The Rothmund-Thomson syndrome helicase RECQL4 is essential for hematopoiesis

Genomic Instability Resulting from Blm Deficiency Compromises Development, Maintenance, and Function of the B Cell Lineage

(2014) H. Babbe et al.   JOURNAL OF IMMUNOLOGY

Bioinformatic analysis of RecQ4 helicases reveals the presence of a RQC domain and a Zn knuckle

(2013) Francesca Marino et al.   BIOPHYSICAL CHEMISTRY

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

(2013) J. Liu et al.   BLOOD

Clonal Analysis Unveils Self-Renewing Lineage-Restricted Progenitors Generated Directly from Hematopoietic Stem Cells

(2013) Ryo Yamamoto et al.   CELL

Deciphering Hematopoietic Stem Cells in Their Niches: A Critical Appraisal of Genetic Models, Lineage Tracing, and Imaging Strategies

(2013) Chacko Joseph et al.   Cell Stem Cell

Removal of myeloid cytokines from the cellular environment enhances T-cell development in vitro

(2013) Monique F. M. A. Smeets et al.   INTERNATIONAL IMMUNOLOGY

Platelet-biased stem cells reside at the apex of the haematopoietic stem-cell hierarchy

(2013) Alejandra Sanjuan-Pla et al.   NATURE

Fli-1 Overexpression in Hematopoietic Progenitors Deregulates T Cell Development and Induces Pre-T Cell Lymphoblastic Leukaemia/Lymphoma

(2013) Monique F. M. A. Smeets et al.   PLoS One

Titration of Four Replication Factors Is Essential for the Xenopus laevis Midblastula Transition

(2013) C. Collart et al.   SCIENCE

Diagnosis of acquired aplastic anemia

(2012) A Rovó et al.   BONE MARROW TRANSPLANTATION

The helicase domain and C-terminus of human RecQL4 facilitate replication elongation on DNA templates damaged by ionizing radiation

(2012) Masaoki Kohzaki et al.   CARCINOGENESIS

Bone Marrow Failure in Fanconi Anemia Is Triggered by an Exacerbated p53/p21 DNA Damage Response that Impairs Hematopoietic Stem and Progenitor Cells

(2012) Raphael Ceccaldi et al.   Cell Stem Cell

Cyclin D3 coordinates the cell cycle during differentiation to regulate erythrocyte size and number

(2012) V. G. Sankaran et al.   GENES & DEVELOPMENT

Molecular pathogenesis and clinical management of Fanconi anemia

(2012) Younghoon Kee et al.   JOURNAL OF CLINICAL INVESTIGATION

Granulomatous skin lesions complicating Varicella infection in a patient with Rothmund-Thomson syndrome and immune deficiency: case report

(2012) Lien De Somer et al.   Orphanet Journal of Rare Diseases

Gene Expression Commons: An Open Platform for Absolute Gene Expression Profiling

(2012) Jun Seita et al.   PLoS One

The N-terminal region of RECQL4 lacking the helicase domain is both essential and sufficient for the viability of vertebrate cells

(2011) Takuya Abe et al.   BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH

Erythropoietin couples erythropoiesis, B-lymphopoiesis, and bone homeostasis within the bone marrow microenvironment

(2011) S. Singbrant et al.   BLOOD

Therapy-related myelodysplasia in a patient with Rothmund-Thomson syndrome

(2011) Aaron M. Carlson et al.   EUROPEAN JOURNAL OF HAEMATOLOGY

Diagnosis and Management of Aplastic Anemia

(2011) E. C. Guinan   Hematology-American Society of Hematology Education Program

Conserved helicase domain of human RecQ4 is required for strand annealing-independent DNA unwinding

(2010) Marie L. Rossi et al.   DNA REPAIR

MCM10 mediates RECQ4 association with MCM2-7 helicase complex during DNA replication

(2009) Xiaohua Xu et al.   EMBO JOURNAL

Dual DNA unwinding activities of the Rothmund–Thomson syndrome protein, RECQ4

(2009) Xiaohua Xu et al.   EMBO JOURNAL

FANCM Connects the Genome Instability Disorders Bloom's Syndrome and Fanconi Anemia

(2009) Andrew J. Deans et al.   MOLECULAR CELL

Bone-marrow adipocytes as negative regulators of the haematopoietic microenvironment

(2009) Olaia Naveiras et al.   NATURE

Drosophila homologue of the Rothmund–Thomson syndrome gene: Essential function in DNA replication during development

(2008) Jianhong Wu et al.   DEVELOPMENTAL BIOLOGY

The mutation spectrum in RECQL4 diseases

(2008) H Annika Siitonen et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Rb intrinsically promotes erythropoiesis by coupling cell cycle exit with mitochondrial biogenesis

(2008) V. G. Sankaran et al.   GENES & DEVELOPMENT

Conditional mouse osteosarcoma, dependent on p53 loss and potentiated by loss of Rb, mimics the human disease

(2008) C. R. Walkley et al.   GENES & DEVELOPMENT

ADAR1 is essential for the maintenance of hematopoiesis and suppression of interferon signaling

(2008) Jochen C Hartner et al.   NATURE IMMUNOLOGY