-
1
-
-
0034644185
-
Environmental and heritable factors in the causation of cancer-analyses of cohorts of twins from Sweden, Denmark, and Finland
-
Lichtenstein P, Holm NV, Verkasalo PK, Iliadou A, Kaprio J, Koskenvuo M, Pukkala E, Skytthe A, Hemminki K. Environmental and heritable factors in the causation of cancer-analyses of cohorts of twins from Sweden, Denmark, and Finland. N Engl J Med 2000;343:78-85.
-
(2000)
N Engl J Med
, vol.343
, pp. 78-85
-
-
Lichtenstein, P.1
Holm, N.V.2
Verkasalo, P.K.3
Iliadou, A.4
Kaprio, J.5
Koskenvuo, M.6
Pukkala, E.7
Skytthe, A.8
Hemminki, K.9
-
2
-
-
0025909734
-
Identification of a gene located at chromosome 5q21 that is mutated in colorectal cancers
-
Kinzler KW, Nilbert MC, Vogelstein B, Bryan TM, Levy DB, Smith KJ, Preisinger AC, Hamilton SR, Hedge P, Markham A, et al. Identification of a gene located at chromosome 5q21 that is mutated in colorectal cancers. Science 1991;251:1366-70.
-
(1991)
Science
, vol.251
, pp. 1366-1370
-
-
Kinzler, K.W.1
Nilbert, M.C.2
Vogelstein, B.3
Bryan, T.M.4
Levy, D.B.5
Smith, K.J.6
Preisinger, A.C.7
Hamilton, S.R.8
Hedge, P.9
Markham, A.10
-
3
-
-
0030592517
-
Lessons from hereditary colorectal cancer
-
Kinzler KW, Vogelstein B. Lessons from hereditary colorectal cancer. Cell 1996;87:159-70.
-
(1996)
Cell
, vol.87
, pp. 159-170
-
-
Kinzler, K.W.1
Vogelstein, B.2
-
5
-
-
0029066689
-
Inactivation of the type II TGF-beta receptor in colon cancer cells with microsatellite instability
-
Markowitz S, Wang J, Myeroff L, Parsons R, Sun L, Lutterbaugh J, Fan RS, Zborowska E, Kinzler KW, Vogelstein B, et al. Inactivation of the type II TGF-beta receptor in colon cancer cells with microsatellite instability. Science 1995;268:1336-8.
-
(1995)
Science
, vol.268
, pp. 1336-1338
-
-
Markowitz, S.1
Wang, J.2
Myeroff, L.3
Parsons, R.4
Sun, L.5
Lutterbaugh, J.6
Fan, R.S.7
Zborowska, E.8
Kinzler, K.W.9
Vogelstein, B.10
-
6
-
-
33846332027
-
Explaining the familial colorectal cancer risk associated with mismatch repair (MMR)-deficient and MMR-stable tumors
-
DOI 10.1158/1078-0432.CCR-06-1256
-
Aaltonen L, Johns L, Jarvinen H, Mecklin JP, Houlston R. Explaining the familial colorectal cancer risk associated with mismatch repair (MMR)-deficient and MMR-stable tumors. Clin Cancer Res 2007;13:356-61. (Pubitemid 46121890)
-
(2007)
Clinical Cancer Research
, vol.13
, Issue.1
, pp. 356-361
-
-
Aaltonen, L.1
Johns, L.2
Jarvinen, H.3
Mecklin, J.-P.4
Houlston, R.5
-
7
-
-
56749176944
-
Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer
-
Colorectal Cancer Association Study Consortium CoRGI Consortium, International Colorectal Cancer Genetic Association Consortium
-
Houlston RS, Webb E, Broderick P, Pittman AM, Di Bernardo MC, Lubbe S, Chandler I, Vijayakrishnan J, Sullivan K, Penegar S, Colorectal Cancer Association Study ConsortiumCarvajal-Carmona L, Howarth K, Jaeger E, Spain SL, Walther A, Barclay E, Martin L, Gorman M, Domingo E, Teixeira AS, CoRGI Consortium, Kerr D, Cazier JB, Niittymäki I, Tuupanen S, Karhu A, Aaltonen LA, Tomlinson IP, Farrington SM, Tenesa A, Prendergast JG, Barnetson RA, Cetnarskyj R, Porteous ME, Pharoah PD, Koessler T, Hampe J, Buch S, Schafmayer C, Tepel J, Schreiber S, Völzke H, Chang-Claude J, Hoffmeister M, Brenner H, Zanke BW, Montpetit A, Hudson TJ, Gallinger S, International Colorectal Cancer Genetic Association ConsortiumCampbell H, Dunlop MG. Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer. Nat Genet 2008;40:1426-35.
