Diamond-Blackfan anemia (DBA) is an inherited bone marrow failure syndrome associated with ribosomal protein (RP) gene mutations. Recent studies have also demonstrated an increased risk of cancer predisposition among DBA patients. In this study, we report the formation of soft tissue sarcoma in the Rpl5 and Rps24 heterozygous mice. Our observation suggests that even though one wild-type allele of the Rpl5 or Rps24 gene prevents anemia in these mice, it still predisposes them to cancer development
AbstractRhabdomyosarcoma (RMS) is the most common soft tissue sarcoma in children. Recent work prese...
MDM2, an E3 ubiquitin ligase, is an important negative regulator of tumor suppressor p53. In turn th...
Diamond-Blackfan anemia (DBA) is an inherited bone marrow failure syndrome characterized by anemia, ...
Diamond-Blackfan anemia (DBA) is characterized by anemia and cancer susceptibility and is caused by ...
SummaryDiamond-Blackfan anemia (DBA) is characterized by anemia and cancer susceptibility and is cau...
International audienceVariants in ribosomal protein (RP) genes drive Diamond-Blackfan anemia (DBA), ...
Diamond-Blackfan anemia (DBA), an inherited bone marrow failure syndrome characterized by anemia tha...
Diamond-Blackfan anemia (DBA), an inherited bone marrow failure syndrome characterized by anemia tha...
Diamond-Blackfan anemia (DBA) is a rare congenital bone marrow failure syndrome characterized by def...
Diamond-Blackfan anemia (DBA) is a congenital erythroid hypoplasia caused by a functional haploinsuf...
The ribosomal protein S19 (RPS19) is located in the small (40S) subunit and is one of 79 ribosomal p...
Diamond-Blackfan anemia (DBA) is a severe congenital anemia characterized by a defect in red blood c...
Diamond-Blackfan anemia (DBA) is a rare bone marrow failure syndrome accompanied by cardiovascular, ...
Ribosome dysfunction underlies the pathogenesis of many cancers and heritable ribosomopathies. Here,...
Defects in ribosome biogenesis are associated with a group of diseases called the ribosomopathies, o...
AbstractRhabdomyosarcoma (RMS) is the most common soft tissue sarcoma in children. Recent work prese...
MDM2, an E3 ubiquitin ligase, is an important negative regulator of tumor suppressor p53. In turn th...
Diamond-Blackfan anemia (DBA) is an inherited bone marrow failure syndrome characterized by anemia, ...
Diamond-Blackfan anemia (DBA) is characterized by anemia and cancer susceptibility and is caused by ...
SummaryDiamond-Blackfan anemia (DBA) is characterized by anemia and cancer susceptibility and is cau...
International audienceVariants in ribosomal protein (RP) genes drive Diamond-Blackfan anemia (DBA), ...
Diamond-Blackfan anemia (DBA), an inherited bone marrow failure syndrome characterized by anemia tha...
Diamond-Blackfan anemia (DBA), an inherited bone marrow failure syndrome characterized by anemia tha...
Diamond-Blackfan anemia (DBA) is a rare congenital bone marrow failure syndrome characterized by def...
Diamond-Blackfan anemia (DBA) is a congenital erythroid hypoplasia caused by a functional haploinsuf...
The ribosomal protein S19 (RPS19) is located in the small (40S) subunit and is one of 79 ribosomal p...
Diamond-Blackfan anemia (DBA) is a severe congenital anemia characterized by a defect in red blood c...
Diamond-Blackfan anemia (DBA) is a rare bone marrow failure syndrome accompanied by cardiovascular, ...
Ribosome dysfunction underlies the pathogenesis of many cancers and heritable ribosomopathies. Here,...
Defects in ribosome biogenesis are associated with a group of diseases called the ribosomopathies, o...
AbstractRhabdomyosarcoma (RMS) is the most common soft tissue sarcoma in children. Recent work prese...
MDM2, an E3 ubiquitin ligase, is an important negative regulator of tumor suppressor p53. In turn th...
Diamond-Blackfan anemia (DBA) is an inherited bone marrow failure syndrome characterized by anemia, ...