Pages that link to "Q59093916"
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The following pages link to Chromosomal localization of the human rhabdomyosarcoma locus by mitotic recombination mapping (Q59093916):
Displaying 50 items.
- Rhabdomyosarcoma-associated locus and MYOD1 are syntenic but separate loci on the short arm of human chromosome 11 (Q24558740) (← links)
- Localization of the MEN1 gene to a small region within chromosome 11q13 by deletion mapping in tumors (Q24558744) (← links)
- Transcriptional map of 170-kb region at chromosome 11p15.5: Identification and mutational analysis of the BWR1A gene reveals the presence of mutations in tumor samples (Q24681580) (← links)
- The human ASM (adult skeletal muscle) gene: expression and chromosomal assignment to 11p15 (Q28249052) (← links)
- Tumor cell growth arrest caused by subchromosomal transferable DNA fragments from chromosome 11 (Q28267975) (← links)
- Global gene expression profiling of PAX-FKHR fusion-positive alveolar and PAX-FKHR fusion-negative embryonal rhabdomyosarcomas (Q28300128) (← links)
- Loss-of-function screen in rhabdomyosarcoma identifies CRKL-YES as a critical signal for tumor growth (Q30009946) (← links)
- A model for embryonal rhabdomyosarcoma tumorigenesis that involves genome imprinting (Q30450833) (← links)
- The ninth Gordon Hamilton-Fairley memorial lecture. Hereditary cancers: clues to mechanisms of carcinogenesis (Q30486894) (← links)
- Loss of allelic heterozygosity at a second locus on chromosome 11 in sporadic Wilms' tumor cells (Q30501796) (← links)
- Distal deletion of chromosome Ip in ductal carcinoma of the breast (Q30541684) (← links)
- Expression and loss of alleles in cultured mouse embryonic fibroblasts and stem cells carrying allelic fluorescent protein genes (Q33260513) (← links)
- Small interfering RNA library screen of human kinases and phosphatases identifies polo-like kinase 1 as a promising new target for the treatment of pediatric rhabdomyosarcomas (Q33514778) (← links)
- The short arm of chromosome 11 is a "hot spot" for hypermethylation in human neoplasia (Q33636876) (← links)
- Loss of heterozygosity in human skin (Q33699908) (← links)
- Mechanisms of p53 loss in human sarcomas (Q33722859) (← links)
- Common mechanisms of osteosarcoma and Paget's disease (Q33746136) (← links)
- Allele loss on chromosome 16 associated with progression of human hepatocellular carcinoma (Q33772796) (← links)
- Mitotic recombination of chromosome 17 in astrocytomas (Q33851092) (← links)
- Tumor-specific loss of 11p15.5 alleles in del11p13 Wilms tumor and in familial adrenocortical carcinoma (Q33853617) (← links)
- Loss of heterozygosity for the short arm of chromosome 1 in human neuroblastomas: correlation with N-myc amplification (Q33858202) (← links)
- Evidence for mitotic recombination in Wei/+ heterozygous mice. (Q33956516) (← links)
- Regulatory regions of the homeotic gene proboscipedia are sensitive to chromosomal pairing (Q33965317) (← links)
- Genitourinary rhabdomyosarcoma. Treatment options (Q34031417) (← links)
- Review and hypotheses: somatic mosaicism: observations related to clinical genetics (Q34164134) (← links)
- Activation of an imprinted allele of the insulin-like growth factor II gene implicated in rhabdomyosarcoma (Q34236278) (← links)
- Differential DNA sequence deletions from chromosomes 3, 11, 13, and 17 in squamous-cell carcinoma, large-cell carcinoma, and adenocarcinoma of the human lung (Q34287423) (← links)
- The 11p15.5 ribonucleotide reductase M1 subunit locus is not imprinted in Wilms' tumour and hepatoblastoma (Q34355833) (← links)
- Genetic analysis of tumorigenesis: a conserved region in the human and Chinese hamster genomes contains genetically identified tumor-suppressor genes (Q34379385) (← links)
- Uniparental paternal disomy in a genetic cancer-predisposing syndrome (Q34535432) (← links)
- High-dose chemotherapy in soft tissue sarcoma in children (Q34539538) (← links)
- Primary rhabdomyosarcoma of the diaphragm: case report and literature review. (Q34618356) (← links)
- Polymorphisms of H-ras-1 and p53 in breast cancer and lung cancer: a meta-analysis (Q34638831) (← links)
- Oncogenes and tumor-suppressor genes (Q35034093) (← links)
- GLI inhibitor GANT-61 diminishes embryonal and alveolar rhabdomyosarcoma growth by inhibiting Shh/AKT-mTOR axis (Q35067950) (← links)
- Cytogenetic studies in subgroups of rhabdomyosarcoma (Q35165751) (← links)
- Localization of HeLa cell tumor-suppressor gene to the long arm of chromosome II. (Q35197594) (← links)
- Familial Wiedemann-Beckwith syndrome and a second Wilms tumor locus both map to 11p15.5. (Q35248366) (← links)
- Molecular genetic characterization of CNS tumor oncogenesis (Q35251504) (← links)
- Three tumor-suppressor regions on chromosome 11p identified by high-resolution deletion mapping in human non-small-cell lung cancer (Q35477427) (← links)
- Mouse chromosome 7. (Q35675706) (← links)
- Strong immunostaining for myogenin in rhabdomyosarcoma is significantly associated with tumors of the alveolar subclass (Q35745424) (← links)
- The long and short of chromosome 11 in breast cancer (Q35753162) (← links)
- All histological types of primary human rhabdomyosarcoma express alpha-cardiac and not alpha-skeletal actin messenger RNA. (Q35833613) (← links)
- Management of paranasal sinus malignancy (Q35989790) (← links)
- Chromosomal localisation of two putative 11p oncosuppressor genes involved in human ovarian tumours (Q35994651) (← links)
- Inhibition of MDM2 by RG7388 confers hypersensitivity to X-radiation in xenograft models of childhood sarcoma (Q36040768) (← links)
- Histone Deacetylase Inhibitors Inhibit Rhabdomyosarcoma by Reactive Oxygen Species-Dependent Targeting of Specificity Protein Transcription Factors (Q36201075) (← links)
- Head and Neck Rhabdomyosarcoma: Clinical and Pathologic Characterization of Seven Cases. (Q36206424) (← links)
- Structural alterations of the RB1 gene in human soft tissue tumours (Q36467187) (← links)