Elevated STAT3 expression in ovarian cancer ascites promotes invasion and metastasis: a potential therapeutic target von Saini, U, Naidu, S, ElNaggar, A C, Bid, H K, Wallbillich, J J, Bixel, K, Bolyard, C, Suarez, A A, Kaur, B, Kuppusamy, P, Hays, J, Goodfellow, P J, Cohn, D E, Selvendiran, K

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Frequent activating FGFR2 mutations in endometrial carcinomas parallel germline mutations associated with craniosynostosis and skeletal dysplasia syndromes von Pollock, P M, Gartside, M G, Dejeza, L C, Powell, M A, Mallon, M A, Davies, H, Mohammadi, M, Futreal, P A, Stratton, M R, Trent, J M, Goodfellow, P J

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Preferences for return of incidental findings from genome sequencing among women diagnosed with breast cancer at a young age von Kaphingst, K.A., Ivanovich, J., Biesecker, B.B., Dresser, R., Seo, J., Dressler, L.G., Goodfellow, P.J., Goodman, M.S.

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MLH1 Promoter Methylation and Gene Silencing is the Primary Cause of Microsatellite Instability in Sporadic Endometrial Cancers von Simpkins, Sally B., Bocker, Tina, Swisher, Elizabeth M., Mutch, David G., Gersell, Deborah J., Kovatich, Albert J., Palazzo, Juan P., Fishel, Richard, Goodfellow, Paul J.

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The mutational spectrum of FOXA2 in endometrioid endometrial cancer points to a tumor suppressor role von Smith, B, Neff, R, Cohn, D.E, Backes, F.J, Suarez, A.A, Mutch, D.G, Rush, C.M, Walker, C.J, Goodfellow, P.J

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Single Missense Mutation in the Tyrosine Kinase Catalytic Domain of the RET Protooncogene is Associated with Multiple Endocrine Neoplasia Type 2B von Carlson, Katrin M., Dou, Shenshen, Chi, David, Scavarda, Nancy, Toshima, Koji, Jackson, Charles E., Wells, Samuel A., Goodfellow, Paul J., Donis-Keller, Helen

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Confirmation that chromosome 18q allelic loss in colon cancer is a prognostic indicator von OGUNBIYI, O. A, GOODFELLOW, P. J, HERFARTH, K, GAGLIARDI, G, SWANSON, P. E, BIRNBAUM, E. H, READ, T. E, FLESHMAN, J. W, KODNER, I. J, MOLEY, J. F

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Mlh1 deficiency accelerates myeloid leukemogenesis in neurofibromatosis 1 (Nf1) heterozygous mice von Gutmann, D H, Winkeler, E, Kabbarah, O, Hedrick, N, Dudley, S, Goodfellow, P J, Liskay, R M

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Allelic loss of sequences from the long arm of chromosome 10 and replication errors in endometrial cancers von PEIFFER, S. L, HERZOG, T. J, TRIBUNE, D. J, MUTCH, D. G, GERSELL, D. J, GOODFELLOW, P. J

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Microsatellite Instability, MLH1 Promoter Methylation, and Loss of Mismatch Repair in Endometrial Cancer and Concomitant Atypical Hyperplasia von Horowitz, N., Pinto, K., Mutch, D.G., Herzog, T.J., Rader, J.S., Gibb, R., Bocker-Edmonston, T., Goodfellow, P.J.

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Parent-of-origin effects in multiple endocrine neoplasia type 2B von Carlson, K M, Bracamontes, J, Jackson, C E, Clark, R, Lacroix, A, Wells, Jr, S A, Goodfellow, P J

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Prevalence of Defective DNA Mismatch Repair and MSH6 Mutation in an Unselected Series of Endometrial Cancers von Goodfellow, Paul J., Buttin, Barbara M., Herzog, Thomas J., Rader, Janet S., Gibb, Randall K., Swisher, Elizabeth, Look, Katherine, Walls, Ken C., Fan, Ming-Yu, Mutch, David G.

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Assignment of a second Charcot-Marie-Tooth type II locus to chromosome 3q von KWON, J. M, ELLIOTT, J. L, WOON-CHEE YEE, IVANOVICH, J, SCAVARDA, N. J, MOOLSINTONG, P. J, GOODFELLOW, P. J

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RET Gene and Its Implications for Cancer von Goodfellow, Paul J., Wells, Samuel A.

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The T-box transcription factor gene TBX22 is mutated in X-linked cleft palate and ankyloglossia von Braybrook, Claire, Doudney, Kit, Marçano, Ana Carolina B., Arnason, Alfred, Bjornsson, Arni, Patton, Michael A., Goodfellow, Paul J., Moore, Gudrun E., Stanier, Philip

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Prognostic value of chromosome 1p allelic loss in colon cancer von Ogunbiyi, OA, Goodfellow, PJ, Gagliardi, G, Swanson, PE, Birnbaum, EH, Fleshman, JW, Kodner, IJ, Moley, JF

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A Drosophila Model of Multiple Endocrine Neoplasia Type 2 von Read, Renee D, Goodfellow, Paul J, Mardis, Elaine R, Novak, Nancy, Armstrong, Jon R, Cagan, Ross L

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A Pseudoautosomal Gene in Man von Goodfellow, Paul J., Darling, Susan M., Thomas, Nicholas S., Goodfellow, Peter N.

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Assignment of multiple endocrine neoplasia type 2A to chromosome 10 by linkage von SIMPSON, N. E, KIDD, K. K, CASTIGLIONE, C, GENEL, M, GERTNER, J, GREENBERG, C. R, GUSELLA, J. F, HOLDEN, J. J. A, WHITE, B. N, GOODFELLOW, P. J, MCDERMID, H, MYERS, S, KIDD, J. R, JACKSON, C. E, DUNCAN, A. M. V, FARRER, L. A, BRASCH, K

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CDKN1A and CDKN1B polymorphisms and risk of advanced prostate carcinoma von KIBEL, Adam S, SUAREZ, Brian K, BELANI, Jay, OH, Joe, WEBSTER, Raul, BROPHY-EBBERS, Michele, CHAN GUO, CATALONA, William J, PICUS, Joel, GOODFELLOW, Paul J

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