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

Martin Poot

Showing results (51-60 of 100) with videos related to

Pageof 10
Sort By:
American Journal of Medical Genetics. Part A|March 16, 2013
Antisense may make sense of 1q44 deletions, seizures, and HNRNPUMartin Poot, Martien J Kas
Experimental Cell Research|September 6, 2002
Distinct patterns of mitochondrial changes precede induction of apoptosis by all-trans-retinoic acid and N-(4-hydroxyphenyl)retinamide in MCF7 breast cancer cellsMartin Poot, Suzanne Hosier, Karen Swisshelm
European Journal of Medical Genetics|August 5, 2008
AKT3 as a candidate gene for corpus callosum anomalies in patients with 1q44 deletionsMartin Poot, Hester Y Kroes, Ron Hochstenbach
Aging|February 6, 2020
Lessons for aging from Werner syndrome epigeneticsGeorge M Martin, Martin Poot, Thomas Haaf
Cytometry|July 13, 2002
A novel flow cytometric technique for drug cytotoxicity gives results comparable to colony-forming assaysMartin Poot, John R Silber, Peter S Rabinovitch
European Journal of Human Genetics : EJHG|January 5, 2006
Microarray-based genome investigation: molecular karyotyping or segmental aneuploidy profiling?Ron Hochstenbach, Hans Kristian Ploos van Amstel, Martin Poot
Plos One|May 17, 2011
Identifying human disease genes through cross-species gene mapping of evolutionary conserved processesMartin Poot, Alexandra Badea, Robert W Williams, et al.
European Journal of Medical Genetics|December 2, 2008
Three de novo losses and one insertion within a pericentric inversion of chromosome 6 in a patient with complete absence of expressive speech and reduced pain perceptionMartin Poot, Ruben van't Slot, Romina Leupert, et al.
Experimental Cell Research|May 20, 2004
Distinct functions for WRN and TP53 in a shared pathway of cellular response to 1-beta-D-arabinofuranosylcytosine and bleomycinMartin Poot, Xiaoyang Jin, Juliane P Hill, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|April 30, 2002
Werner syndrome diploid fibroblasts are sensitive to 4-nitroquinoline-N-oxide and 8-methoxypsoralen: implications for the disease phenotypeMartin Poot, Katherine A Gollahon, Mary J Emond, et al.
Pageof 10

Showing results (51-60 of 100) with videos related to

Sort By:
Pageof 10
American Journal of Medical Genetics. Part A|March 16, 2013
Antisense may make sense of 1q44 deletions, seizures, and HNRNPUMartin Poot, Martien J Kas
Experimental Cell Research|September 6, 2002
Distinct patterns of mitochondrial changes precede induction of apoptosis by all-trans-retinoic acid and N-(4-hydroxyphenyl)retinamide in MCF7 breast cancer cellsMartin Poot, Suzanne Hosier, Karen Swisshelm
European Journal of Medical Genetics|August 5, 2008
AKT3 as a candidate gene for corpus callosum anomalies in patients with 1q44 deletionsMartin Poot, Hester Y Kroes, Ron Hochstenbach
Aging|February 6, 2020
Lessons for aging from Werner syndrome epigeneticsGeorge M Martin, Martin Poot, Thomas Haaf
Cytometry|July 13, 2002
A novel flow cytometric technique for drug cytotoxicity gives results comparable to colony-forming assaysMartin Poot, John R Silber, Peter S Rabinovitch
European Journal of Human Genetics : EJHG|January 5, 2006
Microarray-based genome investigation: molecular karyotyping or segmental aneuploidy profiling?Ron Hochstenbach, Hans Kristian Ploos van Amstel, Martin Poot
Plos One|May 17, 2011
Identifying human disease genes through cross-species gene mapping of evolutionary conserved processesMartin Poot, Alexandra Badea, Robert W Williams, et al.
European Journal of Medical Genetics|December 2, 2008
Three de novo losses and one insertion within a pericentric inversion of chromosome 6 in a patient with complete absence of expressive speech and reduced pain perceptionMartin Poot, Ruben van't Slot, Romina Leupert, et al.
Experimental Cell Research|May 20, 2004
Distinct functions for WRN and TP53 in a shared pathway of cellular response to 1-beta-D-arabinofuranosylcytosine and bleomycinMartin Poot, Xiaoyang Jin, Juliane P Hill, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|April 30, 2002
Werner syndrome diploid fibroblasts are sensitive to 4-nitroquinoline-N-oxide and 8-methoxypsoralen: implications for the disease phenotypeMartin Poot, Katherine A Gollahon, Mary J Emond, et al.
Pageof 10