Research graph
References from Prostate Cancer Aggressiveness Locus on Chromosome 7832-q33 Identified by Linkage and Allelic Imbalance Studies. Local targets link to admitted publications; unresolved targets remain external evidence.
Unresolved reference
2000 · External reference
Major susceptibility locus for prostate cancer on chromosome 1 suggested by a genome-wide search
10.1126/science.274.5291.1371 · 1996 · External reference
Evidence for a rare prostate cancersusceptibility locus at chromosome l p36
10.1086/302287 · 1999 · External reference
Predisposing gene for early-onset prostate cancer, localized on chromosome
10.1086/301879 · 1998 · External reference
Linkage and association studies of prostate cancer susceptibility: evidence for linkage at 8p22-23
10.1086/321967 · 2001 · External reference
A candidate prostate cancer susceptibility gene at chromosome 17p
10.1038/84808 · 2001 · External reference
A genome screen of multiplex sibships with prostate cancer
10.1086/302818 · 2000 · External reference
Evidence for a prostate cancer-susceptibility locus on chromosome 20
10.1086/302994 · 2000 · External reference
A genetic epidemiological study of hereditary prostate cancer
2000 · External reference
PCAP is the major known prostate cancer predisposing locus in families from south and west Europe
10.1038/sj.ejhg.5200592 · 2001 · External reference
Association of HPC2/ELAC2 genotypes and prostate cancer
10.1086/303096 · 2000 · External reference
Prostate cancer susceptibility locus on chromosome 1q: a confirmatory study
10.1093/jnci/89.13.955 · 1997 · External reference
Early age at diagnosis in families providing evidence of linkage to the hereditary prostate cancer locus
1997 · External reference
In Swedish families with hereditary prostate cancer, linkage to the HPCl locus on chromosome lg24-25 is restricted to families with earlyonset prostate cancer
10.1086/302447 · 1999 · External reference
Prostate cancer susceptibility locus HPCl in Utah high-risk pedigrees
10.1093/hmg/8.13.2437 · 1999 · External reference
Identification and fine mapping of a region showing a high frequency of allelic imbalance on chromosome 16823.2 that corresponds to a prostate cancer susceptibility locus
2000 · External reference
Combined analysis of hereditary prostate cancer linkage to 1g24-25: results from 772 hereditary prostate cancer families from the International Consortium for Prostate Cancer Genetics
10.1086/302807 · 2000 · External reference
Evidence for a prostate cancer linkage to chromosome 20 in 159 hereditary prostate cancer families
10.1007/s004390100513 · 2001 · External reference
Analysis of HPC1, HPCX, PCaP in Icelandic hereditary prostate cancer
10.1007/s004390000384 · 2000 · External reference
Analysis of the prostate cancer susceptibility locus HPC20 in 172 families affected by prostate cancer
10.1086/318797 · 2001 · External reference
Linkage analysis of 150 high risk prostate cancer families at 1824-25
10.1002/(sici)1098-2272(200003)18:3<251::aid-gepi5>3.0.co;2-x · 2000 · External reference
Linkage analysis of 49 high-risk families does not support a common familial prostate cancer-susceptibility gene at lg24-25
10.1086/514853 · 1997 · External reference
Replication linkage study for prostate cancer susceptibility genes
10.1002/1097-0045(20001001)45:2<106::aid-pros4>3.0.co;2-h · 2000 · External reference
No evidence of linkage for chromosome lg42.2-43 in prostate cancer
10.1086/302457 · 1999 · External reference
Evaluation of linkage and association of HPC2/ELAC2 in patients with familial or sporadic prostate cancer
10.1086/319513 · 2001 · External reference
Genetics of prostate cancer: too many loci, too few genes
10.1086/316916 · 2000 · External reference
Genomewide scan for prostate cancer-aggressiveness loci
10.1086/302960 · 2000 · External reference
Histologic grading of prostate cancer: a perspective
10.1016/0046-8177(92)90108-f · 1992 · External reference
Loss of heterozygosity at 7g31 is a frequent and early event in prostate cancer
1995 · External reference
Loss of heterozygosity in human primary prostate carcinomas: a possible tumor suppressor gene at 7g31.1
1994 · External reference
(C-Am microsatellite repeat D7S522 is the most commonly deleted region in human primary breast cancer