-
(2008)
Nat Genet
, vol.40
, pp. 1426-1435
-
-
Houlston, R.S.1
Webb, E.2
Broderick, P.3
Pittman, A.M.4
Di Bernardo, M.C.5
Lubbe, S.6
Chandler, I.7
Vijayakrishnan, J.8
Sullivan, K.9
Penegar, S.10
Carvajal-Carmona, L.11
Howarth, K.12
Jaeger, E.13
Spain, S.L.14
Walther, A.15
Barclay, E.16
Martin, L.17
Gorman, M.18
Domingo, E.19
Teixeira, A.S.20
Kerr, D.21
Cazier, J.B.22
Niittymäki, I.23
Tuupanen, S.24
Karhu, A.25
Aaltonen, L.A.26
Tomlinson, I.P.27
Farrington, S.M.28
Tenesa, A.29
Prendergast, J.G.30
Barnetson, R.A.31
Cetnarskyj, R.32
Porteous, M.E.33
Pharoah, P.D.34
Koessler, T.35
Hampe, J.36
Buch, S.37
Schafmayer, C.38
Tepel, J.39
Schreiber, S.40
Völzke, H.41
Chang-Claude, J.42
Hoffmeister, M.43
Brenner, H.44
Zanke, B.W.45
Montpetit, A.46
Hudson, T.J.47
Gallinger, S.48
Campbell, H.49
Dunlop, M.G.50
more..
-
8
-
-
70849136880
-
Birt-Hogg-Dube syndrome: Diagnosis and management
-
European BHD Consortium
-
Menko FH, van Steensel MAM, Giraud S, Friis-Hansen L, Richard S, Ungari S, Nordenskjöld M, Hansen TV, Solly J, Maher EREuropean BHD Consortium. Birt-Hogg-Dube syndrome: diagnosis and management. Lancet Oncology 2009;10:1199-206.
-
(2009)
Lancet Oncology
, vol.10
, pp. 1199-1206
-
-
Menko, F.H.1
Van Steensel, M.A.M.2
Giraud, S.3
Friis-Hansen, L.4
Richard, S.5
Ungari, S.6
Nordenskjöld, M.7
Hansen, T.V.8
Solly, J.9
Maher, E.R.10
-
9
-
-
0034821623
-
Birt-Hogg-Dube syndrome, a genodermatosis associated with spontaneous pneumothorax and kidney neoplasia, maps to chromosome 17p11.2
-
Schmidt LS, Warren MB, Nickerson ML, Weirich G, Matrosova V, Toro JR, Turner ML, Duray P, Merino M, Hewitt S, Pavlovich CP, Glenn G, Greenberg CR, Linehan WM, Zbar B. Birt-Hogg-Dube syndrome, a genodermatosis associated with spontaneous pneumothorax and kidney neoplasia, maps to chromosome 17p11.2. Am J Hum Genet 2001;69:876-82.
