#sarah grünewald

[mumblingsofmemory]

Sarah Grünewald

#Sarah Grünewald #smoking

[kreuzfahrttester]

Ankündigung Schiffstaufe MSC Euribia in Kopenhagen

heute möchten wir Sie über die bevorstehende Schiffstaufe der “MSC Euribia” informieren. Das neue Kreuzfahrtschiff, das von der renommierten Reederei “MSC Cruises” in Auftrag gegeben wurde, wird am 8. Juni 2023 in einer feierlichen Zeremonie im Hafen von Kopenhagen getauft. Oscar-Preisträgerin Sophia Loren wird zum 19. Mal die Rolle der Taufpatin für ein Schiff von MSC Cruises übernehmen Die…

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#Bilder vom Schiff #bob Sinclar #kopenhagen #kreuzfahrt news #MSC Cruises #msc euribia #MSC-Kreuzfahrten #nachrichten Kreuzfahrt #news #Sarah Grünewald #Sophia Loren #Taufe #Taufpatin

[opcaoturismo]

Cerimónia de nomeação do MSC Euribia em Copenhaga

A menos de um mês da inauguração, a MSC Cruzeiros revelou mais detalhes da Cerimónia de Nomeação para a inauguração do navio mais avançado do ponto de vista ambiental até à data, o MSC Euribia, que terá lugar no dia 08 de junho em Copenhaga, Dinamarca. O MSC Euribia simboliza a visão da companhia em assegurar um futuro sustentável e um profundo respeito e compromisso para com a proteção e preservação do ambiente marinho. O MSC Euribia foi “construído para o futuro” e é o navio de cruzeiro com maior eficiência energética alguma vez construído. O navio é o segundo da frota da MSC Cruzeiros a ser movido a LNG, o combustível mais limpo e eficiente disponível atualmente à escala comercial. O navio também apresentará outras tecnologias ambientais de última geração, incluindo sistemas avançados de tratamento de águas residuais a bordo, gestão de resíduos, medidas de eficiência energética, bem como sistemas inovadores de gestão de ruído irradiado subaquático para reduzir o potencial impacto no ambiente marinho.

Uma noite para recordar Comemorando a inauguração deste novo e inovador navio, a MSC Cruzeiros convidará os  seus passageiros para a Cerimónia de Nomeação do mais recente navio emblemático a juntar-se à frota, reunindo dignatários locais, principais parceiros agentes de viagens, meios de comunicação social de todo o mundo e vários nomes conhecidos, incluindo a ícone de Hollywood e a atriz vencedora de um Óscar, Sophia Loren, que mantém uma relação pessoal de longa data com a Companhia e desempenhará o seu papel como madrinha do seu 19.º navio da MSC Cruzeiros. Para apresentar as atuações, Sarah Grünewald, conhecida apresentadora de televisão dinamarquesa, atriz e modelo será a mestre de Cerimónia. Durante todo o evento, os passageiros podem contar com a tradição de se partir uma garrada de champanhe na proa do navio, um belo jantar de gala, bem como entretenimento e espetáculos ao vivo, incluindo um DJ set especial para encerrar a noite, do mundialmente famoso DJ francês e produtor musical de renome, Bob Sinclar. A seguir ao evento, o MSC Euribia começará a navegar no Norte da Europa este Verão, com itinerários de 7 noites de Kiel, Alemanha e Copenhaga, Dinamarca, para os cativantes fiordes noruegueses, incluindo Geiranger, Ålesund e Flaam. A MSC Cruzeiros disponibilizará um pacote especial com voos Lisboa-Copenhaga-Lisboa, podendo ficar a conhecer a capital dinamarquesa, navegando a bordo do MSC Euribia, mas também do MSC Poesia. Read the full article

#cerimonia #dinamarca #msceuribia #sofia

[natbult]

Faith and art (Dump station)

typed " contemporary art and spirituality"

Article about why faith and art are on the rise.

“The resurgence of spirituality is more present than ever in contemporary art,” Iranian artist Parviz Tanavoli said in a recent interview. “Wars, conflicts, and consumerism seem to have prompted a desire for transcendence, for refuge, for essence. Increasingly, artists are aiming for the essence of spirituality in their work.” Undoubtedly—regardless of their personal religious beliefs—artists are turning to spiritual philosophies and theological iconography to examine their own beliefs and make sense of the current moment.

