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Mitoferrin is essential for erythroid iron assimilation

Nature, 2006-03, Vol.440 (7080), p.96-100

2006

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Differential effects of RASA3 mutations on hematopoiesis are profoundly influenced by genetic background and molecular variant

PLoS genetics, 2020-12, Vol.16 (12), p.e1008857-e1008857

2020

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Absence of Erythroblast Macrophage Protein (Emp) Leads to Failure of Erythroblast Nuclear Extrusion

The Journal of biological chemistry, 2006-07, Vol.281 (29), p.20181-20189

2006

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Targeted deletion of βIII spectrin impairs synaptogenesis and generates ataxic and seizure phenotypes

Proceedings of the National Academy of Sciences - PNAS, 2010-03, Vol.107 (13), p.6022-6027

2010

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Critical function for the Ras-GTPase activating protein RASA3 in vertebrate erythropoiesis and megakaryopoiesis

Proceedings of the National Academy of Sciences - PNAS, 2012-07, Vol.109 (30), p.12099-12104

2012

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Identification of Distal cis-Regulatory Elements at Mouse Mitoferrin Loci Using Zebrafish Transgenesis

Molecular and Cellular Biology, 2011-04, Vol.31 (7), p.1344-1356

2011

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Targeted Disruption of the β Adducin Gene (Add2) Causes Red Blood Cell Spherocytosis in Mice

Proceedings of the National Academy of Sciences - PNAS, 1999-09, Vol.96 (19), p.10717-10722

1999

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Reduced pigmentation (rp), a mouse model of Hermansky-Pudlak syndrome, encodes a novel component of the BLOC-1 complex

Blood, 2004-11, Vol.104 (10), p.3181-3189

2004

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Mild spherocytosis and altered red cell ion transport in protein 4.2–null mice

The Journal of clinical investigation, 1999-06, Vol.103 (11), p.1527-1537

1999

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Reversal of pathology in murine mucopolysaccharidosis type VII by somatic cell gene transfer

Nature (London), 1992-12, Vol.360 (6406), p.749-753

1992

Volltextzugriff (PDF)

Intracisternal A-Particle Element Transposition into the Murine β-Glucuronidase Gene Correlates with Loss of Enzyme Activity: a New Model for β-Glucuronidase Deficiency in the C3H Mouse

Molecular and Cellular Biology, 1998-11, Vol.18 (11), p.6474-6481

1998

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Defects in the cappuccino (cno) gene on mouse chromosome 5 and human 4p cause Hermansky-Pudlak syndrome by an AP-3–independent mechanism

Blood, 2000-12, Vol.96 (13), p.4227-4235

2000

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TMEM14C is required for erythroid mitochondrial heme metabolism

The Journal of clinical investigation, 2014-10, Vol.124 (10), p.4294-4304

2014

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Failure of Erythropoiesis and Megakaryocytopoiesis in RASA3 Mutant Scat Mice

Blood, 2011-11, Vol.118 (21), p.680-680

2011

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Iron Regulatory Protein-1 Protects against Mitoferrin-1-deficient Porphyria

The Journal of biological chemistry, 2014-03, Vol.289 (11), p.7835-7843

2014

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Targeted deletion of α-adducin results in absent β- and γ-adducin, compensated hemolytic anemia, and lethal hydrocephalus in mice

Blood, 2008-11, Vol.112 (10), p.4298-4307

2008

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Downeast Anemia (dea), a New Mouse Model of Severe Nonspherocytic Hemolytic Anemia Caused by Hexokinase (HKI) Deficiency

Blood cells, molecules, & diseases, 2001-09, Vol.27 (5), p.850-860

2001

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Tmem14c Plays An Essential Role In Mitochondrial Heme Metabolism

Blood, 2013-11, Vol.122 (21), p.427-427

2013

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Iron regulatory protein-1 protects against mitoferrin-1-deficient porphyria

The Journal of biological chemistry, 2014-05, Vol.289 (20), p.13707-13707

2014

Volltextzugriff (PDF)

