Pesquisa | BVS IEC

1.

Dissecting the loci controlling fetal haemoglobin production on chromosomes 11p and 6q by the regressive approach.

Craig, J E; Rochette, J; Fisher, C A; Weatherall, D J; Marc, S; Lathrop, G M; Demenais, F; Thein, S.

Nat Genet ; 12(1): 58-64, 1996 Jan.

Artigo em Inglês | MEDLINE | ID: mdl-8528252

2.

Interaction of malaria with a common form of severe thalassemia in an Asian population.

O'Donnell, A; Premawardhena, A; Arambepola, M; Samaranayake, R; Allen, S J; Peto, T E A; Fisher, C A; Cook, J; Corran, P H; Olivieri, Nancy F; Weatherall, D J.

Proc Natl Acad Sci U S A ; 106(44): 18716-21, 2009 Nov 03.

Artigo em Inglês | MEDLINE | ID: mdl-19841268

3.

Surface antigen expression on Plasmodium falciparum-infected erythrocytes is modified in alpha- and beta-thalassemia.

Luzzi, G A; Merry, A H; Newbold, C I; Marsh, K; Pasvol, G; Weatherall, D J.

J Exp Med ; 173(4): 785-91, 1991 Apr 01.

Artigo em Inglês | MEDLINE | ID: mdl-2007853

4.

Isolation and immunocytochemical characterization of human bone marrow stromal macrophages in hemopoietic clusters.

Lee, S H; Crocker, P R; Westaby, S; Key, N; Mason, D Y; Gordon, S; Weatherall, D J.

J Exp Med ; 168(3): 1193-8, 1988 Sep 01.

Artigo em Inglês | MEDLINE | ID: mdl-3049905

5.

The alpha thalassaemias.

Higgs, D R; Weatherall, D J.

Cell Mol Life Sci ; 66(7): 1154-62, 2009 Apr.

Artigo em Inglês | MEDLINE | ID: mdl-19020805

6.

Molecular medicine; the road to the better integration of the medical sciences in the twenty-first century.

Weatherall, D J.

Notes Rec R Soc Lond ; 64 Suppl 1: S5-15, 2010 Sep 20.

Artigo em Inglês | MEDLINE | ID: mdl-20973344

7.

Linkage analysis of nondeletion hereditary persistence of fetal hemoglobin.

Old, J M; Ayyub, H; Wood, W G; Clegg, J B; Weatherall, D J.

Science ; 215(4535): 981-2, 1982 Feb 19.

Artigo em Inglês | MEDLINE | ID: mdl-6186021

8.

Genetic variation and susceptibility to infection: the red cell and malaria.

Weatherall, D J.

Br J Haematol ; 141(3): 276-86, 2008 May.

Artigo em Inglês | MEDLINE | ID: mdl-18410566

9.

Is the beta thalassaemia trait of clinical importance?

Premawardhena, A; Arambepola, M; Katugaha, N; Weatherall, D J.

Br J Haematol ; 141(3): 407-10, 2008 May.

Artigo em Inglês | MEDLINE | ID: mdl-18341640

10.

Gene therapy: repairing haemoglobin disorders with ribozymes.

Weatherall, D J.

Curr Biol ; 8(19): R696-8, 1998 Sep 24.

Artigo em Inglês | MEDLINE | ID: mdl-9768357

11.

Different hematologic phenotypes are associated with the leftward (-alpha 4.2) and rightward (-alpha 3.7) alpha+-thalassemia deletions.

Bowden, D K; Hill, A V; Higgs, D R; Oppenheimer, S J; Weatherall, D J; Clegg, J B.

J Clin Invest ; 79(1): 39-43, 1987 Jan.

Artigo em Inglês | MEDLINE | ID: mdl-3793931

12.

Alpha thalassemia changes erythrocyte heterogeneity in sickle cell disease.

Noguchi, C T; Dover, G J; Rodgers, G P; Serjeant, G R; Antonarakis, S E; Anagnou, N P; Higgs, D R; Weatherall, D J; Schechter, A N.

J Clin Invest ; 75(5): 1632-7, 1985 May.

Artigo em Inglês | MEDLINE | ID: mdl-2581999

13.