I find this interesting becauste this is much differnent than what I was finding. Maybe because this is more general sense of spirituality>> I was looking very specifically at Christian artists. So that could be worth noting. Ope yup these are just talking about work in general sense of imbuing a sense of spirituality.

Although it’s nearly impossible to settle on one reason for today’s resurgence of spirituality in contemporary art, for numerous artists, it’s a matter of turning to their work to reflect on personal beliefs, religious or not. They may draw on theology to explore metaphysical themes or reinterpret religious iconography to discuss meaningful secular issues. Time will tell if the revival of these themes is merely a symptom of the present or a new path forward. 

Ann Agee

The feminist artist Ann Agee, known for her deft, hand-built ceramic sculptures, makes use of religious iconography without ascribing any sort of spiritual meaning to her work. “Spirituality is a word that puts me off a little bit,” Agee said. “It feels like there’s an implication to live the right way or the wrong way. And I dislike anything that tells you how to live.” Agee has also been a long-time devotee to religious aesthetics, though she carefully avoids dogma and instead focuses on technical elements like the use of color and light. In her words, “There was a time when artists could not survive if they didn’t make religious iconography, so a lot of really wonderful paintings were made with these stories.”

Good article for definitions!! This also has links to books at the bottom!!!

“Spirituality” is a term that is often used vaguely to refer to an attitude or approach toward life that involves a search for meaning.

Sheldrake also describes the study of spirituality as an academic discipline and discourse. 

The second term that needs qualification is “contemporary” in the sense of contemporary art. 

today’s artists are—unlike Grünewald—far more likely to disclose the broadly numinous rather than the explicitly incarnational, and are far more likely to offer generalised religious experience rather than Christian revelation. In doing so they, like Rothko and other abstract expressionists before them, move religious art beyond its traditionally didactic and narrative intentions towards the primarily experiential.25

Sarah Lucas’s tongue-in-cheek Christ You Know It Ain’t Easy (2003) uses the figure of Christ, composed of cigarette butts, to provoke humor in what resembles an advertising slogan.

Good commentary on this topic.

Art and Fauth Makoto Fuimura

Very important in my work!!

He talks about making in Christainity lense. But his work is not exactly about what his book talks about (so it appears on his site).

[albertehandbergnilsson]

Under min 2 ugers praktik hos Ekstra Bladet fik jeg mulighed for komme med ind og live-dække Vild Med Dans. Det var den aften, hvor Sarah Grünewald gjorde entré i den uges mest omtalte kjole: nemlig Helle Thornings gallakjole fra dronningens jubilæumstaffel. Jeg havde selv tidligere skrevet Ekstra Bladets artikel om kjolen, så derfor blev jeg sat til at interviewe Sarah Grünewald efter showet. Her fik jeg prøvet kræfter med at skulle filme og interviewe samtidig, samt efterfølgende at skrue en artikel sammen på en kort deadline, inden pressen blev sendt hjem.

[trautmans-legs]

Sarah Grünewald

#sarah grünewald #sarah grunewald #legs #bare legs #long legs #high heels #girls #models #dress #long dress #fashion #blonde #blue eyes #elegant #high resolution #sexy #trautmanslegs

[theoutcastrogue]

Prisons in Ancient Rome 

by Invicta

What was it like to go to prison in ancient Rome? In this history documentary we  begin with an overview of how prisons were present since the earliest civilizations but did not function the same as today. Justice did not involve locking people up. Rather, justice was built around the idea of vengeance and the philosophy of "an eye for an eye". In this context, prisons served merely as temporary holding cells while people awaited trial or their punishment.

In ancient Rome we see this with the Mamertine prison which was built during the early monarchy. Consisting of a small dungeon, it never saw widespread use and was instead reserved for mostly high profile figures like war captives. Notable prisoners include Vercingetorix, Simon Gioras, and the Catiline Conspirators. During the late Republic however the demand for prisons increased as reforms to the criminal justice system meant more people were going to court. More public prisons were built as well as growing trend in private prisons. During the transition to the Roman Empire however the consolidation of power prompted a crackdown against private prisons and shifting the focus back to public prisons. These would continue to see use a temporary holdings cells but now also housed enemies of Rome. For the most part however, corporal punishment still remained the norm. This trend would continue through the medieval era and its only with the age of Enlightenment that we start to see justice systems shift to mass incarceration as the preferred vessel for justice.

