-
1
-
-
0035893365
-
Identification and purification of two distinct complexes containing the five RAD51 paralogs
-
Masson J-Y, Tarsounas MC, Stasiak AZ, Stasiak A, Shah R, et al. (2001) Identification and purification of two distinct complexes containing the five RAD51 paralogs. Genes & Development 15: 3296-3307.
-
(2001)
Genes & Development
, vol.15
, pp. 3296-3307
-
-
Masson, J.-Y.1
Tarsounas, M.C.2
Stasiak, A.Z.3
Stasiak, A.4
Shah, R.5
-
2
-
-
16844383231
-
Extensive Chromosomal Instability in Rad51d-Deficient Mouse Cells
-
Smiraldo PG, Gruver AM, Osborn JC, Pittman DL, (2005) Extensive Chromosomal Instability in Rad51d-Deficient Mouse Cells. Cancer Research 65: 2089-2096.
-
(2005)
Cancer Research
, vol.65
, pp. 2089-2096
-
-
Smiraldo, P.G.1
Gruver, A.M.2
Osborn, J.C.3
Pittman, D.L.4
-
3
-
-
80052264429
-
Germline mutations in RAD51D confer susceptibility to ovarian cancer
-
Loveday C, Turnbull C, Ramsay E, Hughes D, Ruark E, et al. (2011) Germline mutations in RAD51D confer susceptibility to ovarian cancer. Nat Genet 43: 879-882.
-
(2011)
Nat Genet
, vol.43
, pp. 879-882
-
-
Loveday, C.1
Turnbull, C.2
Ramsay, E.3
Hughes, D.4
Ruark, E.5
-
4
-
-
84859649798
-
Mutation analysis of RAD51D in non-BRCA1/2 ovarian and breast cancer families
-
Osher DJ, De Leeneer K, Michils G, Hamel N, Tomiak E, et al. (2012) Mutation analysis of RAD51D in non-BRCA1/2 ovarian and breast cancer families. Br J Cancer 106: 1460-1463.
-
(2012)
Br J Cancer
, vol.106
, pp. 1460-1463
-
-
Osher, D.J.1
De Leeneer, K.2
Michils, G.3
Hamel, N.4
Tomiak, E.5
-
5
-
-
84864314189
-
A Finnish founder mutation in RAD51D: analysis in breast, ovarian, prostate, and colorectal cancer
-
Pelttari LM, Kiiski J, Nurminen R, Kallioniemi A, Schleutker J, et al. (2012) A Finnish founder mutation in RAD51D: analysis in breast, ovarian, prostate, and colorectal cancer. J Med Genet.
-
(2012)
J Med Genet
-
-
Pelttari, L.M.1
Kiiski, J.2
Nurminen, R.3
Kallioniemi, A.4
Schleutker, J.5
-
6
-
-
79955478110
-
Frequencies of BRCA1 and BRCA2 mutations among 1,342 unselected patients with invasive ovarian cancer
-
Zhang S, Royer R, Li S, McLaughlin JR, Rosen B, et al. (2011) Frequencies of BRCA1 and BRCA2 mutations among 1,342 unselected patients with invasive ovarian cancer. Gynecol Oncol 121: 353-357.
-
(2011)
Gynecol Oncol
, vol.121
, pp. 353-357
-
-
Zhang, S.1
Royer, R.2
Li, S.3
McLaughlin, J.R.4
Rosen, B.5
-
7
-
-
84864026311
-
BRCA Mutation Frequency and Patterns of Treatment Response in BRCA Mutation-Positive Women With Ovarian Cancer: A Report From the Australian Ovarian Cancer Study Group
-
Alsop K, Fereday S, Meldrum C, deFazio A, Emmanuel C, et al. (2012) BRCA Mutation Frequency and Patterns of Treatment Response in BRCA Mutation-Positive Women With Ovarian Cancer: A Report From the Australian Ovarian Cancer Study Group. Journal of Clinical Oncology.
