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Results: 1 to 20 of 35

1.

Clonal distribution of BCR-ABL1 mutations and splice isoforms by single-molecule long-read RNA sequencing.

Cavelier L, Ameur A, Häggqvist S, Höijer I, Cahill N, Olsson-Strömberg U, Hermanson M.

BMC Cancer. 2015 Feb 12;15:45. doi: 10.1186/s12885-015-1046-y.

2.

Methods of Reprogramming to iPSC Associated with Chromosomal Integrity and Delineation of a Chromosome 5q Candidate Region for Growth Advantage.

Sobol M, Raykova D, Cavelier L, Khalfallah A, Schuster J, Dahl N.

Stem Cells Dev. 2015 May 18. [Epub ahead of print]

PMID:
25867454
3.

DNA methylation-based subtype prediction for pediatric acute lymphoblastic leukemia.

Nordlund J, Bäcklin CL, Zachariadis V, Cavelier L, Dahlberg J, Öfverholm I, Barbany G, Nordgren A, Övernäs E, Abrahamsson J, Flaegstad T, Heyman MM, Jónsson ÓG, Kanerva J, Larsson R, Palle J, Schmiegelow K, Gustafsson MG, Lönnerholm G, Forestier E, Syvänen AC.

Clin Epigenetics. 2015 Feb 17;7(1):11. doi: 10.1186/s13148-014-0039-z. eCollection 2015.

4.

Donor or recipient origin of posttransplant lymphoproliferative disorders following solid organ transplantation.

Kinch A, Cavelier L, Bengtsson M, Baecklund E, Enblad G, Backlin C, Thunberg U, Sundström C, Pauksens K.

Am J Transplant. 2014 Dec;14(12):2838-45. doi: 10.1111/ajt.12990. Epub 2014 Oct 10.

PMID:
25307322
5.

Splicing in the human brain.

Zaghlool A, Ameur A, Cavelier L, Feuk L.

Int Rev Neurobiol. 2014;116:95-125. doi: 10.1016/B978-0-12-801105-8.00005-9. Review.

PMID:
25172473
6.

Clinical and genetic features of pediatric acute lymphoblastic leukemia in Down syndrome in the Nordic countries.

Lundin C, Forestier E, Klarskov Andersen M, Autio K, Barbany G, Cavelier L, Golovleva I, Heim S, Heinonen K, Hovland R, Johannsson JH, Kjeldsen E, Nordgren A, Palmqvist L, Johansson B; Nordic Society of Pediatric Hematology Oncology (NOPHO); Swedish Cytogenetic Leukemia Study Group (SCLSG); NOPHO Leukemia Cytogenetic Study Group (NLCSG).

J Hematol Oncol. 2014 Apr 11;7:32. doi: 10.1186/1756-8722-7-32.

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.

BMC Biotechnol. 2013 Nov 13;13:99. doi: 10.1186/1472-6750-13-99.

8.

High modal number and triple trisomies are highly correlated favorable factors in childhood B-cell precursor high hyperdiploid acute lymphoblastic leukemia treated according to the NOPHO ALL 1992/2000 protocols.

Paulsson K, Forestier E, Andersen MK, Autio K, Barbany G, Borgström G, Cavelier L, Golovleva I, Heim S, Heinonen K, Hovland R, Johannsson JH, Kjeldsen E, Nordgren A, Palmqvist L, Johansson B; Nordic Society of Pediatric Hematology and Oncology (NOPHO); Swedish Cytogenetic Leukemia Study Group (SCLSG); NOPHO Leukemia Cytogenetic Study Group (NLCSG).

Haematologica. 2013 Sep;98(9):1424-32. doi: 10.3324/haematol.2013.085852. Epub 2013 May 3.

9.

The impact of robotic surgery in urology.

Giedelman CA, Abdul-Muhsin H, Schatloff O, Palmer K, Lee L, Sanchez-Salas R, Cathelineau X, Dávila H, Cavelier L, Rueda M, Patel V.