Bibliography and suggested readings:

The Oxford History of the Prison Penal Practice and Penal Policy in Ancient Rome Crime and Punishment in Ancient Rome Prison, Punishment, and Penance in Late Antiquity The Cambridge Companion to Roman Law

May I add to this bibliography, with an always crucial in these matters view from the lower rungs:

Sarah E. Bond, Trade and Taboo: Disreputable Professions in the Roman Mediterranean (2016, University of Michigan Press)

Robert C. Knapp, Invisible Romans: Prostitutes, Outlaws, Slaves, Gladiators and Others (2011, Profile Books)

Wilfried Nippel, Public Order in Ancient Rome (1995, Cambridge University Press)

Wilfried Nippel, “Policing Rome” (1984, The Journal of Roman Studies, Vol. 74)

Aaron L. Beek, “Peirates, Leistai, Boukoloi, and Hostes Gentium of the Classical World : The Portrayal of Pirates in Literature and the Reality of Contemporary Piratical Actions.” (2006, Classics Honors Projects. Paper 4.)

Brent, D. Shaw, “Bandits in the Roman Empire” (1984, Past & Present, No. 105)

Thomas Grünewald, Bandits in the Roman Empire: Myth and Reality (1999, Routledge)

#theory #prison #Invicta #rome #I fought the law #swinging from the gallows tree #bibliography

[yde-copenhagen]

Sarah Grünewald in YDE

#yde #ole yde #yde copenhagen #sarah grünewald #sarah grunewald #design #dress #fashion #luzury #style

[mulheresemtodasascores-blog]

Isadora Duncan, coreógrafa e bailarina precursora da dança moderna. Ilustrada por: Isadora Zeferino

Isadora Duncan nasceu em  27 de maio de 1877 e faleceu em 1927. Ela foi uma bailarina norte-americana, e pioneira da dança moderna. Criou uma dança livre das técnicas do balé clássico e se apresentava com trajes esvoaçantes, cabelos soltos e pés descalços.

Filha do poeta Joseph Charles e da pianista e professora de música Dora Gray Duncanon, desde cedo conviveu com a arte. Ainda adolescente Isadora começou a criar um estilo de dança que iria quebrar todas as convenções do balé clássico. Com 14 anos começou a dar aulas de dança.

Sua técnica tinha como base os movimentos naturais do corpo, como o andar, correr e saltar. Inspirada nas roupas da Grécia Antiga usava trajes drapeados e esvoaçantes, provocou verdadeira revolução no panorama da dança de espetáculo. Trabalhava com músicas não convencionais para a dança da época, como peças de Chopin e Wagner. Com 21 anos fez sua estreia no Teatro Sarah Bemhardt, em Paris. Deu início a uma turnê pela Europa, mas seu novo estilo teve maior aceitação na Alemanha e na Hungria. Em 1904, fixou residência na Grécia, para onde levou seus irmãos Elizabeth e Raymond. Esteve em Viena, na Áustria, onde apresentou “As Suplicantes”, de Ésquilo, com um coro de crianças gregas. Nesse mesmo ano, fundou sua primeira escola de dança, em Grünewald, subúrbio de Berlim, para crianças de classes mais pobres.

Em 1908, foi para Nova Iorque onde apresentou o espetáculo “Ifigênia”, de Gluck. Em seguida retornou a Paris. Nessa época, passou a viver com o coreógrafo inglês Gordon Graig, com quem teve um filho. Depois de separada, viveu com o milionário francês Eugéne Singer, com quem teve seu segundo filho. Em 1913, perdeu seus filhos em um acidente, quando o carro em que estavam caiu no rio Sena.

Em 1919, realizou uma excursão pela América do Sul, apresentando-se no Brasil, Argentina e Uruguai. Após a Primeira Guerra, foi para Moscou. Em 1922 se casa com o poeta soviético Serguei Iessenin. Em 1925, seu marido se suicida. Muda-se então para a França, onde em 1927 morre tragicamente, estrangulada por sua echarpe que enrolou na roda do automóvel que dirigia em alta velocidade na Riviera Francesa.

