Browsing by Author Skarratt, K

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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
2005Gene Dosage Determines the Negative Effects of Polymorphic Alleles of the P2X7 Receptor on Adenosine Triphosphate–Mediated Killing of Mycobacteria by Human MacrophagesBritton, Warwick; Fernando, Sujatha; Saunders, Bernadette; Skarratt, K; Sluyter, Ronald; Wiley, James; Central Clinical School: Centenary Institute; School of Rural Health: Medicine; Central Clinical School: Centenary Institute; Nepean Clinical School: Medicine; School of Medical Sciences: Pathology; Nepean Clinical School: MedicineGene Dosage Determines the Negative Effects of Polymorphic Alleles of the P2X7 Receptor on Adenosine Triphosphate–Mediated Killing of Mycobacteria by Human Macrophages, The Journal of Infectious Diseases 2005, vol.192,(1),2005,pp 149-155
2009Genetics of the P2X7 receptor and human diseaseFuller, Stephen; Gu, Baijun (Ben); Skarratt, K; Stokes, Leanne; Wiley, James; Nepean Clinical School: Medicine; Nepean Clinical School: Medicine; Nepean Clinical School: Medicine; Nepean Clinical School: Medicine; Nepean Clinical School: MedicineGenetics of the P2X7 receptor and human disease, Purinergic Signalling, vol.5,(2),2009,pp 257-262
2005Human Epidermal and Monocyte-Derived Langerhans Cells Express Functional P2X7 ReceptorsChristopherson, Richard; Fuller, Stephen; Georgiou, Jennifer; Martin, Christopher; Skarratt, K; Sluyter, Ronald; Wiley, James; Molecular & Microbial Bioscien; Northern Clinical School: Medicine; Nepean Clinical School: Medicine; Nepean Clinical School: Surgery; Nepean Clinical School: Medicine; School of Medical Sciences: Pathology; Nepean Clinical School: MedicineHuman Epidermal and Monocyte-Derived Langerhans Cells Express Functional P2X7 Receptors, THE JOURNAL OF INVESTIGATIVE DERMATOLOGY 2005, vol.125,(3),2005,pp 482-490
2006A Polymorphism in the P2X7 Gene Increases Susceptibility to Extrapulmonary Tuberculosis.Britton, Warwick; Fernando, Suran; Goldburg, Hazel; Marks, Guy; Saunders, Bernadette; Skarratt, K; Sluyter, Ronald; Wiley, James; Central Clinical School: Centenary Institute; Central Clinical School: Medicine; Central Clinical School: Medicine; Central Clinical School: Woolcock Inst. of Medical Research; Central Clinical School: Centenary Institute; Nepean Clinical School: Medicine; School of Medical Sciences: Pathology; Nepean Clinical School: MedicineA Polymorphism in the P2X7 Gene Increases Susceptibility to Extrapulmonary Tuberculosis., AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE 2005, vol.175,(4),2006,pp 360-366
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