-
1
-
-
0028818286
-
Modulation of radiation-induced chromosomal damage by inhibitors of DNA repair and flow cytometric analysis in ataxia telangiectasia cells with 'intermediate radiosensitivity'
-
ANTOCCIA, A., CHESSA, L., RICORDY, R. and TANZARELLA, C., 1995, Modulation of radiation-induced chromosomal damage by inhibitors of DNA repair and flow cytometric analysis in ataxia telangiectasia cells with 'intermediate radiosensitivity'. Mutagenesis, 10, 523-529.
-
(1995)
Mutagenesis
, vol.10
, pp. 523-529
-
-
Antoccia, A.1
Chessa, L.2
Ricordy, R.3
Tanzarella, C.4
-
2
-
-
0031028857
-
Chromosomal radiosensitivity to clastogenic agents and cell cycle perturbations in Nijmegen Breakage Syndrome lymphoblastoid cell lines
-
ANTOCCIA, A., RICORDY, R., MARASCHIO, P., PRUDENTE, S. and TANZARELLA, C., 1997, Chromosomal radiosensitivity to clastogenic agents and cell cycle perturbations in Nijmegen Breakage Syndrome lymphoblastoid cell lines. International Journal of Radiation Biology, 71, 41-49.
-
(1997)
International Journal of Radiation Biology
, vol.71
, pp. 41-49
-
-
Antoccia, A.1
Ricordy, R.2
Maraschio, P.3
Prudente, S.4
Tanzarella, C.5
-
3
-
-
0028788337
-
The role of the ataxia-telangiectasia gene in the p53, WAF1/CIP1(p21) and GADD45-mediated response to ionising radiation
-
ARTUSO, M., ESTEVE, A., BRESIL, H., VUILLAUME, M. and HALL, J., 1995, The role of the ataxia-telangiectasia gene in the p53, WAF1/CIP1(p21) and GADD45-mediated response to ionising radiation. Oncogene, 11, 1427-1435.
-
(1995)
Oncogene
, vol.11
, pp. 1427-1435
-
-
Artuso, M.1
Esteve, A.2
Bresil, H.3
Vuillaume, M.4
Hall, J.5
-
4
-
-
0025874254
-
Chromosome instability and X-ray hypersensitivity in a microcephalic and growth-retarded child
-
BARBI, G., SCHERES, J. M., SCHINDLER, D., TAALMAN, R. D., RODENS, K., MEHNERT, K., MULLER, M. and SEYSCHAB, H., 1991, Chromosome instability and X-ray hypersensitivity in a microcephalic and growth-retarded child. American Journal of Medical Genetics, 40, 44-50.
-
(1991)
American Journal of Medical Genetics
, vol.40
, pp. 44-50
-
-
Barbi, G.1
Scheres, J.M.2
Schindler, D.3
Taalman, R.D.4
Rodens, K.5
Mehnert, K.6
Muller, M.7
Seyschab, H.8
-
5
-
-
0028213350
-
Radiosensitivity in ataxia telangiectasia: Anomalies in radiation-induced cell cycle delay
-
BEAMISH, H. and LAVIN, M. F., 1994, Radiosensitivity in ataxia telangiectasia: anomalies in radiation-induced cell cycle delay. International Journal of Radiation Biology, 65, 175-184.
-
(1994)
International Journal of Radiation Biology
, vol.65
, pp. 175-184
-
-
Beamish, H.1
Lavin, M.F.2
-
6
-
-
0028171182
-
The p53-dependent GI cell cycle checkpoint pathway and ataxia telangiectasia
-
CANMAN, C. E., WOLFF, A. C., CHEN, C., FORNAGE, A. J. and KASTAN, M. B., 1994, The p53-dependent GI cell cycle checkpoint pathway and ataxia telangiectasia. Cancer Research, 54, 5054-5058.
