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1

Stavrakakis, Emmanouil. "Ventris’ Grids." Bulletin of the Institute of Classical Studies 67, no. 1 (2024): 75–92. https://doi.org/10.1093/bics/qbae033.

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ABSTRACT What is the relationship between Michael Ventris’ decipherment of Linear B and his architecture? The British architect who—against all philologists, archaeologists, and linguists—deciphered the ancient script is still renowned as a decipherer but a long-forgotten figure in the realm of architecture. This article compares the two operations; deciphering (writing) and drawing with the use of a series of his drawings (many of which have never been published before). Through a formal analysis of the various types of grids coming from his work on architecture and on the decipherment, this
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2

Thompson, R. J. E. "THE VENTRIS–CHADWICK CORRESPONDENCE AND THE DECIPHERMENT OF LINEAR B: A DENIER, A DISSENTER AND A DUBIOUS CONCLUSION." Cambridge Classical Journal 65 (September 25, 2019): 173–99. http://dx.doi.org/10.1017/s1750270519000058.

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The correspondence between Michael Ventris and John Chadwick, housed in the Mycenaean Epigraphy Room in the Faculty of Classics, Cambridge, provides valuable insights into the decipherment of Linear B and the collaboration between the two men which produced first ‘Evidence for Greek dialect in the Mycenaean archives’ (Ventris and Chadwick (1953)) and then Documents in Mycenaean Greek (Ventris and Chadwick (1956)). The letters also reveal interesting information about the relationship between Ventris and Chadwick and other scholars of the day. This article examines their relationship with Arthu
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MATHEY, Kosta. "Peristeriones: An Architecture not made for People?" EKISTICS The problems and science of human settlements 61, no. 368/369 (1994): 343–53. https://doi.org/10.5281/zenodo.8423090.

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More than 1000 dovecots are spread over the Greek Island of Tinos (Cyclades). As form and decoration are mostly determined by the owner-builder, they represent a unique variety of Vernacular Architecture. However, Their appearance is also partly influences by the topography, decorative elements derived from the surrounding nature, limitations due to the building materials, believe, religion and fashion. Equally interesting is the historical setting in the rivalry between orthodox and catholic churches, and the liberation movement of Greeks against Turkish occupation. The underlying resear
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4

Palaima, Thomas G. "The Man Who Deciphered Linear B: The Story of Michael Ventris. By Andrew Robinson." American Journal of Archaeology 107, no. 2 (2003): 296–97. http://dx.doi.org/10.1086/ajs40026094.

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Torralvo, Ana Claudia. "Linear B: a especificidade de uma evidência e sua contribuição para os estudos micênicos." Classica - Revista Brasileira de Estudos Clássicos 11, no. 11/12 (2017): 149. http://dx.doi.org/10.24277/classica.v11i11/12.454.

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Temos dois momentos na história da arqueologia proto-histórica grega, divididos em antes e depois da descoberta dos três tipos de escrita egeana. Com o deciframento do Linear B em 1952, por Michael Ventris, e a importantíssima constatação de que a língua grafada nessa escrita era o grego, ocorre uma verdadeira revolução no quadro histórico até então estabelecido pelos arqueólogos: Creta, onde se desenvolveu a cultura minóica e cuja língua nos é desconhecida até hoje, em um certo momento de sua história, foi dominada pelos micênicos, falantes de grego vindos do continente. A partir daí, os arqu
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6

Bendall, L. M. "(A.) Robinson The Man who Deciphered Linear B. The Story of Michael Ventris. London: Thames and Hudson, 2002. Pp. 168, illus. £12.95. 0500510776." Journal of Hellenic Studies 125 (November 2005): 203–5. http://dx.doi.org/10.1017/s0075426900007564.

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7

Gartrell, B.D., L. Argilla, S. Finlayson, et al. "Ventral dermatitis in rowi (Apteryx rowi) due to cutaneous larval migrans." International Journal for Parasitology: Parasites and Wildlife 4, no. 1 (2015): 1–10. https://doi.org/10.1016/j.ijppaw.2014.11.001.

