References
- 1. Wade RH. On and around microtubules: an overview. Mol Biotechnol. 2009;43(2):177-91.
- 2. Fırat-Karalar EN, Stearns T. The centriole duplication cycle. Philos Trans R Soc Lond B Biol Sci. 2014;369(1650): pii: 20130460.
- 3. Gardner MK, Zanic M, Howard J. Microtubule catastrophe and rescue. Curr Opin Cell Biol. 2013;25(1):14-22.
- 4. Kamath K, Oroudjev E, Jordan MA. Determination of microtubule dynamic instability in living cells. Methods Cell Biol. 2010;97:1-14.
- 5. Bryantseva SA, Zhapparova ON. Bidirectional transport of organelles: unity and struggle of opposing motors. Cell Biol Int. 2012;36(1):1-6.
- 6. Inaba K. Molecular basis of sperm flagellar axonemes: structural and evolutionary aspects. Ann N Y Acad Sci. 2007;1101:506-26.
- 7. Romaniello R, Arrigoni F, Bassi MT, Borgatti R. Mutations in α- and β-tubulin encoding genes: implications in brain malformations. Brain Dev. 2015;37(3):273-80.
- 8. Sohal AP, Montgomery T, Mitra D, Ramesh V. TUBA1A mutation-associated lissencephaly: case report and review of the literature. Pediatr Neurol. 2012;46(2):127-31.
- 9. Keays DA, Tian G, Poirier K, Huang GJ, Siebold C, Cleak J, et al. Mutations in alpha-tubulin cause abnormal neuronal migration in mice and lissencephaly in humans. Cell. 2007;128(1):45-57.
- 10. Smith BN, Ticozzi N, Fallini C, Gkazi AS, Topp S, Kenna KP, et al. Exome-wide rare variant analysis identifies TUBA4A mutations associated with familial ALS. Neuron. 2014;84(2):324-31.
- 11. Simons C, Wolf NI, McNeil N, Caldovic L, Devaney JM, Takanohashi A et al. A de novo mutation in the β-tubulin gene TUBB4A results in the leukoencephalopathy hypomyelination with atrophy of the basal ganglia and cerebellum. Am J Hum Genet. 2013;92(5):767-73.
- 12. Yuba-Kubo A, Kubo A, Hata M, Tsukita S. Gene knockout analysis of two gamma-tubulin isoforms in mice. Dev Biol. 2005;282(2):361-73.
- 13. Poirier K, Lebrun N, Broix L, Tian G, Saillour Y, Boscheron C et al. Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephaly. Nat Genet. 2013;45(6):639-47.
- 14. Brandt R. The tau proteins in neuronal growth and development. Front Biosci. 1996;1:d118-30.
- 15. Lei P, Ayton S, Moon S, Zhang Q, Volitakis I, Finkelstein DI et al. Motor and cognitive deficits in aged tau knockout mice in two background strains. Mol Neurodegener. 2014;9:29.
- 16. McMurray CT. Neurodegeneration: diseases of the cytoskeleton? Nature. 2000;7(10):861-5.
- 17. Kovacs GG. Invited review: Neuropathology of tauopathies: principles and practice. Neuropathol Appl Neurobiol. 2015;41(1):3-23.
- 18. Bartoli KM, Jakovljevic J, Woolford JL Jr, Saunders WS. Kinesin molecular motor Eg5 functions during polypeptide synthesis. Mol Biol Cell. 2011;22(18):3420-30.
- 19. Mirzaa GM, Enyedi L, Parsons G, Collins S, Medne L, Adams C et al. Congenital microcephaly and chorioretinopathy due to de novo heterozygous KIF11 mutations: five novel mutations and review of the literature. Am J Med Genet A. 2014;164A(11):2879-86.
- 20. Dagoneau N, Goulet M, Geneviève D, Sznajer Y, Martinovic J, Smithson S et al. DYNC2H1 mutations cause asphyxiating thoracic dystrophy and short rib-polydactyly syndrome, type III. Am J Hum Genet. 2009;84(5):706-11.
- 21. Schmidts M, Arts HH, Bongers EM, Yap Z, Oud MM, Antony D et al. Exome sequencing identifies DYNC2H1 mutations as a common cause of asphyxiating thoracic dystrophy (Jeune syndrome) without major polydactyly, renal or retinal involvement. J Med Genet. 2013;50(5):309-23.
- 22. Huber C, Cormier-Daire V. Ciliary disorder of the skeleton. Am J Med Genet C Semin Med Genet. 2012;160C(3):165-74.
- 23. Leigh MW, Pittman JE, Carson JL, Ferkol TW, Dell SD, Davis SD et al. Clinical and genetic aspects of primary ciliary dyskinesia/Kartagener syndrome. Genet Med. 2009;11(7):473-87.
- 24. Stanislavov R, Marinova Ts, Markova M. [The electron microscopic pathology of human spermatozoa]. Akush Ginekol (Sofiia). 1998;37(3):44-6. Bulgarian
- 25. McGrath J, Brueckner M. Cilia are at the heart of vertebrate left-right asymmetry. Curr Opin Genet Dev. 2003;13(4):385-92.
- 26. Kurkowiak M, Ziętkiewicz E, Witt M. Recent advances in primary ciliary dyskinesia genetics. J Med Genet. 2015;52(1):1-9.
- 27. Rauch A, Thiel CT, Schindler D, Wick U, Crow YJ, Ekici AB et al. Mutations in the pericentrin (PCNT) gene cause primordial dwarfism. Science. 2008;319(5864):816-9.
- 28. Lange R, Krause W, Engel W. Analyses of meiotic chromosomes in testicular biopsies of infertile patients. Hum Reprod. 1997;12(10):2154-8.
- 29. Mrazek M, Fulka J Jr. Failure of oocyte maturation: possible mechanisms for oocyte maturation arrest. Hum Reprod. 2003;18(11):2249-52.
- 30. Schmiady H, Neitzel H. Arrest of human oocytes during meiosis I in two sisters of consanguineous parents: first evidence for an autosomal recessive trait in human infertility: Case report. Hum Reprod. 2002;17(10):2556-9.
- 31. Nikolova V, Chakarova I, Zhivkova R, Markova M, Dimitrov R, Delimitreva S. [Comparison of in vitro matured oocytes from two inbred mouse strains and their F1 hybrids]. Embryologia (Sofia). 2012;7(1):10-14. Bulgarian