159 related articles for article (PubMed ID: 36806726)
1. The NBN founder mutation-Evidence for a country specific difference in age at cancer manifestation.
Chrzanowska KH; Seemanova E; Varon R; Digweed M; Piekutowska-Abramczuk D; Sperling K; Seeman P
Cancer Rep (Hoboken); 2023 Feb; 6(2):e1700. PubMed ID: 36806726
[TBL] [Abstract][Full Text] [Related]
2. Cancer risk of heterozygotes with the NBN founder mutation.
Seemanová E; Jarolim P; Seeman P; Varon R; Digweed M; Swift M; Sperling K
J Natl Cancer Inst; 2007 Dec; 99(24):1875-80. PubMed ID: 18073374
[TBL] [Abstract][Full Text] [Related]
3. The Slavic NBN Founder Mutation: A Role for Reproductive Fitness?
Seemanova E; Varon R; Vejvalka J; Jarolim P; Seeman P; Chrzanowska KH; Digweed M; Resnick I; Kremensky I; Saar K; Hoffmann K; Dutrannoy V; Karbasiyan M; Ghani M; Barić I; Tekin M; Kovacs P; Krawczak M; Reis A; Sperling K; Nothnagel M
PLoS One; 2016; 11(12):e0167984. PubMed ID: 27936167
[TBL] [Abstract][Full Text] [Related]
4. [Heterozygous carriers of Slavic mutation 657del5 of NBN gene in patients with colorectal cancer].
Seemanová E; Hoch J; Seeman P
Cas Lek Cesk; 2011; 150(2):97-9. PubMed ID: 21560448
[TBL] [Abstract][Full Text] [Related]
5. Cleavage of the BRCT tandem domains of nibrin by the 657del5 mutation affects the DNA damage response less than the Arg215Trp mutation.
Mendez G; Cilli D; Berardinelli F; Viganotti M; Ascenzi P; Tanzarella C; Antoccia A; di Masi A
IUBMB Life; 2012 Oct; 64(10):853-61. PubMed ID: 22941933
[TBL] [Abstract][Full Text] [Related]
6. Identification of the interactors of human nibrin (NBN) and of its 26 kDa and 70 kDa fragments arising from the NBN 657del5 founder mutation.
Cilli D; Mirasole C; Pennisi R; Pallotta V; D'Alessandro A; Antoccia A; Zolla L; Ascenzi P; di Masi A
PLoS One; 2014; 9(12):e114651. PubMed ID: 25485873
[TBL] [Abstract][Full Text] [Related]
7. Impact of heterozygous c.657-661del, p.I171V and p.R215W mutations in NBN on nibrin functions.
Dzikiewicz-Krawczyk A; Mosor M; Januszkiewicz D; Nowak J
Mutagenesis; 2012 May; 27(3):337-43. PubMed ID: 22131123
[TBL] [Abstract][Full Text] [Related]
8. Nijmegen breakage syndrome (NBS) with neurological abnormalities and without chromosomal instability.
Seemanová E; Sperling K; Neitzel H; Varon R; Hadac J; Butova O; Schröck E; Seeman P; Digweed M
J Med Genet; 2006 Mar; 43(3):218-24. PubMed ID: 16033915
[TBL] [Abstract][Full Text] [Related]
9. Heterozygous germ-line mutations in the NBN gene predispose to medulloblastoma in pediatric patients.
Ciara E; Piekutowska-Abramczuk D; Popowska E; Grajkowska W; Barszcz S; Perek D; Dembowska-Bagińska B; Perek-Polnik M; Kowalewska E; Czajńska A; Syczewska M; Czornak K; Krajewska-Walasek M; Roszkowski M; Chrzanowska KH
Acta Neuropathol; 2010 Mar; 119(3):325-34. PubMed ID: 19908051
[TBL] [Abstract][Full Text] [Related]
10. Unique morphological spectrum of lymphomas in Nijmegen breakage syndrome (NBS) patients with high frequency of consecutive lymphoma formation.
