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Publication Listing for the MeSH term region. Found 37 abstracts

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Jakubowska A, Rozkrut D, Antoniou A, Hamann U, Scott RJ, McGuffog L, Healy S, Sinilnikova OM, Rennert G, Lejbkowicz F, Flugelman A, Andrulis IL, Glendon G, Ozcelik H, Thomassen M, Paligo M, Aretini P, Kantala J, Aroer B, Von Wachenfeldt A, Liljegren A, Loman N, Herbst K, Kristoffersson U, Rosenquist R, Karlsson P, Stenmark-Askmalm M, Melin B, Nathanson KL, Domchek SM, Byrski T, Huzarski T, Gronwald J, Menkiszak J, Cybulski C, Serrano P, Osorio A, Cajal TR, Tsitlaidou M, Benitez J, Gilbert M, Rookus M, Aalfs CM, Kluijt I, Boessenkool-Pape JL, Meijers-Heijboer HE, Oosterwijk JC, van Asperen CJ, Blok MJ, Nelen MR, van den Ouweland AM, Seynaeve C, van der Luijt RB, Devilee P, Easton DF, Peock S, Frost D, Platte R, Ellis SD, Fineberg E, Evans DG, Lalloo F, Eeles R, Jacobs C, Adlard J, Davidson R, Eccles D, Cole T, Cook J, Godwin A, Bove B, Stoppa-Lyonnet D, Caux-Moncoutier V, Belotti M, Tirapo C, Mazoyer S, Barjhoux L, Boutry-Kryza N, Pujol P, Coupier I, Peyrat JP, Vennin P, Muller D, Fricker JP, Venat-Bouvet L, Johannsson O, Isaacs C, Schmutzler R, Wappenschmidt B, Meindl A, Arnold N, Varon-Mateeva R, Niederacher D, Sutter C, Deissler H, Preisler-Adams S, Simard J, Soucy P, Durocher F, Chenevix-Trench G, Beesley J, Chen X, Rebbeck T, Couch F, Wang X, Lindor N, Fredericksen Z, Pankratz VS, Peterlongo P, Bonanni B, Fortuzzi S, Peissel B, Szabo C, Mai PL, Loud JT, Lubinski J. Association of PHB 1630 C > T and MTHFR 677 C > T polymorphisms with breast and ovarian cancer risk in BRCA1/2 mutation carriers: results from a multicenter study. British Journal of Cancer. 2012 Jun;106(12):2016-24.   PMCID: PMC3388557
Maradeo ME, Cairns P. Translational application of epigenetic alterations: Ovarian cancer as a model. Febs Letters. 2011 Jul;585(13):2112-20.   PMCID: PMC3129436
Nie H, Evans AA, London WT, Block TM, Ren XD, Rman Wf VP. Quantification of complex precore mutations of hepatitis B virus by SimpleProbe real time PCR and dual melting analysis. Journal of Clinical Virology. 2011 Aug;51(4):230-6.   PMCID: PMC3133867
Calin GA, Trapasso F, Shimizu M, Dumitru CD, Yendamuri S, Godwin AK, Ferracin M, Bernardi G, Chatterjee D, Baldassarre G, Rattan S, Alder H, Mabuchi H, Shiraishi T, Hansen LL, Overgaard J, Herlea V, Mauro FR, Dighiero G, Movsas B, Rassenti L, Kipps T, Baffa R, Fusco A, Mori M, Russo G, Liu CG, Neuberg D, Bullrich F, Negrini M, Croce CM. Familial cancer associated with a polymorphism in ARLTS1. New England Journal of Medicine. 2005 Apr 21;352(16):1667-76.
Nunez M, Ludes-Meyers J, Abba M, Kil H, Abbey N, Page R, Sahin A, Klein-Szanto A, Aldaz C. Frequent loss of WWOX expression in breast cancer: correlation with estrogen receptor status. Breast Cancer Research and Treatment. 2005 Jan;89(2):99-105.
Sarti M, Sevignani C, Calin GA, Aqeilan R, Shimizu M, Pentimalli F, Picchio MC, Godwin A, Rosenberg A, Drusco A, Negrini M, Croce CM. Adenoviral transduction of TESTIN gene into breast and uterine cancer cell lines promotes apoptosis and tumor reduction in vivo. Clinical Cancer Research. 2005 Jan 15;11(2):806-13.
