Search Results - "Foot, N. J."

ALK rearrangements in EBUS-derived transbronchial needle aspiration cytology in lung cancer by Neat, M. J., Foot, N. J., Hicks, A., Breen, R., Wilkins, B., McLean, E., Santis, G.

“…Objectives Patients with non‐small cell lung cancer (NSCLC) positive for anaplastic lymphoma kinase (ALK) gene rearrangements may be treated successfully with…”
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Recent Advances into Understanding Some Aspects of the Structure and Function of Mammalian and Avian Lungs by Maina, J. N., West, J. B., Orgeig, S., Foot, N. J., Daniels, C. B., Kiama, S. G., Gehr, P., Mühlfeld, C., Blank, F., Müller, L., Lehmann, A., Brandenberger, C., Rothen‐Rutishauser, B.

“…Recent findings are reported about certain aspects of the structure and function of the mammalian and avian lungs that include (a) the architecture of the air…”
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Drosophila Ndfip is a novel regulator of Notch signaling by Dalton, H E, Denton, D, Foot, N J, Ho, K, Mills, K, Brou, C, Kumar, S

“…In the Drosophila wing, the Nedd4 ubiquitin ligases (E3s), dNedd4 and Su(dx), are important negative regulators of Notch signaling; they ubiquitinate Notch,…”
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Detection of Chromosome Abnormalities Pre–High-Dose Treatment in Patients Developing Therapy-Related Myelodysplasia and Secondary Acute Myelogenous Leukemia After Treatment for Non-Hodgkin’s Lymphoma by LILLINGTON, Debra M, MICALLEF, Ivana N. M, CARPENTER, Emily, NEAT, Michael J, AMESS, John A. L, MATTHEWS, Janet, FOOT, Nicola J, YOUNG, Bryan D, LISTER, T. Andrew, ROHATINER, Ama Z. S

“…To assess whether pre-high-dose therapy (HDT)-related factors play a critical role in the development of therapy-related myelodysplasia (tMDS) or secondary…”
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The most frequent constitutional translocation in humans, the t(11;22)(q23;q11) is due to a highly specific Alu-mediated recombination by HILL, A. S, FOOT, N. J, CHAPLIN, T. L, YOUNG, B. D

“…The t(11;22) is the most common recurrent non-Robertsonian constitutional translocation in humans, having been reported in more than 160 unrelated families…”
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The characterisation of the lymphoma cell line U937, using comparative genomic hybridisation and multi-plex FISH by Strefford, J C, Foot, N J, Chaplin, T, Neat, M J, Oliver, R T, Young, B D, Jones, L K

“…The cell line U937, which has been used extensively for studies of myeloid differentiation, bears the t(10;11)(p13;q14) translocation which results in a fusion…”
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Molecular characterisation of the t(1;15)(p22;q22) translocation in the prostate cancer cell line LNCaP by Strefford, J C, Lane, T M, Hill, A, LeRoux, L, Foot, N J, Shipley, J, Oliver, R T D, Lu, Y-J, Young, B D

“…Although chromosome translocations are well-documented recurrent events in hematological malignancies and soft tissue sarcomas, their significance in…”
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Genetic susceptibility to Hodgkin's disease and secondary neoplasias: FISH analysis reveals patients at high risk of developing secondary neoplasia by Lillington, D. M., Micallef, I. N. M., Carpenter, E., Neat, M. J., Amess, J. A. L., Matthews, J., Foot, N. J., Lister, T. A., Young, B. D., Rohatiner, A. Z. S.

“…Background: Cytotoxic drugs administered before high‐dose therapy (HDT) represent a significant factor in the development of leukemic complications in patients…”
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Novel mutations and polymorphisms in the Fanconi anemia group C gene by Gibson, Rachel A., Morgan, Neil V., Goldstein, Laura H., Pearson, Ian C., Kesterton, Ian P., Foot, Nicola J., Jansen, Stander, Havenga, Charmaine, Pearson, Thomas, de Ravel, Thomy J., Cohn, Richard J., Marques, Isabel M., Dokal, Inderjeet, Roberts, Irene, Marsh, Judith, Ball, Sarah, Milner, R. David, Llerena Jr, Juan C., Samochatova, Elena, Mohan, Sheila P., Vasudevan, Pushpa, Birjandi, Farkondeh, Hajianpour, Atieh, Murer-Orlando, Manuela, Mathew, Christopher G.

“…Fanconi anemia (FA) is an autosomal recessive disorder associated with hypersensitivity to DNA cross‐linking agents and bone marrow failure. At least four…”
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Genome-wide single nucleotide polymorphism analysis reveals frequent partial uniparental disomy due to somatic recombination in acute myeloid leukemias by RAGHAVAN, Manoj, LILLINGTON, Debra M, SKOULAKIS, Spyros, DEBERNARDI, Silvana, CHAPLIN, Tracy, FOOT, Nicola J, LISTER, T. Andrew, YOUNG, Bryan D

“…Genome-wide analysis of single nucleotide polymorphisms in 64 acute myeloid leukemias has revealed that approximately 20% exhibited large regions of…”
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Genomewide single nucleotide polymorphism microarray mapping in basal cell carcinomas unveils uniparental disomy as a key somatic event by TEH, Muy-Teck, BLAYDON, Diana, KELSELL, David P, CHAPLIN, Tracy, FOOT, Nicola J, SKOULAKIS, Spyros, RAGHAVAN, Manoj, HARWOOD, Catherine A, PROBY, Charlotte M, PHILPOTT, Michael P, YOUNG, Bryan D

“…Basal cell carcinoma is the most common human cancer with increasing incidence reported worldwide. Despite the aberrant signaling role of the Hedgehog pathway,…”
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3′ CBFβ deletion associated with inv(16) in acute myeloid leukemia by Kelly, Johanna, Foot, Nicola J., Conneally, Eibhlin, Enright, Helen, Humphreys, Mervyn, Saunders, Karen, Neat, Michael J.

“…Recent reports have shown that concomitant submicroscopic deletions can occur in association with chromosomal translocations/inversions in several leukemia…”
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