-
(1994)
Cancer Research
, vol.54
, pp. 5054-5058
-
-
Canman, C.E.1
Wolff, A.C.2
Chen, C.3
Fornage, A.J.4
Kastan, M.B.5
-
7
-
-
0032076248
-
The hMMre11/hRad50 protein complex and Nijmegen breakage syndrome: Linkage of double-strand break repair to the cellular DNA damage response
-
CARNEY, J. P., MASER, R. S., OLIVARES, H., DAVIS, E. M., LE BEAU, M., YATES, J. R. III, HAYES, L., MORGAN, VV. F. and PETRINI, J. H. J., 1998, The hMMre11/hRad50 protein complex and Nijmegen breakage syndrome: linkage of double-strand break repair to the cellular DNA damage response. Cell, 93, 477-486.
-
(1998)
Cell
, vol.93
, pp. 477-486
-
-
Carney, J.P.1
Maser, R.S.2
Olivares, H.3
Davis, E.M.4
Le Beau, M.5
Yates J.R. III6
Hayes, L.7
Morgan, V.V.F.8
Petrini, J.H.J.9
-
8
-
-
0029056905
-
Eleven Polish patients with microcephaly, immunodeficency, and chromosomal instability: The Nijmegen breakage syndrome
-
CHRZANOWSKA, K. H., KLEIJER, VV. J., KRAJEWSKA WALASEK, M., BIALECKA, M., GUTKOWSKA, A., GORYLUK KOZAKIEWICZ, B., MlCHALKIEWICZ, J., STACHOWSKI, J., GREGOREK, H., LYSON-WOJCIECHOSWSKA, G., JAHOWICZ, W. and JOZWIAK, S., 1995, Eleven Polish patients with microcephaly, immunodeficency, and chromosomal instability: the Nijmegen breakage syndrome. American Journal of Medical Semetics, 57, 462-471.
-
(1995)
American Journal of Medical Semetics
, vol.57
, pp. 462-471
-
-
Chrzanowska, K.H.1
Kleijer, V.V.J.2
Krajewska Walasek, M.3
Bialecka, M.4
Gutkowska, A.5
Goryluk Kozakiewicz, B.6
Michalkiewicz, J.7
Stachowski, J.8
Gregorek, H.9
Lyson-Wojciechoswska, G.10
Jahowicz, W.11
Jozwiak, S.12
-
9
-
-
0022479925
-
A chromosome breakage syndrome with profound immunodeficency
-
CONLEY, M. E., SPINNER, N. B., EMANUEL, B. S., NOWELL, P. C. and NICKOLS, W. W., 1986, A chromosome breakage syndrome with profound immunodeficency. Blood, 67, 1251-1256.
-
(1986)
Blood
, vol.67
, pp. 1251-1256
-
-
Conley, M.E.1
Spinner, N.B.2
Emanuel, B.S.3
Nowell, P.C.4
Nickols, W.W.5
-
10
-
-
0029938657
-
The relationship between p53 status, DNA repair, and chromatid aberration induction in G2 mouse embryo fibroblast cells treated with bleomycin
-
DONNER, E. M. and PRESTON, R. J., 1996, The relationship between p53 status, DNA repair, and chromatid aberration induction in G2 mouse embryo fibroblast cells treated with bleomycin. Carcinogenesis, 17, 1161-1165.
-
(1996)
Carcinogenesis
, vol.17
, pp. 1161-1165
-
-
Donner, E.M.1
Preston, R.J.2
-
11
-
-
0027359827
-
WAFI, a potential mediator of p53 tumor suppression
-
EL-DEIRY, W., TOKINO, T., VELCULESCU, V. E., LEVY, D. B., PARSONS, R., TRENT, J. M., LIN, D., MERCER, W. E., KINZLER, K., W. and VOGELSTEIN, B., 1993, WAFI, a potential mediator of p53 tumor suppression. Cel, 75, 817-825.
