Intraspecific variation in responses to extreme and moderate temperature stress in the wild species, Solanum carolinense (Solanaceae) von Chandler, Emma K, Travers, Steven E

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Prenatal exome sequencing analysis in fetal structural anomalies detected by ultrasonography (PAGE): a cohort study von Lord, Jenny, McMullan, Dominic J, Eberhardt, Ruth Y, Rinck, Gabriele, Hamilton, Susan J, Quinlan-Jones, Elizabeth, Prigmore, Elena, Carey, Georgina K, Mellis, Rhiannon, Robart, Sarah, Berry, Ian R, Chandler, Kate E, Cilliers, Deirdre, Cresswell, Lara, Edwards, Sandra L, Gardiner, Carol, Henderson, Alex, Holden, Simon T, Homfray, Tessa, Lester, Tracy, Newbury-Ecob, Ruth, Prescott, Katrina, Quarrell, Oliver W, Ramsden, Simon C, Roberts, Eileen, Tapon, Dagmar, Tooley, Madeleine J, Vasudevan, Pradeep C, Weber, Astrid P, Wellesley, Diana G, Westwood, Paul, White, Helen, Parker, Michael, Williams, Denise, Jenkins, Lucy, Scott, Richard H, Kilby, Mark D, Chitty, Lyn S, Hurles, Matthew E, Maher, Eamonn R, Bateman, Mark, Best, Sunayna K, Campbell, Carolyn, Carey, Georgina, Chitty, Lyn S, Cilliers, Deirdre, Cohen, Kelly, Collingwood, Emma, Constantinou, Panayiotis, Cresswell, Lara, Delmege, Catherine, Edwards, Sandra L, Ellis, Richard, Evans, Jerry, Everett, Thomas, Pinto, Clare F, Forrester, Natalie, Fowler, Emma, Gardiner, Carol, Hamilton, Susan, Healey, Karen, Henderson, Alex, Holden, Simon T, Homfray, Tessa, Hudson, Rebecca, Hurles, Matthew E, Jenkins, Lucy, Keelagher, Rebecca, Kilby, Mark D, Lester, Tracey, Lewis, Rebecca, Lord, Jenny, Maher, Eamonn R, Marton, Tamas, McMullan, Dominic J, Mehta, Sarju, Mellis, Rhiannon, Newbury-Ecob, Ruth, Park, Soo-Mi, Parker, Michael, Prescott, Katrina, Prigmore, Elena, Quarrell, Oliver W, Quinlan-Jones, Elizabeth, Ramsden, Simon C, Rinck, Gabriele, Robart, Sarah, Roberts, Eileen, Rowland, Jayne, Steer, James, Tapon, Dagmar, Taylor, Emma J, Tooley, Madeleine J, Vasudevan, Pradeep C, Weber, Astrid P, Wellesley, Diana G, Westwood, Paul, White, Helen, Williams, Denise, Wilson, Elizabeth

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Mutations in PRDM5 in Brittle Cornea Syndrome Identify a Pathway Regulating Extracellular Matrix Development and Maintenance von BURKITT WRIGHT, Emma M. M, SPENCER, Helen L, MADDEN, Colm, DODDS, Annabel, CHANDLER, Kate E, BANKA, Siddharth, AU, Leon, CLAYTON-SMITH, Jill, KHAN, Naz, BIESECKER, Leslie G, WILSON, Meredith, ROHRBACH, Marianne, DALY, Sarah B, COLOMBI, Marina, GIUNTA, Cecilia, BLACK, Graeme C. M, MANSON, Forbes D. C, ZEEF, Leo A. H, URQUHART, Jill, ZOPPI, Nicoletta, BONSHEK, Richard, TOSOUNIDIS, Ioannis, MOHAN, Meyyammai

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Aortic tissue stiffness and tensile strength are correlated with density changes following proteolytic treatment von Gueldner, Pete H., Darvish, Cyrus J., Chickanosky, Isabelle K.M., Ahlgren, Emma E., Fortunato, Ronald, Chung, Timothy K., Rajagopal, Keshava, Benjamin, Chandler C., Maiti, Spandan, Rajagopal, Kumbakonam R., Vorp, David A.

