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Now showing items 1-20 of 36
A Nationwide Registry-Based Study on Mortality Due to Rare Congenital Anomalies
A new small supernumerary marker chromosome, generating mosaic pure trisomy 16q11.1-q12.1 in a healthy man
Age-associated hydroxymethylation in human bone-marrow mesenchymal stem cells
AKT and JUN are differentially activated in mesenchymal stem cells after infection with human and canine oncolytic adenoviruses.
Alpha-1 antitrypsin deficiency: outstanding questions and future directions
Alternative transcripts of the SERPINA1 gene in alpha-1 antitrypsin deficiency
c-Fos induces chondrogenic tumor formation in immortalized human mesenchymal progenitor cells
Characterization of Novel Missense Variants of SERPINA1 Gene Causing Alpha-1 Antitrypsin Deficiency.
Chronic fatigue syndrome: aetiology, diagnosis and treatment
Combination of single-photon emission computed tomography and magnetic resonance imaging to track 111in-oxine-labeled human mesenchymal stem cells in neuroblastoma-bearing mice.
DNA Methylomes Reveal Biological Networks Involved in Human Eye Development, Functions and Associated Disorders
Efficacy of ATR inhibitors as single agents in Ewing sarcoma
EWS-FLI1 confers exquisite sensitivity to NAMPT inhibition in Ewing sarcoma cells
EWS-FLI1-mediated suppression of the RAS-antagonist Sprouty 1 (SPRY1) confers aggressiveness to Ewing sarcoma
EWS/FLI1 Target Genes and Therapeutic Opportunities in Ewing Sarcoma
Expanding the genotypic and phenotypic spectrum of severe serine biosynthesis disorders.
Five new cases of syndromic intellectual disability due to KAT6A mutations: widening the molecular and clinical spectrum
Genome-wide profiling of non-smoking-related lung cancer cells reveals common RB1 rearrangements associated with histopathologic transformation in EGFR-mutant tumors.
H3K4me1 marks DNA regions hypomethylated during aging in human stem and differentiated cells.
Hedgehog Pathway Inhibition Hampers Sphere and Holoclone Formation in Rhabdomyosarcoma.