Gładkowska-Dura M; Dzierzanowska-Fangrat K; Dura WT; van Krieken JH; Chrzanowska KH; van Dongen JJ; Langerak AW
J Pathol; 2008 Nov; 216(3):337-44. PubMed ID: 18788073
[TBL] [Abstract][Full Text] [Related]
11. Nijmegen breakage syndrome (NBS).
Chrzanowska KH; Gregorek H; Dembowska-Bagińska B; Kalina MA; Digweed M
Orphanet J Rare Dis; 2012 Feb; 7():13. PubMed ID: 22373003
[TBL] [Abstract][Full Text] [Related]
12. Secondary acute monocytic leukemia positive for 11q23 rearrangement in Nijmegen breakage syndrome.
Pastorczak A; Szczepanski T; Trelinska J; Finalet Ferreiro J; Wlodarska I; Mycko K; Polucha A; Sedek L; Meyer C; Marschalek R; Młynarski W
Pediatr Blood Cancer; 2014 Aug; 61(8):1469-71. PubMed ID: 24619942
[TBL] [Abstract][Full Text] [Related]
13. Clinical variability and expression of the NBN c.657del5 allele in Nijmegen Breakage Syndrome.
Lins S; Kim R; Krüger L; Chrzanowska KH; Seemanova E; Digweed M
Gene; 2009 Nov; 447(1):12-7. PubMed ID: 19635536
[TBL] [Abstract][Full Text] [Related]
14. Geographical Distribution, Incidence, Malignancies, and Outcome of 136 Eastern Slavic Patients With Nijmegen Breakage Syndrome and
Sharapova SO; Pashchenko OE; Bondarenko AV; Vakhlyarskaya SS; Prokofjeva T; Fedorova AS; Savchak I; Mareika Y; Valiev TT; Popa A; Tuzankina IA; Vlasova EV; Sakovich IS; Polyakova EA; Rumiantseva NV; Naumchik IV; Kulyova SA; Aleshkevich SN; Golovataya EI; Minakovskaya NV; Belevtsev MV; Latysheva EA; Latysheva TV; Beznoshchenko AG; Akopyan H; Makukh H; Kozlova O; Varabyou DS; Ballow M; Ong MS; Walter JE; Kondratenko IV; Kostyuchenko LV; Aleinikova OV
Front Immunol; 2020; 11():602482. PubMed ID: 33488600
[TBL] [Abstract][Full Text] [Related]
15. Telomere attrition and dysfunction: a potential trigger of the progeroid phenotype in nijmegen breakage syndrome.
Habib R; Kim R; Neitzel H; Demuth I; Chrzanowska K; Seemanova E; Faber R; Digweed M; Voss R; Jäger K; Sperling K; Walter M
Aging (Albany NY); 2020 Jun; 12(12):12342-12375. PubMed ID: 32564008
[TBL] [Abstract][Full Text] [Related]
16. Regional distribution of heterozygous 657del5 mutation carriers of the NBS1 gene in Wielkopolska province (Poland).
Ziółkowska I; Mosor M; Nowak J
J Appl Genet; 2006; 47(3):269-72. PubMed ID: 16877808
[TBL] [Abstract][Full Text] [Related]
17. [Nijmegen breakage syndrome in Slovakia].
Seemanová E; Pohanka V; Seeman P; Misovicová N; Behunová J; Kvasnicová M; Dlholucký S; Valachová A; Cisarik F; Veghová E; Varon R; Sperling K
Cas Lek Cesk; 2004; 143(8):538-41; discussion 542. PubMed ID: 15446459
[TBL] [Abstract][Full Text] [Related]
18. High prevalence of the NBN gene mutation c.657-661del5 in Southeast Germany.
Maurer MH; Hoffmann K; Sperling K; Varon R
J Appl Genet; 2010; 51(2):211-4. PubMed ID: 20453309
[TBL] [Abstract][Full Text] [Related]
19. NBN 657del5 heterozygous mutations and colorectal cancer risk in the Czech Republic.
Pardini B; Naccarati A; Polakova V; Smerhovsky Z; Hlavata I; Soucek P; Novotny J; Vodickova L; Tomanova V; Landi S; Vodicka P
Mutat Res; 2009 Jun; 666(1-2):64-7. PubMed ID: 19393249
[TBL] [Abstract][Full Text] [Related]
20. Hsp90α regulates ATM and NBN functions in sensing and repair of DNA double-strand breaks.
Pennisi R; Antoccia A; Leone S; Ascenzi P; di Masi A
FEBS J; 2017 Aug; 284(15):2378-2395. PubMed ID: 28631426
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]