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Items: 15

1.

Best Practices for Illumina Library Preparation.

Bronner IF, Quail MA.

Curr Protoc Hum Genet. 2019 Jun;102(1):e86. doi: 10.1002/cphg.86.

PMID:
31216112
2.

Combined Genome and Transcriptome (G&T) Sequencing of Single Cells.

Bronner IF, Lorenz S.

Methods Mol Biol. 2019;1979:319-362. doi: 10.1007/978-1-4939-9240-9_20.

PMID:
31028647
3.

Assembly of transgenic human P301S Tau is necessary for neurodegeneration in murine spinal cord.

Macdonald JA, Bronner IF, Drynan L, Fan J, Curry A, Fraser G, Lavenir I, Goedert M.

Acta Neuropathol Commun. 2019 Mar 18;7(1):44. doi: 10.1186/s40478-019-0695-5.

4.

PiggyBac Transposon-Based Insertional Mutagenesis in Mice.

Friedrich MJ, Bronner IF, Liu P, Bradley A, Rad R.

Methods Mol Biol. 2019;1907:171-183. doi: 10.1007/978-1-4939-8967-6_14.

PMID:
30543000
5.

Uncovering the essential genes of the human malaria parasite Plasmodium falciparum by saturation mutagenesis.

Zhang M, Wang C, Otto TD, Oberstaller J, Liao X, Adapa SR, Udenze K, Bronner IF, Casandra D, Mayho M, Brown J, Li S, Swanson J, Rayner JC, Jiang RHY, Adams JH.

Science. 2018 May 4;360(6388). pii: eaap7847. doi: 10.1126/science.aap7847.

6.

Genome-wide transposon screening and quantitative insertion site sequencing for cancer gene discovery in mice.

Friedrich MJ, Rad L, Bronner IF, Strong A, Wang W, Weber J, Mayho M, Ponstingl H, Engleitner T, Grove C, Pfaus A, Saur D, Cadiñanos J, Quail MA, Vassiliou GS, Liu P, Bradley A, Rad R.

Nat Protoc. 2017 Feb;12(2):289-309. doi: 10.1038/nprot.2016.164. Epub 2017 Jan 12.

PMID:
28079877
7.

Quantitative insertion-site sequencing (QIseq) for high throughput phenotyping of transposon mutants.

Bronner IF, Otto TD, Zhang M, Udenze K, Wang C, Quail MA, Jiang RH, Adams JH, Rayner JC.

Genome Res. 2016 Jul;26(7):980-9. doi: 10.1101/gr.200279.115. Epub 2016 May 10.

8.

A conditional piggyBac transposition system for genetic screening in mice identifies oncogenic networks in pancreatic cancer.

Rad R, Rad L, Wang W, Strong A, Ponstingl H, Bronner IF, Mayho M, Steiger K, Weber J, Hieber M, Veltkamp C, Eser S, Geumann U, Öllinger R, Zukowska M, Barenboim M, Maresch R, Cadiñanos J, Friedrich M, Varela I, Constantino-Casas F, Sarver A, Ten Hoeve J, Prosser H, Seidler B, Bauer J, Heikenwälder M, Metzakopian E, Krug A, Ehmer U, Schneider G, Knösel T, Rümmele P, Aust D, Grützmann R, Pilarsky C, Ning Z, Wessels L, Schmid RM, Quail MA, Vassiliou G, Esposito I, Liu P, Saur D, Bradley A.

Nat Genet. 2015 Jan;47(1):47-56. doi: 10.1038/ng.3164. Epub 2014 Dec 8.

PMID:
25485836
9.

Improved Protocols for Illumina Sequencing.

Bronner IF, Quail MA, Turner DJ, Swerdlow H.

Curr Protoc Hum Genet. 2014 Jan 21;80:18.2.1-42. doi: 10.1002/0471142905.hg1802s80.

PMID:
26270174
10.

Comprehensive mRNA expression profiling distinguishes tauopathies and identifies shared molecular pathways.

Bronner IF, Bochdanovits Z, Rizzu P, Kamphorst W, Ravid R, van Swieten JC, Heutink P.

PLoS One. 2009 Aug 28;4(8):e6826. doi: 10.1371/journal.pone.0006826.

11.

Distinct genetic forms of frontotemporal dementia.

Seelaar H, Kamphorst W, Rosso SM, Azmani A, Masdjedi R, de Koning I, Maat-Kievit JA, Anar B, Donker Kaat L, Breedveld GJ, Dooijes D, Rozemuller JM, Bronner IF, Rizzu P, van Swieten JC.

Neurology. 2008 Oct 14;71(16):1220-6. doi: 10.1212/01.wnl.0000319702.37497.72. Epub 2008 Aug 13.

PMID:
18703462
12.

Progranulin mutations in Dutch familial frontotemporal lobar degeneration.

Bronner IF, Rizzu P, Seelaar H, van Mil SE, Anar B, Azmani A, Donker Kaat L, Rosso S, Heutink P, van Swieten JC.

Eur J Hum Genet. 2007 Mar;15(3):369-74. Epub 2007 Jan 17.

13.

The DeltaK280 mutation in MAP tau favors exon 10 skipping in vivo.

van Swieten JC, Bronner IF, Azmani A, Severijnen LA, Kamphorst W, Ravid R, Rizzu P, Willemsen R, Heutink P.

J Neuropathol Exp Neurol. 2007 Jan;66(1):17-25.

PMID:
17204933
14.

Hereditary Pick's disease with the G272V tau mutation shows predominant three-repeat tau pathology.

Bronner IF, ter Meulen BC, Azmani A, Severijnen LA, Willemsen R, Kamphorst W, Ravid R, Heutink P, van Swieten JC.

Brain. 2005 Nov;128(Pt 11):2645-53. Epub 2005 Jul 13.

PMID:
16014652
15.

The DJ-1L166P mutant protein associated with early onset Parkinson's disease is unstable and forms higher-order protein complexes.

Macedo MG, Anar B, Bronner IF, Cannella M, Squitieri F, Bonifati V, Hoogeveen A, Heutink P, Rizzu P.

Hum Mol Genet. 2003 Nov 1;12(21):2807-16. Epub 2003 Sep 2.

PMID:
12952867

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