Inhibition of metastatic tumor growth in nude mice by portal vein infusions of matrix-targeted retroviral vectors bearing a cytocidal cyclin G1 construct von GORDON, E. M, PENG XUAN LIU, ZHEN HAI CHEN, LING LIU, WHITLEY, M. D, GEE, C, GROSHEN, S, HINTON, D. B, BEART, R. W, HALL, F. L

Volltext

Visit-level Acuity and Resource-based Relative Value Unit Utilization in a Pediatric Emergency Department von Pershad, Jay, Whitley, Michelle, Herman, Martin

Volltext

Systemic administration of a matrix-targeted retroviral vector is efficacious for cancer gene therapy in mice von GORDON, Erlinda M, ZHEN HAI CHEN, HALL, Frederick L, LING LIU, WHITLEY, Michelle, LIQIONG LIU, WEI, Denice, GROSHEN, Susan, HINTON, David R, ANDERSON, W. French, BEART, Robert W

Volltext

There are two mechanisms of achiasmate segregation in Drosophila females, one of which requires heterochromatic homology von Hawley, R.S. (University of California, Davis), Irick, H, Zitron, A.E, Haddox, D.A, Lohe, A, New, C, Whitley, M.D, Arbel, T, Jang, J, McKim, K

Volltext

Genomic diagnosis for children with intellectual disability and/or developmental delay von Bowling, Kevin M, Thompson, Michelle L, Amaral, Michelle D, Finnila, Candice R, Hiatt, Susan M, Engel, Krysta L, Cochran, J Nicholas, Brothers, Kyle B, East, Kelly M, Gray, David E, Kelley, Whitley V, Lamb, Neil E, Lose, Edward J, Rich, Carla A, Simmons, Shirley, Whittle, Jana S, Weaver, Benjamin T, Nesmith, Amy S, Myers, Richard M, Barsh, Gregory S, Bebin, E Martina, Cooper, Gregory M

Volltext

Family Influence in Recovery from Severe Mental Illness von Aldersey, Heather Michelle, Whitley, Rob

Volltext

Characterization of two related Erwinia myoviruses that are distant relatives of the PhiKZ-like Jumbo phages von Arens, Daniel K, Brady, T Scott, Carter, John L, Pape, Jenny A, Robinson, David M, Russell, Kerri A, Staley, Lyndsay A, Stettler, Jason M, Tateoka, Olivia B, Townsend, Michelle H, Whitley, Kiara V, Wienclaw, Trevor M, Williamson, Taryn L, Johnson, Steven M, Grose, Julianne H

Volltext

When in the lifecourse? Socioeconomic position across the lifecourse and biological health score von Whitley, Elise, Benzeval, Michaela, Kelly-Irving, Michelle, Kumari, Meena

Volltext

Genome sequencing as a first-line diagnostic test for hospitalized infants von Bowling, Kevin M., Thompson, Michelle L., Finnila, Candice R., Hiatt, Susan M., Latner, Donald R., Amaral, Michelle D., Lawlor, James M.J., East, Kelly M., Cochran, Meagan E., Greve, Veronica, Kelley, Whitley V., Gray, David E., Felker, Stephanie A., Meddaugh, Hannah, Cannon, Ashley, Luedecke, Amanda, Jackson, Kelly E., Hendon, Laura G., Janani, Hillary M., Johnston, Marla, Merin, Lee Ann, Deans, Sarah L., Tuura, Carly, Williams, Heather, Laborde, Kelly, Neu, Matthew B., Patrick-Esteve, Jessica, Hurst, Anna C.E., Kandasamy, Jegen, Carlo, Wally, Brothers, Kyle B., Kirmse, Brian M., Savich, Renate, Superneau, Duane, Spedale, Steven B., Knight, Sara J., Barsh, Gregory S., Korf, Bruce R., Cooper, Gregory M.

