Browsing by Author Zhang, Katharine Y

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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
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
2015Novel TBK1 truncating mutation in a familial amyotrophic lateral sclerosis patient of Chinese originNicholson, Garth; Blair, Ian P.; Duncan, Emma; Fifita, Jennifer A.; Leo, Paul; Marshall, M S; McCann, Emily P.; Rowe, Dominic B.; Williams, Kelly; Zhang, Katharine Y; Concord Clinical School: ANZAC Research InstituteNovel TBK1 truncating mutation in a familial amyotrophic lateral sclerosis patient of Chinese origin, Neurobiology of Aging, vol.36, 12, 2015,pp 3334.e1-3334.e5
2017Postnatal Development of Spasticity Following Transgene Insertion in the Mouse (beta)IV Spectrin Gene (SPTBN4)Das, Shannon; Kichkin, Eva; Lovicu, Frank; Phillips, William; Shu, Daisy; Visvanathan, Archunan; Blair, Ian P.; McCann, Emily P.; Reddel, Stephen; Williams, Kelly; Zhang, Katharine Y; School of Medical Sciences: Bosch Institute; School of Medical Sciences: Physiology; School of Medical Sciences: Anatomy & Histology; School of Medical Sciences: Physiology; SAHCS: Clinical Ophthalmology and Eye Health; PsychologyPostnatal Development of Spasticity Following Transgene Insertion in the Mouse (beta)IV Spectrin Gene (SPTBN4), Journal of Neuromuscular Diseases, vol.4, 2, 2017,pp 159-164