182 related articles for article (PubMed ID: 32537088)
21. Clinical course and therapeutic implications for lymphoid malignancies in Nijmegen breakage syndrome.
Pastorczak A; Szczepanski T; Mlynarski W;
Eur J Med Genet; 2016 Mar; 59(3):126-32. PubMed ID: 26826318
[TBL] [Abstract][Full Text] [Related]
22. 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]
23. A rare case of primary gastric Hodgkin lymphoma in an adolescent with Nijmegen breakage syndrome.
Batiuk E; Bassett M; Hakar M; Lin HC; Hunter AK
BMC Pediatr; 2023 Apr; 23(1):189. PubMed ID: 37085783
[TBL] [Abstract][Full Text] [Related]
24. 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]
25. The role of nibrin in doxorubicin-induced apoptosis and cell senescence in Nijmegen Breakage Syndrome patients lymphocytes.
Alster O; Bielak-Zmijewska A; Mosieniak G; Moreno-Villanueva M; Dudka-Ruszkowska W; Wojtala A; Kusio-Kobiałka M; Korwek Z; Burkle A; Piwocka K; Siwicki JK; Sikora E
PLoS One; 2014; 9(8):e104964. PubMed ID: 25119968
[TBL] [Abstract][Full Text] [Related]
26. 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]
27. A case of premature ovarian insufficiency in Nijmegen breakage syndrome patient and review of literature. From gene mutation to clinical management.
Szeliga A; Zysnarska A; Szklarska Z; Truszkowska E; Podfigurna A; Czyzyk A; Genazzani AR; Chrzanowska K; Meczekalski B
Gynecol Endocrinol; 2019 Nov; 35(11):999-1002. PubMed ID: 31187634
[No Abstract] [Full Text] [Related]
28. DNA damage in Nijmegen Breakage Syndrome cells leads to PARP hyperactivation and increased oxidative stress.
Krenzlin H; Demuth I; Salewsky B; Wessendorf P; Weidele K; Bürkle A; Digweed M
PLoS Genet; 2012; 8(3):e1002557. PubMed ID: 22396666
[TBL] [Abstract][Full Text] [Related]
29. Nijmegen breakage syndrome. The International Nijmegen Breakage Syndrome Study Group.
The I
Arch Dis Child; 2000 May; 82(5):400-6. PubMed ID: 10799436
[TBL] [Abstract][Full Text] [Related]
30. Chromosomal Instability and Molecular Defects in Induced Pluripotent Stem Cells from Nijmegen Breakage Syndrome Patients.
Halevy T; Akov S; Bohndorf M; Mlody B; Adjaye J; Benvenisty N; Goldberg M
Cell Rep; 2016 Aug; 16(9):2499-511. PubMed ID: 27545893
[TBL] [Abstract][Full Text] [Related]
31. The R215W mutation in NBS1 impairs gamma-H2AX binding and affects DNA repair: molecular bases for the severe phenotype of 657del5/R215W Nijmegen breakage syndrome patients.
di Masi A; Viganotti M; Polticelli F; Ascenzi P; Tanzarella C; Antoccia A
Biochem Biophys Res Commun; 2008 May; 369(3):835-40. PubMed ID: 18328813
[TBL] [Abstract][Full Text] [Related]
32. Reduced-intensity conditioning umbilical cord blood transplantation in Nijmegen breakage syndrome.
Woźniak M; Krzywoń M; Hołda MK; Goździk J
Pediatr Transplant; 2015 Mar; 19(2):E51-5. PubMed ID: 25523867
[TBL] [Abstract][Full Text] [Related]
33. Impaired p53-Mediated DNA Damage Response Contributes to Microcephaly in Nijmegen Breakage Syndrome Patient-Derived Cerebral Organoids.
Martins S; Erichsen L; Datsi A; Wruck W; Goering W; Chatzantonaki E; de Amorim VCM; Rossi A; Chrzanowska KH; Adjaye J
Cells; 2022 Feb; 11(5):. PubMed ID: 35269426
[TBL] [Abstract][Full Text] [Related]
34. Genetic heterogeneity for a Nijmegen breakage-like syndrome.
Maraschio P; Spadoni E; Tanzarella C; Antoccia A; Di Masi A; Maghnie M; Varon R; Demuth I; Tiepolo L; Danesino C
Clin Genet; 2003 Apr; 63(4):283-90. PubMed ID: 12702161
[TBL] [Abstract][Full Text] [Related]
35. Rhabdomyosarcoma in Nijmegen breakage syndrome: strong association with perianal primary site.
Meyer S; Kingston H; Taylor AM; Byrd PJ; Last JI; Brennan BM; Trueman S; Kelsey A; Taylor GM; Eden OB
Cancer Genet Cytogenet; 2004 Oct; 154(2):169-74. PubMed ID: 15474156
[TBL] [Abstract][Full Text] [Related]
36. Mutations in the Nijmegen breakage syndrome gene in medulloblastomas.
Huang J; Grotzer MA; Watanabe T; Hewer E; Pietsch T; Rutkowski S; Ohgaki H
Clin Cancer Res; 2008 Jul; 14(13):4053-8. PubMed ID: 18593981
[TBL] [Abstract][Full Text] [Related]
37. The defect in humoral immunity in patients with Nijmegen breakage syndrome is explained by defects in peripheral B lymphocyte maturation.
Piątosa B; van der Burg M; Siewiera K; Pac M; van Dongen JJ; Langerak AW; Chrzanowska KH; Bernatowska E
Cytometry A; 2012 Oct; 81(10):835-42. PubMed ID: 22851427
[TBL] [Abstract][Full Text] [Related]
38. 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; Stöckl L; Varon R; Herceg Z; Sperling K; Wang ZQ; Digweed M
Hum Mol Genet; 2004 Oct; 13(20):2385-97. PubMed ID: 15333589
[TBL] [Abstract][Full Text] [Related]
39. Nijmegen breakage syndrome complicated with primary cutaneous tuberculosis.
Erdös M; Tóth B; Veres I; Kiss M; Remenyik E; Maródi L
Pediatr Infect Dis J; 2011 Apr; 30(4):359-60. PubMed ID: 20924312
[TBL] [Abstract][Full Text] [Related]
40. Human RAD50 deficiency: Confirmation of a distinctive phenotype.
Ragamin A; Yigit G; Bousset K; Beleggia F; Verheijen FW; de Wit MY; Strom TM; Dörk T; Wollnik B; Mancini GMS
Am J Med Genet A; 2020 Jun; 182(6):1378-1386. PubMed ID: 32212377
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]