Rapid disuse and denervation atrophy involve transcriptional changes similar to those of muscle wasting during systemic diseases
暂无分享,去创建一个
A. Goldberg | R. Roy | V. Reggie Edgerton | A. Raffaello | S. Lecker | J. Sacheck | J. Hyatt | R. Thomas Jagoe
[1] Jiandie D. Lin,et al. PGC-1α protects skeletal muscle from atrophy by suppressing FoxO3 action and atrophy-specific gene transcription , 2006, Proceedings of the National Academy of Sciences.
[2] G. Lanfranchi,et al. Denervation in murine fast-twitch muscle: short-term physiological changes and temporal expression profiling. , 2006, Physiological genomics.
[3] D. Attaix,et al. Altered responses in skeletal muscle protein turnover during aging in anabolic and catabolic periods. , 2005, The international journal of biochemistry & cell biology.
[4] Wei Wei,et al. Novel aspects on the regulation of muscle wasting in sepsis. , 2005, The international journal of biochemistry & cell biology.
[5] Richard T. Lee,et al. Transgenic Overexpression of Locally Acting Insulin-Like Growth Factor-1 Inhibits Ubiquitin-Mediated Muscle Atrophy in Chronic Left-Ventricular Dysfunction , 2005, Circulation research.
[6] J. Babraj,et al. Selective activation of AMPK‐PGC‐1α or PKB‐TSC2‐mTOR signaling can explain specific adaptive responses to endurance or resistance training‐like electrical muscle stimulation , 2005, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
[7] P. Giresi,et al. Identification of a molecular signature of sarcopenia. , 2005, Physiological genomics.
[8] S. Powers,et al. Mechanisms of disuse muscle atrophy: role of oxidative stress. , 2005, American journal of physiology. Regulatory, integrative and comparative physiology.
[9] Hsin C. Lin,et al. Insulin-like Growth Factor-1 (IGF-1) Inversely Regulates Atrophy-induced Genes via the Phosphatidylinositol 3-Kinase/Akt/Mammalian Target of Rapamycin (PI3K/Akt/mTOR) Pathway* , 2005, Journal of Biological Chemistry.
[10] S. Tågerud,et al. Denervation‐induced alterations in gene expression in mouse skeletal muscle , 2005, The European journal of neuroscience.
[11] W. Frontera,et al. IKKβ/NF-κB Activation Causes Severe Muscle Wasting in Mice , 2004, Cell.
[12] A. Goldberg,et al. IGF-I stimulates muscle growth by suppressing protein breakdown and expression of atrophy-related ubiquitin ligases, atrogin-1 and MuRF1. , 2004, American journal of physiology. Endocrinology and metabolism.
[13] Hiroyuki Aburatani,et al. Skeletal Muscle FOXO1 (FKHR) Transgenic Mice Have Less Skeletal Muscle Mass, Down-regulated Type I (Slow Twitch/Red Muscle) Fiber Genes, and Impaired Glycemic Control*[boxs] , 2004, Journal of Biological Chemistry.
[14] K. Reue,et al. Lipin Expression Preceding Peroxisome Proliferator-activated Receptor-γ Is Critical for Adipogenesis in Vivo and in Vitro* , 2004, Journal of Biological Chemistry.
[15] G. Yancopoulos,et al. The IGF-1/PI3K/Akt pathway prevents expression of muscle atrophy-induced ubiquitin ligases by inhibiting FOXO transcription factors. , 2004, Molecular cell.
[16] Marco Sandri,et al. Foxo Transcription Factors Induce the Atrophy-Related Ubiquitin Ligase Atrogin-1 and Cause Skeletal Muscle Atrophy , 2004, Cell.
[17] A. Goldberg,et al. Multiple types of skeletal muscle atrophy involve a common program of changes in gene expression , 2004, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
[18] V. Edgerton,et al. Effects of a mild weight-lifting program on the progress of glucocorticoid-induced atrophy in rat hindlimb muscles , 1980, Pflügers Archiv.
[19] W. Kraus,et al. PGC-1alpha mRNA expression is influenced by metabolic perturbation in exercising human skeletal muscle. , 2004, Journal of applied physiology.
[20] W. Kraus,et al. PGC-1α mRNA expression is influenced by metabolic perturbation in exercising human skeletal muscle , 2004 .
[21] A. Russell,et al. Endurance training in humans leads to fiber type-specific increases in levels of peroxisome proliferator-activated receptor-gamma coactivator-1 and peroxisome proliferator-activated receptor-alpha in skeletal muscle. , 2003, Diabetes.
[22] Peyton Cook,et al. Accurate and statistically verified quantification of relative mRNA abundances using SYBR Green I and real-time RT-PCR. , 2003, Journal of immunological methods.
[23] V. Edgerton,et al. Nerve activity-independent regulation of skeletal muscle atrophy: role of MyoD and myogenin in satellite cells and myonuclei. , 2003, American journal of physiology. Cell physiology.
