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Johan Staaf

Showing results (61-70 of 175) with videos related to

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Melanoma Research|September 18, 2010
Multiple metastases from cutaneous malignant melanoma patients may display heterogeneous genomic and epigenomic patternsKatja Harbst, Johan Staaf, Anna Måsbäck, et al.
Peerj|March 11, 2015
Loss of CITED1, an MITF regulator, drives a phenotype switch in vitro and can predict clinical outcome in primary melanoma tumoursJillian Howlin, Helena Cirenajwis, Barbara Lettiero, et al.
Cancers|July 26, 2020
Methylation Patterns and Chromatin Accessibility in Neuroendocrine Lung CancerElsa Arbajian, Mattias Aine, Anna Karlsson, et al.
Journal of Experimental & Clinical Cancer Research : CR|August 18, 2021
Complement inhibitor CSMD1 modulates epidermal growth factor receptor oncogenic signaling and sensitizes breast cancer cells to chemotherapyChrysostomi Gialeli, Emre Can Tuysuz, Johan Staaf, et al.
Journal of Experimental & Clinical Cancer Research : CR|May 29, 2023
Correction: Complement inhibitor CSMD1 modulates epidermal growth factor receptor oncogenic signaling and sensitizes breast cancer cells to chemotherapyChrysostomi Gialeli, Emre Can Tuysuz, Johan Staaf, et al.
International Journal of Cancer|October 2, 2012
Landscape of somatic allelic imbalances and copy number alterations in human lung carcinomaJohan Staaf, Sofi Isaksson, Anna Karlsson, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|October 4, 2014
Genome-wide DNA methylation analysis of lung carcinoma reveals one neuroendocrine and four adenocarcinoma epitypes associated with patient outcomeAnna Karlsson, Mats Jönsson, Martin Lauss, et al.
British Journal of Haematology|February 16, 2008
Array-CGH reveals hidden gene dose changes in children with acute lymphoblastic leukaemia and a normal or failed karyotype by G-bandingEkaterina Kuchinskaya, Mats Heyman, Ann Nordgren, et al.
Genome Biology|September 18, 2008
Segmentation-based detection of allelic imbalance and loss-of-heterozygosity in cancer cells using whole genome SNP arraysJohan Staaf, David Lindgren, Johan Vallon-Christersson, et al.
Cancer Informatics|May 21, 2009
Tumor genome wide DNA alterations assessed by array CGH in patients with poor and excellent survival following operation for colorectal cancerKristina K Lagerstedt, Johan Staaf, Göran Jönsson, et al.
Pageof 18

Showing results (61-70 of 175) with videos related to

Sort By:
Pageof 18
Melanoma Research|September 18, 2010
Multiple metastases from cutaneous malignant melanoma patients may display heterogeneous genomic and epigenomic patternsKatja Harbst, Johan Staaf, Anna Måsbäck, et al.
Peerj|March 11, 2015
Loss of CITED1, an MITF regulator, drives a phenotype switch in vitro and can predict clinical outcome in primary melanoma tumoursJillian Howlin, Helena Cirenajwis, Barbara Lettiero, et al.
Cancers|July 26, 2020
Methylation Patterns and Chromatin Accessibility in Neuroendocrine Lung CancerElsa Arbajian, Mattias Aine, Anna Karlsson, et al.
Journal of Experimental & Clinical Cancer Research : CR|August 18, 2021
Complement inhibitor CSMD1 modulates epidermal growth factor receptor oncogenic signaling and sensitizes breast cancer cells to chemotherapyChrysostomi Gialeli, Emre Can Tuysuz, Johan Staaf, et al.
Journal of Experimental & Clinical Cancer Research : CR|May 29, 2023
Correction: Complement inhibitor CSMD1 modulates epidermal growth factor receptor oncogenic signaling and sensitizes breast cancer cells to chemotherapyChrysostomi Gialeli, Emre Can Tuysuz, Johan Staaf, et al.
International Journal of Cancer|October 2, 2012
Landscape of somatic allelic imbalances and copy number alterations in human lung carcinomaJohan Staaf, Sofi Isaksson, Anna Karlsson, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|October 4, 2014
Genome-wide DNA methylation analysis of lung carcinoma reveals one neuroendocrine and four adenocarcinoma epitypes associated with patient outcomeAnna Karlsson, Mats Jönsson, Martin Lauss, et al.
British Journal of Haematology|February 16, 2008
Array-CGH reveals hidden gene dose changes in children with acute lymphoblastic leukaemia and a normal or failed karyotype by G-bandingEkaterina Kuchinskaya, Mats Heyman, Ann Nordgren, et al.
Genome Biology|September 18, 2008
Segmentation-based detection of allelic imbalance and loss-of-heterozygosity in cancer cells using whole genome SNP arraysJohan Staaf, David Lindgren, Johan Vallon-Christersson, et al.
Cancer Informatics|May 21, 2009
Tumor genome wide DNA alterations assessed by array CGH in patients with poor and excellent survival following operation for colorectal cancerKristina K Lagerstedt, Johan Staaf, Göran Jönsson, et al.
Pageof 18