A 2.5-Mb transcript map of a tumor-suppressing subchromosomal transferable fragment from 11p15.5, and isolation and sequence analysis of three novel genes.
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A. Feinberg | G. Landes | L. Johnson | T. Burn | T. Connors | K. Su | A P Feinberg | T C Burn | R J Hu | M P Lee | T D Connors | L A Johnson | K Su | G M Landes | R. Hu | M. P. Lee | Kui Su | Maxwell P. Lee
[1] D. Gerhard,et al. Localization of a tumor suppressor gene in 11p15.5 using the G401 Wilms' tumor assay. , 1996, Human molecular genetics.
[2] H. Safaii,et al. Molecular genetic changes associated with ovarian cancer. , 1994, Gynecologic oncology.
[3] A. Reeve,et al. Loss of allelic heterozygosity at a second locus on chromosome 11 in sporadic Wilms' tumor cells , 1989, Molecular and cellular biology.
[4] A. Feinberg,et al. A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity. , 1983, Analytical biochemistry.
[5] A. Feinberg,et al. Fusion of the nucleoporin gene NUP98 to HOXA9 by the chromosome translocation t(7;11)(p15;p15) in human myeloid leukaemia , 1996, Nature Genetics.
[6] W. Cavenee,et al. Familial Wiedemann-Beckwith syndrome and a second Wilms tumor locus both map to 11p15.5. , 1989, American journal of human genetics.
[7] C. Begley,et al. Molecular cloning of a novel human gene (D11S4896E) at chromosomal region 11p15.5. , 1996, Genomics.
[8] R. Kobayashi,et al. The p55 subunit of Drosophila chromatin assembly factor 1 is homologous to a histone deacetylase-associated protein , 1996, Molecular and cellular biology.
[9] Keisuke Toyama,et al. The t(7;11)(p15;p15) translocation in acute myeloid leukaemia fuses the genes for nucleoporin NUP96 and class I homeoprotein HOXA9 , 1996, Nature Genetics.
[10] David J. Anderson,et al. Two rat homologues of Drosophila achaete-scute specifically expressed in neuronal precursors , 1990, Nature.
[11] E. Myers,et al. Basic local alignment search tool. , 1990, Journal of molecular biology.
[12] K. Klinger,et al. Generation of a transcriptional map for a 700-kb region surrounding the polycystic kidney disease type 1 (PKD1) and tuberous sclerosis type 2 (TSC2) disease genes on human chromosome 16p3.3. , 1996, Genome research.
[13] S. Antonarakis,et al. Localization of 102 exons to a 2.5 Mb region involved in Down syndrome. , 1995, Human molecular genetics.
[14] R. Weksberg,et al. Mapping of the gene encoding the integrin-linked kinase, ILK, to human chromosome 11p15.5-p15.4. , 1997, Genomics.
[15] R. Lothe,et al. Frequent loss of 11p13 and 11p15 loci in male germ cell tumours , 1993, Genes, chromosomes & cancer.
[16] Y. Qian,et al. A retinoblastoma-binding protein related to a negative regulator of Ras in yeast , 1993, Nature.
[17] S. Gregory,et al. The generation of ordered sets of cosmid DNA clones from human chromosome region 11p. , 1992, Genomics.
[18] R. Levy,et al. TAPA-1, the target of an antiproliferative antibody, defines a new family of transmembrane proteins , 1990, Molecular and cellular biology.
[19] C. Park,et al. A novel gene product that couples TCR signaling to Fas(CD95) expression in activation-induced cell death. , 1996, Immunity.
[20] G. Bepler,et al. Delineation of the centromeric and telomeric chromosome segment 11p15.5 lung cancer suppressor regions LOH11A and LOH11B , 1997, Genes, chromosomes & cancer.
[21] G. Landes,et al. Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias , 1996, Nature Genetics.
[22] D. Gerhard,et al. A fine-structure deletion map of human chromosome 11p: Analysis of J1 series hybrids , 1989, Somatic cell and molecular genetics.
[23] A. Feinberg,et al. Tumor cell growth arrest caused by subchromosomal transferable DNA fragments from chromosome 11 , 1993, Science.
[24] G. Bepler,et al. Three tumor-suppressor regions on chromosome 11p identified by high-resolution deletion mapping in human non-small-cell lung cancer. , 1994, Proceedings of the National Academy of Sciences of the United States of America.
[25] F. Couch,et al. Construction of a transcription map surrounding the BRCA1 locus of human chromosome 17. , 1995, Genomics.
[26] E. Russell,et al. Fas expression and function in normal and malignant breast cell lines. , 1996, Cancer research.
[27] S. Elledge,et al. p57KIP2, a structurally distinct member of the p21CIP1 Cdk inhibitor family, is a candidate tumor suppressor gene. , 1995, Genes & development.
[28] A. Feinberg,et al. Low frequency of p57KIP2 mutation in Beckwith-Wiedemann syndrome. , 1997, American journal of human genetics.
[29] R. Kobayashi,et al. Nucleosome Assembly by a Complex of CAF-1 and Acetylated Histones H3/H4 , 1996, Cell.
[30] S. Schreiber,et al. A Mammalian Histone Deacetylase Related to the Yeast Transcriptional Regulator Rpd3p , 1996, Science.
[31] Y. Fukushima,et al. An imprinted gene p57KIP2 is mutated in Beckwith–Wiedemann syndrome , 1996, Nature Genetics.
[32] F. Guillemot,et al. The human Achaete-Scute homologue 2 (ASCL2,HASH2) maps to chromosome 11p15.5, close to IGF2 and is expressed in extravillus trophoblasts. , 1997, Human molecular genetics.
[33] A. Feinberg,et al. A novel human homologue of yeast nucleosome assembly protein, 65 kb centromeric to the p57KIP2 gene, is biallelically expressed in fetal and adult tissues. , 1996, Human molecular genetics.
[34] G. Blobel,et al. The peptide repeat domain of nucleoporin Nup98 functions as a docking site in transport across the nuclear pore complex , 1995, Cell.
[35] G. Hampton,et al. Loss of heterozygosity for chromosome 11 in primary human breast tumors is associated with poor survival after metastasis. , 1995, Cancer research.
[36] J. Massagué,et al. Cloning of p57KIP2, a cyclin-dependent kinase inhibitor with unique domain structure and tissue distribution. , 1995, Genes & development.
[37] B. Stillman. Chromatin assembly during SV40 DNA replication in vitro , 1986, Cell.
[38] M. Knowles,et al. Deletion mapping of chromosome II in carcinoma of the bladder , 1995 .
[39] A. Feinberg,et al. Human KVLQT1 gene shows tissue-specific imprinting and encompasses Beckwith-Wiedemann syndrome chromosomal rearrangements , 1997, Nature Genetics.
[40] L. Simms,et al. Three non‐overlapping regions of chromosome arm 11p allele loss identified in infantile tumors of adrenal and liver , 1993, Genes, chromosomes & cancer.
[41] M. Pazin,et al. What's Up and Down with Histone Deacetylation and Transcription? , 1997, Cell.
[42] A. Feinberg,et al. Multiple genetic loci within 11p15 defined by Beckwith-Wiedemann syndrome rearrangement breakpoints and subchromosomal transferable fragments. , 1995, Proceedings of the National Academy of Sciences of the United States of America.