Mechanical effects of human cardiac troponin C mutation Gly159Asp in exchanged rabbit psoas fibres

Mechanical effects of human cardiac troponin C mutation Gly159Asp in exchanged rabbit psoas fibres

التفاصيل البيبلوغرافية
المؤلفون الرئيسيون:	Preston, L, Lipscomb, S, Robinson, P, Watkins, H, Redwood, C, Mogensen, J, Ashley, C
التنسيق:	Conference item
منشور في:	2004

مواد مشابهة

Functional effects of the DCM mutant Gly159Asp troponin C in skinned muscle fibres.
حسب: Preston, L, وآخرون
منشور في: (2007)

DCM troponin C mutant Gly159Asp blunts the response to troponin phosphorylation.
حسب: Preston, L, وآخرون
منشور في: (2007)

Mutations in fast skeletal troponin I, troponin T, and beta-tropomyosin that cause distal arthrogryposis all increase contractile function.
حسب: Robinson, P, وآخرون
منشور في: (2007)

A revised method of troponin exchange in permeabilised cardiac trabeculae using vanadate: functional consequences of a HCM-causing mutation in troponin I.
حسب: Preston, L, وآخرون
منشور في: (2006)

Effects of hypertrophic cardiomyopathy mutations in troponin I on contractility of skinned cardiac muscle fibres
حسب: Burton, D, وآخرون
منشور في: (2002)

Effects of troponin C isoform on the action of the cardiotonic agent EMD 57033.
حسب: Lipscomb, S, وآخرون
منشور في: (2005)

Effect of hypertrophic cardiomyopathy mutations in human cardiac muscle alpha -tropomyosin (Asp175Asn and Glu180Gly) on the regulatory properties of human cardiac troponin determined by in vitro motility assay.
حسب: Bing, W, وآخرون
منشور في: (2000)

Dilated cardiomyopathy causing mutations in cardiac troponin T (TNT), cardiac troponin C (TNC), and alpha tropomyosin (TM) reduce CA(2+) sensitivity and maximum calcium activation
حسب: Redwood, C, وآخرون
منشور في: (2004)

Structure-function relationships of eight mutations in troponin and tropomyosin that cause dilated cardiomyopathy
حسب: Mirza, M, وآخرون
منشور في: (2004)

The effect of HCM mutations in troponin T and troponin I on the calcium binding of human cardiac troponin
حسب: Redwood, C, وآخرون
منشور في: (2001)

Using fluorescence emission spectroscopy to asses the Ca2+ affinity of reconstituted troponin and thin filaments containing cardiomyopathy causing mutations of troponin and alpha-tropomyosin
حسب: Robinson, P, وآخرون
منشور في: (2007)

CD14 C-159T and toll-like receptor 4 Asp299Gly polymorphisms in surviving meningococcal disease patients.
حسب: Ariane Biebl, وآخرون
منشور في: (2009-10-01)

The effect of the Asp175Asn and Glu180Gly TPM1 mutations on actin-myosin interaction during the ATPase cycle.
حسب: Rysev, N, وآخرون
منشور في: (2012)

Hypertrophic and dilated cardiomyopathycausing mutations of troponin and alpha-tropomyosin have opposite effects on thin filament calcium binding
حسب: Robinson, P, وآخرون
منشور في: (2007)

Investigating the Effect of Cardiomyopathy-Causing Mutations in Cardiac Troponin-T on Calcium Buffering In Situ
حسب: Robinson, P, وآخرون
منشور في: (2010)

Functional effects of mutations in troponin T and tropomyosin which cause dilated cardiomyopathy
حسب: Robinson, P, وآخرون
منشور في: (2003)

Altered inhibitory and troponin C-binding activities in cardiac troponin I mutants known to cause hypertrophic cardiomyopathy
حسب: Elliott, K, وآخرون
منشور في: (2000)

Mutations in fast skeletal troponin I, troponin T and beta-tropomyosin that cause distal arthrogryposis all enhance thin filament activation
حسب: Robinson, P, وآخرون
منشور في: (2005)

Dilated and hypertrophic cardiomyopathy mutations in troponin and alpha-tropomyosin have opposing effects on the calcium affinity of cardiac thin filaments.
حسب: Robinson, P, وآخرون
منشور في: (2007)

