A

Antony, H., Wiegmans, A.P., Wei, M.Q., Chernoff, Y.O., Khanna, K.K., and Munn, A.L. (2012) Potential roles for prions and protein-only inheritance in cancer. Cancer and Metastasis Reviews, 31 (1-2). pp. 1-19.

Abu-Daya, Anita, Steer, Wendy M., Trollope, Alexandra F., Friedeberg, Christine E., Patient, Roger K., Thorne, Alan W., and Guille, Matthew J. (2005) Zygotic nucleosome assembly protein-like 1 has a specific, non-cell autonomous role in hematopoiesis. Blood, 106 (2). pp. 514-520.

C

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.

Caine, Jo, Sankovich, Sonia, Antony, Helma, Waddington, Lynne, Macreadie, Peter, Varghese, Jose, and Macreadie, Ian (2007) Alzheimer's Aβ fused to green fluorescent protein induces growth stress and a heat shock response. FEMS Yeast Research, 7 (8). pp. 1230-1236.

E

Eguether, Thibaut, San Agustin, Jovenal T., Keady, Brian T., Jonassen, Julie A., Liang, Yinwen, Francis, Richard, Tobita, Kimimasa, Johnson, Colin A., Abdelhamed, Zakia A., Lo, Cecilia W., and Pazour, Gregory J. (2014) IFT27 links the BBSome to IFT for maintenance of the ciliary signaling compartment. Developmental Cell, 31 (3). pp. 279-290.

G

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.

Gutirrèz-Mecinas, María, Trollope, Alexandra F., Collins, Andrew, Morfett, Hazel, Hesketh, Shirley A., Kersanté, Flavie, and Reul, Johannes M.H.M. (2011) Long-lasting behavioral responses to stress involve a direct interaction of glucocorticoid receptors with ERK1/2–MSK1–Elk-1 signaling. Proceedings of the National Academy of Sciences of the United States of America, 108 (33). pp. 13806-13811.

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.

H

Heimann, Kirsten (2013) Algal cell biology: important tools to understand metal and herbicide toxicity. In: Heimann, Kirsten, and Katsaros, Christos, (eds.) Advances in Algal Cell Biology. Marine and Freshwater Botany . Walter de Gruyter, Berlin, Germany, pp. 191-210.

Hotokezaka, Hitoshi, Sakai, Eiko, Ohara, Naoya, Hotokezaka, Yuka, Gonzales, Carmen, Matsuo, Ken-ichiro, Fujimura, Yuji, Yoshida, Noriaki, and Nakayama, Koji (2007) Molecular analysis of RANKL-independent cell fusion of osteoclast-like cells Induced by TNF-α, lipopolysaccharide, or peptidoglycan. Journal of Cellular Biochemistry, 101 (1). pp. 122-134.

K

Khoo, Chin Meng, Leow, Melvin Khee-Shing, Sadananthan, Suresh Arnand, Lim, Radiance, Venkataraman, Kavita, Khoo, Eric Yin Hao, Velan, S. Sendhil, Ong, Yu Ting, Kambadur, Ravi, McFarlane, Craig, Gluckman, Peter D., Lee, Yung Seng, Chong, Yap Seng, and Tai, E. Shyong (2014) Body fat partitioning does not explain the interethnic variation in insulin sensitivity among Asian ethnicity: the Singapore adults metabolism study. Diabetes, 63. pp. 1093-1102.

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.

L

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.

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.

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.

M

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.

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.

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.

Mollah, Zia U.A., Pai, Saparna, Moore, Craig, O'Sullivan, Brendan J., Harrison, Matthew J., Peng, Judy, Phillips, Karen, Prins, Johannes B., Cardinal, John, and Thomas, Ramjeny (2008) Abnormal NF-κB function characterizes human type 1 diabetes dendritic cells and monocytes. The Journal of Immunology, 180 (5). pp. 3166-3175.

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.

