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  • American Association for the Advancement of Science (AAAS)  (15)
  • 1
    Online Resource
    Online Resource
    American Association for the Advancement of Science (AAAS) ; 2010
    In:  Science Vol. 327, No. 5966 ( 2010-02-05), p. 697-701
    In: Science, American Association for the Advancement of Science (AAAS), Vol. 327, No. 5966 ( 2010-02-05), p. 697-701
    Abstract: Over the past two decades, HIV resistance to antiretroviral drugs (ARVs) has risen to high levels in the wealthier countries of the world, which are able to afford widespread treatment. We have gained insights into the evolution and transmission dynamics of ARV resistance by designing a biologically complex multistrain network model. With this model, we traced the evolutionary history of ARV resistance in San Francisco and predict its future dynamics. By using classification and regression trees, we identified the key immunologic, virologic, and treatment factors that increase ARV resistance. Our modeling shows that 60% of the currently circulating ARV-resistant strains in San Francisco are capable of causing self-sustaining epidemics, because each individual infected with one of these strains can cause, on average, more than one new resistant infection. It is possible that a new wave of ARV-resistant strains that pose a substantial threat to global public health is emerging.
    Type of Medium: Online Resource
    ISSN: 0036-8075 , 1095-9203
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    Language: English
    Publisher: American Association for the Advancement of Science (AAAS)
    Publication Date: 2010
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  • 2
    In: Science, American Association for the Advancement of Science (AAAS), Vol. 360, No. 6395 ( 2018-06-22)
    Abstract: Disorders of the brain can exhibit considerable epidemiological comorbidity and often share symptoms, provoking debate about their etiologic overlap. We quantified the genetic sharing of 25 brain disorders from genome-wide association studies of 265,218 patients and 784,643 control participants and assessed their relationship to 17 phenotypes from 1,191,588 individuals. Psychiatric disorders share common variant risk, whereas neurological disorders appear more distinct from one another and from the psychiatric disorders. We also identified significant sharing between disorders and a number of brain phenotypes, including cognitive measures. Further, we conducted simulations to explore how statistical power, diagnostic misclassification, and phenotypic heterogeneity affect genetic correlations. These results highlight the importance of common genetic variation as a risk factor for brain disorders and the value of heritability-based methods in understanding their etiology.
    Type of Medium: Online Resource
    ISSN: 0036-8075 , 1095-9203
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    Language: English
    Publisher: American Association for the Advancement of Science (AAAS)
    Publication Date: 2018
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  • 3
    In: Science, American Association for the Advancement of Science (AAAS), Vol. 370, No. 6517 ( 2020-11-06), p. 712-715
    Abstract: The Arctic is entering a new ecological state, with alarming consequences for humanity. Animal-borne sensors offer a window into these changes. Although substantial animal tracking data from the Arctic and subarctic exist, most are difficult to discover and access. Here, we present the new Arctic Animal Movement Archive (AAMA), a growing collection of more than 200 standardized terrestrial and marine animal tracking studies from 1991 to the present. The AAMA supports public data discovery, preserves fundamental baseline data for the future, and facilitates efficient, collaborative data analysis. With AAMA-based case studies, we document climatic influences on the migration phenology of eagles, geographic differences in the adaptive response of caribou reproductive phenology to climate change, and species-specific changes in terrestrial mammal movement rates in response to increasing temperature.
    Type of Medium: Online Resource
    ISSN: 0036-8075 , 1095-9203
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    Language: English
    Publisher: American Association for the Advancement of Science (AAAS)
    Publication Date: 2020
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  • 4
    In: Science, American Association for the Advancement of Science (AAAS), Vol. 375, No. 6584 ( 2022-03-04)
    Abstract: Drosophila melanogaster has had a fruitful history in biological research because it has contributed to many key discoveries in genetics, development, and neurobiology. The fruit fly genome contains ~14,000 protein-coding genes, ~63% of which have human orthologs. Single-cell RNA-sequencing has recently been applied to multiple Drosophila tissues and developmental stages. However, these data have been generated by different laboratories on different genetic backgrounds with different dissociation protocols and sequencing platforms, which has hindered the systematic comparison of gene expression across cells and tissues. RATIONALE We aimed to establish a cell atlas for the entire adult Drosophila with the same genetic background, dissociation protocol, and sequencing platform to (i) obtain a comprehensive categorization of cell types, (ii) integrate single-cell transcriptome data with existing knowledge about gene expression and cell types, (iii) systematically compare gene expression across the entire organism and between males and females, and (iv) identify cell type–specific markers across the entire organism. We chose single-nucleus RNA-sequencing (snRNA-seq) to circumvent the difficulties of dissociating cells that are embedded in the cuticle (e.g., sensory neurons) or that are multinucleated (e.g., muscle cells). We took two complementary strategies: sequencing nuclei from dissected tissues to know the identity of the tissue source and