α thalassaemia in British people

α thalassaemia in British people

Although α thalassaemia is rare in north Europeans, it has been identified in British people with no known foreign ancestry. Twelve such patients were studied, of whom eight shared a distinctive molecular defect, which was clearly different from defects seen in subjects of Mediterranean or South Eas...

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Príomhchruthaitheoirí:	Higgs, DR, Ayyub, H, Clegg, J, Hill, A, Nicholls, R, Teal, H, Wainscoat, J, Weatherall, D
Formáid:	Journal article
Teanga:	English
Foilsithe / Cruthaithe:	1985

Míreanna comhchosúla

Alpha thalassaemia in British people.
de réir: Higgs, D, et al.
Foilsithe / Cruthaithe: (1985)

Alpha-thalassaemia and the malaria hypothesis.
de réir: Hill, A, et al.
Foilsithe / Cruthaithe: (1987)

The alpha thalassaemias.
de réir: Higgs, D, et al.
Foilsithe / Cruthaithe: (2009)

THE ALPHA-3.7 AND ALPHA-4.2 DELETION FORMS OF ALPHA+-THALASSAEMIA DIFFER IN SEVERITY
de réir: Hill, A, et al.
Foilsithe / Cruthaithe: (1985)

Molecular rearrangements of the human alpha-globin gene cluster.
de réir: Higgs, D, et al.
Foilsithe / Cruthaithe: (1985)

α-thalassaemia
de réir: Higgs Douglas R, et al.
Foilsithe / Cruthaithe: (2010-05-01)

Alpha-thalassaemia caused by a polyadenylation signal mutation.
de réir: Higgs, D, et al.
Foilsithe / Cruthaithe: (1983)

High frequency of beta thalassaemia in a small island population in Melanesia.
de réir: Bowden, D, et al.
Foilsithe / Cruthaithe: (1987)

Characterization of a new α° thalassaemia defect in the South African population
de réir: Vandenplas, S, et al.
Foilsithe / Cruthaithe: (1987)

The interaction of alpha thalassaemia and sickle cell-beta zero thalassaemia.
de réir: Vyas, P, et al.
Foilsithe / Cruthaithe: (1988)

Splenic size in homozygous alpha+ thalassaemia.
de réir: Williams, T, et al.
Foilsithe / Cruthaithe: (1998)

Alpha-thalassaemia in Nigeria: Its interaction with sickle-cell disease
de réir: Falusi, A, et al.
Foilsithe / Cruthaithe: (2009)

Identification of acquired somatic mutations in the chromatin remodelling factor ATRX in the a thalassaemia myelodysplasia syndrome (ATMDS)
de réir: Gibbons, R, et al.
Foilsithe / Cruthaithe: (2003)

Analysis of the human alpha-globin gene cluster reveals a highly informative genetic locus.
de réir: Higgs, D, et al.
Foilsithe / Cruthaithe: (1986)

Alpha thalassaemia is associated with increased soluble transferrin receptor levels.
de réir: Rees, D, et al.
Foilsithe / Cruthaithe: (1998)

Thalassaemia.
de réir: Higgs, D, et al.
Foilsithe / Cruthaithe: (2012)

Thalassaemia
de réir: Higgs, D, et al.
Foilsithe / Cruthaithe: (2011)

A newly defined X linked mental retardation syndrome associated with alpha thalassaemia.
de réir: Gibbons, R, et al.
Foilsithe / Cruthaithe: (1991)

Thalassaemia in Sri Lanka: implications for the future health burden of Asian populations. Sri Lanka Thalassaemia Study Group.
de réir: de Silva, S, et al.
Foilsithe / Cruthaithe: (2000)

Alpha-thalassaemia.
de réir: Harteveld, C, et al.
Foilsithe / Cruthaithe: (2010)

Thalassaemia in Sri Lanka: A molecular basis.
de réir: Fisher, C, et al.
Foilsithe / Cruthaithe: (1999)

De novo deletion within the telomeric region flanking the human alpha globin locus as a cause of alpha thalassaemia.
de réir: Viprakasit, V, et al.
Foilsithe / Cruthaithe: (2003)

Red blood cell phenotypes in the alpha + thalassaemias from early childhood to maturity.
de réir: Williams, T, et al.
Foilsithe / Cruthaithe: (1996)

Hb H hydrops fetalis syndrome associated with the interaction of two common determinants of alpha thalassaemia (--MED/(alpha)TSaudi(alpha)).
de réir: Viprakasit, V, et al.
Foilsithe / Cruthaithe: (2002)

The effect of α (^+) - thalassaemia on the incidence of malaria and other diseases in children living on the coast of Kenya
de réir: Wambua, S, et al.
Foilsithe / Cruthaithe: (2006)

Survival and desferrioxamine in thalassaemia major.
de réir: Modell, B, et al.
Foilsithe / Cruthaithe: (1982)

Thalassaemia in Vanuatu, south-west Pacific: frequency and haematological phenotypes of young children.
de réir: Ganczakowski, M, et al.
Foilsithe / Cruthaithe: (1995)

GEOGRAPHIC-DISTRIBUTION OF ALPHA-GLOBIN AND BETA-GLOBIN GENE-CLUSTER POLYMORPHISMS
de réir: Wainscoat, J, et al.
Foilsithe / Cruthaithe: (1989)

Epistasis and the sensitivity of phenotypic screens for beta thalassaemia
de réir: Penman, B, et al.
Foilsithe / Cruthaithe: (2014)

Prevalence and molecular basis of alpha-thalassaemia in a malaria endemic region of Vietnam
de réir: Nguyen, N, et al.
Foilsithe / Cruthaithe: (2007)

Thalassaemia
de réir: William H Adams
Foilsithe / Cruthaithe: (2003-01-01)

Anaemia among females in child-bearing age: Relative contributions, effects and interactions of α- and β-thalassaemia
de réir: Mettananda, S, et al.
Foilsithe / Cruthaithe: (2018)

Direct cloning of specific genomic DNA sequences in plasmid libraries following fragment enrichment.
de réir: Nicholls, R, et al.
Foilsithe / Cruthaithe: (1985)

Alpha globin genotypes in two North European populations.
de réir: Flint, J, et al.
Foilsithe / Cruthaithe: (1986)

Alpha thalassaemia mental retardation (ATR-X): an atypical family.
de réir: Logie, L, et al.
Foilsithe / Cruthaithe: (1994)

Relative roles of genetic factors, dietary deficiency, and infection in anaemia in Vanuatu, South-West Pacific.
de réir: Bowden, D, et al.
Foilsithe / Cruthaithe: (1985)

Independent recombination events between the duplicated human alpha globin genes; implications for their concerted evolution.
de réir: Higgs, D, et al.
Foilsithe / Cruthaithe: (1984)

The interaction of alpha thalassaemia with malaria.
de réir: Oppenheimer, S, et al.
Foilsithe / Cruthaithe: (1987)

Synergistic silencing of α-globin and induction of γ-globin by histone deacetylase inhibitor, vorinostat as a potential therapy for β-thalassaemia
de réir: Mettananda, S, et al.
Foilsithe / Cruthaithe: (2019)

Different hematologic phenotypes are associated with the leftward (-alpha 4.2) and rightward (-alpha 3.7) alpha+-thalassemia deletions.
de réir: Bowden, D, et al.
Foilsithe / Cruthaithe: (1987)