-
1
-
-
0029861118
-
Fanconi's anemia and malignancies
-
Alter BP (1996) Fanconi's anemia and malignancies. Am J Hematol 53: 99-110
-
(1996)
Am J Hematol
, vol.53
, pp. 99-110
-
-
Alter, B.P.1
-
2
-
-
0029558476
-
E-cadherin is a tumour invasion suppressor gene mutated in human lobular breast cancers
-
Berx G, Cleton-Jansen AM, Nollet F, De Leeuw WJF, Van de Vijver MJ, Cornelisse C and Van Roy F (1995) E-cadherin is a tumour invasion suppressor gene mutated in human lobular breast cancers. EMBO J 14: 6107-6115
-
(1995)
EMBO J
, vol.14
, pp. 6107-6115
-
-
Berx, G.1
Cleton-Jansen, A.M.2
Nollet, F.3
De Leeuw, W.J.F.4
Van De Vijver, M.J.5
Cornelisse, C.6
Van Roy, F.7
-
3
-
-
0029951738
-
E-cadherin is inactivated in a majority of invasive human lobular breast cancers by truncation mutations throughout its extracellular domain
-
Berx G, Cleton-Jansen AM, Strumane K, De Leeuw WJF, Nollet F, Van Roy F and Cornelisse C (1996) E-cadherin is inactivated in a majority of invasive human lobular breast cancers by truncation mutations throughout its extracellular domain. Oncogene 13: 1919-1925
-
(1996)
Oncogene
, vol.13
, pp. 1919-1925
-
-
Berx, G.1
Cleton-Jansen, A.M.2
Strumane, K.3
De Leeuw, W.J.F.4
Nollet, F.5
Van Roy, F.6
Cornelisse, C.7
-
4
-
-
0028959056
-
Mapping of regions of physical deletion on chromosome 16q in prostate cancer cells by fluorescence in situ hybridization (FISH)
-
Cher ML, Ito T, Weidner N, Carroll PR and Jensen RH (1995) Mapping of regions of physical deletion on chromosome 16q in prostate cancer cells by fluorescence in situ hybridization (FISH). J Urol 153: 249-254
-
(1995)
J Urol
, vol.153
, pp. 249-254
-
-
Cher, M.L.1
Ito, T.2
Weidner, N.3
Carroll, P.R.4
Jensen, R.H.5
-
5
-
-
0027982971
-
At least two different regions are involved in allelic imbalance on chromosome arm 16q in breast cancer
-
Cleton-Jansen AM, Moerland EW, Kuipers-Dijkshoorn NJ, Callen DF, Sutherland GR, Hansen B, Devilee P and Cornelisse CJ (1994) At least two different regions are involved in allelic imbalance on chromosome arm 16q in breast cancer. Genes Chrom Cancer 9: 101-107
-
(1994)
Genes Chrom Cancer
, vol.9
, pp. 101-107
-
-
Cleton-Jansen, A.M.1
Moerland, E.W.2
Kuipers-Dijkshoorn, N.J.3
Callen, D.F.4
Sutherland, G.R.5
Hansen, B.6
Devilee, P.7
Cornelisse, C.J.8
-
6
-
-
0025832422
-
Allelotype of human breast carcinoma: A second major site for loss of heterozygosity is on chromosome 6q
-
Devilee P, Van Vliet M, van Sloun P, Kuipers Dijkshoorn N, Hermans J, Pearson PL and Cornelisse CJ (1991) Allelotype of human breast carcinoma: a second major site for loss of heterozygosity is on chromosome 6q. Oncogene 6: 1705-1711
-
(1991)
Oncogene
, vol.6
, pp. 1705-1711
-
-
Devilee, P.1
Van Vliet, M.2
Van Sloun, P.3
