Pages that link to "Q68097060"
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The following pages link to Germline mutations of the p53 tumor-suppressor gene in children and young adults with second malignant neoplasms (Q68097060):
Displaying 50 items.
- Li-fraumeni syndrome (Q22241780) (← links)
- Study design: evaluating gene-environment interactions in the etiology of breast cancer - the WECARE study (Q24794680) (← links)
- Osteosarcoma: Cells-of-Origin, Cancer Stem Cells, and Targeted Therapies (Q26745742) (← links)
- Solid tumor second primary neoplasms: who is at risk, what can we do? (Q27026266) (← links)
- An African-specific polymorphism in the TP53 gene impairs p53 tumor suppressor function in a mouse model (Q27853369) (← links)
- Analysis of germline and in vivo somatic mutations in the human adenine phosphoribosyltransferase gene: Mutational hot spots at the intron 4 splice donor site and at codon 87 (Q28298034) (← links)
- Inherited predisposition to glioma. (Q30477902) (← links)
- Soft tissue sarcoma of the extremities. A multimodality diagnostic and therapeutic approach (Q33585746) (← links)
- Simultaneous adrenocortical carcinoma and ganglioneuroblastoma in a child with Turner syndrome and germline p53 mutation (Q33680565) (← links)
- MGMT promoter hypermethylation and K-RAS, PTEN and TP53 mutations in tamoxifen-exposed and non-exposed endometrial cancer cases (Q33750187) (← links)
- Germline p53 mutations in a cohort with childhood sarcoma: sex differences in cancer risk (Q33905119) (← links)
- Germline p53 mutations are frequently detected in young children with rhabdomyosarcoma (Q34207682) (← links)
- Screening women at high risk of breast cancer on the basis of evidence (Q34299930) (← links)
- Spontaneous and carcinogen-induced tumorigenesis in p53-deficient mice. (Q34347328) (← links)
- A simple p53 functional assay for screening cell lines, blood, and tumors (Q34397902) (← links)
- Li-Fraumeni syndrome – a molecular and clinical review (Q34432117) (← links)
- Gene mutation as a target for early detection in cancer diagnosis. (Q34460648) (← links)
- Polymorphisms of H-ras-1 and p53 in breast cancer and lung cancer: a meta-analysis (Q34638831) (← links)
- A database of germline p53 mutations in cancer-prone families (Q34651275) (← links)
- Defective osteogenic differentiation in the development of osteosarcoma (Q34700590) (← links)
- Genetic counselling and testing for susceptibility to breast, ovarian and colon cancer: where are we today? (Q34713375) (← links)
- Genetic predisposition and screening in pediatric cancer (Q35064135) (← links)
- Pediatric cancer survivors: Past history and future challenges (Q35128211) (← links)
- Late effects of treatment for cancer during childhood and adolescence (Q35128215) (← links)
- Updates on the cytogenetics and molecular genetics of bone and soft tissue tumors: osteosarcoma and related tumors (Q35186715) (← links)
- Functional studies of a germ-line polymorphism at codon 47 within the p53 gene (Q35195008) (← links)
- Molecular basis of inherited diseases: a structural perspective (Q35212660) (← links)
- A clinical and genetic analysis of multiple primary cancer referrals to genetics services (Q35477924) (← links)
- Cancer risks from germline p53 mutations (Q35513831) (← links)
- Germ-line p53 mutations in 15 families with Li-Fraumeni syndrome. (Q35643184) (← links)
- Identification of Medically Actionable Secondary Findings in the 1000 Genomes (Q35762437) (← links)
- Tumors associated with p53 germline mutations: a synopsis of 91 families. (Q35765327) (← links)
- Mutations of cell cycle regulators. Biological and clinical implications for human neoplasia (Q35798342) (← links)
- Occurrence of Neuroblastoma among TP53 p.R337H Carriers (Q35801794) (← links)
- Using germ-line genetic variation to investigate and treat cancer (Q35829133) (← links)
- Chromosome 17 abnormalities and TP53 mutations in adult soft tissue sarcomas. (Q35833993) (← links)
- Highly penetrant hereditary cancer syndromes. (Q35868041) (← links)
- Prognostic significance of TP53 alterations in breast carcinoma (Q35976693) (← links)
- Molecular epidemiology studies of cancer in families (Q35977161) (← links)
- Multiple primary tumours in a population-based series of patients with histopathologically peer-reviewed sarcomas (Q35977560) (← links)
- Cancer experience in the relatives of an unselected series of breast cancer patients. (Q36079492) (← links)
- Mutation hotspots due to sunlight in the p53 gene of nonmelanoma skin cancers. (Q36287125) (← links)
- Two Li-Fraumeni syndrome families with novel germline p53 mutations: loss of the wild-type p53 allele in only 50% of tumours (Q36292302) (← links)
- p53 gene mutations and protein accumulation in human ovarian cancer (Q36328863) (← links)
- Spontaneous in vitro immortalization of breast epithelial cells from a patient with Li-Fraumeni syndrome (Q36567058) (← links)
- P53 germline mutations in childhood cancers and cancer risk for carrier individuals (Q36621004) (← links)
- Leiomyosarcoma as a second metachronous malignant neoplasm following colon adenocarcinoma. A case report and review of the literature. (Q36674053) (← links)
- ARCAD: a method for estimating age-dependent disease risk associated with mutation carrier status from family data (Q36699828) (← links)
- Radiotherapy-induced malignancies: review of clinical features, pathobiology, and evolving approaches for mitigating risk (Q36736612) (← links)
- Osteosarcoma development and stem cell differentiation (Q36803600) (← links)