-
1
-
-
0032076190
-
Nibrin, a novel DNA double-strand break repair protein, is mutated in Nijmegen breakage syndrome
-
Varon R, Vissinga C, Platzer M, Cerosaletti KM, Chrzanowska KH, Saar K, Beckmann G, Seemanova E, Cooper PR, Nowak NJ, Stumm M, Weemaes CM, et al. Nibrin, a novel DNA double-strand break repair protein, is mutated in Nijmegen breakage syndrome. Cell 1998;93:467-76.
-
(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.12
-
2
-
-
0000770165
-
Nijmegen breakage syndrome
-
The International Nijmegen Breakage Syndrome Study Group
-
The International Nijmegen Breakage Syndrome Study Group. Nijmegen breakage syndrome. Arch Dis Child 2000;82:400-6.
-
(2000)
Arch Dis Child
, vol.82
, pp. 400-406
-
-
-
3
-
-
3242892589
-
Nijmegen breakage syndrome: Clinical manifestation of defective response to DNA double-strand breaks
-
Digweed M, Sperling K. Nijmegen breakage syndrome: clinical manifestation of defective response to DNA double-strand breaks. DNA Repair 2004;3:1207-17.
-
(2004)
DNA Repair
, vol.3
, pp. 1207-1217
-
-
Digweed, M.1
Sperling, K.2
-
4
-
-
0033710938
-
Clinical ascertainment of Nijmegen breakage syndrome (NBS) and prevalence of the major mutation, 657del5, in three Slavic populations
-
Varon R, Seemanova E, Chrzanowska K, Hnateyko O, Piekutowska-Abramczuk D, Krajewska-Walasek M, Sykut-Cegielska J, Sperling K, Reis A. Clinical ascertainment of Nijmegen breakage syndrome (NBS) and prevalence of the major mutation, 657del5, in three Slavic populations. Eur J Hum Genet 2000;8:900-2.
-
(2000)
Eur J Hum Genet
, vol.8
, pp. 900-902
-
-
Varon, R.1
Seemanova, E.2
Chrzanowska, K.3
Hnateyko, O.4
Piekutowska-Abramczuk, D.5
Krajewska-Walasek, M.6
Sykut-Cegielska, J.7
Sperling, K.8
Reis, A.9
-
5
-
-
0034938838
-
High frequency of spontaneous translocations revealed by FISH in cells from patients with the cancer-prone syndromes ataxia telangiectasia and Nijmegen breakage syndrome
-
Stumm M, Neubauer S, Keindorff S, Wegner RD, Wieacker P, Sauer R. High frequency of spontaneous translocations revealed by FISH in cells from patients with the cancer-prone syndromes ataxia telangiectasia and Nijmegen breakage syndrome. Cytogenet Cell Genet 2001;92:186-91.
-
(2001)
Cytogenet Cell Genet
, vol.92
, pp. 186-191
-
-
Stumm, M.1
Neubauer, S.2
Keindorff, S.3
Wegner, R.D.4
Wieacker, P.5
Sauer, R.6
-
6
-
-
3042818662
-
Increased cancer risk of heterozygotes with NBS1 germline mutations in Poland
-
Steffen J, Varon R, Mosor M, Maneva G, Maurer M, Stumm M, Nowakowska D, Rubach M, Kosakowska E, Ruka W, Nowecki Z, Rutkowski P, et al. Increased cancer risk of heterozygotes with NBS1 germline mutations in Poland. Int J Cancer 2004;111:67-71.
-
(2004)
Int J Cancer
, vol.111
, pp. 67-71
-
-
Steffen, J.1
Varon, R.2
Mosor, M.3
Maneva, G.4
Maurer, M.5
Stumm, M.6
Nowakowska, D.7
Rubach, M.8
Kosakowska, E.9
Ruka, W.10
Nowecki, Z.11
Rutkowski, P.12
-
7
-
-
0034085362
-
No evidence for a major role of heterozygous deletion 657del5 within the NBS1 gene in the pathogenesis of non-Hodgkin's lymphoma of childhood and adolescence
-
Stanulla M, Stumm M, Dieckvoss BO, Seidemann K, Schemmel V, Muller Brechlin A, Schrappe M, Welte K, Reiter A. No evidence for a major role of heterozygous deletion 657del5 within the NBS1 gene in the pathogenesis of non-Hodgkin's lymphoma of childhood and adolescence. Br J Haematol 2000;109:117-20.
