Items where Subject is "Gene mapping"

B

Bar, Merav and Wyman, Stacia K. and Fritz, Brian R. and Qi, Junlin and Garg, Kavita S. and Parkin, Rachael K. and Kroh, Evan M. and Bendoraite, Ausra and Mitchell, Patrick S. and Nelson, Angelique and Ruzzo, Walter L. and Ware, Carol and Radich, Jerald P. and Gentleman, Robert and Ruohola-Baker, Hannele and Tewari, Muneesh (2008) MicroRNA discovery and profiling in human embryonic stem cells by deep sequencing of small RNA libraries. Stem Cells. ISSN 1066-5099

C

Coyle, Susan M and Huntingford, Felicity A and Peichel, Catherine L (2007) Parallel evolution of Pitx1 underlies pelvic reduction in Scottish threespine stickleback (Gasterosteus aculeatus). The Journal of Heredity, 98 (6). pp. 581-586. ISSN 0022-1503

D

Dreger, R T and Harris, M J and Peichel, Catherine L and Vogt, T F and Juriloff, D M (1995) The first arch (Far) mutation in mice recombines with Hoxd and Mdk. Mammalian genome : official journal of the International Mammalian Genome Society, 6 (9). pp. 662-663. ISSN 0938-8990

E

Edelhoff, S and Ayer, D E and Zervos, A S and Steingrímsson, E and Jenkins, N A and Copeland, N G and Eisenman, R N and Brent, R and Disteche, C M (1994) Mapping of two genes encoding members of a distinct subfamily of MAX interacting proteins: MAD to human chromosome 2 and mouse chromosome 6, and MXI1 to human chromosome 10 and mouse chromosome 19. Oncogene, 9 (2). pp. 665-668. ISSN 0950-9232

F

FitzGerald, Liesel M. and Kwon, Erika M. and Koopmeiners, Joseph S. and Salinas, Claudia A. and Stanford, Janet L. and Ostrander, Elaine A. (2009) Analysis of recently identified prostate cancer susceptibility loci in a population-based study: Associations with family history and clinical features. Clinical Cancer Research, 15 (9). pp. 3231-3237. ISSN 1557-3265

G

Gilladoga, A D and Edelhoff, S and Blackwood, E M and Eisenman, R N and Disteche, C M (1992) Mapping of MAX to human chromosome 14 and mouse chromosome 12 by in situ hybridization. Oncogene, 7 (6). pp. 1249-1251. ISSN 0950-9232

O

Orian, Amir and van Steensel, Bas and Delrow, Jeffrey and Bussemaker, Harmen J and Li, Ling and Sawado, Tomoyuki and Williams, Eleanor and Loo, Lenora W M and Cowley, Shaun M and Yost, Cynthia and Pierce, Sarah and Edgar, Bruce A and Parkhurst, Susan M and Eisenman, Robert N (2003) Genomic binding by the Drosophila Myc, Max, Mad/Mnt transcription factor network. Genes & development, 17 (9). pp. 1101-1114. ISSN 0890-9369

P

Palmiter, R D and Gagnon, J and Vogt, V M and Ripley, S and Eisenman, R N (1978) The NH2-terminal sequence of the avian oncovirus gag precursor polyprotein (Pr76gag). Virology, 91 (2). pp. 423-433. ISSN 0042-6822

Peichel, Catherine L and Abbott, C M and Vogt, T F (1996) Genetic and physical mapping of the mouse Ulnaless locus. Genetics, 144 (4). pp. 1757-1767. ISSN 0016-6731

Peichel, Catherine L and Kozak, C A and Luyten, F P and Vogt, T F (1998) Evaluation of mouse Sfrp3/Frzb1 as a candidate for the lst, Ul, and Far mutants on chromosome 2. Mammalian genome : official journal of the International Mammalian Genome Society, 9 (5). pp. 385-387. ISSN 0938-8990

Peichel, Catherine L and Scherer, S W and Tsui, L C and Beier, D R and Vogt, T F (1993) Mapping the midkine family of developmentally regulated signaling molecules. Mammalian genome : official journal of the International Mammalian Genome Society, 4 (11). pp. 632-638. ISSN 0938-8990

S

Song, Honglin and Ramus, Susan J and Tyrer, Jonathan and Bolton, Kelly L and Gentry-Maharaj, Aleksandra and Wozniak, Eva and Anton-Culver, Hoda and Chang-Claude, Jenny and Cramer, Daniel W and DiCioccio, Richard and Dörk, Thilo and Goode, Ellen L and Goodman, Marc T and Schildkraut, Joellen M and Sellers, Thomas and Baglietto, Laura and Beckmann, Matthias W and Beesley, Jonathan and Blaakaer, Jan and Carney, Michael E and Chanock, Stephen and Chen, Zhihua and Cunningham, Julie M and Dicks, Ed and Doherty, Jennifer A and Dürst, Matthias and Ekici, Arif B and Fenstermacher, David and Fridley, Brooke L and Giles, Graham and Gore, Martin E and De Vivo, Immaculata and Hillemanns, Peter and Hogdall, Claus and Hogdall, Estrid and Iversen, Edwin S and Jacobs, Ian J and Jakubowska, Anna and Li, Dong and Lissowska, Jolanta and Lubiński, Jan and Lurie, Galina and McGuire, Valerie and McLaughlin, John and Medrek, Krzysztof and Moorman, Patricia G and Moysich, Kirsten and Narod, Steven and Phelan, Catherine and Pye, Carole and Risch, Harvey and Runnebaum, Ingo B and Severi, Gianluca and Southey, Melissa and Stram, Daniel O and Thiel, Falk C and Terry, Kathryn L and Tsai, Ya-Yu and Tworoger, Shelley S and Van Den Berg, David J and Vierkant, Robert A and Wang-Gohrke, Shan and Webb, Penelope M and Wilkens, Lynne R and Wu, Anna H and Yang, Hannah and Brewster, Wendy and Ziogas, Argyrios and Houlston, Richard and Tomlinson, Ian and Whittemore, Alice S and Rossing, Mary Anne and Ponder, Bruce A J and Pearce, Celeste Leigh and Ness, Roberta B and Menon, Usha and Kjaer, Susanne Krüger and Gronwald, Jacek and Garcia-Closas, Montserrat and Fasching, Peter A and Easton, Douglas F and Chenevix-Trench, Georgia and Berchuck, Andrew and Pharoah, Paul D P and Gayther, Simon A (2009) A genome-wide association study identifies a new ovarian cancer susceptibility locus on 9p22.2. Nature genetics, 41 (9). pp. 996-1000. ISSN 1546-1718