Publications by: Mridula Sharma

Also publishes as (M. Sharma)

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Number of items: 25.

Peker, Nesibe, Donipadi, Vinay, Sharma, Mridula, McFarlane, Craig, and Kambadur, Ravi (2018) Loss of Parkin impairs mitochondrial function and leads to muscle atrophy. American Journal of Physiology: cell physiology, 315 (2). C164-C185.

Musarrat, Maisha Reza, Subramaniyam, Nathiya, Sim, Chu Ming, Ge, Xiaojia, Sathiakumar, Durgalakshmi, McFarlane, Craig, Sharma, Mridula, and Kambadur, Ravi (2017) Irisin is a pro-myogenic factor that induces skeletal muscle hypertrophy and rescues denervation-induced atrophy. Nature Communications, 8. 1104.

Reza, Musarrat Maisha, Sim, Chu Ming, Subramaniyam, Nathiya, Ge, Xiaojia, Sharma, Mridula, Kambadur, Ravi, and McFarlane, Craig (2017) Irisin treatment improves healing of dystrophic skeletal muscle. Oncotarget, 8. pp. 98553-98566.

Chandrashekar, Preeti, Manickam, Ravikumar, Ge, Xiaojia, Bonala, Sabeera, McFarlane, Craig, Sharma, Mridula, Wahli, Walter, and Kambadur, Ravi (2015) Inactivation of PPARβ/δ adversely affects satellite cells and reduces postnatal myogenesis. American Journal of Physiology-Endocrinology and Metabolism, 309. E122-E131.

Sharma, Mridula, McFarlane, Craig, Kambador, Ravi, Kukreti, Himani, Bonala, Sabeera, and Srinivasan, Shruti (2015) Myostatin: expanding horizons. IUBMB Life, 67 (8). pp. 589-600.

Shenoy P., Sudheer, Bose, Bipasha, Sharma, Mridula, McFarlane, Craig, and Kambadur, Ravi (2014) Lack of Myostatin reduces MyoD induced myogenic potential of primary muscle fibroblasts. Journal of Cellular Biochemistry, 115 (11). pp. 1908-1917.

Sharma, Mridula, Juvvuna, Prasanna Kumar, Kukreti, Himani, and McFarlane, Craig (2014) Mega roles of microRNAs in regulation of skeletal muscle health and disease. Frontiers in Physiology, 5. 239.

Sharma, Mridula, Kambadur, Ravi, Sriram, Sandhya, Lokireddy, Sudarsanareddy, and McFarlane, Craig (2014) Molecular targets of cancer cachexia: opportunities for pharmanutritional approaches. PharmaNutrition, 2 (3). pp. 126-128.

Sriram, Sandhya, Subramanian, Subha, Juvvuna, Prasanna Kumar, Ge, Xiaojia, Lokireddy, Sudarsanareddy, McFarlane, Craig Desmond, Wahli, Walter, Kambadur, Ravi, and Sharma, Mridula (2014) Myostatin augments muscle-specific ring finger protein-1 expression through an NF-kB independent mechanism in SMAD3 null muscle. Molecular Endocrinology, 28 (3). pp. 317-330.

McFarlane, Craig, Vajjala, Anuradha, Arigela, Harikumar, Lokireddy, Sudarsanareddy, Ge, Xiaojia, Bonala, Sabeera, Manickam, Ravikumar, Kambadur, Ravi, and Sharma, Mridula (2014) Negative auto-regulation of myostatin expression is mediated by Smad3 and MicroRNA-27. PLoS ONE, 9 (1). e87687. e87687.

Kukreti, Himani, Amuthavalli, Kottaiswamy, Harikumar, Arigela, Sathiyamoorthy, Sushmitha, Feng, Peng Zhao, Anantharaj, Rengaraj, Tan, Suan Liang Kelvin, Lokireddy, Sudarsanareddy, Bonala, Sabeera, Sriram, Sandhya, McFarlane, Craig, Kambadur, Ravi, and Sharma, Mridula (2013) Muscle-specific microRNA1 (miR1) targets heat shock protein 70 (HSP70) during dexamethasone-mediated atrophy. Journal of Biological Chemistry, 288 (9). pp. 6663-6678.

Lokireddy, Sudarsanareddy, Wijesoma, Isuru Wijerupage, Sze, Siu Kwan, McFarlane, Craig, Kambadur, Ravi, and Sharma, Mridula (2012) Identification of atrogin-1-targeted proteins during the myostatin-induced skeletal muscle wasting. American Journal of Physiology: cell physiology, 303 (5). C512-C529.