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Gartrell, B.D., Argilla, L., Finlayson, S., Gedye, K., Argandona, A.K. Gonzalez, Graham, I., Howe, L., Hunter, S., Lenting, B., Makan, T., McInnes, K., Michael, S., Morgan, K.J., Scott, I., Sijbranda, D., Zyl, N. van, Ward, J.M. (2015): Ventral dermatitis in rowi (Apteryx rowi) due to cutaneous larval migrans. International Journal for Parasitology: Parasites and Wildlife 4 (1): 1-10, DOI: 10.1016/j.ijppaw.2014.11.001, URL: http://dx.doi.org/10.1016/j.ijppaw.2014.11.001
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8

Graziano, Michael S. A., Xin Tian Hu, and Charles G. Gross. "Visuospatial Properties of Ventral Premotor Cortex." Journal of Neurophysiology 77, no. 5 (1997): 2268–92. http://dx.doi.org/10.1152/jn.1997.77.5.2268.

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Graziano, Michael S. A., Xin Tian Hu, and Charles G. Gross. Visuospatial properties of ventral premotor cortex. J. Neurophysiol. 77: 2268–2292, 1997. In macaque ventral premotor cortex, we recorded the activity of neurons that responded to both visual and tactile stimuli. For these bimodal cells, the visual receptive field extended from the tactile receptive field into the adjacent space. Their tactile receptive fields were organized topographically, with the arms represented medially, the face represented in the middle, and the inside of the mouth represented laterally. For many neurons, both
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9

Duhamel, Jean-René, Carol L. Colby, and Michael E. Goldberg. "Ventral Intraparietal Area of the Macaque: Congruent Visual and Somatic Response Properties." Journal of Neurophysiology 79, no. 1 (1998): 126–36. http://dx.doi.org/10.1152/jn.1998.79.1.126.

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Duhamel, Jean-René, Carol L. Colby, and Michael E. Goldberg. Ventral intraparietal area of the macaque: congruent visual and somatic response properties. J. Neurophysiol. 79: 126–136, 1998. In a previous report, we described the visual response properties in the ventral intraparietal area (area VIP) of the awake macaque. Here we describe the somatosensory response properties in area VIP and the patterns of correspondence between the responses of single neurons to independently administered tactile and visual stimulation. VIP neurons responded to visual stimulation only or to visual and tactile
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10

Ferragamo, Michael J., Nace L. Golding, and Donata Oertel. "Synaptic Inputs to Stellate Cells in the Ventral Cochlear Nucleus." Journal of Neurophysiology 79, no. 1 (1998): 51–63. http://dx.doi.org/10.1152/jn.1998.79.1.51.

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Ferragamo, Michael J., Nace L Golding, and Donata Oertel. Synaptic inputs to stellate cells in the ventral cochlear nucleus. J. Neurophysiol. 79: 51–63, 1998. Auditory information is carried from the cochlear nuclei to the inferior colliculi through six parallel ascending pathways, one of which is through stellate cells of the ventral cochlear nuclei (VCN) through the trapezoid body. To characterize and identify the synaptic influences on T stellate cells, intracellular recordings were made from anatomically identified stellate cells in parasagittal slices of murine cochlear nuclei. Shocks to
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11

Ischenko, R. V., I. E. Sedakov, V. N. Antipov, et al. "Whipple procedure for ampulla of Vater cancer in a patient with situs inversus (clinical case)." Annaly khirurgicheskoy gepatologii = Annals of HPB Surgery 26, no. 1 (2021): 115–20. http://dx.doi.org/10.16931/1995-5464.20211115-120.

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A clinical case of a rare combination of complete transposition of internal organs (situs inversus totalis) with adenocarcinoma of the major duodenal papilla is presented. In addition to situs vicserum inversus, the patient has a special variant of vascular anatomy that is not included in the generally accepted classification of variants of arterial liver anatomy according to Michaels N.A. (1955), namely: separate separation of the left and right hepatic arteries from the ventral trunk. After individual preoperative planning, a patient with a complete reverse position of the abdominal organs a
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12

Calenda, Davide. "David E. Morrison, Matthew Kieran, Michael Svennevig & Sarah Ventress, Media & Values: Intimate Transgressions in a Changing Moral and Cultural Landscape." Information, Communication & Society 11, no. 8 (2008): 1183–84. http://dx.doi.org/10.1080/13691180802382348.

