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Chemotype

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27 documents available in our comprehensive collection of Chemotype resources. Find practical guides, tutorials, and documentation to enhance your knowledge.

Preview of Phenotype Optimization
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Phenotype Optimization (12918_2012_1106_MOESM5_ESM.pdf)

43 KBCihanEN 1 page
Mathematical model is unable to capture several phenotypes initially, so optimize model parameters, quantify competition between phenotypes, identify...
Preview of Wax-less Phenotype Genetics
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Wax-less Phenotype Genetics (12870_2023_4424_ReviewerReport_V8_R4.pdf)

8 KBEN 2 pages
The authors identified a new allele of BraA09g066480.3C controlling the wax-less phenotype in Chinese cabbage using QTL-seq and DNA markers.
Preview of electronic edition @ ceur-ws.org (open access)
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electronic edition @ ceur-ws.org (open access) (paper_22.pdf)

284 KBEN 3 pages
The Human Phenotype Ontology (HP) and Mammalian Phenotype (MP) Ontology represent information about abnormal phenotypes in human diseases and mammalian...
Preview of View publication
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View publication (nutrients_11_02399.pdf)

561 KBEN 15 pages
Frailty is a complex condition characterized by increased vulnerability to adverse health outcomes, and it can be measured using the physical frailty phenotype...
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PDF (ajtr0146688.pdf)

1.96 MBEN 14 pages
Depletion of the m6A demethylases FTO and ALKBH5 impairs growth and metastatic capacity through EMT phenotype change in clear cell renal cell carcinoma.
Preview of Macrophage Differentiation Model
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Macrophage Differentiation Model (12950_2015_60_MOESM1_ESM.pdf)

126 KBNora LieggiEN 1 page
HBPMCs differentiate into macrophages in 8 days when stimulated with 100 ng/ml M-CSF, transitioning from a classical monocyte phenotype to immature macrophages...
Preview of CoQ10 & Retinitis Pigmentosa
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CoQ10 & Retinitis Pigmentosa (Jurkute_Coq10_pathway_NPJ_Genomic_med_2022.pdf)

2.38 MBNeringa JurkuteEN 12 pages
Biallelic variants in coenzyme Q10 biosynthesis pathway genes cause a retinitis pigmentosa phenotype in 13 individuals from 12 unrelated families, with defects...
Preview of A New Look at XXYY Syndrome: Medical and Psychological Features
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A New Look at XXYY Syndrome: Medical and Psychological Features (A-New-Look-at-XXYY-Syndrome.pdf)

276 KBEN 14 pages
XXYY syndrome occurs in approximately 1:18,000-1:40,000 males, with a similar physical phenotype to 47,XXY Klinefelter syndrome, but with additional medical...
Preview of Supplementary Figures
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Supplementary Figures (41587_2013_BFnbt2749_MOESM26_ESM.pdf)

6.5 MBJoshua C DennyEN 55 pages
Supplementary figures and tables are provided, including a flowchart of analysis, replication of NHGRI Catalog phenotypes, receiver operator characteristic...
Preview of [doi]
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[doi] (paper16.pdf)

261 KBEN 10 pages
Registries of domain-relevant semantic reference models help bootstrap interoperability in domains with fragmented data resources, such as rare diseases, by...
Preview of Shear Stress on DCs
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Shear Stress on DCs (Shear-stress-evaluation-on-dendritic-cells-viability-Rbeihat-EACR-2023.pdf)

1.08 MBKoen BeyersEN 1 page
Researchers evaluated the effect of shear stress on tolerogenic dendritic cells (tolDCs) using the VAX-ID® intradermal drug delivery device with various needle...
Preview of Gènes & Évolution
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Gènes & Évolution (2009_Jorge_FDLS_diversit molculaire 02_1.pdf)

2.17 MBVéronique Jorge, Catherine Bastien, Olivier Bertel, Vanina Guérin, Leopoldo Sanchez Rodriguez, MarcFR 2 pages
Les gènes supports de l'hérédité et mémoire de l'évolution : l'apparence d'un arbre est déterminée par son patrimoine génétique (génotype) et l'environnement,...
Preview of electronic edition @ stanford.edu (open access)
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electronic edition @ stanford.edu (open access) (intro-innovative.pdf)

553 KBTiffany MurrayEN 3 pages
The increasing use of Whole Genome Sequencing (WGS) and Whole Exome Sequencing (WES) in clinical settings has made it difficult to determine the causal variant...
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PDF (rsos.181227.pdf)