-
(2000)
Br J Haematol
, vol.109
, pp. 117-120
-
-
Stanulla, M.1
Stumm, M.2
Dieckvoss, B.O.3
Seidemann, K.4
Schemmel, V.5
Muller Brechlin, A.6
Schrappe, M.7
Welte, K.8
Reiter, A.9
-
8
-
-
0033902941
-
The common deletion 657del5 in the Nibrin gene is not a major risk factor for B or T non-Hodgkin lymphoma in a pediatric population
-
Rischewski J, Bismarck PV, Kabisch H, Janka-Schaub G, Obser T, Schneppenheim R. The common deletion 657del5 in the Nibrin gene is not a major risk factor for B or T non-Hodgkin lymphoma in a pediatric population. Leukemia 2000;14:1528-9.
-
(2000)
Leukemia
, vol.14
, pp. 1528-1529
-
-
Rischewski, J.1
Bismarck, P.V.2
Kabisch, H.3
Janka-Schaub, G.4
Obser, T.5
Schneppenheim, R.6
-
9
-
-
0033869097
-
Absence of mutations in the NBS1 gene in B-cell malignant lymphoma patients
-
Hama S, Matsuura S, Tauchi H, Sawada J, Kato C, Yamasaki F, Yoshioka H, Sugiyama K, Arita K, Kurisu K, Kamada N, Heike Y, et al. Absence of mutations in the NBS1 gene in B-cell malignant lymphoma patients. Anticancer Res 2000;20:1897-900.
-
(2000)
Anticancer Res
, vol.20
, pp. 1897-1900
-
-
Hama, S.1
Matsuura, S.2
Tauchi, H.3
Sawada, J.4
Kato, C.5
Yamasaki, F.6
Yoshioka, H.7
Sugiyama, K.8
Arita, K.9
Kurisu, K.10
Kamada, N.11
Heike, Y.12
-
10
-
-
0141918879
-
Correspondence re: "R. Varon, et al. Mutations in the Nijmegen breakage syndrome gene (NBS1) in childhood acute lymphoblastic leukemia. Cancer Res 61:3570-2, 2001"
-
Taylor GM, O'Brien HP, Greaves MF, Ravetto PF, Eden OB. Correspondence re: "R. Varon, et al. Mutations in the Nijmegen breakage syndrome gene (NBS1) in childhood acute lymphoblastic leukemia. Cancer Res 61:3570-2, 2001". Cancer Res 2003;63:6563-4.
-
(2003)
Cancer Res
, vol.63
, pp. 6563-6564
-
-
Taylor, G.M.1
O'Brien, H.P.2
Greaves, M.F.3
Ravetto, P.F.4
Eden, O.B.5
-
11
-
-
0036836572
-
Mutations and molecular variants of the NBS1 gene in non-Hodgkin lymphoma
-
Cerosaletti KM, Morrison VA, Sabath DE, Willerford MD, Concannon P. Mutations and molecular variants of the NBS1 gene in non-Hodgkin lymphoma. Genes Chromosomes Cancer 2002;35:282-6.
-
(2002)
Genes Chromosomes Cancer
, vol.35
, pp. 282-286
-
-
Cerosaletti, K.M.1
Morrison, V.A.2
Sabath, D.E.3
Willerford, M.D.4
Concannon, P.5
-
12
-
-
0038074370
-
Multiplex single-tube screening for mutations in the Nijmegen breakage syndrome (NBS1) gene in Hodgkin's and non-Hodgkin's lymphoma patients of Slavic origin
-
Soucek P, Gut I, Trneny M, Skovlund E, Grenaker Alnaes G, Kristensen T, Borresen-Dale AL, Kristensen VN. Multiplex single-tube screening for mutations in the Nijmegen breakage syndrome (NBS1) gene in Hodgkin's and non-Hodgkin's lymphoma patients of Slavic origin. Eur J Hum Genet 2003;11:416-9.
-
(2003)
Eur J Hum Genet
, vol.11
, pp. 416-419
-
-
Soucek, P.1
Gut, I.2
Trneny, M.3
Skovlund, E.4
Grenaker Alnaes, G.5
Kristensen, T.6
Borresen-Dale, A.L.7
Kristensen, V.N.8
-
13
-
-
10744226677
-
657del5 mutation in the gene for the Nijmegen breakage syndrome (NBS1) in a cohort of Russian children with lymphoid tissue malignancies and controls
-
Resnick IB, Kondratenko I, Pashanov E, Maschan AA, Karachunsky A, Togoev O, Timakov A, Polyakov A, Tverskaya S, Evgrafov O, Roumiantsev AG. 657del5 mutation in the gene for the Nijmegen breakage syndrome (NBS1) in a cohort of Russian children with lymphoid tissue malignancies and controls. Am J Med Genet A 2003;120:174-9.
