The role of creatine kinase in inhibition of mitochondrial permeability transition

[1]  P. Tittmann,et al.  Crystalline mitochondrial inclusion bodies isolated from creatine depleted rat soleus muscle. , 1997, Journal of cell science.

[2]  T. Wallimann,et al.  In vivo brain phosphocreatine and ATP regulation in mice fed a creatine analog. , 1997, The American journal of physiology.

[3]  A. Koretsky,et al.  Expression of functional mitochondrial creatine kinase in liver of transgenic mice. , 1997, The American journal of physiology.

[4]  V. Skulachev.  Why are mitochondria involved in apoptosis? Permeability transition pores and apoptosis as selective mechanisms to eliminate superoxide‐producing mitochondria and cell , 1996, FEBS letters.

[5]  W. Welte,et al.  Complexes between kinases, mitochondrial porin and adenylate translocator in rat brain resemble the permeability transition pore , 1996, FEBS letters.

[6]  Guido Kroemer,et al.  Mitochondria and programmed cell death: back to the future , 1996, FEBS letters.

[7]  G. Kroemer,et al.  Bcl-2 inhibits the mitochondrial release of an apoptogenic protease , 1996, The Journal of experimental medicine.

[8]  Theo Wallimann,et al.  Changes of creatine kinase structure upon ligand binding as seen by small-angle scattering☆ , 1996 .

[9]  T. Wallimann,et al.  Differential effects of creatine depletion on the regulation of enzyme activities and on creatine-stimulated mitochondrial respiration in skeletal muscle, heart, and brain. , 1996, Biochimica et biophysica acta.

[10]  B. Chance,et al.  Induction of endotoxin tolerance in transgenic mouse liver expressing creatine kinase , 1996, Hepatology.

[11]  D. Zorov,et al.  Mitochondrial damage as a source of diseases and aging: a strategy of how to fight these. , 1996, Biochimica et biophysica acta.

[12]  M. Klingenberg,et al.  Mitochondrial ADP/ATP carrier can be reversibly converted into a large channel by Ca2+. , 1996, Biochemistry.

[13]  A. Halestrap,et al.  Chaotropic agents and increased matrix volume enhance binding of mitochondrial cyclophilin to the inner mitochondrial membrane and sensitize the mitochondrial permeability transition to [Ca2+]. , 1996, Biochemistry.

[14]  G. Radda,et al.  The utilisation of creatine and its analogues by cytosolic and mitochondrial creatine kinase. , 1996, Biochimica et biophysica acta.

[15]  B. Chance,et al.  Energy metabolism and regeneration in transgenic mouse liver expressing creatine kinase after major hepatectomy. , 1996, Gastroenterology.

[16]  M. Zoratti,et al.  The mitochondrial permeability transition. , 1995, Biochimica et biophysica acta.

[17]  A. Halestrap,et al.  Recruitment of mitochondrial cyclophilin to the mitochondrial inner membrane under conditions of oxidative stress that enhance the opening of a calcium-sensitive non-specific channel. , 1994, The Biochemical journal.

[18]  M. Crompton,et al.  On the interactions of Ca2+ and cyclosporin A with a mitochondrial inner membrane pore: a study using cobaltammine complex inhibitors of the Ca2+ uniporter. , 1994, The Biochemical journal.

[19]  S. Houser,et al.  ENHANCEMENT OF THE RECOVERY OF RAT HEARTS AFTER PROLONGED COLD STORAGE BY CYCLOCREATINE PHOSPHATE1,2 , 1994, Transplantation.

[20]  V. Skulachev,et al.  Ion permeability induced in artificial membranes by the ATP/ADP antiporter , 1994, FEBS letters.

[21]  T. Wallimann,et al.  Kinetics of assembly and dissociation of the mitochondrial creatine kinase octamer. A fluorescence study. , 1993, Biochemistry.

[22]  A. Koretsky,et al.  Phosphocreatine protects transgenic mouse liver expressing creatine kinase from hypoxia and ischemia. , 1993, The American journal of physiology.

[23]  N. Takeyama,et al.  Oxidative damage to mitochondria is mediated by the Ca(2+)-dependent inner-membrane permeability transition. , 1993, The Biochemical journal.

[24]  A. Halestrap,et al.  Purification and N-terminal sequencing of peptidyl-prolyl cis-trans-isomerase from rat liver mitochondrial matrix reveals the existence of a distinct mitochondrial cyclophilin. , 1992, The Biochemical journal.

[25]  P. Bernardi.  Modulation of the mitochondrial cyclosporin A-sensitive permeability transition pore by the proton electrochemical gradient. Evidence that the pore can be opened by membrane depolarization. , 1992, The Journal of biological chemistry.

[26]  A. Koretsky,et al.  Phosphocreatine protects ATP from a fructose load in transgenic mouse liver expressing creatine kinase. , 1991, The American journal of physiology.

[27]  H. Eppenberger,et al.  Adult rat cardiomyocytes cultured in creatine-deficient medium display large mitochondria with paracrystalline inclusions, enriched for creatine kinase , 1991, The Journal of cell biology.

[28]  A. Koretsky,et al.  Free ADP levels in transgenic mouse liver expressing creatine kinase. Effects of enzyme activity, phosphagen type, and substrate concentration. , 1990, The Journal of biological chemistry.

[29]  V A Saks,et al.  Creatine kinase of rat heart mitochondria. The demonstration of functional coupling to oxidative phosphorylation in an inner membrane-matrix preparation. , 1985, The Journal of biological chemistry.

[30]  H. Eppenberger,et al.  Function of M-line-bound creatine kinase as intramyofibrillar ATP regenerator at the receiving end of the phosphorylcreatine shuttle in muscle. , 1984, The Journal of biological chemistry.

[31]  G. R. Griffiths,et al.  Accumulation of analgo of phosphocreatine in muscle of chicks fed 1-carboxymethyl-2-iminoimidazolidine (cyclocreatine). , 1976, The Journal of biological chemistry.

[32]  G. L. Kenyon,et al.  On the specificity of creatine kinase. New glycocyamines and glycocyamine analogs related to creatine. , 1971, Journal of the American Chemical Society.

[33]  J. Dickinson,et al.  Localization of Encephalitogenic Basic Protein in the Intraperiod Line of Lamellar Myelin , 1970, Nature.

[34]  U. K. Laemmli,et al.  Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4 , 1970, Nature.

[35]  M. Wyss,et al.  Intracellular compartmentation, structure and function of creatine kinase isoenzymes in tissues with high and fluctuating energy demands: the 'phosphocreatine circuit' for cellular energy homeostasis. , 1992, The Biochemical journal.