Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 1 to 20 of 22

1.

Characterization of two novel FANCG mutations in Indian Fanconi anemia patients.

Solanki A, Kumar Selvaa C, Sheth F, Radhakrishnan N, Kalra M, Vundinti BR.

Leuk Res. 2017 Feb;53:50-56. doi: 10.1016/j.leukres.2016.11.013. Epub 2016 Nov 29.

PMID:
28024295
2.

Cell Killing Mechanisms and Impact on Gene Expression by Gemcitabine and 212Pb-Trastuzumab Treatment in a Disseminated i.p. Tumor Model.

Yong KJ, Milenic DE, Baidoo KE, Brechbiel MW.

PLoS One. 2016 Jul 28;11(7):e0159904. doi: 10.1371/journal.pone.0159904. eCollection 2016.

3.

Profiling Fanconi Anemia Gene Mutations among Iranian Patients.

Esmail Nia G, Fadaee M, Royer R, Najmabadi H, Akbari MR.

Arch Iran Med. 2016 Apr;19(4):236-40. doi: 0161904/AIM.003.

4.

Low Dose Iron Treatments Induce a DNA Damage Response in Human Endothelial Cells within Minutes.

Mollet IG, Patel D, Govani FS, Giess A, Paschalaki K, Periyasamy M, Lidington EC, Mason JC, Jones MD, Game L, Ali S, Shovlin CL.

PLoS One. 2016 Feb 11;11(2):e0147990. doi: 10.1371/journal.pone.0147990. eCollection 2016.

5.

Diadenosine 5', 5'''-P(1),P(4)-tetraphosphate (Ap4A) is synthesized in response to DNA damage and inhibits the initiation of DNA replication.

Marriott AS, Copeland NA, Cunningham R, Wilkinson MC, McLennan AG, Jones NJ.

DNA Repair (Amst). 2015 Sep;33:90-100. doi: 10.1016/j.dnarep.2015.06.008. Epub 2015 Jun 29.

PMID:
26204256
6.

Clinical aspects of Fanconi anemia individuals with the same mutation of FANCF identified by next generation sequencing.

Nicchia E, Benedicenti F, De Rocco D, Greco C, Bottega R, Inzana F, Faleschini M, Bonin S, Cappelli E, Mogni M, Stanzial F, Svahn J, Dufour C, Savoia A.

Birth Defects Res A Clin Mol Teratol. 2015 Dec;103(12):1003-10. doi: 10.1002/bdra.23388. Epub 2015 Jun 2.

PMID:
26033879
7.

Functional Significance of Nuclear α Spectrin.

Lambert MW.

J Cell Biochem. 2015 Sep;116(9):1816-30. doi: 10.1002/jcb.25123.

PMID:
25757157
8.

Founder haplotype analysis of Fanconi anemia in the Korean population finds common ancestral haplotypes for a FANCG variant.

Park J, Kim M, Jang W, Chae H, Kim Y, Chung NG, Lee JW, Cho B, Jeong DC, Park IY, Park MS.

Ann Hum Genet. 2015 May;79(3):153-61. doi: 10.1111/ahg.12097. Epub 2015 Feb 20.

9.

Candidate gene analysis of BRCA1/2 mutation-negative high-risk Russian breast cancer patients.

Sokolenko AP, Preobrazhenskaya EV, Aleksakhina SN, Iyevleva AG, Mitiushkina NV, Zaitseva OA, Yatsuk OS, Tiurin VI, Strelkova TN, Togo AV, Imyanitov EN.

Cancer Lett. 2015 Apr 10;359(2):259-61. doi: 10.1016/j.canlet.2015.01.022. Epub 2015 Jan 22.

PMID:
25619955
10.

Hematological consequences of a FANCG founder mutation in Black South African patients with Fanconi anemia.

Feben C, Kromberg J, Wainwright R, Stones D, Poole J, Haw T, Krause A.

Blood Cells Mol Dis. 2015 Mar;54(3):270-4. doi: 10.1016/j.bcmd.2014.11.011. Epub 2014 Nov 27.

PMID:
25477267
11.

RNA-seq profiling of a radiation resistant and radiation sensitive prostate cancer cell line highlights opposing regulation of DNA repair and targets for radiosensitization.

Young A, Berry R, Holloway AF, Blackburn NB, Dickinson JL, Skala M, Phillips JL, Brettingham-Moore KH.

