Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Bekim Sadikovic

Showing results (31-40 of 228) with videos related to

Pageof 23
Sort By:
Neoplasia (New York, N.Y.)|May 14, 2008
Decitabine-induced demethylation of 5' CpG island in GADD45A leads to apoptosis in osteosarcoma cellsKhaldoun Al-Romaih, Bekim Sadikovic, Maisa Yoshimoto, et al.
Genes|August 26, 2022
Examining the Diagnostic Yield of Tumour Testing and Qualifying Germline Concordance for Hereditary Cancer Variants in Patients with High-Grade Serous CarcinomaEmily A Goebel, Jennifer Kerkhof, Oleksandra Dzyubak, et al.
Research and Practice in Thrombosis and Haemostasis|May 12, 2021
A case of congenital prothrombin deficiency with two concurrent mutations in the prothrombin geneEman M Mansory, Pratibha Bhai, Alan Stuart, et al.
Human Molecular Genetics|March 17, 2009
Identification of interactive networks of gene expression associated with osteosarcoma oncogenesis by integrated molecular profilingBekim Sadikovic, Maisa Yoshimoto, Susan Chilton-MacNeill, et al.
Plos One|August 14, 2008
In vitro analysis of integrated global high-resolution DNA methylation profiling with genomic imbalance and gene expression in osteosarcomaBekim Sadikovic, Maisa Yoshimoto, Khaldoun Al-Romaih, et al.
Journal of Molecular Medicine (Berlin, Germany)|July 19, 2023
Genotypic analysis of a large cohort of patients with suspected atypical hemolytic uremic syndromeDervla M Connaughton, Pratibha Bhai, Paul Isenring, et al.
European Journal of Human Genetics : EJHG|September 22, 2023
Methylation signatures in clinically variable syndromic disorders: a familial DNMT3A variant in two adults with Tatton-Brown-Rahman syndromeCandy Kumps, Erika D'haenens, Jennifer Kerkhof, et al.
Journal of Internal Medicine|September 20, 2023
Sodium-glucose cotransporter-2 inhibitor-associated erythrocytosis: A retrospective cohort studyJessica Liu, Benjamin Chin-Yee, Ian H Chin-Yee, et al.
Canadian Journal of Gastroenterology & Hepatology|February 24, 2015
Examining the clinical use of hemochromatosis genetic testingMatthew B Lanktree, Bruce B Lanktree, Guillaume Paré, et al.
Epigenomics|December 20, 2022
DNA methylation episignatures: insight into copy number variationLiselot van der Laan, Kathleen Rooney, Tessa Ma Trooster, et al.
Pageof 23

Showing results (31-40 of 228) with videos related to

Sort By:
Pageof 23
Neoplasia (New York, N.Y.)|May 14, 2008
Decitabine-induced demethylation of 5' CpG island in GADD45A leads to apoptosis in osteosarcoma cellsKhaldoun Al-Romaih, Bekim Sadikovic, Maisa Yoshimoto, et al.
Genes|August 26, 2022
Examining the Diagnostic Yield of Tumour Testing and Qualifying Germline Concordance for Hereditary Cancer Variants in Patients with High-Grade Serous CarcinomaEmily A Goebel, Jennifer Kerkhof, Oleksandra Dzyubak, et al.
Research and Practice in Thrombosis and Haemostasis|May 12, 2021
A case of congenital prothrombin deficiency with two concurrent mutations in the prothrombin geneEman M Mansory, Pratibha Bhai, Alan Stuart, et al.
Human Molecular Genetics|March 17, 2009
Identification of interactive networks of gene expression associated with osteosarcoma oncogenesis by integrated molecular profilingBekim Sadikovic, Maisa Yoshimoto, Susan Chilton-MacNeill, et al.
Plos One|August 14, 2008
In vitro analysis of integrated global high-resolution DNA methylation profiling with genomic imbalance and gene expression in osteosarcomaBekim Sadikovic, Maisa Yoshimoto, Khaldoun Al-Romaih, et al.
Journal of Molecular Medicine (Berlin, Germany)|July 19, 2023
Genotypic analysis of a large cohort of patients with suspected atypical hemolytic uremic syndromeDervla M Connaughton, Pratibha Bhai, Paul Isenring, et al.
European Journal of Human Genetics : EJHG|September 22, 2023
Methylation signatures in clinically variable syndromic disorders: a familial DNMT3A variant in two adults with Tatton-Brown-Rahman syndromeCandy Kumps, Erika D'haenens, Jennifer Kerkhof, et al.
Journal of Internal Medicine|September 20, 2023
Sodium-glucose cotransporter-2 inhibitor-associated erythrocytosis: A retrospective cohort studyJessica Liu, Benjamin Chin-Yee, Ian H Chin-Yee, et al.
Canadian Journal of Gastroenterology & Hepatology|February 24, 2015
Examining the clinical use of hemochromatosis genetic testingMatthew B Lanktree, Bruce B Lanktree, Guillaume Paré, et al.
Epigenomics|December 20, 2022
DNA methylation episignatures: insight into copy number variationLiselot van der Laan, Kathleen Rooney, Tessa Ma Trooster, et al.
Pageof 23