Nrf2 expands the intracellular pool of the chaperone AHSP in a cellular model of β-thalassemia

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(2021) Ali T. Taher et al.   NEW ENGLAND JOURNAL OF MEDICINE

The Molecular Mechanisms Regulating the KEAP1-NRF2 Pathway

(2020) Liam Baird et al.   MOLECULAR AND CELLULAR BIOLOGY

Reactive oxygen species (ROS) as pleiotropic physiological signalling agents

(2020) Helmut Sies et al.   NATURE REVIEWS MOLECULAR CELL BIOLOGY

NRF2 activation promotes aggressive lung cancer and associates with poor clinical outcomes

(2020) Anju Singh et al.   CLINICAL CANCER RESEARCH

Hemolysis transforms liver macrophages into antiinflammatory erythrophagocytes

(2020) Marc Pfefferlé et al.   JOURNAL OF CLINICAL INVESTIGATION

Abnormal red blood cell morphological changes in thalassaemia associated with iron overload and oxidative stress

(2019) Pornthip Chaichompoo et al.   JOURNAL OF CLINICAL PATHOLOGY

Association of alpha hemoglobin–stabilizing protein (AHSP) gene mutation and disease severity among HbE—beta thalassemia patients

(2019) Rudra Ray et al.   ANNALS OF HEMATOLOGY

CPUY192018, a potent inhibitor of the Keap1-Nrf2 protein-protein interaction, alleviates renal inflammation in mice by restricting oxidative stress and NF-κB activation

(2019) Meng-Chen Lu et al.   Redox Biology

Prediction of potent shRNAs with a sequential classification algorithm

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Oxidative stress in β-thalassaemia and sickle cell disease

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Multistage Mass Spectrometric Analysis of Human Hemoglobin Glutathionylation: Correlation with Cigarette Smoking

(2014) Hauh-Jyun Candy Chen et al.   CHEMICAL RESEARCH IN TOXICOLOGY

The α-Thalassemias

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Quantitative analysis of murine terminal erythroid differentiation in vivo: novel method to study normal and disordered erythropoiesis

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α-Hemoglobin-stabilizing Protein (AHSP) Perturbs the Proximal Heme Pocket of Oxy-α-hemoglobin and Weakens the Iron-Oxygen Bond

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Insights into Hemoglobin Assembly throughin VivoMutagenesis of α-Hemoglobin Stabilizing Protein

(2012) Eugene Khandros et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Kinetics of α-Globin Binding to α-Hemoglobin Stabilizing Protein (AHSP) Indicate Preferential Stabilization of Hemichrome Folding Intermediate

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An integrated encyclopedia of DNA elements in the human genome

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Nrf2–MafG heterodimers contribute globally to antioxidant and metabolic networks

(2012) Yosuke Hirotsu et al.   NUCLEIC ACIDS RESEARCH

Altered Vascular Function, Arterial Stiffness, and Antioxidant Gene Responses in Pediatric Thalassemia Patients

(2012) Pantipa Detchaporn et al.   PEDIATRIC CARDIOLOGY

 -thalassemia: a model for elucidating the dynamic regulation of ineffective erythropoiesis and iron metabolism

(2011) Y. Ginzburg et al.   BLOOD

α-Haemoglobin stabilising protein expression is influenced by mean cell haemoglobin and HbF levels in HbE/β-thalassaemia individuals

(2011) Wai Feng Lim et al.   BLOOD CELLS MOLECULES AND DISEASES

Transgenic Human α-Hemoglobin Stabilizing Protein Could Partially Relieve βIVS-2-654-Thalassemia Syndrome in Model Mice

(2010) Baobin Wang et al.   HUMAN GENE THERAPY

Forward genetics inCandida albicansthat reveals the Arp2/3 complex is required for hyphal formation, but not endocytosis

(2010) Elias Epp et al.   MOLECULAR MICROBIOLOGY

Differential regulation of redox proteins and chaperones in HbEβ-thalassemia erythrocyte proteome

(2010) Dipankar Bhattacharya et al.   Proteomics Clinical Applications

Stress-Activated Cap'n'collar Transcription Factors in Aging and Human Disease

(2010) G. P. Sykiotis et al.   Science Signaling

Nrf2:INrf2 (Keap1) signaling in oxidative stress

(2009) James W. Kaspar et al.   FREE RADICAL BIOLOGY AND MEDICINE

Oxidative Stress in the Regulation of Normal and Neoplastic Hematopoiesis

(2008) Saghi Ghaffari   ANTIOXIDANTS & REDOX SIGNALING

A novel transgenic mouse model produced from lentiviral germline integration for the study of  -thalassemia gene therapy

(2008) W. Li et al.   HAEMATOLOGICA

An Iron Responsive Element-like Stem-Loop Regulates α-Hemoglobin-stabilizing Protein mRNA

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