Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Harsha Rajasimha"'
Autor:
Hossain Shahriar, Evbusogie Sogbesan, Lorna Migiro, Temitope Balogun, Sweta Sneha, Harsha Rajasimha, Arleen Joy Patinga, Masrura Tasnim
Publikováno v:
International Journal of Applied Research on Public Health Management. 8:1-24
Clinical research management systems are mainly used by both pharmaceutical companies and biotechnology companies to manage the clinical trial process from start to finish. Due to the very nature and complexity of the clinical research process, havin
Autor:
Lindsay A. Farrer, Chi-Chao Chan, Lana M. Olson, Barbara E.K. Klein, Andrew J. Lotery, Jacqueline Ramke, Kyu Hyung Park, Yuri V. Sergeev, Felix Grassmann, John C. Merriam, Debra A. Schaumberg, Gonçalo R. Abecasis, Evangelia E. Tsironi, Anand Swaroop, Tammy M. Martin, Kari Branham, Naushin Waseem, Mohammad Othman, Donald J. Zack, Albert O. Edwards, Hendrik P. N. Scholl, Xiaowei Zhan, David Zipprer, Margaret A. Pericak-Vance, Harsha Rajasimha, Bingshan Li, José Sahel, Ronald Klein, Matthew P. Johnson, Michael B. Gorin, Thierry Léveillard, Denise J. Morgan, Stephanie A. Hagstrom, Mark Lathrop, Giuliana Silvestri, Ivana K. Kim, Robert N. Fariss, Barbara Truitt, Dwight Stambolian, James S. Friedman, Jonathan L. Haines, Arvydas Maminishkis, Yoichiro Kamatani, Robert P. Igo, Rinki Ratnapriya, Yvette P. Conley, Margaux A. Morrison, Rando Allikmets, Robert V. Baron, Jingsheng Tuo, Christina Chakarova, Bernhard H. F. Weber, Matthew Brooks, Gerald A. Fishman, Michael L. Klein, Shomi S. Bhattacharya, Joanna E. Merriam, Eric H Souied, Samuel G. Jacobson, Daniel E. Weeks, John R. Heckenlively, Emily Y. Chew, Neal S. Peachey, Margaret M. DeAngelis, Maria M Campos, Sudha K. Iyengar, Yingda Jiang
Publikováno v:
Human molecular genetics, vol 23, iss 21
Neurodegenerative diseases affecting the macula constitute a major cause of incurable vision loss and exhibit considerable clinical and genetic heterogeneity, from early-onset monogenic disease to multifactorial late-onset age-related macular degener
Autor:
Kohei Homma, Satoshi Okamoto, Wei Li, Shan Chen, Michiko Mandai, Harsha Rajasimha, Masayo Takahashi, Tiziana Cogliati, Norimoto Gotoh, Yi Sheng Chang, Anand Swaroop
Publikováno v:
Stem Cells. 31:1149-1159
Replacement of dysfunctional or dying photoreceptors offers a promising approach for retinal neurodegenerative diseases, including age-related macular degeneration and retinitis pigmentosa. Several studies have demonstrated the integration and differ
Autor:
Hans Henrik M. Dahl, Jeffrey R. Mann, Lynsey M. Cree, David C. Samuels, Passorn Wonnapinij, Susana M. Chuva de Sousa Lopes, Patrick F. Chinnery, Harsha Rajasimha
Publikováno v:
Nature Genetics. 40:249-254
Mammalian mitochondrial DNA (mtDNA) is inherited principally down the maternal line, but the mechanisms involved are not fully understood. Females harboring a mixture of mutant and wild-type mtDNA (heteroplasmy) transmit a varying proportion of mutan
Autor:
Matthew E. Monroe, Kenneth Verheggen, Brynn H. Voy, Allison Heath, Gordon A. Anderson, Alexander Kel, Dmitrij Frishman, Srikanth Rapole, Larry Smarr, Imre Janko, Gilbert S. Omenn, Louise Warnich, Natali Kolker, Vural Ozdemir, Ancha Baranova, Elizabeth Stewart, Lihua Jiang, Sanjeeva Srivastava, John Choiniere, Lennart Martens, Wu-chun Feng, Isaac S. Kohane, Geoffrey C. Fox, Harsha Rajasimha, Preveen Ramamoorthy, Jean-Claude Marshall, Jerry Sheehan, Nathaniel Anderson, Stefano Toppo, Eugene Kolker, William S. Hancock, Shawn R. Campagna, Santosh Noronha, Lynnette R. Ferguson, Paola Masuzzo, Charles V. Smith, Alexey I. Nesvizhskii, Robert L. Grossman, Gregory Yandl, Rui Chen, Joseph W. Kemnitz, Elaine Lee, Stephen P. Dearth, Michael Snyder, Elizabeth Montague, Roger Higdon, Andrey Lisitsa, Weizhong Li, Sean D. Mooney, Adrián LLerena, Courtney MacNealy-Koch, Mara H. Hutz, Doron Lancet, George I. Mias, Todd M. Smith, Sanjay Joshi, Amanda L. May, Sukru Aynacioglu, Steven W. Wilhelm, Larissa Stanberry, Peter Uetz
Publikováno v:
Omics : a journal of integrative biology. 18(1)
Biological processes are fundamentally driven by complex interactions between biomolecules. Integrated high-throughput omics studies enable multifaceted views of cells, organisms, or their communities. With the advent of new post-genomics technologie