-
(2001)
Am J Hum Genet
, vol.69
, pp. 876-882
-
-
Schmidt, L.S.1
Warren, M.B.2
Nickerson, M.L.3
Weirich, G.4
Matrosova, V.5
Toro, J.R.6
Turner, M.L.7
Duray, P.8
Merino, M.9
Hewitt, S.10
Pavlovich, C.P.11
Glenn, G.12
Greenberg, C.R.13
Linehan, W.M.14
Zbar, B.15
-
10
-
-
0035939821
-
Birt-Hogg-Dube syndrome: Mapping of a novel hereditary neoplasia gene to chromosome 17p12-q11.2
-
Khoo SK, Bradley M, Wong FK, Hedblad MA, Nordenskjöld M, Teh BT. Birt-Hogg-Dube syndrome: mapping of a novel hereditary neoplasia gene to chromosome 17p12-q11.2. Oncogene 2001;20:5239-42.
-
(2001)
Oncogene
, vol.20
, pp. 5239-5242
-
-
Khoo, S.K.1
Bradley, M.2
Wong, F.K.3
Hedblad, M.A.4
Nordenskjöld, M.5
Teh, B.T.6
-
11
-
-
0000939691
-
Mutations in a novel gene lead to kidney tumors, lung wall defects, and benign tumors of the hair follicle in patients with the Birt-Hogg-Dube syndrome
-
Nickerson ML, Warren MB, Toro JR, Matrosova V, Glenn G, Turner ML, Duray P, Merino M, Choyke P, Pavlovich CP, Sharma N, Walther M, Munroe D, Hill R, Maher E, Greenberg C, Lerman MI, Linehan WM, Zbar B, Schmidt LS. Mutations in a novel gene lead to kidney tumors, lung wall defects, and benign tumors of the hair follicle in patients with the Birt-Hogg-Dube syndrome. Cancer Cell 2002;2:157-64.
-
(2002)
Cancer Cell
, vol.2
, pp. 157-164
-
-
Nickerson, M.L.1
Warren, M.B.2
Toro, J.R.3
Matrosova, V.4
Glenn, G.5
Turner, M.L.6
Duray, P.7
Merino, M.8
Choyke, P.9
Pavlovich, C.P.10
Sharma, N.11
Walther, M.12
Munroe, D.13
Hill, R.14
Maher, E.15
Greenberg, C.16
Lerman, M.I.17
Linehan, W.M.18
Zbar, B.19
Schmidt, L.S.20
more..
-
12
-
-
0036909242
-
Clinical and genetic studies of Birt-Hogg-Dube syndrome
-
Khoo SK, Giraud S, Kahnoski K, Chen J, Motorna O, Nickolov R, Binet O, Lambert D, Friedel J, Lévy R, Ferlicot S, Wolkenstein P, Hammel P, Bergerheim U, Hedblad MA, Bradley M, Teh BT, Nordenskjöld M, Richard S. Clinical and genetic studies of Birt-Hogg-Dube syndrome. J Med Genet 2002;39:906-12.
-
(2002)
J Med Genet
, vol.39
, pp. 906-912
-
-
Khoo, S.K.1
Giraud, S.2
Kahnoski, K.3
Chen, J.4
Motorna, O.5
Nickolov, R.6
Binet, O.7
Lambert, D.8
Friedel, J.9
Lévy, R.10
Ferlicot, S.11
Wolkenstein, P.12
Hammel, P.13
Bergerheim, U.14
Hedblad, M.A.15
Bradley, M.16
Teh, B.T.17
Nordenskjöld, M.18
Richard, S.19
-
13
-
-
21044457377
-
Germline BHD-mutation spectrum and phenotype analysis of a large cohort of families with Birt-Hogg-Dube syndrome
-
Schmidt LS, Nickerson ML, Warren MB, Glenn GM, Toro JR, Merino MJ, Turner ML, Choyke PL, Sharma N, Peterson J, Morrison P, Maher ER, Walther MM, Zbar B, Linehan WM. Germline BHD-mutation spectrum and phenotype analysis of a large cohort of families with Birt-Hogg-Dube syndrome. Am J Hum Genet 2005;76:1023-33.
