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Comparing the two leading erythroid lines BEL-A and HUDEP-2

Haematologica (Roma), 2020-08, Vol.105 (8), p.e389

2020

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Disruption of the tumour-associated EMP3 enhances erythroid proliferation and causes the MAM-negative phenotype

Nature communications, 2020-07, Vol.11 (1), p.3569-3569, Article 3569

2020

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Induction of adult levels of β-globin in human erythroid cells that intrinsically express embryonic or fetal globin by transduction with KLF1 and BCL11A-XL

Haematologica (Roma), 2014-11, Vol.99 (11), p.1677

2014

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Mutations in EKLF/KLF1 form the molecular basis of the rare blood group In(Lu) phenotype

Blood, 2008-09, Vol.112 (5), p.2081-2088

2008

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Mutations in the second zinc finger of human EKLF reduce promoter affinity but give rise to benign and disease phenotypes

Blood, 2011-09, Vol.118 (11), p.3137-3145

2011

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Blood group type A secretors are associated with a higher risk of COVID‐19 cardiovascular disease complications

EJHaem, 2021-05, Vol.2 (2), p.175-187

2021

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Autophagy facilitates organelle clearance during differentiation of human erythroblasts: Evidence for a role for ATG4 paralogs during autophagosome maturation

Autophagy, 2013-06, Vol.9 (6), p.881-893

2013

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Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approach

Nature genetics, 2011-04, Vol.43 (4), p.295-301

2011

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Blood group phenotypes resulting from mutations in erythroid transcription factors

Current opinion in hematology, 2012-11, Vol.19 (6), p.486-493

2012

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A novel GATA1 mutation (Stop414Arg) in a family with the rare X‐linked blood group Lu(a‐b‐) phenotype and mild macrothrombocytic thrombocytopenia

British journal of haematology, 2013-04, Vol.161 (1), p.139-142

2013

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New mutations in C1GALT1C1 in individuals with Tn positive phenotype

British journal of haematology, 2008-08, Vol.142 (4), p.657-667

2008

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Clustered DNA damage leads to complex genetic changes in irradiated human cells

Cancer research (Chicago, Ill.), 2002-11, Vol.62 (21), p.6263-6269

2002

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McLeod syndrome resulting from a novel XK mutation

British journal of haematology, 2003-08, Vol.122 (4), p.682-685

2003

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Ex vivo Engineering of Red Blood Cells

Blood, 2019-11, Vol.134 (Supplement_1), p.SCI-5-SCI-5

2019

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Characterization and evolutionary origin of novel C 2 H 2 zinc finger protein (ZNF648) required for both erythroid and megakaryocyte differentiation in humans

Haematologica (Roma), 2021-11, Vol.106 (11), p.2859

2021

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The presence of an RHD pseudogene containing a 37 base pair duplication and a nonsense mutation in Africans with the Rh D-negative blood group phenotype

Blood, 2000, Vol.95 (1), p.12-18

2000

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A novel GATA 1 mutation ( S top414 A rg) in a family with the rare X ‐linked blood group L u(a‐b‐) phenotype and mild macrothrombocytic thrombocytopenia

British journal of haematology, 2013-04, Vol.161 (1), p.139-142

2013

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Combined immunodeficiency associated with increased apoptosis of lymphocytes and radiosensitivity of fibroblasts

Cancer research (Chicago, Ill.), 1999-07, Vol.59 (14), p.3454-3460

1999

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A Novel GATA1 Mutation (Ter414Arg) in a Family with the Rare X-Linked Blood Group Lu(a-b-) Phenotype

Blood, 2009-11, Vol.114 (22), p.1979-1979

2009

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A Novel EKLF Mutation in a Patient with Dyserythropoietic Anemia: The First Association of EKLF with Disease in Man

Blood, 2009-11, Vol.114 (22), p.162-162

2009

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C1GALT1C1 (COSMC) Mutations in Four Individuals with Tn+ Phenotype

Blood, 2007-11, Vol.110 (11), p.1727-1727

2007

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Mutations in EKLFIKLF1 form the molecular basis of the rare blood group In(Lu) phenotype. Commentary

Blood, 2008, Vol.112 (5)

2008

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McLeod syndrome resulting from a novel XK mutation

British journal of haematology, 2003-08, Vol.122 (4), p.682

2003

Volltextzugriff (PDF)

The presence of an RHD pseudogene containing a 37 base pair duplication and a nonsense mutation in Africans with the Rh D-negative blood group phenotype

Blood, 2000-01, Vol.95 (1), p.12-18

2000

Volltextzugriff (PDF)

A novel GATA1 mutation (Stop414Arg) in a family with the rare X-linked blood group Lu(a-b-) phenotype and mild macrothrombocytic thrombocytopenia

British journal of haematology, 2013, Vol.161 (1), p.139-142

2013

Volltextzugriff (PDF)

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Comparing the two leading erythroid lines BEL-A and HUDEP-2

Disruption of the tumour-associated EMP3 enhances erythroid proliferation and causes the MAM-negative phenotype

Induction of adult levels of β-globin in human erythroid cells that intrinsically express embryonic or fetal globin by transduction with KLF1 and BCL11A-XL

Mutations in EKLF/KLF1 form the molecular basis of the rare blood group In(Lu) phenotype

Mutations in the second zinc finger of human EKLF reduce promoter affinity but give rise to benign and disease phenotypes

Blood group type A secretors are associated with a higher risk of COVID‐19 cardiovascular disease complications

Autophagy facilitates organelle clearance during differentiation of human erythroblasts: Evidence for a role for ATG4 paralogs during autophagosome maturation

Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approach

Blood group phenotypes resulting from mutations in erythroid transcription factors

A novel GATA1 mutation (Stop414Arg) in a family with the rare X‐linked blood group Lu(a‐b‐) phenotype and mild macrothrombocytic thrombocytopenia

New mutations in C1GALT1C1 in individuals with Tn positive phenotype

Clustered DNA damage leads to complex genetic changes in irradiated human cells

McLeod syndrome resulting from a novel XK mutation

Ex vivo Engineering of Red Blood Cells

Characterization and evolutionary origin of novel C 2 H 2 zinc finger protein (ZNF648) required for both erythroid and megakaryocyte differentiation in humans

The presence of an RHD pseudogene containing a 37 base pair duplication and a nonsense mutation in Africans with the Rh D-negative blood group phenotype

A novel GATA 1 mutation ( S top414 A rg) in a family with the rare X ‐linked blood group L u(a‐b‐) phenotype and mild macrothrombocytic thrombocytopenia

Combined immunodeficiency associated with increased apoptosis of lymphocytes and radiosensitivity of fibroblasts

A Novel GATA1 Mutation (Ter414Arg) in a Family with the Rare X-Linked Blood Group Lu(a-b-) Phenotype

A Novel EKLF Mutation in a Patient with Dyserythropoietic Anemia: The First Association of EKLF with Disease in Man

C1GALT1C1 (COSMC) Mutations in Four Individuals with Tn+ Phenotype

Mutations in EKLFIKLF1 form the molecular basis of the rare blood group In(Lu) phenotype. Commentary

McLeod syndrome resulting from a novel XK mutation

The presence of an RHD pseudogene containing a 37 base pair duplication and a nonsense mutation in Africans with the Rh D-negative blood group phenotype

A novel GATA1 mutation (Stop414Arg) in a family with the rare X-linked blood group Lu(a-b-) phenotype and mild macrothrombocytic thrombocytopenia

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