Extreme reconfiguration of plastid genomes in the angiosperm family Geraniaceae: rearrangements, repeats, and codon usage von Guisinger, Mary M, Kuehl, Jennifer V, Boore, Jeffrey L, Jansen, Robert K

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Dynamic queuosine changes in tRNA couple nutrient levels to codon choice in Trypanosoma brucei von Dixit, Sameer, Kessler, Alan C, Henderson, Jeremy, Pan, Xiaobei, Zhao, Ruoxia, D’Almeida, Gabriel Silveira, Kulkarni, Sneha, Rubio, Mary Anne T, Hegedűsová, Eva, Ross, Robert L, Limbach, Patrick A, Green, Brian D, Paris, Zdeněk, Alfonzo, Juan D

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A paradoxical genotype-phenotype relationship: Low level of GOSR2 translation from a non-AUG start codon in a family with profound hearing loss von Aburayyan, Amal, Carlson, Ryan J, Rabie, Grace N, Lee, Ming K, Gulsuner, Suleyman, Walsh, Tom, Avraham, Karen B, Kanaan, Moien N, King, Mary-Claire

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Association of p53 codon 72 polymorphism with weight and metabolic diseases in a Central Indian population von Abraham, Jessy, Mahapatra, Deepak, Agrawal, Pratishtha, James, Mary Jovita

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Platelet-Derived Codon-Optimized Hyperfunctional FIX Gene Therapy of Hemophilia B Mice von Schroeder, Jocelyn A., Jozwiak, Mary A., Monahan, Paul E., Shi, Qizhen

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LATE BREAKING NEWS E-POSTER PRESENTATION: LBP 11 Congenital Muscular Dystrophy Type 1D (α-Dystroglycanopathy) in a Family of Labrador Retrievers with a Stop Codon Mutation in LARGE1 Gene von Shelton, G. Diane, Minor, Kate M., Guo, Ling T., Friedenberg, Steven G., Cullen, Jonah N., Hord, Jeffrey M., Venzke, David, Anderson, Mary E., Devereaux, Megan, Handelman, Caryl, Campbell, Kevin P., Mickelson, James R.

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BRCA2 Polymorphic Stop Codon K3326X and the Risk of Breast, Prostate, and Ovarian Cancers von Barrowdale, Daniel, Nathanson, Katherine L, Liang, Dong, Hildebrant, Michelle AT, Modugno, Francesmary, Thompson, Pamela J, Hahnen, Eric, Nevanlinna, Heli, Buys, Saundra S, Bogdanova, Natalia V, Dörk, Thilo, Margolin, Sara, Mannermaa, Arto, Hopper, John L, Neven, Patrick, Claes, Kathleen BM, VanMaerken, Tom, Chang-Claude, Jenny, Flesch-Janys, Dieter, Heitz, Florian, Radice, Paolo, Southey, Melissa C, Viel, Alessandra, Manoukian, Siranoush, Peixoto, Ana, Hallberg, Emily, Olson, Janet E, Shimelis, Hermela, Milne, Roger L, James, Paul A, Goldberg, Mark S, Eccles, Diana M, Pylkäs, Katri, va nder Ouweland, Ans MW, Winqvist, Robert, Greene, Mark H, Broeks, Annegien, Czene, Kamila, McNeish, Iain, Siddiquil, Nadeem, Kwong, Ava, Park, Sue K, Teo, Soo Hwang, Matsuo, Keitaro, Schmidt, Marjanka K, etova, Lenka, Rappaport-Feurhauser, Christine, Laitman, Yael, Koppert, Linetta B, Kiemeney, Lambertus A, Massuger, Leon FAG, Cook, Linda S, Beckman, Matthias W, Pejovic, Tanja, Rossing, Mary Anne, Wentzensen, Nicolas, Cross, Simon S, Fasching, Peter A, Shah, Mitul, Torres, Diana, Jakubowska, Anna, Gronwald, Jacek, Slager, Susan, Antoniou, Antonis C, Berchuck, Andrew, Dunning, Alison M, Easton, Douglas F, Couch, Fergus J, Riboli, Elio, Menon, Usha, Hamann, Ute, Rudolph, Anja, Tworoger, Shelley S, vanRensburg, Elizabeth J, Truong, Thérèse, Stoppa-Lyonnet, Dominique, Damiola, Francesca, Sinilnikova, Olga M, Gerdes, Anne-Marie, Hansen, Thomas VO, Kjaer, Susanne K, Hogdall, Claus, Hogdall, Estrid, Pedersen, Inge Sokilde, González-Neira, Anna, Osorio, Ana, Anton-Culver, Hoda, Eunjung, Lee, Neuhausen, Susan L, Karlan, Beth Y, Wu, Anna, Gayther, Simon, Ramus, Susan J, Whittermore, Alice S, Phelan, Catherine M, Offit, Kenneth, Robson, Mark, Cannioto, Rikki, Olson, Sara H, Daly, Mary B

