-
1
-
-
0032555020
-
Incidence of hereditary nonpolyposis colorectal cancer and the feasibility of molecular screening for the disease
-
Aaltonen LA, Salovaara R, Kristo P, Canzian F, Hemminki A, Peltomäki P, Chadwick RB, Kääriäinen H, Eskelinen M, Järvinen H, Mecklin JP, de la Chapelle A. 1998. Incidence of hereditary nonpolyposis colorectal cancer and the feasibility of molecular screening for the disease. N Engl J Med 338:1481-1487.
-
(1998)
N Engl J Med
, vol.338
, pp. 1481-1487
-
-
Aaltonen, L.A.1
Salovaara, R.2
Kristo, P.3
Canzian, F.4
Hemminki, A.5
Peltomäki, P.6
Chadwick, R.B.7
Kääriäinen, H.8
Eskelinen, M.9
Järvinen, H.10
Mecklin, J.P.11
de la Chapelle, A.12
-
2
-
-
0037113938
-
A complex of the Srb8, -9, -10, and -11 transcriptional regulatory proteins from yeast
-
Borggrefe T, Davis R, Erdjument-Bromage H, Tempst P, Kornberg RD. 2002. A complex of the Srb8, -9, -10, and -11 transcriptional regulatory proteins from yeast. J Biol Chem 277:44202-44207.
-
(2002)
J Biol Chem
, vol.277
, pp. 44202-44207
-
-
Borggrefe, T.1
Davis, R.2
Erdjument-Bromage, H.3
Tempst, P.4
Kornberg, R.D.5
-
3
-
-
84863922124
-
Comprehensive molecular characterization of human colon and rectal cancer
-
Cancer Genome Atlas Network.
-
Cancer Genome Atlas Network. 2012. Comprehensive molecular characterization of human colon and rectal cancer. Nature 487:330-337.
-
(2012)
Nature
, vol.487
, pp. 330-337
-
-
-
4
-
-
0037245894
-
High cumulative incidence of uterine leiomyoma in black and white women: ultrasound evidence
-
Day Baird D, Dunson DB, Hill MC, Cousins D, Schectman JM. 2003. High cumulative incidence of uterine leiomyoma in black and white women: ultrasound evidence. Am J Obstet Gynecol 188:100-107.
-
(2003)
Am J Obstet Gynecol
, vol.188
, pp. 100-107
-
-
Day Baird, D.1
Dunson, D.B.2
Hill, M.C.3
Cousins, D.4
Schectman, J.M.5
-
5
-
-
84880325091
-
Mediator complex subunit 12 exon 2 mutation analysis in different subtypes of smooth muscle tumors confirms genetic heterogeneity
-
de Graaff MA, Cleton-Jansen AM, Szuhai K, Bovee JV. 2013. Mediator complex subunit 12 exon 2 mutation analysis in different subtypes of smooth muscle tumors confirms genetic heterogeneity. Hum Pathol 44:1597-1604.
-
(2013)
Hum Pathol
, vol.44
, pp. 1597-1604
-
-
de Graaff, M.A.1
Cleton-Jansen, A.M.2
Szuhai, K.3
Bovee, J.V.4
-
6
-
-
33748779351
-
Health care resource use for uterine fibroid tumors in the United States
-
Flynn M, Jamison M, Datta S, Myers E. 2006. Health care resource use for uterine fibroid tumors in the United States. Am J Obstet Gynecol 195:955-964.
-
(2006)
Am J Obstet Gynecol
, vol.195
, pp. 955-964
-
-
Flynn, M.1
Jamison, M.2
Datta, S.3
Myers, E.4
-
7
-
-
75549087826
-
COSMIC (the Catalogue of Somatic Mutations in Cancer): a resource to investigate acquired mutations in human cancer
-
Forbes SA, Tang G, Bindal N, Bamford S, Dawson E, Cole C, Kok CY, Jia M, Ewing R, Menzies A, Teaque JW, Stratton MR, et al. 2010. COSMIC (the Catalogue of Somatic Mutations in Cancer): a resource to investigate acquired mutations in human cancer. Nucleic Acids Res 38:D652-D657.