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Health communication campaigns to drive demand for evidence-based practices and reduce stigma in the HEALing communities study von Lefebvre, R. Craig, Chandler, Redonna K., Helme, Donald W., Kerner, Robin, Mann, Sarah, Stein, Michael D., Reynolds, Jennifer, Slater, Michael D., Anakaraonye, Amarachi R., Beard, Dacia, Burrus, Olivia, Frkovich, Jenna, Hedrick, Haley, Lewis, Nicky, Rodgers, Emma

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Effects of fluoxetine on functional outcomes after acute stroke (FOCUS): a pragmatic, double-blind, randomised, controlled trial von Perry, David, Dinsmore, Lynn, Kambafwile, Mary, Idrovo, Luis, Hurley, Lisa, Kerwood, Lauriane, Merritt, Carley, Duty, Suzanna, Lindert, Ralf, Meegada, Madana, Maguire, Holly, Hiden, Joanne, Brodie, Fiona, Barcroft, Heather, Wightman, John, O Neill, Mark, Siddiqui, Amber, Rashmi, Sindhu, Wilson, Laura, Cullen, Claire, Keeling, Alison, Hindle, Julia, Maguire, Stuart, Hamid, Umair, Gaba, Waqar, Mohammed, Niaz, Robinson, Rianne, Mathieson, Philip, Jones, Val, Lush, Audrey, Bell, Jo, Badiani, Bhavna, Guo, Fenglin, Chamberlain, Angela, Donaldson, Dave, Melikyan, Elina, Oconnell, Susan, Hurdowar, Steve, Johnson, Matthew, Moore, Kimberley, Stevens, Angela, Burnip, Rachel, Beranova, Eva, Walker, Susannah, Cain, Rebecca, Willmot, Mark, Bates, Michelle, Pitt Ford, Alexandra, Aubrey, Beth, Howard, Joanne, Dhar, Saikat, Howard-Brown, Jennifer, Imam, Javed, Whitworth, Simon, Mcgee, Joanne, Hannon, Niamh, Mokoena, Langanani, Smart, Amanda, Donaldson, Fiona, Graham, Libby, Rowe, Joy, Munuswamy Vaiyapuri, Elangovan, Thomas, Lisa, Sharon, Storton, Jones, Paul, Johnston, Stuart, Pusalkar, Aparna, Broughton, David, Tryambake, Dinesh, Skotnicka, Agnieszka, Thompson, Jane, Annamalai, Arunkumar, Wilkinson, Peter, Young, Emma, Pereira, Rita, Drummond, Graham, Austin, Duncan, Funnell, Sarah, Jones, Stephanie, Vassallo, Joseph, Leonard, Dee, Wynter, Inez, Janbieh, Joumana, Wade, Lynne, Otter, Linda, Fleming, Amy, Jones, Rhian, Williams, Richard, Mavinamane, Sunanda, Hunt, Lorraine, Haque, Kashif, Gibson, Elspeth, Neves-Silva, Yara, Thompson, Alastair, Ritchings, Andrew, Mcredmond, Catherine, Goulding, Alicia, Punnoose, Sunil, Gordon, Laura, Tarkas, Tillana

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PD-L1 correlates with chemokines and cytokines in gingival crevicular fluid from healthy and diseased sites in subjects with periodontitis von Shelby, Andrew, Pendleton, Chandler, Thayer, Emma, Johnson, Georgia K, Xie, Xian Jin, Brogden, Kim A

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GABAA Alpha 2,3 Modulation Improves Select Phenotypes in a Mouse Model of Fragile X Syndrome von Schaefer, Tori L., Ashworth, Amy A., Tiwari, Durgesh, Tomasek, Madison P., Parkins, Emma V., White, Angela R., Snider, Andrew, Davenport, Matthew H., Grainger, Lindsay M., Becker, Robert A., Robinson, Chandler K., Mukherjee, Rishav, Williams, Michael T., Gibson, Jay R., Huber, Kimberly M., Gross, Christina, Erickson, Craig A.