Kuipers Dijkshoorn, N.4
Hermans, J.5
Pearson, P.L.6
Cornelisse, C.J.7
-
7
-
-
0028784565
-
Allelic imbalance stidu of 16q in human primary breast carcinomas using microsatellite markers
-
Dorion-Bonnet F, Mautalen S, Hostein I and Longy M (1995) Allelic imbalance stidu of 16q in human primary breast carcinomas using microsatellite markers. Genes Chrom Cancer 14: 171-181
-
(1995)
Genes Chrom Cancer
, vol.14
, pp. 171-181
-
-
Dorion-Bonnet, F.1
Mautalen, S.2
Hostein, I.3
Longy, M.4
-
8
-
-
0030293337
-
Positional cloning of the Fanconi anaemia group A gene
-
Fanconi Anemia/Breast Cancer Consortium (1996) Positional cloning of the Fanconi anaemia group A gene. Nat Genet 14: 324-328
-
(1996)
Nat Genet
, vol.14
, pp. 324-328
-
-
-
9
-
-
19244364472
-
A locus for Fanconi anemia on 16q determined by homozygosity mapping
-
Gschwend M, Levran O, Kruglyak L, Ranade K, Verlander PC, Shen S, Faure S, Weissenbach J, Altay C, Lander ES, Auerbach AD and Botstein D (1996) A locus for Fanconi anemia on 16q determined by homozygosity mapping. Am J Hum Genet 59: 377-384
-
(1996)
Am J Hum Genet
, vol.59
, pp. 377-384
-
-
Gschwend, M.1
Levran, O.2
Kruglyak, L.3
Ranade, K.4
Verlander, P.C.5
Shen, S.6
Faure, S.7
Weissenbach, J.8
Altay, C.9
Lander, E.S.10
Auerbach, A.D.11
Botstein, D.12
-
10
-
-
17544391773
-
The genomic organization of the Fanconi anemia group A (FAA) gene
-
Ianzano L, D'Apolito M, Centra M, Savino M, Levran O, Auerbach AD, Cleton-Jansen AM, Doggett NA, Pronk JC, Tipping AJ, Gibson RA, Mathew CG, Whitmore SA, Apostolou S, Callen DF, Zelante L and Savoia A (1997) The genomic organization of the Fanconi anemia group A (FAA) gene. Genomics 41: 309-314
-
(1997)
Genomics
, vol.41
, pp. 309-314
-
-
Ianzano, L.1
D'Apolito, M.2
Centra, M.3
Savino, M.4
Levran, O.5
Auerbach, A.D.6
Cleton-Jansen, A.M.7
Doggett, N.A.8
Pronk, J.C.9
Tipping, A.J.10
Gibson, R.A.11
Mathew, C.G.12
Whitmore, S.A.13
Apostolou, S.14
Callen, D.F.15
Zelante, L.16
Savoia, A.17
-
11
-
-
0031014544
-
Localization of a breast cancer tumour-suppressor gene to a 3-cM interval within chromosomal region 16q22.1
-
Iida A, Yoshimoto M, Kasumi F, Nakamura Y and Emi M (1997) Localization of a breast cancer tumour-suppressor gene to a 3-cM interval within chromosomal region 16q22.1. Br J Cancer 75: 264-267
-
(1997)
Br J Cancer
, vol.75
, pp. 264-267
-
-
Iida, A.1
Yoshimoto, M.2
Kasumi, F.3
Nakamura, Y.4
Emi, M.5
-
12
-
-
0030995091
-
Loss of heterozygosity at chromosome 16q in prostate adenocarcinoma: Identification of three independent regions
-
Latil A, Cussenot O, Fournier G, Driouch K and Lidereau R (1997) Loss of heterozygosity at chromosome 16q in prostate adenocarcinoma: identification of three independent regions. Cancer Res 57: 1058-1062
-
