Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Jonathan Bingham"'
Publikováno v:
Indian Dermatology Online Journal, Vol 6, Iss 7, Pp 33-36 (2015)
We describe a case of Mevalonate Kinase Deficiency (MKD) also known as Hyperimmunoglobulinemia D Syndrome (HIDS) presenting as a Sweet-like syndrome in a 5-week-old with multiple erythematous plaques, fever, aseptic meningitis, and bronchiolitis. The
Externí odkaz:
https://doaj.org/article/7868ee3a181b462aa81cc098835b4cd0
Autor:
Susan E. Swogger, Karen T. Snider, Yasir Rehman, Shalini Bhatia, Barbara Senger, Robert Johnston, Jonathan Bingham, Jonathon Kirsch
Publikováno v:
International Journal of Osteopathic Medicine. 42:76-82
Background Osteopathic manipulative treatment (OMT) has been increasingly adopted by osteopathic practitioners to treat dizziness from neuro-otologic disorders. However, no systematic review has investigated effectiveness of OMT on benefit outcomes a
Autor:
Yasir Rehman, Jonathon Kirsch, Mary Ying-Fang Wang, Hannah Ferguson, Jonathan Bingham, Barbara Senger, Susan E. Swogger, Robert Johnston, Karen T. Snider
Publikováno v:
Journal of osteopathic medicineReferences.
Context Osteopathic manipulative treatment (OMT) has been utilized by osteopathic clinicians as primary or adjunctive management for dizziness caused by neuro-otologic disorders. To our knowledge, no current systematic reviews provide pooled estimate
Autor:
Matthew Bookman, Suzanne M. Paquette, Varsha Dhankani, Michael Miller, Kalle Leinonen, Nicole A. Deflaux, Mark Backus, Todd Pihl, Madelyn Reyes, Sheila Reynolds, Joseph Slagel, Jonathan Bingham, David L Gibbs, David Pot, William J.R. Longabaugh, Abigail Hahn, Zack Rodebaugh, Ilya Shmulevich, Phyliss Lee
Publikováno v:
Cancer Research. 77:e7-e10
The ISB Cancer Genomics Cloud (ISB-CGC) is one of three pilot projects funded by the National Cancer Institute to explore new approaches to computing on large cancer datasets in a cloud environment. With a focus on Data as a Service, the ISB-CGC offe
Autor:
Gregory McInnes, Jonathan Bingham, Cuiping Pan, Philip S. Tsao, Michael Snyder, Nicole A. Deflaux, Somalee Datta
Publikováno v:
Bioinformatics. 33:3709-3715
Motivation Large scale genomic sequencing is now widely used to decipher questions in diverse realms such as biological function, human diseases, evolution, ecosystems, and agriculture. With the quantity and diversity these data harbor, a robust and
Autor:
Christian R. Marshall, Annette Estes, John Wei, Janet A. Buchanan, Jennifer L. Howe, Christina Chrysler, Weili Li, Tara Paton, Fiona Tsoi, Zhuozhi Wang, Brendan J. Frey, Eric Deneault, Edwin H. Cook, William Van Etten, Stephen W. Scherer, Mohammed Uddin, Mayada Elsabbagh, Emily Kirby, Sylvia Lamoureux, Cheryl Cytrynbaum, Bhooma Thiruvahindrapuram, Mathew T. Pletcher, Lonnie Zwaigenbaum, Wilson W L Sung, Angie Fedele, Daniele Merico, Bartha Maria Knoppers, Ryan K. C. Yuen, Marc Woodbury-Smith, Worrawat Engchuan, Vicki Seifer, Isabel M. Smith, Barbara Kellam, Bonnie Mackinnon Modi, Stephanie Koyanagi, Bridget A. Fernandez, James T. Robinson, Karen Ho, Edward J Higginbotham, Joe Whitney, Krissy A.R. Doyle-Thomas, Beth A. Malow, Susan Walker, Jeremy R. Parr, Louise Gallagher, Rob Nicolson, Jonathan Bingham, Thomas Nalpathamkalam, Lia D’Abate, Sanne Jilderda, Matt Bookman, Jessica Brian, Sarah J. Spence, Ann Thompson, Jonathan Leef, Rosanna Weksberg, Jacob A. S. Vorstman, Tal Savion-Lemieux, Anne Marie Tassé, Peter Szatmari, Alana Iaboni, Xudong Liu, Evdokia Anagnostou, Jeffrey R. MacDonald, Ny Hoang, Mehdi Zarrei, Lizhen Xu, Simon N. Twigger, Robert H. Ring, Stephen R. Dager, Melissa T. Carter, Irene Drmic, Michael J. Szego, Wendy Roberts, Lili Senman, Giovanna Pellecchia, Rohan V. Patel, Sergio L. Pereira, Joachim Hallmayer, David Glazer, Lisa J. Strug, Ada J.S. Chan, Nicole A. Deflaux
Publikováno v:
Nature Neuroscience, 20(4), 602. Nature Publishing Group
Paediatrics Publications
Paediatrics Publications
We are performing whole genome sequencing (WGS) of families with Autism Spectrum Disorder (ASD) to build a resource, named MSSNG, to enable the sub-categorization of phenotypes and underlying genetic factors involved. Here, we report WGS of 5,205 sam
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b63f8e721122ea3d6acab7f7535d5d8f
https://europepmc.org/articles/PMC5501701/
https://europepmc.org/articles/PMC5501701/
Publikováno v:
Current Drug Discovery Technologies. 9:77-80
Genome-wide RNA splicing (with gene expression) can be used to discover variations that drive specific diseases and / or change the susceptibility in individuals to drug responses including tissue specific toxicities. Evidence linking causative SNPs
Autor:
Somalee Datta, Jonathan Bingham, Nicole A. Deflaux, Philip S. Tsao, Michael Snyder, Cuiping Pan, Gregory McInnes
Large scale genomic sequencing is now widely used to decipher questions in diverse realms such as biological function, human diseases, evolution, ecosystems, and agriculture. With the quantity and diversity these data harbor, a robust and scalable da
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f9ca7eb68bec93cacaf4ac41775c6e9a
Autor:
Subha Srinvasan, Jonathan Bingham, Patricia E. Carrigan, Teresa A. Brentnall, Laurence J. Miller
Publikováno v:
Pancreas. 40:281-288
Alternative splicing provides proteomic diversity that can have profound effects. The extent, pattern, and roles of alternative splicing in pancreatic cancer have not been systematically investigated. We have utilized a spliceoform-specific microarra
Publikováno v:
Pediatric dermatology. 31(6)
Microcystic adnexal carcinoma (MAC) is an uncommon adnexal neoplasm with a predilection for the head and neck. The tumor rarely metastasizes but is locally aggressive and commonly demonstrates perineural invasion. MAC occurs most often in older adult