[24] P. Giresi,et al. Global analysis of gene expression patterns during disuse atrophy in rat skeletal muscle , 2003, The Journal of physiology.
[25] V. Edgerton,et al. Atrophy responses to muscle inactivity. I. Cellular markers of protein deficits. , 2003, Journal of applied physiology.
[26] P. Hasselgren,et al. Sepsis upregulates the gene expression of multiple ubiquitin ligases in skeletal muscle. , 2003, The international journal of biochemistry & cell biology.
[27] E. Hoffman,et al. Patterns of global gene expression in rat skeletal muscle during unloading and low-intensity ambulatory activity. , 2003, Physiological genomics.
[28] K. Ogawa,et al. Regulation of TG-interacting factor by transforming growth factor-beta. , 2003, The Biochemical journal.
[29] R. Paules,et al. An integrated stress response regulates amino acid metabolism and resistance to oxidative stress. , 2003, Molecular cell.
[30] M. Caligiuri,et al. Tumor Necrosis Factor-regulated Biphasic Activation of NF-κB Is Required for Cytokine-induced Loss of Skeletal Muscle Gene Products* , 2002, The Journal of Biological Chemistry.
[31] V. Edgerton,et al. Atrophy responses to muscle inactivity. II. Molecular markers of protein deficits. , 2003, Journal of applied physiology.
[32] L. Nolte,et al. Adaptations of skeletal muscle to exercise: rapid increase in the transcriptional coactivator PGC‐1 , 2002, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
[33] D. Maclennan,et al. Sarcolipin Overexpression in Rat Slow Twitch Muscle Inhibits Sarcoplasmic Reticulum Ca2+ Uptake and Impairs Contractile Function* , 2002, The Journal of Biological Chemistry.
[34] A. Goldberg,et al. Patterns of gene expression in atrophying skeletal muscles: response to food deprivation , 2002, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
[35] G. Taylor,et al. P311 induces a TGF-beta1-independent, nonfibrogenic myofibroblast phenotype. , 2002, The Journal of clinical investigation.
[36] Hui Zhong,et al. Mechanical properties of the electrically silent adult rat soleus muscle , 2002, Muscle & nerve.
[37] Jiandie D. Lin,et al. Transcriptional co-activator PGC-1α drives the formation of slow-twitch muscle fibres , 2002, Nature.
[38] S. Kandarian,et al. Activation of an alternative NF‐ΚB pathway in skeletal muscle during disuse atrophy , 2002, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
[39] Jiandie D. Lin,et al. Transcriptional co-activator PGC-1 alpha drives the formation of slow-twitch muscle fibres. , 2002, Nature.
[40] A. Goldberg,et al. Atrogin-1, a muscle-specific F-box protein highly expressed during muscle atrophy , 2001, Proceedings of the National Academy of Sciences of the United States of America.
[41] D J Glass,et al. Identification of Ubiquitin Ligases Required for Skeletal Muscle Atrophy , 2001, Science.
[42] Yi-Ping Li,et al. Tumor necrosis factor-α and muscle wasting: a cellular perspective , 2001, Respiratory research.
[43] J. Frystyk,et al. Liver-specific igf-1 gene deletion leads to muscle insulin insensitivity. , 2001, Diabetes.
[44] M. Pfaffl,et al. A new mathematical model for relative quantification in real-time RT-PCR. , 2001, Nucleic acids research.
[45] V. Edgerton,et al. Temporal effects of inactivty on myosin heavy chain gene expression in rat slow muscle , 2001, Muscle & nerve.
[46] Yudong D. He,et al. Functional Discovery via a Compendium of Expression Profiles , 2000, Cell.
[47] V. Edgerton,et al. Persistence of myosin heavy chain‐based fiber types in innervated but silenced rat fast muscle , 2000, Muscle & nerve.
[48] Simpkins Co,et al. Metallothionein in human disease. , 2000 .
[49] T. Pritts,et al. The gene expression of ubiquitin ligase E3alpha is upregulated in skeletal muscle during sepsis in rats-potential role of glucocorticoids. , 2000, Biochemical and biophysical research communications.
[50] C. Simpkins. Metallothionein in human disease. , 2000, Cellular and molecular biology.
[51] A. Goldberg,et al. Ubiquitin conjugation by the N-end rule pathway and mRNAs for its components increase in muscles of diabetic rats. , 1999, The Journal of clinical investigation.
[52] J. Weiner,et al. Novel Dendritic Kinesin Sorting Identified by Different Process Targeting of Two Related Kinesins: KIF21A and KIF21B , 1999, The Journal of cell biology.
[53] P. Hasselgren. Glucocorticoids and muscle catabolism. , 1999, Current opinion in clinical nutrition and metabolic care.