-
(2005)
Am J Hum Genet
, vol.76
, pp. 1023-1033
-
-
Schmidt, L.S.1
Nickerson, M.L.2
Warren, M.B.3
Glenn, G.M.4
Toro, J.R.5
Merino, M.J.6
Turner, M.L.7
Choyke, P.L.8
Sharma, N.9
Peterson, J.10
Morrison, P.11
Maher, E.R.12
Walther, M.M.13
Zbar, B.14
Linehan, W.M.15
-
14
-
-
45249103326
-
BHD mutations, clinical and molecular genetic investigations of Birt-Hogg-Dube syndrome: A new series of 50 families and a review of published reports
-
Toro JR, Wei MH, Glenn GM, Weinreich M, Toure O, Vocke C, Turner M, Choyke P, Merino MJ, Pinto PA, Steinberg SM, Schmidt LS, Linehan WM. BHD mutations, clinical and molecular genetic investigations of Birt-Hogg-Dube syndrome: a new series of 50 families and a review of published reports. J Med Genet 2008;45:321-31.
-
(2008)
J Med Genet
, vol.45
, pp. 321-331
-
-
Toro, J.R.1
Wei, M.H.2
Glenn, G.M.3
Weinreich, M.4
Toure, O.5
Vocke, C.6
Turner, M.7
Choyke, P.8
Merino, M.J.9
Pinto, P.A.10
Steinberg, S.M.11
Schmidt, L.S.12
Linehan, W.M.13
-
15
-
-
53249113792
-
Familial non-VHL clear cell (conventional) renal cell carcinoma: Clinical features, segregation analysis, and mutation analysis of FLCN
-
Woodward ER, Ricketts C, Killick P, Gad S, Morris MR, Kavalier F, Hodgson SV, Giraud S, Bressac-de Paillerets B, Chapman C, Escudier B, Latif F, Richard S, Maher ER. Familial non-VHL clear cell (conventional) renal cell carcinoma: clinical features, segregation analysis, and mutation analysis of FLCN. Clin Cancer Res 2008;14:5925-30.
-
(2008)
Clin Cancer Res
, vol.14
, pp. 5925-5930
-
-
Woodward, E.R.1
Ricketts, C.2
Killick, P.3
Gad, S.4
Morris, M.R.5
Kavalier, F.6
Hodgson, S.V.7
Giraud, S.8
Bressac-De Paillerets, B.9
Chapman, C.10
Escudier, B.11
Latif, F.12
Richard, S.13
Maher, E.R.14
-
16
-
-
0017138187
-
Generalized dermal perifollicular fibromas with polyps of the colon
-
Hornstein OP. Generalized dermal perifollicular fibromas with polyps of the colon. Hum Genet 1976;33:193-7.
-
(1976)
Hum Genet
, vol.33
, pp. 193-197
-
-
Hornstein, O.P.1
-
17
-
-
0017760671
-
Hereditary multiple fibrofolliculomas with trichodiscomas and acrochordons
-
Birt AR, Hogg GR, Dube WJ. Hereditary multiple fibrofolliculomas with trichodiscomas and acrochordons. Arch Dermatol 1977;113:1674-7.
-
(1977)
Arch Dermatol
, vol.113
, pp. 1674-1677
-
-
Birt, A.R.1
Hogg, G.R.2
Dube, W.J.3
-
18
-
-
0030115744
-
Perifollicular fibroma of the skin and colonic polyps: Hornstein-Knickenberg syndrome
-
Schachtschabel AA, Kuster W, Happle R. Perifollicular fibroma of the skin and colonic polyps: Hornstein-Knickenberg syndrome. Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete 1996;47:304-6.
