scholarly article | Q13442814 |
P2093 | author name string | Fu W | |
Mihatsch MJ | |||
Moch H | |||
Sauter G | |||
Gasser T | |||
Kononen J | |||
Wilber K | |||
Schraml P | |||
Struckmann K | |||
Bednar R | |||
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Mutational analysis of CDKN2 (CDK4I/MTS1) gene in tissues and cell lines of human prostate cancer | Q41332196 | ||
Homozygous deletions within 9p21-p22 identify a small critical region of chromosomal loss in human malignant mesotheliomas | Q41520737 | ||
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Genetic aberrations detected by comparative genomic hybridization are associated with clinical outcome in renal cell carcinoma. | Q46525301 | ||
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Loss of heterozygosity of microsatellite loci on chromosome 9p in astrocytic tumors and its prognostic implications | Q48909013 | ||
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Contribution of Chromosome 9p21‐22 Deletion to the Progression of Human Renal Cell Carcinoma | Q55388589 | ||
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Frequent loss of heterozygosity on chromosome 9 in adenocarcinoma and squamous cell carcinoma of the esophagus. | Q55481521 | ||
Haplotype analysis of two recurrentCDKN2A mutations in 10 melanoma families: Evidence for common founders and independent mutations | Q56438205 | ||
Mutations in the CDKN2A ( p16INK4a ) gene in microdissected sporadic primary melanomas | Q57664941 | ||
Retinoblastoma-protein-dependent cell-cycle inhibition by the tumour suppressor p16 | Q59082348 | ||
Histopathology and classification of renal cell tumors (adenomas, oncocytomas and carcinomas). The basic cytological and histopathological elements and their use for diagnostics | Q69578343 | ||
Genomic alterations and instabilities in renal cell carcinomas and their relationship to tumor pathology | Q70786914 | ||
Accumulation of p16CDKN2A in response to ultraviolet irradiation correlates with late S-G(2)-phase cell cycle delay | Q71129121 | ||
Frequency of homozygous deletion at p16/CDKN2 in primary human tumours | Q71721193 | ||
Frequent allele loss on 9p21-22 defines a smallest common region in the vicinity of the CDKN2 gene in sporadic breast cancer | Q71722021 | ||
Inactivation of the CDKN2/p16/MTS1 gene is frequently associated with aberrant DNA methylation in all common human cancers | Q71729088 | ||
Methylation of the 5' CpG island of the p16/CDKN2 tumor suppressor gene in normal and transformed human tissues correlates with gene silencing | Q71729092 | ||
Chromosome-9 loss detected by fluorescence in situ hybridization in bladder cancer | Q71891260 | ||
Rates of p16 (MTS1) mutations in primary tumors with 9p loss | Q72041274 | ||
Homozygous deletions of 9p21 in primary human bladder tumors detected by comparative multiplex polymerase chain reaction | Q72313814 | ||
Localization of tumor suppressor loci on chromosome 9 in primary human renal cell carcinomas | Q72388328 | ||
MTS1/CDKN2 gene mutations are rare in primary human astrocytomas with allelic loss of chromosome 9p | Q72529989 | ||
Frequent loss of chromosome 9 in human primary non-small cell lung cancer | Q72769107 | ||
Increased expression of cyclin-dependent kinase inhibitor 2 (CDKN2A) gene product P16INK4A in ovarian cancer is associated with progression and unfavourable prognosis | Q73081846 | ||
Alteration of p16 and p15 genes in common epithelial ovarian tumors | Q73302855 | ||
Chromosome 9p deletions in invasive and noninvasive nonfunctional pituitary adenomas: the deleted region involves markers outside of the MTS1 and MTS2 genes | Q73470634 | ||
Loss of Heterozygosity at Chromosome 9p21 in Primary Neuroblastomas: Evidence for Two Deleted Regions | Q73496858 | ||
A comparison of p53 and p16 expression in human tumor cells treated with hyperthermia or ionizing radiation | Q73503269 | ||
Allelic loss at the D9S171 locus on chromosome 9p13 is associated with progression of papillary renal cell carcinoma | Q73504522 | ||
Homozygous deletions at 9p21 in childhood acute lymphoblastic leukemia detected by microsatellite analysis | Q73767278 | ||
G1 control gene status is frequently altered in resectable non-small cell lung cancer | Q73841999 | ||
