Canlyniadau Chwilio - Garner, Terence
- Dangos 1 - 10 canlyniadau o 10
-
1
-
2
-
3
-
4
-
5
-
6
Identification of human glucocorticoid response markers using integrated multi-omic analysis from a randomized crossover trial gan Chantzichristos, Dimitrios, Svensson, Per-Arne, Garner, Terence, Glad, Camilla AM, Walker, Brian R, Bergthorsdottir, Ragnhildur, Ragnarsson, Oskar, Trimpou, Penelope, Stimson, Roland H, Borresen, Stina W, Feldt-Rasmussen, Ulla, Jansson, Per-Anders, Skrtic, Stanko, Stevens, Adam, Johannsson, Gudmundur
Cyhoeddwyd 2021Text -
7
Gene expression signatures predict response to therapy with growth hormone gan Stevens, Adam, Murray, Philip, De Leonibus, Chiara, Garner, Terence, Koledova, Ekaterina, Ambler, Geoffrey, Kapelari, Klaus, Binder, Gerhard, Maghnie, Mohamad, Zucchini, Stefano, Bashnina, Elena, Skorodok, Julia, Yeste, Diego, Belgorosky, Alicia, Siguero, Juan-Pedro Lopez, Coutant, Regis, Vangsøy-Hansen, Eirik, Hagenäs, Lars, Dahlgren, Jovanna, Deal, Cheri, Chatelain, Pierre, Clayton, Peter
Cyhoeddwyd 2021Text -
8
EVI1 phosphorylation at S436 regulates interactions with CtBP1 and DNMT3A and promotes self-renewal gan Paredes, Roberto, Kelly, James R., Geary, Bethany, Almarzouq, Batool, Schneider, Marion, Pearson, Stella, Narayanan, Prakrithi, Williamson, Andrew, Lovell, Simon C., Wiseman, Daniel H., Chadwick, John A., Jones, Nigel J., Kustikova, Olga, Schambach, Axel, Garner, Terence, Amaral, Fabio M. R., Pierce, Andrew, Stevens, Adam, Somervaille, Tim C. P., Whetton, Anthony D., Meyer, Stefan
Cyhoeddwyd 2020Text -
9
Correction: A restricted spectrum of missense KMT2D variants cause a multiple malformations disorder distinct from Kabuki syndrome gan Cuvertino, Sara, Hartill, Verity, Colyer, Alice, Garner, Terence, Nair, Nisha, Al-Gazali, Lihadh, Canham, Natalie, Faundes, Victor, Flinter, Frances, Hertecant, Jozef, Holder-Espinasse, Muriel, Jackson, Brian, Lynch, Sally Ann, Nadat, Fatima, Narasimhan, Vagheesh M., Peckham, Michelle, Sellers, Robert, Seri, Marco, Montanari, Francesca, Southgate, Laura, Squeo, Gabriella Maria, Trembath, Richard, van Heel, David, Venuto, Santina, Weisberg, Daniel, Stals, Karen, Ellard, Sian, Barton, Anne, Kimber, Susan J., Sheridan, Eamonn, Merla, Giuseppe, Stevens, Adam, Johnson, Colin A., Banka, Siddharth
Cyhoeddwyd 2020Text -
10
A restricted spectrum of missense KMT2D variants cause a multiple malformations disorder distinct from Kabuki syndrome gan Cuvertino, Sara, Hartill, Verity, Colyer, Alice, Garner, Terence, Nair, Nisha, Al-Gazali, Lihadh, Canham, Natalie, Faundes, Victor, Flinter, Frances, Hertecant, Jozef, Holder-Espinasse, Muriel, Jackson, Brian, Lynch, Sally Ann, Nadat, Fatima, Narasimhan, Vagheesh M., Peckham, Michelle, Sellers, Robert, Seri, Marco, Montanari, Francesca, Southgate, Laura, Squeo, Gabriella Maria, Trembath, Richard, van Heel, David, Venuto, Santina, Weisberg, Daniel, Stals, Karen, Ellard, Sian, Barton, Anne, Kimber, Susan J., Sheridan, Eamonn, Merla, Giuseppe, Stevens, Adam, Johnson, Colin A., Banka, Siddharth
Cyhoeddwyd 2020Text