BMC Cancer. 2014 Nov 4;14:808. doi: 10.1186/1471-2407-14-808.

12.

K63-linked ubiquitination of FANCG is required for its association with the Rap80-BRCA1 complex to modulate homologous recombination repair of DNA interstand crosslinks.

Zhu B, Yan K, Li L, Lin M, Zhang S, He Q, Zheng D, Yang H, Shao G.

Oncogene. 2015 May 28;34(22):2867-78. doi: 10.1038/onc.2014.229. Epub 2014 Aug 18.

PMID:
25132264
13.

Modularized functions of the Fanconi anemia core complex.

Huang Y, Leung JW, Lowery M, Matsushita N, Wang Y, Shen X, Huong D, Takata M, Chen J, Li L.

Cell Rep. 2014 Jun 26;7(6):1849-57. doi: 10.1016/j.celrep.2014.04.029. Epub 2014 Jun 5. Erratum in: Cell Rep. 2016 Mar 22;14(11):2761-3.

14.

Assessing the function of homologous recombination DNA repair in malignant pleural effusion (MPE) samples.

Patterson MJ, Sutton RE, Forrest I, Sharrock R, Lane M, Kaufmann A, O'Donnell R, Edmondson RJ, Wilson BT, Curtin NJ.

Br J Cancer. 2014 Jul 8;111(1):94-100. doi: 10.1038/bjc.2014.261. Epub 2014 May 27.

15.

MicroRNA regulation of DNA repair gene expression in 4-aminobiphenyl-treated HepG2 cells.

Huan LC, Wu JC, Chiou BH, Chen CH, Ma N, Chang CY, Tsen YK, Chen SC.

Toxicology. 2014 Aug 1;322:69-77. doi: 10.1016/j.tox.2014.05.003. Epub 2014 May 23.

PMID:
24857880
16.

Differential radiosensitivity phenotypes of DNA-PKcs mutations affecting NHEJ and HRR systems following irradiation with gamma-rays or very low fluences of alpha particles.

Lin YF, Nagasawa H, Little JB, Kato TA, Shih HY, Xie XJ, Wilson PF Jr, Brogan JR, Kurimasa A, Chen DJ, Bedford JS, Chen BP.

PLoS One. 2014 Apr 8;9(4):e93579. doi: 10.1371/journal.pone.0093579. eCollection 2014.

17.

Molecular analysis of Fanconi anemia: the experience of the Bone Marrow Failure Study Group of the Italian Association of Pediatric Onco-Hematology.

De Rocco D, Bottega R, Cappelli E, Cavani S, Criscuolo M, Nicchia E, Corsolini F, Greco C, Borriello A, Svahn J, Pillon M, Mecucci C, Casazza G, Verzegnassi F, Cugno C, Locasciulli A, Farruggia P, Longoni D, Ramenghi U, Barberi W, Tucci F, Perrotta S, Grammatico P, Hanenberg H, Della Ragione F, Dufour C, Savoia A; Bone Marrow Failure Study Group of the Italian Association of Pediatric Onco-Hematology.

Haematologica. 2014 Jun;99(6):1022-31. doi: 10.3324/haematol.2014.104224. Epub 2014 Feb 28. Erratum in: Haematologica. 2014 Sep;99(9):1532.

18.

Fanconi anaemia in black South African patients heterozygous for the FANCG c.637-643delTACCGCC founder mutation.

Wainstein T, Kerr R, Mitchell CL, Madaree S, Essop FB, Vorster E, Wainwright R, Poole J, Krause A.

S Afr Med J. 2013 Oct 11;103(12 Suppl 1):970-3. doi: 10.7196/samj.7215.

PMID:
24300640
19.

Lymphocytes of patients with Alzheimer's disease display different DNA damage repair kinetics and expression profiles of DNA repair and stress response genes.

Leandro GS, Lobo RR, Oliveira DV, Moriguti JC, Sakamoto-Hojo ET.

Int J Mol Sci. 2013 Jun 10;14(6):12380-400. doi: 10.3390/ijms140612380.

20.

Testing the utility of an integrated analysis of copy number and transcriptomics datasets for inferring gene regulatory relationships.

Goh XY, Newton R, Wernisch L, Fitzgerald R.

PLoS One. 2013 May 30;8(5):e63780. doi: 10.1371/journal.pone.0063780. Print 2013.

Supplemental Content

Loading ...
Support Center