Feuk L - Search Results

1

A Role for the Chromatin-Remodeling Factor BAZ1A in Neurodevelopment.

Zaghlool A, Halvardson J, Zhao JJ, Etemadikhah M, Kalushkova A, Konska K, Jernberg-Wiklund H, Thuresson AC, Feuk L. Zaghlool A, et al. Among authors: feuk l. Hum Mutat. 2016 Sep;37(9):964-75. doi: 10.1002/humu.23034. Epub 2016 Jul 8. Hum Mutat. 2016. PMID: 27328812 Free PMC article.

2

Characterization of copy number-stable regions in the human genome.

Johansson AC, Feuk L. Johansson AC, et al. Among authors: feuk l. Hum Mutat. 2011 Aug;32(8):947-55. doi: 10.1002/humu.21524. Epub 2011 Jul 20. Hum Mutat. 2011. PMID: 21542059

3

Total RNA sequencing reveals nascent transcription and widespread co-transcriptional splicing in the human brain.

Ameur A, Zaghlool A, Halvardson J, Wetterbom A, Gyllensten U, Cavelier L, Feuk L. Ameur A, et al. Among authors: feuk l. Nat Struct Mol Biol. 2011 Nov 6;18(12):1435-40. doi: 10.1038/nsmb.2143. Nat Struct Mol Biol. 2011. PMID: 22056773

4

Exome RNA sequencing reveals rare and novel alternative transcripts.

Halvardson J, Zaghlool A, Feuk L. Halvardson J, et al. Among authors: feuk l. Nucleic Acids Res. 2013 Jan 7;41(1):e6. doi: 10.1093/nar/gks816. Epub 2012 Aug 31. Nucleic Acids Res. 2013. PMID: 22941640 Free PMC article.

5

RNA-binding protein QKI regulates Glial fibrillary acidic protein expression in human astrocytes.

Radomska KJ, Halvardson J, Reinius B, Lindholm Carlström E, Emilsson L, Feuk L, Jazin E. Radomska KJ, et al. Among authors: feuk l. Hum Mol Genet. 2013 Apr 1;22(7):1373-82. doi: 10.1093/hmg/dds553. Epub 2013 Jan 15. Hum Mol Genet. 2013. PMID: 23321059

6

Welander distal myopathy caused by an ancient founder mutation in TIA1 associated with perturbed splicing.

Klar J, Sobol M, Melberg A, Mäbert K, Ameur A, Johansson AC, Feuk L, Entesarian M, Orlén H, Casar-Borota O, Dahl N. Klar J, et al. Among authors: feuk l. Hum Mutat. 2013 Apr;34(4):572-7. doi: 10.1002/humu.22282. Hum Mutat. 2013. PMID: 23348830

7

Efficient cellular fractionation improves RNA sequencing analysis of mature and nascent transcripts from human tissues.

Zaghlool A, Ameur A, Nyberg L, Halvardson J, Grabherr M, Cavelier L, Feuk L. Zaghlool A, et al. Among authors: feuk l. BMC Biotechnol. 2013 Nov 13;13:99. doi: 10.1186/1472-6750-13-99. BMC Biotechnol. 2013. PMID: 24225116 Free PMC article.

8

Deleterious mutation in FDX1L gene is associated with a novel mitochondrial muscle myopathy.

Spiegel R, Saada A, Halvardson J, Soiferman D, Shaag A, Edvardson S, Horovitz Y, Khayat M, Shalev SA, Feuk L, Elpeleg O. Spiegel R, et al. Among authors: feuk l. Eur J Hum Genet. 2014 Jul;22(7):902-6. doi: 10.1038/ejhg.2013.269. Epub 2013 Nov 27. Eur J Hum Genet. 2014. PMID: 24281368 Free PMC article. Clinical Trial.

9

Splicing in the human brain.

Zaghlool A, Ameur A, Cavelier L, Feuk L. Zaghlool A, et al. Among authors: feuk l. Int Rev Neurobiol. 2014;116:95-125. doi: 10.1016/B978-0-12-801105-8.00005-9. Int Rev Neurobiol. 2014. PMID: 25172473 Review.

10

Transcriptome Profiling Reveals Degree of Variability in Induced Pluripotent Stem Cell Lines: Impact for Human Disease Modeling.

Schuster J, Halvardson J, Pilar Lorenzo L, Ameur A, Sobol M, Raykova D, Annerén G, Feuk L, Dahl N. Schuster J, et al. Among authors: feuk l. Cell Reprogram. 2015 Oct;17(5):327-37. doi: 10.1089/cell.2015.0009. Epub 2015 Sep 8. Cell Reprogram. 2015. PMID: 26348590

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