Ge, Xiaojia, Vajjala, Anuradha, McFarlane, Craig, Wahli, Walter, Sharma, Mridula, and Kambadur, Ravi (2012) Lack of Smad3 signaling leads to impaired skeletal muscle regeneration. American Journal of Physiology-Endocrinology and Metabolism, 303. E90-E102.

Zhang, Chen, Tan, Chek Kun, McFarlane, Craig, Sharma, Mridula, Tan, Nguan Soon, and Kambadur, Ravi (2012) Myostatin-null mice exhibit delayed skin wound healing through the blockade of transforming growth factor-β signaling by decorin. American Journal of Physiology: cell physiology, 302. C1213-C1225.

McFarlane, Craig, Hui, Gu Zi, Amanda, Wong Zhi Wei, Lau, Hiu Yeung, Lokireddy, Sudarsanareddy, Ge, Xiaojia, Mouly, Vincent, Butler-Browne, Gillian, Gluckman, Peter, Sharma, Mridula, and Kambadur, Ravi (2011) Human myostatin negatively regulates human myoblast growth and differentiation. American Journal of Physiology: cell physiology, 301 (1). C195-C203.

Sriram, Sandhya, Subramanian, Subha, Sathiakumar, Durga, Venkatesh, Rithika, Salerno, Monica S., McFarlane, Craig, Kambadur, Ravi, and Sharma, Mridula (2011) Modulation of reactive oxygen species in skeletal muscle by myostatin is mediated through NF-κB. Aging Cell, 10 (6). pp. 931-948.

Lokireddy, Sudarsanareddy, Mouly, Vincent, Butler-Browne, Gillian, Gluckman, Peter D., Sharma, Mridula, Kambadur, Ravi, and McFarlane, Craig (2011) Myostatin promotes the wasting of human myoblast cultures through promoting ubiquitin-proteasome pathway-mediated loss of sarcomeric proteins. American Journal of Physiology: cell physiology, 301 (6). C1316-C1324.

Zhang, C., McFarlane, C., Lokireddy, S., Bonala, S., Ge, X., Masuda, S., Gluckman, P.D., Sharma, M., and Kambadur, R. (2011) Myostatin-deficient mice exhibit reduced insulin resistance through activating the AMP-activated protein kinase signalling pathway. Diabetologia, 54 (6). pp. 1491-1501.

Ge, Xiaojia, McFarlane, Craig, Vajjala, Anuradha, Lokireddy, Sudarsanareddy, Ng, Zhi Hui, Tan, Chek Kun, Tan, Nguan Soon, Wahli, Walter, Sharma, Mridula, and Kambadur, Ravi (2011) Smad3 signaling is required for satellite cell function and myogenic differentiation of myoblasts. Cell Research, 21. pp. 1591-1604.

McFarlane, Craig, Sharma, Mridula, and Kambadur, Ravi (2010) Role of myostatin in skeletal muscle growth and cevelopment: implications for sarcopenia. In: Lynch, Gordon S., (ed.) Sarcopenia - Age-Related Muscle Wasting and Weakness: mechanisms and treatments. Springer, London, UK, pp. 419-447.

McFarlane, Craig, Sharma, Mridula, and Kambadur, Ravi (2008) Myostatin is a procachectic growth factor during postnatal myogenesis. Current Opinion in Clinical Nutrition and Metabolic Care, 11 (4). pp. 422-427.

McFarlane, Craig, Hennebry, Alex, Thomas, Mark, Plummer, Erin, Ling, Nicholas, Sharma, Mridula, and Kambadur, Ravi (2008) Myostatin signals through Pax7 to regulate satellite cell self-renewal. Experimental Cell Research, 314 (2). pp. 317-329.

McFarlane, Craig McFarlane, Plummer, Erin, Thomas, Mark, Hennebry, Alex, Ashby, Murray, Ling, Nicholas, Smith, Heather, Sharma, Mridula, and Kambadur, Ravi (2006) Myostatin induces cachexia by activating the ubiquitin proteolytic system through an NF-κB-independent, FoxO1-dependent mechanism. Journal of Cellular Physiology, 209 (2). pp. 501-514.

McFarlane, Craig, Langley, Brett, Thomas, Mark, Hennebry, Alex, Plummer, Erin, Nicholas, Gina, McMahon, Chris, Sharma, Mridula, and Kambadur, Ravi (2005) Proteolytic processing of myostatin is auto-regulated during myogenesis. Developmental Biology, 283 (1). pp. 58-69.

Langley, Brett, Thomas, Mark, McFarlane, Craig, Gilmour, Stewart, Sharma, Mridula, and Kambadur, Ravi (2004) Myostatin inhibits rhabdomyosarcoma cell proliferation through an Rb-independent pathway. Oncogene, 23. pp. 524-534.

This list was generated on Wed Dec 25 04:56:52 2024 AEST.