Partial deletion of the α-globin structural gene in human α-thalassaemia

3

Transcript of Partial deletion of the α-globin structural gene in human α-thalassaemia

Page 1: Partial deletion of the α-globin structural gene in human α-thalassaemia
Page 2: Partial deletion of the α-globin structural gene in human α-thalassaemia

© Nature Publishing Group1980

Page 3: Partial deletion of the α-globin structural gene in human α-thalassaemia

© Nature Publishing Group1980


DIAGNOSIS OF THE THALASSAEMIA SYNDROMES: …users.unimi.it/barb/public/UploadAttach/metting VI HbA2... ·  · 2012-12-04DIAGNOSIS OF THE THALASSAEMIA SYNDROMES: MEASUREMENT OF HAEMOGLOBIN

DIAGNOSIS OF THE THALASSAEMIA SYNDROMES: …users.unimi.it/barb/public/UploadAttach/metting VI HbA2... ·  · 2012-12-04DIAGNOSIS OF THE THALASSAEMIA SYNDROMES: MEASUREMENT OF HAEMOGLOBIN

Conditional deletion of AP-2β in mouse cranial neural crest …dmm.biologists.org/content/dmm/9/8/849.full.pdf · deletion of Tfap2b in NCCs resulted in post-natal ocular defects

Conditional deletion of AP-2β in mouse cranial neural crest …dmm.biologists.org/content/dmm/9/8/849.full.pdf · deletion of Tfap2b in NCCs resulted in post-natal ocular defects

Non-deletional alpha thalassaemia: a review · 2020. 6. 29. · thalassaemia. Keywords: α-Thalassaemia, Molecular basis, Non-deletional mutations, Genotype-phenotype correlation

Non-deletional alpha thalassaemia: a review · 2020. 6. 29. · thalassaemia. Keywords: α-Thalassaemia, Molecular basis, Non-deletional mutations, Genotype-phenotype correlation

DNase I hypersensitivity in the γ globin gene locus of K562 cells

DNase I hypersensitivity in the γ globin gene locus of K562 cells

-globin subunits for hemoglobin synthesis · to the α thalassemia silent carrier strain, termed α-globin*α/αα, which lacks 1 of 4 α- globin genes and exhibits minimal erythroid

-globin subunits for hemoglobin synthesis · to the α thalassemia silent carrier strain, termed α-globin*α/αα, which lacks 1 of 4 α- globin genes and exhibits minimal erythroid

Haemoglobinopathies A group of genetic disorders of Hb synthesis characterized by either a reduction of the rate of synthesis of globin chains ( Thalassaemias.

Haemoglobinopathies A group of genetic disorders of Hb synthesis characterized by either a reduction of the rate of synthesis of globin chains ( Thalassaemias.

1 Genetics and Biosynthesis of Human Hemoglobin The α-like globin genes The β-like genes.

1 Genetics and Biosynthesis of Human Hemoglobin The α-like globin genes The β-like genes.

Francis Brown, CNRS (Institut de Math´ematiques de Jussieu ...brown/Amplitudes2012.pdf · By contraction-deletion, the polynomials Ψ1,1 and Ψ1 are linear in the next variable,

Francis Brown, CNRS (Institut de Math´ematiques de Jussieu ...brown/Amplitudes2012.pdf · By contraction-deletion, the polynomials Ψ1,1 and Ψ1 are linear in the next variable,

Alpha Thalassaemia

Alpha Thalassaemia

Alfa thalassaemia

Alfa thalassaemia

Hepatic deletion of SIRT1 decreases HNF1α/FXR signaling and ...

Hepatic deletion of SIRT1 decreases HNF1α/FXR signaling and ...

Deletion of GSK-3β in mice leads to hypertrophic ...dm5migu4zj3pb.cloudfront.net/manuscripts/36000/36245/JCI083624… · The hypertrophic myopathy was caused by cardio-myocyte hyperproliferation

Deletion of GSK-3β in mice leads to hypertrophic ...dm5migu4zj3pb.cloudfront.net/manuscripts/36000/36245/JCI083624… · The hypertrophic myopathy was caused by cardio-myocyte hyperproliferation

Non-transfusion-dependent thalassemias - SAH · Hemoglobin Bart’s hydrops fetalis (α-thalassemia major) is caused by deletion of all four α-globin genes, and patients often die

Non-transfusion-dependent thalassemias - SAH · Hemoglobin Bart’s hydrops fetalis (α-thalassemia major) is caused by deletion of all four α-globin genes, and patients often die

BONE MARROW TRANSPLANTATION (BMT) in β-thalassaemia · This leaflet contains important information for β-thalassaemia patients on hematopoietic stem cell transplantation (HSCT),

BONE MARROW TRANSPLANTATION (BMT) in β-thalassaemia · This leaflet contains important information for β-thalassaemia patients on hematopoietic stem cell transplantation (HSCT),

Immunostick Test for Detecting ζ-Globin Chains and ...

Immunostick Test for Detecting ζ-Globin Chains and ...

RESEARCH ARTICLE Open Access Neuronal deletion of GSK3β … · 2017. 8. 29. · RESEARCH ARTICLE Open Access Neuronal deletion of GSK3β increases microtubule speed in the growth

RESEARCH ARTICLE Open Access Neuronal deletion of GSK3β … · 2017. 8. 29. · RESEARCH ARTICLE Open Access Neuronal deletion of GSK3β increases microtubule speed in the growth

In the name of God. A 23-years old β-thalassaemia major woman with resistant hypocalcemia.

In the name of God. A 23-years old β-thalassaemia major woman with resistant hypocalcemia.

Departmental seminar Genetic determinants of b-thalassaemia phenotype

Departmental seminar Genetic determinants of b-thalassaemia phenotype

5-17-2018 Deletion of Endo-β-1,4-Xylanase the Virulence of ...

5-17-2018 Deletion of Endo-β-1,4-Xylanase the Virulence of ...

Editing an α-globin enhancer in primary human ...repositorio.insa.pt/bitstream/10400.18/4791/1/Mettananda S et al... · ARTICLE Editing an α-globin enhancer in primary human hematopoietic

Editing an α-globin enhancer in primary human ...repositorio.insa.pt/bitstream/10400.18/4791/1/Mettananda S et al... · ARTICLE Editing an α-globin enhancer in primary human hematopoietic