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TNNI1 encodes a protein that is a subunit of troponin, which is a regulatory complex located on the thin filament of the sarcomere. 再加上，我们可以发TNNI1 抗体 (61) 和 TNNI1 蛋白 (14)和数多这个蛋白质的别的产品。
Showing 8 out of 47 products:
Human TNNI1 ELISA Kit for Sandwich ELISA - ABIN418922
King, Abreu, Cheng, Chertoff, Brotto, Kelly, Brotto: A multimodal assessment of balance in elderly and young adults. in Oncotarget 2016
High TNNT1 expression is associated with breast cancer.
This study describes the first TNNT1 mutation that transmits in an autosomal dominant fashion to cause nemaline myopathy.
investigated the effects of one of these mutations, K247R of TnT, on the picosecond dynamics of the Tn core domain (Tn-CD), consisting of TnC (显示 TNC ELISA试剂盒), TnI (显示 TNNI2 ELISA试剂盒) and TnT2 (183-288 residues of TnT), by carrying out the quasielastic neutron scattering measurements on the reconstituted Tn-CD containing either the wild-type TnT2 (wtTn-CD) or the mutant TnT2 (K247R-Tn-CD) in the absence and presence of Ca(2 (显示 CA2 ELISA试剂盒)+)
Data suggest that mutations in troponin C (TnC, A8V) and troponin T (TnT, delta14-TnT) found in patients with hypertrophic cardiomyopathy together fully stabilize the active M state of regulated actin (the actin-tropomyosin-troponin complex).
pathogenesis of TNNT1 myopathies
Copeptin (显示 AVP ELISA试剂盒) and troponin T measurement could potentially improve the prehospital diagnostic and prognostic classification of patients with a suspected AMI (显示 CFD ELISA试剂盒).
TNNT1 genetic and epigenetic variations are associated with HDL (显示 HSD11B1 ELISA试剂盒)-C levels and coronary artery disease.
Three homologous genes have evolved in vertebrates to encode three muscle type-specific TnT isoforms: TNNT1 for slow skeletal muscle TnT, TNNT2 for cardiac muscle TnT, and TNNT3 for fast skeletal muscle TnT.
Nemaline body myopathy Palestinian patients were found to have a novel mutation in troponin T1.
troponin T and creatinine kinase isoenzyme (CK-MB) have roles in combined renal and myocardial injuries in asphyxiated infants
Mouse tumor endothelial cells express troponin T.
demonstrated that ssTnT deficiency resulted in significantly decreased levels of other slow fibre-specific myofilament proteins whereas fast fibre-specific myofilament proteins were increased correspondingly
the induction of Tnnt1 gene expression in adult mouse brains by ketamine may illustrate the genes involved in the metabolic syndromes observed in neuropsychiatric disorders
Data show that cardiac expression of slow skeletal troponin T (Tnnt1) strictly depends on the physical interaction between GATA4-FOG2 in the myocardium of both atria and ventricles.
This gene encodes a protein that is a subunit of troponin, which is a regulatory complex located on the thin filament of the sarcomere. This complex regulates striated muscle contraction in response to fluctuations in intracellular calcium concentration. This complex is composed of three subunits: troponin C, which binds calcium, troponin T, which binds tropomyosin, and troponin I, which is an inhibitory subunit. This protein is the slow skeletal troponin T subunit. Mutations in this gene cause nemaline myopathy type 5, also known as Amish nemaline myopathy, a neuromuscular disorder characterized by muscle weakness and rod-shaped, or nemaline, inclusions in skeletal muscle fibers which affects infants, resulting in death due to respiratory insufficiency, usually in the second year. Multiple transcript variants encoding different isoforms have been found for this gene.
nemaline myopathy type 5
, slow skeletal muscle troponin T
, troponin T, slow skeletal muscle
, troponin-T1, skeletal, slow
, troponin I, skeletal, slow
, troponin I type 1 (skeletal, slow)
, troponin I, skeletal, slow 1
, troponin T1, skeletal, slow
, troponin T slow type isoform sTnT1
, skeletal muscle slow-twitch TnT