Volltext

Gradient of Developmental and Injury Response transcriptional states defines functional vulnerabilities underpinning glioblastoma heterogeneity von Richards, Laura M, Whitley, Owen K N, MacLeod, Graham, Cavalli, Florence M G, Coutinho, Fiona J, Jaramillo, Julia E, Svergun, Nataliia, Riverin, Mazdak, Croucher, Danielle C, Kushida, Michelle, Yu, Kenny, Guilhamon, Paul, Rastegar, Naghmeh, Ahmadi, Moloud, Bhatti, Jasmine K, Bozek, Danielle A, Li, Naijin, Lee, Lilian, Che, Clare, Luis, Erika, Park, Nicole I, Xu, Zhiyu, Ketela, Troy, Moore, Richard A, Marra, Marco A, Spears, Julian, Cusimano, Michael D, Das, Sunit, Bernstein, Mark, Haibe-Kains, Benjamin, Lupien, Mathieu, Luchman, H Artee, Weiss, Samuel, Angers, Stephane, Dirks, Peter B, Bader, Gary D, Pugh, Trevor J

Volltext

Wnt activation as a therapeutic strategy in medulloblastoma von Manoranjan, Branavan, Venugopal, Chitra, Bakhshinyan, David, Adile, Ashley A., Richards, Laura, Kameda-Smith, Michelle M., Whitley, Owen, Dvorkin-Gheva, Anna, Subapanditha, Minomi, Savage, Neil, Tatari, Nazanin, McKenna, Dillon, Bassey-Archibong, Blessing, Winegarden, Neil, Hallett, Robin, Provias, John P., Yarascavitch, Blake, Ajani, Olufemi, Fleming, Adam, Bader, Gary D., Pugh, Trevor J., Doble, Bradley W., Singh, Sheila K.

Volltext

De novo variants in CNOT9 cause a neurodevelopmental disorder with or without epilepsy von von Wintzingerode, Lydia, Ben-Zeev, Bruria, Cesario, Claudia, Chan, Katie M., Depienne, Christel, Elpeleg, Orly, Iascone, Maria, Kelley, Whitley V., Nassogne, Marie-Cécile, Niceta, Marcello, Pezzani, Lidia, Rahner, Nils, Revencu, Nicole, Bekheirnia, Mir Reza, Santiago-Sim, Teresa, Tartaglia, Marco, Thompson, Michelle L., Trivisano, Marina, Hentschel, Julia, Sticht, Heinrich, Abou Jamra, Rami, Oppermann, Henry

Volltext

Open versus Endovascular Repair of Abdominal Aortic Aneurysm von Lederle, Frank A, Kyriakides, Tassos C, Stroupe, Kevin T, Freischlag, Julie A, Padberg, Frank T, Matsumura, Jon S, Huo, Zhiping, Johnson, Gary R

Volltext

Dose-Dependent Prevention of Metabolic and Neurologic Disease in Murine MPS II by ZFN-Mediated In Vivo Genome Editing von Laoharawee, Kanut, DeKelver, Russell C., Podetz-Pedersen, Kelly M., Rohde, Michelle, Sproul, Scott, Nguyen, Hoang-Oanh, Nguyen, Tam, St. Martin, Susan J., Ou, Li, Tom, Susan, Radeke, Robert, Meyer, Kathleen E., Holmes, Michael C., Whitley, Chester B., Wechsler, Thomas, McIvor, R. Scott

Volltext

The Effect of Bariatric Surgery on Post-Operative Outcomes After Hysterectomy [6D] von Whitley, Julia, Voltzke, Kristin, Louie, Michelle Yee

Volltext

Poison exon annotations improve the yield of clinically relevant variants in genomic diagnostic testing von Felker, Stephanie A., Lawlor, James M.J., Hiatt, Susan M., Thompson, Michelle L., Latner, Donald R., Finnila, Candice R., Bowling, Kevin M., Bonnstetter, Zachary T., Bonini, Katherine E., Kelly, Nicole R., Kelley, Whitley V., Hurst, Anna C.E., Rashid, Salman, Kelly, Melissa A., Nakouzi, Ghunwa, Hendon, Laura G., Bebin, E. Martina, Kenny, Eimear E., Cooper, Gregory M.