-
(1996)
Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und Verwandte Gebiete
, vol.47
, pp. 304-306
-
-
Schachtschabel, A.A.1
Kuster, W.2
Happle, R.3
-
19
-
-
0032942317
-
Birt-Hogg-Dube syndrome and Hornstein-Knickenberg syndrome are the same. Different sectioning technique as the cause of different histology
-
Schulz T, Hartschuh W. Birt-Hogg-Dube syndrome and Hornstein-Knickenberg syndrome are the same. Different sectioning technique as the cause of different histology. J Cutan Pathol 1999;26:55-61.
-
(1999)
J Cutan Pathol
, vol.26
, pp. 55-61
-
-
Schulz, T.1
Hartschuh, W.2
-
20
-
-
0029948120
-
Multiple lipomas, angiolipomas, and parathyroid adenomas in a patient with Birt-Hogg-Dube syndrome
-
Chung JY, Ramos-Caro FA, Beers B, Ford MJ, Flowers F. Multiple lipomas, angiolipomas, and parathyroid adenomas in a patient with Birt-Hogg-Dube syndrome. Int J Dermatol 1996;35:365-7. (Pubitemid 126479842)
-
(1996)
International Journal of Dermatology
, vol.35
, Issue.5
, pp. 365-367
-
-
Chung, J.Y.1
Ramos-Caro, F.A.2
Beers, B.3
Ford, M.J.4
Flowers, F.5
-
21
-
-
0024587286
-
Fibrofolliculomas, tricodiscomas and acrochordons (Birt-Hogg-Dube) associated with intestinal polyposis
-
Rongioletti F, Hazini R, Gianotti G, Rebora A. Fibrofolliculomas, tricodiscomas and acrochordons (Birt-Hogg-Dube) associated with intestinal polyposis. Clin Exp Dermatol 1989;14:72-4.
-
(1989)
Clin Exp Dermatol
, vol.14
, pp. 72-74
-
-
Rongioletti, F.1
Hazini, R.2
Gianotti, G.3
Rebora, A.4
-
22
-
-
0036122090
-
Risk of renal and colonic neoplasms and spontaneous pneumothorax in the Birt-Hogg-Dube syndrome
-
Zbar B, Alvord WG, Glenn G, Turner M, Pavlovich CP, Schmidt L, Walther M, Choyke P, Weirich G, Hewitt SM, Duray P, Gabril F, Greenberg C, Merino MJ, Toro J, Linehan WM. Risk of renal and colonic neoplasms and spontaneous pneumothorax in the Birt-Hogg-Dube syndrome. Cancer Epidemiol Biomarkers Prev 2002;11:393-400.
-
(2002)
Cancer Epidemiol Biomarkers Prev
, vol.11
, pp. 393-400
-
-
Zbar, B.1
Alvord, W.G.2
Glenn, G.3
Turner, M.4
Pavlovich, C.P.5
Schmidt, L.6
Walther, M.7
Choyke, P.8
Weirich, G.9
Hewitt, S.M.10
Duray, P.11
Gabril, F.12
Greenberg, C.13
Merino, M.J.14
Toro, J.15
Linehan, W.M.16
-
23
-
-
0037562904
-
Mutations of the Birt-Hogg-Dube (BHD) gene in sporadic colorectal carcinomas and colorectal carcinoma cell lines with microsatellite instability
-
Shin JH, Shin YK, Ku JL, Jeong SY, Hong SH, Park SY, Kim WH, Park JG. Mutations of the Birt-Hogg-Dube (BHD) gene in sporadic colorectal carcinomas and colorectal carcinoma cell lines with microsatellite instability. J Med Genet 2003;40:364-7.