-
(2003)
Am J Med Genet A
, vol.120
, pp. 174-179
-
-
Resnick, I.B.1
Kondratenko, I.2
Pashanov, E.3
Maschan, A.A.4
Karachunsky, A.5
Togoev, O.6
Timakov, A.7
Polyakov, A.8
Tverskaya, S.9
Evgrafov, O.10
Roumiantsev, A.G.11
-
14
-
-
31844434470
-
Carrier frequency of mutation 657del5 in the NBS1 gene in a population of Polish pediatric patients with sporadic lymphoid malignancies
-
Chrzanowska KH, Piekutowska-Abramczuk D, Popowska E, Gladkowska-Dura M, Maldyk J, Syczewska M, Krajewska-Walasek M, Goryluk-Kozakiewicz B, Bubala H, Gadomski A, Gaworczyk A, Kazanowska B, et al. Carrier frequency of mutation 657del5 in the NBS1 gene in a population of Polish pediatric patients with sporadic lymphoid malignancies. Int J Cancer 2006;118:1269-74.
-
(2006)
Int J Cancer
, vol.118
, pp. 1269-1274
-
-
Chrzanowska, K.H.1
Piekutowska-Abramczuk, D.2
Popowska, E.3
Gladkowska-Dura, M.4
Maldyk, J.5
Syczewska, M.6
Krajewska-Walasek, M.7
Goryluk-Kozakiewicz, B.8
Bubala, H.9
Gadomski, A.10
Gaworczyk, A.11
Kazanowska, B.12
-
15
-
-
0035328489
-
Mutations in the Nijmegen breakage syndrome gene (NBS1) in childhood acute lymphoblastic leukemia (ALL)
-
Varon R, Reis A, Henze G, von Einsiedel H, Sperling K, Seeger K. Mutations in the Nijmegen breakage syndrome gene (NBS1) in childhood acute lymphoblastic leukemia (ALL). Cancer Res 2001;61:3570-2.
-
(2001)
Cancer Res
, vol.61
, pp. 3570-3572
-
-
Varon, R.1
Reis, A.2
Henze, G.3
Von Einsiedel, H.4
Sperling, K.5
Seeger, K.6
-
16
-
-
33645125102
-
Nijmegen breakage syndrome (NBS) with neurological abnormalities and without chromosomal instability
-
Seemanova E, Sperling K, Neitzel H, Varon R, Hadac J, Butova O, Schrock E, Seeman P, Digweed M. Nijmegen breakage syndrome (NBS) with neurological abnormalities and without chromosomal instability. J Med Genet 2006;43:218-24.
-
(2006)
J Med Genet
, vol.43
, pp. 218-224
-
-
Seemanova, E.1
Sperling, K.2
Neitzel, H.3
Varon, R.4
Hadac, J.5
Butova, O.6
Schrock, E.7
Seeman, P.8
Digweed, M.9
-
17
-
-
0032784783
-
World Health Organization classification of neoplastic diseases of the hematopoietic and lymphoid tissues: Report of the Clinical Advisory Committee meeting - Airlie House, Virginia, November 1997
-
Harris NL, Jaffe ES, Diebold J, Flandrin G, Muller-Hermelink HK, Vardiman J, Lister TA, Bloomfield CD. World Health Organization classification of neoplastic diseases of the hematopoietic and lymphoid tissues: report of the Clinical Advisory Committee meeting - Airlie House, Virginia, November 1997. J Clin Oncol 1999;17:3835-49.
-
(1999)
J Clin Oncol
, vol.17
, pp. 3835-3849
-
-
Harris, N.L.1
Jaffe, E.S.2
Diebold, J.3
Flandrin, G.4
Muller-Hermelink, H.K.5
Vardiman, J.6
Lister, T.A.7
Bloomfield, C.D.8
-
18
-
-
0242610857
-
Nbn heterozygosity renders mice susceptible to tumor formation and ionizing radiation-induced tumorigenesis
-
Dumon-Jones V, Frappart PO, Tong WM, Sajithlal G, Hulla W, Schmid G, Herceg Z, Digweed M, Wang ZQ. Nbn heterozygosity renders mice susceptible to tumor formation and ionizing radiation-induced tumorigenesis. Cancer Res 2003;63:7263-9.