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13

Weinzapfel, Ellen N., Keith E. Maier, Matthew R. Marunde, et al. "Abstract P17: Epigenomic fingerprinting of limited primary immune cells using automated CUT&RUN." Blood Cancer Discovery 5, no. 2_Supplement (2024): P17. http://dx.doi.org/10.1158/2643-3249.bcdsymp24-p17.

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Abstract Chromatin structure drives gene expression programs during immune cell development and in cancer, making it central to the advancement of precision medicine. Indeed, the study of chromatin regulation has provided valuable insight on effector cell differentiation and function, anti-tumor immune responses, and therapeutic resistance. Epigenomic features – such as histone post-translational modifications (PTMs) and chromatin-associated proteins – mark distinct genomic compartments (e.g., promoters, enhancers) and regulate chromatin function/gene expression. Mapping the genomic distributi
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14

Sava, Laura. "David E. Morrison, Matthew Kieran, Michael Svennevig and Sarah Ventress (2007) Media & Values. Intimate Transgressions in a Changing Moral and Cultural Landscape." Film-Philosophy 14, no. 1 (2010): 361–66. http://dx.doi.org/10.3366/film.2010.0019.

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15

Deuchars, Susan A., K. Michael Spyer, and Michael P. Gilbey. "Stimulation Within the Rostral Ventrolateral Medulla Can Evoke Monosynaptic GABAergic IPSPs in Sympathetic Preganglionic Neurons In Vitro." Journal of Neurophysiology 77, no. 1 (1997): 229–35. http://dx.doi.org/10.1152/jn.1997.77.1.229.

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Deuchars, Susan A., K. Michael Spyer, and Michael P. Gilbey. Stimulation within the rostral ventrolateral medulla can evoke monosynaptic GABAergic IPSPs in sympathetic preganglionic neurons in vitro. J. Neurophysiol. 77: 229–235, 1997. The inhibitory responses of identified sympathetic preganglionic neurons (SPNs) to stimulation within the rostral ventrolateral medulla (RVLM) were studied to determine their nature and pharmacology. Whole cell patch-clamp recordings were made from 36 SPNs in the upper thoracic segments of the spinal cord in a neonatal rat brain stem-spinal cord preparation. Neu
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16

Leuzzi, Giuseppe, Alessandro Vasciaveo, Angelo Taglialatela, et al. "Abstract PR009: SMARCAL1 is a dual regulator of innate immune signaling and PD-L1 expression that promotes tumor immune evasion." Cancer Research 84, no. 1_Supplement (2024): PR009. http://dx.doi.org/10.1158/1538-7445.dnarepair24-pr009.

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Abstract Genomic instability can trigger cancer-intrinsic innate immune responses that promote tumor rejection. However, cancer cells often evade these responses by overexpressing immune checkpoint regulators, such as PD-L1. Here, we identify the SNF2-family DNA translocase SMARCAL1 as a factor that favors tumor immune evasion by a dual mechanism involving both the suppression of innate immune signaling and the induction of PD-L1-mediated immune checkpoint responses. Mechanistically, SMARCAL1 relieves endogenous DNA damage and suppresses cGAS-STING-dependent immune signaling during cancer cell
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17

Husby, Natalia L., Lu Sun, Hannah Willis, et al. "Abstract B015: Versatile biochemical and genomic platforms for drug discovery in chromatin remodeling research." Cancer Research 82, no. 23_Supplement_2 (2022): B015. http://dx.doi.org/10.1158/1538-7445.cancepi22-b015.

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Abstract Chromatin remodeling, driven by ATP-dependent remodeling enzymes, plays key roles in regulating gene expression, genome replication and repair. Aberrant nucleosome organization can severely disrupt these important processes, driving various cancers and developmental disorders. Remarkably, nearly 20% of all human cancers contain mutations in subunits from the SWI/SNF family of chromatin remodeling complexes, making them attractive therapeutic targets and interests of basic research. However, studies on the remodeling enzymes (and their multi-subunit complexes) in vitro are challenging
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18

Spengler, Jen, Bryan J. Venters, Vishnu U. Sunitha Kumary, et al. "Abstract 210: Direct multiomic mapping of chromatin proteins and DNA methylation." Cancer Research 85, no. 8_Supplement_1 (2025): 210. https://doi.org/10.1158/1538-7445.am2025-210.