-
(1993)
Cel
, vol.75
, pp. 817-825
-
-
El-Deiry, W.1
Tokino, T.2
Velculescu, V.E.3
Levy, D.B.4
Parsons, R.5
Trent, J.M.6
Lin, D.7
Mercer, W.E.8
Kinzler, K.W.9
Vogelstein, B.10
-
12
-
-
0029878308
-
Gytogenetic damage and the radiation-induced G1-phase checkpoint
-
GUPTA, N. V. R., HAAS-KOGAN, D. A., ISRAEL, M. A., DEEN, D. F. and MORGAN, W. F., 1996, Gytogenetic damage and the radiation-induced G1-phase checkpoint. Radiation Research, 145, 289-298.
-
(1996)
Radiation Research
, vol.145
, pp. 289-298
-
-
Gupta, N.V.R.1
Haas-Kogan, D.A.2
Israel, M.A.3
Deen, D.F.4
Morgan, W.F.5
-
13
-
-
0027496935
-
The p21 Cdk-interacting protein Cip 1 is a potent inhibitor of G1 cyclin dependent kinases
-
HARPER, J. W., ADAMI, G. R., WEI, N., KEYOMARSI, K. and ELLEDGE, S. J., 1993, The p21 Cdk-interacting protein Cip 1 is a potent inhibitor of G1 cyclin dependent kinases. Cell, 75, 805-816.
-
(1993)
Cell
, vol.75
, pp. 805-816
-
-
Harper, J.W.1
Adami, G.R.2
Wei, N.3
Keyomarsi, K.4
Elledge, S.J.5
-
14
-
-
0030786912
-
Nijmegen Breakage Syndrome cells fail to induce the p53-mediated DNA damage response following exposure to ionizing radiation
-
JONGMANS, W., VUILLAUME, M., CHRZANOWSKA, K. A., SMEETS, D., SPERLING, K. and HALL, J., 1997, Nijmegen Breakage Syndrome cells fail to induce the p53-mediated DNA damage response following exposure to ionizing radiation. Molecular and Cellular Biology, 17, 5016-5022.
-
(1997)
Molecular and Cellular Biology
, vol.17
, pp. 5016-5022
-
-
Jongmans, W.1
Vuillaume, M.2
Chrzanowska, K.A.3
Smeets, D.4
Sperling, K.5
Hall, J.6
-
15
-
-
0026496885
-
A mammalian cell cycle checkpoint pathway utilizing p53 and GADD45 is defective in ataxia telangiectasia
-
KASTAN, M. B., ZHAN, Q., EL-DEIRY, W. S., CARRIER, F., JACKS, T., WALSH, W. V., PLUNKETT, B. S., VOGELSTEIN, B. and FORNACE, A. J. J., 1992, A mammalian cell cycle checkpoint pathway utilizing p53 and GADD45 is defective in ataxia telangiectasia. Cell, 71, 587-597.
-
(1992)
Cell
, vol.71
, pp. 587-597
-
-
Kastan, M.B.1
Zhan, Q.2
El-Deiry, W.S.3
Carrier, F.4
Jacks, T.5
Walsh, W.V.6
Plunkett, B.S.7
Vogelstein, B.8
Fornace, A.J.J.9
-
16
-
-
0027486024
-
Ionizing radiation and UV induction of p53 protein by different pathways in ataxia-telangiectasia cells
-
KHANNA, K. K., and LAVIN, M. K., 1993, Ionizing radiation and UV induction of p53 protein by different pathways in ataxia-telangiectasia cells. Oncogene, 8, 3307-3312.
-
(1993)
Oncogene
, vol.8
, pp. 3307-3312
-
-
Khanna, K.K.1
Lavin, M.K.2
-
17
-
-
0026656853
-
Wild-type p53 is a cell cycle checkpoint determinant following irradiation
-
KUERBITZ, S. J., PLUNKETT, B. S., WALSH, W. V. and KASTAN, M. B., 1992, Wild-type p53 is a cell cycle checkpoint determinant following irradiation. Proceedings of the National Academy of Sciences, USA, 89, 7491-7495.