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A Premature Stop Codon in RAF1 Is the Priority Candidate Causative Mutation of the Inherited Chicken Wingless-2 Developmental Syndrome von Youngworth, Ingrid, Delany, Mary E

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C to U editing of the anticodon of imported mitochondrial tRNA(Trp) allows decoding of the UGA stop codon in Leishmania tarentolae von Alfonzo, J D, Blanc, V, Estévez, A M, Rubio, M A, Simpson, L

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Adaptor protein-2 sigma subunit mutations causing familial hypocalciuric hypercalcaemia type 3 (FHH3) demonstrate genotype-phenotype correlations, codon bias and dominant-negative effects von Hannan, Fadil M, Howles, Sarah A, Rogers, Angela, Cranston, Treena, Gorvin, Caroline M, Babinsky, Valerie N, Reed, Anita A, Thakker, Clare E, Bockenhauer, Detlef, Brown, Rosalind S, Connell, John M, Cook, Jacqueline, Darzy, Ken, Ehtisham, Sarah, Graham, Una, Hulse, Tony, Hunter, Steven J, Izatt, Louise, Kumar, Dhavendra, McKenna, Malachi J, McKnight, John A, Morrison, Patrick J, Mughal, M Zulf, O'Halloran, Domhnall, Pearce, Simon H, Porteous, Mary E, Rahman, Mushtaqur, Richardson, Tristan, Robinson, Robert, Scheers, Isabelle, Siddique, Haroon, Van't Hoff, William G, Wang, Timothy, Whyte, Michael P, Nesbit, M Andrew, Thakker, Rajesh V

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Codon usage in plant genes von MURRAY, E. E, LOTZER, J, EBERLE, M

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A Selection of Macrocyclic Peptides That Bind STING From an mRNA‐Display Library With Split Degenerate Codons von Lin, Chi‐Wang, Harner, Mary J., Douglas, Andrew E., Lafont, Virginie, Yu, Fei, Lee, Ving G., Poss, Michael A., Swain, Joanna F., Wright, Martin, Lipovšek, Daša

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Pathogenic missense variants altering codon 336 of GARS1 lead to divergent dominant phenotypes von Meyer, Alayne P., Forrest, Megan E., Nicolau, Stefan, Wiszniewski, Wojciech, Bland, Mary Pat, Tsao, Chang‐Yong, Antonellis, Anthony, Abreu, Nicolas J.

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Novel premature termination codon in the FOXP3 gene as the cause of familial hydrops fetalis in males von Goodhue, Brighton, Smith, MaryLou, Bennett, Kelly, Grace, Matthew

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HER2 codon 655 polymorphism and breast cancer : results from kin-cohort and case- control analyses von MILLIKAN, Robert C, HUMMER, Amanda J, WOLFF, Mary S, HISHIDA, Asahi, BEGG, Colin B

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In Arabidopsis thaliana codon volatility scores reflect GC3 composition rather than selective pressure von O'Connell, Mary J, Doyle, Aisling M, Juenger, Thomas E, Donoghue, Mark T A, Keshavaiah, Channa, Tuteja, Reetu, Spillane, Charles

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A Simple Combinatorial Codon Mutagenesis Method for Targeted Protein Engineering von Belsare, Ketaki D, Andorfer, Mary C, Cardenas, Frida S, Chael, Julia R, Park, Hyun June, Lewis, Jared C

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Frontispiece: A Selection of Macrocyclic Peptides That Bind STING From an mRNA‐Display Library With Split Degenerate Codons von Lin, Chi‐Wang, Harner, Mary J., Douglas, Andrew E., Lafont, Virginie, Yu, Fei, Lee, Ving G., Poss, Michael A., Swain, Joanna F., Wright, Martin, Lipovšek, Daša

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Interaction of Hb South Florida (codon 1; GTG1ATG) and HbE, with b-thalassemia (IVS1-1; G1A): expression of different clinical phenotypes von Tan, Jin-Ai Mary Anne, Tan, Kim-Lian, Omar, Khairul Zaman, Chan, Lee-Lee, Wee, Yong-Chui, George, Elizabeth

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Correlation between the development of extracolonic manifestations in FAP patients and mutations beyond codon 1403 in the APC gene von Dobbie, Z, Spycher, M, Mary, J L, Häner, M, Guldenschuh, I, Hürliman, R, Amman, R, Roth, J, Müller, H, Scott, R J

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