Shwachman–Bodian–Diamond syndrome (SBDS) protein deficiency impairs translation re-initiation fromC/EBPαandC/EBPβmRNAs

eIF6 anti-association activity is required for ribosome biogenesis, translational control and tumor progression

(2015) Daniela Brina et al.   Biochimica et Biophysica Acta-Gene Regulatory Mechanisms

Deficiency in mTORC1-controlled C/EBP -mRNA translation improves metabolic health in mice

(2015) L. M. Zidek et al.   EMBO REPORTS

Deficiency of the ribosome biogenesis gene Sbds in hematopoietic stem and progenitor cells causes neutropenia in mice by attenuating lineage progression in myelocytes

(2015) N. A. Zambetti et al.   HAEMATOLOGICA

In Vivo Senescence in the Sbds-Deficient Murine Pancreas: Cell-Type Specific Consequences of Translation Insufficiency

(2015) Marina E. Tourlakis et al.   PLoS Genetics

Deficiency of the ribosome biogenesis gene Sbds in hematopoietic stem and progenitor cells causes neutropenia in mice by attenuating lineage progression in myelocytes

(2015) N. A. Zambetti et al.   HAEMATOLOGICA

DENR–MCT-1 promotes translation re-initiation downstream of uORFs to control tissue growth

(2014) Sibylle Schleich et al.   NATURE

TOR and S6K1 promote translation reinitiation of uORF-containing mRNAs via phosphorylation of eIF3h

(2013) Mikhail Schepetilnikov et al.   EMBO JOURNAL

Impaired ribosomal subunit association in Shwachman-Diamond syndrome

(2012) N. Burwick et al.   BLOOD

Draft consensus guidelines for diagnosis and treatment of Shwachman-Diamond syndrome

(2011) Yigal Dror et al.   Annals of the New York Academy of Sciences

The ribosome-related protein, SBDS, is critical for normal erythropoiesis

(2011) S. Sen et al.   BLOOD

Defective ribosome assembly in Shwachman-Diamond syndrome

(2011) C. C. Wong et al.   BLOOD

Uncoupling of GTP hydrolysis from eIF6 release on the ribosome causes Shwachman-Diamond syndrome

(2011) A. J. Finch et al.   GENES & DEVELOPMENT

Sbds is required for Rac2-mediated monocyte migration and signaling downstream of RANK during osteoclastogenesis

(2010) R. Leung et al.   BLOOD

Ribosomopathies: human disorders of ribosome dysfunction

(2010) A. Narla et al.   BLOOD

Nucleolar retention of a translational C/EBPα isoform stimulates rDNA transcription and cell size

(2010) Christine Müller et al.   EMBO JOURNAL

C/EBP  uORF mice--a genetic model for uORF-mediated translational control in mammals

(2010) K. Wethmar et al.   GENES & DEVELOPMENT

The Role of ABCE1 in Eukaryotic Posttermination Ribosomal Recycling

(2010) Andrey V. Pisarev et al.   MOLECULAR CELL

Hematopoietic Stem Cell Expansion Precedes the Generation of Committed Myeloid Leukemia-Initiating Cells in C/EBPα Mutant AML

(2009) Oxana Bereshchenko et al.   CANCER CELL

The Cell Cycle and Myc Intersect with Mechanisms that Regulate Pluripotency and Reprogramming

(2009) Amar M. Singh et al.   Cell Stem Cell

Shwachman-Bodian Diamond syndrome is a multi-functional protein implicated in cellular stress responses

(2009) Heather L. Ball et al.   HUMAN MOLECULAR GENETICS

SBDS Expression and Localization at the Mitotic Spindle in Human Myeloid Progenitors

(2009) Claudia Orelio et al.   PLoS One

Modeling of C/EBPα Mutant Acute Myeloid Leukemia Reveals a Common Expression Signature of Committed Myeloid Leukemia-Initiating Cells

(2008) Peggy Kirstetter et al.   CANCER CELL

SBDS-deficient cells undergo accelerated apoptosis through the Fas-pathway

(2008) P. Rujkijyanont et al.   HAEMATOLOGICA

Mitotic spindle destabilization and genomic instability in Shwachman-Diamond syndrome

(2008) Karyn M. Austin et al.   JOURNAL OF CLINICAL INVESTIGATION

Dysregulation of the C/EBPα Differentiation Pathway in Human Cancer

(2008) Steffen Koschmieder et al.   JOURNAL OF CLINICAL ONCOLOGY

AGC kinases regulate phosphorylation and activation of eukaryotic translation initiation factor 4B

(2008) A G M van Gorp et al.   ONCOGENE