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DNA methylation (DNAme) is a class of epigenetic marks that includes the methylation of cytosine residues (5mC) within CpG islands. In addition to well characterized roles regulating gene expression, imprinting, and silencing parasitic DNA elements, misregulation of DNAme is implicated in multiple cancers. Evidence is emerging that DNAme is not an independent epigenetic mark but rather closely linked to chromatin proteins. However, examining the relationships between DNAme and chromatin proteins is hampered by correlative analyses that cannot establish a direct mechanistic link. Furthermore, t
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19

Johnstone, Andrea L., Danielle N. Maryanski, Keli L. Rodriguez, et al. "Abstract A022: A field survey of histone PTM antibodies in epigenomic mapping approaches reveals widespread liabilities: Best practices and resources for reliable epigenetic studies." Cancer Research 82, no. 23_Supplement_2 (2022): A022. http://dx.doi.org/10.1158/1538-7445.cancepi22-a022.

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Abstract Histone post-translational modifications (PTMs) play a critical role in chromatin regulation. It has long been suspected that the poorly understood capability of ‘PTM-specific’ antibodies (i.e., their specificity and efficiency) is a prime driver of the reproducibility crisis in biomedical research. Here we confirm the validity of this concern as it applies to epigenomic mapping studies. Extensive spike-in panels of PTM-defined DNA-barcoded nucleosome standards show that >70% of >500 commercial antibodies (and >80% of the most highly cited) to >50 histone l
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20

Kew, John J. M., Peter W. Halligan, John C. Marshall, et al. "Abnormal Access of Axial Vibrotactile Input to Deafferented Somatosensory Cortex in Human Upper Limb Amputees." Journal of Neurophysiology 77, no. 5 (1997): 2753–64. http://dx.doi.org/10.1152/jn.1997.77.5.2753.

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Kew, John J. M., Peter W. Halligan, John C. Marshall, Richard E. Passingham, John C. Rothwell, Michael C. Ridding, C. David Marsden, and David J. Brooks. Abnormal access of axial vibrotactile input to deafferented somatosensory cortex in human upper limb amputees. J. Neurophysiol. 77: 2753–2764, 1997. We studied two human subjects with total deafferentation of one upper limb secondary to traumatic multiple cervical root avulsions. Both subjects developed a phantom limb and underwent elective amputation of the paralyzed, deafferentated limb. Psychophysical study revealed in each subject an area
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21

Sun, Lu, Hannah Willis, Matthew R. Marunde, et al. "Abstract 4728: Biochemical and genomic approaches for high throughput drug discovery in chromatin remodeling research." Cancer Research 83, no. 7_Supplement (2023): 4728. http://dx.doi.org/10.1158/1538-7445.am2023-4728.

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Abstract Chromatin remodeling is mediated by ATP-dependent enzymes that play key roles regulating gene expression and genome replication/repair. Aberrant nucleosome organization from dysregulated chromatin remodeling can severely alter chromatin accessibility and disrupt these important processes, thereby driving various cancers. Remarkably, nearly 20% of all human cancers contain mutations in subunits from the SWI/SNF family of chromatin remodeling complexes, making them of great interest to basic research and therapeutic intervention. In vitro studies on the remodeling enzymes (and their mul
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22

Simmons, Alysha, Eva Oswald, Georg Kuales, et al. "Abstract 4413: Identifying genome-wide histone profiles in patient derived models of AML for predictive biomarker development." Cancer Research 84, no. 6_Supplement (2024): 4413. http://dx.doi.org/10.1158/1538-7445.am2024-4413.

