Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 20

1.

Limiting replication stress during somatic cell reprogramming reduces genomic instability in induced pluripotent stem cells.

Ruiz S, Lopez-Contreras AJ, Gabut M, Marion RM, Gutierrez-Martinez P, Bua S, Ramirez O, Olalde I, Rodrigo-Perez S, Li H, Marques-Bonet T, Serrano M, Blasco MA, Batada NN, Fernandez-Capetillo O.

Nat Commun. 2015 Aug 21;6:8036. doi: 10.1038/ncomms9036.

2.

Aberrant DNA methylation reprogramming during induced pluripotent stem cell generation is dependent on the choice of reprogramming factors.

Planello AC, Ji J, Sharma V, Singhania R, Mbabaali F, Müller F, Alfaro JA, Bock C, De Carvalho DD, Batada NN.

Cell Regen (Lond). 2014 Feb 7;3(1):4. doi: 10.1186/2045-9769-3-4. eCollection 2014.

3.

SET8 methyltransferase activity during the DNA double-strand break response is required for recruitment of 53BP1.

Dulev S, Tkach J, Lin S, Batada NN.

EMBO Rep. 2014 Nov;15(11):1163-74. doi: 10.15252/embr.201439434. Epub 2014 Sep 24.

4.

Antioxidant supplementation reduces genomic aberrations in human induced pluripotent stem cells.

Ji J, Sharma V, Qi S, Guarch ME, Zhao P, Luo Z, Fan W, Wang Y, Mbabaali F, Neculai D, Esteban MA, McPherson JD, Batada NN.

Stem Cell Reports. 2014 Jan 2;2(1):44-51. doi: 10.1016/j.stemcr.2013.11.004. eCollection 2014 Jan 14.

5.

Frequent mutations in TP53 and CDKN2A found by next-generation sequencing of head and neck cancer cell lines.

Nichols AC, Yoo J, Palma DA, Fung K, Franklin JH, Koropatnick J, Mymryk JS, Batada NN, Barrett JW.

Arch Otolaryngol Head Neck Surg. 2012 Aug;138(8):732-9. doi: 10.1001/archoto.2012.1558.

PMID:
22911296
6.

Elevated coding mutation rate during the reprogramming of human somatic cells into induced pluripotent stem cells.

Ji J, Ng SH, Sharma V, Neculai D, Hussein S, Sam M, Trinh Q, Church GM, McPherson JD, Nagy A, Batada NN.

Stem Cells. 2012 Mar;30(3):435-40. doi: 10.1002/stem.1011.

7.

Copy number variation and selection during reprogramming to pluripotency.

Hussein SM, Batada NN, Vuoristo S, Ching RW, Autio R, Närvä E, Ng S, Sourour M, Hämäläinen R, Olsson C, Lundin K, Mikkola M, Trokovic R, Peitz M, Brüstle O, Bazett-Jones DP, Alitalo K, Lahesmaa R, Nagy A, Otonkoski T.

Nature. 2011 Mar 3;471(7336):58-62. doi: 10.1038/nature09871.

8.

Chromatin- and transcription-related factors repress transcription from within coding regions throughout the Saccharomyces cerevisiae genome.

Cheung V, Chua G, Batada NN, Landry CR, Michnick SW, Hughes TR, Winston F.

PLoS Biol. 2008 Nov 11;6(11):e277. doi: 10.1371/journal.pbio.0060277.

9.

The impact of the nucleosome code on protein-coding sequence evolution in yeast.

Warnecke T, Batada NN, Hurst LD.

PLoS Genet. 2008 Nov;4(11):e1000250. doi: 10.1371/journal.pgen.1000250. Epub 2008 Nov 7.

10.

Chromatin remodelling is a major source of coexpression of linked genes in yeast.

Batada NN, Urrutia AO, Hurst LD.

Trends Genet. 2007 Oct;23(10):480-4. Epub 2007 Sep 5.

PMID:
17822800
11.
12.

Still stratus not altocumulus: further evidence against the date/party hub distinction.

Batada NN, Reguly T, Breitkreutz A, Boucher L, Breitkreutz BJ, Hurst LD, Tyers M.

PLoS Biol. 2007 Jun;5(6):e154. No abstract available.

13.

Stratus not altocumulus: a new view of the yeast protein interaction network.

Batada NN, Reguly T, Breitkreutz A, Boucher L, Breitkreutz BJ, Hurst LD, Tyers M.

PLoS Biol. 2006 Oct;4(10):e317.

14.

Evolutionary and physiological importance of hub proteins.

Batada NN, Hurst LD, Tyers M.

PLoS Comput Biol. 2006 Jul 14;2(7):e88. Epub 2006 Jun 5.

15.

Comprehensive curation and analysis of global interaction networks in Saccharomyces cerevisiae.

Reguly T, Breitkreutz A, Boucher L, Breitkreutz BJ, Hon GC, Myers CL, Parsons A, Friesen H, Oughtred R, Tong A, Stark C, Ho Y, Botstein D, Andrews B, Boone C, Troyanskya OG, Ideker T, Dolinski K, Batada NN, Tyers M.

J Biol. 2006;5(4):11. Epub 2006 Jun 8.

16.

Spatial regulation and the rate of signal transduction activation.

Batada NN, Shepp LA, Siegmund DO, Levitt M.

PLoS Comput Biol. 2006 May;2(5):e44. Epub 2006 May 12.

17.

Spines and neurite branches function as geometric attractors that enhance protein kinase C action.

Craske ML, Fivaz M, Batada NN, Meyer T.

J Cell Biol. 2005 Sep 26;170(7):1147-58.

18.

Diffusion of nucleoside triphosphates and role of the entry site to the RNA polymerase II active center.

Batada NN, Westover KD, Bushnell DA, Levitt M, Kornberg RD.

Proc Natl Acad Sci U S A. 2004 Dec 14;101(50):17361-4. Epub 2004 Dec 1.

19.

Stochastic model of protein-protein interaction: why signaling proteins need to be colocalized.

Batada NN, Shepp LA, Siegmund DO.

Proc Natl Acad Sci U S A. 2004 Apr 27;101(17):6445-9. Epub 2004 Apr 19.

20.

CNplot: visualizing pre-clustered networks.

Batada NN.

Bioinformatics. 2004 Jun 12;20(9):1455-6. Epub 2004 Feb 10.

PMID:
14871859

Supplemental Content

Loading ...
Support Center