Browsing by Author Yang, Shu

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Issue DateTitleAuthor(s)Citation
2016CCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementiaCole, Nicholas; Nicholson, Garth; Williams, Kelly; et al, Various; Farrawell, Natalie E.; Fifita, Jennifer A.; Hu, Xun; Smith, Bradley; Topp, Simon; Vance, Caroline; Warraich, Sadaf T.; Yang, Shu; Zhang, Katharine Y; School of Medical Sciences: Anatomy & Histology; Concord Clinical School: ANZAC Research Institute; Concord Clinical School: ANZAC Research InstituteCCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementia, Nature Communications, vol.7, N/A, 2016,pp 1-8
2016CCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementiaCole, Nicholas; Nicholson, Garth; Williams, Kelly; et al, Various; Farrawell, Natalie E.; Fifita, Jennifer A.; Hu, Xun; Smith, Bradley; Topp, Simon; Vance, Caroline; Warraich, Sadaf T.; Yang, Shu; Zhang, Katharine Y; School of Medical Sciences: Anatomy & Histology; Concord Clinical School: ANZAC Research Institute; Concord Clinical School: ANZAC Research InstituteCCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementia, Nature Communications, vol.7, N/A, 2016,pp 1-8
2015Evaluation of Skin Fibroblasts from Amyotrophic Lateral Sclerosis Patients for the Rapid Study of Pathological FeaturesBlair, Ian; Nicholson, Garth; Bax, Monique; Fifita, Jennifer A; Kariawasam, Ruvini; Ooi, Lezanne; Yang, Shu; Yerbury, Justin J.; Zhang, Katharine Y; Concord Clinical School: ANZAC Research Institute; Concord Clinical School: ANZAC Research InstituteEvaluation of Skin Fibroblasts from Amyotrophic Lateral Sclerosis Patients for the Rapid Study of Pathological Features, Neurotoxicity Research, vol.28, 2, 2015,pp 138-146
2010Fused in sarcoma/translocated in liposarcoma: a multifunctional DNA/RNA binding protein.Blair, Ian; Nicholson, Garth; Warraich, Sadaf; Yang, Shu; Concord Clinical School: Medicine; Concord Clinical School: ANZAC Research Institute; Concord Clinical School: MedicineFused in sarcoma/translocated in liposarcoma: a multifunctional DNA/RNA binding protein., The International Journal of Biochemistry & Cell Biology, vol.42, 9,pp 1408-1411
2017Genetic and Pathological Assessment of hnRNPA1, hnRNPA2/B1, and hnRNPA3 in Familial and Sporadic Amyotrophic Lateral SclerosisNicholson, Garth; Pamphlett, Roger; Bauer, Denis; Blair, Ian P.; Fifita, Jennifer A; Galper, Jasmin; Hogan, Alison L; McCann, Emily P.; Rowe, Dominic; Saunders, Neil; Tarr, I; Williams, Kelly L; Yang, Shu; Zhang, Katharine Y; Concord Clinical School: ANZAC Research Institute; School of Medical Sciences: PathologyGenetic and Pathological Assessment of hnRNPA1, hnRNPA2/B1, and hnRNPA3 in Familial and Sporadic Amyotrophic Lateral Sclerosis, Neurodegenerative Diseases, vol.17, 6, 2017,pp 304-312
2013Mutation analysis and immunopathological studies of PFN1 in familial and sporadic amyotrophic lateral sclerosisBlair, Ian; Nicholson, Garth; Pamphlett, Roger; Warraich, Sadaf; Williams, Kelly; Fifita, Jennifer; Yang, Shu; Concord Clinical School: ANZAC Research Institute; Concord Clinical School: ANZAC Research Institute; School of Medical Sciences: Pathology; Concord Clinical School: Medicine; Concord Clinical School: ANZAC Research InstituteMutation analysis and immunopathological studies of PFN1 in familial and sporadic amyotrophic lateral sclerosis, Neurobiology of Aging, vol.34, 9, 2013,pp 2235.e7-2235.e10
2012Mutation analysis of the optineurin gene in familial amyotrophic lateral sclerosisBlair, Ian; Nicholson, Garth; Williams, Kelly; Solski, Jennifer; Yang, Shu; Concord Clinical School: ANZAC Research Institute; Concord Clinical School: ANZAC Research Institute; Concord Clinical School: ANZAC Research InstituteMutation analysis of the optineurin gene in familial amyotrophic lateral sclerosis, Neurobiology of Aging: age-related phenomena, neurodegeneration and neuropathology, vol.33, 1, 2012,pp 210.e9-210.e10
2012A novel TARDBP insertion/deletion mutation in the flail arm variant of amyotrophic lateral sclerosisBlair, Ian; Luquin, Natasha; Nicholson, Garth; Pamphlett, Roger; Williams, Kelly; Fernando, Ruvini; Solski, Jennifer; Yang, Shu; Concord Clinical School: Medicine; School of Medical Sciences: Anatomy & Histology; Concord Clinical School: ANZAC Research Institute; School of Medical Sciences: Pathology; Concord Clinical School: ANZAC Research InstituteA novel TARDBP insertion/deletion mutation in the flail arm variant of amyotrophic lateral sclerosis, Amyotrophic Lateral Sclerosis, vol.13, 5, 2012,pp 465-470
2010TDP-43: a DNA and RNA binding protein with roles in neurodegenerative diseasesBlair, Ian; Nicholson, Garth; Warraich, Sadaf; Yang, Shu; Concord Clinical School: Medicine; Concord Clinical School: ANZAC Research Institute; Concord Clinical School: MedicineTDP-43: a DNA and RNA binding protein with roles in neurodegenerative diseases, The International Journal of Biochemistry & Cell Biology, vol.42, 10,pp 1606-1609
2012UBQLN2/ubiquilin 2 mutation and pathology in familial amyotrophic lateral sclerosisBlair, Ian; Nicholson, Garth; Warraich, Sadaf; Williams, Kelly; Fernando, Ruvini; Rouleau, Guy A.; Solski, Jennifer; Yang, Shu; Concord Clinical School: ANZAC Research Institute; Concord Clinical School: ANZAC Research Institute; Concord Clinical School: Medicine; Concord Clinical School: ANZAC Research InstituteUBQLN2/ubiquilin 2 mutation and pathology in familial amyotrophic lateral sclerosis, Neurobiology of Aging, vol.33, 10, 2012,pp 2527.e3-2527.e10