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Abstract Acute myeloid leukemia (AML) is a complex disease with highly individualized treatment plans for patients. Mostly these are based on genetic and phenotypic markers of the disease, but the patient’s overall condition is playing a significant role as well. To develop innovative drugs for a broad patient cohort, it is essential to understand the biological implications of these differences and to model them preclinically. In this study, we are assessing the utility of EpiCypher’s CUT&Tag-FFPE platform to characterize the epigenome of AML PDX samples. CUT&Tag-FFPE is an epigenome
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23

Maier, Keith E., Vishnu U. Sunitha Kumary, Bryan J. Venters, et al. "Abstract 7027: Direct multi-omics for the masses: Linking DNA methylation to chromatin targets via TEM-seq." Cancer Research 84, no. 6_Supplement (2024): 7027. http://dx.doi.org/10.1158/1538-7445.am2024-7027.

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Abstract DNA methylation (DNAme) is an epigenetic mark that includes the modification of cytosine resides (5mC) within CpG islands. In addition to well characterized roles regulating gene expression, imprinting and silencing parasitic DNA elements, the misregulation of DNAme is implicated in multiple diseases. Evidence is emerging that DNAme is not an independent epigenetic mark but rather closely linked to the post translational modification (PTM) of histone proteins. However, examining the relationship between 5mC and PTMs are hampered by the usual approach of independent analyses that canno
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24

Kumary, Vishnu Sunitha, Allison Hickman, Bryan J. Venters, et al. "Abstract A009: Direct multi-omics for the masses: Linking DNA methylation to chromatin targets via CUT&RUN-EM." Cancer Research 85, no. 3_Supplement (2025): A009. https://doi.org/10.1158/1538-7445.dnamethylation-a009.

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Abstract Localized DNA methylation (DNAme), particularly 5-methylcytosine (5mC), contributes to the regulation of gene expression, imprinting, and the silencing of parasitic DNA elements, with dysregulation implicated in multiple diseases including cancer. Understanding how DNAme signaling drives physiological dysfunction has great potential to reveal novel biomarkers for therapeutic strategies. Despite growing evidence that DNAme is functionally linked to various histone post translational modifications (PTMs), these entities are generally independently genomic mapped, with the resulting data
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Venters, Bryan J., Paul W. Hook, Vishnu S. Kumary, et al. "Abstract 7026: Multi-omic genomic mapping with long read sequencing." Cancer Research 84, no. 6_Supplement (2024): 7026. http://dx.doi.org/10.1158/1538-7445.am2024-7026.

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Abstract Gene transcription is regulated by the complex interplay between histone post-translational modifications (PTMs), chromatin associated proteins (CAPs), and DNA methylation (DNAme). Mapping their genomic locations and examining the relationships between these chromatin elements is a powerful approach to decipher mechanisms of disease, thereby enabling discovery of novel biomarkers and therapeutics. Leading epigenomic mapping technologies (e.g., ChIP-seq, CUT&RUN) rely upon DNA fragmentation to isolate regions of interest for sequencing on short read platforms (e.g., Illumina). This
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26

Weinzapfel, Ellen N., Alysha E. Simmons, Eva Brill, et al. "Abstract 214: Chromatin profiling from formalin-fixed paraffin-embedded samples for precision oncology." Cancer Research 85, no. 8_Supplement_1 (2025): 214. https://doi.org/10.1158/1538-7445.am2025-214.

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Abstract As the oncology field moves towards a precision medicine model of patient care, understanding and profiling the epigenetic landscape is increasingly important. Gene expression and cell function are regulated by epigenomic features, including histone post-translational modifications (PTMs), transcription factors, and other chromatin proteins. Mapping the location of these features provides a powerful approach to study chromatin mechanisms driving disease and can be leveraged for biomarker and drug development. Formalin-fixed paraffin-embedded (FFPE) tissues banked from cancer clinical
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27

James, N. "History of archaeology - Ian Graham. Alfred Maudslay and the Maya: a biography. 323 pages, 83 illustrations. 2002. London: British Museum Press; 0-7141-2561-X hardback $29.99. - James E. Snead Ruins and rivals: the making of Southwest archaeology, xxvii+226 pages, 18 figures. 2001. Tucson (AZ): University of Arizona Press; 08165-2138-7 hardback $35. - Ann Brown with Keith Bennett (ed.). Arthur Evans’s travels in Crete, 1894–1899 (BAR International series S1000). xxxi+509 pages, figures, tables. 2001. Oxford: Archaeopress; 1-84171-281-7 paperback. - Andrew Robinson. The man who deciphered Linear B: the story of Micheal Ventris. 168 pages, illustrations. 2002. London: Thames & Hudson; 0-500-51077-6 hardback £12.95." Antiquity 76, no. 292 (2002): 573–74. http://dx.doi.org/10.1017/s0003598x00119453.

