Browsing by Author Dao-Ung, L

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Issue DateTitleAuthor(s)Citation
2005A 50 intronic splice site polymorphism leads to a null allele of the P2X7 gene in 1–2% of the Caucasian populationDao-Ung, L; Fuller, Stephen; Gu, Baijun (Ben); Skarratt, K; Sluyter, Ronald; Wiley, James; Nepean Clinical School: Medicine; Northern Clinical School: Medicine; Nepean Clinical School: Medicine; Nepean Clinical School: Medicine; School of Medical Sciences: Pathology; Nepean Clinical School: MedicineA 50 intronic splice site polymorphism leads to a null allele of the P2X7 gene in 1–2% of the Caucasian population, FEBS Letters (2005), vol.579,(12),2005,pp 2675-2678
2008Analysis of a large multi-generational family provides insight into the genetics of chronic lymphocytic leukemiaDao-Ung, L; Fuller, Stephen; McKinnon, Leah; Skarratt, K; Wiley, James; Crowther-Swanepoel, Dalemari; Houlston, Richard S.; Papaemmanuil, Elli; Sellick, Gabrielle S; Webb, Emily L.; Nepean Clinical School: Medicine; Northern Clinical School: Medicine; Nepean Clinical School: Medicine; Nepean Clinical School: Medicine; Nepean Clinical School: MedicineAnalysis of a large multi-generational family provides insight into the genetics of chronic lymphocytic leukemia, British Journal of Haematology, vol.142,(2),2008,pp 238-245
2004An Arg307 To Gln Polymorphism Within The Atp-Binding Site Causes Loss Of Function Of The Human P2X7 Receptor.Barden, Julian; Dao-Ung, L; Fuller, Stephen; Gu, Baijun (Ben); Shemon, Anne; Skarratt, K; Sluyter, Ronald; Wiley, James; Clarke, Alison L; Petrou, Steven; School of Medical Sciences: Anatomy & Histology; Nepean Clinical School: Medicine; Northern Clinical School: Medicine; Nepean Clinical School: Medicine; Nepean Clinical School: Medicine; Nepean Clinical School: Medicine; School of Medical Sciences: Pathology; Nepean Clinical School: MedicineAn Arg307 To Gln Polymorphism Within The Atp-Binding Site Causes Loss Of Function Of The Human P2X7 Receptor., Journal of Biological Chemistry, vol.279,(30),2004,pp 31287-31295
2006Chronic gingivitis in a new BTK mutationDao-Ung, L; Liu, Anthony; Nanan, Ralph; McDonald, David; Nepean Clinical School: Medicine; Northern Clinical School: Medicine; Nepean Clinical School: Paediatrics & Child HealthChronic gingivitis in a new BTK mutation, European Journal of Haematology, vol.76,(N/A),2006,pp 171-175
2003An Ile-568 to Asn polymorphism prevents normal trafficking and function of the human P2X7 receptorBarden, Julian; Dao-Ung, L; Fuller, Stephen; Gu, Baijun (Ben); Li, Changping; Shemon, Anne; Sluyter, Ronald; Wiley, James; Petrou, Steven; Smart, Megan L; School of Medical Sciences: Anatomy & Histology; Nepean Clinical School: Medicine; Northern Clinical School: Medicine; Nepean Clinical School: Medicine; Nepean Clinical School: Medicine; Nepean Clinical School: Medicine; School of Medical Sciences: Pathology; Nepean Clinical School: MedicineAn Ile-568 to Asn polymorphism prevents normal trafficking and function of the human P2X7 receptor, Journal of Biological Chemistry, vol.278,(19),2003,pp 17108-17113
2006A Thr(357) to Ser polymorphism in homozygous and compound heterozygous subjects causes absent or reduced P2X(7) function and impairs ATP-induced mycobacterial killing by macrophages.Britton, Warwick; Dao-Ung, L; Fernando, Suran; Fuller, Stephen; Gu, Baijun (Ben); Saunders, Bernadette; Shemon, Anne; Skarratt, K; Sluyter, Ronald; Wiley, James; Clarke, Alison L; Petrou, Steven; Tan, Khai See; Central Clinical School: Centenary Institute; Nepean Clinical School: Medicine; Central Clinical School: Medicine; Northern Clinical School: Medicine; Nepean Clinical School: Medicine; Central Clinical School: Centenary Institute; Nepean Clinical School: Medicine; Nepean Clinical School: Medicine; School of Medical Sciences: Pathology; Nepean Clinical School: MedicineA Thr(357) to Ser polymorphism in homozygous and compound heterozygous subjects causes absent or reduced P2X(7) function and impairs ATP-induced mycobacterial killing by macrophages., Journal of Biological Chemistry, vol.281,(4),2006,pp 2079-2086