Severe disease expression of cardiac troponin C and T mutations in patients with idiopathic dilated cardiomyopathy.
حسب: Mogensen, J, وآخرون
منشور في: (2004)

Comparison of the functional effects of mutations in troponin T which cause dilated and hypertrophic cardiomyopathies
حسب: Robinson, P, وآخرون
منشور في: (2002)

Two mutations in human cardiac troponin I known to cause hypertrophic cardiomyopathy have different effects on cardiac muscle contraction
حسب: Burton, D, وآخرون
منشور في: (2000)

Investigation of troponin I mutations causing familial hypertrophic cardiomyopathy
حسب: Abdulrazzak, H, وآخرون
منشور في: (2001)

Bisphosphonate-functionalized cyclic Arg-Gly-Asp peptidomimetics
حسب: Carmelo Drago, وآخرون
منشور في: (2012-10-01)

Hypertrophic cardiomyopathy-causing Asp175asn and Glu180gly Tpm1 mutations shift tropomyosin strands further towards the open position during the ATPase cycle
حسب: Borovikov, Y, وآخرون
منشور في: (2011)

Hypertrophic cardiomyopathy-causing Asp175asn and Glu180gly Tpm1 mutations shift tropomyosin strands further towards the open position during the ATPase cycle.
حسب: Borovikov, Y, وآخرون
منشور في: (2011)

Tethering of Gly-Arg-Gly-Asp-Ser-Pro-Lys Peptides on Mg-Doped Hydroxyapatite
حسب: Alessandro Pistone, وآخرون
منشور في: (2017-02-01)

Two mutations in troponin I that cause hypertrophic cardiomyopathy have contrasting effects on cardiac muscle contractility.
حسب: Burton, D, وآخرون
منشور في: (2002)

Altered regulatory properties of human cardiac troponin I mutants that cause hypertrophic cardiomyopathy.
حسب: Elliott, K, وآخرون
منشور في: (2000)

Characterizations and molecular docking mechanism of the interactions between peptide FDGDF (Phe-Asp-Gly-Asp-Phe) and SOD enzyme
حسب: C.H.E.N. Wen-Tao, وآخرون
منشور في: (2024-01-01)

A troponin I mutant known to cause hypertrophic cardiomyopathy shows reduced inhibition of Ca2+ independent tension
حسب: Burton, D, وآخرون
منشور في: (2000)

Identification and functional analysis of cardiac troponin I as a novel disease gene in autosomal dominant familial dilated cardiomyopathy
حسب: Carballo, S, وآخرون
منشور في: (2006)

Alterations in thin filament regulation induced by a human cardiac troponin T mutant that causes dilated cardiomyopathy are distinct from those induced by troponin T mutants that cause hypertrophic cardiomyopathy.
حسب: Robinson, P, وآخرون
منشور في: (2002)

Cardiac troponin I is a potential novel substrate for AMP-activated protein kinase
حسب: Oliveira, S, وآخرون
منشور في: (2007)

An Asp7Gly substitution in PPARG is associated with decreased transcriptional activation activity.
حسب: Liushuai Hua, وآخرون
منشور في: (2014-01-01)

Effect of mutation Arg91Gly on the thermal stability of β-tropomyosin
حسب: Nevzorov, I, وآخرون
منشور في: (2008)

Histomorphometry of Ossification in Functionalised Ceramics with Tripeptide Arg-Gly-Asp (RGD): An In Vivo Study
حسب: Filippo Migliorini, وآخرون
منشور في: (2022-05-01)

A single amino acid (Asp159) from the dog prion protein suppresses the toxicity of the mouse prion protein in Drosophila
حسب: J. Sanchez-Garcia, وآخرون
منشور في: (2016-11-01)

Association of IRS1 (Gly972Arg) and IRS2 (Gly1057Asp) genes polymorphisms with OSA and NAFLD in Asian Indians.
حسب: Surya Prakash Bhatt, وآخرون
منشور في: (2021-01-01)

CDH1 ASP187GLY MUTATION IMPAIRS APC/C ACTIVITY LEADING TO PFKFB3 STABILIZATION
حسب: Leticia Sancha, وآخرون
منشور في: (2023-10-01)