[54] Claudine Jurkovitz,et al. Evaluation of signals activating ubiquitin-proteasome proteolysis in a model of muscle wasting. , 1999, American journal of physiology. Cell physiology.
[55] R. Palmiter. The elusive function of metallothioneins. , 1998, Proceedings of the National Academy of Sciences of the United States of America.
[56] L. Baum,et al. Galectins: versatile modulators of cell adhesion, cell proliferation, and cell death , 1998, Journal of Molecular Medicine.
[57] V. Edgerton,et al. Effects of inactivity on myosin heavy chain composition and size of rat soleus fibers , 1998, Muscle & nerve.
[58] A. Goldberg,et al. Inhibitors of the proteasome reduce the accelerated proteolysis in atrophying rat skeletal muscles. , 1997, The Journal of clinical investigation.
[59] F. Haddad,et al. The relationships among IGF-1, DNA content, and protein accumulation during skeletal muscle hypertrophy. , 1996, Journal of applied physiology.
[60] A. Goldberg,et al. Importance of the ATP-Ubiquitin-Proteasome Pathway in the Degradation of Soluble and Myofibrillar Proteins in Rabbit Muscle Extracts* , 1996, The Journal of Biological Chemistry.
[61] L. Phillips,et al. Muscle wasting in insulinopenic rats results from activation of the ATP-dependent, ubiquitin-proteasome proteolytic pathway by a mechanism including gene transcription. , 1996, The Journal of clinical investigation.
[62] V. Preedy,et al. The effect of endotoxin on skeletal muscle protein gene expression in the rat. , 1996, The international journal of biochemistry & cell biology.
[63] W. Mitch,et al. The acidosis of chronic renal failure activates muscle proteolysis in rats by augmenting transcription of genes encoding proteins of the ATP-dependent ubiquitin-proteasome pathway. , 1996, The Journal of clinical investigation.
[64] S. Price,et al. Necessary but not sufficient: the role of glucocorticoids in the acidosis-induced increase in levels of mRNAs encoding proteins of the ATP-dependent proteolytic pathway in rat muscle. , 1996, Mineral and electrolyte metabolism.
[65] L. Henderson,et al. Adaptation of nicotinic acetylcholine receptor, myogenin, and MRF4 gene expression to long-term muscle denervation , 1995, The Journal of cell biology.
[66] A. Goldberg,et al. Activation of the ATP-ubiquitin-proteasome pathway in skeletal muscle of cachectic rats bearing a hepatoma. , 1995, The American journal of physiology.
[67] A. Goldberg,et al. Increase in ubiquitin-protein conjugates concomitant with the increase in proteolysis in rat skeletal muscle during starvation and atrophy denervation. , 1995, The Biochemical journal.
[68] A. Goldberg,et al. Increase in levels of polyubiquitin and proteasome mRNA in skeletal muscle during starvation and denervation atrophy. , 1995, The Biochemical journal.
[69] A. Riggs,et al. Genomic Sequencing , 2010 .
[70] Y. Itokawa,et al. Trace element movement and oxidative stress in skeletal muscle atrophied by immobilization. , 1992, The American journal of physiology.
[71] Hao-ming Shen. Spherical reflector as an electromagnetic‐missile launcher , 1990 .
[72] P. Chase,et al. Different mechanisms of increased proteolysis in atrophy induced by denervation or unweighting of rat soleus muscle. , 1990, Metabolism: clinical and experimental.
[73] A. Goldberg,et al. Role of different proteolytic systems in the degradation of muscle proteins during denervation atrophy. , 1990, The Journal of biological chemistry.
[74] F. Booth,et al. Atrophy of the soleus muscle by hindlimb unweighting. , 1990, Journal of applied physiology.
[75] F. Booth,et al. Protein metabolism and beta-myosin heavy-chain mRNA in unweighted soleus muscle. , 1989, The American journal of physiology.
[76] S. Jaspers,et al. Role of glucocorticoids in the response of rat leg muscles to reduced activity , 1986, Muscle & nerve.
[77] J. Sanes,et al. Denervation supersensitivity in skeletal muscle: analysis with a cloned cDNA probe , 1984, The Journal of cell biology.
[78] N. Robbins,et al. Cell proliferation in denervated muscle: Identity and origin of dividing cells , 1982, Neuroscience.
[79] D. DuBois,et al. A possible role for glucocorticoids in denervation atrophy , 1981, Muscle & nerve.
[80] A. Goldberg,et al. Effects of food deprivation on protein synthesis and degradation in rat skeletal muscles. , 1976, The American journal of physiology.
[81] A. Goldberg. Protein turnover in skeletal muscle. II. Effects of denervation and cortisone on protein catabolism in skeletal muscle. , 1969, The Journal of biological chemistry.
[82] S. S. Tower,et al. Function and structure in the chronically isolated lumbo‐sacral spinal cord of the dog , 1937 .