-
(2012)
Journal of Clinical Oncology
-
-
Alsop, K.1
Fereday, S.2
Meldrum, C.3
deFazio, A.4
Emmanuel, C.5
-
8
-
-
79960815893
-
RAD51C is a susceptibility gene for ovarian cancer
-
Pelttari LM, Heikkinen T, Thompson D, Kallioniemi A, Schleutker J, et al. (2011) RAD51C is a susceptibility gene for ovarian cancer. Hum Mol Genet 20: 3278-3288.
-
(2011)
Hum Mol Genet
, vol.20
, pp. 3278-3288
-
-
Pelttari, L.M.1
Heikkinen, T.2
Thompson, D.3
Kallioniemi, A.4
Schleutker, J.5
-
9
-
-
84857691595
-
Analysis of RAD51C Germline Mutations in High-Risk Breast and Ovarian Cancer Families and Ovarian Cancer Patients
-
Thompson ER, Boyle SE, Johnson J, Ryland GL, Sawyer S, et al. (2011) Analysis of RAD51C Germline Mutations in High-Risk Breast and Ovarian Cancer Families and Ovarian Cancer Patients. Hum Mutat 33: 95.
-
(2011)
Hum Mutat
, vol.33
, pp. 95
-
-
Thompson, E.R.1
Boyle, S.E.2
Johnson, J.3
Ryland, G.L.4
Sawyer, S.5
-
10
-
-
0030041917
-
Localization of an ovarian cancer tumor suppressor gene to a 0.5-cM region between D22S284 and CYP2D, on chromosome 22q
-
Bryan EJ, Watson RH, Davis M, Hitchcock A, Foulkes WD, et al. (1996) Localization of an ovarian cancer tumor suppressor gene to a 0.5-cM region between D22S284 and CYP2D, on chromosome 22q. Cancer Res 56: 719-721.
-
(1996)
Cancer Res
, vol.56
, pp. 719-721
-
-
Bryan, E.J.1
Watson, R.H.2
Davis, M.3
Hitchcock, A.4
Foulkes, W.D.5
-
11
-
-
33644949696
-
Analysis of cancer risk and BRCA1 and BRCA2 mutation prevalence in the kConFab familial breast cancer resource
-
Mann GJ, Thorne H, Balleine RL, Butow PN, Clarke CL, et al. (2006) Analysis of cancer risk and BRCA1 and BRCA2 mutation prevalence in the kConFab familial breast cancer resource. Breast Cancer Res 8: R12.
-
(2006)
Breast Cancer Res
, vol.8
-
-
Mann, G.J.1
Thorne, H.2
Balleine, R.L.3
Butow, P.N.4
Clarke, C.L.5
-
12
-
-
0036195557
-
Transforming growth factor beta receptor 1 polyalanine polymorphism and exon 5 mutation analysis in breast and ovarian cancer
-
Baxter SW, Choong DY, Eccles DM, Campbell IG, (2002) Transforming growth factor beta receptor 1 polyalanine polymorphism and exon 5 mutation analysis in breast and ovarian cancer. Cancer Epidemiol Biomarkers Prev 11: 211-214.
-
(2002)
Cancer Epidemiol Biomarkers Prev
, vol.11
, pp. 211-214
-
-
Baxter, S.W.1
Choong, D.Y.2
Eccles, D.M.3
Campbell, I.G.4
-
13
-
-
55849092083
-
Mutation and methylation analysis of the chromodomain-helicase-DNA binding 5 gene in ovarian cancer
-
Gorringe KL, Choong DY, Williams LH, Ramakrishna M, Sridhar A, et al. (2008) Mutation and methylation analysis of the chromodomain-helicase-DNA binding 5 gene in ovarian cancer. Neoplasia 10: 1253-1258.
-
(2008)
Neoplasia
, vol.10
, pp. 1253-1258
-
-
Gorringe, K.L.1
Choong, D.Y.2
Williams, L.H.3
Ramakrishna, M.4
Sridhar, A.5
-
14
-
-
77951640946
-
A method and server for predicting damaging missense mutations
-
Adzhubei IA, Schmidt S, Peshkin L, Ramensky VE, Gerasimova A, et al. (2010) A method and server for predicting damaging missense mutations. Nat Methods 7: 248-249.