-
(2003)
J Med Genet
, vol.40
, pp. 364-367
-
-
Shin, J.H.1
Shin, Y.K.2
Ku, J.L.3
Jeong, S.Y.4
Hong, S.H.5
Park, S.Y.6
Kim, W.H.7
Park, J.G.8
-
24
-
-
0344010917
-
Analysis of the Birt-Hogg-Dube (BHD) tumour suppressor gene in sporadic renal cell carcinoma and colorectal cancer
-
da Silva NF, Gentle D, Hesson LB, Morton DG, Latif F, Maher ER. Analysis of the Birt-Hogg-Dube (BHD) tumour suppressor gene in sporadic renal cell carcinoma and colorectal cancer. J Med Genet 2003;40:820-4. (Pubitemid 37485492)
-
(2003)
Journal of Medical Genetics
, vol.40
, Issue.11
, pp. 820-824
-
-
Fernandes Da Silva, N.1
Gentle, D.2
Hesson, L.B.3
Morton, D.G.4
Latif, F.5
Maher, E.R.6
-
25
-
-
33744907495
-
Evidence of linkage to chromosome 9q22.33 in colorectal cancer kindreds from the United Kingdom
-
Colorectal Tumour Gene Identification Study Consortium
-
Kemp ZE, Carvajal-Carmona LG, Barclay E, Gorman M, Martin L, Wood W, Rowan A, Donohue C, Spain S, Jaeger E, Evans DG, Maher ER, Bishop T, Thomas H, Houlston R, Tomlinson IColorectal Tumour Gene Identification Study Consortium. Evidence of linkage to chromosome 9q22.33 in colorectal cancer kindreds from the United Kingdom. Cancer Res 2006;66:5003-6.
-
(2006)
Cancer Res
, vol.66
, pp. 5003-5006
-
-
Kemp, Z.E.1
Carvajal-Carmona, L.G.2
Barclay, E.3
Gorman, M.4
Martin, L.5
Wood, W.6
Rowan, A.7
Donohue, C.8
Spain, S.9
Jaeger, E.10
Evans, D.G.11
Maher, E.R.12
Bishop, T.13
Thomas, H.14
Houlston, R.15
Tomlinson, I.16
-
26
-
-
0032830214
-
Mononucleotide microsatellite instability and germline MSH6 mutation analysis in early onset colorectal cancer
-
Verma L, Kane MF, Brassett C, Schmeits J, Evans DG, Kolodner RD, Maher ER. Mononucleotide microsatellite instability and germline MSH6 mutation analysis in early onset colorectal cancer. J Med Genet 1999;36:678-82. (Pubitemid 29433725)
-
(1999)
Journal of Medical Genetics
, vol.36
, Issue.9
, pp. 678-682
-
-
Verma, L.1
Kane, M.F.2
Brassett, C.3
Schmeits, J.4
Evans, D.G.R.5
Kolodner, R.D.6
Maher, E.R.7
-
27
-
-
65549117870
-
Implications of familial colorectal cancer risk profiles and microsatellite instability status
-
Lubbe SJ, Webb EL, Chandler IP, Houlston RS. Implications of familial colorectal cancer risk profiles and microsatellite instability status. J Clin Oncol 2009;27:2238-44.
-
(2009)
J Clin Oncol
, vol.27
, pp. 2238-2244
-
-
Lubbe, S.J.1
Webb, E.L.2
Chandler, I.P.3
Houlston, R.S.4
-
28
-
-
34249697672
-
Colorectal cancer: An overview of the epidemiology, risk factors, symptoms, and screening guidelines
-
quiz 2
-
Bazensky I, Shoobridge-Moran C, Yoder LH. Colorectal cancer: an overview of the epidemiology, risk factors, symptoms, and screening guidelines. Medsurg Nurs 2007;16:46-51; quiz 2.
-
(2007)
Medsurg Nurs
, vol.16
, pp. 46-51
-
-
Bazensky, I.1
Shoobridge-Moran, C.2
Yoder, L.H.3
-
29
-
-
0032718182
-
Birt-Hogg-Dube syndrome: A novel marker of kidney neoplasia
-
Toro JR, Glenn G, Duray P, Darling T, Weirich G, Zbar B, Linehan M, Turner ML. Birt-Hogg-Dube syndrome: a novel marker of kidney neoplasia. Archive Dermatol 1999;135:1195-202.
