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Tom Vulliamy

Showing results (31-40 of 50) with videos related to

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The Lancet. Respiratory Medicine|September 13, 2014
Intermittent montelukast in children aged 10 months to 5 years with wheeze (WAIT trial): a multicentre, randomised, placebo-controlled trialChinedu Nwokoro, Hitesh Pandya, Stephen Turner, et al.
Human Mutation|September 18, 2009
Defining the pathogenic role of telomerase mutations in myelodysplastic syndrome and acute myeloid leukemiaMichael Kirwan, Tom Vulliamy, Anna Marrone, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 9, 2020
A frameshift variant in specificity protein 1 triggers superactivation of Sp1-mediated transcription in familial bone marrow failureHemanth Tummala, Amanda J Walne, Findlay Bewicke-Copley, et al.
American Journal of Human Genetics|June 28, 2016
DNAJC21 Mutations Link a Cancer-Prone Bone Marrow Failure Syndrome to Corruption in 60S Ribosome Subunit MaturationHemanth Tummala, Amanda J Walne, Mike Williams, et al.
British Journal of Haematology|September 26, 2022
Germline ERCC excision repair 6 like 2 (ERCC6L2) mutations lead to impaired erythropoiesis and reshaping of the bone marrow microenvironmentHannah Armes, Findlay Bewicke-Copley, Ana Rio-Machin, et al.
American Journal of Human Genetics|August 5, 2022
Germline thymidylate synthase deficiency impacts nucleotide metabolism and causes dyskeratosis congenitaHemanth Tummala, Amanda Walne, Roberto Buccafusca, et al.
Environment International|September 5, 2016
Air pollution, ethnicity and telomere length in east London schoolchildren: An observational studyRobert T Walton, Ian S Mudway, Isobel Dundas, et al.
American Journal of Medical Genetics. Part A|August 31, 2010
Emberger syndrome-primary lymphedema with myelodysplasia: report of seven new casesSahar Mansour, Fiona Connell, Colin Steward, et al.
The New England Journal of Medicine|October 21, 2011
Inflammatory skin and bowel disease linked to ADAM17 deletionDiana C Blaydon, Paolo Biancheri, Wei-Li Di, et al.
American Journal of Human Genetics|February 21, 2012
Revertant somatic mosaicism by mitotic recombination in dyskeratosis congenitaMarjolijn C J Jongmans, Eugene T P Verwiel, Yvonne Heijdra, et al.
Pageof 5

Showing results (31-40 of 50) with videos related to

Sort By:
Pageof 5
The Lancet. Respiratory Medicine|September 13, 2014
Intermittent montelukast in children aged 10 months to 5 years with wheeze (WAIT trial): a multicentre, randomised, placebo-controlled trialChinedu Nwokoro, Hitesh Pandya, Stephen Turner, et al.
Human Mutation|September 18, 2009
Defining the pathogenic role of telomerase mutations in myelodysplastic syndrome and acute myeloid leukemiaMichael Kirwan, Tom Vulliamy, Anna Marrone, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 9, 2020
A frameshift variant in specificity protein 1 triggers superactivation of Sp1-mediated transcription in familial bone marrow failureHemanth Tummala, Amanda J Walne, Findlay Bewicke-Copley, et al.
American Journal of Human Genetics|June 28, 2016
DNAJC21 Mutations Link a Cancer-Prone Bone Marrow Failure Syndrome to Corruption in 60S Ribosome Subunit MaturationHemanth Tummala, Amanda J Walne, Mike Williams, et al.
British Journal of Haematology|September 26, 2022
Germline ERCC excision repair 6 like 2 (ERCC6L2) mutations lead to impaired erythropoiesis and reshaping of the bone marrow microenvironmentHannah Armes, Findlay Bewicke-Copley, Ana Rio-Machin, et al.
American Journal of Human Genetics|August 5, 2022
Germline thymidylate synthase deficiency impacts nucleotide metabolism and causes dyskeratosis congenitaHemanth Tummala, Amanda Walne, Roberto Buccafusca, et al.
Environment International|September 5, 2016
Air pollution, ethnicity and telomere length in east London schoolchildren: An observational studyRobert T Walton, Ian S Mudway, Isobel Dundas, et al.
American Journal of Medical Genetics. Part A|August 31, 2010
Emberger syndrome-primary lymphedema with myelodysplasia: report of seven new casesSahar Mansour, Fiona Connell, Colin Steward, et al.
The New England Journal of Medicine|October 21, 2011
Inflammatory skin and bowel disease linked to ADAM17 deletionDiana C Blaydon, Paolo Biancheri, Wei-Li Di, et al.
American Journal of Human Genetics|February 21, 2012
Revertant somatic mosaicism by mitotic recombination in dyskeratosis congenitaMarjolijn C J Jongmans, Eugene T P Verwiel, Yvonne Heijdra, et al.
Pageof 5