W. Wood

发表

Characterization of the major regulatory element upstream of the human alpha-globin gene cluster

A. Jarman, D. Higgs, J. Sharpe, 1991, Molecular and cellular biology.

Globin Synthesis During Erythroid Cell Maturation in α Thalrssemia

G. Stamatoyannopoulos, W. Wood, 1976 .

Heterocellular Hereditary Persistence of Fetal Haemoglobin (Heterocellular HPFH) and its Interaction with β Thalassaemia

J. Edwards, J. Clegg, D. Weatherall, 1977, British journal of haematology.

Sickle-,80 Thalassemia in Eastern Saudi Arabia

D. Weatherall, M. Pembrey, W. Wood, 2006 .

Hb F Synthesis in Sickle Cell Anaemia: a Comparison of Saudi Arab Cases with those of African Origin

D. Weatherall, G. Serjeant, M. Pembrey, 1980, British journal of haematology.

Fetal Haemoglobin Production and the Sickle Gene in the Oases of Eastern Saudi Arabia

D. Weatherall, W. Wood, M. Pembrey, 1978, British journal of haematology.

Haemoglobin Synthesis by Fetal Erythroid Cells in an Adult Environment

D. Weatherall, M. Corp, W. Wood, 1981, British journal of haematology.

The Kenya Form of Hereditary Persistence of Fetal Haemoglobin: Structural Studies and Evidence for Homogeneous Distribution of Haemoglobin F using Fluorescent Anti‐haemoglobin F Antibodies

G. Stamatoyannopoulos, P. E. Nute, W. Wood, 1976, British journal of haematology.

Globin Chain Synthesis in the Greek Type (Aγ) of Hereditary Persistence of Fetal Haemoglobin

G. Stamatoyannopoulos, P. E. Nute, W. Wood, 1975 .

X-linked syndrome of platelet dysfunction, thrombocytopenia, and imbalanced globin chain synthesis with hemolysis.

G. Stamatoyannopoulos, A. Thompson, W. Wood, 1977, Blood.

THE CLINICAL AND MOLECULAR HETEROGENEITY OF THE THALASSEMIA SYNDROMES *

J. Clegg, D. Weatherall, D. Higgs, 1980, Annals of the New York Academy of Sciences.

F-cells in the adult: normal values and levels in individuals with hereditary and acquired elevations of Hb F.

G. Stamatoyannopoulos, P. E. Nute, W. Wood, 1975, Blood.

The Heterogeneity of Normal Hb A2‐β Thalassaemia in Greece

D. Weatherall, C. Kattamis, J. Nash, 1979 .

Switch from foetal to adult haemoglobin synthesis in normal and hypophysectomised sheep

J. Clegg, D. Weatherall, G. Dawes, 1976, Nature.

The Patterns of Fetal Haemoglobin Production in Leukaemia

W. McWhirter, J. Clegg, D. Weatherall, 1976, British journal of haematology.

Globin synthesis in fractionated Normoblasts of beta-thalassemia heterozygotes.

G. Stamatoyannopoulos, W. Wood, W G Wood, 1975, The Journal of clinical investigation.

Foetal erythropoiesis in human leukaemia

J. Clegg, D. Weatherall, W. Wood, 1975, Nature.

A new form of hereditary persistence of fetal hemoglobin in blacks and its association with sickle cell trait.

G. Stamatoyannopoulos, T. Papayannopoulou, P. E. Nute, 1975, Blood.

Haemoglobin Synthesis in Human Erythroid Bursts during Ontogeny: Reproducibility and Sensitivity to Culture Conditions

J. Adamson, D. Weatherall, W. Wood, 1981, British journal of haematology.

Occurrence of Gγ Hb F in Greek HPFH: Analysis of Heterozygotes and Compound Heterozygotes with β Thalassaemia

J. Clegg, D. Weatherall, C. Kattamis, 1979 .

Patterns of Globin Chain Synthesis in Erythroid Colonies Grown from Sheep Marrow of Different Developmental Stages

J. Adamson, D. Weatherall, P. Darbre, 1979, British journal of haematology.

The α‐Thalassemias

P. Vyas, A. Wilkie, D. Higgs, 1990, Annals of the New York Academy of Sciences.

Haemoglobin Synthesis during Human Foetal Development

D. Weatherall, W. Wood, D. Weatherall, 1973, Nature.

THE SIGNIFICANCE OF HAEMOGLOBIN H IN PATIENTS WITH MENTAL RETARDATION OR MYELOPROLIFERATIVE DISEASE

J. Clegg, D. Weatherall, W. Wood, 1982, British Journal of Haematology.

δβ‐Thalassaemia in a Chinese Family

J. Clegg, D. Weatherall, W. Wood, 1972 .

A Comparison of the Homozygous States for Gγ and GγAγδβ Thalassaemia

J. Clegg, D. Weatherall, J. White, 1979 .

Globin chain synthesis in the greek type (A gamma) of hereditary persisitence of fetal haemoglobin.

G. Stamatoyannopoulos, P. E. Nute, W. Wood, 1975, British journal of haematology.

Characterization of an Indian (δβ)° thalassaemia

D. Weatherall, J. Wainscoat, J. Old, 1984 .

(Aγδβ)° thalassaemia: similarity of phenotype in four different molecular defects, including one newly described

R. W. Jones, J. Clegg, D. Weatherall, 1984, British journal of haematology.

Molecular basis for acquired haemoglobin H disease

J. Clegg, D. Weatherall, J. Old, 1977, Nature.

association with sickle cell trait A new form of hereditary persistence of fetal hemoglobin in blacks and its

G. Stamatoyannopoulos, T. Papayannopoulou, P. E. Nute, 2011 .

In vitro growth of sheep erythroid progenitors

S. Kelly, W. Wood, 1986, British journal of haematology.

Haemoglobin Synthesis in Suspension Cultures of Human Bone Marrow

W. Wood, 1974, British journal of haematology.

Acquired Haemoglobin H Disease in Leukaemia: Pathophysiology and Molecular Basis

J. Clegg, D. Weatherall, W. Wood, 1978, British journal of haematology.

X-linked syndrome of platelet dysfunction, thrombocytopenia, and imbalanced globin chain synthesis with hemolysis.

G. Stamatoyannopoulos, A. Thompson, W. Wood, 1977, Blood.

A major positive regulatory region located far upstream of the human alpha-globin gene locus.

A. Jarman, D. Higgs, J. Sharpe, 1990, Genes & development.

Analysis of Globin Gene Inversion Reveals Similarities with Immunoglobulin Rearrangement

R. W. Jones, D. Weatherall, W. Wood, 1985, Annals of the New York Academy of Sciences.

Globin gene mapping in normal Hb A2 types of β‐thalassaemia

D. Weatherall, E. Kanavakis, C. Kattamis, 1982, British journal of haematology.