Hypoxia Stimulates Synthesis of Neutrophil Gelatinase-Associated Lipocalin in Aortic Valve Disease

por Swaminathan, Ganesh, Krishnamurthy, Varun K., Sridhar, Swetha, Robson, Denise C., Ning, Yao, Grande-Allen, K. Jane
Publicado 2019

Emerging Nano- and Micro-Technologies Used in the Treatment of Type-1 Diabetes

por Primavera, Rosita, Kevadiya, Bhavesh D, Swaminathan, Ganesh, Wilson, Rudilyn Joyce, De Pascale, Angelo, Decuzzi, Paolo, Thakor, Avnesh S
Publicado 2020

Umbilical cord mesenchymal stromal cells—from bench to bedside

por Chetty, Shashank, Yarani, Reza, Swaminathan, Ganesh, Primavera, Rosita, Regmi, Shobha, Rai, Sravanthi, Zhong, Jim, Ganguly, Abantika, Thakor, Avnesh S
Publicado 2022

Elastin homeostasis is altered with pelvic organ prolapse in cultures of vaginal cells from a lysyl oxidase‐like 1 knockout mouse model

por Jameson, Slater A., Swaminathan, Ganesh, Dahal, Shataakshi, Couri, Bruna, Kuang, Mei, Rietsch, Anna, Butler, Robert S., Ramamurthi, Anand, Damaser, Margot S.
Publicado 2020

Integrated transcriptome-proteome analyses of human stem cells reveal source-dependent differences in their regenerative signature

por Ganguly, Abantika, Swaminathan, Ganesh, Garcia-Marques, Fernando, Regmi, Shobha, Yarani, Reza, Primavera, Rosita, Chetty, Shashank, Bermudez, Abel, Pitteri, Sharon J., Thakor, Avnesh S.
Publicado 2022

Facilitating Collaboration in Rare Genetic Disorders Through Effective Matchmaking in DECIPHER

por Chatzimichali, Eleni A., Brent, Simon, Hutton, Benjamin, Perrett, Daniel, Wright, Caroline F., Bevan, Andrew P., Hurles, Matthew E., Firth, Helen V., Swaminathan, Ganesh J.
Publicado 2015

Discovery of four recessive developmental disorders using probabilistic genotype and phenotype matching among 4,125 families

por 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.
Publicado 2015

Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing

por 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
Publicado 2016