Loss of heterozygosity at chromosomes 8p, 9p, and 14q is associated with stage and grade of non-papillary renal cell carcinomas | Q73923938 | ||
9p21 deletion correlates with recurrence in head and neck cancer | Q74250907 | ||
Retinoblastoma and p16 proteins in mammary carcinoma: their relationship to cyclin D1 and histopathological parameters | Q74292669 | ||
CDKN2A mutations in multiple primary melanomas | Q74357667 | ||
Homozygous deletion of the p16INK4a and the p15INK4b tumour suppressor genes in a subset of human sporadic cutaneous malignant melanoma | Q74425282 | ||
Infrequent mutation of the p16/MTS1 gene and overexpression of cyclin-dependent kinase 4 in human primary soft-tissue sarcoma | Q74490616 | ||
Overexpression of the cyclin-dependent kinase inhibitor p16 is associated with tumor recurrence in human prostate cancer | Q77827926 | ||
Response | Q94596609 | ||
P433 | issue | 2 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 593-601 | |
P577 | publication date | 2001-02-01 | |
P1433 | published in | The American Journal of Pathology | Q4744259 |
P1476 | title | CDKNA2A mutation analysis, protein expression, and deletion mapping of chromosome 9p in conventional clear-cell renal carcinomas: evidence for a second tumor suppressor gene proximal to CDKN2A. | |
P478 | volume | 158 |
Q55298720 | Aberrations of the p14(ARF) and p16(INK4a) genes in renal cell carcinomas. |
Q28253911 | An automated procedure to identify biomedical articles that contain cancer-associated gene variants |
Q41815800 | Analysis of p16 expression and allelic imbalance / loss of heterozygosity of 9p21 in cutaneous squamous cell carcinomas |
Q38184386 | Biomarkers in renal cancer |
Q91519122 | Chromosomal deletion of 9p21 is linked to poor patient prognosis in papillary and clear cell kidney cancer |
Q34283721 | Chromosome 9p deletion in clear cell renal cell carcinoma predicts recurrence and survival following surgery |
Q33220432 | Clonal divergence and genetic heterogeneity in clear cell renal cell carcinomas with sarcomatoid transformation |
Q36648942 | Cytogenetic alterations in ovarian clear cell carcinoma detected by comparative genomic hybridisation |
Q38947910 | Downregulation of NDUFB6 due to 9p24.1-p13.3 loss is implicated in metastatic clear cell renal cell carcinoma |
Q26785930 | Genetic and Chromosomal Aberrations and Their Clinical Significance in Renal Neoplasms |
Q37401031 | Genome-wide profiling of chromosomal alterations in renal cell carcinoma using high-density single nucleotide polymorphism arrays |
Q52544535 | INK4a-ARF alterations and p53 mutations in hepatocellular carcinomas. |
Q37728343 | Kinase targets in renal-cell carcinomas: reassessing the old and discovering the new. |
Q34695773 | Loss of chromosome 9p is an independent prognostic factor in patients with clear cell renal cell carcinoma |
Q36730935 | Loss of heterozygosity and copy number abnormality in clear cell renal cell carcinoma discovered by high-density affymetrix 10K single nucleotide polymorphism mapping array |
Q33710257 | Metastatic renal cell carcinoma with undetectable renal mass presenting as lymphadenopathy |
Q54792472 | Multipoint methylation and expression analysis of tumor suppressor genes in human renal cancer cells. |
Q28298079 | Pathological characterization of Kank in renal cell carcinoma |
Q37349768 | Patterns of gene expression and copy-number alterations in von-hippel lindau disease-associated and sporadic clear cell carcinoma of the kidney |
Q35792041 | Relevance of nuclear and cytoplasmic von hippel lindau protein expression for renal carcinoma progression. |
Q37579066 | Significance of CDKN2A gene A148T variant in patients with bladder cancer. |
Q33616134 | Significance of chromosome 9p status in renal cell carcinoma: a systematic review and quality of the reported studies. |
Q36872295 | The VHL/HIF axis in clear cell renal carcinoma |
Q39341646 | Tumour suppressor gene (CDKNA2) status on chromosome 9p in resected renal tissue improves prognosis of localised kidney cancer |
Q53327323 | [Exploration of tumor suppressors p16INK4a and p14ARF in oral leukoplakias]. |
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