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)
Bone marrow cells from patients with Shwachman-Diamond syndrome abnormally express genes involved in ribosome biogenesis and RNA processing
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Shwachman-Diamond syndrome neutrophils have altered chemoattractant-induced F-actin polymerization and polarization characteristics
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HAEMATOLOGICA-THE HEMATOLOGY JOURNAL (2009)
Shwachman-Bodian Diamond syndrome is a multi-functional protein implicated in cellular stress responses
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JNK/c-Jun signaling mediates an anti-apoptotic effect of RANKL in osteoclasts
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JOURNAL OF BONE AND MINERAL RESEARCH (2008)
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JOURNAL OF CLINICAL INVESTIGATION (2008)
Bone remodeling: Multiple cellular interactions required for coupling of bone formation and resorption
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JOURNAL OF BONE AND MINERAL RESEARCH (2008)
The Shwachman-Bodian-Diamond syndrome associated protein interacts with HsNip7 and its down-regulation affects gene expression at the transcriptional and translational levels
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Rac1 and Rac2 differentially regulate actin free barbed end formation downstream of the fMLP receptor
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JOURNAL OF CELL BIOLOGY (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)
Cell-cell fusion
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FEBS LETTERS (2007)
The Shwachman-Bodian-Diamond syndrome protein mediates translational activation of ribosomes in yeast
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NATURE GENETICS (2007)
Shwachman-Diamond Syndrome is not necessary for the terminal maturation of neutrophils but is important for maintaining viability of granulocyte precursors
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EXPERIMENTAL HEMATOLOGY (2007)
Prevalence of oral diseases in Shwachman-Diamond syndrome
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Loss of the mouse ortholog of the Shwachman-Diamond syndrome gene (Sbds) results in early embryonic lethality
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MOLECULAR AND CELLULAR BIOLOGY (2006)
Molecular backgrounds of age-related osteoporosis from mouse genetics approaches
Hiroshi Kawaguchi
REVIEWS IN ENDOCRINE & METABOLIC DISORDERS (2006)
The Shwachman-Bodian-Diamond syndrome gene encodes an RNA-binding protein that localizes to the pseudopod of Dictyostelium amoebae during chemotaxis
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RANKL-RANK signaling in osteoclastogenesis and bone disease
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TRENDS IN MOLECULAR MEDICINE (2006)
The Shwachman-Diamond SBDS protein localizes to the nucleolus
KM Austin et al.
BLOOD (2005)
DC-STAMP is essential for cell-cell fusion in osteoclasts and foreign body giant cells
M Yagi et al.
JOURNAL OF EXPERIMENTAL MEDICINE (2005)
The Shwachman-Bodian-Diamond syndrome protein family is involved in RNA metabolism
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JOURNAL OF BIOLOGICAL CHEMISTRY (2005)
Rac2 regulates neutrophil chemotaxis, superoxide production, and myeloid colony formation through multiple distinct effector pathways
D Carstanjen et al.
JOURNAL OF IMMUNOLOGY (2005)
The chemotaxis defect of Shwachman-Diamond Syndrome leukocytes
V Stepanovic et al.
CELL MOTILITY AND THE CYTOSKELETON (2004)
Skeletal phenotype in patients with Shwachman-Diamond syndrome and mutations in SBDS
O Mäkitie et al.
CLINICAL GENETICS (2004)
RANKL-induced DC-STAMP is essential for osteoclastogenesis
T Kukita et al.
JOURNAL OF EXPERIMENTAL MEDICINE (2004)
Targeted expression of a dominant-negative N-cadherin in vivo delays peak bone mass and increases adipogenesis
CHM Castro et al.
JOURNAL OF CELL SCIENCE (2004)
Osteoclast differentiation and activation
WJ Boyle et al.
NATURE (2003)
Mutations in SBDS are associated with Shwachman-Diamond syndrome
GRB Boocock et al.
NATURE GENETICS (2003)
Transduction of TAT fusion proteins into osteoclasts and osteoblasts
S Dolgilevich et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2002)
Gene expression profiling of osteoclast differentiation by combined suppression subtractive hybridization (SSH) and cDNA microarray analysis
J Rho et al.
DNA AND CELL BIOLOGY (2002)
Human neutrophil immunodeficiency syndrome is associated with an inhibitory Rac2 mutation
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PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2000)
Segregation analysis in Shwachman-Diamond syndrome: Evidence for recessive inheritance
H Ginzberg et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2000)