Arnold Library

Items where Subject is "Mutation"

Group by: Creators | Item Type
Number of items at this level: 28.

Article or Abstract

Blackwood, E M and Lugo, T G and Kretzner, L and King, M W and Street, A J and Witte, O N and Eisenman, R N (1994) Functional analysis of the AUG- and CUG-initiated forms of the c-Myc protein. Molecular biology of the cell, 5 (5). pp. 597-609. ISSN 1059-1524

Carr, Laurie L and Gottschling, Daniel E (2008) Does age influence loss of heterozygosity? Experimental gerontology, 43 (3). pp. 123-129. ISSN 0531-5565

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

Cross, James T. and Poole, Elizabeth M. and Ulrich, Cornelia M. (2008) A review of gene-drug interactions for nonsteroidal anti-inflammatory drug use in preventing colorectal neoplasia. The Pharmacogenomics Journal, 8 (4). pp. 237-247. ISSN 1473-1150

Firzlaff, J M and Lüscher, B and Eisenman, R N (1991) Negative charge at the casein kinase II phosphorylation site is important for transformation but not for Rb protein binding by the E7 protein of human papillomavirus type 16. Proceedings of the National Academy of Sciences of the United States of America, 88 (12). pp. 5187-5191. ISSN 0027-8424

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

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

Hann, S R and Eisenman, R N (1984) Proteins encoded by the human c-myc oncogene: differential expression in neoplastic cells. Molecular and cellular biology, 4 (11). pp. 2486-2497. ISSN 0270-7306

Holt, S.K. and Kwon, E.M. and Peters, U. and Ostrander, E.A. and Stanford, J.L. (2009) Vitamin D Pathway Gene Variants and Prostate Cancer Risk. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 18 (6). pp. 1929-1933. ISSN 1055-9965

Johnatty, Sharon E and Beesley, Jonathan and Chen, Xiaoqing and Spurdle, Amanda B and Defazio, Anna and Webb, Penelope M and Goode, Ellen L and Rider, David N and Vierkant, Robert A and Anderson, Stephanie and Wu, Anna H and Pike, Malcolm and Van Den Berg, David and Moysich, Kirsten and Ness, Roberta and Doherty, Jennifer and Rossing, Mary-Anne and Pearce, Celeste Leigh and Chenevix-Trench, Georgia (2009) Polymorphisms in the FGF2 gene and risk of serous ovarian cancer: results from the ovarian cancer association consortium. Twin research and human genetics : the official journal of the International Society for Twin Studies, 12 (3). pp. 269-275. ISSN 1832-4274

Langeberg, Wendy J and Kwon, Erika M and Koopmeiners, Joseph S and Ostrander, Elaine A and Stanford, Janet L (2010) Population-based study of the association of variants in mismatch repair genes with prostate cancer risk and outcomes. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 19 (1). pp. 258-264. ISSN 1538-7755

Li, Xiaohong and Galipeau, Patricia C and Sanchez, Carissa A and Blount, Patricia L and Maley, Carlo C and Arnaudo, Jessica and Peiffer, Daniel A and Pokholok, Dmitry and Gunderson, Kevin L and Reid, Brian J (2008) Single nucleotide polymorphism-based genome-wide chromosome copy change, loss of heterozygosity, and aneuploidy in Barrett's esophagus neoplastic progression. Cancer prevention research (Philadelphia, Pa.), 1 (6). pp. 413-423. ISSN 1940-6215

Loo, L W M and Ton, C and Wang, Y-W and Grove, D I and Bouzek, H and Vartanian, N and Lin, M-G and Yuan, X and Lawton, T L and Daling, J R and Malone, K E and Li, C I and Hsu, L and Porter, P L (2008) Differential patterns of allelic loss in estrogen receptor-positive infiltrating lobular and ductal breast cancer. Genes, chromosomes & cancer, 47 (12). pp. 1049-1066. ISSN 1098-2264

Mason, W S and Linial, M and Hsu, T W and Eisenman, R N and Townsend, J and Mark, G E and Seal, G and Aldrich, C and Taylor, J M (1982) Alterations in the genomes of avian sarcoma viruses. Virology, 117 (2). pp. 456-474. ISSN 0042-6822

Meshinchi, Soheil and Appelbaum, Frederick R. (2009) Structural and functional Alterations of FLT3 in Acute Myeloid Leukemia. Clinical Cancer Research, 15 (13). pp. 4263-4269. ISSN 1078-0432

Meshinchi, Soheil and Stirewalt, Derek L and Alonzo, Todd A and Boggon, Titus J and Gerbing, Robert B and Rocnik, Jennifer L and Lange, Beverly J and Gilliland, D Gary and Radich, Jerald P (2008) Structural and numerical variation of FLT3/ITD in pediatric AML. Blood, 111 (10). pp. 4930-4933. ISSN 1528-0020

Oehler, VG and Qin, J and Ramakrishnan, R and Facer, G and Ananthnarayan, S and Cummings, C and Deininger, M and Shah, N and McCormick, F and Willis, S and Daridon, A and Unger, M and Radich, J (2008) Absolute quantitative detection of ABL tyrosine kinase domain point mutations in chronic myeloid leukemia using a novel nanofluidic platform and mutation-specific PCR. Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K. ISSN 1476-5551

