33 SCW1 1995 submitted abstracts

• Ambros et al. Biological properties of 1p36.33 in normal development and human malignancies.
• Bièche et al. Loss and gain of distinct regions of chromosome 1q in primary breast cancer.
• Bièche et al. A gene dosage effect is responsible for overexpression of the MUC1 gene in human breast cancer.
• Brodeur Chromosome 1 Rearrangements in Human Cancers
• Buyse et al. Abnomalities of the retinoblastoma-binding protein RIZ on chromosome 1p36 in human cancer.
• Chung et al. Genetic map of 1p31 in region homologous to mid-murine chromosome 4.
• Coleman et al. Mapping of genes on distal mouse chromosome 4.
• Cuttichia et al. The Role of the Genome Data Base at the Chromosome 1 Workshop.
• Denton et al. Genetic and physical mapping of the chromosome 1p36 region surrounding the Charcot-Marie-Tooth disease (CMT) type 2A locus.
• Eskdale et al. A Polymorphic Dinucleotide Repeat in the Human IL-10 Promoter.
• Eudy et al. Construction of NotI linking libraries and YAC contigs to map the critical region of USH2a in 1q41.
• Forus Characterisation of 1q21-q22 amplifications in human sarcomas by CGH and molecular analysis.
• Hey et al. Identification and cloning in yeast artificial chromosomes of a region of elevated loss of heterozygosity on chromosome 1p31.1 in human breast cancer.
• Hofele et al. Analysis of 2 pedigrees with autosomal dominant paroxysmal choreoathetosis: Assignment of a gene locus to probably 2 cM between D1S443 and D1S197 ...
• Marenholz et al. A High Resolution Genomic Restriction Map and a YAC Contig of the Epidermal Differentiation Complex (EDC) on Human Chromosome 1q21.
• Martinsson et al. Analysis of 1p-deletions in neuroblastoma tumors; Delimitation of the critical region with genetically mapped short tandem repeat polymorphisms.
• Martinsson et al. PITSLRE (p58cdc2L1) Genes in Neuroblastoma Cell Genomes: Evidence Against Involvement in Tumorigenesis.
• Menedetter et al. Mapping of DNA sequences frequently deleted in human neoplasms: comparison of physical and genetic data.
• Praml et al. 1p-Alterations in human cancer: Deletions in 1p34.2-pter in colorectal cancer and a reciprocal translocation (1;15) (36.2;q24) in a neuroblastoma cell line define putative loci for tumor-supressor genes.
• Schutte et al. Genetic Maps of Chromosome 1.
• Schutte et al. Mapping of 15 genes near the Van der Woude locus.
• Seldin. Homology relationships between human chromosome 1 and mouse chromosomes.
• Seldin et al. Preliminary Linkage of Peutz-Jegher's Syndrome to chromosome 1p.
• Speleman et al. A putative tumor suppressor gene involved in Merkel cell carcinoma maps between p58 and D1Z2.
• Stephan et al. Rippling muscle disease: genetic and physical mapping of a new locus at 1q41-43.
• Van Camp et al. Localization of the human gap junction protein connexin37 to chromosome 1p35.
• Versteeg et al. Chromosomal region 1p35-36 encodes for several neuroblastoma suppressor loci.
• Vojta et al. Generation of a subchromosomal transferable fragment library for human chromosome 1.
• Weterman et al. Mapping of DNA markers relative to two tumor-associated breakpoints in 1q21.
• White et al. Toward an Integrated Map of 1p35-36.
• Williams et al. Isolation, Sequencing and Mapping of the Gene for Neural Cell Adhesion Molecule tenascin-R Within 1q32.
• Wimmer et al. Mapping of NotI sites on chromosome 1 identified by two-dimensional electrophoresis of genomic restriction fragments.
• Zhao et al. Construction and mapping of a YAC / P1 contig containing the S100 and SPRR gene.