Zobrazeno 1 - 10
of 47
pro vyhledávání: '"V J, Bubb"'
Autor:
Lauren J. McIver, David A. Boothman, L-S Li, V. J. Bubb, J. F. McCormick, C. L. Galindo, Angela C. George, Harold R. Garner, J. P. Quinn
Publikováno v:
Cancer Research. 70:P2-06
Background: There is a strong genetic component to breast cancer, which is the most common neoplasm in women; however current risk markers are few, accounting for less than 10% of breast cancer cases. This means that the majority of familial breast c
Publikováno v:
Current topics in behavioral neurosciences. 12
The serotonin transporter is a key regulator of the bioavailability of serotonin and therefore any modulation in the expression or action of the transporter would be expected to have consequences on behaviour. The transporter has therefore become a t
Autor:
J. F. McCormick, Michael A. Skinner, Angela C. George, V. J. Bubb, Long Shan Li, J. P. Quinn, D. H. Abid Alkadem, David A. Boothman, Lauren J. McIver, Harold R. Garner, Cristi L. Galindo
We sequenced the 5′ UTR of the estrogen-related receptor gamma gene (ERR-γ) in ~500 patient and volunteer samples and found that longer alleles of the (AAAG) n microsatellite were statistically and significantly more likely to exist in the germlin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f0bd56835ffdc7ab25b7acd9e61382c8
https://europepmc.org/articles/PMC3374865/
https://europepmc.org/articles/PMC3374865/
Publikováno v:
Histology and histopathology. 23(3)
Activity-dependent neuroprotective protein (ADNP) is a VIP-regulated gene, which is essential for brain development. A synthetic peptide (NAP) derived from the ADNP sequence is highly neuroprotective, therefore it has been hypothesised that ADNP has
Publikováno v:
The European journal of neuroscience. 17(2)
We have demonstrated that a variable number tandem repeat domain (VNTR) within intron 2 of the serotonin transporter gene is a transcriptional regulatory domain which is potentially correlated with a predisposition to affective disorders and other be
Publikováno v:
Histopathology. 39(6)
Members of the cadherin and catenin families are involved in chondrogenesis and catenin gene mutations have been detected in malignant tumours of bone. This study was undertaken to assess in detail expression of cadherin, beta-catenin and the associa
Autor:
A H, Wyllie, C O, Bellamy, V J, Bubb, A R, Clarke, S, Corbet, L, Curtis, D J, Harrison, M L, Hooper, N, Toft, S, Webb, C C, Bird
Publikováno v:
British journal of cancer. 80
Apoptosis has long been known to be effected through a common sequence of structural changes, despite the wide variety of initiating stimuli. These common structural events appear to depend upon activation of a set of enzymes (caspases) which direct
Autor:
C A, Midgley, S, White, R, Howitt, V, Save, M G, Dunlop, P A, Hall, D P, Lane, A H, Wyllie, V J, Bubb
Publikováno v:
The Journal of pathology. 181(4)
The tumour suppressor gene APC codes for a 2843-amino acid protein whose precise functions are still poorly understood. This paper describes the development of two new antisera to APC (to amino- and carboxy-terminal epitopes) which permit localizatio
Publikováno v:
The Journal of pathology. 181(4)
Codon 12 of the K-ras oncogene was screened for mutations in 65 surgically-resected primary pulmonary adenocarcinomas and in 32 tissue foci of alveolar atypical hyperplasia (AAH) by a polymerase chain reaction (PCR)-based method. Mutations in either
Autor:
C A, Cooper, V J, Bubb, N, Smithson, R L, Carter, S, Gledhill, D, Lamb, A H, Wyllie, F A, Carey
Publikováno v:
The Journal of pathology. 180(1)
Four genetic polymorphisms in the APC and MCC genes at chromosome 5q21 were analysed for loss of heterozygosity (LOH) in 97 primary squamous carcinomas and adenocarcinomas of the lung. LOH was identified in at least two polymorphic loci in 41 percent