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R Higgs

Showing results (301-310 of 469) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|July 5, 2007
Structural consequences of disease-causing mutations in the ATRX-DNMT3-DNMT3L (ADD) domain of the chromatin-associated protein ATRXAnthony Argentaro, Ji-Chun Yang, Lynda Chapman, et al.
Hemoglobin|January 22, 2011
Hb S-β-thalassemia: molecular, hematological and clinical comparisonsGraham R Serjeant, Beryl E Serjeant, Raphael A Fraser, et al.
British Journal of Haematology|May 1, 1982
Inadequacy of Hb Bart's as an indicator of alpha thalassaemiaD R Higgs, J Lamb, B E Aldridge, et al.
Annals of the New York Academy of Sciences|January 1, 1980
The clinical and molecular heterogeneity of the thalassemia syndromesD J Weatherall, J B Clegg, W G Wood, et al.
Cell Reports|February 17, 2021
Persistence of RNA transcription during DNA replication delays duplication of transcription start sites until G2/MJianming Wang, Patricia Rojas, Jingwen Mao, et al.
Nature Communications|July 7, 2015
Suppression of the alternative lengthening of telomere pathway by the chromatin remodelling factor ATRXDavid Clynes, Clare Jelinska, Barbara Xella, et al.
Journal of Medical Genetics|January 1, 1987
High resolution gene mapping of the human alpha globin locusR D Nicholls, J A Jonasson, J O McGee, et al.
Leukemia|May 23, 2008
Familial essential thrombocythemia with spontaneous megakaryocyte colony formation and acquired JAK2 mutationsJ R Higgs, I Sadek, P E Neumann, et al.
Lancet (London, England)|August 11, 1979
Negro alpha-thalassaemia is caused by deletion of a single alpha-globin geneD R Higgs, L Pressley, J M Old, et al.
Annals of the New York Academy of Sciences|January 1, 1985
Molecular rearrangements of the human alpha-globin gene clusterD R Higgs, A V Hill, R Nicholls, et al.
Pageof 47

Showing results (301-310 of 469) with videos related to

Sort By:
Pageof 47
Proceedings of the National Academy of Sciences of the United States of America|July 5, 2007
Structural consequences of disease-causing mutations in the ATRX-DNMT3-DNMT3L (ADD) domain of the chromatin-associated protein ATRXAnthony Argentaro, Ji-Chun Yang, Lynda Chapman, et al.
Hemoglobin|January 22, 2011
Hb S-β-thalassemia: molecular, hematological and clinical comparisonsGraham R Serjeant, Beryl E Serjeant, Raphael A Fraser, et al.
British Journal of Haematology|May 1, 1982
Inadequacy of Hb Bart's as an indicator of alpha thalassaemiaD R Higgs, J Lamb, B E Aldridge, et al.
Annals of the New York Academy of Sciences|January 1, 1980
The clinical and molecular heterogeneity of the thalassemia syndromesD J Weatherall, J B Clegg, W G Wood, et al.
Cell Reports|February 17, 2021
Persistence of RNA transcription during DNA replication delays duplication of transcription start sites until G2/MJianming Wang, Patricia Rojas, Jingwen Mao, et al.
Nature Communications|July 7, 2015
Suppression of the alternative lengthening of telomere pathway by the chromatin remodelling factor ATRXDavid Clynes, Clare Jelinska, Barbara Xella, et al.
Journal of Medical Genetics|January 1, 1987
High resolution gene mapping of the human alpha globin locusR D Nicholls, J A Jonasson, J O McGee, et al.
Leukemia|May 23, 2008
Familial essential thrombocythemia with spontaneous megakaryocyte colony formation and acquired JAK2 mutationsJ R Higgs, I Sadek, P E Neumann, et al.
Lancet (London, England)|August 11, 1979
Negro alpha-thalassaemia is caused by deletion of a single alpha-globin geneD R Higgs, L Pressley, J M Old, et al.
Annals of the New York Academy of Sciences|January 1, 1985
Molecular rearrangements of the human alpha-globin gene clusterD R Higgs, A V Hill, R Nicholls, et al.
Pageof 47