-
(1992)
Proceedings of the National Academy of Sciences, U S A
, vol.89
, pp. 7491-7495
-
-
Kuerbitz, S.J.1
Plunkett, B.S.2
Walsh, W.V.3
Kastan, M.B.4
-
18
-
-
0027285380
-
p53 mutations increase resistance to ionizing radiation
-
LEE, J. M. and BERNSTEIN, A., 1993, p53 mutations increase resistance to ionizing radiation. Proceedings of the National Academy of Sciences, U S A, 90, 5742-5746.
-
(1993)
Proceedings of the National Academy of Sciences, U S A
, vol.90
, pp. 5742-5746
-
-
Lee, J.M.1
Bernstein, A.2
-
19
-
-
0027332996
-
Differential induction of transcriptionally active p53 following UV or ionizing radiation: Defects in chromosome instability syndromes?
-
LU, X. and LANE, D. P., 1993, Differential induction of transcriptionally active p53 following UV or ionizing radiation: defects in chromosome instability syndromes? Cell, 75, 765-778.
-
(1993)
Cell
, vol.75
, pp. 765-778
-
-
Lu, X.1
Lane, D.P.2
-
20
-
-
0032567642
-
Radiation induction of p53 in cells from Nijmegen Breakage Syndrome is defective but not similar to ataxia-telangiectasia
-
MATSUURA, K., BALMUKHANOV, T., TAUCHI, H., WEEMAES, C., SMEETS, D., CHRZANOWSKA, K. A., ENDOU, S., MATSUURA, S. and KOMATSU, K., 1998b, Radiation induction of p53 in cells from Nijmegen Breakage Syndrome is defective but not similar to ataxia-telangiectasia. Biochemical and Biophysical Research Communications, 242, 602-007.
-
(1998)
Biochemical and Biophysical Research Communications
, vol.242
, pp. 602-1007
-
-
Matsuura, K.1
Balmukhanov, T.2
Tauchi, H.3
Weemaes, C.4
Smeets, D.5
Chrzanowska, K.A.6
Endou, S.7
Matsuura, S.8
Komatsu, K.9
-
21
-
-
17344372572
-
Positional cloning of the gene for Nijmegen breakage syndrome
-
MATSUURA, S., TAUCHI, H., NAKAMURA, A., KONDO, N., SAKAMOTO, S., ENDO, S., SMEETS, D., SOLDER, B., BELOHRADSKY, B. H., DER KALOUSTIAN, V. M., OSHIMURA, M, ISOMURA, M., NAKAMURA, Y. and KOMATSU, K., 1998a, Positional cloning of the gene for Nijmegen breakage syndrome. Nature Genetics, 19, 179-181.
-
(1998)
Nature Genetics
, vol.19
, pp. 179-181
-
-
Matsuura, S.1
Tauchi, H.2
Nakamura, A.3
Kondo, N.4
Sakamoto, S.5
Endo, S.6
Smeets, D.7
Solder, B.8
Belohradsky, B.H.9
Der Kaloustian, V.M.10
Oshimura, M.11
Isomura, M.12
Nakamura, Y.13
Komatsu, K.14
-
22
-
-
16944367119
-
Genetic mapping using microcell-mediated chromosome fragment suggests a locus for Nijmegen breakage syndrome at chromosome 8q21-24
-
MATSUURA, S., WEEMAES, C., SMEETS, D., TAKAMI, H., KONDO, N., SAKAMOTO, S., YANO, N., NAKAMURA, A., TAUCHI, H., ENDOU, S., OSHIMURA, M. and KOMATSU, K., 1997, Genetic mapping using microcell-mediated chromosome fragment suggests a locus for Nijmegen breakage syndrome at chromosome 8q21-24. American Journal of Human Genetics, 60, 1487-1494.
