-
1
-
-
0029985255
-
Hereditary nonpolyposis colorectal cancer: Review of clinical, molecular genetics, and counseling aspects
-
Bellacosa A, Genuardi M, Anti M, Viel A, Ponz de Leon M (1996) Hereditary nonpolyposis colorectal cancer: review of clinical, molecular genetics, and counseling aspects. Am J Med Genet 62:353-364
-
(1996)
Am J Med Genet
, vol.62
, pp. 353-364
-
-
Bellacosa, A.1
Genuardi, M.2
Anti, M.3
Viel, A.4
Ponz de Leon, M.5
-
2
-
-
0030054894
-
Analysis of alternative splicing patterns in the cystic fibrosis transmembrane conductance regulator gene using mRNA derived from lymphoblastoid cells of cystic fibrosis patients
-
Bienvenu T, Beldjord C, Chelly J, Fonknechten N, Hubert D, Dusser D, Kaplan JC (1996) Analysis of alternative splicing patterns in the cystic fibrosis transmembrane conductance regulator gene using mRNA derived from lymphoblastoid cells of cystic fibrosis patients. Eur J Hum Genet 4: 127-134
-
(1996)
Eur J Hum Genet
, vol.4
, pp. 127-134
-
-
Bienvenu, T.1
Beldjord, C.2
Chelly, J.3
Fonknechten, N.4
Hubert, D.5
Dusser, D.6
Kaplan, J.C.7
-
3
-
-
0029955269
-
Molecular genetics of hereditary non-polyposis colorectal cancer (HNPCC)
-
Cama A, Genuardi M, Guanti G, Radice P, Varesco L (1996) Molecular genetics of hereditary non-polyposis colorectal cancer (HNPCC). Tumori 82: 122-135
-
(1996)
Tumori
, vol.82
, pp. 122-135
-
-
Cama, A.1
Genuardi, M.2
Guanti, G.3
Radice, P.4
Varesco, L.5
-
4
-
-
0028907311
-
Alternative splicing of MLH1 messenger RNA in human normal cells
-
Charbonnier F, Martin C, Scotte M, Sibert L, Moreau V, Frebourg T (1995) Alternative splicing of MLH1 messenger RNA in human normal cells. Cancer Res 55 :1839-1841
-
(1995)
Cancer Res
, vol.55
, pp. 1839-1841
-
-
Charbonnier, F.1
Martin, C.2
Scotte, M.3
Sibert, L.4
Moreau, V.5
Frebourg, T.6
-
5
-
-
0023277545
-
Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction
-
Chomczynski P, Sacchi N (1987) Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction. Anal Biochem 162: 156-159
-
(1987)
Anal Biochem
, vol.162
, pp. 156-159
-
-
Chomczynski, P.1
Sacchi, N.2
-
6
-
-
0028916722
-
A frequent hMSH2 mutation in hereditary non-polyposis colon cancer syndrome
-
Froggatt NJ, Joyce JA, Davies R, Evans DGR., Ponder BAJ, Barton DE, Maher ER (1995) A frequent hMSH2 mutation in hereditary non-polyposis colon cancer syndrome. Lancet 345 : 727
-
(1995)
Lancet
, vol.345
, pp. 727
-
-
Froggatt, N.J.1
Joyce, J.A.2
Davies, R.3
Evans, D.G.R.4
Ponder, B.A.J.5
Barton, D.E.6
Maher, E.R.7
-
7
-
-
0027959827
-
Intron splice acceptor site sequence variations in the hereditary non-polyposis colorectal cancer gene hMSH2
-
Hall NR, Taylor GR, Finan PJ, Kolodner RD, Bodmer WF, Cottrell SE, Frayling I, Bishop DT (1994) Intron splice acceptor site sequence variations in the hereditary non-polyposis colorectal cancer gene hMSH2. Eur J Cancer 30 A : 1550-1552
-
(1994)
Eur J Cancer
, vol.30 A
, pp. 1550-1552
-
-
Hall, N.R.1
Taylor, G.R.2
Finan, P.J.3
Kolodner, R.D.4
Bodmer, W.F.5
Cottrell, S.E.6
Frayling, I.7
Bishop, D.T.8
-
8
-
-
0028966917
-
Genomic structure of human mismatch repair gene, hMLH1, and its mutation analysis in patients with hereditary non-polyposis colorectal cancer (HNPCC)
-
Han H-J, Maruyama M, Baba S, Park J-G, Nakamura Y (1995) Genomic structure of human mismatch repair gene, hMLH1, and its mutation analysis in patients with hereditary non-polyposis colorectal cancer (HNPCC). Hum Mol Genet 4:237-242
-
(1995)
Hum Mol Genet
, vol.4
, pp. 237-242
-
-
Han, H.-J.1
Maruyama, M.2
Baba, S.3
