يعرض 1 - 5 نتائج من 5 نتيجة بحث عن '"Menzel, Stephan"', وقت الاستعلام: 0.98s تنقيح النتائج
  1. 1
    دورية أكاديمية
    Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approach

    المؤلفون: Giardine, Belinda, Borg, Joseph, Higgs, Douglas R, Peterson, Kenneth, Philipsen, Sjaak, Maglott, Donna, Singleton, Belinda, Anstee, David J, Basak, Nazli, Clark, Barnaby, Costa, Flavia C, Faustino, Paula, Fedosyuk, Halyna, Felice, Alex E, Francina, Alain, Galanello, Renzo, Gallivan, Monica VE, Georgitsi, Marianthi, Gibbons, Richard J, Giordano, Piero C, Harteveld, Cornelis L, Hoyer, James D, Jarvis, Martin, Joly, Philippe, Kanavakis, Emmanuel, Kollia, Panagoula, Menzel, Stephan, Miller, Webb, Moradkhani, Kamran, Old, John, Papachatzopoulou, Adamantia, Papadakis, Manoussous N, Papadopoulos, Petros, Pavlovic, Sonja, Perseu, Lucia, Radmilovic, Milena, Riemer, Cathy, Satta, Stefania, Schrijver, Iris, Stojiljkovic, Maja, Thein, Swee Lay, Traeger-Synodinos, Jan, Tully, Ray, Wada, Takahito, Wayne, John S, Wiemann, Claudia, Zukic, Branda, Chui, David HK, Wajcman, Henri, Hardison, Ross C, Patrinos, George P

    مصطلحات موضوعية: hemoglobinopathies, thalassemia, locus-specific databases, microattribution, Doenças Genéticas

    العلاقة: info:eu-repo/grantAgreement/EC/FP7/200754; Nat Genet. 2011 Mar 20;43(4):295-301; http://hdl.handle.net/10400.18/105Test

    الإتاحة: http://hdl.handle.net/10400.18/105Test

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  2. 2
    دورية أكاديمية
    Discovering the genetics underlying foetal haemoglobin production in adults.

    المؤلفون: Thein, Swee Lay1,2 sl.thein@kcl.ac.uk, Menzel, Stephan1

    المصدر: British Journal of Haematology. May2009, Vol. 145 Issue 4, p455-467. 13p. 2 Diagrams, 1 Chart, 1 Graph.

    مصطلحات موضوعية: *SICKLE cell anemia, *GLOBIN genes, *HEMOGLOBINS, *THALASSEMIA, *HEMOGLOBINOPATHY


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  3. 3
    دورية أكاديمية
    Circulating DNA: a potential marker of sickle cell crisis.

    المؤلفون: Vasavda, Nisha, Ulug, Pinar, Kondaveeti, Sheila, Ramasamy, Karthik, Sugai, Taku, Cheung, Gordon, Rees, David C., Awogbade, Moji, Bannister, Sybil, Cunningham, Juliette, Menzel, Stephan, Thein, Swee Lay

    المصدر: British Journal of Haematology; Oct2007, Vol. 139 Issue 2, p331-336, 6p, 1 Chart, 3 Graphs

    مصطلحات موضوعية: DNA, CELL death, SICKLE cell anemia, POLYMERASE chain reaction, THALASSEMIA, C-reactive protein


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  4. 4
    دورية أكاديمية
    Intergenic variants of HBS1L-MYB are responsible for a major quantitative trait locus on chromosome 6q23 influencing fetal hemoglobin levels in adults.

    المؤلفون: Thein, Swee Lay1,2 sl.thein@kcl.ac.uk, Menzel, Stephan1, Xu Peng3, Best, Steve1, Jie Jiang1, Close, James1,4, Silver, Nicholas1, Gerovasilli, Ageliki1, Chen Ping4, Yamaguchi, Masao4, Wahlberg, Karin1, Ulug, Pinar1, Spector, Tim D.5, Garner, Chad6, Matsuda, Fumihiko4, Farrall, Martin7, Lathrop, Mark3

    المصدر: Proceedings of the National Academy of Sciences of the United States of America. 7/3/2007, Vol. 104 Issue 27, p11346-11351. 6p. 1 Diagram, 1 Chart, 1 Graph.

    مصطلحات موضوعية: *HEMOGLOBINS, *THALASSEMIA, *GUANOSINE triphosphate, *CARRIER proteins, *SICKLE cell anemia, *HEMOGLOBINOPATHY, *PURE red cell aplasia

    النص الكامل

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  5. 5
    دورية أكاديمية
    α-Haemoglobin stabilising protein is a quantitative trait gene that modifies the phenotype of β-thalassaemia.

    المؤلفون: Lai, Mei I., Jiang, Jie, Silver, Nicholas, Best, Steve, Menzel, Stephan, Mijovic, Aleksandar, Colella, Stefano, Ragoussis, Jiannis, Garner, Chad, Weiss, Mitchell J., Thein, Swee L.

    المصدر: British Journal of Haematology; Jun2006, Vol. 133 Issue 6, p675-682, 8p

    مصطلحات موضوعية: THALASSEMIA, HEMOGLOBINS, PHENOTYPES, POLYMERASE chain reaction, DNA polymerases, HEMOLYTIC anemia


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