Apparatus and method for determining a characteristic of a material von MACHIN, Tom, WEI, Kent

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APPARATUS AND METHOD FOR DETERMINING A CHARACTERISTIC OF A MATERIAL von WEI, KENT, MACHIN, TOM

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APPARATUS AND METHOD FOR DETERMINING A CHARACTERISTIC OF A MATERIAL von MACHIN, Tom, WEI, Kent

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APARELHOS PARA DETERMINAR UMA CARACTERÍSTICA DE UM MATERIAL DENTRO DE UMA REGIÃO E DE PROCESSAMENTO INDUSTRIAL, SISTEMA DE MEDIÇÃO DE DENSIDADE, MÉTODOS IMPLEMENTADO POR COMPUTADOR... von TOM MACHIN, KENT WEI

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Fellowship of the rings: a saga of strigolactones and other small signals von Machin, Darren C., Hamon-Josse, Maxime, Bennett, Tom

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International Terror Attacks and Local Out-Group Hate Crimes von Ivandic, Ria, Kirchmaier, Tom, Machin, Stephen

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Diagnosis of large vessel vasculitis in the community: a specific benefit from a non-specific symptom pathway von Machin, Russell, Sulkin, Tom, Maskell, Giles, Hughes, Mark

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Germline ERCC excision repair 6 like 2 (ERCC6L2) mutations lead to impaired erythropoiesis and reshaping of the bone marrow microenvironment von Armes, Hannah, Bewicke‐Copley, Findlay, Rio‐Machin, Ana, Di Bella, Doriana, Philippe, Céline, Wozniak, Anna, Tummala, Hemanth, Wang, Jun, Ezponda, Teresa, Prosper, Felipe, Dokal, Inderjeet, Vulliamy, Tom, Kilpivaara, Outi, Wartiovaara‐Kautto, Ulla, Fitzgibbon, Jude, Rouault‐Pierre, Kevin

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The International Neuroblastoma Risk Group (INRG) Classification System: An INRG Task Force Report von COHN, Susan L, PEARSON, Andrew D. J, MOSSERI, Veronique, SIMON, Thorsten, GARAVENTA, Alberto, CASTEL, Victoria, MATTHAY, Katherine K, LONDON, Wendy B, MONCLAIR, Tom, AMBROS, Peter F, BRODEUR, Garrett M, FALDUM, Andreas, HERO, Barbara, IEHARA, Tomoko, MACHIN, David

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Two routes to germinate a seed von Machin, Darren C., Bennett, Tom

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Prices, Policing and Policy: The Dynamics of Crime Booms and Busts von Kirchmaier, Tom, Machin, Stephen, Sandi, Matteo, Witt, Robert

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The utility of beta-2-microglobulin testing as a human cellular control in COVID-19 testing von Davies, Emma, Whitfield, Tom, Machin, Nicholas, Ahmad, Shazaad

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GATA2 monoallelic expression underlies reduced penetrance in inherited GATA2-mutated MDS/AML von Al Seraihi, Ahad F., Rio-Machin, Ana, Tawana, Kiran, Bödör, Csaba, Wang, Jun, Nagano, Ai, Heward, James A., Iqbal, Sameena, Best, Steven, Lea, Nicholas, McLornan, Donal, Kozyra, Emilia J., Wlodarski, Marcin W., Niemeyer, Charlotte M., Scott, Hamish, Hahn, Chris, Ellison, Alicia, Tummala, Hemanth, Cardoso, Shirleny Romualdo, Vulliamy, Tom, Dokal, Inderjeet, Butler, Tom, Smith, Matthew, Cavenagh, Jamie, Fitzgibbon, Jude