-
(2003)
Cancer Res
, vol.63
, pp. 7263-7269
-
-
Dumon-Jones, V.1
Frappart, P.O.2
Tong, W.M.3
Sajithlal, G.4
Hulla, W.5
Schmid, G.6
Herceg, Z.7
Digweed, M.8
Wang, Z.Q.9
-
19
-
-
19544389992
-
An inducible null mutant murine model of Nijmegen breakage syndrome proves the essential function of NBS1 in chromosomal stability and cell viability
-
Demuth I, Frappart PO, Hildebrand G, Melchers A, Lobitz S, Stockl L, Varon R, Herceg Z, Sperling K, Wang ZQ, Digweed M. An inducible null mutant murine model of Nijmegen breakage syndrome proves the essential function of NBS1 in chromosomal stability and cell viability. Hum Mol Genet 2004;13:2385-97.
-
(2004)
Hum Mol Genet
, vol.13
, pp. 2385-2397
-
-
Demuth, I.1
Frappart, P.O.2
Hildebrand, G.3
Melchers, A.4
Lobitz, S.5
Stockl, L.6
Varon, R.7
Herceg, Z.8
Sperling, K.9
Wang, Z.Q.10
Digweed, M.11
-
20
-
-
16844384184
-
DNA lesion-specific colocalization of the Mre11/Rad50/Nbs1 (MRN) complex and replication protein A (RPA) to repair foci
-
Robinson JG, Lu L, Dixon K, Bissler JJ. DNA lesion-specific colocalization of the Mre11/Rad50/Nbs1 (MRN) complex and replication protein A (RPA) to repair foci. J Biol Chem 2005;280:12927-34.
-
(2005)
J Biol Chem
, vol.280
, pp. 12927-12934
-
-
Robinson, J.G.1
Lu, L.2
Dixon, K.3
Bissler, J.J.4
-
21
-
-
0037086702
-
Targeted disruption of NBS1 reveals its roles in mouse development and DNA repair
-
Kang J, Bronson RT, Xu Y. Targeted disruption of NBS1 reveals its roles in mouse development and DNA repair. EMBO J 2002;21:1447-55.
-
(2002)
EMBO J
, vol.21
, pp. 1447-1455
-
-
Kang, J.1
Bronson, R.T.2
Xu, Y.3
-
22
-
-
13444281917
-
Nibrin functions in Ig class-switch recombination
-
Kracker S, Bergmann Y, Demuth I, Frappart PO, Hildebrand G, Christine R, Wang ZQ, Sperling K, Digweed M, Radbruch A. Nibrin functions in Ig class-switch recombination. Proc Natl Acad Sci USA 2005;102:1584-9.
-
(2005)
Proc Natl Acad Sci USA
, vol.102
, pp. 1584-1589
-
-
Kracker, S.1
Bergmann, Y.2
Demuth, I.3
Frappart, P.O.4
Hildebrand, G.5
Christine, R.6
Wang, Z.Q.7
Sperling, K.8
Digweed, M.9
Radbruch, A.10
-
23
-
-
13444309097
-
Genomic instability, endoreduplication, and diminished Ig class-switch recombination in B cell lacking Nbsl
-
Reina-San-Martin B, Nussenzweig MC, Nussenzweig A, Difilippantonio S. Genomic instability, endoreduplication, and diminished Ig class-switch recombination in B cell lacking Nbsl. Proc Natl Acad Sci USA 2005;102:1590-5.
-
(2005)
Proc Natl Acad Sci USA
, vol.102
, pp. 1590-1595
-
-
Reina-San-Martin, B.1
Nussenzweig, M.C.2
Nussenzweig, A.3
Difilippantonio, S.4
-
24
-
-
22144485580
-
The MRE11-RAD50-NBS1 complex accelerates somatic hypermutation and gene conversion of immunoglobulin variable regions
-
Yabuki M, Fujii MM, Maizels N. The MRE11-RAD50-NBS1 complex accelerates somatic hypermutation and gene conversion of immunoglobulin variable regions. Nat Immunol 2005;6:730-6.
-
(2005)
Nat Immunol
, vol.6
, pp. 730-736
-
-
Yabuki, M.1
Fujii, M.M.2
Maizels, N.3
-
25
-
-
0028019444
-
Gastrointestinal lymphoma
-
Isaacson PG. Gastrointestinal lymphoma. Hum Pathol 1994;25:1020-9.
-
(1994)
Hum Pathol
, vol.25
, pp. 1020-1029
-
-
Isaacson, P.G.1
-
26
-
-
0030923385
-
Primary extranodal non-Hodgkin's lymphomas, Part 1: Gastrointestinal, cutaneous and genito-urinary lymphomas
-
Zucca E, Roggero E, Bertoni F, Cavalli F. Primary extranodal non-Hodgkin's lymphomas, Part 1: Gastrointestinal, cutaneous and genito-urinary lymphomas. Ann Oncol 1997;8:727-37.
