Search Results - "Stanton, V. P"

The translocation t(8;16)(p11;p13) of acute myeloid leukaemia fuses a putative acetyltransferase to the CREB-binding protein by Chaganti, Raju S. K, Andresen, J. Michael, Stanton, Vincent P, Behm, Frederick G, Frischauf, Anna Marie, Housman, David E, Watmore, Ann E, Horsman, Doug, Disteche, Christine, Volinia, Stefano, Civin, Curt I, Becher, Reinhard, Mitelman, Felix, Borrow, Julian, Dubé, Ian

“…The recurrent translocation t(8;16)(p11;p13) is a cytogenetic hallmark for the M4/M5 subtype of acute myeloid leukaemia. Here we identify the…”
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The t(7;11)(p15;p15) translocation in acute myeloid leukaemia fuses the genes for nucleoporin NUP98 and class I homeoprotein HOXA9 by BORROW, J, SHEARMAN, A. M, OHYASHIKI, K, TOYAMA, K, ROWLEY, J, HOUSMAN, D. E, STANTON, V. P, BECHER, R, COLLINS, T, WILLIAMS, A. J, DUBE, I, KATZ, F, KWONG, Y. L, MORRIS, C

“…The t(7;11)(p15;p15) translocation is a recurrent chromosomal abnormality associated primarily with acute myeloid leukaemia (FAB M2 and M4). We present here…”
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The peripheral myelin gene PMP-22/GAS-3 is duplicated in Charcot-Marie-Tooth disease type 1A by Valentijn, L. J, Bolhuis, P. A, Zorn, I, Hoogendijk, J. E, van den Bosch, N, Hensels, G. W, Stanton, V. P, Housman, D. E, Fischbeck, K. H, Ross, D. A, Nicholson, G. A, Meershoek, E. J, Dauwerse, H. G, van Ommen, G. -J. B, Baas, F

“…Charcot-Marie-Tooth disease type 1A (CMT1A) is associated with a DNA duplication at chromosome 17p11.2. In view of the point mutation in the gene for…”
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Single-Nucleotide Polymorphisms Can Cause Different Structural Folds of mRNA by Shen, Ling X., Basilion, James P., Stanton, Vincent P.

“…Single-nucleotide polymorphisms (SNPs) are the most common type of genetic variation in man. Genes containing one or more SNPs can give rise to two or more…”
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Definition of the human raf amino-terminal regulatory region by deletion mutagenesis by STANTON, V. P. JR, NICHOLS, D. W, LAUDANO, A. P, COOPER, G. M

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Ordered Restriction Endonuclease Maps of Yeast Artificial Chromosomes Created by Optical Mapping on Surfaces by Cai, Weiwen, Aburatani, Hiroyuki, Stanton, Vincent P., Housman, David E., Wang, Yu-Ker, Schwartz, David C.

“…We have developed a surface mounting technology for the rapid construction of ordered restriction maps from individual DNA molecules. Optical restriction maps…”
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Clinical and genetic studies of renal cell carcinomas in a family with a constitutional chromosome 3;8 translocation : genetics of familial renal carcinoma by LI, F. P, DECKER, H.-J. H, BROWN, R. S, ZBAR, B, STANTON, V. P, KOVACS, G, SEIZINGER, B. R, ABURATANI, H, SANDBERG, A. A, BERG, S, HOSOE, S

“…To describe the clinical course and genetic studies of renal carcinoma in members of a family with the constitutional chromosome translocation, t(3;8)…”
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Activation of human raf transforming genes by deletion of normal amino-terminal coding sequences by STANTON, V. P. JR, COOPER, G. M

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High-Resolution Physical Mapping by Combined Alu-Hybridization/PCR Screening: Construction of a Yeast Artificial Chromosome Map Covering 31 Centimorgans in 3p21-p14 by Aburatani, Hiroyuki, Stanton, Vincent P., Housman, David E.

