Výsledky vyhledávání - Nadat, Fatima

SARS-CoV-2 diagnostics: Towards a more comprehensive approach to routine patient testing Autor Carter, Clive, Hughes, Pamela, McHugh, Anna, Nadat, Fatima, Lewthwaite, Penny, Savic, Sinisa, Clark, Brendan

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Identification of a novel MAGT1 mutation supports a diagnosis of XMEN disease Autor Watson, Christopher M., Nadat, Fatima, Ahmed, Sammiya, Crinnion, Laura A., O’Riordan, Sean, Carter, Clive, Savic, Sinisa

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Fresh versus frozen PMBC using the SARS CoV-2 T-SPOT.COVID test. Which works best? Autor Nadat, Fatima, Morbey, James, Clark, Brendan, Welbury Smith, Matthew, Daga, Sunil, Ahmed, Ahmed, Chimakurthi, Chenchu, Carter, Clive

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An Atypical Autoinflammatory Disease Due to an LRR Domain NLRP3 Mutation Enhancing Binding to NEK7 Autor Caseley, Emily A., Lara-Reyna, Samuel, Poulter, James A., Topping, Joanne, Carter, Clive, Nadat, Fatima, Spickett, Gavin P., Savic, Sinisa, McDermott, Michael F.

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A missense variant in specificity protein 6 (SP6) is associated with amelogenesis imperfecta Autor Smith, Claire E L, Whitehouse, Laura L E, Poulter, James A, Wilkinson Hewitt, Laura, Nadat, Fatima, Jackson, Brian R, Manfield, Iain W, Edwards, Thomas A, Rodd, Helen D, Inglehearn, Chris F, Mighell, Alan J

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Selective Affimers Recognise the BCL‐2 Family Proteins BCL‐x(L) and MCL‐1 through Noncanonical Structural Motifs Autor Miles, Jennifer A., Hobor, Fruzsina, Trinh, Chi H., Taylor, James, Tiede, Christian, Rowell, Philip R., Jackson, Brian R., Nadat, Fatima A., Ramsahye, Pallavi, Kyle, Hannah F., Wicky, Basile I. M., Clarke, Jane, Tomlinson, Darren C., Wilson, Andrew J., Edwards, Thomas A.

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Zinc-dependent multimerization of mutant calreticulin is required for MPL binding and MPN pathogenesis Autor Rivera, Jeanne F., Baral, April J., Nadat, Fatima, Boyd, Grace, Smyth, Rachael, Patel, Hershna, Burman, Emma L., Alameer, Ghadah, Boxall, Sally A., Jackson, Brian R., Baxter, E. Joanna, Laslo, Peter, Green, Anthony R., Kent, David G., Mullally, Ann, Chen, Edwin

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Effectiveness of SARS-CoV-2 vaccination in patients with rheumatoid arthritis (RA) on DMARDs: as determined by antibody and T cell responses Autor Saleem, Benazir, Ross, Rebecca L, Bissell, Lesley-Anne, Aslam, Aamir, Mankia, Kulveer, Duquenne, Laurence, Corsadden, Diane, Carter, Clive, Hughes, Pam, Nadat, Fatima A, Mulipa, Panji, Lobb, Mark, Clarke, Brendan, Mbara, Katie, Morton, Ruth, Dibb, Sophie, Chowdhury, Rahaymin, Newton, Darren, Pike, Alexandra, Kakkar, Vishal, Savic, Sinisia, DelGaldo, Francesco, Emery, Paul

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Correction: A restricted spectrum of missense KMT2D variants cause a multiple malformations disorder distinct from Kabuki syndrome Autor 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

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A restricted spectrum of missense KMT2D variants cause a multiple malformations disorder distinct from Kabuki syndrome Autor 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

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