588 KBEN 9 pages
A global cline in a colour polymorphism suggests a limited contribution of gene flow towards the recovery of a heavily exploited marine mammal.
Preview of ATBox OAEI 2021 Results
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ATBox OAEI 2021 Results (oaei21_paper5.pdf)

599 KBEN 7 pages
ATBox is a system for matching instances and schema of two given Knowledge Graphs (KGs), focusing on scalability for large tasks like Knowledge Graph and Large...
Preview of Cancer Biomarkers
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Cancer Biomarkers (pdf-71505-8737)

581 KBEN 8 pages
Researchers investigated chromosomal instability, γ-H2AX foci, polymorphisms in DNA repair genes, and apoptosis as potential biomarkers for prostate and...
Preview of Changes in the AM program
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Changes in the AM program (EM-meeting-2015-pres2.pdf)

187 KBYourNameEN 3 pages
The Acceptable Mismatch (AM) program currently includes patients with a (v)PRA > 85% due to cytotoxic antibody reactivity.
Preview of Alcohol Lung Damage
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Alcohol Lung Damage (article04.pdf)

234 KBNational Institute on Alcohol Abuse and Alcoholism (NIAAA)EN 12 pages
Alcohol use disorder (AUD) renders people susceptible to lung damage through alterations in host defenses, disruption of alveolar epithelial barrier integrity,...
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URL (PDF10.pdf)

1001 KBEN 11 pages
Researchers investigated error awareness in adults with attention-deficit hyperactivity disorder (ADHD) using a Go/No-Go response inhibition task and...
Preview of Download (583kB)
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Download (583kB) (Published_Version.pdf)

569 KBEN 8 pages
Researchers investigated the factors contributing to the success of an antibiotic resistance plasmid, pCT, which has spread globally.
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PDF (2UnqAZMsagtENmXA6lqJlLqn8hZzbwhJKwmchqXe.pdf)

113 KB微软中国EN 6 pages
Research on frailty in elderly people with osteoporosis in the community is increasing due to the rising incidence of these conditions.
Preview of Toller Coat Color Genetics
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Toller Coat Color Genetics (COAT-COLOR-IN-THE-TOLLER.pdf)

1.04 MBAmanda CraneEN 11 pages
Coat color in the Nova Scotia Duck Tolling Retriever is determined by genetics, with various genes controlling pigment production and distribution.
Preview of The_pyriproxyfen_metabolite_4_OH_PPF_disrupts_thyroid_hormone_signaling_in_neural_stem_cells_modifying_neurodevelopmental_genes_
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The_pyriproxyfen_metabolite_4_OH_PPF_disrupts_thyroid_hormone_signaling_in_neural_stem_cells_modifying_neurodevelopmental_genes_ (The_pyriproxyfen_metabolite_4_OH_PPF_disrupts_thyroid_hormone_signaling_in_neural_stem_cells_modifying_neurodevelopmental_genes_affected_by_ZIKA_virus_infection.pdf)

7.42 MBPieter VancampEN 12 pages
The pyriproxyfen metabolite, 4′–OH–PPF, disrupts thyroid hormone signaling in neural stem cells, modifying neurodevelopmental genes affected by ZIKA virus...
Preview of Sarcoglycanopathies: molecular pathogenesis and therapeutic prospects
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Sarcoglycanopathies: molecular pathogenesis and therapeutic prospects (Sandona_Sarcoglycanopathies_molecular_pathogenesis_and_therapeutic_prospects.pdf)

1.18 MBDorianna Sandonà, Romeo BettoEN 27 pages
Sarcoglycanopathies are autosomal recessive muscle-wasting disorders caused by genetic defects in one of four cell membrane glycoproteins: a-, b-, g-, or...
Preview of Télécharger le fichier
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Télécharger le fichier (Manuscript.pdf)

1.33 MBEN 24 pages
This study presents an integro-differential model to investigate how individuals and populations adapt to fluctuating environments, focusing on the...
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PDF (article-pdf-1662802292-71.pdf)

352 KBBrian BurnettEN 8 pages
Researchers evaluated 56 pregnancies with early onset fetal growth restriction (FGR) diagnosed before 30 weeks' gestation and delivered before 34 weeks.
Preview of Download (6MB)
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Download (6MB) (2022AntonopoulosPhD.pdf)

6.18 MBAlistair AntonopoulosEN 313 pages
Sustainable use of levamisole through elucidation of genetic markers of resistance and molecular diagnostics in Haemonchus contortus," investigates the use of...

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