-
(1997)
American Journal of Human Genetics
, vol.60
, pp. 1487-1494
-
-
Matsuura, S.1
Weemaes, C.2
Smeets, D.3
Takami, H.4
Kondo, N.5
Sakamoto, S.6
Yano, N.7
Nakamura, A.8
Tauchi, H.9
Endou, S.10
Oshimura, M.11
Komatsu, K.12
-
23
-
-
0030969423
-
Fragments of ATM which have dominant-negative or complementing activity
-
MORGAN, S. E., LOVLY, C., PANDITA, T. K., SHILOH, Y. and KASTAN, M. B., 1997, Fragments of ATM which have dominant-negative or complementing activity. Molecular and Cellular Biology, 17, 2020-2029.
-
(1997)
Molecular and Cellular Biology
, vol.17
, pp. 2020-2029
-
-
Morgan, S.E.1
Lovly, C.2
Pandita, T.K.3
Shiloh, Y.4
Kastan, M.B.5
-
24
-
-
0028932603
-
Cell cycle regulation in response to DNA damage in mammalian cells: A historical perspective
-
MURNAME, J. P., 1995, Cell cycle regulation in response to DNA damage in mammalian cells: a historical perspective. Cancer and Metastasis Reviews, 14, 17-29.
-
(1995)
Cancer and Metastasis Reviews
, vol.14
, pp. 17-29
-
-
Murname, J.P.1
-
25
-
-
0030895204
-
When checkpoints fail
-
PAULOVICH, A. G., TOCZYSKI, D. and HARTWELL, L. H., 1997, When Checkpoints fail. Cell, 88, 315-321.
-
(1997)
Cell
, vol.88
, pp. 315-321
-
-
Paulovich, A.G.1
Toczyski, D.2
Hartwell, L.H.3
-
26
-
-
0027143217
-
The mdm-2 gene is induced in response to UV-light in a p53-dependent manner
-
PERRY, M. E., PIETTE, J., ZANWADZIKI, J. A., HARVEY, D. and LEVINE, A. J., 1993, The mdm-2 gene is induced in response to UV-light in a p53-dependent manner. Proceedings of the National Academy of Sciences, U S A, 90, 11 623-11 627.
-
(1993)
Proceedings of the National Academy of Sciences, U S A
, vol.90
, pp. 11623-11627
-
-
Perry, M.E.1
Piette, J.2
Zanwadziki, J.A.3
Harvey, D.4
Levine, A.J.5
-
27
-
-
16944366639
-
The gene for the ataxia-telangiectasia variant, Nijmegen breakage syndrome, maps to a 1-cM interval on chromosome 8q21
-
SAAR, K., CHRZANOWSKA, K. A., STUMM, M., JUNG, M., NURNBERG, G., WlENKER, T. F., SEEMANOVA, E., WEGNER, R. D., REIS, A. and SPERLING, K., 1997, The gene for the ataxia-telangiectasia variant, Nijmegen breakage syndrome, maps to a 1-cM interval on chromosome 8q21. American Journal of Human Genetics, 60, 605-610.
-
(1997)
American Journal of Human Genetics
, vol.60
, pp. 605-610
-
-
Saar, K.1
Chrzanowska, K.A.2
Stumm, M.3
Jung, M.4
Nurnberg, G.5
Wlenker, T.F.6
Seemanova, E.7
Wegner, R.D.8
Reis, A.9
Sperling, K.10
-
28
-
-
0029057336
-
A single ataxia telangiectasia gene with a product similar to PI-3kinase
-
SAVITSKY, K., BAR-SHIRA, A., GILAND, S., ROTMAN, G., ZIV, Y., VANAGAITE, L., TAGLE, D. A., SMITH, S., UZIEL, T., SFEZ, S., ASHKENAZI, M., PECKER, I., FRYDMAN, M., HARNIK, R., PATANJALI, S. R., SIMMONS, A., CLINES, G. A., SARTIEL, A., GATTI, R. A., CHESSA, L., SANAL, O., LAVIN, M. F., JASPERS, N. G. J., TAYLOR, A. M. R., ARLETT, C. F., MIKI, T., WEISSMAN, S., LOVETT, M., COLLINS, F. S. and SHILOH, Y., 1995, A single ataxia telangiectasia gene with a product similar to PI-3kinase. Science, 268, 1749-1753.