Battaglieri M, Anciant E, Anghinolfi M, De Vita R, Golovach E, Laget JM, Mokeev V, Ripani M, Adams G, Amaryan MJ, Armstrong DS, Asavapibhop B, Asryan G, Audit G, Auger T, Avakian H, Barrow S, Beard K, Bektasoglu M, Berman BL, Bianchi N, Biselli AS, Boiarinov S, Branford D, Briscoe WJ, Brooks WK, Burkert VD, Calarco JR, Capitani GP, Carman DS, Carnahan B, Cazes A, Cetina C, Cole PL, Coleman A, Cords D, Corvisiero P, Crabb D, Crannell H, Cummings JP, DeSanctis E, Degtyarenko PV, Demirchyan R, Denizli H, Dennis L, Dharmawardane KV, Dhuga KS, Djalali C, Dodge GE, Doughty D, Dragovitsch P, Dugger M, Dytman S, Eckhause M, Egiyan H, Egiyan KS, Elouadrhiri L, Farhi L, Feuerbach RJ, Ficenec J, Forest TA, Freyberger AP, Frolov V, Funsten H, Gaff SJ, Gai M, Gilad S, Gilfoyle GP, Giovanetti KL, Griffioen K, Guidal M, Guillo M, Gyurjyan V, Hancock D, Hardie J, Heddle D, Hersman FW, Hicks K, Hicks RS, Holtrop M, Hyde-Wright CE, Ito MM, Joo K, Kelley JH, Khandaker M, Kim W, Klein A, Klein FJ, Klusman M, Kossov M, Kramer LH, Kuang Y, Kuhn SE, Lawrence D, Lucas M, Lukashin K, Major RW, Manak JJ, Marchand C, McAleer S, McCarthy J, McNabb JW, Mecking BA, Mestayer MD, Meyer CA, Mikhailov K, Minehart R, Mirazita M, Miskimen R, Muccifora V, Mueller J, Mutchler GS, Napolitano J, Nelson SO, Niczyporuk BB, Niyazov RA, O'Brien JT, Opper AK, Peterson G, Philips SA, Pivnyuk N, Pocanic D, Pogorelko O, Polli E, Preedom BM, Price JW, Protopopescu D, Qin LM, Raue BA, Reolon AR, Riccardi G, Ricco G, Ritchie BG, Ronchetti F, Rossi P, Rowntree D, Rubin PD, Sabourov K, Salgado C, Sanzone-Arenhovel M, Sapunenko V, Schumacher RA, Serov VS, Shafi A, Sharabian YG, Shaw J, Skabelin AV, Smith ES, Smith T, Smith LC, Sober DI, Spraker M, Stavinsky A, Stepanyan S, Stoler P, Taiuti M, Taylor S, Tedeschi DJ, Todor L, Thompson R, Vineyard MF, Vlassov AV, Weinstein LB, Weisberg A, Weller H, Weygand DP, Whisnant CS, Wolin E, Wood M, Yegneswaran A, Yun J, Zhang B, Zhao J, Zhou Z, CLAS Collaboration. Photoproduction of the rho(0) meson on the proton at large momentum transfer. Physical review letters. 2001 Oct 22;8717(17):-.
Jaiswal AK, Bell DW, Radjendirane V, Testa JR. Localization of human NQO1 gene to chromosome 16q22 and NQO2- 6p25 and associated polymorphisms. Pharmacogenetics. 1999 Jun;9(3):413-8.
Rondinelli RH, Tricoli JV. CLAR1, a novel gene that exhibits enhanced expression in advanced human prostate cancer. Clinical Cancer Research. 1999 Jun;5(6):1595-602.
Zekri AR, Bahnassi AA, Bove B, Huang YJ, Russo IH, Rogatko A, Shaarawy S, Shawki OA, Hamza MR, Omer S, Khaled HM, Russo J. Allelic instability as a predictor of survival in Egyptian breast cancer patients. International Journal of Oncology. 1999 Oct;15(4):757-67.
Laing NM, Belinsky MG, Kruh GD, Bell DW, Boyd JT, Barone L, Testa JR, Tew KD. Amplification of the ATP-Binding cassette 2 transporter gene is functionally linked with enhanced efflux of estramustine in ovarian carcinoma cells. Cancer Research. 1998 Apr;58(7):1332-7.
Pea M, Bonetti F, Martignoni G, Henske EP, Manfrin E, Colato C, Bernstein J. Apparent renal cell carcinomas in tuberous sclerosis are heterogeneous - The identification of malignant epithelioid angiomyolipoma. American Journal of Surgical Pathology. 1998 Feb;22(2):180-7.
Smolarek TA, Wessner LL, McCormack FX, Mylet JC, Menon AG, Henske EP. Evidence that lymphangiomyomatosis is caused by TSC2 mutations: Chromosome 16p13 loss of heterozygosity in angiomyolipomas and lymph nodes from women with lymphangiomyomatosis. American journal of human genetics. 1998 Apr;62(4):810-5.
