-
1
-
-
0023807680
-
A simple method for DNA purification from peripheral blood
-
Ciulla TA, Sklar RM, Hauser SL (1988) A simple method for DNA purification from peripheral blood. Anal Biochem 174: 485-488
-
(1988)
Anal Biochem
, vol.174
, pp. 485-488
-
-
Ciulla, T.A.1
Sklar, R.M.2
Hauser, S.L.3
-
2
-
-
7144251865
-
A highly conserved processed pseudogene is located on chromosome band 9p21
-
Dahia PLM, Fitzgerald MG, Zhang X, Marsh DJ, Zheng Z, Pietsch T, von Deimling A, Haluska FG, Haber DA, Eng C (1998) A highly conserved processed pseudogene is located on chromosome band 9p21. Oncogene 16:2403-2406
-
(1998)
Oncogene
, vol.16
, pp. 2403-2406
-
-
Dahia, P.L.M.1
Fitzgerald, M.G.2
Zhang, X.3
Marsh, D.J.4
Zheng, Z.5
Pietsch, T.6
Von Deimling, A.7
Haluska, F.G.8
Haber, D.A.9
Eng, C.10
-
3
-
-
0033843623
-
Differential nuclear and cytoplasmic expression of PTEN in normal thyroid tissue, and benign and malignant epithelial thyroid tumours
-
Gimm O, Perren A, Weng LP, Marsh DJ, Yeh JJ, Ziebold, U, Gil E, Hinze R, Delbridge L, Lees JA, Mutter GL, Robinson BG, Komminoth P, Dralle H, Eng C (2000) Differential nuclear and cytoplasmic expression of PTEN in normal thyroid tissue, and benign and malignant epithelial thyroid tumours Am J Pathol 156:1693-1700
-
(2000)
Am J Pathol
, vol.156
, pp. 1693-1700
-
-
Gimm, O.1
Perren, A.2
Weng, L.P.3
Marsh, D.J.4
Yeh, J.J.5
Ziebold, U.6
Gil, E.7
Hinze, R.8
Delbridge, L.9
Lees, J.A.10
Mutter, G.L.11
Robinson, B.G.12
Komminoth, P.13
Dralle, H.14
Eng, C.15
-
4
-
-
0030936323
-
PTEN, a putative protein tyrosine phosphatase gene mutated in human brain, breast, and prostate cancer
-
Li J, Yen C, Liaw D, Podsypanina K, Bose S, Wang SI, Pue J, Miliaresis C, Rodgers L, McCombie R, Bigner SH, Giovanella BC, Ittmann M, Tycko B, Hibshoosh H, Wigler MH, Parsons R (1997) PTEN, a putative protein tyrosine phosphatase gene mutated in human brain, breast, and prostate cancer. Science 275:1943-1947
-
(1997)
Science
, vol.275
, pp. 1943-1947
-
-
Li, J.1
Yen, C.2
Liaw, D.3
Podsypanina, K.4
Bose, S.5
Wang, S.I.6
Pue, J.7
Miliaresis, C.8
Rodgers, L.9
McCombie, R.10
Bigner, S.H.11
Giovanella, B.C.12
Ittmann, M.13
Tycko, B.14
Hibshoosh, H.15
Wigler, M.H.16
Parsons, R.17
-
5
-
-
0031004088
-
Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndrome
-
Liaw D, Marsh DJ, Li J, Dahia PLM, Wang SI, Zheng Z, Bose S, Call KM, Tsou HC, Peacocke M, Eng C, Parsons R (1997) Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndrome. Nat Genet 16: 64-67
-
(1997)
Nat Genet
, vol.16
, pp. 64-67
-
-
Liaw, D.1
Marsh, D.J.2
Li, J.3
Dahia, P.L.M.4
Wang, S.I.5
Zheng, Z.6
Bose, S.7
Call, K.M.8
Tsou, H.C.9
Peacocke, M.10
Eng, C.11
Parsons, R.12
-
6
-
-
17344363637
-
Inherited mutations in PTEN that are associated with breast cancer, Cowden disease, and juvenile polyposis
-
Lynch ED, Ostermeyer EA, Lee MK, Arena F, Ji HL, Dann J, Swisshelm K, Suchard D, MacLeod PM, Kvinnsland S, Gjertsen BT, Heimdal K, Lubs H, Moller P, King MC (1997) Inherited mutations in PTEN that are associated with breast cancer, Cowden disease, and juvenile polyposis. Am J Hum Genet 61: 1254-1260
-
(1997)
Am J Hum Genet
, vol.61
, pp. 1254-1260
-
-
Lynch, E.D.1
Ostermeyer, E.A.2
Lee, M.K.3
Arena, F.4
Ji, H.L.5
Dann, J.6
Swisshelm, K.7
Suchard, D.8
MacLeod, P.M.9
Kvinnsland, S.10
Gjertsen, B.T.11
Heimdal, K.12
Lubs, H.13
Moller, P.14
King, M.C.15
-
7
-
-
6844252284
-
Mutation spectrum and genotype-phenotype analyses in Cowden disease and Bannayan-Zonana syndromes with germline PTEN mutation
-
Marsh DJ, Coulon V, Lunetta KL, Rocca-Serra P, Dahia PL, Zheng Z, Liaw D, Caron S, Duboue B, Lin AY, Richardson AL, Bonnetblanc JM, Bressieux JM, Cabarrot-Moreau A, Chompret A, Demange L, Eeles RA, Yahanda AM, Fearon ER, Fricker JP, Gorlin RJ, Hodgson SV, Huson S, Lacombe D, Eng C. et al (1998) Mutation spectrum and genotype-phenotype analyses in Cowden disease and Bannayan-Zonana syndromes with germline PTEN mutation. Hum Mol Genet 7:507-515
-
(1998)
Hum Mol Genet
, vol.7
, pp. 507-515
-
-
Marsh, D.J.1
Coulon, V.2
Lunetta, K.L.3
Rocca-Serra, P.4
Dahia, P.L.5
Zheng, Z.6
Liaw, D.7
Caron, S.8
Duboue, B.9
Lin, A.Y.10
Richardson, A.L.11
Bonnetblanc, J.M.12
Bressieux, J.M.13
Cabarrot-Moreau, A.14
Chompret, A.15
Demange, L.16
Eeles, R.A.17
Yahanda, A.M.18
Fearon, E.R.19
Fricker, J.P.20
Gorlin, R.J.21
Hodgson, S.V.22
Huson, S.23
Lacombe, D.24
Eng, C.25
more..