Park, J.-G.4
Nakamura, Y.5
-
9
-
-
0345198560
-
RNA-based mutation screening in hereditary nonpolyposis colorectal cancer
-
Kohonen-Corish M, Ross VL, Doe WF, Kool DA, Edkins E, Faragher I, Wijnen J, Khan PM, Macrae F, St John DJ (1996) RNA-based mutation screening in hereditary nonpolyposis colorectal cancer. Am. J. Hum. Genet 59 : 818-824
-
(1996)
Am. J. Hum. Genet
, vol.59
, pp. 818-824
-
-
Kohonen-Corish, M.1
Ross, V.L.2
Doe, W.F.3
Kool, D.A.4
Edkins, E.5
Faragher, I.6
Wijnen, J.7
Khan, P.M.8
Macrae, F.9
St John, D.J.10
-
10
-
-
0028106776
-
HMSH2 mutations in hereditary nonpolyposis colorectal cancer kindreds
-
Liu B, Parsons RE, Hamilton SR, Petersen GM, Lynch HT, Watson P, Markowitz S, Willson JKV, Green J, de la Chapelle A, Kinzler KW, Vogelstein B (1994) hMSH2 mutations in hereditary nonpolyposis colorectal cancer kindreds. Cancer Res 54 : 4590-4594
-
(1994)
Cancer Res
, vol.54
, pp. 4590-4594
-
-
Liu, B.1
Parsons, R.E.2
Hamilton, S.R.3
Petersen, G.M.4
Lynch, H.T.5
Watson, P.6
Markowitz, S.7
Willson, J.K.V.8
Green, J.9
De la Chapelle, A.10
Kinzler, K.W.11
Vogelstein, B.12
-
11
-
-
0028915223
-
Genetic instability occurs in the majority of young patients with colorectal cancer
-
Liu B, Farrington SM, Petersen GM, Hamilton SR, Parsons R, Papadopoulos N, Fujiwara T, Jen J, Kinzler KW, Wyllie AH, Vogelstein B, Dunlop MG (1995) Genetic instability occurs in the majority of young patients with colorectal cancer. Nat Med 1 : 348-352
-
(1995)
Nat Med
, vol.1
, pp. 348-352
-
-
Liu, B.1
Farrington, S.M.2
Petersen, G.M.3
Hamilton, S.R.4
Parsons, R.5
Papadopoulos, N.6
Fujiwara, T.7
Jen, J.8
Kinzler, K.W.9
Wyllie, A.H.10
Vogelstein, B.11
Dunlop, M.G.12
-
12
-
-
2942569549
-
Analysis of mismatch repair genes in hereditary non-polyposis colorectal cancer patients
-
Liu B, Parsons RE, Papadopolous N, Nicolaides NC, Lynch HT, Watson P, Jass JR, Dunlop M, Wyllie A, Peltomäki P, de la Chapelle A, Hamilton SR, Vogelstein B, Kinzler KW (1996) Analysis of mismatch repair genes in hereditary non-polyposis colorectal cancer patients. Nat Med 2: 169-174
-
(1996)
Nat Med
, vol.2
, pp. 169-174
-
-
Liu, B.1
Parsons, R.E.2
Papadopolous, N.3
Nicolaides, N.C.4
Lynch, H.T.5
Watson, P.6
Jass, J.R.7
Dunlop, M.8
Wyllie, A.9
Peltomäki, P.10
De la Chapelle, A.11
Hamilton, S.R.12
Vogelstein, B.13
Kinzler, K.W.14
-
13
-
-
0029164415
-
In vitro transcription/translation assay for the screening of hMLH1 and hMSH2 mutations in familial colon cancer
-
Luce MC, Marra G, Chauchan DP, Laghi L, Carethers JM, Cherian SP, Hawn M, Binnie CG, Kam-Morgan LNW, Cayouette MC, Koi M, Boland CR (1995) In vitro transcription/translation assay for the screening of hMLH1 and hMSH2 mutations in familial colon cancer. Gastroenterology, 109: 1368-1374
-
(1995)
Gastroenterology
, vol.109
, pp. 1368-1374
-
-
Luce, M.C.1
Marra, G.2
Chauchan, D.P.3
Laghi, L.4
Carethers, J.M.5
Cherian, S.P.6
Hawn, M.7
Binnie, C.G.8
Kam-Morgan, L.N.W.9
Cayouette, M.C.10
Koi, M.11
Boland, C.R.12
-
14
-
-
0029089259
-
Hereditary nonpolyposis colorectal cancer: The syndrome, the genes, and historical perspectives
-
Marra G, Boland CR (1995) Hereditary nonpolyposis colorectal cancer: the syndrome, the genes, and historical perspectives. J Natl Cancer Inst 87 : 1114-1124
-
(1995)
J Natl Cancer Inst
, vol.87
, pp. 1114-1124
-
-
Marra, G.1
Boland, C.R.2
-
15
-
-
0030892133
-
Alternative splicing of HMSH2 in normal human tissues
-
Mori Y, Shiwaku H, Fukushige S, Wakatsuki S, Sato M, Nukiwa T, Horii A (1997) Alternative splicing of HMSH2 in normal human tissues. Hum Genet 99:590-595
