Výsledky vyhledávání - Swaminathan, Ganesh
- Zobrazuji výsledky 1 - 15 z 15
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Magnetically Responsive Bone Marrow Mesenchymal Stem Cell-Derived Smooth Muscle Cells Maintain Their Benefits to Augmenting Elastic Matrix Neoassembly Autor Swaminathan, Ganesh, Sivaraman, Balakrishnan, Moore, Lee, Zborowski, Maciej, Ramamurthi, Anand
Vydáno 2016Text -
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Elastin homeostasis is altered with pelvic organ prolapse in cultures of vaginal cells from a lysyl oxidase‐like 1 knockout mouse model Autor Jameson, Slater A., Swaminathan, Ganesh, Dahal, Shataakshi, Couri, Bruna, Kuang, Mei, Rietsch, Anna, Butler, Robert S., Ramamurthi, Anand, Damaser, Margot S.
Vydáno 2020Text -
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Smooth Muscle Progenitor Cells Derived From Human Pluripotent Stem Cells Induce Histologic Changes in Injured Urethral Sphincter Autor Li, Yanhui, Wen, Yan, Wang, Zhe, Wei, Yi, Wani, Prachi, Green, Morgaine, Swaminathan, Ganesh, Ramamurthi, Anand, Pera, Renee Reijo, Chen, Bertha
Vydáno 2016Text -
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A Dense Poly(ethylene glycol) Coating Improves Penetration of Large Polymeric Nanoparticles within Brain Tissue Autor Nance, Elizabeth A., Woodworth, Graeme F., Sailor, Kurt A., Shih, Ting-Yu, Xu, Qingguo, Swaminathan, Ganesh, Xiang, Dennis, Eberhart, Charles, Hanes, Justin
Vydáno 2012Text -
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Protein-Functionalized Poly(ethylene glycol) Hydrogels as Scaffolds for Monolayer Organoid Culture Autor Wilson, Reid L., Swaminathan, Ganesh, Ettayebi, Khalil, Bomidi, Carolyn, Zeng, Xi-Lei, Blutt, Sarah E., Estes, Mary K., Grande-Allen, K. Jane
Vydáno 2021Text -
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Facilitating Collaboration in Rare Genetic Disorders Through Effective Matchmaking in DECIPHER Autor Chatzimichali, Eleni A., Brent, Simon, Hutton, Benjamin, Perrett, Daniel, Wright, Caroline F., Bevan, Andrew P., Hurles, Matthew E., Firth, Helen V., Swaminathan, Ganesh J.
Vydáno 2015Text -
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DECIPHER: web-based, community resource for clinical interpretation of rare variants in developmental disorders Autor Swaminathan, Ganesh J., Bragin, Eugene, Chatzimichali, Eleni A., Corpas, Manuel, Bevan, A. Paul, Wright, Caroline F., Carter, Nigel P., Hurles, Matthew E., Firth, Helen V.
Vydáno 2012Text -
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Noninvasive delivery of stealth, brain-penetrating nanoparticles across the blood-brain barrier using MRI-guided focused ultrasound Autor Nance, Elizabeth, Timbie, Kelsie, Miller, G. Wilson, Song, Ji, Louttit, Cameron, Klibanov, Alexander L, Shih, Ting-Yu, Swaminathan, Ganesh, Tamargo, Rafael J., Woodworth, Graeme F., Hanes, Justin, Price, Richard J.