Isadora Duncan faleceu em Nice, na França, no dia 14 de setembro de 1927.

Fonte:  https://www.ebiografia.com/isadora_duncan/ http://www.lpm.com.br/site/default.asp?TroncoID=805134&SecaoID=948848&SubsecaoID=0&Template=../livros/layout_autor.asp&AutorID=806181

[fxj8760]

Book Design: À rebours — Joris-Karl Huysmans Text in Adobe Caslon (by Carol Twombly), chapter number is set in Nostra Stream. Book Design by Sarah Martinon, art director and illustrator based in Paris.

“On the occasion of the exhibition Huysmans. De Degas à Grünewald taking place at the Musée d’Orsay in Paris, an illustrated version of the French novelist and art critic’s most famous text was published. Sarah Martinon, art director and illustrator based in Paris, was in charge of the book’s layout as well as the creation of original marble-inspired illustrations used as chapter openers. These mesmerising patterns complement the text, now considered to be the ultimate example of Decadent literature, with a main character described by its author as “soaring upwards into dream, seeking refuge in illusions of extravagant fantasy.”

Source: https://fontsinuse.com/uses/31030/a-rebours-joris-karl-huysmans

#adobecaslon #typeinuse

[dvisage]

Sarah Grünewald

#woman #beautiful face #beautiful eyes #portrait #sarah grunewald #attractive #beautiful woman #gorgeous #charm #beauty

[abbkineeu]

New Post has been published on Biotech Advisers

New Post has been published on http://www.bioadvisers.com/new-method-analyze-cell-membrane-proteins-situ-using-mass-spectrometry/

A new method to analyze cell membrane proteins in situ by using mass spectrometry

The cell membrane is a biological membrane that separates the interior of all cells from the outside environment which protects the cell from its environment consisting of a lipid bilayer with embedded proteins. The cell membrane controls the movement of substances in and out of cells and organelles. In this way, it is selectively permeable to ions and organic molecules. In addition, cell membranes are involved in a variety of cellular processes such as cell adhesion, ion conductivity and cell signalling and serve as the attachment surface for several extracellular structures, including the cell wall, the carbohydrate layer called the glycocalyx, and the intracellular network of protein fibers called the cytoskeleton.

Membranes protect all of our cells and the organelles inside them, including the mitochondria – the powerhouse of the cell. These membranes are studded with biological machinery made of proteins that enable molecular cargo to pass in and out.

Studying these membrane-embedded machines in their native state is crucial to understanding mechanisms of disease and providing new goals for treatments. However, current methods for studying them involve removing them from the membrane, which can compromise the integrity of membrane proteins and alter their structure and functional properties.

Recently, researchers have developed a new technique to analyse cell membrane proteins in situ which could revolutionise the way in which we study diseases, such as cancer, metabolic and heart diseases. In this work, they ejected intact assemblies from membranes, without chemical disruption, and used mass spectrometry to define their composition. This research will enable the development of mass spectrometry in biology to be taken to a new level, enabling new discoveries that would not have been possible before.

The technique could dramatically affect our understanding of both how cell membrane complexes work, and in the process, our approach to healthcare research. From Escherichia coli outer membranes, scientists identified a chaperone-porin association and lipid interactions in the β-barrel assembly machinery. They observed efflux pumps bridging inner and outer membranes, and from inner membranes they identified a pentameric pore of TonB, as well as the protein-conducting channel SecYEG in association with F1FO adenosine triphosphate (ATP) synthase. Intact mitochondrial membranes from Bos taurus yielded respiratory complexes and fatty acid–bound dimers of the ADP (adenosine diphosphate)/ATP translocase (ANT-1). These results highlight the importance of native membrane environments for retaining small-molecule binding, subunit interactions, and associated chaperones of the membrane proteome.

The technique involves vibrating the sample at ultrasonic frequencies so that the cell begins to fall apart. Electrical currents then applied an electric field to eject the protein machines out of the membrane and directly into a mass spectrometer – an instrument that can detect a molecule’s chemical ‘signature’, based on its mass.

Not only did the membrane protein machines survive the ejection; the analysis also revealed how they communicate with each other, are guided to their final location and transport their molecular cargo into the cell. With the development of this method, the application of mass spectrometry in biology will be taken to a new level, using it to make discoveries that would not have been possible before.