sequencing nuclei from the entire head and body to ensure that all cells are sampled. Experts from 40 laboratories participated in crowd annotation to assign transcriptomic cell types with the best knowledge available. RESULTS We sequenced 570,000 cells using droplet-based 10x Genomics from 15 dissected tissues as well as whole heads and bodies, separately in females and males. We also sequenced 10,000 cells from dissected tissues using the plate-based Smart-seq2 platform, providing deeper coverage per cell. We developed reproducible analysis pipelines using NextFlow and implemented a distributed cell-type annotation system with controlled vocabularies in SCope. Crowd-based annotations of transcriptomes from dissected tissues identified 17 main cell categories and 251 detailed cell types linked to FlyBase ontologies. Many of these cell types are characterized for the first time, either because they emerged only after increasing cell coverage or because they reside in tissues that had not been previously subjected to scRNA-seq. The excellent correspondence of transcriptomic clusters from whole body and dissected tissues allowed us to transfer annotations and identify a few cuticular cell types not detected in individual tissues. Cross-tissue analysis revealed location-specific subdivisions of muscle cells and heterogeneity within blood cells. We then determined cell type–specific marker genes and transcription factors with different specificity levels, enabling the construction of gene regulatory networks. Finally, we explored sexual dimorphism, finding a link between sex-biased expression and the presence of doublesex , and investigated tissue dynamics through trajectory analyses. CONCLUSION Our Fly Cell Atlas (FCA) constitutes a valuable resource for the Drosophila community as a reference for studies of gene function at single-cell resolution. All the FCA data are freely available for further analysis through multiple portals and can be downloaded for custom analyses using other single-cell tools. The ability to annotate cell types by sequencing the entire head and body will facilitate the use of Drosophila in the study of biological processes and in modeling human diseases at a whole-organism level with cell-type resolution. All data with annotations can be accessed from www.flycellatlas.org , which provides links to SCope, ASAP, and cellxgene portals. Tabula Drosophilae . In this single-cell atlas of the adult fruit fly, 580,000 cells were sequenced and 〉 250 cell types were annotated. They are from 15 individually dissected sexed tissues as well as the entire head and body. All data are freely available for visualization and download, with featured analyses shown at the bottom right.
    Type of Medium: Online Resource
    ISSN: 0036-8075 , 1095-9203
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    Language: English
    Publisher: American Association for the Advancement of Science (AAAS)
    Publication Date: 2022
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  • 5
    In: Science, American Association for the Advancement of Science (AAAS), Vol. 361, No. 6398 ( 2018-07-13)
    Type of Medium: Online Resource
    ISSN: 0036-8075 , 1095-9203
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    Language: English
    Publisher: American Association for the Advancement of Science (AAAS)
    Publication Date: 2018
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  • 6
    In: Science, American Association for the Advancement of Science (AAAS), Vol. 296, No. 5573 ( 2002-05-31), p. 1661-1671
    Abstract: The high degree of similarity between the mouse and human genomes is demonstrated through analysis of the sequence of mouse chromosome 16 (Mmu 16), which was obtained as part of a whole-genome shotgun assembly of the mouse genome. The mouse genome is about 10% smaller than the human genome, owing to a lower repetitive DNA content. Comparison of the structure and protein-coding potential of Mmu 16 with that of the homologous segments of the human genome identifies regions of conserved synteny with human chromosomes (Hsa) 3, 8, 12, 16, 21, and 22. Gene content and order are highly conserved between Mmu 16 and the syntenic blocks of the human genome. Of the 731 predicted genes on Mmu 16, 509 align with orthologs on the corresponding portions of the human genome, 44 are likely paralogous to these genes, and 164 genes have homologs elsewhere in the human genome; there are 14 genes for which we could find no human counterpart.
    Type of Medium: Online Resource
    ISSN: 0036-8075 , 1095-9203
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    Language: English
    Publisher: American Association for the Advancement of Science (AAAS)
    Publication Date: 2002
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  • 7
    In: Science, American Association for the Advancement of Science (AAAS), Vol. 380, No. 6650 ( 2023-06-16), p. 1155-1160
    Abstract: Overfishing is driving common coral reef sharks toward global extinction and shifting reefs to ray-dominated assemblages.
    Type of Medium: Online Resource
    ISSN: 0036-8075 , 1095-9203
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    Language: English
    Publisher: American Association for the Advancement of Science (AAAS)
    Publication Date: 2023
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  • 8
    In: Science, American Association for the Advancement of Science (AAAS), Vol. 360, No. 6386 ( 2018-04-20), p. 280-282
    Type of Medium: Online Resource
    ISSN: 0036-8075 , 1095-9203
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    Language: English
    Publisher: American Association for the Advancement of Science (AAAS)
    Publication Date: 2018
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  • 9
    In: Science Advances, American Association for the Advancement of Science (AAAS), Vol. 8, No. 34 ( 2022-08-26)
    Abstract: Compositions seen by SuperCam show progressive primitive to evolved transition along the first 286 days of Perseverance’s mission.
