Isolation, characterization, and gene expression analysis of Wharton’s jelly-derived mesenchymal stem cells under xeno-free culture conditions

por Venugopal, Parvathy, Balasubramanian, Sudha, Majumdar, Anish Sen, Ta, Malancha
Publicado 2011

Increased Proliferation and Analysis of Differential Gene Expression in Human Wharton's Jelly-derived Mesenchymal Stromal Cells under Hypoxia

por Nekanti, Usha, Dastidar, Sumitava, Venugopal, Parvathy, Totey, Satish, Ta, Malancha
Publicado 2010

Glycosylation in SARS-CoV-2 variants: A path to infection and recovery

por Aloor, Arya, Aradhya, Rajaguru, Venugopal, Parvathy, Gopalakrishnan Nair, Bipin, Suravajhala, Renuka
Publicado 2022

Multiple functions of the scaffold protein Discs large 5 in the control of growth, cell polarity and cell adhesion in Drosophila melanogaster

por Venugopal, Parvathy, Veyssière, Hugo, Couderc, Jean-Louis, Richard, Graziella, Vachias, Caroline, Mirouse, Vincent
Publicado 2020

Are serum-free and xeno-free culture conditions ideal for large scale clinical grade expansion of Wharton’s jelly derived mesenchymal stem cells? A comparative study

por Swamynathan, Priyanka, Venugopal, Parvathy, Kannan, Suresh, Thej, Charan, Kolkundar, Udaykumar, Bhagwat, Swaroop, Ta, Malancha, Majumdar, Anish Sen, Balasubramanian, Sudha
Publicado 2014

Two monogenic disorders masquerading as one: severe congenital neutropenia with monocytosis and non-syndromic sensorineural hearing loss

por Venugopal, Parvathy, Gagliardi, Lucia, Forsyth, Cecily, Feng, Jinghua, Phillips, Kerry, Babic, Milena, Poplawski, Nicola K., Rienhoff, Hugh Young, Schreiber, Andreas W., Hahn, Christopher N., Brown, Anna L., Scott, Hamish S.
Publicado 2020

Revealing Missing Human Protein Isoforms Based on Ab Initio Prediction, RNA-seq and Proteomics

por Hu, Zhiqiang, Scott, Hamish S., Qin, Guangrong, Zheng, Guangyong, Chu, Xixia, Xie, Lu, Adelson, David L., Oftedal, Bergithe E., Venugopal, Parvathy, Babic, Milena, Hahn, Christopher N., Zhang, Bing, Wang, Xiaojing, Li, Nan, Wei, Chaochun
Publicado 2015

GATA2 deficiency syndrome: A decade of discovery

por Homan, Claire C., Venugopal, Parvathy, Arts, Peer, Shahrin, Nur H., Feurstein, Simone, Rawlings, Lesley, Lawrence, David M., Andrews, James, King‐Smith, Sarah L., Harvey, Natasha L., Brown, Anna L., Scott, Hamish S., Hahn, Christopher N.
Publicado 2021

Allogeneic hematopoietic stem cell transplant outcomes in adults with inherited myeloid malignancies

por Saygin, Caner, Roloff, Gregory, Hahn, Christopher N., Chhetri, Rakchha, Gill, Saar, Elmariah, Hany, Talati, Chetasi, Nunley, Emma, Gao, Guimin, Kim, Aelin, Bishop, Michael, Kosuri, Satyajit, Das, Soma, Singhal, Deepak, Venugopal, Parvathy, Homan, Claire C., Brown, Anna, Scott, Hamish S., Hiwase, Devendra, Godley, Lucy A.
Publicado 2022

Somatic mutational landscape of hereditary hematopoietic malignancies caused by germline variants in RUNX1, GATA2, and DDX41

por Homan, Claire C., Drazer, Michael W., Yu, Kai, Lawrence, David M., Feng, Jinghua, Arriola-Martinez, Luis, Pozsgai, Matthew J., McNeely, Kelsey E., Ha, Thuong, Venugopal, Parvathy, Arts, Peer, King-Smith, Sarah L., Cheah, Jesse, Armstrong, Mark, Wang, Paul, Bödör, Csaba, Cantor, Alan B., Cazzola, Mario, Degelman, Erin, DiNardo, Courtney D., Duployez, Nicolas, Favier, Remi, Fröhling, Stefan, Rio-Machin, Ana, Klco, Jeffery M., Krämer, Alwin, Kurokawa, Mineo, Lee, Joanne, Malcovati, Luca, Morgan, Neil V., Natsoulis, Georges, Owen, Carolyn, Patel, Keyur P., Preudhomme, Claude, Raslova, Hana, Rienhoff, Hugh, Ripperger, Tim, Schulte, Rachael, Tawana, Kiran, Velloso, Elvira, Yan, Benedict, Kim, Erika, Sood, Raman, Hsu, Amy P., Holland, Steven M., Phillips, Kerry, Poplawski, Nicola K., Babic, Milena, Wei, Andrew H., Forsyth, Cecily, Mar Fan, Helen, Lewis, Ian D., Cooney, Julian, Susman, Rachel, Fox, Lucy C., Blombery, Piers, Singhal, Deepak, Hiwase, Devendra, Phipson, Belinda, Schreiber, Andreas W., Hahn, Christopher N., Scott, Hamish S., Liu, Paul, Godley, Lucy A., Brown, Anna L.
Publicado 2023