202 papers found
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Antisense telomerase treatment: induction of two distinct pathways, apoptosis and differentiation
Loss of heterozygosity for the short arm of chromosome 7 in sporadic Wilms tumour
NB4S, a Member of the TBC1 Domain Family of Genes, is Truncated as a Result of a Constitutional t(1;10)(p22;q21) Chromosome Translocation in a Patient with Stage 4S Neuroblastoma
Targeted therapy of human malignant glioma in a mouse model by 2-5A antisense directed against telomerase RNA. Oncogene 16: 3323-30
A novel missense mutation in patients from a retinoblastoma pedigree showing only mild expression of the tumor phenotype
Inhibition of telomerase increases the susceptibility of human malignant glioblastoma cells to cisplatin-induced apoptosis
Characterization of the breakpoints in a t(8;13)(p11;q12) translocation from a patient with myeloproliferative disease using fluorescence in situ hybridization
Molecular characterization of the 1p22 breakpoint region spanning the constitutional translocation breakpoint in a neuroblastoma patient with a t(1;10)(p22;q21)
Molecular Characterization of the t(8; 13)(p11;q12) Translocation Associated With an Atypical Myeloproliferative Disorder: Evidence for Three Discrete Loci Involved in Myeloid Leukemias on 8p11
Direct isolation of human transcribed sequences from yeast artificial chromosomes through the application of RNA fingerprinting
Cloning of the human Gfi-1 gene and its mapping to chromosome region 1p22
Regional Localization of 192 Genic Markers on Human Chromosome 1
The Expression Pattern of Wilms' Tumour Gene (Wt1) Product in Normal Tissues and Paediatric Renal Tumours
Germline mutations in theRB1 gene in patients with hereditary retinoblastoma
A Yeast Artificial Chromosome Contig That Spans the RB1-D13S31 Interval on Human Chromosome 13 and Encompasses the Frequently Deleted Region in B-cell Chronic Lymphocytic Leukemia
Molecular characterization of a (1;10)(p22;q21) constitutional translocation from a patient with neuroblastoma
Integration of the Physical and Genetic Linkage Map for Human Chromosome 13
Localization of the 8;13 translocation breakpoint associated with myeloproliferative disease to a 1.5 mbp region of chromosome 13
Assignment of 55 Novel Cosmids to Seven Subregions of Chromosome 13 Using Fluorescence in Situ Hybridization
Frequent Constitutional C to T Mutations in CGA-Arginine Codons in the RB1 Gene Produce Premature Stop Codons in Patients with Bilateral (Hereditary) Retinoblastoma
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