-
(1995)
Science
, vol.268
, pp. 1749-1753
-
-
Savitsky, K.1
Bar-Shira, A.2
Giland, S.3
Rotman, G.4
Ziv, Y.5
Vanagaite, L.6
Tagle, D.A.7
Smith, S.8
Uziel, T.9
Sfez, S.10
Ashkenazi, M.11
Pecker, I.12
Frydman, M.13
Harnik, R.14
Patanjali, S.R.15
Simmons, A.16
Clines, G.A.17
Sartiel, A.18
Gatti, R.A.19
Chessa, L.20
Sanal, O.21
Lavin, M.F.22
Jaspers, N.G.J.23
Taylor, A.M.R.24
Arlett, C.F.25
Miki, T.26
Weissman, S.27
Lovett, M.28
Collins, F.S.29
Shiloh, Y.30
more..
-
29
-
-
0021946340
-
Familial microcephaly with normal intelligence, immunodeficency, and risk for lyrnphoreticular malignancies: A new autosomal recessive disorder
-
SEEMANOVA, E., PASSARGE, E., BENESKOVA, D., HOUSTEK, J., KASAL, P. and SEVCIKOVA, M., 1985, Familial microcephaly with normal intelligence, immunodeficency, and risk for lyrnphoreticular malignancies: a new autosomal recessive disorder. American Journal of Medical Genetics, 20, 639-648.
-
(1985)
American Journal of Medical Genetics
, vol.20
, pp. 639-648
-
-
Seemanova, E.1
Passarge, E.2
Beneskova, D.3
Houstek, J.4
Kasal, P.5
Sevcikova, M.6
-
30
-
-
0031466618
-
Ataxia telangiectasia and the Nijmegen Breakage Syndrome: Related disorders but genes a part
-
SHILOH, Y., 1997, Ataxia telangiectasia and the Nijmegen Breakage Syndrome: related disorders but genes a part. Annual Review of Genetics, 31, 635-662.
-
(1997)
Annual Review of Genetics
, vol.31
, pp. 635-662
-
-
Shiloh, Y.1
-
31
-
-
0028919069
-
Involvement of the p53 tumor suppressor in repair of u.v.-type DNA damage
-
SMITH, M. L., CHEN, I. T., ZHAN, Q., O'CONNOR, P. M. and FORNACE, A. J. J., 1995, Involvement of the p53 tumor suppressor in repair of u.v.-type DNA damage. Oncogene, 10, 1053-1059.
-
(1995)
Oncogene
, vol.10
, pp. 1053-1059
-
-
Smith, M.L.1
Chen, I.T.2
Zhan, Q.3
O'Connor, P.M.4
Fornace, A.J.J.5
-
32
-
-
0029112755
-
The ataxia-telangiectasia-variant genes 1 and 2 are distinct from the ataxia-telangiectasia gene on chromosome 11q23.1
-
STUMM, M., GATTI, R. A., REIS, A., UDAR, N., CHRZANOWSKA, K., SEEMANOVA, E., SPERLING, K. and WEGNER, R. D., 1995, The ataxia-telangiectasia-variant genes 1 and 2 are distinct from the ataxia-telangiectasia gene on chromosome 11q23.1. American Journal of Human Genetics, 57, 960-962.
-
(1995)
American Journal of Human Genetics
, vol.57
, pp. 960-962
-
-
Stumm, M.1
Gatti, R.A.2
Reis, A.3
Udar, N.4
Chrzanowska, K.5
Seemanova, E.6
Sperling, K.7
Wegner, R.D.8
-
33
-
-
0030955042
-
Noncomplementation of radiation induced chromosome aberrations in ataxia telangiectasia variant heterodikaryons
-
STUMM, M., SPERLING, K. and WEGNER, R. D., 1997, Noncomplementation of radiation induced chromosome aberrations in ataxia telangiectasia variant heterodikaryons. American Journal of Human Genetics, 60, 1246-1251.