Henske EP, Wessner LL, Golden J, Scheithauer BW, Vortmeyer AO, Zhuang ZP, KleinSzanto AJ, Kwiatkowski DJ, Yeung RS. Loss of tuberin in both subependymal giant cell astrocytomas and angiomyolipomas supports a two-hit model for the pathogenesis of tuberous sclerosis tumors. American Journal of Pathology. 1997 Dec;151(6):1639-47.
Cryer JE, Johnson SW, Engelsberg BN, Billings PC. Analysis of HMG protein binding to DNA modified with the anticancer drug cisplatin. Cancer Chemotherapy and Pharmacology. 1996 Jun;38(2):163-8.
Gastier JM, Brody T, Pulido JC, Businga T, Sunden S, Hu XT, Maitra S, Buetow KH, Murray JC, Sheffield VC, Boguski M, Duyk GM, Hudson TJ. Development of a screening set for New (CAG/CTG)(n) dynamic mutations. Genomics. 1996 Feb 15;32(1):75-85.
Katz RA, Merkel G, Skalka AM. Targeting of retroviral integrase by fusion to a heterologous DNA binding domain: In vitro activities and incorporation of a fusion protein into viral particles. Virology. 1996 Mar;217(1):178-90.
Yeung RS, Buetow KH, ScherpbierHeddema T, Bell DW, Testa JR. A genetic, physical, and comparative map of rat Chromosome 10. Mammalian Genome. 1996 Jun;7(6):425-8.
Altomare DA, Guo K, Cheng JQ, Sonoda G, Walsh K, Testa JR. Cloning, Chromosomal Localization and Expression Analysis of the Mouse Akt2 Oncogene. Oncogene. 1995 Sep 21;11(6):1055-60.
Franke TF, Yang SI, Chan TO, Datta K, Kazlauskas A, Morrison DK, Kaplan DR, Tsichlis PN. The Protein-Kinase Encoded by the Akt Protooncogene Is a Target of the Pdgf-Activated Phosphatidylinositol 3-Kinase. Cell. 1995 Jun 02;81(5):727-36.
The above publications are sorted by year, faculty last name, and first author. Click on any highlighted author listed to find all publications attributed to that individual. Click on the publication title to see the abstract. First authors who are faculty are highlighted like this. Last authors who are faculty are highlighted like this. Other authors who are faculty are highlighted like this.

MeSH cloud from publications including the MeSH term region

region gene expression heterozygosity homology resistance tumor-suppressor gene sequence cancer protein identification breast cancer growth suppressor linkage map kidney molecular-cloning renal angiomyolipomas sequence-independent amplification mutagenicity hiv-1 microrna expression profiles trinucleotide repeats eker allelotype WWOX renal sarcomas hydrocephalus mice microsatellite instability estrogen receptor human breast-cancer tuberous-sclerosis-2 tsc2 gene genotype cells expansion rna Quantification reductase dioxin NQO2 renal cell carcinoma excitation death e-antigen dna methylation specificity chromosome ovarian cancer risk dt-diaphorase gene mapping hmb-45 reactivity seroconversion human genome dimerization deletions somatic mosaicism subfamily risk receptors chromosome 13q12-q13 damaged dna angiomyolipoma 16q tuberous sclerosis human-immunodeficiency-virus photon tuberous sclerosis complex molecular markers loci HMG proteins mismatch repair deficiency kinase e-cadherin fra7g tumor-suppressor locus BRCA1 deletion 7q312 susceptibility locus messenger-rna Methylation ovarian-cancer Mutation pulmonary lymphangiomyomatosis electroproduction down-regulation chronic lymphocytic-leukemia oncogene recombination qPCR chromosome-17 lung poor-prognosis qcd polymerase chain-reaction lesions brca1 promoter association Ovarian cancer v-akt 13q14 mouse carcinogenesis basal core promoter glycoprotein lymphangioleiomyomatosis folate status prognostic factors nervous-system lesions progression-free survival antimitotic drug stem-like cells rat model site sporadic breast oxidoreductase integrase FRA16D PHB 1630 C > T polymorphism 2 mutation carriers-MTHFR 677 C > T polymorphism-breast invitro carcinomas NQO1 lim domain Precore SimpleProbe growth-factor myotonic-dystrophy chemotherapy lexa binding triplet repeat immunohistochemistry brca2 carcinoma in-situ modulation common mutation caveolin-1 peptides liver-disease allelic loss pion CDDP-DNA smooth-muscle zyxin localization protein- exclusive photoproduction hamartomas quinones
Last updated on Wednesday, August 12, 2020