    Type of Medium: Online Resource
    ISSN: 2375-2548
    Language: English
    Publisher: American Association for the Advancement of Science (AAAS)
    Publication Date: 2022
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  • 10
    In: Science, American Association for the Advancement of Science (AAAS), Vol. 381, No. 6660 ( 2023-08-25)
    Abstract: It has been known for more than 100 years that human cancers exhibit pervasive aneuploidy, or chromosome copy number changes. For instance, about 25% of cancers exhibit gains of the q arm of chromosome 1. However, despite the prevalence of aneuploidy across cancer types, its role in tumorigenesis has remained poorly defined. Our ability to uncover the function of these large-scale copy number alterations has been hampered by our inability to experimentally manipulate chromosome dosage in cancer. Nonetheless, as aneuploidy is common across malignancies but rare in normal tissue, drugs that exhibit selective toxicity toward aneuploid cells could be useful anticancer agents. RATIONALE Although aneuploidies have resisted close analysis, previous research has led to the discovery of a phenomenon called “oncogene addiction.” An oncogene-addicted cancer is dependent on the expression of an individual oncogene for continued malignant growth, and loss or inhibition of that oncogene is sufficient to induce cancer regression. As specific aneuploidies such as the gain of chromosome 1q are frequent events in diverse cancer types, we hypothesized that certain aneuploidies could themselves represent oncogene-like cancer addictions. To test this hypothesis, we developed ReDACT (Restoring Disomy in Aneuploid cells using CRISPR Targeting), a set of chromosome engineering tools that allow us to eliminate individual aneuploid chromosomes from cancer genomes. Using ReDACT, we created and then characterized a panel of isogenic cells that have or lack common cancer aneuploidies. RESULTS We found that eliminating the trisomy of chromosome 1q from cancer cell lines harboring this alteration almost completely abolished anchorage-independent growth and xenograft formation. Similarly, eliminating the 1q trisomy from a nonmalignant cell line blocked RAS -mediated transformation. Prolonged growth in vitro or in vivo after aneuploidy elimination in cancer cell lines led to karyotype evolution, and 1q-disomic cells were eventually outcompeted by cells that had recovered the 1q trisomy. In contrast, removing other trisomic chromosomes from cancer cells had variable effects on malignant growth, demonstrating that different aneuploidies have distinct phenotypic consequences for cancer development. An analysis of clinical sequencing data demonstrated that chromosome 1q gains arise early during tumorigenesis and are mutually exclusive with mutations in the tumor suppressor TP53 , suggesting that 1q trisomies could represent a mutation-independent mechanism for blocking p53 signaling. Consistent with this, we demonstrated that ReDACT-mediated elimination of chromosome 1q trisomies increased the expression of p53 target genes in TP53 wild-type cell lines. We traced this suppression of p53 function to the triplication of MDM4 , a p53 inhibitor encoded on chromosome 1q, and we found that deleting a single copy of MDM4 impaired the growth of 1q-trisomic cells, whereas moderate overexpression of MDM4 rescued the growth of 1q-disomic cells. Finally, we demonstrated that chromosome 1q gains result in the overexpression of UCK2 , a nucleotide kinase encoded on chromosome 1q that is also required for the cytotoxicity of certain anticancer nucleotide analogs. We determined that several different 1q-trisomic cell lines displayed enhanced sensitivity to these compounds owing to the up-regulation of UCK2 , revealing that 1q aneuploidy can also represent a tractable cancer vulnerability. CONCLUSION Certain aneuploidies that are commonly found in tumor genomes play a central role in cancer development, and eliminating these aneuploidies compromises malignant growth potential. At the same time, aneuploidy causes collateral therapeutic vulnerabilities that can be targeted to selectively eliminate cells with chromosome dosage imbalances. The development of flexible chromosome engineering methodologies like ReDACT will enable additional experiments to further unravel the consequences of aneuploidy in development and disease. Chromosomal engineering to investigate the effects of aneuploidy. ( A ) ReDACT enables the targeted deletion of aneuploid chromosomes. ( B ) Loss of an extra copy of chromosome 1q compromises malignant growth. ( C ) MDM4 and BCL9 are dosage-sensitive drivers of chromosome 1q gain in cancer. ( D ) Chromosome 1q gain can be targeted therapeutically with UCK2-specific nucleotide analogs.
    Type of Medium: Online Resource
    ISSN: 0036-8075 , 1095-9203
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    Language: English
    Publisher: American Association for the Advancement of Science (AAAS)
    Publication Date: 2023
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