O

O’Sullivan, Brendan J., Pai, Saparna, Street, Shayna, An, Xiayou, MacDonald, Kelli P.A., Wong, Michele, Strutton, Geoffrey, Gerondakis, Steve, Steptoe, Raymond J., Fazekas de St. Groth, Barbara, Hill, Geoffrey R., and Thomas, Ranjeny (2011) Immunotherapy with costimulatory dendritic cells to control autoimmune inflammation. Journal of Immunology, 187 (8). pp. 4018-4030.

O'Sullivan, B.J., Thomas, H.E., Pai, S., Santamaria, P., Iwakura, Y., Steptoe, R.J., Kay, T.W.H., and Thomas, R. (2006) IL-1 breaks tolerance through expansion of CD25+ effector T cells. The Journal of Immunology, 176 (12). pp. 7278-7287.

P

Pai, Saparna, and Thomas, R. (2008) Dendritic cells. In: Hochberg, Marc, Silman, Alan, Smolen, Josef, Weinblatt, Michael, and Weisman, Michael, (eds.) Rheumatoid Arthritis. Mosby, Philadelphia, USA, pp. 116-123.

Pai, Saparna, and Thomas, Ranjeny (2008) Dentritic cells. In: Hochberg, Mark, Silman, Alan, Smolen, Josef, Weinblatt, Michael, and Weisman, Michael, (eds.) Rheumatoid Arthritis. Elsevier, Philadelphia, USA, pp. 116-123.

Pai, Saparna, and Thomas, Ranjeny (2008) Immune deficiency or hyperactivity-Nf-κb illuminates autoimmunity. Journal of Autoimmunity, 31 (3). pp. 245-251.

Pai, Saparna, O'Sullivan, Brendan, Abdul-Jabbar, Ibtissam, Peng, Judy, Connoly, Geoff, Khanna, Rajiv, Thomas, Ranjeny, and thomas, ran (2007) Nasopharyngeal carcinoma-associated Epstein–Barr virus-encoded oncogene latent membrane protein 1 potentiates regulatory T-cell function. Immunology and Cell Biology, 85 (5). pp. 370-377.

Peng, Judy C., Hyde, Claire, Pai, Saparna, O'Sullivan, Brendan J., Nielsen, Lars K., and Thomas, Ranjeny (2006) Monocyte-derived DC primed with TLR agonists secrete IL-12p70 in a CD40-dependent manner under hyperthermic conditions. Journal of Immunotherapy, 29 (6). pp. 606-615.

Pai, Saparna, O'Sullivan, Brendan J., Cooper, Leanne, Thomas, Ranjeny, and Khanna, Rajiv (2002) RelB nuclear translocation mediated by C-terminal activator regions of Epstein-Barr virus-encoded latent membrane protein 1 and its effect on antigen-presenting function in B cells. Journal of Virology, 76 (4). pp. 1914-1921.

S

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.

Sakata-Goto, Tomoko, Takahashi, Katsu, Kiso, Honoka, Huang, Boyen, Tsukamoto, Hiroko, Takemoto, Mitsuru, Hayashi, Tatsunari, Sugai, Manabu, Nakamura, Takashi, Yokota, Yoshifumi, Shimizu, Akira, Slavkin, Harold, and Bessho, Kazuhisa (2012) Id2 controls chondrogenesis acting downstream of BMP signaling during maxillary morphogenesis. Bone, 50 (1). pp. 69-78.

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.

U

Ukolova, Svetlana (2012) Characterization of the Wnt signalling system in the coral Acropora millepora. PhD thesis, James Cook University.

V

Vangaveti, V., and Kennedy, L. (2009) Regulation of stearoyl-coa desaturase by hydroxyoctadecadienoic acids. In: Abstracts from the Australian Society for Medical Research Queensland Postgraduate Student Conference. From: Australian Society for Medical Research Queensland Postgraduate Student Conference, 26 May 2009, Brisbane, QLD, Australia.

Z

Zhang, C., McFarlane, C., Lokireddy, S., Masuda, S., Ge, X., Gluckman, P.D., Sharma, M., and Kambadur, R. (2012) Inhibition of myostatin protects against diet-induced obesity by enhancing fatty acid oxidation and promoting a brown adipose phenotype in mice. Diabetologia, 55 (1). pp. 183-193.

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.

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.