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Items: 1 to 20 of 126


Absence of GP130 cytokine receptor signaling causes extended Stüve-Wiedemann syndrome.

Chen YH, Grigelioniene G, Newton PT, Gullander J, Elfving M, Hammarsjö A, Batkovskyte D, Alsaif HS, Kurdi WIY, Abdulwahab F, Shanmugasundaram V, Devey L, Bacrot S, Brodszki J, Huber C, Hamel B, Gisselsson D, Papadogiannakis N, Jedrycha K, Gürtl-Lackner B, Chagin AS, Nishimura G, Aschenbrenner D, Alkuraya FS, Laurence A, Cormier-Daire V, Uhlig HH.

J Exp Med. 2020 Mar 2;217(3). pii: e20191306. doi: 10.1084/jem.20191306.


Multidimensional intratumour heterogeneity in neuroblastoma.

von Stedingk K, Gisselsson D, Bexell D.

Oncotarget. 2019 Jan 1;10(1):3-5. doi: 10.18632/oncotarget.26524. eCollection 2019 Jan 1. No abstract available.


Changes in the Prevalence of Embryologic Remnants in Umbilical Cord With Gestational Age.

Grottling E, Gisselsson D.

Pediatr Dev Pathol. 2019 Jul-Aug;22(4):288-291. doi: 10.1177/1093526618813663. Epub 2018 Dec 12.


Clonal evolution through genetic bottlenecks and telomere attrition: Potential threats to in vitro data reproducibility.

Gisselsson D, Lichtenzstejn D, Kachko P, Karlsson J, Manor E, Mai S.

Genes Chromosomes Cancer. 2019 Jul;58(7):452-461. doi: 10.1002/gcc.22685. Epub 2018 Nov 29. Review.


The Iroquois homeobox proteins IRX3 and IRX5 have distinct roles in Wilms tumour development and human nephrogenesis.

Holmquist Mengelbier L, Lindell-Munther S, Yasui H, Jansson C, Esfandyari J, Karlsson J, Lau K, Hui CC, Bexell D, Hopyan S, Gisselsson D.

J Pathol. 2019 Jan;247(1):86-98. doi: 10.1002/path.5171. Epub 2018 Nov 29.


Neuroblastoma with flat genomic profile: a question of representativity?

Valind A, Öra I, Mertens F, Gisselsson D.

BMJ Case Rep. 2018 Sep 8;2018. pii: bcr-2018-225568. doi: 10.1136/bcr-2018-225568.


Patient-Derived Xenograft Models Reveal Intratumor Heterogeneity and Temporal Stability in Neuroblastoma.

Braekeveldt N, von Stedingk K, Fransson S, Martinez-Monleon A, Lindgren D, Axelson H, Levander F, Willforss J, Hansson K, Øra I, Backman T, Börjesson A, Beckman S, Esfandyari J, Berbegall AP, Noguera R, Karlsson J, Koster J, Martinsson T, Gisselsson D, Påhlman S, Bexell D.

Cancer Res. 2018 Oct 15;78(20):5958-5969. doi: 10.1158/0008-5472.CAN-18-0527. Epub 2018 Aug 28.


Convergent evolution of 11p allelic loss in multifocal Wilms tumors arising in WT1 mutation carriers.

Valind A, Wessman S, Pal N, Karlsson J, Jonson T, Sandstedt B, Gisselsson D.

Pediatr Blood Cancer. 2018 Nov;65(11):e27301. doi: 10.1002/pbc.27301. Epub 2018 Jul 3.


Four evolutionary trajectories underlie genetic intratumoral variation in childhood cancer.

Karlsson J, Valind A, Holmquist Mengelbier L, Bredin S, Cornmark L, Jansson C, Wali A, Staaf J, Viklund B, Øra I, Börjesson A, Backman T, Braekeveldt N, Sandstedt B, Pal N, Isaksson A, Lackner BG, Jonson T, Bexell D, Gisselsson D.

Nat Genet. 2018 Jul;50(7):944-950. doi: 10.1038/s41588-018-0131-y. Epub 2018 Jun 4.


Neuroblastoma patient-derived xenograft cells cultured in stem-cell promoting medium retain tumorigenic and metastatic capacities but differentiate in serum.

Persson CU, von Stedingk K, Bexell D, Merselius M, Braekeveldt N, Gisselsson D, Arsenian-Henriksson M, Påhlman S, Wigerup C.

