Zobrazeno 1 - 10
of 53
pro vyhledávání: '"Nicholas T Potter"'
Autor:
David A Johnson, Robert L Barclay, Klaus Mergener, Gunter Weiss, Thomas König, Jürgen Beck, Nicholas T Potter
Publikováno v:
PLoS ONE, Vol 9, Iss 6, p e98238 (2014)
BACKGROUND:Screening improves outcomes related to colorectal cancer (CRC); however, suboptimal participation for available screening tests limits the full benefits of screening. Non-invasive screening using a blood based assay may potentially help re
Externí odkaz:
https://doaj.org/article/e0da240968644dea9a7e7722de6e05aa
Autor:
Klaus Mergener, Nicholas T. Potter
Publikováno v:
JAMA. 316(16)
Autor:
Hrishikesh M. Rao, Nicholas T. Potter, Lawrence G. Appelbaum, David J. Zielinski, Regis Kopper
Publikováno v:
VR
Here we explore a visual display technique for low frame rate virtual environments called low persistence (LP). This involves displaying the rendered frame for a single display frame and blanking the screen while waiting for the next frame to be gene
Autor:
Elayna Kirsch, Marc A. Sommer, Jillian M. Clements, Regis Kopper, Lawrence G. Appelbaum, Hrishikesh M. Rao, Nicholas T. Potter
Publikováno v:
Journal of Vision. 18:432
Autor:
Nicholas T. Potter, Mary C. Phelan, Donald C. Henley, Eric Crawford, Tracey Cato, Chris E. Ramsey, Toni Jago, James E. Hewitt, Sara K. Farrell, Sarah Dodson, O. George Negrea, Christine A. Green, Ron V. Lee
Publikováno v:
Laboratory Medicine. 40:79-86
Autor:
Melinda L. Moseley, William K. Seltzer, Joline C. Dalton, T. Ashizawa, Massimo Pandolfo, John W. Day, Nicholas T. Potter, Laura P.W. Ranum, John B. Vincent, Kathy Gardner, Aubrey Milunsky, Yoshio Ikeda, Mikio Shoji, Thomas D. Bird
Publikováno v:
The American Journal of Human Genetics. 75(1):3-16
We reported elsewhere that an untranslated CTG expansion causes the dominantly inherited neurodegenerative disorder spinocerebellar ataxia type 8 (SCA8). SCA8 shows a complex inheritance pattern with extremes of incomplete penetrance, in which often
Autor:
Stanley Fahn, Astrid Rasmussen, Juliette Harris, Adam Rosenblatt, Jayalakshmi S. Mysore, Thomas D. Bird, Takayoshi Shimohata, Shoji Tsuji, Yoshiki Adachi, Ruth H. Walker, E. Almqvist, Christopher A. Ross, Nicholas T. Potter, Amanda Krause, Penny Greenstein, Tetsuo Ashizawa, Kazuhiro Nakaso, William K. Seltzer, Michael R. Hayden, Marcy E. MacDonald, Lisa Gourley, Susan E. Holmes, Kenji Nakashima, Elizabeth O'Hearn, Russell L. Margolis
Publikováno v:
Annals of Neurology. 56:670-674
Huntington's Disease-like 2 (HDL2) is a progressive, autosomal dominant, neurodegenerative disorder with marked clinical and pathological similarities to Huntington's disease (HD). The causal mutation is a CTG/CAG expansion mutation on chromosome 16q
Autor:
Neil B. Quigley, Nicholas T. Potter, Thomas Koenig, Gunter Weiss, Mary N. White, Kara D. Whitlock, Patrick Hurban, Reimo Tetzner, Catherine Lofton-Day
Publikováno v:
Clinical chemistry. 60(9)
BACKGROUND Epi proColon® is a new blood-based colorectal cancer (CRC) screening test designed to determine the methylation status of a promoter region of the SEPT9 (septin 9) gene in cell-free DNA isolated from plasma. We describe the analytical and
Autor:
Robert L. Barclay, Thomas König, David A. Johnson, Jürgen Beck, Gunter Weiss, Klaus Mergener, Nicholas T. Potter
Publikováno v:
PLoS ONE, Vol 9, Iss 6, p e98238 (2014)
PLoS ONE
PLoS ONE
Background Screening improves outcomes related to colorectal cancer (CRC); however, suboptimal participation for available screening tests limits the full benefits of screening. Non-invasive screening using a blood based assay may potentially help re
Autor:
Martha Nance, Nicholas T. Potter
Publikováno v:
Molecular Diagnosis. 5:91-99
The Ataxia Molecular Diagnostics Testing Group was established to generate quantitative proficiency and outcomes data regarding molecular testing for the autosomal dominant cerebellar ataxias (spinocerebellar ataxia types 1 [SCA-1] through -3, -6, an