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Emergence delirium in children: a randomized trial to compare total intravenous anesthesia with propofol and remifentanil to inhalational sevoflurane anesthesia von Chandler, John R., Myers, Dorothy, Mehta, Disha, Whyte, Emma, Groberman, Michelle K., Montgomery, Carolyne J., Ansermino, J. Mark

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A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3 von Koessler, Thibaud, Chandler, Ian, Buch, Stephan, Agúndez, Jose AG, Caldés, Trinidad, Howarth, Kimberley, Walther, Axel, Ladero, Jose M, Morreau, Hans, Giles, Graham G, Cazier, Jean-Baptiste, Castells, Antoni, Maher, Eamonn R, Wood, Wendy, Försti, Asta, Southey, Melissa C, Broderick, Peter, Hopper, John L, de la Hoya, Miguel, Webb, Emily, Wijnen, Juul T, Aaltonen, Lauri, Dunlop, Malcolm G, John, Ulrich, Fielding, Sarah, Barnetson, Rebecca A, Barclay, Ella, Martin, Lynn, Bishop, D Timothy, Tuupanen, Sari, Tenesa, Albert, Jaeger, Emma, Cheng, K K, Niittymäki, Iina, Karhu, Auli, Schreiber, Stefan, Peto, Julian, Völzke, Henry, Schafmayer, Clemens, Luk, J, Vodicka, Pavel, Vijayakrishnan, Jayaram, Carracedo, Angel, Houlston, Richard S, Tomlinson, Ian PM, Rowan, Andrew, Ruiz-Ponte, Clara, Ho, Judy WC, Kemp, Zoe, Lipton, Lara, Sullivan, Kate, Penegar, Steven, Prendergast, James GD, Carvajal-Carmona, Luis, Hampe, Jochen, Sham, Pak C, Kerr, David, Pharoah, Paul, Severi, Gianluca, Campbell, Harry, Pittman, Alan M, Gray, Richard, Castellví-Bel, Sergi, Spain, Sarah, Domingo, Enric, Hemminki, Kari, Lubbe, Steven, Thomas, Huw, van Wezel, Tom, Naccarati, Alessio, Gorman, Maggie, Lucassen, Anneke, Farrington, Susan M, Qureshi, Mobshra, Evans, D Gareth R

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A Randomized Trial Comparing Part-time Patching with Observation for Intermittent Exotropia in Children 12 to 35 Months of Age von Mohney, Brian G., MD, Cotter, Susan A., OD, MS, Chandler, Danielle L., MSPH, Holmes, Jonathan M., BM, BCh, Chen, Angela M., OD, MS, Melia, Michele, ScM, Donahue, Sean P., MD, PhD, Wallace, David K., MD, MPH, Kraker, Raymond T., MSPH, Christian, Melanie L., COA, Suh, Donny W., MD

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Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy von Abou Jamra, Rami, Accogli, Andrea, Amburgey, Kimberly, Basinger, Alice A., Ceulemans, Sophia, Charles, Perrine, McRae, Jeremy F., Rajan, Diana, Ambridge, Kirsty, Jones, Philip, Jones, Wendy D., Ahmed, Munaza, Anjum, Uruj, Armstrong, Ruth, Barnicoat, Angela, Bennett, Chris, Blair, Edward, Blyth, Moira, Bourdon, Louise, Brady, Angela, Burn, John, Canham, Natalie, Cilliers, Deirdre, Clayton-Smith, Jill, Coates, Andrea, Cooper, Nicola, Dabir, Tabib, Davies, Sally, Dean, John, Devlin, Gemma, Donnai, Dian, Donnelly, Carina, Evans, Karenza, Fendick, Tina, Goodship, Judith, Green, Andrew, Harrison, Lucy, Holden, Simon, Jarvis, Joanna, Johnson, Diana, Jones, Elizabeth, Kumar, V. K. Ajith, Lachlan, Katherine, Langman, Caroline, Maye, Una, McMullan, Dominic J., McWilliam, Catherine, Metcalfe, Kay, Norman, Andrew, Ogilvie, Caroline, Park, Soo-Mi, Phipps, Julie, Prescott, Katrina, Procter, Annie, Purnell, Hellen, Ross, Alison, Sampson, Julian, Shannon, Nora, Skitt, Zara, Stewart, Fiona, Stewart, Helen, Swaminathan, Ganesh Jawahar, Taylor, Cat, Tein, Mark, Treacy, Becky, Vandersteen, Anthony, Wallwark, Sarah, Waters, Jonathon, Weber, Astrid, Whiteford, Margo, Widaa, Sara, Wilcox, Sarah, Wilkinson, Emily, Parker, Michael, FitzPatrick, David R., Demurger, Florence, Eiset, Saga Elise, Ferrarini, Alessandra, Haack, Tobias B., Hashim, Mona, Jonasson, Amy R., Kok, Fernando, Marcelis, Carlo L.M., McWalter, Kirsty, Mercimek-Andrews, Saadet, Person, Richard, Ramelli, Gian Paolo, Rauch, Anita, Sanchez-Valle, Amarilis, Sattar, Shifteh, Saunders, Carol, Steindl, Katharina, Syrbe, Steffen, Taylor, Jenny C., Trauner, Doris A., Vogel, Ida, Widjaja, Elysa, Zak, Jaroslav, Banka, Siddharth, Rodan, Lance H.

