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137 REFERENCES Abe, Masashi, and Nancy M. Bonini. 2013. “MicroRNAs and Neurodegeneration: Role and Impact.” Trends in Cell Biology 23 (1): 30–36. doi:10.1016/j.tcb.2012.08.013. Adachi, Naoko, Takeshi Kobayashi, Hideyuki Takahashi, Takumi Kawasaki, Yasuhito Shirai, Takehiko Ueyama, Toshio Matsuda, Takahiro Seki, Norio Sakai, and Naoaki Saito. 2008. “Enzymological Analysis of Mutant Protein Kinase Cgamma Causing Spinocerebellar Ataxia Type 14 and Dysfunction in Ca2+ Homeostasis.” The Journal of Biological Chemistry 283 (28): 19854– 63. doi:10.1074/jbc.M801492200. Airaksinen, Matti S., Jens Eilers, Olga Garaschuk, Hans Thoenen, Arthur Konnerth, and Michael Meyer. 1997. “Ataxia and Altered Dendritic Calcium Signaling in Mice Carrying a Targeted Null Mutation of the Calbindin D28k Gene.” Proceedings of the National Academy of Sciences 94 (4): 1488–93. Ames, Robert S., Yi Li, Henry M. Sarau, Paru Nuthulaganti, James J. Foley, Catherine Ellis, Zhizhen Zeng, et al. 1996. “Molecular Cloning and Characterization of the Human Anaphylatoxin C3a Receptor.” Journal of Biological Chemistry 271 (34): 20231–34. doi:10.1074/jbc.271.34.20231. Anders, Simon, Paul Theodor Pyl, and Wolfgang Huber. 2014. “HTSeq – A Python Framework to Work with High-Throughput Sequencing Data.” bioRxiv, February. doi:10.1101/002824. Arndt, Greg M., Lesley Dossey, Lara M. Cullen, Angela Lai, Riki Druker, Michael Eisbacher, Chunyan Zhang, et al. 2009. “Characterization of Global microRNA Expression Reveals Oncogenic Potential of miR-145 in Metastatic Colorectal Cancer.” BMC Cancer 9: 374. doi:10.1186/1471-2407-9-374. Arosio, Beatrice, Claudio D’Addario, Cristina Gussago, Martina Casati, Enzo Tedone, Evelyn Ferri, Paola Nicolini, Paolo D. Rossi, Mauro Maccarrone, and Daniela Mari. 2014. “Peripheral Blood Mononuclear Cells as a Laboratory to Study Dementia in the Elderly.” BioMed Research International 2014 (April): e169203. doi:10.1155/2014/169203. Ashizawa, Tetsuo, Karla P. Figueroa, Susan L. Perlman, Christopher M. Gomez, George R. Wilmot, Jeremy D. Schmahmann, Sarah H. Ying, et al. 2013. “Clinical Characteristics of Patients with Spinocerebellar Ataxias 1, 2, 3 and 6 in the US; a Prospective Observational Study.” Orphanet Journal of Rare Diseases 8: 177. doi:10.1186/1750-1172-8-177. Avila-Figueroa, Amalia, Douglas Cattie, and Sarah Delaney. 2011. “A Small Unstructured Nucleic Acid Disrupts a Trinucleotide Repeat Hairpin.” Biochemical and Biophysical Research Communications 413 (4): 532–36. doi:10.1016/j.bbrc.2011.08.130. Bahl, S., K. Virdi, U. Mittal, M. P. Sachdeva, A. K. Kalla, S. E. Holmes, E. O’Hearn, et al. 2005. “Evidence of a Common Founder for SCA12 in the Indian Population.” Annals of Human Genetics 69 (Pt 5): 528–34. doi:10.1046/j.1529-8817.2005.00173.x. Bakalkin, Georgy, Hiroyuki Watanabe, Justyna Jezierska, Cloë Depoorter, Corien Verschuuren-Bemelmans, Igor Bazov, Konstantin A. Artemenko, et al. 2010. “Prodynorphin Mutations Cause the Neurodegenerative Disorder Spinocerebellar Ataxia Type 23.” The American Journal of Human Genetics 87 (5): 593–603. doi:10.1016/j.ajhg.2010.10.001. Banfi, S., A. Servadio, M. Chung, F. Capozzoli, L. A. Duvick, R. Elde, H. Y. Zoghbi, and H. T. Orr. 1996a. “Cloning and Developmental Expression Analysis of the

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Page 1: Thesis Dhanya final sept2015 - INFLIBNETshodhganga.inflibnet.ac.in/bitstream/10603/75345/16/16_bibliography.pdf · Nayana Lahiri, Elsa Raibon, et al. 2008a. “A Novel Pathogenic

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REFERENCES Abe, Masashi, and Nancy M. Bonini. 2013. “MicroRNAs and Neurodegeneration:

Role and Impact.” Trends in Cell Biology 23 (1): 30–36. doi:10.1016/j.tcb.2012.08.013.