“A longstanding question on the structure of one membrane machine from mitochondria has now been solved using this technique.” said Dr Sarah Rouse, from the Department of Life Sciences at Imperial. The results are particularly exciting for mitochondrial membranes—we managed to catch a translocator in action—passing metabolites. Because mitochondrial therapeutics target a wide range of debilitating diseases, we now have a new way of assessing their effects.

Source: http://www.ox.ac.uk/news/2018-11-16-new-way-look-cell-membranes-could-change-way-we-study-disease

Article: Title: Protein assemblies ejected directly from native membranes yield complexes for mass spectrometry Authors: Dror S. Chorev, Lindsay A. Baker, Di Wu, Victoria Beilsten-Edmands, Sarah L. Rouse, Tzviya Zeev-Ben-Mordehai, Chimari Jiko, Firdaus Samsudin, Christoph Gerle, Syma Khalid, Alastair G. Stewart, Stephen J. Matthews, Kay Grünewald, Carol V. Robinson

[bioadvisers]

Bioadvisers shared on Biotech Advisers

A new method to analyze cell membrane proteins in situ by using mass spectrometry

The cell membrane is a biological membrane that separates the interior of all cells from the outside environment which protects the cell from its environment consisting of a lipid bilayer with embedded proteins. The cell membrane controls the movement of substances in and out of cells and organelles. In this way, it is selectively permeable to ions and organic molecules. In addition, cell membranes are involved in a variety of cellular processes such as cell adhesion, ion conductivity and cell signalling and serve as the attachment surface for several extracellular structures, including the cell wall, the carbohydrate layer called the glycocalyx, and the intracellular network of protein fibers called the cytoskeleton.

Membranes protect all of our cells and the organelles inside them, including the mitochondria – the powerhouse of the cell. These membranes are studded with biological machinery made of proteins that enable molecular cargo to pass in and out.

Studying these membrane-embedded machines in their native state is crucial to understanding mechanisms of disease and providing new goals for treatments. However, current methods for studying them involve removing them from the membrane, which can compromise the integrity of membrane proteins and alter their structure and functional properties.

Recently, researchers have developed a new technique to analyse cell membrane proteins in situ which could revolutionise the way in which we study diseases, such as cancer, metabolic and heart diseases. In this work, they ejected intact assemblies from membranes, without chemical disruption, and used mass spectrometry to define their composition. This research will enable the development of mass spectrometry in biology to be taken to a new level, enabling new discoveries that would not have been possible before.

The technique could dramatically affect our understanding of both how cell membrane complexes work, and in the process, our approach to healthcare research. From Escherichia coli outer membranes, scientists identified a chaperone-porin association and lipid interactions in the β-barrel assembly machinery. They observed efflux pumps bridging inner and outer membranes, and from inner membranes they identified a pentameric pore of TonB, as well as the protein-conducting channel SecYEG in association with F1FO adenosine triphosphate (ATP) synthase. Intact mitochondrial membranes from Bos taurus yielded respiratory complexes and fatty acid–bound dimers of the ADP (adenosine diphosphate)/ATP translocase (ANT-1). These results highlight the importance of native membrane environments for retaining small-molecule binding, subunit interactions, and associated chaperones of the membrane proteome.

The technique involves vibrating the sample at ultrasonic frequencies so that the cell begins to fall apart. Electrical currents then applied an electric field to eject the protein machines out of the membrane and directly into a mass spectrometer – an instrument that can detect a molecule’s chemical ‘signature’, based on its mass.

Not only did the membrane protein machines survive the ejection; the analysis also revealed how they communicate with each other, are guided to their final location and transport their molecular cargo into the cell. With the development of this method, the application of mass spectrometry in biology will be taken to a new level, using it to make discoveries that would not have been possible before.

“A longstanding question on the structure of one membrane machine from mitochondria has now been solved using this technique.” said Dr Sarah Rouse, from the Department of Life Sciences at Imperial. The results are particularly exciting for mitochondrial membranes—we managed to catch a translocator in action—passing metabolites. Because mitochondrial therapeutics target a wide range of debilitating diseases, we now have a new way of assessing their effects.