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28

"The man who deciphered Linear B: the story of Michael Ventris." Choice Reviews Online 40, no. 05 (2003): 40–2614. http://dx.doi.org/10.5860/choice.40-2614.

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29

Loptson, Peter. "Giacomo Tripodi (ed.), Iliad and Odyssey in the North of Europe – Proceedings of the Workshop “Toija and the roots of European civilisation”, Toija, Finland, August 10th 2007 (Messina: Armando Siciliano Editore, 2009)." Nordicum-Mediterraneum 5, no. 1 (2010). http://dx.doi.org/10.33112/nm.5.1.24.

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Classical scholarship has profited, upon occasion, from the contributions of talented or inspired outsiders. Particularly notable in these regards, in the case of Homeric studies, have been the insights, and the detailed work, of Heinrich Schliemann, Milman Parry, and Michael Ventris. One wants never to disavow or disdain what may prove to be brilliant or helpful additions to the inevitably partly speculative domains of investigation into the early literature and the archaeology of the Hellenic peoples. At the same time these same territories have attracted more than their share of wild, somet
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30

Zhang, Linlin, Shifang Cui, Hongyan Bi, et al. "The research focus and frontiers in surgical treatment of essential tremor." Frontiers in Neurology 15 (December 11, 2024). https://doi.org/10.3389/fneur.2024.1499652.

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BackgroundEssential tremor (ET) is one of the most prevalent neurodegenerative disorders, with surgery serving as the principal treatment option. This paper presents a bibliometric analysis of research in the field of ET surgery from 2004 to 2024, aiming to identify current research hotspots and inform future research directions.MethodsThis study employs CiteSpace to analyze publication trends, countries/institutions, authors, keywords, and co-cited references in ET surgery, using the Web of Science core database from 2004 to 2024 to delineate the research pathways.ResultsA total of 1,362 publ
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Mistry, Nikhil, Max Solish, Lindsay Cahill, et al. "Cardiovascular adaptations to moderate anemia maintain cerebral perfusion but are inadequate to prevent renal and splanchnic tissue hypoxia." FASEB Journal 31, S1 (2017). http://dx.doi.org/10.1096/fasebj.31.1_supplement.700.1.

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Mild to moderate anemia is associated with increased organ injury and mortality in surgical patients by undefined mechanisms. We hypothesize that anemia‐induced tissue hypoxia is a potential unifying mechanism. A transgenic mouse model, with luciferase fused to hypoxia inducible factor (HIF ODD‐Luciferase) was utilized to assess the impact of acute antibody‐mediated anemia on adaptive cardiovascular responses, tissue PO2 (PtO2), and HIF expression. A red blood cell (RBC)‐specific antibody (TER119) induced anemia, reducing hemoglobin concentrations from 144±9 to 94±11 g/L (p<0.006) via intra
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Stevens, Ian. "The Epistemological Consequences of Artificial Intelligence, Precision Medicine, and Implantable Brain-Computer Interfaces." Voices in Bioethics 10 (June 30, 2024). http://dx.doi.org/10.52214/vib.v10i.12654.

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ABSTRACT I argue that this examination and appreciation for the shift to abductive reasoning should be extended to the intersection of neuroscience and novel brain-computer interfaces too. This paper highlights the implications of applying abductive reasoning to personalized implantable neurotechnologies. Then, it explores whether abductive reasoning is sufficient to justify insurance coverage for devices absent widespread clinical trials, which are better applied to one-size-fits-all treatments. INTRODUCTION In contrast to the classic model of randomized-control trials, often with a large num
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