Hematologic and biosynthetic studies in homozygous hemoglobin Constant Spring.

Derry, S; Wood, W G; Pippard, M; Clegg, J B; Weatherall, D J; Wickramasinghe, S N; Darley, J; Fucharoen, S; Wasi, P.

J Clin Invest ; 73(6): 1673-82, 1984 Jun.

Artigo em Inglês | MEDLINE | ID: mdl-6725554

14.

The quiet art revisited.

Weatherall, D J.

Lancet ; 377(9781): 1912-3, 2011 Jun 04.

Artigo em Inglês | MEDLINE | ID: mdl-21648122

15.

Hydroxycarbamide for sickle-cell anaemia in infancy.

Weatherall, D J.

Lancet ; 377(9778): 1628-30, 2011 May 14.

Artigo em Inglês | MEDLINE | ID: mdl-21571132

16.

Commentary on "The modifying effect of Xmn1-HBG2 on thalassemic phenotype is associated with its linked elements in the beta globin locus control region, including the palindromic site at 5' HS4" by M. Neishabury et al.

Weatherall, D J.

Blood Cells Mol Dis ; 48(1): 6, 2012 Jan 15.

Artigo em Inglês | MEDLINE | ID: mdl-22136729

17.

Haemoglobin E beta thalassaemia in Sri Lanka.

Premawardhena, A; Fisher, C A; Olivieri, N F; de Silva, S; Arambepola, M; Perera, W; O'Donnell, A; Peto, T E A; Viprakasit, V; Merson, L; Muraca, G; Weatherall, D J.

Lancet ; 366(9495): 1467-70, 2005.

Artigo em Inglês | MEDLINE | ID: mdl-16243092

18.

The clinical and pathophysiological features of malarial anaemia.

Roberts, D J; Casals-Pascual, C; Weatherall, D J.

Curr Top Microbiol Immunol ; 295: 137-67, 2005.

Artigo em Inglês | MEDLINE | ID: mdl-16265890

19.

Muscle cell injury, haemolysis and dark urine in children with falciparum malaria in Papua New Guinea.

O'Donnell, A; Weatherall, D J; Taylor, A M; Reeder, J C; Allen, S J.

Trans R Soc Trop Med Hyg ; 100(9): 817-25, 2006 Sep.

Artigo em Inglês | MEDLINE | ID: mdl-16527319

20.

Thalassemia--a global public health problem.

Weatherall, D J; Clegg, J B.

Nat Med ; 2(8): 847-9, 1996 Aug.

Artigo em Inglês | MEDLINE | ID: mdl-8705845

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Dissecting the loci controlling fetal haemoglobin production on chromosomes 11p and 6q by the regressive approach.

Interaction of malaria with a common form of severe thalassemia in an Asian population.

Surface antigen expression on Plasmodium falciparum-infected erythrocytes is modified in alpha- and beta-thalassemia.

Isolation and immunocytochemical characterization of human bone marrow stromal macrophages in hemopoietic clusters.

The alpha thalassaemias.

Molecular medicine; the road to the better integration of the medical sciences in the twenty-first century.

Linkage analysis of nondeletion hereditary persistence of fetal hemoglobin.

Genetic variation and susceptibility to infection: the red cell and malaria.

Is the beta thalassaemia trait of clinical importance?

Gene therapy: repairing haemoglobin disorders with ribozymes.

Different hematologic phenotypes are associated with the leftward (-alpha 4.2) and rightward (-alpha 3.7) alpha+-thalassemia deletions.

Alpha thalassemia changes erythrocyte heterogeneity in sickle cell disease.

Hematologic and biosynthetic studies in homozygous hemoglobin Constant Spring.

The quiet art revisited.

Hydroxycarbamide for sickle-cell anaemia in infancy.

Commentary on "The modifying effect of Xmn1-HBG2 on thalassemic phenotype is associated with its linked elements in the beta globin locus control region, including the palindromic site at 5' HS4" by M. Neishabury et al.

Haemoglobin E beta thalassaemia in Sri Lanka.

The clinical and pathophysiological features of malarial anaemia.

Muscle cell injury, haemolysis and dark urine in children with falciparum malaria in Papua New Guinea.

Thalassemia--a global public health problem.