10.1073/pnas.91.25.12155 · 1994 · External reference
Chromosome 7q allelic losses in pancreatic carcinoma
1996 · External reference
Commonly deleted region on the long arm of chromosome 7 in differentiated adenocarcinoma of the stomach
10.1038/bjc.1997.598 · 1997 · External reference
Differential loss of heterozygosity at 7g31.2 in follicular and papillary thyroid tumors
10.1038/sj.onc.1201996 · 1998 · External reference
Loss of heterozygosity on chromosomes 7p, 7% 9p and l lq is an early event in ovarian tumorigenesis
10.1038/sj.onc.1201945 · 1998 · External reference
Frequent loss of heterozygosity at 7g31.1 in primary prostate cancer is associated with tumor aggressiveness and progression
1995 · External reference
Prognostic significance of allelic imbalance of chromosome arms 7% 8p, 168, 18q in stage T3NOMO prostate cancer
10.1002/(sici)1098-2264(199802)21:2<131::aid-gcc9>3.0.co;2-1 · 1998 · External reference
Mutational and functional analyses reveal that ST7 is a highly conserved tumorsuppressor gene on human chromosome 7g31
10.1038/86891 · 2001 · External reference
A radiation hybrid map of the human genome
10.1093/hmg/5.3.339 · 1996 · External reference
Overview of QTL mapping software and introduction to map manager QT
10.1007/s003359900997 · 1999 · External reference
Four regions of allelic imbalance on 17gl2-gter associated with high-grade breast tumors
10.1002/(sici)1098-2264(199712)20:4<354::aid-gcc6>3.0.co;2-0 · 1997 · External reference
Haseman and Elston revisited
10.1002/1098-2272(200007)19:1<1::aid-gepi1>3.0.co;2-e · 2000 · External reference
Familial chordoma, a tumor of notochordal remnants, is linked to chromosome 7833
10.1086/321982 · 2001 · External reference
Chordomas: pathological features; ploidy and silver nucleolar organizing region analysis
10.1007/bf00296357 · 1995 · External reference
A tumor suppressor locus in familial and sporadic chordoma maps to l p36
10.1002/1097-0215(20000701)87:1<68::aid-ijc10>3.0.co;2-v · 2000 · External reference
Molecular characterization of a common fragile site
1998 · External reference
Construction of a physical and transcript map flanking the imprinted MEST/PEGl region at 7832
10.1006/geno.2000.6206 · 2000 · External reference
The FHIT gene, spanning the chromosome 3pl4.2 fragile site and renal carcinoma-associated t(3;8) breakpoint, is abnormal in digestive tract cancers
10.1016/s0092-8674(00)81034-x · 1996 · External reference
Definitive functional evidence for a tumor suppressor gene on human chromosome 7g31.1 neighboring the Fra7G site
10.1038/sj.onc.1203488 · 2000 · External reference
Chromosomal fragile site FRA16D and DNA instability in cancer
2000 · External reference
A 700-kb physical map of a region of 16823.2 homozygously deleted in multiple cancers and spanning the common fragile site FRA16D
2000 · External reference
cDNA cloning of human muskelin and localisation of the muskelin
1999 · External reference
Muskelin, a novel intracellular mediator of cell adhesive and cytoskeletal responses to thrombospondin-1
10.1093/emboj/17.17.4964 · 1998 · External reference
Control of angiogenesis in fibroblasts by p53 regulation of thrombospondin-1
10.1126/science.7521539 · 1994 · External reference
Regulation of tumor growth and metastasis by thrombospondin-1
10.1096/fasebj.10.10.8751720 · 1996 · External reference
Independent association of angiogenesis index with outcome in prostate cancer
2001 · External reference
Molecular cloning and characterization of human podocalyxin-like protein
1997 · External reference
Human testicular germ cell tumor marker, gp200, identified as podocalyxin-like protein
2000 · External reference
Domains in plexins: links to integrins and transcription factors
10.1016/s0968-0004(99)01416-4 · 1999 · External reference
Plexins are a large family of receptors for transmembrane, secreted, GPI-anchored semaphorins in vertebrates
10.1016/s0092-8674(00)80063-x · 1999 · External reference
Transcription of a novel mouse semaphorin gene, M-semaH, correlates with the metastatic ability of mouse tumor cell lines
1998 · External reference
Control of invasive growth by hepatocyte growth factor
10.1016/s1359-6101(97)00007-5 · 1997 · External reference
