OXIDATIVE PHOSPHORYLATION DEFICIENCY
\ˈɒksɪdətˌɪv fˌɒsfɔːɹɪlˈe͡ɪʃən dɪfˈɪʃənsi], \ˈɒksɪdətˌɪv fˌɒsfɔːɹɪlˈeɪʃən dɪfˈɪʃənsi], \ˈɒ_k_s_ɪ_d_ə_t_ˌɪ_v f_ˌɒ_s_f_ɔː_ɹ_ɪ_l_ˈeɪ_ʃ_ə_n d_ɪ_f_ˈɪ_ʃ_ə_n_s_i]\
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Diseases caused by abnormal function of the MITOCHONDRIA. They may be caused by mutations, acquired or inherited, in mitochondrial DNA or in nuclear genes that code for mitochondrial components. They may also be the result of acquired mitochondria dysfunction due to adverse effects of drugs, infections, or other environmental causes.
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.-.
Nearby Words
- oxidative
- oxidative burst
- oxidative bursts
- oxidative phosphorylation
- oxidative phosphorylation deficiencies
- Oxidative Phosphorylation Deficiency
- oxidative phosphorylations
- oxidative stress
- oxidative stresses
- oxidator
- oxide