Search Results - Daniel Doherty
Daniel Doherty
Daniel Doherty is a San Franciscan street artist. He is widely known for creating graffiti murals in the Mission District. Clarion Alley Mural Project participates in spreading awareness of heroes worldwide. Every year, 200,000 people visit these murals in San Francisco's Mission District. In 2011, Doherty painted an informative mural of Mohamed Bouazizi. The mural consists of a painting of Bouazizi surrounded by an explanation of how he became a catalyst for the Tunisian Revolution. Laura Lengel, author of "Symbolic Interaction and New Social Media," mention the significance of Doherty's mural of Mohamed Bouazizi. They describe Doherty's work of art as an "alternative offline media form." Doherty's mural educated each visitor about this Tunisian martyr while promoting local art, helping spread Bouazizi's actions worldwide. Doherty has created several murals that consist of a local homeless man. These images touch on social problems. In one of them titles "Everything Must Go!" a bookstore filled with books about San Francisco is going out of business. He has also captured a famous location in San Francisco, Dolores Park, where he used pointillism. Provided by Wikipedia- Showing 1 - 9 results of 9
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Role of the larval feeding morphology and digestive enzyme activity in the early development of the polychaete Boccardia wellingtonensis by Daniel Doherty-Weason, Fernanda X. Oyarzun, Luciano Vera, Miguel Bascur, Fabián Guzmán, Francisco Silva, Ángel Urzúa, Antonio Brante
Published in PeerJ (2019-01-01)Get full text
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Sleep and breathing in children with Joubert syndrome and a review of other rare congenital hindbrain malformations by Jia-Der Ju-Wang, Jennifer C. Dempsey, Cristian Zhang, Daniel Doherty, Manisha Witmans, Mary Anne Tablizo, Maida Lynn Chen
Published in Therapeutic Advances in Respiratory Disease (2025-01-01)Get full text
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P591: Parental needs during pediatric whole genome sequencing for developmental disorders: An interview study by Priyanka Murali, Joon-Ho Yu, Kate MacDuffie, Michael Bamshad, Daniel Doherty, Olivia Sommerland, Betty Cohn, Tesla Theoryn, Sara Wang, Paul Kruszka
Published in Genetics in Medicine Open (2025-01-01)Get full text
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P214: SeqFirst DDi: Early whole genome sequencing improves access to early precise genetic diagnosis for children with developmental differences by Katrina Dipple, Daniel Doherty, Kailyn Anderson, Olivia Sommers, Tara Wenger, Kate MacDuffie, Alexandra Keefe, Abbey Scott, Lukas Kruidenier, Jamie Love-Nichols, Heidi Gildersleeve, Chayna Davis, Kati Buckingham, Jessica Chong, David Veenstra, Danny Miller, Deborah Copenheaver, Jane Juusola, Kyle Retterer, Kirsty McWalter, Paul Kruszka, Joon-Ho Yu, Michael Bamshad
Published in Genetics in Medicine Open (2024-01-01)Get full text
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Pulses of ocean acidification at the Triassic–Jurassic boundary by Molly Trudgill, James W. B. Rae, Ross Whiteford, Markus Adloff, Jessica Crumpton-Banks, Michael Van Mourik, Andrea Burke, Marieke Cuperus, Frank Corsetti, Daniel Doherty, William Gray, Rosanna Greenop, Wei-Li Hong, Aivo Lepland, Andrew McIntyre, Noor Neiroukh, Catherine V. Rose, Micha Ruhl, David Saunders, Magali M.F.R. Siri, Robert C. J. Steele, Eva E. Stüeken, A. Joshua West, Martin Ziegler, Sarah E. Greene
Published in Nature Communications (2025-07-01)Get full text
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Dominant‐negative variant in SLC1A4 causes an autosomal dominant epilepsy syndrome by Jonai Pujol‐Giménez, Ghayda Mirzaa, Elizabeth E. Blue, Giuseppe Albano, Danny E. Miller, Aimee Allworth, James T. Bennett, Peter H. Byers, Sirisak Chanprasert, Jingheng Chen, Daniel Doherty, Andrew B. Folta, Madelyn A. Gillentine, Ian Glass, Anne Hing, Martha Horike‐Pyne, Kathleen A. Leppig, Azma Parhin, Jane Ranchalis, Wendy H. Raskind, Elisabeth A. Rosenthal, Ulrike Schwarze, Sam Sheppeard, Samuel Strohbehn, Virginia P. Sybert, Andrew Timms, Mark Wener, University of Washington Center for Mendelian Genomics (UW‐CMG)a, Undiagnosed Diseases Network (UDN), Michael J. Bamshad, Fuki M. Hisama, Gail P. Jarvik, Katrina M. Dipple, Matthias A. Hediger, Andrew B. Stergachis
Published in Annals of Clinical and Translational Neurology (2023-06-01)Get full text
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Dual diagnosis of UQCRFS1-related mitochondrial complex III deficiency and recessive GJA8-related cataracts by Elizabeth E. Blue, Samuel J. Huang, Alyna Khan, Katie Golden-Grant, Brenna Boyd, Elisabeth A. Rosenthal, Madelyn A. Gillentine, Leah R. Fleming, David R. Adams, Lynne Wolfe, Aimee Allworth, Michael J. Bamshad, Nikeisha J. Caruana, Sirisak Chanprasert, Jingheng Chen, Nitsuh Dargie, Daniel Doherty, Marisa W. Friederich, Fuki M. Hisama, Martha Horike-Pyne, Jessica C. Lee, Tonia E. Donovan, Daniella H. Hock, Kathleen A. Leppig, Danny E. Miller, Ghayda Mirzaa, Jane Ranchalis, Wendy H. Raskind, Cole R. Michel, Richard Reisdorph, Ulrike Schwarze, Sam Sheppeard, Samuel Strohbehn, David A. Stroud, Virginia P. Sybert, Mark H. Wener, Andrew B. Stergachis, Christina T. Lam, Gail P. Jarvik, Katrina M. Dipple, Johan L.K. Van Hove, Ian A. Glass
Published in Rare (2024-01-01)Get full text
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