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Elucidating the clinical spectrum and molecular basis of HYAL2 deficiency von Fasham, James, Lin, Siying, Ghosh, Promita, Radio, Francesca Clementina, Farrow, Emily G., Thiffault, Isabelle, Kussman, Jennifer, Zhou, Dihong, Hemming, Rick, Zahka, Kenneth, Chioza, Barry A., Rawlins, Lettie E., Wenger, Olivia K., Gunning, Adam C., Pizzi, Simone, Onesimo, Roberta, Zampino, Giuseppe, Barker, Emily, Osawa, Natasha, Rodriguez, Megan Christine, Neuhann, Teresa M., Zackai, Elaine H., Keena, Beth, Capasso, Jenina, Levin, Alex V., Bhoj, Elizabeth, Li, Dong, Hakonarson, Hakon, Wentzensen, Ingrid M., Jackson, Adam, Chandler, Kate E., Coban-Akdemir, Zeynep H., Posey, Jennifer E., Banka, Siddharth, Lupski, James R., Sheppard, Sarah E., Tartaglia, Marco, Triggs-Raine, Barbara, Crosby, Andrew H., Baple, Emma L.

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Bi-allelic Loss-of-Function CACNA1B Mutations in Progressive Epilepsy-Dyskinesia von Reich, Adi, Cross, J. Helen, Scheffer, Ingrid E., Krishnappa, Netravathi, Awada, Jana, Baralle, Diana, Bernhard, Birgitta, Clasper, Susan, Clayton-Smith, Jill, Cresswell, Lara, Donaldson, Alan, Ellis, Ian, Gaunt, Lorraine, He, Liu, Hewitt, Sarah, Hurst, Jane, Kirk, Claire, Kivuva, Emma, Kumar, Dhavendra, Mansour, Sahar, McCann, Emma, McKee, Shane, Mugalaasi, Hood, Murphy, Helen, Newbury-Ecob, Ruth, Pilz, Daniela T., Pollard, Martin, Pridham, Abigail, Saggar, Anand, Scott, Richard, Shearing, Emma, Smithson, Sarah, Sneddon, Linda, Suri, Mohnish, Tatton-Brown, Kate, Thomson, Jenny, Torokwa, Audrey, Varghese, Vinod, Yau, Michael, Artigas, Maria Soler, Boustred, Chris, Evans, David, Flicek, Paul, Hart, Deborah, Langford, Cordelia, Lawson, Daniel, Li, Rui, O'Donnovan, Michael, Parker, Victoria, Parr, Jeremy R., Paunio, Tiina, Rehnström, Karola, Sun, Jianping, Suvisaari, Jaana, Tachmazidou, Ionna, Williamson, Kathleen A., Wong, Kim, Alachkar, Hana, Ambegaonkar, Gautum, Attwood, Antony, Austin, Steve, Bennett, David, Bibi, Shahnaz, Bleda, Marta, Boggard, Harm, Bradley, John R., Browning, Michael, Clement, Emma, Doffinger, Rainer, Drewe, Elizabeth, Frary, Amy, Ghataorhe, Pavandeep K., Greenhalgh, Alan, Hackett, Scott, Hadinnapola, Charaka, Heemskerk, Johan W.M., Humbert, Marc, James, Roger, Krishnakumar, Deepa, Lawrie, Allan, Lentaigne, Claire, Maimaris, Jesmeen, Maw, Anna, Megy, Karyn, Moledina, Shahin, Morrell, Nicholas, Nejentsev, Sergey, Polwarth, Gary, Quinti, Isabella, Raymond, F. Lucy, Samarghitean, Crina, Sanchis-Juan, Alba, Southgate, Laura, Stauss, Hans, Thrasher, Adrian, Trembath, Richard, Turro, Ernest, Williamson, Catherine, Yeatman, Nigel, Millichap, John J.

