STUART PROWER DEFICIENCY
\stjˈuːət pɹˈa͡ʊə dɪfˈɪʃənsi], \stjˈuːət pɹˈaʊə dɪfˈɪʃənsi], \s_t_j_ˈuː_ə_t p_ɹ_ˈaʊ_ə d_ɪ_f_ˈɪ_ʃ_ə_n_s_i]\
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Blood coagulation disorder usually inherited as an autosomal recessive trait, though it can be acquired. It is characterized by defective activity in both the intrinsic and extrinsic pathways, impaired thromboplastin time, and impaired prothrombin consumption.
By DataStellar Co., Ltd
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Proto Oncogene Proteins c erbB 2
- cell surface protein-tyrosine kinase that is found to be overexpressed in significant number adenocarcinomas. It has extensive homology can heterodimerize EGF EPIDERMAL GROWTH FACTOR), 3 receptor (RECEPTOR, 3) and the 4 receptor. Activation of erbB-2 receptor occurs during heterodimer formation with a ligand-bound erbB family members. EC 2.7.11.-.