Adachi, Naoko, Takeshi Kobayashi, Hideyuki Takahashi, Takumi Kawasaki, Yasuhito Shirai, Takehiko Ueyama, Toshio Matsuda, Takahiro Seki, Norio Sakai, and Naoaki Saito. 2008. “Enzymological Analysis of Mutant Protein Kinase Cgamma Causing Spinocerebellar Ataxia Type 14 and Dysfunction in Ca2+ Homeostasis.” The Journal of Biological Chemistry 283 (28): 19854–63. doi:10.1074/jbc.M801492200.

Airaksinen, Matti S., Jens Eilers, Olga Garaschuk, Hans Thoenen, Arthur Konnerth, and Michael Meyer. 1997. “Ataxia and Altered Dendritic Calcium Signaling in Mice Carrying a Targeted Null Mutation of the Calbindin D28k Gene.” Proceedings of the National Academy of Sciences 94 (4): 1488–93.

Ames, Robert S., Yi Li, Henry M. Sarau, Paru Nuthulaganti, James J. Foley, Catherine Ellis, Zhizhen Zeng, et al. 1996. “Molecular Cloning and Characterization of the Human Anaphylatoxin C3a Receptor.” Journal of Biological Chemistry 271 (34): 20231–34. doi:10.1074/jbc.271.34.20231.

Anders, Simon, Paul Theodor Pyl, and Wolfgang Huber. 2014. “HTSeq – A Python Framework to Work with High-Throughput Sequencing Data.” bioRxiv, February. doi:10.1101/002824.

Arndt, Greg M., Lesley Dossey, Lara M. Cullen, Angela Lai, Riki Druker, Michael Eisbacher, Chunyan Zhang, et al. 2009. “Characterization of Global microRNA Expression Reveals Oncogenic Potential of miR-145 in Metastatic Colorectal Cancer.” BMC Cancer 9: 374. doi:10.1186/1471-2407-9-374.

Arosio, Beatrice, Claudio D’Addario, Cristina Gussago, Martina Casati, Enzo Tedone, Evelyn Ferri, Paola Nicolini, Paolo D. Rossi, Mauro Maccarrone, and Daniela Mari. 2014. “Peripheral Blood Mononuclear Cells as a Laboratory to Study Dementia in the Elderly.” BioMed Research International 2014 (April): e169203. doi:10.1155/2014/169203.

Ashizawa, Tetsuo, Karla P. Figueroa, Susan L. Perlman, Christopher M. Gomez, George R. Wilmot, Jeremy D. Schmahmann, Sarah H. Ying, et al. 2013. “Clinical Characteristics of Patients with Spinocerebellar Ataxias 1, 2, 3 and 6 in the US; a Prospective Observational Study.” Orphanet Journal of Rare Diseases 8: 177. doi:10.1186/1750-1172-8-177.

Avila-Figueroa, Amalia, Douglas Cattie, and Sarah Delaney. 2011. “A Small Unstructured Nucleic Acid Disrupts a Trinucleotide Repeat Hairpin.” Biochemical and Biophysical Research Communications 413 (4): 532–36. doi:10.1016/j.bbrc.2011.08.130.

Bahl, S., K. Virdi, U. Mittal, M. P. Sachdeva, A. K. Kalla, S. E. Holmes, E. O’Hearn, et al. 2005. “Evidence of a Common Founder for SCA12 in the Indian Population.” Annals of Human Genetics 69 (Pt 5): 528–34. doi:10.1046/j.1529-8817.2005.00173.x.

Bakalkin, Georgy, Hiroyuki Watanabe, Justyna Jezierska, Cloë Depoorter, Corien Verschuuren-Bemelmans, Igor Bazov, Konstantin A. Artemenko, et al. 2010. “Prodynorphin Mutations Cause the Neurodegenerative Disorder Spinocerebellar Ataxia Type 23.” The American Journal of Human Genetics 87 (5): 593–603. doi:10.1016/j.ajhg.2010.10.001.

Banfi, S., A. Servadio, M. Chung, F. Capozzoli, L. A. Duvick, R. Elde, H. Y. Zoghbi, and H. T. Orr. 1996a. “Cloning and Developmental Expression Analysis of the

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