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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 ATRX
Anthony Argentaro, Ji-Chun Yang, Lynda Chapman, et al.
Hemoglobin
|
January 22, 2011
Hb S-β-thalassemia: molecular, hematological and clinical comparisons
Graham 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 thalassaemia
D 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 syndromes
D 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/M
Jianming 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 ATRX
David Clynes, Clare Jelinska, Barbara Xella, et al.
Journal of Medical Genetics
|
January 1, 1987
High resolution gene mapping of the human alpha globin locus
R 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 mutations
J 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 gene
D 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 cluster
D R Higgs, A V Hill, R Nicholls, et al.
Page
of 47
Search research articles
Search
Showing results (301-310 of 469) with videos related to
Sort By:
Page
of 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 ATRX
Anthony Argentaro, Ji-Chun Yang, Lynda Chapman, et al.
Hemoglobin
|
January 22, 2011
Hb S-β-thalassemia: molecular, hematological and clinical comparisons
Graham 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 thalassaemia
D 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 syndromes
D 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/M
Jianming 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 ATRX
David Clynes, Clare Jelinska, Barbara Xella, et al.
Journal of Medical Genetics
|
January 1, 1987
High resolution gene mapping of the human alpha globin locus
R 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 mutations
J 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 gene
D 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 cluster
D R Higgs, A V Hill, R Nicholls, et al.
Page
of 47