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Patrik Georgii-Hemming

Showing results (1-10 of 10) with videos related to

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Studies in Health Technology and Informatics|September 12, 2009
Representing a chemotherapy guideline using openEHR and rulesRong Chen, Patrik Georgii-Hemming, Hans Ahlfeldt
European Journal of Haematology|October 9, 2002
Expression of the bcl-2 family of pro- and anti-apoptotic genes in multiple myeloma and normal plasma cells: regulation during interleukin-6(IL-6)-induced growth and survivalHelena Spets, Thomas Strömberg, Patrik Georgii-Hemming, et al.
Gynecologic Oncology|July 16, 2015
The gynecological surveillance of women with Lynch syndrome in SwedenGerasimos Tzortzatos, Emil Andersson, Maria Soller, et al.
Human Mutation|June 6, 2017
Reduced cell surface levels of GPI-linked markers in a new case with PIGG loss of functionJin James Zhao, Jonatan Halvardson, Alexej Knaus, et al.
Medical Oncology (Northwood, London, England)|May 30, 2015
Picropodophyllin inhibits proliferation and survival of diffuse large B-cell lymphoma cellsThomas Strömberg, Xiaoying Feng, Maryam Delforoush, et al.
Journal of Medical Genetics|June 24, 2016
Mutations in HECW2 are associated with intellectual disability and epilepsyJonatan Halvardson, Jin J Zhao, Ammar Zaghlool, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|October 10, 2017
Exome sequencing reveals NAA15 and PUF60 as candidate genes associated with intellectual disabilityJin J Zhao, Jonatan Halvardson, Cecilia S Zander, et al.
Health Informatics Journal|October 11, 2024
Smart variant filtering - A blueprint solution for massively parallel sequencing-based variant analysisOrlinda Brahimllari, Sandra Eloranta, Patrik Georgii-Hemming, et al.
The Journal of Pathology|July 13, 2012
Transcriptional profiling of human glioblastoma vessels indicates a key role of VEGF-A and TGFβ2 in vascular abnormalizationLothar C Dieterich, Sofie Mellberg, Elise Langenkamp, et al.
Genome Medicine|November 8, 2019
From cytogenetics to cytogenomics: whole-genome sequencing as a first-line test comprehensively captures the diverse spectrum of disease-causing genetic variation underlying intellectual disabilityAnna Lindstrand, Jesper Eisfeldt, Maria Pettersson, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
Studies in Health Technology and Informatics|September 12, 2009
Representing a chemotherapy guideline using openEHR and rulesRong Chen, Patrik Georgii-Hemming, Hans Ahlfeldt
European Journal of Haematology|October 9, 2002
Expression of the bcl-2 family of pro- and anti-apoptotic genes in multiple myeloma and normal plasma cells: regulation during interleukin-6(IL-6)-induced growth and survivalHelena Spets, Thomas Strömberg, Patrik Georgii-Hemming, et al.
Gynecologic Oncology|July 16, 2015
The gynecological surveillance of women with Lynch syndrome in SwedenGerasimos Tzortzatos, Emil Andersson, Maria Soller, et al.
Human Mutation|June 6, 2017
Reduced cell surface levels of GPI-linked markers in a new case with PIGG loss of functionJin James Zhao, Jonatan Halvardson, Alexej Knaus, et al.
Medical Oncology (Northwood, London, England)|May 30, 2015
Picropodophyllin inhibits proliferation and survival of diffuse large B-cell lymphoma cellsThomas Strömberg, Xiaoying Feng, Maryam Delforoush, et al.
Journal of Medical Genetics|June 24, 2016
Mutations in HECW2 are associated with intellectual disability and epilepsyJonatan Halvardson, Jin J Zhao, Ammar Zaghlool, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|October 10, 2017
Exome sequencing reveals NAA15 and PUF60 as candidate genes associated with intellectual disabilityJin J Zhao, Jonatan Halvardson, Cecilia S Zander, et al.
Health Informatics Journal|October 11, 2024
Smart variant filtering - A blueprint solution for massively parallel sequencing-based variant analysisOrlinda Brahimllari, Sandra Eloranta, Patrik Georgii-Hemming, et al.
The Journal of Pathology|July 13, 2012
Transcriptional profiling of human glioblastoma vessels indicates a key role of VEGF-A and TGFβ2 in vascular abnormalizationLothar C Dieterich, Sofie Mellberg, Elise Langenkamp, et al.
Genome Medicine|November 8, 2019
From cytogenetics to cytogenomics: whole-genome sequencing as a first-line test comprehensively captures the diverse spectrum of disease-causing genetic variation underlying intellectual disabilityAnna Lindstrand, Jesper Eisfeldt, Maria Pettersson, et al.
Pageof 1