Search Results - "NOWAK, N. J"

Identification and characterisation of constitutional chromosome abnormalities using arrays of bacterial artificial chromosomes by COWELL, J. K, WANG, Y. D, HEAD, K, CONROY, J, MCQUAID, D, NOWAK, N. J

“…Constitutional chromosome deletions and duplications frequently predispose to the development of a wide variety of cancers. We have developed a microarray of…”
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Array comparative genomic hybridisation (aCGH) analysis of premenopausal breast cancers from a nuclear fallout area and matched cases from Western New York by VARMA, G, VARMA, R, MOYSICH, K, FALKNER, K. L, GERADTS, J, HUANG, H, PRYSHCHEPAVA, A, GROTH, J, FLEMING, D, NOWAK, N. J, MCQUAID, D, CONROY, J, MAHONEY, M

“…High-resolution array comparative genomic hybridisation (aCGH) analysis of DNA copy number aberrations (CNAs) was performed on breast carcinomas in…”
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Alterations in chromatin accessibility and DNA methylation in clear cell renal cell carcinoma by Buck, M J, Raaijmakers, L M, Ramakrishnan, S, Wang, D, Valiyaparambil, S, Liu, S, Nowak, N J, Pili, R

“…Recent studies have demonstrated that in clear cell renal cell carcinoma (ccRCC) several chromatin remodeling enzymes are genetically inactivated. Although,…”
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A gene expression atlas of the central nervous system based on bacterial artificial chromosomes by Hatten, Mary E, Heintz, Nathaniel, Gong, Shiaoching, Zheng, Chen, Doughty, Martin L, Losos, Kasia, Didkovsky, Nicholas, Schambra, Uta B, Nowak, Norma J, Joyner, Alexandra, Leblanc, Gabrielle

“…The mammalian central nervous system (CNS) contains a remarkable array of neural cells, each with a complex pattern of connections that together generate…”
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MAGOH Interacts with a Novel RNA-Binding Protein by Zhao, Xian-Feng, Nowak, Norma J., Shows, Thomas B., Aplan, Peter D.

“…MAGOH is the human homologue of Drosophila mago nashi, a protein that is required for normal germ plasm development in the Drosophila embryo. Using human MAGOH…”
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Bestrophin Gene Mutations in Patients with Best Vitelliform Macular Dystrophy by Caldwell, Germaine M., Kakuk, Laura E., Griesinger, Irina B., Simpson, Stacey A., Nowak, Norma J., Small, Kent W., Maumenee, Irene H., Rosenfeld, Philip J., Sieving, Paul A., Shows, Thomas B., Ayyagari, Radha

“…Best vitelliform macular dystrophy (VMD2) is an autosomal dominant dystrophy with a juvenile age of onset. Mutations in the Bestrophin gene were shown in…”
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Familial 4.3 Mb duplication of 21q22 sheds new light on the Down syndrome critical region by Ronan, Anne, Fagan, Kerry, Christie, Louise, Conroy, Jeffrey, Nowak, Norma J, Turner, Gillian

“…A 4.3 Mb duplication of chromosome 21 bands q22.13–q22.2 was diagnosed by interphase fluorescent in-situ hybridisation (FISH) in a 31-week gestational age baby…”
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Comparative Morphological Development of Divergent Flowering Types of Annual Bluegrass and Tillering Types of Creeping Bentgrass by Cattani, D. J., Struik, P. C., Nowak, J. N.

“…Annual bluegrass (AB; Poa annua L.) competition in creeping bentgrass [CB; Agrostis palustris Huds. = A stolonifera var. palustris (Huds.) Farw.] turf under…”
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Linkage-disequilibrium mapping without genotyping by Cheung, Vivian G, Gregg, Jeffrey P, Gogolin-Ewens, Kathryn J, Bandong, Jonathan, Stanley, Charles A, Baker, Lester, Higgins, Michael J, Nowak, Norma J, Shows, Thomas B, Ewens, Warren J, Nelson, Stanley F, Spielman, Richard S

“…Genomic mismatch scanning (GMS) is a technique that enriches for regions of identity by descent (IBD) between two individuals without the need for genotyping…”
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Divergently Transcribed Overlapping Genes Expressed in Liver and Kidney and Located in the 11p15.5 Imprinted Domain by Cooper, Paul R., Smilinich, Nancy J., Day, Colleen D., Nowak, Norma J., Reid, Laura H., Pearsall, R.Scott, Reece, Mark, Prawitt, Dirk, Landers, John, Housman, David E., Winterpacht, Andreas, Zabel, Bernhard U., Pelletier, Jerry, Weissman, Bernard E., Shows, Thomas B., Higgins, Michael J.

