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CDAN1 gene

Known as: DISCS LOST, DROSOPHILA, HOMOLOG OF, CODANIN 1, DLT 
This gene may be involved in nuclear membrane maintenance.
National Institutes of Health

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CDAN1 wt Allele
Codanin-1Congenital dyserythropoietic anemiaCongenital dyserythropoietic anemia, type ICongenital dyserythropoietic anemia, type II

Papers overview

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2017
2017
Longitudinal analysis of hepatic transcriptome and serum metabolome demonstrates altered lipid metabolism following the onset of hyperglycemia in spontaneously diabetic biobreeding rats
Type 1 diabetes is associated with abberations of fat metabolism before and after the clinical onset of disease. It has been… 
2017
2017
OC-045 Efficacy & safety of dose adjustment & delayed response to ustekinumab in moderate–severe crohn’s disease patients: results from im-uniti maintenance study
Introduction Ustekinumab (UST) induced/maintained clinical response (CR) and remission (CRM) in mod-severe Crohn’s disease (CD… 
2017
2017
Non-myeloablative allogeneic stem cell transplant with post-transplant cyclophosphamide cures the first adult patient with congenital dyserythropoietic anemia
Non-myeloablative allogeneic stem cell transplant with post-transplant cyclophosphamide cures the first adult patient with… 
2015
2015
Congenital Dyserythropoietic Anemia Type 1: A New Variant Pathogenic CDAN1 Mutation
Introduction: Congenital dyserythropoietic anemia (CDA) is a rare autosomal recessive condition that results in dyserythropoiesis… 
Review
2012
Review
2012
Methionine Restriction and Modification of Epithelial Tight Junction Barrier Function and Permeability
It is well known that caloric restriction leads to an increased longevity by forestalling age-related diseases. Dietary… 
2009
2009
Roles of DLT in fine modulation on brassinosteroid response in rice
Accumulated evidences suggest that brassinosteroid (BR) response is fine-tuned by multiple strategies. Recently, a GRAS protein… 
Review
2006
Review
2006
Linkage and mutational analysis of the CDAN1 gene reveals genetic heterogeneity in congenital dyserythropoietic anemia type I.
The congenital dyserythropoietic anemias (CDAs) are a heterogeneous group of genetic disorders of erythropoiesis characterized by… 
1993
1993
Hepatic removal of 125I‐DLT gelatin after burn injury: a model of soluble collagenous debris that interacts with plasma fibronectin
The decline of plasma fibronectin after surgery, trauma, and burn, as well as during severe sepsis after injury, appears to limit… 
1992
1992
Imaging of Thrombi With Tissue‐Type Plasminogen Activator Rendered Enzymatically Inactive and Conjugated to a Residualizing Label
BackgroundContemporary cardiovascular practice relies increasingly on thrombolysis as a therapeutic modality. Its optimal use… 
1988
1988
The sites of catabolism of murine monomeric IgA.
The tissue sites of monomeric IgA (mIgA) catabolism were determined in a BALB/c mouse model. Mouse mIgA myeloma proteins were… 
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