Shwachman-Bodian-Diamond syndrome is an autosomal recessive genetic syndrome with pleiotropic phenotypes, including pancreatic deficiencies, bone marrow dysfunctions with increased risk of myelodysplasia or leukemia, and skeletal abnormalities. This syndrome has been associated with mutations in the SBDS gene, which encodes a conserved protein showing orthologs in Archaea and eukaryotes. The Shwachman-Bodian-Diamond syndrome pleiotropic phenotypes may be an indication of different cell type requirements for a fully functional SBDS protein. RNA-binding activity has been predicted for archaeal and yeast SBDS orthologs, with the latter also being implicated in ribosome biogenesis. However, full-length SBDS orthologs function in a species-speci...
Shwachman-Diamond Syndrome (SDS) is an autosomal recessive disorder whose patients present mutations...
Mutations that target the ubiquitous process of ribosome assembly paradoxically cause diverse tissue...
Shwachman-Diamond syndrome (SDS) is an autosomal recessive disease characterized by growth retardati...
Shwachman-Bodian-Diamond syndrome is an autosomal recessive genetic syndrome with pleiotropic phenot...
RIGHTS : This article is licensed under the BioMed Central licence at http://www.biomedcentral.com/...
This is a freely-available open access publication. Please cite the published version which is avail...
The functional correlation of missense mutations which cause disease remains a challenge to understa...
The Shwachman-Bodian-Diamond syndrome (SDS) is an autosomal disorder with pleiotropic phenotypes inc...
Olga VasievaInstitute of Integrative Biology, University of Liverpool, Liverpool, United Kingdom; Fe...
AbstractThe Shwachman–Bodian–Diamond syndrome (SBDS) protein family occurs widely in nature, althoug...
The Shwachman-Diamond Syndrome (SDS) is a disorder arising from mutations in the genes encoding for ...
Shwachman-Diamond Syndrome (SDS) is a rare inherited disease caused by mutations in the SBDS gene. H...
Shwachman-Diamond Syndrome (SDS) is a rare inherited disease caused by mutations in the SBDS gene. H...
BACKGROUND: Shwachman-Diamond syndrome (SDS) is an autosomal recessive ribosomopathy caused mainly b...
Background: Shwachman-Diamond Syndrome (SDS) is a hereditary disease caused by mutations in the SBDS...
Shwachman-Diamond Syndrome (SDS) is an autosomal recessive disorder whose patients present mutations...
Mutations that target the ubiquitous process of ribosome assembly paradoxically cause diverse tissue...
Shwachman-Diamond syndrome (SDS) is an autosomal recessive disease characterized by growth retardati...
Shwachman-Bodian-Diamond syndrome is an autosomal recessive genetic syndrome with pleiotropic phenot...
RIGHTS : This article is licensed under the BioMed Central licence at http://www.biomedcentral.com/...
This is a freely-available open access publication. Please cite the published version which is avail...
The functional correlation of missense mutations which cause disease remains a challenge to understa...
The Shwachman-Bodian-Diamond syndrome (SDS) is an autosomal disorder with pleiotropic phenotypes inc...
Olga VasievaInstitute of Integrative Biology, University of Liverpool, Liverpool, United Kingdom; Fe...
AbstractThe Shwachman–Bodian–Diamond syndrome (SBDS) protein family occurs widely in nature, althoug...
The Shwachman-Diamond Syndrome (SDS) is a disorder arising from mutations in the genes encoding for ...
Shwachman-Diamond Syndrome (SDS) is a rare inherited disease caused by mutations in the SBDS gene. H...
Shwachman-Diamond Syndrome (SDS) is a rare inherited disease caused by mutations in the SBDS gene. H...
BACKGROUND: Shwachman-Diamond syndrome (SDS) is an autosomal recessive ribosomopathy caused mainly b...
Background: Shwachman-Diamond Syndrome (SDS) is a hereditary disease caused by mutations in the SBDS...
Shwachman-Diamond Syndrome (SDS) is an autosomal recessive disorder whose patients present mutations...
Mutations that target the ubiquitous process of ribosome assembly paradoxically cause diverse tissue...
Shwachman-Diamond syndrome (SDS) is an autosomal recessive disease characterized by growth retardati...