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Browsing by Author Douglas R. Higgs

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Showing results 1 to 7 of 7
Issue DateTitleAuthor(s)
22-Dec-2009Adventitious changes in long-range gene expression caused by polymorphic structural variation and promoter competitionKaren M. Lower; Jim R. Hughes; Marco De Gobbi; Shirley Henderson; Vip Viprakasit; Chris Fisher; Anne Goriely; Helena Ayyub; Jackie Sloane-Stanley; Douglas Vernimmen; Cordelia Langford; David Garrick; Richard J. Gibbons; Douglas R. Higgs; John Radcliffe Hospital; Oxford Radcliffe Hospitals NHS Trust; Mahidol University; Wellcome Trust Sanger Institute
29-Oct-2010ATR-X syndrome protein targets tandem repeats and influences allele-specific expression in a size-dependent mannerMartin J. Law; Karen M. Lower; Hsiao P.J. Voon; Jim R. Hughes; David Garrick; Vip Viprakasit; Matthew Mitson; Marco De Gobbi; Marco Marra; Andrew Morris; Aaron Abbott; Steven P. Wilder; Stephen Taylor; Guilherme M. Santos; Joe Cross; Helena Ayyub; Steven Jones; Jiannis Ragoussis; Daniela Rhodes; Ian Dunham; Douglas R. Higgs; Richard J. Gibbons; John Radcliffe Hospital; Mahidol University; Wellcome Trust Centre for Human Genetics; Wellcome Trust; The Medical Research Council Laboratory of Molecular Biology; The University of British Columbia
1-Mar-2004Co-inheritance of Hb Pak Num Po, a Novel α1 Gene Mutation, and α<sup>0</sup>Thalassemia Associated with Transfusion-Dependent Hb H DiseaseVip Viprakasit; Voravarn S. Tanphaichitr; Gavivann Veerakul; Worrawut Chinchang; Siripan Petrarat; Parichat Pung-Amritt; Douglas R. Higgs; Mahidol University; University of Oxford; John Radcliffe Hospital
1-May-2004Evaluation of alpha hemoglobin stabilizing protein (AHSP) as a genetic modifier in patients with β thalassemiaVip Viprakasit; Voravarn S. Tanphaichitr; Worrawut Chinchang; Pakarat Sangkla; Mitchell J. Weiss; Douglas R. Higgs; Mahidol University
9-Mar-2017An international registry of survivors with Hb Bart's hydrops fetalis syndromeDuantida Songdej; Christian Babbs; Douglas R. Higgs; Weatherall Institute of Molecular Medicine; Mahidol University
6-Mar-2014Mutations in Krüppel-like factor 1 cause transfusion-dependent hemolytic anemia and persistence of embryonic globin gene expressionVip Viprakasit; Supachai Ekwattanakit; Suchada Riolueang; Nipon Chalaow; Chris Fisher; Karen Lower; Hitoshi Kanno; Kalaya Tachavanich; Sasithorn Bejrachandra; Jariya Saipin; Monthana Juntharaniyom; Kleebsabai Sanpakit; Voravarn S. Tanphaichitr; Duantida Songdej; Christian Babbs; Richard J. Gibbons; Sjaak Philipsen; Douglas R. Higgs; Mahidol University; Weatherall Institute of Molecular Medicine; Flinders University; Tokyo Women's Medical University; Khon Kaen Regional Hospital; Erasmus University Medical Center
26-May-2006A regulatory SNP causes a human genetic disease by creating a new transcriptional promoterMarco De Gobbi; Vip Viprakasit; Jim R. Hughes; Chris Fisher; Veronica J. Buckle; Helena Ayyub; Richard J. Gibbons; Douglas Vernimmen; Yuko Yoshinaga; Pieter De Jong; Jan Fang Cheng; Edward M. Rubin; William G. Wood; Don Bowden; Douglas R. Higgs; John Radcliffe Hospital; Mahidol University; Children's Hospital Oakland Research Institute; Lawrence Berkeley National Laboratory; Monash University