Browsing by Author Whittle, Belinda L

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Issue DateTitleAuthor(s)Citation
2013Autoimmunity in primary antibody deficiency is associated with protein tyrosine phosphatase nonreceptor type 22 (PTPN22)Adelstein, Stephen; Garsia, Roger; Chew, Gary Y.; Cook, Matthew C.; DeMalmanche, Theo; French, Martyn; Fulcher, David; Gatenby, Paul; Hissaria, Pravin; Kirkpatrick, Philippa; Riminton, D. Sean; Sinha, Umang; Whittle, Belinda L; Wilson, Anastasia; Central Clinical School: Medicine; Central Clinical School: MedicineAutoimmunity in primary antibody deficiency is associated with protein tyrosine phosphatase nonreceptor type 22 (PTPN22), Journal of Allergy and Clinical Immunology, vol.131, 4, 2013,pp 1130-1135
2014Autosomal-dominant B-cell deficiency with alopecia due to a mutation in NFKB2 that results in nonprocessible p100Fulcher, David; Andrews, T. Daniel; Chand, Rochna; Cook, Matthew C.; Fewings, N; Field, Matthew; Goodnow, Christopher C.; Lee, Cindy; Whittle, Belinda L; Western Clinical School: Medicine (Westmead)Autosomal-dominant B-cell deficiency with alopecia due to a mutation in NFKB2 that results in nonprocessible p100, Blood, vol.124, 19, 2014,pp 2964-2972
2013Single Nucleotide Variants (SNVs) Define Senescence-Accelerated SAMP8 Mice, a Model of a Geriatric ConditionDelerue, Fabien; Goetz, Jurgen; Kruger, Sarah; Andrews, Dan; Sjollema, Geoff; Whittle, Belinda L; School of Medical Sciences: Brain & Mind Research Institute; School of Medical Sciences: Brain & Mind Research Institute; School of Medical Sciences: Brain & Mind Research InstituteSingle Nucleotide Variants (SNVs) Define Senescence-Accelerated SAMP8 Mice, a Model of a Geriatric Condition, Journal of Alzheimer's Disease, vol.36, 2, 2013,pp 349-363