-
(1997)
Ann Oncol
, vol.8
, pp. 727-737
-
-
Zucca, E.1
Roggero, E.2
Bertoni, F.3
Cavalli, F.4
-
27
-
-
0011329911
-
Lymphoproliferative diseases associated with primary immune disorders
-
Jaffe ES, Harris NL, Stein H, Vardiman JW, eds. Lyon: IARC Press
-
Borisch B, Raphael M, Swerdlow SH, Jaffe ES. Lymphoproliferative diseases associated with primary immune disorders. In: Jaffe ES, Harris NL, Stein H, Vardiman JW, eds. World Health Organization Classification of Tumours: Pathology and Genetics of Tumours of Haematopoietic and Lymphoid Tissues. Lyon: IARC Press, 2001. 257-9.
-
(2001)
World Health Organization Classification of Tumours: Pathology and Genetics of Tumours of Haematopoietic and Lymphoid Tissues
, pp. 257-259
-
-
Borisch, B.1
Raphael, M.2
Swerdlow, S.H.3
Jaffe, E.S.4
-
28
-
-
0025935635
-
Helicobacter pylori-associated gastritis and primary B-cell gastric lymphoma
-
Wotherspoon AC, Ortiz-Hidalgo C, Falzon MR, Isaacson PG. Helicobacter pylori-associated gastritis and primary B-cell gastric lymphoma. Lancet 1991;338:1175-6.
-
(1991)
Lancet
, vol.338
, pp. 1175-1176
-
-
Wotherspoon, A.C.1
Ortiz-Hidalgo, C.2
Falzon, M.R.3
Isaacson, P.G.4
-
29
-
-
0026031788
-
Histopathologic features of high-grade non-Hodgkin's lymphomas in acquired immunodeficiency syndrome
-
The French Study Group of Pathology for Human Immunodeficiency Virus-Associated Tumors
-
Raphael M, Gentilhomme O, Tulliez M, Byron PA, Diebold J. Histopathologic features of high-grade non-Hodgkin's lymphomas in acquired immunodeficiency syndrome. The French Study Group of Pathology for Human Immunodeficiency Virus-Associated Tumors. Arch Pathol Lab Med 1991;115:15-20.
-
(1991)
Arch Pathol Lab Med
, vol.115
, pp. 15-20
-
-
Raphael, M.1
Gentilhomme, O.2
Tulliez, M.3
Byron, P.A.4
Diebold, J.5
-
31
-
-
0027279758
-
In situ demonstration of Epstein-Barr virus small RNAs (EBER 1) in acquired immunodeficiency syndrome-related lymphomas: Correlation with tumor morphology and primary site
-
Hamilton-Dutoit SJ, Raphael M, Audouin J, Diebold J, Lisse I, Pedersen C, Oksenhendler E, Marelle L, Pallesen G. In situ demonstration of Epstein-Barr virus small RNAs (EBER 1) in acquired immunodeficiency syndrome-related lymphomas: correlation with tumor morphology and primary site. Blood 1993;82:619-24.
-
(1993)
Blood
, vol.82
, pp. 619-624
-
-
Hamilton-Dutoit, S.J.1
Raphael, M.2
Audouin, J.3
Diebold, J.4
Lisse, I.5
Pedersen, C.6
Oksenhendler, E.7
Marelle, L.8
Pallesen, G.9
-
32
-
-
0029901549
-
Additional neoplasms and HCV infection in low-grade lymphoma of MALT type
-
Luppi M, Longo G, Ferrari MG, Ferrara L, Marasca R, Barozzi P, Morselli M, Emilia G, Torelli G. Additional neoplasms and HCV infection in low-grade lymphoma of MALT type. Br J Haematol 1996;94:373-5.
-
(1996)
Br J Haematol
, vol.94
, pp. 373-375
-
-
Luppi, M.1
Longo, G.2
Ferrari, M.G.3
Ferrara, L.4
Marasca, R.5
Barozzi, P.6
Morselli, M.7
Emilia, G.8
Torelli, G.9
-
34
-
-
0025853003
-
Is adult-onset coeliac disease due to a low-grade lymphoma of intraepithelial T lymphocytes?
-
Wright DH, Jones DB, Clark H, Mead GM, Hodges E, Howell WM. Is adult-onset coeliac disease due to a low-grade lymphoma of intraepithelial T lymphocytes? Lancet 1991;337:1373-4.
-
(1991)
Lancet
, vol.337
, pp. 1373-1374
-
-
Wright, D.H.1
Jones, D.B.2
Clark, H.3
Mead, G.M.4
Hodges, E.5
Howell, W.M.6
|