Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Michael Neat"'
Autor:
Daniel Johnathan Hughes, Gary JR Cook, Emma McLean, Daniel Smith, Juliet King, Athanasios Diamantopoulos, Aled Jones, Michael Neat, George Santis, James Spicer, Eleni Karapanagiotou, Alexandros Georgiou
Publikováno v:
Current Problems in Cancer: Case Reports, Vol 4, Iss , Pp 100106- (2021)
Activating epidermal growth factor receptor gene mutations (EGFRm) are relatively common in non-small cell lung cancer (NSCLC) and are predictive of superior outcomes with EGFR tyrosine kinase inhibitors (TKIs). Eventually, acquired genetic or phenot
Externí odkaz:
https://doaj.org/article/151bb1b481df4a83a33de03e0521dbf0
Publikováno v:
Oncology Reports
Subjectivity in oral dysplasia grading has prompted evaluation of molecular‑based tests to predict malignant transformation. Aneuploidy detected by DNA image‑based cytometry (ICM) is currently the best predictor but fails to detect certain high r
Autor:
Andrea Bille, Leanne Harling, Rosamond Nuamah, Michael Neat, Alka Saxena, Wen Ng, Federica Torricelli, Alessia Ciarrocchi, James Spicer
Publikováno v:
European journal of cancer (Oxford, England : 1990). 132
Background Malignant pleural mesothelioma (MPM) is an aggressive tumour with poor prognosis. The aim of this study was to identify genetic mutations associated with poor or extended survival in patients who received palliative chemotherapy. Methods A
Autor:
Majid Kazmi, Michael Neat, Inas El-Najjar, Ieuan Walker, Alice Coady, Reuben Benjamin, Matthew Streetly, Steve Schey, Darius Ladon
Publikováno v:
British Journal of Haematology. 180:451-454
Autor:
Alka Saxena, Wen Ng, R. Nuamah, Alessia Ciarrocchi, Michael Neat, Federica Torricelli, James Spicer, Andrea Bille, Leanne Harling
Publikováno v:
Journal of Thoracic Oncology. 14:S296-S297
Publikováno v:
The American Journal of Dermatopathology. 33:1-16
Advances made within the field of genomics and proteomics have facilitated the emergence of a new era of molecular diagnostics. However, ongoing rapid developments in molecular methodology ensure that this remains a complex field, accessible primaril
Autor:
Alexandra, Clipson, Sharon, Barrans, Naiyan, Zeng, Simon, Crouch, Nicholas F, Grigoropoulos, Hongxiang, Liu, Sylvia, Kocialkowski, Ming, Wang, Yuanxue, Huang, Lisa, Worrillow, John, Goodlad, Jenny, Buxton, Michael, Neat, Paul, Fields, Bridget, Wilkins, John W, Grant, Penny, Wright, Hesham, Ei-Daly, George A, Follows, Eve, Roman, A James, Watkins, Peter W M, Johnson, Andrew, Jack, Ming-Qing, Du
Publikováno v:
The Journal of Pathology: Clinical Research
A proportion of MYC translocation positive diffuse large B‐cell lymphomas (DLBCL) harbour a BCL2 and/or BCL6 translocation, known as double‐hit DLBCL, and are clinically aggressive. It is unknown whether there are other genetic abnormalities that
Autor:
James Spicer, Tom Newsom-Davies, Karim El-Shakankery, Guillermina Nickless, Michael Neat, Sarah Hunter, Daniel J. Smith, Gillian Brand, E. Karapanagiotou, Ana Montes, Nadia Yousaf, Marianne Nicolson
Publikováno v:
Journal of Clinical Oncology. 35:e20678-e20678
e20678 Background: The clinical significance of common epidermal growth factor receptor (EGFR) mutations (exon 19 deletions and exon 21 L858 mutations) in non-small cell lung cancer is well known1. However, 2-8% of NSCLC patients harbour an uncommon
Autor:
Fiona Child, Nita Agar, Alya Abdul-Wahab, Sean Whittaker, E. Mary Wain, Alistair Robson, Stephen Morris, J. Scarisbrick, Soo-Yong Tang, Michael Neat
Publikováno v:
Journal of the American Academy of Dermatology. 70(6)
Background The t(14;18)(q32;q21) chromosomal translocation is found in the majority of nodal follicular lymphomas but only rarely in primary cutaneous follicle center cell lymphomas (PCFCL). Recent studies have postulated that the translocation is mo
Publikováno v:
Clinical Lymphoma Myeloma and Leukemia. 15:e116
e116 expressed on multiple myeloma cells. However expression of CD138 is reduced in some patients during their clinical courses. To clarify the clinical significance of this phenomenon, we evaluated correlation between CD138 expression levels by flow