-
(1999)
Archive Dermatol
, vol.135
, pp. 1195-1202
-
-
Toro, J.R.1
Glenn, G.2
Duray, P.3
Darling, T.4
Weirich, G.5
Zbar, B.6
Linehan, M.7
Turner, M.L.8
-
30
-
-
0026894053
-
Somatic mutations of the APC gene in colorectal tumors: Mutation cluster region in the APC gene
-
Miyoshi Y, Nagase H, Ando H, Horii A, Ichii S, Nakatsuru S, Aoki T, Miki Y, Mori T, Nakamura Y. Somatic mutations of the APC gene in colorectal tumors: mutation cluster region in the APC gene. Hum Mol Genet 1992;1:229-33.
-
(1992)
Hum Mol Genet
, vol.1
, pp. 229-233
-
-
Miyoshi, Y.1
Nagase, H.2
Ando, H.3
Horii, A.4
Ichii, S.5
Nakatsuru, S.6
Aoki, T.7
Miki, Y.8
Mori, T.9
Nakamura, Y.10
-
31
-
-
0032970571
-
Mutations of the VHL gene in sporadic renal cell carcinoma: Definition of a risk factor for VHL patients to develop an RCC
-
Gallou C, Joly D, Mejean A, Staroz F, Martin N, Tarlet G, Orfanelli MT, Bouvier R, Droz D, Chrétien Y, Maréchal JM, Richard S, Junien C, Béroud C. Mutations of the VHL gene in sporadic renal cell carcinoma: definition of a risk factor for VHL patients to develop an RCC. Hum Mutat 1999;13:464-75.
-
(1999)
Hum Mutat
, vol.13
, pp. 464-475
-
-
Gallou, C.1
Joly, D.2
Mejean, A.3
Staroz, F.4
Martin, N.5
Tarlet, G.6
Orfanelli, M.T.7
Bouvier, R.8
Droz, D.9
Chrétien, Y.10
Maréchal, J.M.11
Richard, S.12
Junien, C.13
Béroud, C.14
-
32
-
-
0038502078
-
Alterations of the Birt-Hogg-Dube gene (BHD) in sporadic colorectal tumours
-
Kahnoski K, Khoo SK, Nassif NT, Chen J, Lobo GP, Segelov E, Teh BT. Alterations of the Birt-Hogg-Dube gene (BHD) in sporadic colorectal tumours. J Med Genet 2003;40:511-15. (Pubitemid 36843073)
-
(2003)
Journal of Medical Genetics
, vol.40
, Issue.7
, pp. 511-515
-
-
Kahnoski, K.1
Khoo, S.K.2
Nassif, N.T.3
Chen, J.4
Lobo, G.P.5
Segelov, E.6
Teh, B.T.7
-
33
-
-
69549121814
-
The folliculin mutation database: An online database of mutations associated with Birt-Hogg-Dube syndrome
-
Wei MH, Blake PW, Shevchenko J, Toro RJ. The folliculin mutation database: an online database of mutations associated with Birt-Hogg-Dube syndrome. Hum Mutat 2009;30:E880-90.
-
(2009)
Hum Mutat
, vol.30
-
-
Wei, M.H.1
Blake, P.W.2
Shevchenko, J.3
Toro, R.J.4
-
34
-
-
16144368515
-
Microsatellite instability in the insulin-like growth factor II receptor gene in gastrointestinal tumours
-
Souza RF, Appel R, Yin J, Wang S, Smolinski KN, Abraham JM, Zou TT, Shi YQ, Lei J, Cottrell J, Cymes K, Biden K, Simms L, Leggett B, Lynch PM, Frazier M, Powell SM, Harpaz N, Sugimura H, Young J, Meltzer SJ. Microsatellite instability in the insulin-like growth factor II receptor gene in gastrointestinal tumours. Nat Genet 1996;14:255-7.
