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Tom Vulliamy

Showing results (11-20 of 50) with videos related to

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British Journal of Haematology|April 27, 2012
Marked genetic heterogeneity in familial myelodysplasia/acute myeloid leukaemiaHarriet Holme, Upal Hossain, Michael Kirwan, et al.
Nature Genetics|April 21, 2004
Disease anticipation is associated with progressive telomere shortening in families with dyskeratosis congenita due to mutations in TERCTom Vulliamy, Anna Marrone, Richard Szydlo, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 5, 2008
Mutations in the telomerase component NHP2 cause the premature ageing syndrome dyskeratosis congenitaTom Vulliamy, Richard Beswick, Michael Kirwan, et al.
Haematologica|February 8, 2006
The role of the G6PD AEth376G/968C allele in glucose-6-phosphate dehydrogenase deficiency in the seerer population of SenegalCarla De Araujo, Florence Migot-Nabias, Juliette Guitard, et al.
Journal of Human Genetics|September 7, 2005
Characterization of G6PD deficiency in southern Croatia: description of a new variant, G6PD SplitMarin Barišić, Jelena Korać, Ivana Pavlinac, et al.
Oncogene|October 26, 2002
Targeted disruption of Dkc1, the gene mutated in X-linked dyskeratosis congenita, causes embryonic lethality in miceJun He, Sandra Navarrete, Murek Jasinski, 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.
Blood|September 6, 2007
Telomerase reverse-transcriptase homozygous mutations in autosomal recessive dyskeratosis congenita and Hoyeraal-Hreidarsson syndromeAnna Marrone, Amanda Walne, Hannah Tamary, et al.
Biochemistry|October 20, 2009
Single-molecule analysis of the human telomerase RNA.dyskerin interaction and the effect of dyskeratosis congenita mutationsBeth Ashbridge, Angel Orte, Justin A Yeoman, et al.
Pageof 5

Showing results (11-20 of 50) with videos related to

Sort By:
Pageof 5
British Journal of Haematology|April 27, 2012
Marked genetic heterogeneity in familial myelodysplasia/acute myeloid leukaemiaHarriet Holme, Upal Hossain, Michael Kirwan, et al.
Nature Genetics|April 21, 2004
Disease anticipation is associated with progressive telomere shortening in families with dyskeratosis congenita due to mutations in TERCTom Vulliamy, Anna Marrone, Richard Szydlo, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 5, 2008
Mutations in the telomerase component NHP2 cause the premature ageing syndrome dyskeratosis congenitaTom Vulliamy, Richard Beswick, Michael Kirwan, et al.
Haematologica|February 8, 2006
The role of the G6PD AEth376G/968C allele in glucose-6-phosphate dehydrogenase deficiency in the seerer population of SenegalCarla De Araujo, Florence Migot-Nabias, Juliette Guitard, et al.
Journal of Human Genetics|September 7, 2005
Characterization of G6PD deficiency in southern Croatia: description of a new variant, G6PD SplitMarin Barišić, Jelena Korać, Ivana Pavlinac, et al.
Oncogene|October 26, 2002
Targeted disruption of Dkc1, the gene mutated in X-linked dyskeratosis congenita, causes embryonic lethality in miceJun He, Sandra Navarrete, Murek Jasinski, 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.
Blood|September 6, 2007
Telomerase reverse-transcriptase homozygous mutations in autosomal recessive dyskeratosis congenita and Hoyeraal-Hreidarsson syndromeAnna Marrone, Amanda Walne, Hannah Tamary, et al.
Biochemistry|October 20, 2009
Single-molecule analysis of the human telomerase RNA.dyskerin interaction and the effect of dyskeratosis congenita mutationsBeth Ashbridge, Angel Orte, Justin A Yeoman, et al.
Pageof 5