-
(1997)
Hum Genet
, vol.99
, pp. 590-595
-
-
Mori, Y.1
Shiwaku, H.2
Fukushige, S.3
Wakatsuki, S.4
Sato, M.5
Nukiwa, T.6
Horii, A.7
-
16
-
-
0345050350
-
DNA mismatch repair gene mutations in 55 kindreds with verified or putative hereditary non-polyposis colorectal cancer
-
Nyström-Lahti M, Wu Y, Moisio A-L, Hofstra RMW, Osinga J, Mecklin J-P, Järvinen HJ, Leisti J, Buys CHCM, de la Chapelle A, Peltomäki P (1996) DNA mismatch repair gene mutations in 55 kindreds with verified or putative hereditary non-polyposis colorectal cancer. Hum Mol Genet 5:763-769
-
(1996)
Hum Mol Genet
, vol.5
, pp. 763-769
-
-
Nyström-Lahti, M.1
Wu, Y.2
Moisio, A.-L.3
Hofstra, R.M.W.4
Osinga, J.5
Mecklin, J.-P.6
Järvinen, H.J.7
Leisti, J.8
Buys, C.H.C.M.9
De la Chapelle, A.10
Peltomäki, P.11
-
17
-
-
0029100951
-
Alternatively spliced adenomatous polyposis coli (APC) gene transcripts that delete exons mutated in attenuated APC
-
Samowitz WS, Thliveris A, Spirio LN, White R (1995) Alternatively spliced adenomatous polyposis coli (APC) gene transcripts that delete exons mutated in attenuated APC. Cancer Res 55:3732-3734
-
(1995)
Cancer Res
, vol.55
, pp. 3732-3734
-
-
Samowitz, W.S.1
Thliveris, A.2
Spirio, L.N.3
White, R.4
-
18
-
-
0031023545
-
Characterization of MSH2 and MLH1 mutations in Italian families with hereditary nonpolyposis colorectal cancer
-
Viel A, Genuardi M, Capozzi E, Leonardi F, Bellacosa A, Paravatou-Petsotas M, Pomponi MG, Fornasarig M, Percesepe A, Roncucci L, Tamassia MG, Benatti P, Ponz de Leòn M, Valenti A, Covino M, Anti M, Foletto M, Boiocchi M, Neri G (1997) Characterization of MSH2 and MLH1 mutations in Italian families with hereditary nonpolyposis colorectal cancer. Genes Chromosomes Cancer 18:8-18
-
(1997)
Genes Chromosomes Cancer
, vol.18
, pp. 8-18
-
-
Viel, A.1
Genuardi, M.2
Capozzi, E.3
Leonardi, F.4
Bellacosa, A.5
Paravatou-Petsotas, M.6
Pomponi, M.G.7
Fornasarig, M.8
Percesepe, A.9
Roncucci, L.10
Tamassia, M.G.11
Benatti, P.12
Ponz de Leòn, M.13
Valenti, A.14
Covino, M.15
Anti, M.16
Foletto, M.17
Boiocchi, M.18
Neri, G.19
-
19
-
-
19144365420
-
Majority of hMLH1 mutations responsible for hereditary nonpolyposis colorectal cancer (HNPCC) cluster at the exonic region 15-16
-
Wijnen J, Khan PM, Vasen H, Menko FH, van der Klift H. van den Broek M, van Leeuwen-Cornelisse I, Nagengast F, MeijersHeijboer A, Lindhout D, Griffioen G, Cats A. Kleibeuker J, Varesco L, Bertario L, Bisgaard M-L, Mohr J, Kolodner R, Fodde R (1996) Majority of hMLH1 mutations responsible for hereditary nonpolyposis colorectal cancer (HNPCC) cluster at the exonic region 15-16. Am J Hum Genet 58:300-307
-
(1996)
Am J Hum Genet
, vol.58
, pp. 300-307
-
-
Wijnen, J.1
Khan, P.M.2
Vasen, H.3
Menko, F.H.4
Van der Klift, H.5
Van den Broek, M.6
Van Leeuwen-Cornelisse, I.7
Nagengast, F.8
Meijersheijboer, A.9
Lindhout, D.10
Griffioen, G.11
Cats, A.12
Kleibeuker, J.13
Varesco, L.14
Bertario, L.15
Bisgaard, M.-L.16
Mohr, J.17
Kolodner, R.18
Fodde, R.19
-
20
-
-
0029994784
-
A truncated hMSH2 transcript occurs as a common variant in the population: Implications for genetic diagnosis
-
Xia L, Shen W, Ritacca F, Mitri A, Madlensky L, Berk T, Cohen Z, Gallinger S, Bapat B (1996) A truncated hMSH2 transcript occurs as a common variant in the population: implications for genetic diagnosis. Cancer Res 56:2289-2292
-
(1996)
Cancer Res
, vol.56
, pp. 2289-2292
-
-
Xia, L.1
Shen, W.2
Ritacca, F.3
Mitri, A.4
Madlensky, L.5
Berk, T.6
Cohen, Z.7
Gallinger, S.8
Bapat, B.9
|