Source: http://www.ox.ac.uk/news/2018-11-16-new-way-look-cell-membranes-could-change-way-we-study-disease

Article: Title: Protein assemblies ejected directly from native membranes yield complexes for mass spectrometry Authors: Dror S. Chorev, Lindsay A. Baker, Di Wu, Victoria Beilsten-Edmands, Sarah L. Rouse, Tzviya Zeev-Ben-Mordehai, Chimari Jiko, Firdaus Samsudin, Christoph Gerle, Syma Khalid, Alastair G. Stewart, Stephen J. Matthews, Kay Grünewald, Carol V. Robinson

[abbkine]

BioAdvisers said on Biotech Advisers

A new method to analyze cell membrane proteins in situ by using mass spectrometry

The cell membrane is a biological membrane that separates the interior of all cells from the outside environment which protects the cell from its environment consisting of a lipid bilayer with embedded proteins. The cell membrane controls the movement of substances in and out of cells and organelles. In this way, it is selectively permeable to ions and organic molecules. In addition, cell membranes are involved in a variety of cellular processes such as cell adhesion, ion conductivity and cell signalling and serve as the attachment surface for several extracellular structures, including the cell wall, the carbohydrate layer called the glycocalyx, and the intracellular network of protein fibers called the cytoskeleton.

Membranes protect all of our cells and the organelles inside them, including the mitochondria – the powerhouse of the cell. These membranes are studded with biological machinery made of proteins that enable molecular cargo to pass in and out.

Studying these membrane-embedded machines in their native state is crucial to understanding mechanisms of disease and providing new goals for treatments. However, current methods for studying them involve removing them from the membrane, which can compromise the integrity of membrane proteins and alter their structure and functional properties.

Recently, researchers have developed a new technique to analyse cell membrane proteins in situ which could revolutionise the way in which we study diseases, such as cancer, metabolic and heart diseases. In this work, they ejected intact assemblies from membranes, without chemical disruption, and used mass spectrometry to define their composition. This research will enable the development of mass spectrometry in biology to be taken to a new level, enabling new discoveries that would not have been possible before.

The technique could dramatically affect our understanding of both how cell membrane complexes work, and in the process, our approach to healthcare research. From Escherichia coli outer membranes, scientists identified a chaperone-porin association and lipid interactions in the β-barrel assembly machinery. They observed efflux pumps bridging inner and outer membranes, and from inner membranes they identified a pentameric pore of TonB, as well as the protein-conducting channel SecYEG in association with F1FO adenosine triphosphate (ATP) synthase. Intact mitochondrial membranes from Bos taurus yielded respiratory complexes and fatty acid–bound dimers of the ADP (adenosine diphosphate)/ATP translocase (ANT-1). These results highlight the importance of native membrane environments for retaining small-molecule binding, subunit interactions, and associated chaperones of the membrane proteome.

The technique involves vibrating the sample at ultrasonic frequencies so that the cell begins to fall apart. Electrical currents then applied an electric field to eject the protein machines out of the membrane and directly into a mass spectrometer – an instrument that can detect a molecule’s chemical ‘signature’, based on its mass.

Not only did the membrane protein machines survive the ejection; the analysis also revealed how they communicate with each other, are guided to their final location and transport their molecular cargo into the cell. With the development of this method, the application of mass spectrometry in biology will be taken to a new level, using it to make discoveries that would not have been possible before.

“A longstanding question on the structure of one membrane machine from mitochondria has now been solved using this technique.” said Dr Sarah Rouse, from the Department of Life Sciences at Imperial. The results are particularly exciting for mitochondrial membranes—we managed to catch a translocator in action—passing metabolites. Because mitochondrial therapeutics target a wide range of debilitating diseases, we now have a new way of assessing their effects.

Source: http://www.ox.ac.uk/news/2018-11-16-new-way-look-cell-membranes-could-change-way-we-study-disease

Article: Title: Protein assemblies ejected directly from native membranes yield complexes for mass spectrometry Authors: Dror S. Chorev, Lindsay A. Baker, Di Wu, Victoria Beilsten-Edmands, Sarah L. Rouse, Tzviya Zeev-Ben-Mordehai, Chimari Jiko, Firdaus Samsudin, Christoph Gerle, Syma Khalid, Alastair G. Stewart, Stephen J. Matthews, Kay Grünewald, Carol V. Robinson