Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Nicholas Telford"'
Autor:
Stefan Meyer, Rachel Dixon, Robert F Wynn, Andrew M Will, Denise Bonney, Jamie M Ellingford, Bronwyn Kerr, Ben Adams, Nicholas Telford, Graeme C.M. Black, Jill E. Urquhart
Publikováno v:
Cancer genetics.
Pathogenic germ-line variants in GATA2 (GATA2-deficiency) can cause childhood myelodysplastic syndrome (MDS) and acute myeloid leukaemia (AML), and can be associated with distinct clinical syndromic features. However, penetrance and genotype-phenotyp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::64bdf34d157840c1abd638966169323e
https://pubmed.ncbi.nlm.nih.gov/33957466
https://pubmed.ncbi.nlm.nih.gov/33957466
Autor:
Ian Fillis, Nicholas Telford
This timely and incisive Handbook provides critical contemporary insights into the theory and practice of entrepreneurship and marketing in the twenty-first century. Bringing together rich and varied contributions from prominent international researc
Autor:
M Tariq, Nicholas Telford, Claire L Attwooll, John Coyne, Martin Harris, Brian P Eyden, Anthony J. Freemont, M Atkinson, Jennifer Varley
Publikováno v:
The American Journal of Surgical Pathology. 24:1020-1026
A case of extraskeletal myxoid chondrosarcoma (EMC) in which there was histochemical, immunohistochemical, and ultrastructural evidence of neuroendocrine differentiation is reported. Genetic investigations showed the recently described novel transloc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b5b3a63d5a29ea433a5eea64c9affb7c
https://doi.org/10.1097/00000478-200007000-00015
https://doi.org/10.1097/00000478-200007000-00015
Autor:
Federico Garrido, Claire S Brady, Ann-Margaret Little, Deborah J. Burt, Francisco Ruiz-Cabello, Peter L. Stern, Pilar Jiménez, Jennifer S. Bartholomew, Margaret F Duggan-Keen, Suzanne Glenville, Nicholas Telford, Judith A Davidson
Publikováno v:
Tissue Antigens. 55:401-411
The consistent dysregulation of HLA expression in cervical neoplasia is likely to influence the natural history of the disease and prospects for cell-mediated vaccine therapies. We have studied the underlying mechanisms in eight new cervical cancer c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ba25cee21bd76b02ae14e34d94707d42
https://doi.org/10.1034/j.1399-0039.2000.550502.x
https://doi.org/10.1034/j.1399-0039.2000.550502.x
Publikováno v:
Oncogene. 18:7599-7601
A proportion of extraskeletal myxoid chondrosarcomas (EMC) have been shown to have a characteristic translocation t(9;22)(q22;q12) involving the EWS gene at 22q12 and the CHN orphan nuclear receptor gene at 9q22. This translocation appears to be larg
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c9671916ac75717657c1d7b8f8fc068
https://doi.org/10.1038/sj.onc.1203156
https://doi.org/10.1038/sj.onc.1203156
Publikováno v:
Cancer genetics and cytogenetics. 151(2)
Deletion of the long arm of chromosome 15 has been described as a recurrent chromosomal abnormality in myeloid malignancies. We present here some additional case reports of deletion 15 including two cases with an extra copy of the deleted chromosome,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d0ed0d3312f167530aa812a3cd42e834
https://pubmed.ncbi.nlm.nih.gov/15172752
https://pubmed.ncbi.nlm.nih.gov/15172752
Autor:
Joan, Cunningham, Mark, Sales, Andrew, Pearce, Julie, Howard, Ray, Stallings, Nicholas, Telford, Rosalie, Wilkie, Brian, Huntly, Angela, Thomas, Aengus, O'Marcaigh, Andrew, Will, Norman, Pratt
Publikováno v:
British journal of haematology. 119(4)
We report on nine children with Shwachman-Diamond syndrome (SDS), eight of whom had clonal abnormalities of chromosome 7. Seven children had an isochromosome 7 [i(7)(q10)] and one a derivative chromosome 7, all with an apparently identical (centromer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4372ac6ee472b66a50507b4fed8ed22b
https://pubmed.ncbi.nlm.nih.gov/12472589
https://pubmed.ncbi.nlm.nih.gov/12472589