Vydáno 2014Text -
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Effect of Substrate Stiffness on Human Intestinal Enteroids’ Infectivity by Enteroaggregative Escherichia coli Autor Swaminathan, Ganesh, Kamyabi, Nabiollah, Carter, Hannah E., Rajan, Anubama, Karandikar, Umesh, Criss, Zachary K., Shroyer, Noah F., Robertson, Matthew J., Coarfa, Cristian, Huang, Chenlin, Shannon, Tate E., Tadros, Madeleine, Estes, Mary K., Maresso, Anthony W., Grande-Allen, K. Jane
Vydáno 2021Text -
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Drivers of transcriptional variance in human intestinal epithelial organoids Autor Criss, Zachary K., Bhasin, Nobel, Di Rienzi, Sara C., Rajan, Anubama, Deans-Fielder, Kali, Swaminathan, Ganesh, Kamyabi, Nabiollah, Zeng, Xi-Lei, Doddapaneni, Harsha, Menon, Vipin K., Chakravarti, Deepavali, Estrella, Clarissa, Yu, Xiaomin, Patil, Ketki, Petrosino, Joseph F., Fleet, James C., Verzi, Michael P., Christakos, Sylvia, Helmrath, Michael A., Arimura, Sumimasa, DePinho, Ronald A., Britton, Robert A., Maresso, Anthony W., Grande-Allen, K. Jane, Blutt, Sarah E., Crawford, Sue E., Estes, Mary K., Ramani, Sasirekha, Shroyer, Noah F.
Vydáno 2021Text -
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Discovery of four recessive developmental disorders using probabilistic genotype and phenotype matching among 4,125 families Autor Akawi, Nadia, McRae, Jeremy, Ansari, Morad, Balasubramanian, Meena, Blyth, Moira, Brady, Angela F., Clayton, Stephen, Cole, Trevor, Deshpande, Charu, Fitzgerald, Tomas W., Foulds, Nicola, Francis, Richard, Gabriel, George, Gerety, Sebastian S., Goodship, Judith, Hobson, Emma, Jones, Wendy D., Joss, Shelagh, King, Daniel, Klena, Nikolai, Kumar, Ajith, Lees, Melissa, Lelliott, Chris, Lord, Jenny, McMullan, Dominic, O'Regan, Mary, Osio, Deborah, Piombo, Virginia, Prigmore, Elena, Rajan, Diana, Rosser, Elisabeth, Sifrim, Alejandro, Smith, Audrey, Swaminathan, Ganesh J., Turnpenny, Peter, Whitworth, James, Wright, Caroline F., Firth, Helen V., Barrett, Jeffrey C., Lo, Cecilia W., FitzPatrick, David R., Hurles, Matthew E.
Vydáno 2015Text -
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Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing Autor Sifrim, Alejandro, Hitz, Marc-Phillip, Wilsdon, Anna, Breckpot, Jeroen, Al Turki, Saeed H., Thienpont, Bernard, McRae, Jeremy, Fitzgerald, Tomas W, Singh, Tarjinder, Swaminathan, Ganesh Jawahar, Prigmore, Elena, Rajan, Diana, Abdul-Khaliq, Hashim, Banka, Siddharth, Bauer, Ulrike M. M., Bentham, Jamie, Berger, Felix, Bhattacharya, Shoumo, Bu'Lock, Frances, Canham, Natalie, Colgiu, Irina-Gabriela, Cosgrove, Catherine, Cox, Helen, Daehnert, Ingo, Daly, Allan, Danesh, John, Fryer, Alan, Gewillig, Marc, Hobson, Emma, Hoff, Kirstin, Homfray, Tessa, Kahlert, Anne-Karin, Ketley, Ami, Kramer, Hans-Heiner, Lachlan, Katherine, Lampe, Anne Katrin, Louw, Jacoba J., Manickara, Ashok Kumar, Manase, Dorin, McCarthy, Karen P., Metcalfe, Kay, Moore, Carmel, Newbury-Ecob, Ruth, Omer, Seham Osman, Ouwehand, Willem H., Park, Soo-Mi, Parker, Michael J., Pickardt, Thomas, Pollard, Martin O., Robert, Leema, Roberts, David J., Sambrook, Jennifer, Setchfield, Kerry, Stiller, Brigitte, Thornborough, Chris, Toka, Okan, Watkins, Hugh, Williams, Denise, Wright, Michael, Mital, Seema, Daubeney, Piers E. F., Keavney, Bernard, Goodship, Judith, Abu-Sulaiman, Riyadh Mahdi, Klaassen, Sabine, Wright, Caroline F., Firth, Helen V., Barrett, Jeffrey C., Devriendt, Koenraad, FitzPatrick, David R., Brook, J. David, Hurles, Matthew
Vydáno 2016Text