Browsing by Author Chapman, G.

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Issue DateTitleAuthor(s)Citation
2016Gestational stress induces the unfolded protein response, resulting in heart defectsChapman, Bogdan; Grieve, Stuart; Bewes, Therese; Chapman, G.; Dunwoodie, Sally; Graham, Robert M; Moreau, Julie; O'Reilly, Victoria; Shi, Hongjun; Sparrow, D. B.; Stocker, Roland; Yam, Michelle; Molecular Bioscience; Central Clinical School: MedicineGestational stress induces the unfolded protein response, resulting in heart defects, Development, vol.143, 14, 2016,pp 2561-2572
2004Identification Of Two Novel Hla Class Ii Alleles, Dqb1*0311 And Dqb1*0620.Chapman, G.; Dunckley, Heather; Greville, W.; Hogbin, J; Kennedy, A.; Velickovic, Zlatibor; Central Clinical School: Australian Red Cross Blood Service; Central Clinical School: Australian Red Cross Blood Service; Central Clinical School: Australian Red Cross Blood Service; Molecular & Microbial Bioscien; Central Clinical School: Australian Red Cross Blood Service; MedicineIdentification Of Two Novel Hla Class Ii Alleles, Dqb1*0311 And Dqb1*0620., Tissue Antigens, vol.64,(4),2004,pp 515-517
2004New Hla-B Alleles Detected By Polymerase Chain Reaction-Sequence-Specific Oligonucleotide Typing: Hla-B*0725, B*0728, And B*3808.Chapman, G.; Dunckley, Heather; Greville, W.; Kennedy, A.; Wallace, Ross; Dodd, R.; Hersee, J.; Le, T.; Taverniti, A.; Central Clinical School: Australian Red Cross Blood Service; Central Clinical School: Australian Red Cross Blood Service; Central Clinical School: Australian Red Cross Blood Service; Central Clinical School: Australian Red Cross Blood Service; Central Clinical School: AnaesthesiaNew Hla-B Alleles Detected By Polymerase Chain Reaction-Sequence-Specific Oligonucleotide Typing: Hla-B*0725, B*0728, And B*3808., Tissue Antigens, vol.63,(6),2004,pp 598-599
2015NKX2-5 mutations causative for congenital heart disease retain functionality and are directed to hundreds of targetsWaardenberg, Ashley; Bhattacharya, Shoumo; Blanpain, Cedric; Bondue, Antoine; Bouveret, Romaric; Chapman, G.; Chen, Chiann-mun; de Jong, Danielle; Doan, Tram; Dunwoodie, Sally; Fonoudi, Hananeh; Harvey, R; Kaur, Gurpreet; Mohamed, Stephanie; Plachta, Nicolas; Ramialison, Mirana; Schonrock, Nicole; Wouters, Merridee A.; Childrens Medical Research Institute (CMRI)NKX2-5 mutations causative for congenital heart disease retain functionality and are directed to hundreds of targets, eLife, vol.4, N/A, 2015,pp 1-30