-
8
-
-
0030140025
-
Localization of the gene for Cowden disease to chromosome 10q22-23
-
Nelen MR, Padberg GW, Peeters, EA, Lin AY, van den Helm B, Frants RR, Coulon V, Goldstein AM, van Reen MM, Easton DF, Eeles RA, Hodgsen S, Mulvihill JJ, Murday VA, Tucker MA, Mariman EC, Starink TM, Ponder BA, Ropers HH, Kremer H, Longy M, Eng C (1996) Localization of the gene for Cowden disease to chromosome 10q22-23. Nat Genet 13:114-116
-
(1996)
Nat Genet
, vol.13
, pp. 114-116
-
-
Nelen, M.R.1
Padberg, G.W.2
Peeters, E.A.3
Lin, A.Y.4
Van Den Helm, B.5
Frants, R.R.6
Coulon, V.7
Goldstein, A.M.8
Van Reen, M.M.9
Easton, D.F.10
Eeles, R.A.11
Hodgsen, S.12
Mulvihill, J.J.13
Murday, V.A.14
Tucker, M.A.15
Mariman, E.C.16
Starink, T.M.17
Ponder, B.A.18
Ropers, H.H.19
Kremer, H.20
Longy, M.21
Eng, C.22
more..
-
9
-
-
0032905101
-
Novel PTEN mutations in patients with Cowden disease: Absence of clear genotype-phenolype correlations
-
Nelen MR, Kremer H, Konings IB, Schoute F, van Essen AJ, Koch R, Woods CG, Fryns JP, Hamel B, Hoefsloot LH, Peeters EA, Padberg GW (1999) Novel PTEN mutations in patients with Cowden disease: absence of clear genotype-phenolype correlations. Eur J Hum Genet 7:267-273
-
(1999)
Eur J Hum Genet
, vol.7
, pp. 267-273
-
-
Nelen, M.R.1
Kremer, H.2
Konings, I.B.3
Schoute, F.4
Van Essen, A.J.5
Koch, R.6
Woods, C.G.7
Fryns, J.P.8
Hamel, B.9
Hoefsloot, L.H.10
Peeters, E.A.11
Padberg, G.W.12
-
10
-
-
0032410074
-
Identification of a novel PTEN mutation (L139X) in a patient with Cowden disease and Sjogren syndrome
-
Raizis AM, Ferguson MM, Robinson BA, Atkinson CH, George P (1998) Identification of a novel PTEN mutation (L139X) in a patient with Cowden disease and Sjogren syndrome. J Clin Pathol 51:339-341
-
(1998)
J Clin Pathol
, vol.51
, pp. 339-341
-
-
Raizis, A.M.1
Ferguson, M.M.2
Robinson, B.A.3
Atkinson, C.H.4
George, P.5
-
11
-
-
0033624869
-
A novel 5′ (40̂41 InsA) mutation in a patient with numerous manifestations of Cowden disease
-
Raizis AM, Ferguson MM, George P (2000) A novel 5′ (40̂41 InsA) mutation in a patient with numerous manifestations of Cowden disease. J Invest Dermatol 114:597
-
(2000)
J Invest Dermatol
, vol.114
, pp. 597
-
-
Raizis, A.M.1
Ferguson, M.M.2
George, P.3
-
12
-
-
17144436629
-
Identification of a candidate tumour suppressor gene, MMAC1, at chromosome 10q23.3 that is mutated in multiple advanced cancers
-
Steck PA, Pershouse MA, Jasser SA, Yung WK, Lin H, Ligon AH, Langford LA, Baumgard ML, Hattier T, Davis T, Frye C, Hu R, Swedlund B, Teng DH, Tavtigian SV (1997) Identification of a candidate tumour suppressor gene, MMAC1, at chromosome 10q23.3 that is mutated in multiple advanced cancers. Nat Genet 15:356-362
-
(1997)
Nat Genet
, vol.15
, pp. 356-362
-
-
Steck, P.A.1
Pershouse, M.A.2
Jasser, S.A.3
Yung, W.K.4
Lin, H.5
Ligon, A.H.6
Langford, L.A.7
Baumgard, M.L.8
Hattier, T.9
Davis, T.10
Frye, C.11
Hu, R.12
Swedlund, B.13
Teng, D.H.14
Tavtigian, S.V.15
|