Sci Rep. 2017 Aug 31;7(1):10274. doi: 10.1038/s41598-017-09662-8.


Cancer - An Insurgency of Clones.

Gisselsson D, Egnell R.

Trends Cancer. 2017 Feb;3(2):73-75. doi: 10.1016/j.trecan.2016.11.010. Epub 2016 Dec 23. Review.


Mosaicism in health and disease - clones picking up speed.

Forsberg LA, Gisselsson D, Dumanski JP.

Nat Rev Genet. 2017 Feb;18(2):128-142. doi: 10.1038/nrg.2016.145. Epub 2016 Dec 12. Review.


Gain of 1q As a Prognostic Biomarker in Wilms Tumors (WTs) Treated With Preoperative Chemotherapy in the International Society of Paediatric Oncology (SIOP) WT 2001 Trial: A SIOP Renal Tumours Biology Consortium Study.

Chagtai T, Zill C, Dainese L, Wegert J, Savola S, Popov S, Mifsud W, Vujanić G, Sebire N, Le Bouc Y, Ambros PF, Kager L, O'Sullivan MJ, Blaise A, Bergeron C, Mengelbier LH, Gisselsson D, Kool M, Tytgat GA, van den Heuvel-Eibrink MM, Graf N, van Tinteren H, Coulomb A, Gessler M, Williams RD, Pritchard-Jones K.

J Clin Oncol. 2016 Sep 10;34(26):3195-203. doi: 10.1200/JCO.2015.66.0001. Epub 2016 Jul 18. Erratum in: J Clin Oncol. 2017 Jun 20;35(18):2100.


The fetal thymus has a unique genomic copy number profile resulting from physiological T cell receptor gene rearrangement.

Valind A, Haikal C, Klasson ME, Johansson MC, Gullander J, Soller M, Baldetorp B, Gisselsson D.

Sci Rep. 2016 Mar 24;6:23500. doi: 10.1038/srep23500.


Neuroblastoma patient-derived orthotopic xenografts reflect the microenvironmental hallmarks of aggressive patient tumours.

Braekeveldt N, Wigerup C, Tadeo I, Beckman S, Sandén C, Jönsson J, Erjefält JS, Berbegall AP, Börjesson A, Backman T, Øra I, Navarro S, Noguera R, Gisselsson D, Påhlman S, Bexell D.

Cancer Lett. 2016 Jun 1;375(2):384-389. doi: 10.1016/j.canlet.2016.02.046. Epub 2016 Mar 18.


Aberrant epigenetic regulation in clear cell sarcoma of the kidney featuring distinct DNA hypermethylation and EZH2 overexpression.

Karlsson J, Valind A, Jansson C, O'Sullivan MJ, Holmquist Mengelbier L, Gisselsson D.

Oncotarget. 2016 Mar 8;7(10):11127-36. doi: 10.18632/oncotarget.7152.


Comprehensive genetic analysis of a paediatric pleomorphic myxoid liposarcoma reveals near-haploidization and loss of the RB1 gene.

Hofvander J, Jo VY, Ghanei I, Gisselsson D, Mårtensson E, Mertens F.

Histopathology. 2016 Jul;69(1):141-147. doi: 10.1111/his.12913. Epub 2016 Feb 9.


BCOR internal tandem duplication and YWHAE-NUTM2B/E fusion are mutually exclusive events in clear cell sarcoma of the kidney.

Karlsson J, Valind A, Gisselsson D.

Genes Chromosomes Cancer. 2016 Feb;55(2):120-3. doi: 10.1002/gcc.22316. Epub 2015 Oct 23.


Genetic heterogeneity in rhabdomyosarcoma revealed by SNP array analysis.

Walther C, Mayrhofer M, Nilsson J, Hofvander J, Jonson T, Mandahl N, Øra I, Gisselsson D, Mertens F.

Genes Chromosomes Cancer. 2016 Jan;55(1):3-15. doi: 10.1002/gcc.22285. Epub 2015 Oct 20.


Gene fusion detection in formalin-fixed paraffin-embedded benign fibrous histiocytomas using fluorescence in situ hybridization and RNA sequencing.

Walther C, Hofvander J, Nilsson J, Magnusson L, Domanski HA, Gisselsson D, Tayebwa J, Doyle LA, Fletcher CD, Mertens F.

Lab Invest. 2015 Sep;95(9):1071-6. doi: 10.1038/labinvest.2015.83. Epub 2015 Jun 29.

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