-
(1996)
Nat Genet
, vol.14
, pp. 255-257
-
-
Souza, R.F.1
Appel, R.2
Yin, J.3
Wang, S.4
Smolinski, K.N.5
Abraham, J.M.6
Zou, T.T.7
Shi, Y.Q.8
Lei, J.9
Cottrell, J.10
Cymes, K.11
Biden, K.12
Simms, L.13
Leggett, B.14
Lynch, P.M.15
Frazier, M.16
Powell, S.M.17
Harpaz, N.18
Sugimura, H.19
Young, J.20
Meltzer, S.J.21
more..
-
36
-
-
33750293584
-
Folliculin encoded by the BHD gene interacts with a binding protein, FNIP1, and AMPK, and is involved in AMPK and mTOR signaling
-
Baba M, Hong SB, Sharma N, Warren MB, Nickerson ML, Iwamatsu A, Esposito D, Gillette WK, Hopkins RF 3rd, Hartley JL, Furihata M, Oishi S, Zhen W, Burke TR Jr, Linehan WM, Schmidt LS, Zbar B. Folliculin encoded by the BHD gene interacts with a binding protein, FNIP1, and AMPK, and is involved in AMPK and mTOR signaling. Proc Natl Acad Sci U S A 2006;103:15552-7.
-
(2006)
Proc Natl Acad Sci U S A
, vol.103
, pp. 15552-15557
-
-
Baba, M.1
Hong, S.B.2
Sharma, N.3
Warren, M.B.4
Nickerson, M.L.5
Iwamatsu, A.6
Esposito, D.7
Gillette, W.K.8
Hopkins III, R.F.9
Hartley, J.L.10
Furihata, M.11
Oishi, S.12
Zhen, W.13
Burke Jr., T.R.14
Linehan, W.M.15
Schmidt, L.S.16
Zbar, B.17
-
37
-
-
64049090204
-
The role of the Birt-Hogg-Dube protein in mTOR activation and renal tumorigenesis
-
Hartman TR, Nicolas E, Klein-Szanto A, Al-Saleem T, Cash TP, Simon MC, Henske EP. The role of the Birt-Hogg-Dube protein in mTOR activation and renal tumorigenesis. Oncogene 2009;28:1594-604.
-
(2009)
Oncogene
, vol.28
, pp. 1594-1604
-
-
Hartman, T.R.1
Nicolas, E.2
Klein-Szanto, A.3
Al-Saleem, T.4
Cash, T.P.5
Simon, M.C.6
Henske, E.P.7
-
38
-
-
63449094233
-
Gastrointestinal polyposis with esophageal polyposis is useful for early diagnosis of Cowden's disease
-
Umemura K, Takagi S, Ishigaki Y, Iwabuchi M, Kuroki S, Kinouchi Y, Shimosegawa T. Gastrointestinal polyposis with esophageal polyposis is useful for early diagnosis of Cowden's disease. World J Gastroenterol 2008;14:5755-9.
-
(2008)
World J Gastroenterol
, vol.14
, pp. 5755-5759
-
-
Umemura, K.1
Takagi, S.2
Ishigaki, Y.3
Iwabuchi, M.4
Kuroki, S.5
Kinouchi, Y.6
Shimosegawa, T.7
-
39
-
-
51649126752
-
Inhibition of the mTORC1 pathway suppresses intestinal polyp formation and reduces mortality in ApcDelta716 mice
-
Fujishita T, Aoki K, Lane HA, Aoki M, Taketo MM. Inhibition of the mTORC1 pathway suppresses intestinal polyp formation and reduces mortality in ApcDelta716 mice. Proc Natl Acad Sci U S A 2008;105:13544-9.
-
(2008)
Proc Natl Acad Sci U S A
, vol.105
, pp. 13544-13549
-
-
Fujishita, T.1
Aoki, K.2
Lane, H.A.3
Aoki, M.4
Taketo, M.M.5
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