-
(2010)
Nucleic Acids Res
, vol.38
-
-
Forbes, S.A.1
Tang, G.2
Bindal, N.3
Bamford, S.4
Dawson, E.5
Cole, C.6
Kok, C.Y.7
Jia, M.8
Ewing, R.9
Menzies, A.10
Teaque, J.W.11
Stratton, M.R.12
-
8
-
-
73549099794
-
Nationwide use of laparoscopic hysterectomy compared with abdominal and vaginal approaches
-
Jacoby VL, Autry A, Jacobson G, Domush R, Nakagawa S, Jacoby A. 2009. Nationwide use of laparoscopic hysterectomy compared with abdominal and vaginal approaches. Obstet Gynecol 114:1041-1048.
-
(2009)
Obstet Gynecol
, vol.114
, pp. 1041-1048
-
-
Jacoby, V.L.1
Autry, A.2
Jacobson, G.3
Domush, R.4
Nakagawa, S.5
Jacoby, A.6
-
9
-
-
84864138141
-
Mutational analysis of MED12 exon 2 in uterine leiomyoma and other common tumors
-
Je EM, Kim MR, Min KO, Yoo NJ, Lee SH. 2012. Mutational analysis of MED12 exon 2 in uterine leiomyoma and other common tumors. Int J Cancer 2012:E1044-E1047.
-
(2012)
Int J Cancer
, vol.2012
-
-
Je, E.M.1
Kim, M.R.2
Min, K.O.3
Yoo, N.J.4
Lee, S.H.5
-
10
-
-
84869029053
-
Somatic MED12 mutations in uterine leiomyosarcoma and colorectal cancer
-
Kämpjärvi K, Mäkinen N, Kilpivaara O, Arola J, Heinonen HR, Böhm J, Abdel-Wahab O, Lehtonen HJ, Pelttari LM, Mehine M, Schrewe H, Nevanlinna H, et al. 2012. Somatic MED12 mutations in uterine leiomyosarcoma and colorectal cancer. Br J Cancer 107:1761-1765.
-
(2012)
Br J Cancer
, vol.107
, pp. 1761-1765
-
-
Kämpjärvi, K.1
Mäkinen, N.2
Kilpivaara, O.3
Arola, J.4
Heinonen, H.R.5
Böhm, J.6
Abdel-Wahab, O.7
Lehtonen, H.J.8
Pelttari, L.M.9
Mehine, M.10
Schrewe, H.11
Nevanlinna, H.12
-
11
-
-
33646580781
-
Mediator is a transducer of Wnt/beta-catenin signaling
-
Kim S, Xu X, Hecht A, Boyer TG. 2006. Mediator is a transducer of Wnt/beta-catenin signaling. J Biol Chem 281:14066-14075.
-
(2006)
J Biol Chem
, vol.281
, pp. 14066-14075
-
-
Kim, S.1
Xu, X.2
Hecht, A.3
Boyer, T.G.4
-
12
-
-
0037102441
-
Few FH mutations in sporadic counterparts of tumor types observed in hereditary leiomyomatosis and renal cell cancer families
-
Kiuru M, Lehtonen R, Arola J, Salovaara R, Järvinen H, Aittomäki K, Sjöberg J, Visakorpi T, Knuutila S, Isola J, Delahunt B, Herva R, et al. 2002. Few FH mutations in sporadic counterparts of tumor types observed in hereditary leiomyomatosis and renal cell cancer families. Cancer Res 62:4554-4557.
-
(2002)
Cancer Res
, vol.62
, pp. 4554-4557
-
-
Kiuru, M.1
Lehtonen, R.2
Arola, J.3
Salovaara, R.4
Järvinen, H.5
Aittomäki, K.6
Sjöberg, J.7
Visakorpi, T.8
Knuutila, S.9
Isola, J.10
Delahunt, B.11
Herva, R.12
-
13
-
-
80054097980
-
MED12, the mediator complex subunit 12 gene, is mutated at high frequency in uterine leiomyomas
-
Mäkinen N, Mehine M, Tolvanen J, Kaasinen E, Li Y, Lehtonen HJ, Gentile M, Yan J, Enge M, Taipale M, Aavikko M, Katainen R, et al. 2011a. MED12, the mediator complex subunit 12 gene, is mutated at high frequency in uterine leiomyomas. Science 334:252-255.
-
(2011)
Science
, vol.334
, pp. 252-255
-
-
Mäkinen, N.1
Mehine, M.2
Tolvanen, J.3
Kaasinen, E.4
Li, Y.5
Lehtonen, H.J.6
Gentile, M.7
Yan, J.8
Enge, M.9
Taipale, M.10
Aavikko, M.11
Katainen, R.12
-
14
-
-
84858059395
-
MED12 exon 2 mutations are common in uterine leiomyomas from South African patients
-
Mäkinen N, Heinonen HR, Moore S, Tomlinson IP, van der Spuy ZM, Aaltonen LA. 2011b. MED12 exon 2 mutations are common in uterine leiomyomas from South African patients. Oncotarget 2:966-969.