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The complex genetic landscape of familial MDS and AML reveals pathogenic germline variants von Rio-Machin, Ana, Vulliamy, Tom, Hug, Nele, Walne, Amanda, Tawana, Kiran, Cardoso, Shirleny, Ellison, Alicia, Pontikos, Nikolas, Wang, Jun, Tummala, Hemanth, Al Seraihi, Ahad Fahad H., Alnajar, Jenna, Bewicke-Copley, Findlay, Armes, Hannah, Barnett, Michael, Bloor, Adrian, Bödör, Csaba, Bowen, David, Fenaux, Pierre, Green, Andrew, Hallahan, Andrew, Hjorth-Hansen, Henrik, Hossain, Upal, Killick, Sally, Lawson, Sarah, Layton, Mark, Male, Alison M., Marsh, Judith, Mehta, Priyanka, Mous, Rogier, Nomdedéu, Josep F., Owen, Carolyn, Pavlu, Jiri, Payne, Elspeth M., Protheroe, Rachel E., Preudhomme, Claude, Pujol-Moix, Nuria, Renneville, Aline, Russell, Nigel, Saggar, Anand, Sciuccati, Gabriela, Taussig, David, Toze, Cynthia L., Uyttebroeck, Anne, Vandenberghe, Peter, Schlegelberger, Brigitte, Ripperger, Tim, Steinemann, Doris, Wu, John, Mason, Joanne, Page, Paula, Akiki, Susanna, Reay, Kim, Cavenagh, Jamie D., Plagnol, Vincent, Caceres, Javier F., Fitzgibbon, Jude, Dokal, Inderjeet

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Myelodysplasia and liver disease extend the spectrum of RTEL1 related telomeropathies von Cardoso, Shirleny R, Ellison, Alicia C M, Walne, Amanda J, Cassiman, David, Raghavan, Manoj, Kishore, Bhuvan, Ancliff, Philip, Rodríguez-Vigil, Carmen, Dobbels, Bieke, Rio-Machin, Ana, Al Seraihi, Ahad F H, Pontikos, Nikolas, Tummala, Hemanth, Vulliamy, Tom, Dokal, Inderjeet

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Synthesis of the Evidence on What Works for Whom in Telemental Health: Rapid Realist Review von Schlief, Merle, Saunders, Katherine R K, Appleton, Rebecca, Barnett, Phoebe, Vera San Juan, Norha, Foye, Una, Olive, Rachel Rowan, Machin, Karen, Shah, Prisha, Chipp, Beverley, Lyons, Natasha, Tamworth, Camilla, Persaud, Karen, Badhan, Monika, Black, Carrie-Ann, Sin, Jacqueline, Riches, Simon, Graham, Tom, Greening, Jeremy, Pirani, Farida, Griffiths, Raza, Jeynes, Tamar, McCabe, Rose, Lloyd-Evans, Brynmor, Simpson, Alan, Needle, Justin J, Trevillion, Kylee, Johnson, Sonia

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Acquired somatic variants in inherited myeloid malignancies von Armes, Hannah, Rio-Machin, Ana, Krizsán, Szilvia, Bödör, Csaba, Kaya, Fadimana, Bewicke-Copley, Findlay, Alnajar, Jenna, Walne, Amanda, Péterffy, Borbála, Tummala, Hemanth, Rouault-Pierre, Kevin, Dokal, Inderjeet, Vulliamy, Tom, Fitzgibbon, Jude

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Neutrophil to lymphocyte count ratio as an early indicator of blood stream infection in the emergency department von Lowsby, Richard, Gomes, Clint, Jarman, Ian, Lisboa, Paulo, Nee, Patrick A, Vardhan, Madhur, Eckersley, Tom, Saleh, Roshan, Mills, Hannah

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A frameshift variant in specificity protein 1 triggers superactivation of Sp1-mediated transcription in familial bone marrow failure von Tummala, Hemanth, Walne, Amanda J., Bewicke-Copley, Findlay, Ellison, Alicia, Pontikos, Nikolas, Bridger, Maria G., Rio-Machin, Ana, Sidhu, Jasmin K., Wang, Jun, Hasle, Henrik, Fitzgibbon, Jude, Vulliamy, Tom, Dokal, Inderjeet

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Genome instability is a consequence of transcription deficiency in patients with bone marrow failure harboring biallelic ERCC6L2 variants von Tummala, Hemanth, Dokal, Arran D., Walne, Amanda, Ellison, Alicia, Cardoso, Shirleny, Amirthasigamanipillai, Saranha, Kirwan, Michael, Browne, Isobel, Sidhu, Jasmin K., Rajeeve, Vinothini, Rio-Machin, Ana, Seraihi, Ahad Al, Duncombe, Andrew S., Jenner, Matthew, Smith, Owen P., Enright, Helen, Norton, Alice, Aksu, Tekin, Özbek, Namık Yaşar, Pontikos, Nikolas, Cutillas, Pedro, Dokal, Inderjeet, Vulliamy, Tom

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