Actas Urol Esp. 2013 Nov-Dec;37(10):652-7. doi: 10.1016/j.acuro.2012.11.015. Epub 2013 Apr 22. Review.

PMID:
23618511
10.

Genome-wide sequencing for the identification of rearrangements associated with Tourette syndrome and obsessive-compulsive disorder.

Hooper SD, Johansson AC, Tellgren-Roth C, Stattin EL, Dahl N, Cavelier L, Feuk L.

BMC Med Genet. 2012 Dec 19;13:123. doi: 10.1186/1471-2350-13-123.

11.

Sequence based analysis of U-2973, a cell line established from a double-hit B-cell lymphoma with concurrent MYC and BCL2 rearrangements.

Hooper SD, Jiao X, Sundström E, Rehman FL, Tellgren-Roth C, Sjöblom T, Cavelier L.

BMC Res Notes. 2012 Nov 22;5:648. doi: 10.1186/1756-0500-5-648.

12.

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.

Nat Struct Mol Biol. 2011 Nov 6;18(12):1435-40. doi: 10.1038/nsmb.2143.

PMID:
22056773
13.

Paediatric B-cell precursor acute lymphoblastic leukaemia with t(1;19)(q23;p13): clinical and cytogenetic characteristics of 47 cases from the Nordic countries treated according to NOPHO protocols.

Andersen MK, Autio K, Barbany G, Borgström G, Cavelier L, Golovleva I, Heim S, Heinonen K, Hovland R, Johannsson JH, Johansson B, Kjeldsen E, Nordgren A, Palmqvist L, Forestier E.

Br J Haematol. 2011 Oct;155(2):235-43. doi: 10.1111/j.1365-2141.2011.08824.x. Epub 2011 Sep 9.

PMID:
21902680
14.

The frequency and prognostic impact of dic(9;20)(p13.2;q11.2) in childhood B-cell precursor acute lymphoblastic leukemia: results from the NOPHO ALL-2000 trial.

Zachariadis V, Gauffin F, Kuchinskaya E, Heyman M, Schoumans J, Blennow E, Gustafsson B, Barbany G, Golovleva I, Ehrencrona H, Cavelier L, Palmqvist L, Lönnerholm G, Nordenskjöld M, Johansson B, Forestier E, Nordgren A; Nordic Society of Pediatric Hematology, Oncology (NOPHO); Swedish Cytogenetic Leukemia Study Group (SCLSG).

Leukemia. 2011 Apr;25(4):622-8. doi: 10.1038/leu.2010.318. Epub 2011 Jan 18.

PMID:
21242996
15.

Identification of novel exons and transcribed regions by chimpanzee transcriptome sequencing.

Wetterbom A, Ameur A, Feuk L, Gyllensten U, Cavelier L.

Genome Biol. 2010;11(7):R78. doi: 10.1186/gb-2010-11-7-r78. Epub 2010 Jul 23.

16.

Genome-wide analysis of chimpanzee genes with premature termination codons.

Wetterbom A, Gyllensten U, Cavelier L, Bergström TF.

BMC Genomics. 2009 Jan 29;10:56. doi: 10.1186/1471-2164-10-56.

17.

Comparative genomic analysis of human and chimpanzee indicates a key role for indels in primate evolution.

Wetterbom A, Sevov M, Cavelier L, Bergström TF.

J Mol Evol. 2006 Nov;63(5):682-90. Epub 2006 Oct 29.

PMID:
17075697
18.

Resveratrol regulates the expression of LXR-alpha in human macrophages.

Sevov M, Elfineh L, Cavelier LB.

Biochem Biophys Res Commun. 2006 Sep 29;348(3):1047-54. Epub 2006 Aug 1.

PMID:
16901463
19.
20.

MtDNA mutations in maternally inherited diabetes: presence of the 3397 ND1 mutation previously associated with Alzheimer's and Parkinson's disease.

Cavelier L, Erikson I, Tammi M, Jalonen P, Lindholm E, Jazin E, Smith P, Luthman H, Gyllensten U.

Hereditas. 2001;135(1):65-70.

PMID:
12035616
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