Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Holly, Barker"'
Autor:
Phil Bland, Harry Saville, Abigail Read, Patty Wai, Gareth Muirhead, Lucinda Curnow, Jadwiga Nieminuszczy, Nivedita Ravindran, Marie John, Somaieh Hedayat, Holly Barker, James Wright, Lu Yu, Ioanna Mavrommati, Barrie Peck, Mark Allen, Patrycja Gazinska, Helen Pemberton, Aditi Gulati, Sarah Nash, Farzana Noor, Naomi Guppy, Ioannis Roxanis, Samantha Barlow, Helen Kalirai, Sarah Coupland, Ronan Broderick, Samar Alsafadi, Alexandre Houy, Marc-Henri Stern, Stephen Pettit, Jyoti Choudhary, Syed Haider, Wojciech Niedzwiedz, Christopher Lord, Rachael Natrajan
Publikováno v:
Cancer Research. 83:P6-10
Background: Heterozygous hotspot mutations in the RNA splicing factor SF3B1, occur in 3% of unselected breast cancers and are associated with oestrogen receptor (ER+) breast cancer (BC) where they are enriched in metastatic disease and are associated
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::37dd549b1ea099cf9881e0df9401b989
https://doi.org/10.1158/1538-7445.sabcs22-p6-10-05
https://doi.org/10.1158/1538-7445.sabcs22-p6-10-05
Autor:
Clare L. Scott, Kevin K. Lin, Elizabeth M. Swisher, Iain A. McNeish, Mitch Raponi, Thomas C. Harding, Andrew D. Simmons, Scott H. Kaufmann, Matthew J. Wakefield, Heidi Giordano, David Bowtell, Lara Maloney, Liliane Robillard, James Sun, Amit Oza, David M. O'Malley, Ganessan Kichenadasse, Michael Friedlander, Anne Floquet, Robert L. Coleman, Kara A. Bernstein, Gregory J. Brunette, Meghan R. Sullivan, Elizabeth M. Kass, Rohit Prakash, Maria Jasin, Holly Barker, Gwo-Yaw Ho, Michael J. Kuiper, Maria I. Harrell, Nelson N.H. Teng, Anna V. Tinker, Kristy Shield-Artin, Minh Nguyen, Olga Kondrashova
A list of copy number alterations, rearrangements and short variants detected by Foundation Medicine NGS
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::290d4db2a909f21e74c4707ffaf15b8c
https://doi.org/10.1158/2159-8290.22532014
https://doi.org/10.1158/2159-8290.22532014
Autor:
Clare L. Scott, Kevin K. Lin, Elizabeth M. Swisher, Iain A. McNeish, Mitch Raponi, Thomas C. Harding, Andrew D. Simmons, Scott H. Kaufmann, Matthew J. Wakefield, Heidi Giordano, David Bowtell, Lara Maloney, Liliane Robillard, James Sun, Amit Oza, David M. O'Malley, Ganessan Kichenadasse, Michael Friedlander, Anne Floquet, Robert L. Coleman, Kara A. Bernstein, Gregory J. Brunette, Meghan R. Sullivan, Elizabeth M. Kass, Rohit Prakash, Maria Jasin, Holly Barker, Gwo-Yaw Ho, Michael J. Kuiper, Maria I. Harrell, Nelson N.H. Teng, Anna V. Tinker, Kristy Shield-Artin, Minh Nguyen, Olga Kondrashova
Supplementary Tables, Figures and Video legends, Tables 2,3,5 and all Supplementary Figures. Supplementary Table 2. Confirmation of cis configuration of BRCA1 primary and secondary mutations in case 4 by colony PCR. Supplementary Table 3. IC50 (mirco
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::397e20de6afaeebadb9878c50aa24cdb
https://doi.org/10.1158/2159-8290.22532005
https://doi.org/10.1158/2159-8290.22532005
Autor:
Clare L. Scott, Kevin K. Lin, Elizabeth M. Swisher, Iain A. McNeish, Mitch Raponi, Thomas C. Harding, Andrew D. Simmons, Scott H. Kaufmann, Matthew J. Wakefield, Heidi Giordano, David Bowtell, Lara Maloney, Liliane Robillard, James Sun, Amit Oza, David M. O'Malley, Ganessan Kichenadasse, Michael Friedlander, Anne Floquet, Robert L. Coleman, Kara A. Bernstein, Gregory J. Brunette, Meghan R. Sullivan, Elizabeth M. Kass, Rohit Prakash, Maria Jasin, Holly Barker, Gwo-Yaw Ho, Michael J. Kuiper, Maria I. Harrell, Nelson N.H. Teng, Anna V. Tinker, Kristy Shield-Artin, Minh Nguyen, Olga Kondrashova
Molecular Dynamics Modeling of WT RAD51D monofilament interaction with dsDNA.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c3fba9c22b5a359aa72c1e801f4e7723
https://doi.org/10.1158/2159-8290.22532008
https://doi.org/10.1158/2159-8290.22532008
Autor:
Clare L. Scott, Kevin K. Lin, Elizabeth M. Swisher, Iain A. McNeish, Mitch Raponi, Thomas C. Harding, Andrew D. Simmons, Scott H. Kaufmann, Matthew J. Wakefield, Heidi Giordano, David Bowtell, Lara Maloney, Liliane Robillard, James Sun, Amit Oza, David M. O'Malley, Ganessan Kichenadasse, Michael Friedlander, Anne Floquet, Robert L. Coleman, Kara A. Bernstein, Gregory J. Brunette, Meghan R. Sullivan, Elizabeth M. Kass, Rohit Prakash, Maria Jasin, Holly Barker, Gwo-Yaw Ho, Michael J. Kuiper, Maria I. Harrell, Nelson N.H. Teng, Anna V. Tinker, Kristy Shield-Artin, Minh Nguyen, Olga Kondrashova
Copy number estimation by SNP array in the archival tumor tissue of the patient identified to have a germline RAD51C mutation (c.577C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::916a972cc1b288a8152b36cc181d3f6a
https://doi.org/10.1158/2159-8290.22532011.v1
https://doi.org/10.1158/2159-8290.22532011.v1
Autor:
Mélodie Derome, Sandra Machon, Holly Barker, Petya Kozhuharova, Natasza Orlov, Elenor Morgenroth, Kenneth Hugdahl, Paul Allen
Publikováno v:
European Archives of Psychiatry and Clinical Neuroscience.
Childhood trauma (CT) has been linked to increased risk for psychosis. Moreover, CT has been linked to psychosis phenotypes such as impaired cognitive and sensory functions involved in the detection of novel sensory stimuli. Our objective was to inve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7cedef6600595120a1a16b128087d3e8
https://doi.org/10.1007/s00406-023-01564-3
https://doi.org/10.1007/s00406-023-01564-3