Cappuccino, a mouse model of Hermansky-Pudlak syndrome, encodes a novel protein that is part of the pallidin-muted complex (BLOC-1)

Blood, 2003-06, Vol.101 (11), p.4402-4407

2003

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Cell-specific mitotic defect and dyserythropoiesis associated with erythroid band 3 deficiency

Nature genetics, 2003-05, Vol.34 (1), p.59-64

2003

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Targeted deletion of [beta]III spectrin impairs synaptogenesis and generates ataxic and seizure phenotypes

Proceedings of the National Academy of Sciences - PNAS, 2010-03, Vol.107 (13), p.6022

2010

Volltextzugriff (PDF)

Positional Cloning of the Mouse Scat Mutation Reveals a Critical Role for RASA3, a Ras GTPase Activating Protein, in Vertebrate Erythropoiesis

Blood, 2009-11, Vol.114 (22), p.776-776

2009

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A mouse TRAPP-related protein is involved in pigmentation

Genomics (San Diego, Calif.), 2006-08, Vol.88 (2), p.196-203

2006

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Targeted Deletion of α-Adducin Results in Absent β-Adducin, Compensated Hemolytic Anemia, and Hydrocephalus in Mice

Blood, 2007-11, Vol.110 (11), p.141-141

2007

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Mitoferrin is essential for erythroid iron assimilation

Differential effects of RASA3 mutations on hematopoiesis are profoundly influenced by genetic background and molecular variant

Absence of Erythroblast Macrophage Protein (Emp) Leads to Failure of Erythroblast Nuclear Extrusion

Targeted deletion of βIII spectrin impairs synaptogenesis and generates ataxic and seizure phenotypes

Critical function for the Ras-GTPase activating protein RASA3 in vertebrate erythropoiesis and megakaryopoiesis

Identification of Distal cis-Regulatory Elements at Mouse Mitoferrin Loci Using Zebrafish Transgenesis

Targeted Disruption of the β Adducin Gene (Add2) Causes Red Blood Cell Spherocytosis in Mice

Reduced pigmentation (rp), a mouse model of Hermansky-Pudlak syndrome, encodes a novel component of the BLOC-1 complex

Mild spherocytosis and altered red cell ion transport in protein 4.2–null mice

Reversal of pathology in murine mucopolysaccharidosis type VII by somatic cell gene transfer

Intracisternal A-Particle Element Transposition into the Murine β-Glucuronidase Gene Correlates with Loss of Enzyme Activity: a New Model for β-Glucuronidase Deficiency in the C3H Mouse

Defects in the cappuccino (cno) gene on mouse chromosome 5 and human 4p cause Hermansky-Pudlak syndrome by an AP-3–independent mechanism

TMEM14C is required for erythroid mitochondrial heme metabolism

Failure of Erythropoiesis and Megakaryocytopoiesis in RASA3 Mutant Scat Mice

Iron Regulatory Protein-1 Protects against Mitoferrin-1-deficient Porphyria

Targeted deletion of α-adducin results in absent β- and γ-adducin, compensated hemolytic anemia, and lethal hydrocephalus in mice

Downeast Anemia (dea), a New Mouse Model of Severe Nonspherocytic Hemolytic Anemia Caused by Hexokinase (HKI) Deficiency

Tmem14c Plays An Essential Role In Mitochondrial Heme Metabolism

Iron regulatory protein-1 protects against mitoferrin-1-deficient porphyria

Cappuccino, a mouse model of Hermansky-Pudlak syndrome, encodes a novel protein that is part of the pallidin-muted complex (BLOC-1)

Cell-specific mitotic defect and dyserythropoiesis associated with erythroid band 3 deficiency

Targeted deletion of [beta]III spectrin impairs synaptogenesis and generates ataxic and seizure phenotypes

Positional Cloning of the Mouse Scat Mutation Reveals a Critical Role for RASA3, a Ras GTPase Activating Protein, in Vertebrate Erythropoiesis

A mouse TRAPP-related protein is involved in pigmentation

Targeted Deletion of α-Adducin Results in Absent β-Adducin, Compensated Hemolytic Anemia, and Hydrocephalus in Mice

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