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Mutations in the PP2A regulatory subunit B family genes PPP2R5B, PPP2R5C and PPP2R5D cause human overgrowth von Loveday, Chey, Tatton-Brown, Katrina, Clarke, Matthew, Westwood, Isaac, Renwick, Anthony, Ramsay, Emma, Nemeth, Andrea, Campbell, Jennifer, Joss, Shelagh, Gardner, McKinlay, Zachariou, Anna, Elliott, Anna, Ruark, Elise, van Montfort, Rob, Rahman, Nazneen

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Targeted methylation testing of a patient cohort broadens the epigenetic and clinical description of imprinting disorders von Poole, Rebecca L., Docherty, Louise E., Al Sayegh, Abeer, Caliebe, Almuth, Turner, Claire, Baple, Emma, Wakeling, Emma, Harrison, Lucy, Lehmann, Anna, Temple, I. Karen, Mackay, Deborah J.G.

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The Lancet Commission on self-harm von Moran, Paul, Chandler, Amy, Dudgeon, Pat, Kirtley, Olivia J, Knipe, Duleeka, Pirkis, Jane, Sinyor, Mark, Allister, Rosie, Ansloos, Jeffrey, Ball, Melanie A, Chan, Lai Fong, Darwin, Leilani, Derry, Kate L, Hawton, Keith, Heney, Veronica, Hetrick, Sarah, Li, Ang, Machado, Daiane B, McAllister, Emma, McDaid, David, Mehra, Ishita, Niederkrotenthaler, Thomas, Nock, Matthew K, O'Keefe, Victoria M, Oquendo, Maria A, Osafo, Joseph, Patel, Vikram, Pathare, Soumitra, Peltier, Shanna, Roberts, Tessa, Robinson, Jo, Shand, Fiona, Stirling, Fiona, Stoor, Jon P A, Swingler, Natasha, Turecki, Gustavo, Venkatesh, Svetha, Waitoki, Waikaremoana, Wright, Michael, Yip, Paul S F, Spoelma, Michael J, Kapur, Navneet, O'Connor, Rory C, Christensen, Helen

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Paternal retraction of a fragile X allele to normal size, showing normal function over two generations von Bartlett, Essra, Archibald, Alison D., Francis, David, Ling, Ling, Thomas, Rob, Chandler, Gabrielle, Ward, Lisa, O'Farrell, Gemma, Pandelache, Alison, Delatycki, Martin B., Bennetts, Bruce H., Ho, Gladys, Fisk, Katrina, Baker, Emma K., Amor, David J., Godler, David E.

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The Lancet Commission on self-harm von Moran, Paul, Chandler, Amy, Dudgeon, Pat, Kirtley, Olivia J, Knipe, Duleeka, Pirkis, Jane, Sinyor, Mark, Allister, Rosie, Ansloos, Jeffrey, Ball, Melanie A, Chan, Lai Fong, Darwin, Leilani, Derry, Kate L, Hawton, Keith, Heney, Veronica, Hetrick, Sarah, Li, Ang, Machado, Daiane B, Mcallister, Emma, Mcdaid, David, Mehra, Ishita, Niederkrotenthaler, Thomas, Nock, Matthew K, O'Keefe, Victoria M, Oquendo, Maria A, Osafo, Joseph, Patel, Vikram, Pathare, Soumitra, Peltier, Shanna, Roberts, Tessa, Robinson, Jo, Shand, Fiona, Stirling, Fiona, Stoor, Jon P.A, Swingler, Natasha, Turecki, Gustavo, Venkatesh, Svetha, Waitoki, Waikaremoana, Wright, Michael, Yip, Paul S.F, Spoelma, Michael J, Kapur, Navneet, O'Connor, Rory C, Christensen, Helen

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Germline mutations in the oncogene EZH2 cause Weaver syndrome and increased human height von Tatton-Brown, Katrina, Hanks, Sandra, Ruark, Elise, Zachariou, Anna, Duarte, Silvana Del Vecchio, Ramsay, Emma, Snape, Katie, Murray, Anne, Perdeaux, Elizabeth R, Seal, Sheila, Loveday, Chey, Banka, Siddharth, Clericuzio, Carol, Flinter, Frances, Magee, Alex, McConnell, Vivienne, Patton, Michael, Raith, Wolfgang, Rankin, Julia, Splitt, Miranda, Strenger, Volker, Taylor, Clare, Wheeler, Patricia, Temple, Karen I, Cole, Trevor, Douglas, Jenny, Rahman, Nazneen

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