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

Marcel E Dinger

Showing results (91-100 of 161) with videos related to

Pageof 17
Sort By:
European Journal of Human Genetics : EJHG|March 16, 2017
Gonadal mosaicism of a novel IQSEC2 variant causing female limited intellectual disability and epilepsyLisa J Ewans, Michael Field, Ying Zhu, et al.
Molecular Cancer Research : MCR|February 28, 2019
Lipid Uptake Is an Androgen-Enhanced Lipid Supply Pathway Associated with Prostate Cancer Disease Progression and Bone MetastasisKaylyn D Tousignant, Anja Rockstroh, Atefeh Taherian Fard, et al.
Genome Medicine|February 26, 2021
ClinSV: clinical grade structural and copy number variant detection from whole genome sequencing dataAndre E Minoche, Ben Lundie, Greg B Peters, et al.
Nucleic Acids Research|November 16, 2010
Expression of distinct RNAs from 3' untranslated regionsTim R Mercer, Dagmar Wilhelm, Marcel E Dinger, et al.
Scientific Reports|October 17, 2013
Genome-wide methylated CpG island profiles of melanoma cells reveal a melanoma coregulation networkJian-Liang Li, Joseph Mazar, Cuncong Zhong, et al.
Cell|August 23, 2011
The human mitochondrial transcriptomeTim R Mercer, Shane Neph, Marcel E Dinger, et al.
Oncotarget|February 6, 2016
The long noncoding RNA MALAT1 promotes tumor-driven angiogenesis by up-regulating pro-angiogenic gene expressionAndrew E Tee, Bing Liu, Renhua Song, et al.
Cell Systems|February 4, 2018
Universal Alternative Splicing of Noncoding ExonsIra W Deveson, Marion E Brunck, James Blackburn, et al.
Methods and Protocols|July 2, 2021
A Pathway to Precision Medicine for Aboriginal Australians: A Study ProtocolYeu-Yao Cheng, Jack Nunn, John Skinner, et al.
Molecular Genetics and Metabolism Reports|August 11, 2018
Expanding the spectrum of <i>PEX16</i> mutations and novel insights into disease mechanismsKishore R Kumar, Gautam Wali, Ryan L Davis, et al.
Pageof 17

Showing results (91-100 of 161) with videos related to

Sort By:
Pageof 17
European Journal of Human Genetics : EJHG|March 16, 2017
Gonadal mosaicism of a novel IQSEC2 variant causing female limited intellectual disability and epilepsyLisa J Ewans, Michael Field, Ying Zhu, et al.
Molecular Cancer Research : MCR|February 28, 2019
Lipid Uptake Is an Androgen-Enhanced Lipid Supply Pathway Associated with Prostate Cancer Disease Progression and Bone MetastasisKaylyn D Tousignant, Anja Rockstroh, Atefeh Taherian Fard, et al.
Genome Medicine|February 26, 2021
ClinSV: clinical grade structural and copy number variant detection from whole genome sequencing dataAndre E Minoche, Ben Lundie, Greg B Peters, et al.
Nucleic Acids Research|November 16, 2010
Expression of distinct RNAs from 3' untranslated regionsTim R Mercer, Dagmar Wilhelm, Marcel E Dinger, et al.
Scientific Reports|October 17, 2013
Genome-wide methylated CpG island profiles of melanoma cells reveal a melanoma coregulation networkJian-Liang Li, Joseph Mazar, Cuncong Zhong, et al.
Cell|August 23, 2011
The human mitochondrial transcriptomeTim R Mercer, Shane Neph, Marcel E Dinger, et al.
Oncotarget|February 6, 2016
The long noncoding RNA MALAT1 promotes tumor-driven angiogenesis by up-regulating pro-angiogenic gene expressionAndrew E Tee, Bing Liu, Renhua Song, et al.
Cell Systems|February 4, 2018
Universal Alternative Splicing of Noncoding ExonsIra W Deveson, Marion E Brunck, James Blackburn, et al.
Methods and Protocols|July 2, 2021
A Pathway to Precision Medicine for Aboriginal Australians: A Study ProtocolYeu-Yao Cheng, Jack Nunn, John Skinner, et al.
Molecular Genetics and Metabolism Reports|August 11, 2018
Expanding the spectrum of <i>PEX16</i> mutations and novel insights into disease mechanismsKishore R Kumar, Gautam Wali, Ryan L Davis, et al.
Pageof 17