Zobrazeno 1 - 10
of 155
pro vyhledávání: '"David T Miller"'
Autor:
Charles Hager, David T. Miller
Winner, ISHS Best of Illinois History Award, 2019 In this riveting true story of coming of age in the Chicago Mob, Charles “Charley” Hager is plucked from his rural West Virginia home by an uncle in the 1960s and thrown into an underworld of mone
Autor:
David T. Miller
In a period of budget austerity, prioritization becomes especially important for defense policymakers. In order to determine such priorities, it is first necessary to consider the nature of conflict and missions the U.S. military may face in the futu
Autor:
Ilaria Mannucci, Nghi D. P. Dang, Hannes Huber, Jaclyn B. Murry, Jeff Abramson, Thorsten Althoff, Siddharth Banka, Gareth Baynam, David Bearden, Ana Beleza-Meireles, Paul J. Benke, Siren Berland, Tatjana Bierhals, Frederic Bilan, Laurence A. Bindoff, Geir Julius Braathen, Øyvind L. Busk, Jirat Chenbhanich, Jonas Denecke, Luis F. Escobar, Caroline Estes, Julie Fleischer, Daniel Groepper, Charlotte A. Haaxma, Maja Hempel, Yolanda Holler-Managan, Gunnar Houge, Adam Jackson, Laura Kellogg, Boris Keren, Catherine Kiraly-Borri, Cornelia Kraus, Christian Kubisch, Gwenael Le Guyader, Ulf W. Ljungblad, Leslie Manace Brenman, Julian A. Martinez-Agosto, Matthew Might, David T. Miller, Kelly Q. Minks, Billur Moghaddam, Caroline Nava, Stanley F. Nelson, John M. Parant, Trine Prescott, Farrah Rajabi, Hanitra Randrianaivo, Simone F. Reiter, Janneke Schuurs-Hoeijmakers, Perry B. Shieh, Anne Slavotinek, Sarah Smithson, Alexander P. A. Stegmann, Kinga Tomczak, Kristian Tveten, Jun Wang, Jordan H. Whitlock, Christiane Zweier, Kirsty McWalter, Jane Juusola, Fabiola Quintero-Rivera, Utz Fischer, Nan Cher Yeo, Hans-Jürgen Kreienkamp, Davor Lessel
Publikováno v:
Genome Medicine, Vol 13, Iss 1, Pp 1-19 (2021)
Abstract Background We aimed to define the clinical and variant spectrum and to provide novel molecular insights into the DHX30-associated neurodevelopmental disorder. Methods Clinical and genetic data from affected individuals were collected through
Externí odkaz:
https://doaj.org/article/c447334b912746929ee920eb4139f48f
Autor:
David T. Miller, Michelle J. Semins
Publikováno v:
Frontiers in Surgery, Vol 8 (2021)
It is known that urologic surgeons are at risk of work-place injury due to the physical requirements of operating and exposure to hazards. These hazards include radiation, exposure to body fluids, use of laser energy, and orthopedic injury due to the
Externí odkaz:
https://doaj.org/article/5d888c42c2094646bfed49c5ec8e6728
Autor:
Isidro, Cortes-Ciriano, Christopher D, Steele, Katherine, Piculell, Alyaa, Al-Ibraheemi, Vanessa, Eulo, Marilyn M, Bui, Aikaterini, Chatzipli, Brendan C, Dickson, Dana C, Borcherding, Andrew, Feber, Alon, Galor, Jesse, Hart, Kevin B, Jones, Justin T, Jordan, Raymond H, Kim, Daniel, Lindsay, Colin, Miller, Yoshihiro, Nishida, Paula Z, Proszek, Jonathan, Serrano, R Taylor, Sundby, Jeffrey J, Szymanski, Nicole J, Ullrich, David, Viskochil, Xia, Wang, Matija, Snuderl, Peter J, Park, Adrienne M, Flanagan, Angela C, Hirbe, Nischalan, Pillay, David T, Miller
Publikováno v:
Cancer Discovery. 13:654-671
Malignant peripheral nerve sheath tumor (MPNST), an aggressive soft-tissue sarcoma, occurs in people with neurofibromatosis type 1 (NF1) and sporadically. Whole-genome and multiregional exome sequencing, transcriptomic, and methylation profiling of 9
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af47f0e457c5aa96b953dcac0b29aac9
https://doi.org/10.1158/2159-8290.cd-22-0786
https://doi.org/10.1158/2159-8290.cd-22-0786
Autor:
Erin Rooney Riggs, Taylor I. Bingaman, Carrie-Ann Barry, Andrea Behlmann, Krista Bluske, Bret Bostwick, Alison Bright, Chun-An Chen, Amanda R. Clause, Avinash V. Dharmadhikari, Mythily Ganapathi, Claudia Gonzaga-Jauregui, Andrew R. Grant, Madeline Y. Hughes, Se Rin Kim, Amanda Krause, Jun Liao, Aimé Lumaka, Michelle Mah, Caitlin M. Maloney, Shruthi Mohan, Ikeoluwa A. Osei-Owusu, Emma Reble, Olivia Rennie, Juliann M. Savatt, Hermela Shimelis, Rebecca K. Siegert, Tam P. Sneddon, Courtney Thaxton, Kelly A. Toner, Kien Trung Tran, Ryan Webb, Emma H. Wilcox, Jiani Yin, Xinming Zhuo, Masa Znidarsic, Christa Lese Martin, Catalina Betancur, Jacob A.S. Vorstman, David T. Miller, Christian P. Schaaf