-
(1997)
American Journal of Human Genetics
, vol.60
, pp. 1246-1251
-
-
Stumm, M.1
Sperling, K.2
Wegner, R.D.3
-
34
-
-
0020684242
-
Hypersensitivity, in vitro, to ionizing radiation in a new chromosomal instability syndrome, the Nijmegen Breakage Syndrome
-
TAALMAN, R. D. F. M., JASPERS, N. G. J., SCHERES, J. M. J. C., DE DEWIT, J. and HUSTINX, T. W. J., 1983, Hypersensitivity, in vitro, to ionizing radiation in a new chromosomal instability syndrome, the Nijmegen Breakage Syndrome. Mutation Research, 112, 23-32.
-
(1983)
Mutation Research
, vol.112
, pp. 23-32
-
-
Taalman, R.D.F.M.1
Jaspers, N.G.J.2
Scheres, J.M.J.C.3
De Dewit, J.4
Hustinx, T.W.J.5
-
35
-
-
0016786321
-
Ataxia-telangiectasia, a human mutation with abnormal radiation sensitivity
-
TAYLOR, A. M. R., HARNDEN, D. G., ARLETT, C. F., HARCOURT, A. R., LEHMAN, A. R., STEVENS, F. and BRIDGES, B. A., 1975, Ataxia-telangiectasia, a human mutation with abnormal radiation sensitivity. Nature, 258, 427-429.
-
(1975)
Nature
, vol.258
, pp. 427-429
-
-
Taylor, A.M.R.1
Harnden, D.G.2
Arlett, C.F.3
Harcourt, A.R.4
Lehman, A.R.5
Stevens, F.6
Bridges, B.A.7
-
36
-
-
0031036968
-
Nijmegen Breakage Syndrome with unusual cytogenetic features and intermediate cellular radiosensitivity
-
TUPLER, R., MARSEGLIA, G., STEFANINI, M., PROSPERI, E., CHESSA, L., NARDO, T., MARCHI, A. and MARASCHIO, P., 1997, Nijmegen Breakage Syndrome with unusual cytogenetic features and intermediate cellular radiosensitivity. Journal of Medical Genetics, 34, 190-202.
-
(1997)
Journal of Medical Genetics
, vol.34
, pp. 190-202
-
-
Tupler, R.1
Marseglia, G.2
Stefanini, M.3
Prosperi, E.4
Chessa, L.5
Nardo, T.6
Marchi, A.7
Maraschio, P.8
-
37
-
-
0030022497
-
Nijmegen breakage syndrome
-
VAN DER BURGT, I., CHRZANOWSKA, K., SMEETS, D. and WEEMAES, C., 1996, Nijmegen breakage syndrome. Journal of Medical Genetics, 33, 153-155.
-
(1996)
Journal of Medical Genetics
, vol.33
, pp. 153-155
-
-
Van Der Burgt, I.1
Chrzanowska, K.2
Smeets, D.3
Weemaes, C.4
-
38
-
-
0032076190
-
Nibrin, a novel DNA double-strand break repair protein, is mutated in Nijmegen breakage syndrome
-
VARON, R., VISSINGA, C., PLATZER, M., CEROSALETTI, K. M., CHRZANOWSKA, K. H., SAAR, K., BECKMANN, G., SEEMANOVA, E., COOPER, P. R., NOWAK, N. J., STUMM, M., WEEMAES, C. M. R., GATTI, R. A., WILSON, R. K., DIGWEED, M., ROSENTHAL, A., SPERLING, K., CONCANNON, P. and REIS, A., 1998, Nibrin, a novel DNA double-strand break repair protein, is mutated in Nijmegen breakage syndrome. Cell, 93, 467-476.
