from a single tertiary Centre. DATASET
<p>Database of the paper</p> <p>Gender differences in congenital hypogonadotropic hypogonadism (CHH): an analysis in a large cohort of CHH patients and an insight in female genotype and phenotype</p>
CSF Aβ40 and P-tau181 might differentiate atypical from typical AD phenotypes: preliminary evidence
<p>Data associated with the manuscript "CSF Aβ40 and P-tau181 might differentiate atypical from typical AD phenotypes: preliminary evidence"</p>
Maize phenotypic traits evaluated under synergistic influence of native soil microbial communities (dilution-to-extinction) and biostimulant Azospirillum brasilense Ab-V5
<p>Maize phenotypic traits evaluated under synergistic influence of native soil microbial communities (dilution-to-extinction) and biostimulant Azospirillum brasilense Ab-V5.</p>
Table S1: Fetal phenotype and genotype
<p>Legend to supplementary Table 1</p> <p>This table contains the 28 fetal cases on whom WES was performed. For each case, the fetal phenotype and the organ system involved are described, as well as the sample type from which the DNA was extracted, the applied gene panel and the result. For the positive cases, the gestational age at ultrasound, the affected gene and variant, the inheritance mode, the associated syndrome, the fetal phenotype as described in the literature and the outcome of the pregnancy are listed as well.</p> <p>AC: amniocytes; AD: autosomal dominant; AR: autosomal recessive; CNS: central nervous system; CV: chorionic villi; hom: homozygous; IF: incidental finding; IUGR: intrauterine growth restriction; LB: live birth; norm: normal; NT: nuchal translucency; pat: paternal; path: pathogenic; TOP: termination of pregnancy; US: ultrasound; VSD: ventricular septal defect; WES: whole exome sequencing; WESSD: WES with skeletal dysplasia panel</p>
dat scan IMAGES RELATED TO ARTICLE "Cerebrospinal fluid neuropathological biomarkers in beta-propeller protein-associated neurodegeneration, with complicated parkinsonian phenotype."
<p>DAT SCAN IMAGES</p>
Dataset for Verde et al., Neurol Sci 2023 - Relationship between cerebrospinal fluid/serum albumin quotient and phenotype in amyotrophic lateral sclerosis: a retrospective study on 328 patients
<p>This is the dataset for Verde et al., Neurol Sci 2023 - Relationship between cerebrospinal fluid/serum albumin quotient and phenotype in amyotrophic lateral sclerosis: a retrospective study on 328 patients.</p>
Dataset of "Parts-per-Object Count in Agricultural Images: Solving Phenotyping Problems via a Single Deep Neural Network" paper
<p>This includes the relevant datasets to: </p> <p>Khoroshevsky, F., Khoroshevsky, S., & Bar-Hillel, A. (2021). Parts-per-object count in agricultural images: Solving phenotyping problems via a single deep neural network. Remote Sens. 13(13), 2496.<br> https://doi.org/10.3390/rs13132496<br> </p> <p>Datasets related to wheat and banana are not public since it belongs to the Israel Phenomics consortium.</p> <p>This research was funded by the Generic technological R&D program of the Israel innovation<br> authority-the Phenomics consortium, and the Ministry of Science & Technology, Israel.</p> <p> </p> <p> </p>
Dataset for the article "Phenotypic correlates of serum neurofilament light chain levels in amyotrophic lateral sclerosis" (Verde et al., Front Aging Neurosci 2023)
<p>This is the dataset of the study "Phenotypic correlates of serum neurofilament light chain levels in amyotrophic lateral sclerosis" (Verde et al., Front Aging Neurosci 2023).</p>
phenotyping of patients with Advanced Chronic Liver Disease for better characterization of Cirrhosis Regression
<p>Regression of cirrhosis has been observed in patients with viral and non-viral etiologies of liver disease in whom the underlying cause of liver injury was effectively suppressed. However, the understanding of the factors contributing to reversibility of fibrosis and cirrhosis is limited. Our aim was to assess clinical factors, perform genotyping of known variants, and comprehensive metabolic phenotyping to characterize the regression of fibrosis in patients with compensated advanced chronic liver disease (cACLD).</p> <p>In a case-control pilot study with 60 cACLD patients, we compared individuals exhibiting histological or clinical evidence of cACLD regression ("regressors") with those showing no improvement ("non-regressors") after a minimum of 24 months of successful therapy for the cause of liver disease. </p> <p>A subgroup of 15 patients had paired frozen biopsies (before and after etiologic therapy) preserved and stored. RNA was extracted from those paired liver tissue (30 biopsies). RNA Sequencing data is saved in this repository</p>
Phenotyping long COVID
<p>raw data publication "Phenotyping long COVID"</p>
raw data for "Two novel CACNA1F gene mutations cause two different phenotypes: Aland Eye Disease and Incomplete Congenital Stationary Night Blindness"
<p>DNA and mRNA sequences of two patients affected by CSNB2</p>
Integrated Multi-omics Analysis Reveals Tumor-Suppressive Phenotypes and Associated Transcriptomic Remodeling upon METTL3 Overexpression in A549 Lung Cancer Cells
GEO Series GSE318384. Homo sapiens. 6 samples. Type: Expression profiling by high throughput sequencing.
Data from: Environmental variation predicts patterns of phenotypic and genomic variation in an African tropical forest frog
<p>Central African rainforests are predicted to be disproportionately affected by future climate change. How species will cope with these changes is unclear, but rapid environmental changes will likely impose strong selection pressures. Here we examined environmental drivers of phenotypic and genomic variation in the central African puddle frog (<i>Phrynobatrachus auritus</i>) to identify areas of elevated environmentally-associated turnover where populations may have the greatest capacity to adapt. We also compared current and future climate models to pinpoint areas of high genomic vulnerability where allele frequencies will have to shift the most in order to keep pace with future climate change. Analyses of body size, relative leg length, and head shape suggest that seasonal aspects of temperature and precipitation significantly influence phenotypic variation, whereas geographic distance and precipitation seasonality are the most important drivers of SNP allele frequency variation. However, neither landscape barriers nor the effects of past Pleistocene refugia had any influence on genomic differentiation. Most phenotypic and genomic differentiation coincided with key ecological gradients across the forest-savanna ecotone, montane areas and a coastal to interior rainfall gradient. Areas of greatest vulnerability were found in the lower Sanaga basin and southeastern region of Cameroon. In contrast with past conservation efforts that have focused on hotspots of species richness or endemism, our findings highlight the importance of preserving environmentally heterogeneous landscapes to preserve putatively adaptive variation and ongoing evolutionary processes in the face of climate change.</p>
Heightened DOT1L-AF10 enriches H3K79me3 to promote pro-atherogenic inflammatory endothelial phenotype through NF-κB p65
GEO Series GSE295366. Homo sapiens. 3 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
ScienceDex guides
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
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.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.