Autor:
David C. Samuels, Patrick F. Chinnery, George M.C. Janssen, Raimond B. G. Ravelli, Roshan S. Jahangir Tafrechi, René de Coo, Frans M. van de Rijke, Carolina Wählby, Mats Nilsson, Angela Pyle, Karoly Szuhai, Harsha Rajasimha, Anton K. Raap
Publikováno v:
PLoS ONE
PLoS ONE, Vol 7, Iss 12, p e52080 (2012)
PLoS ONE, 7(12)
PLoS ONE, Vol 7, Iss 12, p e52080 (2012)
PLoS ONE, 7(12)
Many pathogenic mitochondrial DNA mutations are heteroplasmic, with a mixture of mutated and wild-type mtDNA present within individual cells. The severity and extent of the clinical phenotype is largely due to the distribution of mutated molecules be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21b14bf808922de514c5f90c4d244376
https://doi.org/10.1371/journal.pone.0052080
https://doi.org/10.1371/journal.pone.0052080
Publikováno v:
Retinal Development ISBN: 9781617798474
In humans, protein-coding exons constitute 1.5-1.7% of the human genome. Targeted sequencing of all coding exons is termed as exome sequencing. This method enriches for coding sequences at a genome-wide scale from 3 μg of DNA in a hybridization capt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1833a39e830614ae8d344627b768078f
https://doi.org/10.1007/978-1-61779-848-1_24
https://doi.org/10.1007/978-1-61779-848-1_24
Publikováno v:
Retinal Development ISBN: 9781617798474
RNA expression profiles produced by next-generation sequencing (NGS) technology (RNA-seq) allow comprehensive investigation of transcribed sequences within a cell or tissue. RNA-seq is rapidly becoming more cost-effective for transcriptome profiling.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4bcbf3de9c2ea0bb8de9f5a9f9f97ac4
https://doi.org/10.1007/978-1-61779-848-1_23
https://doi.org/10.1007/978-1-61779-848-1_23
Autor:
Margot Sunshine, Frank Schacherer, Nigam H. Shah, Akhilesh Pandey, Harsha Rajasimha, Andrew Finney, Rebecca Tang, Martijn P. van Iersel, Kumaran Kandasamy, Kei-Hoi Cheung, Martina Kutmon, Geeta Joshi-Tope, Matthias Samwald, Dean Ravenscroft, Mustafa H Syed, Vincent Schächter, Michael L. Blinov, Chris Sander, Liya Ren, Guanming Wu, Christian Lemer, Zhenjun Hu, Peter Hornbeck, Andrey Rzhetsky, Nicolas Le Novère, Emek Demir, Shiva Krupa, Michelle Whirl-Carrillo, Ken Fukuda, Alejandra López-Fuentes, Michael P. Cary, Erik Brauner, David Merberg, Julie Leonard, Imran Shah, David W. Kane, Alexander R. Pico, Shannon K. McWeeney, Michael Hucka, Peter D. Karp, Nadia Anwar, Andrea Splendiani, Peter D'Eustachio, Olivier Hubaut, Ugur Dogrusoz, Julio Collado-Vides, Gary D. Bader, Jeremy Zucker, Carl F. Schaefer, Keith Allen, Kam D. Dahlquist, Oliver Reubenacker, Paul Thomas, Mirit I. Aladjem, Victoria Petri, Verónica Jiménez-Jacinto, Igor Rodchenkov, Edgar Wingender, Gopal R. Gopinath, Imre Vastrik, Stan Letovksy, Susumu Goto, Ryan Whaley, Frank Gibbons, Natalia Maltsev, Özgün Babur, Ranjani Ramakrishnan, Robin Haw, Elgar Pichler, Burk Braun, Sylva L. Donaldson, Suzanne M. Paley, Huaiyu Mi, Sarala M. Wimalaratne, Elizabeth M. Glass, Sasha Tkachev, Irma Martínez-Flores, Augustin Luna, Joanne S. Luciano, Debbie Marks, Marc Gillespie, Michael Honig, Ewan Birney, Dan Corwin, Bruno S. Sobral, Kenneth H. Buetow, Li Gong, Eric K. Neumann, Robert N. Goldberg, Peter Murray-Rust
Publikováno v:
Nature biotechnology
Nature Biotechnology
Nature Biotechnology, 28(9), 935-42. Nature Publishing Group
Nature Biotechnology
Nature Biotechnology, 28(9), 935-42. Nature Publishing Group
BioPAX (Biological Pathway Exchange) is a standard language to represent biological pathways at the molecular and cellular level. Its major use is to facilitate the exchange of pathway data (http://www.biopax.org). Pathway data captures our understan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d104cbe5aa6621a4df6eefcda72f4a5
https://resolver.caltech.edu/CaltechAUTHORS:20100929-111828470
https://resolver.caltech.edu/CaltechAUTHORS:20100929-111828470
Publikováno v:
American journal of human genetics. 82(2)
The mutation 3243A--G is the most common heteroplasmic pathogenic mitochondrial DNA (mtDNA) mutation in humans, but it is not understood why the proportion of this mutation decreases in blood during life. Changing levels of mtDNA heteroplasmy are fun