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

Amanda J Walne

Showing results (1-10 of 23) with videos related to

Pageof 3
Sort By:
Cytotechnology|November 13, 2008
Telomerase dysfunction and dyskeratosis congenitaAmanda J Walne, Inderjeet Dokal
British Journal of Haematology|February 12, 2009
Advances in the understanding of dyskeratosis congenitaAmanda J Walne, Inderjeet Dokal
Mechanisms of Ageing and Development|December 7, 2007
Dyskeratosis Congenita: a historical perspectiveAmanda J Walne, Inderjeet Dokal
International Journal of Hematology|October 7, 2005
Dyskeratosis congenita: a disorder of defective telomere maintenance?Amanda J Walne, Anna Marrone, Inderjeet Dokal
Blood|August 2, 2008
TINF2 mutations result in very short telomeres: analysis of a large cohort of patients with dyskeratosis congenita and related bone marrow failure syndromesAmanda J Walne, Tom Vulliamy, Richard Beswick, et al.
Human Molecular Genetics|September 7, 2010
Mutations in C16orf57 and normal-length telomeres unify a subset of patients with dyskeratosis congenita, poikiloderma with neutropenia and Rothmund-Thomson syndromeAmanda J Walne, Tom Vulliamy, Richard Beswick, et al.
American Journal of Human Genetics|March 5, 2013
Constitutional mutations in RTEL1 cause severe dyskeratosis congenitaAmanda J Walne, Tom Vulliamy, Michael Kirwan, et al.
British Journal of Haematology|April 12, 2011
Dyskeratosis congenita and the DNA damage responseMichael Kirwan, Richard Beswick, Amanda J Walne, et al.
British Journal of Haematology|November 28, 2008
Exogenous TERC alone can enhance proliferative potential, telomerase activity and telomere length in lymphocytes from dyskeratosis congenita patientsMichael Kirwan, Richard Beswick, Tom Vulliamy, et al.
American Journal of Human Genetics|May 1, 2012
Exome sequencing identifies autosomal-dominant SRP72 mutations associated with familial aplasia and myelodysplasiaMichael Kirwan, Amanda J Walne, Vincent Plagnol, et al.
Pageof 3

Showing results (1-10 of 23) with videos related to

Sort By:
Pageof 3
Cytotechnology|November 13, 2008
Telomerase dysfunction and dyskeratosis congenitaAmanda J Walne, Inderjeet Dokal
British Journal of Haematology|February 12, 2009
Advances in the understanding of dyskeratosis congenitaAmanda J Walne, Inderjeet Dokal
Mechanisms of Ageing and Development|December 7, 2007
Dyskeratosis Congenita: a historical perspectiveAmanda J Walne, Inderjeet Dokal
International Journal of Hematology|October 7, 2005
Dyskeratosis congenita: a disorder of defective telomere maintenance?Amanda J Walne, Anna Marrone, Inderjeet Dokal
Blood|August 2, 2008
TINF2 mutations result in very short telomeres: analysis of a large cohort of patients with dyskeratosis congenita and related bone marrow failure syndromesAmanda J Walne, Tom Vulliamy, Richard Beswick, et al.
Human Molecular Genetics|September 7, 2010
Mutations in C16orf57 and normal-length telomeres unify a subset of patients with dyskeratosis congenita, poikiloderma with neutropenia and Rothmund-Thomson syndromeAmanda J Walne, Tom Vulliamy, Richard Beswick, et al.
American Journal of Human Genetics|March 5, 2013
Constitutional mutations in RTEL1 cause severe dyskeratosis congenitaAmanda J Walne, Tom Vulliamy, Michael Kirwan, et al.
British Journal of Haematology|April 12, 2011
Dyskeratosis congenita and the DNA damage responseMichael Kirwan, Richard Beswick, Amanda J Walne, et al.
British Journal of Haematology|November 28, 2008
Exogenous TERC alone can enhance proliferative potential, telomerase activity and telomere length in lymphocytes from dyskeratosis congenita patientsMichael Kirwan, Richard Beswick, Tom Vulliamy, et al.
American Journal of Human Genetics|May 1, 2012
Exome sequencing identifies autosomal-dominant SRP72 mutations associated with familial aplasia and myelodysplasiaMichael Kirwan, Amanda J Walne, Vincent Plagnol, et al.
Pageof 3