Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Gillian S. Masters"'
Autor:
Clifford M. Lawrence, Gillian M. Murphy, Pamela Gover, Michael Norman Badminton, Gillian S. Masters, George H. Elder, Ghulam J. Mufti, Sharon D. Whatley, Robert Sarkany, Sally H. Ibbotson
Publikováno v:
Journal of Investigative Dermatology. 131(5):1172-1175
Publikováno v:
Clinical & Laboratory Haematology. 19:61-65
A serum-free method for the culture of megakaryocyte progenitor cells (burst-forming units megakaryocyte, BFU-Mk) from human bone marrow is described, using recombinant cytokines (interleukin[IL]-3, IL-6, IL-11 and stem cell factor [SCF]) to provide
Autor:
Margaretha Van Mourik, Mohamed Khalil, Adele Timbs, Alison May, John M. Old, Shirley Henderson, Anna Schuh, Alice Gallienne, Gillian S. Masters, Janice McCarthy
Publikováno v:
Clinical biochemistry. 42(18)
OBJECTIVES: The aim of this study was to update the incidence data of beta thalassaemia mutations in various populations and compare it to the spectrum of mutations in the United Kingdom (UK) population in order to determine the impact of immigration
Publikováno v:
Journal of Clinical Pathology. 43:937-941
Erythroid colony growth in the presence and absence of erythropoietin was compared in 23 patients with primary proliferative polycythaemia (PPP), nine with idiopathic erythrocytosis, 10 with secondary polycythaemia, 15 with pseudopolycythaemia and in
Autor:
Graham P, Feeney, Kymberley, Carter, Gillian S, Masters, Helen A, Jackson, Ivor, Cavil, Mark, Worwood
Publikováno v:
Haematologica. 90(2)
The HFE protein interacts with the transferrin receptor (TfR) to regulate cellular iron uptake. Nucleated erythroid cells have the highest number of TfR and the greatest iron uptake. The aim of this study was to investigate whether erythroid iron upt
Autor:
Gillian S. Masters, Xiaojun Guo, Alison May, David F. Bishop, Philip D. Cotter, A. I. Al-Sabah, Soumeya Bekri
Publikováno v:
Blood. 102(2)
X-linked sideroblastic anemia (XLSA) is caused by mutations in the erythroid-specific 5-aminolevulinate synthase gene (ALAS2). XLSA was diagnosed in a 32-year-old woman with a mild phenotype and moderately late onset. Pyridoxine therapy had no effect
Publikováno v:
Leukemia research. 19(8)
We have previously reported that serum stem cell factor (SCF) levels are significantly lower in patients with myelodysplastic syndrome (MDS) than normal controls. We have now studied the effects of adding SCF to cultures of blood mononuclear cells fr
Publikováno v:
Blood. 106:3541-3541
A woman of 60yr presented with exhaustion and breathlessness (Hb 89g/L, MCV 102fL, MCH 36.9pg), a palpable spleen (15cm), dyserythropoiesis, sideroblastic change in her bone marrow and a normal karyotype. She had been investigated elsewhere at 27yr f
Autor:
T Gorvett, T Littlewood, P Baines, Gillian S. Masters, Alice K. Jacobs, R Bailey-Wood, P Bentley, H Parry-Jones
Publikováno v:
Journal of Clinical Pathology. 40:87-93
Peripheral blood and bone marrow were studied in 21 men with disseminated untreated bronchial cancer in an attempt to define abnormalities of erythropoiesis associated with the development of anaemia. Haemoglobin concentration at or below 13 g/dl was
Publikováno v:
British journal of haematology. 68(2)
Summary Myeloid and erythroid progenitors from myelodysplastic marrows have been separated from accessory cell populations likely to influence their in-vitro growth. Myeloid colony-forming cells were enriched 23-fold and erythroid progenitors 5-7-fol