(1997)
Cancer Res
, vol.57
, pp. 1058-1062
-
-
Latil, A.1
Cussenot, O.2
Fournier, G.3
Driouch, K.4
Lidereau, R.5
-
13
-
-
0030695440
-
Sequence variation in the Fanconi anemia gene FAA
-
Levran O, Erlich T, Magdalena N, Gregory JJ, Batish SD, Verlander PC and Auerbach AD (1997) Sequence variation in the Fanconi anemia gene FAA. Proc Natl Acad Sci USA 94: 13051-13056
-
(1997)
Proc Natl Acad Sci USA
, vol.94
, pp. 13051-13056
-
-
Levran, O.1
Erlich, T.2
Magdalena, N.3
Gregory, J.J.4
Batish, S.D.5
Verlander, P.C.6
Auerbach, A.D.7
-
14
-
-
1842337370
-
Expression cloning of a cDNA for the major Fanconi anaemia gene, FAA
-
Lo Ten Foe JR, Rooimans MA, Bosnoyan Collins L, Alon N, Wijker M, Parker L, Lightfoot J, Carreau M, Callen DF, Savoia A, Cheng NC, van Berkel CG, Strunk MH, Gille JJ, Pals G, Kruyt FA, Pronk JC, Arwert F, Buchwald M and Joenje H (1996) Expression cloning of a cDNA for the major Fanconi anaemia gene, FAA. Nat Genet 14: 320-323
-
(1996)
Nat Genet
, vol.14
, pp. 320-323
-
-
Lo Ten Foe, J.R.1
Rooimans, M.A.2
Bosnoyan Collins, L.3
Alon, N.4
Wijker, M.5
Parker, L.6
Lightfoot, J.7
Carreau, M.8
Callen, D.F.9
Savoia, A.10
Cheng, N.C.11
Van Berkel, C.G.12
Strunk, M.H.13
Gille, J.J.14
Pals, G.15
Kruyt, F.A.16
Pronk, J.C.17
Arwert, F.18
Buchwald, M.19
Joenje, H.20
more..
-
16
-
-
0031990269
-
Involvement of Brca2 in DNA repair
-
Patel KJ, Yu VPCC, Lee H, Corcoran A, Thistlethwaite FC, Evans MJ, Colledge WH, Friedman LS, Ponder BAJ and Venkitaraman AR (1998) Involvement of Brca2 in DNA repair. Mol Cell 1: 347-357
-
(1998)
Mol Cell
, vol.1
, pp. 347-357
-
-
Patel, K.J.1
Yu, V.P.C.C.2
Lee, H.3
Corcoran, A.4
Thistlethwaite, F.C.5
Evans, M.J.6
Colledge, W.H.7
Friedman, L.S.8
Ponder, B.A.J.9
Venkitaraman, A.R.10
-
17
-
-
0028840709
-
Localisation of the Fanconi anaemia complementation group A gene to chromosome 16q24.3
-
Pronk JC, Gibson RA, Savoia A, Wijker M, Morgan NV, Melchionda S, Ford D, Temtamy S, Ortega JJ, Jansen S, Havenga C, Cohn RJ, De Ravel TJ, Roberts I, Westerveld A, Easton DF, Joenje H, Mathew CG and Arwert F (1995) Localisation of the Fanconi anaemia complementation group A gene to chromosome 16q24.3. Nat Genet 11: 338-340
-
(1995)
Nat Genet
, vol.11
, pp. 338-340
-
-
Pronk, J.C.1
Gibson, R.A.2
Savoia, A.3
Wijker, M.4
Morgan, N.V.5
Melchionda, S.6
Ford, D.7
Temtamy, S.8
Ortega, J.J.9
Jansen, S.10
Havenga, C.11
Cohn, R.J.12
De Ravel, T.J.13
Roberts, I.14
Westerveld, A.15
Easton, D.F.16
Joenje, H.17
Mathew, C.G.18
Arwert, F.19
-
18
-
-
0031472370
-
Association of BRCA1 with Rad51 in mitotic and meiotic cells
-
Scully R, Chen J, Plug A, Xiao Y, Weaver D, Feunteun J, Ashley T, Livingston DM (1997) Association of BRCA1 with Rad51 in mitotic and meiotic cells. Cell 88: 265-275
-
(1997)
Cell