-
(2011)
Oncotarget
, vol.2
, pp. 966-969
-
-
Mäkinen, N.1
Heinonen, H.R.2
Moore, S.3
Tomlinson, I.P.4
van der Spuy, Z.M.5
Aaltonen, L.A.6
-
15
-
-
84885898181
-
MED12 exon 2 mutations in histopathological uterine leiomyoma variants
-
Mäkinen N, Vahteristo P, Kämpjärvi K, Arola J, Bützow R, Aaltonen LA. 2013. MED12 exon 2 mutations in histopathological uterine leiomyoma variants. Eur J Hum Genet 21:1300-1303.
-
(2013)
Eur J Hum Genet
, vol.21
, pp. 1300-1303
-
-
Mäkinen, N.1
Vahteristo, P.2
Kämpjärvi, K.3
Arola, J.4
Bützow, R.5
Aaltonen, L.A.6
-
16
-
-
84864432850
-
MED12 mutations in uterine fibroids-their relationship to cytogenetic subgroups
-
Markowski DN, Bartnitzke S, Loning T, Drieschner N, Helmke BM, Bullerdiek J. 2012a. MED12 mutations in uterine fibroids-their relationship to cytogenetic subgroups. Int J Cancer 131:1528-1536.
-
(2012)
Int J Cancer
, vol.131
, pp. 1528-1536
-
-
Markowski, D.N.1
Bartnitzke, S.2
Loning, T.3
Drieschner, N.4
Helmke, B.M.5
Bullerdiek, J.6
-
17
-
-
84872419881
-
MED12 mutations occurring in benign and malignant mammalian smooth muscle tumors
-
Markowski DN, Huhle S, Nimzyk R, Stenman G, Loning T, Bullerdiek J. 2012b. MED12 mutations occurring in benign and malignant mammalian smooth muscle tumors. Genes Chromosomes Cancer 52:297-304.
-
(2012)
Genes Chromosomes Cancer
, vol.52
, pp. 297-304
-
-
Markowski, D.N.1
Huhle, S.2
Nimzyk, R.3
Stenman, G.4
Loning, T.5
Bullerdiek, J.6
-
18
-
-
84874201565
-
Prevalence of MED12 mutations in uterine and extrauterine smooth muscle tumours
-
Matsubara A, Sekine S, Yoshida M, Yoshida A, Taniguchi H, Kushima R, Tsuda H, Kanai Y. 2012. Prevalence of MED12 mutations in uterine and extrauterine smooth muscle tumours. Histopathology 62:657-661.
-
(2012)
Histopathology
, vol.62
, pp. 657-661
-
-
Matsubara, A.1
Sekine, S.2
Yoshida, M.3
Yoshida, A.4
Taniguchi, H.5
Kushima, R.6
Tsuda, H.7
Kanai, Y.8
-
19
-
-
84858054364
-
Whole exome sequencing in a random sample of North American women with leiomyomas identifies MED12 mutations in majority of uterine leiomyomas
-
McGuire MM, Yatsenko A, Hoffner L, Jones M, Surti U, Rajkovic A. 2012. Whole exome sequencing in a random sample of North American women with leiomyomas identifies MED12 mutations in majority of uterine leiomyomas. PLoS One 7:e33251.
-
(2012)
PLoS One
, vol.7
-
-
McGuire, M.M.1
Yatsenko, A.2
Hoffner, L.3
Jones, M.4
Surti, U.5
Rajkovic, A.6
-
20
-
-
84879771630
-
Characterization of uterine leiomyomas by whole-genome sequencing
-
Mehine M, Kaasinen E, Mäkinen N, Katainen R, Kämpjärvi K, Pitkänen E, Heinonen HR, Bützow R, Kilpivaara O, Kuosmanen A, Ristolainen H, Gentile M, et al. 2013. Characterization of uterine leiomyomas by whole-genome sequencing. N Engl J Med 369:43-53.