-
(2010)
Nat Methods
, vol.7
, pp. 248-249
-
-
Adzhubei, I.A.1
Schmidt, S.2
Peshkin, L.3
Ramensky, V.E.4
Gerasimova, A.5
-
15
-
-
67749137351
-
Functional annotations improve the predictive score of human disease-related mutations in proteins
-
Calabrese R, Capriotti E, Fariselli P, Martelli PL, Casadio R, (2009) Functional annotations improve the predictive score of human disease-related mutations in proteins. Hum Mutat 30: 1237-1244.
-
(2009)
Hum Mutat
, vol.30
, pp. 1237-1244
-
-
Calabrese, R.1
Capriotti, E.2
Fariselli, P.3
Martelli, P.L.4
Casadio, R.5
-
16
-
-
70350671733
-
Automated inference of molecular mechanisms of disease from amino acid substitutions
-
Li B, Krishnan VG, Mort ME, Xin F, Kamati KK, et al. (2009) Automated inference of molecular mechanisms of disease from amino acid substitutions. Bioinformatics 25: 2744-2750.
-
(2009)
Bioinformatics
, vol.25
, pp. 2744-2750
-
-
Li, B.1
Krishnan, V.G.2
Mort, M.E.3
Xin, F.4
Kamati, K.K.5
-
17
-
-
25144496606
-
PMUT: a web-based tool for the annotation of pathological mutations on proteins
-
Ferrer-Costa C, Gelpi JL, Zamakola L, Parraga I, de la Cruz X, et al. (2005) PMUT: a web-based tool for the annotation of pathological mutations on proteins. Bioinformatics 21: 3176-3178.
-
(2005)
Bioinformatics
, vol.21
, pp. 3176-3178
-
-
Ferrer-Costa, C.1
Gelpi, J.L.2
Zamakola, L.3
Parraga, I.4
de la Cruz, X.5
-
18
-
-
77955151784
-
MutationTaster evaluates disease-causing potential of sequence alterations
-
Schwarz JM, Rodelsperger C, Schuelke M, Seelow D, (2010) MutationTaster evaluates disease-causing potential of sequence alterations. Nat Methods 7: 575-576.
-
(2010)
Nat Methods
, vol.7
, pp. 575-576
-
-
Schwarz, J.M.1
Rodelsperger, C.2
Schuelke, M.3
Seelow, D.4
-
19
-
-
66249120367
-
Human Splicing Finder: an online bioinformatics tool to predict splicing signals
-
Desmet FO, Hamroun D, Lalande M, Collod-Beroud G, Claustres M, et al. (2009) Human Splicing Finder: an online bioinformatics tool to predict splicing signals. Nucleic Acids Res 37: e67.
-
(2009)
Nucleic Acids Res
, vol.37
-
-
Desmet, F.O.1
Hamroun, D.2
Lalande, M.3
Collod-Beroud, G.4
Claustres, M.5
-
20
-
-
84868568796
-
Loss of function germline mutations in RAD51D in women with ovarian carcinoma
-
Wickramanyake A, Bernier G, Pennil C, Casadei S, Agnew KJ, et al. (2012) Loss of function germline mutations in RAD51D in women with ovarian carcinoma. Gynecol Oncol 127: 552-555.
-
(2012)
Gynecol Oncol
, vol.127
, pp. 552-555
-
-
Wickramanyake, A.1
Bernier, G.2
Pennil, C.3
Casadei, S.4
Agnew, K.J.5
-
21
-
-
84975742565
-
A map of human genome variation from population-scale sequencing
-
The 1000 Genomes Project Consortium
-
The 1000 Genomes Project Consortium (2010) A map of human genome variation from population-scale sequencing. Nature 467: 1061-1073.
-
(2010)
Nature
, vol.467
, pp. 1061-1073
-
-
-
22
-
-
0016197604
-
Amino acid difference formula to help explain protein evolution
-
Grantham R, (1974) Amino acid difference formula to help explain protein evolution. Science 185: 862-864.
-
(1974)
Science
, vol.185
, pp. 862-864
-
-
Grantham, R.1
|