, vol.88
, pp. 265-275
-
-
Scully, R.1
Chen, J.2
Plug, A.3
Xiao, Y.4
Weaver, D.5
Feunteun, J.6
Ashley, T.7
Livingston, D.M.8
-
19
-
-
0028898357
-
High frequency of allelic imbalance at chromosome region 16q22-23 in human breast cancer: Correlation with high PgR and low S phase
-
Skirnisdottir S, Eiriksdottir G, Baldursson T, Barkardottir RB, Egilsson V and Ingvarsson S (1995) High frequency of allelic imbalance at chromosome region 16q22-23 in human breast cancer: correlation with high PgR and low S phase. Int J Cancer 64: 112-116
-
(1995)
Int J Cancer
, vol.64
, pp. 112-116
-
-
Skirnisdottir, S.1
Eiriksdottir, G.2
Baldursson, T.3
Barkardottir, R.B.4
Egilsson, V.5
Ingvarsson, S.6
-
20
-
-
0030446547
-
Three distinct commonly deleted regions of chromosome arm 16q in human primary and metastatic prostate cancers
-
Suzuki H, Komiya A, Emi M, Kuramochi H, Shiraishi T, Yatani R and Shimazaki J (1996) Three distinct commonly deleted regions of chromosome arm 16q in human primary and metastatic prostate cancers. Genes Chrom Canc 17: 225-233
-
(1996)
Genes Chrom Canc
, vol.17
, pp. 225-233
-
-
Suzuki, H.1
Komiya, A.2
Emi, M.3
Kuramochi, H.4
Shiraishi, T.5
Yatani, R.6
Shimazaki, J.7
-
21
-
-
0028123514
-
Allele loss on chromosome 16q24-qter occurs frequently in breast cancers irrespective of differences in phenotype and extent of spread
-
Tsuda H, Callen DF, Fukutomi T, Nakamura Y and Hirohashi S (1994) Allele loss on chromosome 16q24-qter occurs frequently in breast cancers irrespective of differences in phenotype and extent of spread. Cancer Res 54: 513-517
-
(1994)
Cancer Res
, vol.54
, pp. 513-517
-
-
Tsuda, H.1
Callen, D.F.2
Fukutomi, T.3
Nakamura, Y.4
Hirohashi, S.5
-
22
-
-
0013512335
-
Heterogenous spectrum of mutations in the Fanconi anaemia group A gene
-
in press
-
Wijker M, Morgan NV, Herterich S, van Berkel CGM, Tipping AJ, Gross HJ, Gille JJP, Pals G, Savino M, Altay C, Mohan S, Dokal I, Cavenagh J, Marsh J, van Weel M, Ortega JJ, Schuler D, Samochatova E, Karwachi M, Bekassy AN, Abecasis M, Ebell W, Kwee ML, de Ravel T, Gibson RA, Gluckman E, Arwert F, Joenje H, Savoia A, Hoehn H, Pronk JC and Mathew CG (1998) Heterogenous spectrum of mutations in the Fanconi anaemia group A gene. Eur J Human Genet (in press)
-
(1998)
Eur J Human Genet
-
-
Wijker, M.1
Morgan, N.V.2
Herterich, S.3
Van Berkel, C.G.M.4
Tipping, A.J.5
Gross, H.J.6
Gille, J.J.P.7
Pals, G.8
Savino, M.9
Altay, C.10
Mohan, S.11
Dokal, I.12
Cavenagh, J.13
Marsh, J.14
Van Weel, M.15
Ortega, J.J.16
Schuler, D.17
Samochatova, E.18
Karwachi, M.19
Bekassy, A.N.20
Abecasis, M.21
Ebell, W.22
Kwee, M.L.23
De Ravel, T.24
Gibson, R.A.25
Gluckman, E.26
Arwert, F.27
Joenje, H.28
Savoia, A.29
Hoehn, H.30
Pronk, J.C.31
Mathew, C.G.32
more..
|