-
(2013)
N Engl J Med
, vol.369
, pp. 43-53
-
-
Mehine, M.1
Kaasinen, E.2
Mäkinen, N.3
Katainen, R.4
Kämpjärvi, K.5
Pitkänen, E.6
Heinonen, H.R.7
Bützow, R.8
Kilpivaara, O.9
Kuosmanen, A.10
Ristolainen, H.11
Gentile, M.12
-
21
-
-
34147162657
-
Etiology, symptomatology, and diagnosis of uterine myomas
-
Parker WH. 2007. Etiology, symptomatology, and diagnosis of uterine myomas. Fertil Steril 87:725-736.
-
(2007)
Fertil Steril
, vol.87
, pp. 725-736
-
-
Parker, W.H.1
-
22
-
-
84863096005
-
MED12 alterations in both human benign and malignant uterine soft tissue tumors
-
Perot G, Croce S, Ribeiro A, Lagarde P, Velasco V, Neuville A, Coindre JM, Stoeckle E, Floquet A, Macgrogan G, Chibon F. 2012. MED12 alterations in both human benign and malignant uterine soft tissue tumors. PLoS One 7:e40015.
-
(2012)
PLoS One
, vol.7
-
-
Perot, G.1
Croce, S.2
Ribeiro, A.3
Lagarde, P.4
Velasco, V.5
Neuville, A.6
Coindre, J.M.7
Stoeckle, E.8
Floquet, A.9
Macgrogan, G.10
Chibon, F.11
-
23
-
-
84877010692
-
MED12 mutations in leiomyosarcoma and extrauterine leiomyoma
-
Ravegnini G, Marino-Enriquez A, Slater J, Eilers G, Wang Y, Zhu M, Nucci MR, George S, Angelini S, Raut CP, Fletcher JA. 2012. MED12 mutations in leiomyosarcoma and extrauterine leiomyoma. Mod Pathol 26:743-749.
-
(2012)
Mod Pathol
, vol.26
, pp. 743-749
-
-
Ravegnini, G.1
Marino-Enriquez, A.2
Slater, J.3
Eilers, G.4
Wang, Y.5
Zhu, M.6
Nucci, M.R.7
George, S.8
Angelini, S.9
Raut, C.P.10
Fletcher, J.A.11
-
24
-
-
84879684170
-
Mutation status of the mediator complex subunit 12 (MED12) in uterine leiomyomas and concurrent/metachronous multifocal peritoneal smooth muscle nodules (leiomyomatosis peritonealis disseminata)
-
Rieker RJ, Agaimy A, Moskalev EA, Hebele S, Hein A, Mehlhorn G, Beckmann MW, Hartmann A, Haller F. 2013. Mutation status of the mediator complex subunit 12 (MED12) in uterine leiomyomas and concurrent/metachronous multifocal peritoneal smooth muscle nodules (leiomyomatosis peritonealis disseminata). Pathology 45:388-392.
-
(2013)
Pathology
, vol.45
, pp. 388-392
-
-
Rieker, R.J.1
Agaimy, A.2
Moskalev, E.A.3
Hebele, S.4
Hein, A.5
Mehlhorn, G.6
Beckmann, M.W.7
Hartmann, A.8
Haller, F.9
-
25
-
-
0034129240
-
Population-based molecular detection of hereditary nonpolyposis colorectal cancer
-
Salovaara R, Loukola A, Kristo P, Kääriäinen H, Ahtola H, Eskelinen M, Härkönen N, Julkunen R, Kangas E, Ojala S, Tulikoura J, Valkamo E, et al. 2000. Population-based molecular detection of hereditary nonpolyposis colorectal cancer. J Clin Oncol 18:2193-2200.
-
(2000)
J Clin Oncol
, vol.18
, pp. 2193-2200
-
-
Salovaara, R.1
Loukola, A.2
Kristo, P.3
Kääriäinen, H.4
Ahtola, H.5
Eskelinen, M.6
Härkönen, N.7
Julkunen, R.8
Kangas, E.9
Ojala, S.10
Tulikoura, J.11
Valkamo, E.12
-
26
-
-
0029088063
-
Recurrent rearrangements in the high mobility group protein gene, HMGI-C, in benign mesenchymal tumours
-
Schoenmakers EF, Wanschura S, Mols R, Bullerdiek J, Van den Berghe H, Van de Ven WJ. 1995. Recurrent rearrangements in the high mobility group protein gene, HMGI-C, in benign mesenchymal tumours. Nat Genet 10:436-444.