“…Human chromosomal band 11p15.5 has been shown to contain genes involved in the development of several pediatric and adult tumors and in Beckwith–Wiedemann…”
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Semiautomated clone verification by real-time PCR using molecular beacons by van Schie, R C, Marras, S A, Conroy, J M, Nowak, N J, Catanese, J J, de Jong, P J

“…Conventional, high-throughput PCR analysis of common elements utilizing numerous primer sets and template DNA requires multiple rounds of PCR to ensure optimal…”
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The pericentromeric region of human chromosome 11: evidence for a chromosome-specific duplication by Zhang, J, Qin, S, Sait, S N, Haley, L L, Henry, W M, Higgins, M J, Nowak, N J, Shows, T B, Gerhard, D S

“…We have identified a chromosome duplication in the pericentromeric region of human chromosome 11 located in 11p11 and 11q14. A detailed physical map of each…”
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A 1-Mb Physical Map and PAC Contig of the Imprinted Domain in 11p15.5 That Contains TAPA1 and the BWSCR1/WT2 Region by Reid, Laura H., Davies, Chris, Cooper, Paul R., Crider-Miller, Shyra J., Sait, Sheila N.J., Nowak, Norma J., Evans, Glen, Stanbridge, Eric J., dejong, Pieter, Shows, Thomas B., Weissman, Bernard E., Higgins, Michael J.

“…We have constructed a 1-Mb contig in human chromosomal band 11p15.5, a region implicated in the etiology of several embryonal tumors, including Wilms tumor,…”
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A chromosome 11 YAC library by Qin, S, Zhang, J, Isaacs, C M, Nagafuchi, S, Jani Sait, S N, Abel, K J, Higgins, M J, Nowak, N J, Shows, T B

“…A targeted yeast artificial chromosome (YAC) library for chromosome 11 has been constructed from the J1 cell line that carries a single human chromosome 11…”
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The Human Angiotensinase C Gene (HUMPCP) Maps to 11q14 within 700 kb of D11S901: A Candidate Gene for Essential Hypertension by Watson, Bracie, Nowak, Norma J., Myracle, Angela D., Shows, Thomas B., Warnock, David G.

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Genome-wide allelotyping indicates increased loss of heterozygosity on 9p and 14q in early age of onset colorectal cancer by Weber, T K, Conroy, J, Keitz, B, Rodriguez-Bigas, M, Petrelli, N J, Stoler, D L, Anderson, G R, Shows, T B, Nowak, N J

“…Colorectal cancer remains a significant public health challenge, despite our increased understanding of the genetic mechanisms involved in the initiation and…”
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Transcript Mapping of the Human Chromosome 11q12–q13.1 Gene-Rich Region Identifies Several Newly Described Conserved Genes by Cooper, Paul R., Nowak, Norma J., Higgins, Michael J., Church, Deanna M., Shows, Thomas B.

“…Despite the localization of several human diseases to 11q13, the majority of the genes responsible for these disorders have not yet been cloned. Exon…”
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A 2.8-Mb Clone Contig of the Multiple Endocrine Neoplasia Type 1 (MEN1) Region at 11q13 by Guru, Siradanahalli C., Olufemi, Shodimu-Emmanuel, Manickam, Pachiappan, Cummings, Christiano, Gieser, Linn M., Pike, Brian L., Bittner, Michael L., Jiang, Yuan, Chinault, A.Craig, Nowak, Norma J., Brzozowska, Anna, Crabtree, Judy S., Wang, Yingping, Roe, Bruce A., Weisemann, Jane M., Boguski, Mark S., Agarwal, Sunita K., Burns, A.Lee, Spiegel, Allen M., Marx, Stephen J., Flejter, Wendy L., de Jong, Pieter J., Collins, Francis S., Chandrasekharappa, Settara C.

“…Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant disorder that results in parathyroid, anterior pituitary, and pancreatic and duodenal…”
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A High-Resolution Physical Map of Human Chromosome 11 by Qin, Shizhen, Nowak, Norma J., Zhang, Jialu, Sheila N. J. Sait, Mayers, Peter G., Higgins, Michael J., Cheng, Yi-Jun, Li Li, Munroe, David J., Gerhard, Daniela S., Weber, Bernhard H., Bric, Eva, Housman, David E., Evans, Glen A., Shows, Thomas B.

“…The development of a highly reliable physical map with landmark sites spaced an average of 100 kbp apart has been a central goal of the Human Genome Project…”
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Framework YAC Contig Anchored into a 3.2-Mb High-Resolution Physical Map in Proximal 11q13 by Courseaux, Anouk, Szepetowski, Pierre, Fernandes, Marie, Serizet, Carine, Kawaguchi, Yoshihiko, Grosgeorge, Josiane, Perucca-Lostanlen, Danielle, Shows, Thomas B., Todd, John A., Nowak, Norma J., Gaudray, Patrick

“…Despite the presence on band q13 of chromosome 11 of a number of genes predisposing individuals to various human diseases, most of this genomic region remains…”
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