Related references
Note: Only part of the references are listed.Depletion of the Shwachman-Diamond syndrome gene product, SBDS, leads to growth inhibition and increased expression of OPG and VEGF-A
Abdallah Nihrane et al.
BLOOD CELLS MOLECULES AND DISEASES (2009)
The route to development of myelodysplastic syndrome/acute myeloid leukaemia in Shwachman-Diamond syndrome: the role of ageing, karyotype instability, and acquired chromosome anomalies
Emanuela Maserati et al.
BRITISH JOURNAL OF HAEMATOLOGY (2009)
Comparative Temporal Proteomics of a Response Regulator (SO2426)-Deficient Strain and Wild-Type Shewanella oneidensis MR-1 During Chromate Transformation
Karuna Chourey et al.
JOURNAL OF PROTEOME RESEARCH (2009)
Inhibition of endoplasmic reticulum stress-induced apoptosis of melanoma cells by the ARC protein
Li Hua Chen et al.
CANCER RESEARCH (2008)
SBDS-deficient cells undergo accelerated apoptosis through the Fas-pathway
Piya Rujkijyanont et al.
HAEMATOLOGICA (2008)
Mitotic spindle destabilization and genomic instability in Shwachman-Diamond syndrome
Karyn M. Austin et al.
JOURNAL OF CLINICAL INVESTIGATION (2008)
The Shwachman-Bodian-Diamond syndrome associated protein interacts with HsNip7 and its down-regulation affects gene expression at the transcriptional and translational levels
Cedric Hesling et al.
EXPERIMENTAL CELL RESEARCH (2007)
Lentiviral-mediated RNAi inhibition of Sbds in murine hematopoietic progenitors impairs their hematopoietic potential
Amy S. Rawls et al.
BLOOD (2007)
The human Shwachman-Diamond syndrome protein, SBDS, associates with ribosomal RNA
Karthik A. Ganapathi et al.
BLOOD (2007)
Signal integration in the endoplasmic reticulum unfolded protein response
David Ron et al.
NATURE REVIEWS MOLECULAR CELL BIOLOGY (2007)
The Shwachman-Bodian-Diamond syndrome protein mediates translational activation of ribosomes in yeast
Tobias F. Menne et al.
NATURE GENETICS (2007)
Shwachman-Diamond Syndrome is not necessary for the terminal maturation of neutrophils but is important for maintaining viability of granulocyte precursors
Masafumi Yamaguchi et al.
EXPERIMENTAL HEMATOLOGY (2007)
Severe Shwachman-Diamond syndrome phenotype caused by compound heterozygous missense mutations in the SBDS gene
Melinda Erdos et al.
EXPERIMENTAL HEMATOLOGY (2006)
Loss of the mouse ortholog of the Shwachman-Diamond syndrome gene (Sbds) results in early embryonic lethality
Siyi Zhang et al.
MOLECULAR AND CELLULAR BIOLOGY (2006)
Shwachman syndrome as mutator phenotype responsible for myeloid dysplasia/neoplasia through karyotype instability and chromosomes 7 and 20 anomalies
E Maserati et al.
GENES CHROMOSOMES & CANCER (2006)
Global landscape of protein complexes in the yeast Saccharomyces cerevisiae
NJ Krogan et al.
NATURE (2006)
The Shwachman-Diamond SBDS protein localizes to the nucleolus
KM Austin et al.
BLOOD (2005)
The Shwachman-Bodian-Diamond syndrome protein family is involved in RNA metabolism
A Savchenko et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2005)
Skeletal phenotype in patients with Shwachman-Diamond syndrome and mutations in SBDS
O Mäkitie et al.
CLINICAL GENETICS (2004)
PI 3-kinase related kinases: 'big' players in stress-induced signaling pathways
RT Abraham
DNA REPAIR (2004)
Release of eIF6 (p27BBP) from the 60S subunit allows 80S ribosome assembly
M Ceci et al.
NATURE (2003)
Disruption of the nucleolus mediates stabilization of p53 in response to DNA damage and other stresses
CP Rubbi et al.
EMBO JOURNAL (2003)
PANTHER: A library of protein families and subfamilies indexed by function
PD Thomas et al.
GENOME RESEARCH (2003)
Mutations in SBDS are associated with Shwachman-Diamond syndrome
GRB Boocock et al.
NATURE GENETICS (2003)
Cytoscape: A software environment for integrated models of biomolecular interaction networks
P Shannon et al.
GENOME RESEARCH (2003)
Clonal evolution in marrows of patients with Shwachman-Diamond syndrome: A prospective 5-year follow-up study
Y Dror et al.
EXPERIMENTAL HEMATOLOGY (2002)