-
(1995)
Nat Genet
, vol.10
, pp. 436-444
-
-
Schoenmakers, E.F.1
Wanschura, S.2
Mols, R.3
Bullerdiek, J.4
Van den Berghe, H.5
Van de Ven, W.J.6
-
27
-
-
84890115210
-
MED12 exon 2 mutations in uterine and extrauterine smooth muscle tumors
-
Schwetye KE, Pfeifer JD, Duncavage EJ. 2014. MED12 exon 2 mutations in uterine and extrauterine smooth muscle tumors. Hum Pathol 45:65-70.
-
(2014)
Hum Pathol
, vol.45
, pp. 65-70
-
-
Schwetye, K.E.1
Pfeifer, J.D.2
Duncavage, E.J.3
-
28
-
-
84898646236
-
Proceedings from the third national institutes of health international congress on advances in uterine leiomyoma research: comprehensive review, conference summary and future recommendations
-
Segars JH, Parrott EC, Nagel JD, Guo XC, Gao X, Birnbaum LS, Pinn VW, Dixon D. 2014. Proceedings from the third national institutes of health international congress on advances in uterine leiomyoma research: comprehensive review, conference summary and future recommendations. Hum Reprod Update 20:309-333.
-
(2014)
Hum Reprod Update
, vol.20
, pp. 309-333
-
-
Segars, J.H.1
Parrott, E.C.2
Nagel, J.D.3
Guo, X.C.4
Gao, X.5
Birnbaum, L.S.6
Pinn, V.W.7
Dixon, D.8
-
29
-
-
77954759030
-
The human mediator complex: a versatile, genome-wide regulator of transcription
-
Taatjes DJ. 2010. The human mediator complex: a versatile, genome-wide regulator of transcription. Trends Biochem Sci 35:315-322.
-
(2010)
Trends Biochem Sci
, vol.35
, pp. 315-322
-
-
Taatjes, D.J.1
-
30
-
-
18544365990
-
Germline mutations in FH predispose to dominantly inherited uterine fibroids, skin leiomyomata and papillary renal cell cancer
-
Tomlinson IP, Alam NA, Rowan AJ, Barclay E, Jaeger EE, Kelsell D, Leigh I, Gorman P, Lamlum H, Rahman S, Roylance RR, Olpin S, et al. 2002. Germline mutations in FH predispose to dominantly inherited uterine fibroids, skin leiomyomata and papillary renal cell cancer. Nat Genet 30:406-410.
-
(2002)
Nat Genet
, vol.30
, pp. 406-410
-
-
Tomlinson, I.P.1
Alam, N.A.2
Rowan, A.J.3
Barclay, E.4
Jaeger, E.E.5
Kelsell, D.6
Leigh, I.7
Gorman, P.8
Lamlum, H.9
Rahman, S.10
Roylance, R.R.11
Olpin, S.12
-
31
-
-
84899923205
-
Uterine leiomyoma-linked MED12 mutations disrupt mediator-associated CDK activity
-
Turunen M, Spaeth JM, Keskitalo S, Park MJ, Kivioja T, Clark AD, Mäkinen N, Gao F, Palin K, Nurkkala H, Vähärautio A, Aavikko M, et al. 2014. Uterine leiomyoma-linked MED12 mutations disrupt mediator-associated CDK activity. Cell Rep 7:654-660.
-
(2014)
Cell Rep
, vol.7
, pp. 654-660
-
-
Turunen, M.1
Spaeth, J.M.2
Keskitalo, S.3
Park, M.J.4
Kivioja, T.5
Clark, A.D.6
Mäkinen, N.7
Gao, F.8
Palin, K.9
Nurkkala, H.10
Vähärautio, A.11
Aavikko, M.12
-
32
-
-
33745190319
-
Analysis of fumarate hydratase mutations in a population-based series of early onset uterine leiomyosarcoma patients
-
Ylisaukko-oja SK, Kiuru M, Lehtonen HJ, Lehtonen R, Pukkala E, Arola J, Launonen V, Aaltonen LA. 2006. Analysis of fumarate hydratase mutations in a population-based series of early onset uterine leiomyosarcoma patients. Int J Cancer 119:283-287.
-
(2006)
Int J Cancer
, vol.119
, pp. 283-287
-
-
Ylisaukko-oja, S.K.1
Kiuru, M.2
Lehtonen, H.J.3
Lehtonen, R.4
Pukkala, E.5
Arola, J.6
Launonen, V.7
Aaltonen, L.A.8
|