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Tom Vulliamy

Showing results (1-10 of 50) with videos related to

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Blood Reviews|October 15, 2003
Dyskeratosis congenita: its link to telomerase and aplastic anaemiaInderjeet Dokal, Tom Vulliamy
Blood Reviews|January 1, 2008
Inherited aplastic anaemias/bone marrow failure syndromesInderjeet Dokal, Tom Vulliamy
Seminars in Hematology|July 11, 2006
Dyskeratosis congenitaTom Vulliamy, Inderjeet Dokal
Blood|May 23, 2022
Inherited bone marrow failure in the pediatric patientInderjeet Dokal, Hemanth Tummala, Tom Vulliamy
Lancet (London, England)|July 2, 2002
Association between aplastic anaemia and mutations in telomerase RNATom Vulliamy, Anna Marrone, Inderjeet Dokal, 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.
Blood|August 21, 2004
Heterozygous telomerase RNA mutations found in dyskeratosis congenita and aplastic anemia reduce telomerase activity via haploinsufficiencyAnna Marrone, David Stevens, Tom Vulliamy, et al.
International Ophthalmology|July 21, 2012
Limbal stem cell deficiency in patients with inherited stem cell disorder of dyskeratosis congenitaDeniz Aslan, Rustu F Akata, Harriet Holme, et al.
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.
Pageof 5

Showing results (1-10 of 50) with videos related to

Sort By:
Pageof 5
Blood Reviews|October 15, 2003
Dyskeratosis congenita: its link to telomerase and aplastic anaemiaInderjeet Dokal, Tom Vulliamy
Blood Reviews|January 1, 2008
Inherited aplastic anaemias/bone marrow failure syndromesInderjeet Dokal, Tom Vulliamy
Seminars in Hematology|July 11, 2006
Dyskeratosis congenitaTom Vulliamy, Inderjeet Dokal
Blood|May 23, 2022
Inherited bone marrow failure in the pediatric patientInderjeet Dokal, Hemanth Tummala, Tom Vulliamy
Lancet (London, England)|July 2, 2002
Association between aplastic anaemia and mutations in telomerase RNATom Vulliamy, Anna Marrone, Inderjeet Dokal, 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.
Blood|August 21, 2004
Heterozygous telomerase RNA mutations found in dyskeratosis congenita and aplastic anemia reduce telomerase activity via haploinsufficiencyAnna Marrone, David Stevens, Tom Vulliamy, et al.
International Ophthalmology|July 21, 2012
Limbal stem cell deficiency in patients with inherited stem cell disorder of dyskeratosis congenitaDeniz Aslan, Rustu F Akata, Harriet Holme, et al.
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.
Pageof 5