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 Prabhakaran, B and Vogt, T F (1997) The mouse Ulnaless mutation deregulates posterior HoxD gene expression and alters appendicular patterning. Development (Cambridge, England), 124 (18). pp. 3481-3492. ISSN 0950-1991

Poole, Elizabeth M and Hsu, Li and Xiao, Liren and Kulmacz, Richard J and Carlson, Christopher S and Rabinovitch, Peter S and Makar, Karen W and Potter, John D and Ulrich, Cornelia M (2010) Genetic variation in prostaglandin E2 synthesis and signaling, prostaglandin dehydrogenase, and the risk of colorectal adenoma. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 19 (2). pp. 547-557. ISSN 1538-7755

Radstake, Timothy R D J and Gorlova, Olga and Rueda, Blanca and Martin, Jose-Ezequiel and Alizadeh, Behrooz Z and Palomino-Morales, Rogelio and Coenen, Marieke J and Vonk, Madelon C and Voskuyl, Alexandre E and Scheurwegh, Annemie J and Broen, Jasper C and van Riel, Piet L C M and van 't Slot, Ruben and Italiaander, Annet and Ophoff, Roel A and Riemekasten, Gabriela and Hunzelmann, Nico and Simeon, Carmen P and Ortego-Centeno, Norberto and González-Gay, Miguel A and González-Escribano, María F and Airo, Paolo and van Laar, Jaap and Herrick, Ariane and Worthington, Jane and Hesselstrand, Roger and Smith, Vanessa and de Keyser, Filip and Houssiau, Fredric and Chee, Meng May and Madhok, Rajan and Shiels, Paul and Westhovens, Rene and Kreuter, Alexander and Kiener, Hans and de Baere, Elfride and Witte, Torsten and Padykov, Leonid and Klareskog, Lars and Beretta, Lorenzo and Scorza, Rafaella and Lie, Benedicte A and Hoffmann-Vold, Anna-Maria and Carreira, Patricia and Varga, John and Hinchcliff, Monique and Gregersen, Peter K and Lee, Annette T and Ying, Jun and Han, Younghun and Weng, Shih-Feng and Amos, Christopher I and Wigley, Fredrick M and Hummers, Laura and Nelson, J Lee and Agarwal, Sandeep K and Assassi, Shervin and Gourh, Pravitt and Tan, Filemon K and Koeleman, Bobby P C and Arnett, Frank C and Martin, Javier and Mayes, Maureen D (2010) Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus. Nature genetics, 42 (5). pp. 426-429. ISSN 1546-1718

Rueda, B and Simeon, C and Hesselstrand, R and Herrick, A and Worthington, J and Ortego-Centeno, N and Riemekasten, G and Fonollosa, V and Vonk, MC and van den Hoogen, FHJ and Sanchez-Román, J and Aguirre-Zamorano, MA and García-Portales, R and Pros, A and Camps, MT and Gonzalez-Gay, MA and Coenen, MJ and Lambert, N and Nelson, JL and Radstake, TRDJ and Martin, J (2008) A large multicenter analysis of CTGF -945 promoter polymorphism does not confirm association with Systemic Sclerosis susceptibility or phenotype. Annals of the rheumatic diseases. ISSN 1468-2060

Sakai, Wataru and Swisher, Elizabeth M and Jacquemont, Céline and Chandramohan, Kurapaty Venkatapoorna and Couch, Fergus J and Langdon, Simon P and Wurz, Kaitlyn and Higgins, Jake and Villegas, Emily and Taniguchi, Toshiyasu (2009) Functional restoration of BRCA2 protein by secondary BRCA2 mutations in BRCA2-mutated ovarian carcinoma. Cancer research, 69 (16). pp. 6381-6386. ISSN 1538-7445

Sakai, Wataru and Swisher, Elizabeth M. and Karlan, Beth Y. and Agarwal, Mukesh K. and Higgins, Jake and Friedman, Cynthia and Villegas, Emily and Jacquemont, Céline and Farrugia, Daniel J. and Couch, Fergus J. and Urban, Nicole and Taniguchi, Toshiyasu (2008) Secondary mutations as a mechanism of cisplatin resistance in BRCA2-mutated cancers. Nature, 451 (7182). pp. 1116-1120. ISSN 1476-4687

Saracino, Misty R and Bigler, Jeannette and Schwarz, Yvonne and Chang, Jyh-Lurn and Li, Shiuying and Li, Lin and White, Emily and Potter, John D. and Lampe, Johanna W. (2009) Citrus Fruit Intake Is Associated with Lower Serum Bilirubin Concentration among Women with the UGT1A1*28 Polymorphism. The Journal of nutrition, 139 (3). pp. 555-560. ISSN 1541-6100

Swisher, Elizabeth M. and Sakai, Wataru and Karlan, Beth Y. and Wurz, Kaitlyn and Urban, Nicole and Taniguchi, Toshiyasu (2008) Secondary BRCA1 Mutations in BRCA1-Mutated Ovarian carcinomas with platinum resistance. Cancer Research, 68 (8). pp. 2581-2586. ISSN 1538-7445

Young, Janet M and Endicott, Raelynn M and Parghi, Sean S and Walker, Megan and Kidd, Jeffrey M and Trask, Barbara J (2008) Extensive copy-number variation of the human olfactory receptor gene family. American journal of human genetics, 83 (2). pp. 228-242. ISSN 1537-6605

This list was generated on Thu Mar 28 12:41:26 2024 PDT.