“…We describe an integrated approach to large-scale physical mapping using an Alu-PCR hybridization screening strategy in conjunction with direct PCR-based…”
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Familial predisposition to Wilms tumor does not segregate with the WT1 gene by Schwartz, C E, Haber, D A, Stanton, V P, Strong, L C, Skolnick, M H, Housman, D E

“…Wilms tumor (WT) is one of the more common childhood cancers. A small fraction of WT occurs in association with aniridia, genitourinary abnormalities and…”
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Use of denaturing gradient gel electrophoresis to study conformational transitions in nucleic acids by Abrams, E S, Stanton, Jr, V P

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Selective killing of cancer cells based on loss of heterozygosity and normal variation in the human genome: a new paradigm for anticancer drug therapy by Basilion, J P, Schievella, A R, Burns, E, Rioux, P, Olson, J C, Monia, B P, Lemonidis, K M, Stanton, Jr, V P, Housman, D E

“…Most drugs for cancer therapy are targeted to relative differences in the biological characteristics of cancer cells and normal cells. The therapeutic index of…”
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Rapid and efficient construction of yeast artificial chromosome contigs in the mouse genome with interspersed repetitive sequence PCR (IRS-PCR): generation of a 5-cM, > 5 megabase contig on mouse chromosome 1 by Hunter, K W, Ontiveros, S D, Watson, M L, Stanton, Jr, V P, Gutierrez, P, Bhat, D, Rochelle, J, Graw, S, Ton, C, Schalling, M

“…We have developed a new technique for the generation of YAC contigs in the mouse genome that is based on the ability to detect overlapping clones by…”
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Ordering three DNA polymorphisms on human chromosome 3 by sperm typing by Goradia, T M, Stanton, Jr, V P, Cui, X F, Aburatani, H, Li, H H, Lange, K, Housman, D E, Arnheim, N

“…Three loci on the short arm of human chromosome 3 were ordered by sperm typing to expand the limited genetic map of this region. Almost 300 individual sperm…”
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Large-scale cloning of human chromosome 2-specific yeast artificial chromosomes (YACs) using an interspersed repetitive sequences (IRS)-PCR approach by Liu, Jing, Stanton, Vincent P., Fujiwara, T.Mary, Wang, Jian-Xue, Rezonzew, Rebeca, Crumley, M.Joyce, Morgan, Kenneth, Gros, Philippe, Housman, David, Schurr, Erwin

“…We report here an efficient approach to the establishment of extended YAC contigs on human chromosome 2 by using an interspersed repetitive sequences…”
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Rapid identification of overlapping YACs in the MEN2 region of human chromosome 10 by hybridization with Alu element-mediated PCR products by Moir, D T, Dorman, T E, Xue, F, Ma, N S, Stanton, Jr, V P, Housman, D, Bowden, D W, Noll, W W, Mao, J

“…An overlapping set of 21 yeast artificial chromosomes (YACs) spanning the RET proto-oncogene [Takahashi et al., Oncogene 3 (1988) 571-578] and D10S102 markers…”
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YAC contigs for 4q35 in the region of the facioscapulohumeral muscular dystrophy (FSHD) gene by Weiffenbach, B, Dubois, J, Manning, S, Ma, N S, Schutte, B C, Winokur, S T, Altherr, M R, Jacobsen, S J, Stanton, Jr, V P, Yokoyama, K

“…We report here the construction of a genetic linkage map and an overlapping set of clones containing DNA markers linked to the causative locus for…”
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Phosphorylation occurs in the amino terminus of the Raf-1 protein by McGrew, B R, Nichols, D W, Stanton, Jr, V P, Cai, H, Whorf, R C, Patel, V, Cooper, G M, Laudano, A P

“…The ability of the Raf-1 protein to morphologically transform murine fibroblasts can be activated by amino-terminal deletions or substitutions. We have…”
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Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member by Brook, J D, McCurrach, M E, Harley, H G, Buckler, A J, Church, D, Aburatani, H, Hunter, K, Stanton, V P, Thirion, J P, Hudson, T

“…Using positional cloning strategies, we have identified a CTG triplet repeat that undergoes expansion in myotonic dystrophy patients. This sequence is highly…”
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Sperm typing allows accurate measurement of the recombination fraction between D3S2 and D3S3 on the short arm of human chromosome 3 by Hubert, R, Stanton, Jr, V P, Aburatani, H, Warren, J, Li, H, Housman, D E, Arnheim, N

“…The interval between the D3S2 and D3S3 loci on human chromosome 3p is a frequent site of deletions in a number of different cancers and contains the most…”
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