Publikováno v:
Genetics in Medicine
Genetics in Medicine, 2022, 24 (9), pp.1899-1908. ⟨10.1016/j.gim.2022.05.001⟩
Genetics in Medicine, 2022, 24 (9), pp.1899-1908. ⟨10.1016/j.gim.2022.05.001⟩
International audience; Purpose: Neurodevelopmental disorders (NDDs), such as intellectual disability (ID) and autism spectrum disorder (ASD), exhibit genetic and phenotypic heterogeneity, making them difficult to differentiate without a molecular di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b07ead00b13dfac939c5dc9322d918b8
https://doi.org/10.1016/j.gim.2022.05.001
https://doi.org/10.1016/j.gim.2022.05.001
Autor:
Jillian L, Chen, David T, Miller, Laura S, Schmidt, David, Malkin, Bruce R, Korf, Charis, Eng, David J, Kwiatkowski, Krinio, Giannikou
Publikováno v:
Annual Review of Genomics and Human Genetics. 23:331-361
A mosaic state arises when pathogenic variants are acquired in certain cell lineages during postzygotic development, and mosaic individuals may present with a generalized or localized phenotype. Here, we review the current state of knowledge regardin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::77a03daf094c624cc84e692d2729f8d7
https://doi.org/10.1146/annurev-genom-120121-105450
https://doi.org/10.1146/annurev-genom-120121-105450
Autor:
David T. Miller, Nischalan Pillay, Angela C. Hirbe, Adrienne M. Flanagan, Peter J. Park, Matija Snuderl, Xia Wang, David Viskochil, Nicole J. Ullrich, Jeffrey J. Szymanski, R. Taylor Sundby, Jonathan Serrano, Paula Z. Proszek, Yoshihiro Nishida, Colin Miller, Daniel Lindsay, Raymond H. Kim, Justin T. Jordan, Kevin B. Jones, Jesse Hart, Alon Galor, Andrew Feber, Dana C. Borcherding, Brendan C. Dickson, Aikaterini Chatzipli, Marilyn M. Bui, Vanessa Eulo, Alyaa Al-Ibraheemi, Katherine Piculell, Christopher D. Steele, Isidro Cortes-Ciriano
Supplementary figures provide additional details on the genomic landscape of MPNST and interesting cases within the cohort.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::161b5a8bac5dc55c121b8f13371bedb4
https://doi.org/10.1158/2159-8290.22542121
https://doi.org/10.1158/2159-8290.22542121
Autor:
David T. Miller, Nischalan Pillay, Angela C. Hirbe, Adrienne M. Flanagan, Peter J. Park, Matija Snuderl, Xia Wang, David Viskochil, Nicole J. Ullrich, Jeffrey J. Szymanski, R. Taylor Sundby, Jonathan Serrano, Paula Z. Proszek, Yoshihiro Nishida, Colin Miller, Daniel Lindsay, Raymond H. Kim, Justin T. Jordan, Kevin B. Jones, Jesse Hart, Alon Galor, Andrew Feber, Dana C. Borcherding, Brendan C. Dickson, Aikaterini Chatzipli, Marilyn M. Bui, Vanessa Eulo, Alyaa Al-Ibraheemi, Katherine Piculell, Christopher D. Steele, Isidro Cortes-Ciriano
Supplementary Table 1 includes the metadata on all subjects, including basic demographics and medical history. Supplementary Table 2 provides statistics on chrom 8 gene expression among tumors with H3K27me3 loss. Note: no changes have been made to th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15deb6bdcb75389ac6ff3546033511c4
https://doi.org/10.1158/2159-8290.22542118.v1
https://doi.org/10.1158/2159-8290.22542118.v1
Autor:
David T. Miller, Nischalan Pillay, Angela C. Hirbe, Adrienne M. Flanagan, Peter J. Park, Matija Snuderl, Xia Wang, David Viskochil, Nicole J. Ullrich, Jeffrey J. Szymanski, R. Taylor Sundby, Jonathan Serrano, Paula Z. Proszek, Yoshihiro Nishida, Colin Miller, Daniel Lindsay, Raymond H. Kim, Justin T. Jordan, Kevin B. Jones, Jesse Hart, Alon Galor, Andrew Feber, Dana C. Borcherding, Brendan C. Dickson, Aikaterini Chatzipli, Marilyn M. Bui, Vanessa Eulo, Alyaa Al-Ibraheemi, Katherine Piculell, Christopher D. Steele, Isidro Cortes-Ciriano
Malignant peripheral nerve sheath tumor (MPNST), an aggressive soft-tissue sarcoma, occurs in people with neurofibromatosis type 1 (NF1) and sporadically. Whole-genome and multiregional exome sequencing, transcriptomic, and methylation profiling of 9
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ae70edd78830fc820d4ca5d1771d9b86
https://doi.org/10.1158/2159-8290.c.6549805.v1
https://doi.org/10.1158/2159-8290.c.6549805.v1