-
(1998)
Cell
, vol.93
, pp. 467-476
-
-
Varon, R.1
Vissinga, C.2
Platzer, M.3
Cerosaletti, K.M.4
Chrzanowska, K.H.5
Saar, K.6
Beckmann, G.7
Seemanova, E.8
Cooper, P.R.9
Nowak, N.J.10
Stumm, M.11
Weemaes, C.M.R.12
Gatti, R.A.13
Wilson, R.K.14
Digweed, M.15
Rosenthal, A.16
Sperling, K.17
Concannon, P.18
Reis, A.19
-
39
-
-
0028598517
-
Nijmegen Breakage Syndrome: A progress report
-
WEEMAES, C. M. R., SMEETS, D. F. C. M. and VAN DER BURGT, C. J. A. M., 1994, Nijmegen Breakage Syndrome: a progress report. International Journal of Radiation Biology, 66, 185-188.
-
(1994)
International Journal of Radiation Biology
, vol.66
, pp. 185-188
-
-
Weemaes, C.M.R.1
Smeets, D.F.C.M.2
Van Der Burgt, C.J.A.M.3
-
40
-
-
0019478575
-
A new chromosomal instability disorder: The Nijmegen breakage syndrome
-
WEEMAES, M. R., HUSTINX, T. W. J., SCHERE.S, J. M. J., MUNSTER, P. J., VAN BAKKEREN, J. A. J. and TAALAMAN, R. D. F., 1981, A new chromosomal instability disorder: the Nijmegen breakage syndrome. Acta Paediatrica Scandinavica, 70, 557-564.
-
(1981)
Acta Paediatrica Scandinavica
, vol.70
, pp. 557-564
-
-
Weemaes, M.R.1
Hustinx, T.W.J.2
Scheres, J.M.J.3
Munster, P.J.4
Van Bakkeren, J.A.J.5
Taalaman, R.D.F.6
-
41
-
-
0002229288
-
Ataxia Telangiectasia Variants: In (Nijmegen Breakage Syndrome)
-
edited by Ochs, Smith and Puck (Oxford: Oxford University Press)
-
WEGNER, R. D., CHRZANOWSKA, K., SPERLING, K. and STUMM, M., 1998, Ataxia Telangiectasia Variants: in (Nijmegen Breakage Syndrome), in: Primary Immunodeficency Diseases, A Genetic and Molecular Approach, edited by Ochs, Smith and Puck (Oxford: Oxford University Press).
-
(1998)
Primary Immunodeficency Diseases, A Genetic and Molecular Approach
-
-
Wegner, R.D.1
Chrzanowska, K.2
Sperling, K.3
Stumm, M.4
-
42
-
-
0023846248
-
A new chromosomal instability disorder confirmed by complementation studies
-
WEGNER, R. D., METZGER, M., HANEFELD, F., JASPERS, N. G., BAAN, C., MEGDORF, K., KUNZE, J. and SPERLING, K., 1988, A new chromosomal instability disorder confirmed by complementation studies. Clinical Genetics, 33, 20-32.
-
(1988)
Clinical Genetics
, vol.33
, pp. 20-32
-
-
Wegner, R.D.1
Metzger, M.2
Hanefeld, F.3
Jaspers, N.G.4
Baan, C.5
Megdorf, K.6
Kunze, J.7
Sperling, K.8
-
43
-
-
0032101583
-
Characterization of cell cycle checkpoint response after ionizing radiation in Nijmegen Breakage Syndrome cells
-
YAMAZAKY, V., WEGNER, R. D. and KIRCHGESSNER, C. U., 1998, Characterization of cell cycle checkpoint response after ionizing radiation in Nijmegen Breakage Syndrome cells. Cancer Research, 58, 2316-2322.
-
(1998)
Cancer Research
, vol.58
, pp. 2316-2322
-
-
Yamazaky, V.1
Wegner, R.D.2
Kirchgessner, C.U.3
-
44
-
-
0029127643
-
ATM-related genes: What do they tell us about functions of the human gene?
-
ZAKIAN, V. A., 1995, ATM-related genes: what do they tell us about functions of the human gene? Cell, 82, 685-687.
-
(1995)
Cell
, vol.82
, pp. 685-687
-
-
Zakian, V.A.1
|