Volltext

Long‐term trajectories of self‐reported cognitive function in a cohort of older survivors of breast cancer: CALGB 369901 (Alliance) von Mandelblatt, Jeanne S., Clapp, Jonathan D., Luta, Gheorghe, Faul, Leigh Anne, Tallarico, Michelle D., McClendon, Trina D., Whitley, Jessica A., Cai, Ling, Ahles, Tim A., Stern, Robert A., Jacobsen, Paul B., Small, Brent J., Pitcher, Brandelyn N., Dura‐Fernandis, Estrella, Muss, Hyman B., Hurria, Arti, Cohen, Harvey J., Isaacs, Claudine

Volltext

MARK2 variants cause autism spectrum disorder via the downregulation of WNT/β-catenin signaling pathway von Gong, Maolei, Li, Jiayi, Qin, Zailong, Machado Bressan Wilke, Matheus Vernet, Liu, Yijun, Li, Qian, Liu, Haoran, Liang, Chen, Morales-Rosado, Joel A., Cohen, Ana S.A., Hughes, Susan S., Sullivan, Bonnie R., Waddell, Valerie, van den Boogaard, Marie-José H., van Jaarsveld, Richard H., van Binsbergen, Ellen, van Gassen, Koen L., Wang, Tianyun, Hiatt, Susan M., Amaral, Michelle D., Kelley, Whitley V., Zhao, Jianbo, Feng, Weixing, Ren, Changhong, Yu, Yazhen, Boczek, Nicole J., Ferber, Matthew J., Lahner, Carrie, Elliott, Sherr, Ruan, Yiyan, Mignot, Cyril, Keren, Boris, Xie, Hua, Wang, Xiaoyan, Popp, Bernt, Zweier, Christiane, Piard, Juliette, Coubes, Christine, Mau-Them, Frederic Tran, Safraou, Hana, Innes, A. Micheil, Gauthier, Julie, Michaud, Jacques L., Koboldt, Daniel C., Sylvie, Odent, Willems, Marjolaine, Tan, Wen-Hann, Cogne, Benjamin, Rieubland, Claudine, Braun, Dominique, McLean, Scott Douglas, Platzer, Konrad, Zacher, Pia, Oppermann, Henry, Evenepoel, Lucie, Blanc, Pierre, El Khattabi, Laïla, Haque, Neshatul, Dsouza, Nikita R., Zimmermann, Michael T., Urrutia, Raul, Klee, Eric W., Shen, Yiping, Du, Hongzhen, Rappaport, Leonard, Liu, Chang-Mei, Chen, Xiaoli

Volltext

Genomic sequencing identifies secondary findings in a cohort of parent study participants von Thompson, Michelle L., Finnila, Candice R., Bowling, Kevin M., Brothers, Kyle B., Neu, Matthew B., Amaral, Michelle D., Hiatt, Susan M., East, Kelly M., Gray, David E., Lawlor, James M.J., Kelley, Whitley V., Lose, Edward J., Rich, Carla A., Simmons, Shirley, Levy, Shawn E., Myers, Richard M., Barsh, Gregory S., Bebin, E Martina, Cooper, Gregory M.

Volltext

Identifying rare, medically relevant variation via population-based genomic screening in Alabama: opportunities and pitfalls von Bowling, Kevin M., Thompson, Michelle L., Gray, David E., Lawlor, James M. J., Williams, Kelly, East, Kelly M., Kelley, Whitley V., Moss, Irene P., Absher, Devin M., Partridge, E. Christopher, Hurst, Anna C. E., Edberg, Jeffrey C., Barsh, Gregory S., Korf, Bruce R., Cooper, Gregory M.

Volltext