Papers associated with dnah3 (and tubgcp2)

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	Taxon-specific expansion and loss of tektins inform metazoan ciliary diversity., Bastin BR, Schneider SQ., BMC Evol Biol. January 31, 2019; 19 (1): 40.
	F-Actin nucleated on chromosomes coordinates their capture by microtubules in oocyte meiosis., Burdyniuk M, Callegari A, Mori M, Nédélec F, Lénárt P., J Cell Biol. August 6, 2018; 217 (8): 2661-2674.
	Calaxin establishes basal body orientation and coordinates movement of monocilia in sea urchin embryos., Mizuno K, Shiba K, Yaguchi J, Shibata D, Yaguchi S, Prulière G, Chenevert J, Inaba K., Sci Rep. September 7, 2017; 7 (1): 10751.
	Distinct mechanisms eliminate mother and daughter centrioles in meiosis of starfish oocytes., Borrego-Pinto J, Somogyi K, Karreman MA, König J, Müller-Reichert T, Bettencourt-Dias M, Gönczy P, Schwab Y, Lénárt P., J Cell Biol. March 28, 2016; 212 (7): 815-27.
	Insights into the structure and function of ciliary and flagellar doublet microtubules: tektins, Ca2+-binding proteins, and stable protofilaments., Linck R, Fu X, Lin J, Ouch C, Schefter A, Steffen W, Warren P, Nicastro D., J Biol Chem. June 20, 2014; 289 (25): 17427-44.
	Cryo-electron tomography reveals conserved features of doublet microtubules in flagella., Nicastro D, Fu X, Heuser T, Tso A, Porter ME, Linck RW., Proc Natl Acad Sci U S A. October 18, 2011; 108 (42): E845-53.
	Is the curvature of the flagellum involved in the apparent cooperativity of the dynein arms along the "9+2" axoneme?, Cibert C, Ludu A., J Theor Biol. July 21, 2010; 265 (2): 95-103.
	Dynein pulls microtubules without rotating its stalk., Ueno H, Yasunaga T, Shingyoji C, Hirose K., Proc Natl Acad Sci U S A. December 16, 2008; 105 (50): 19702-7.
	An agent-based model contrasts opposite effects of dynamic and stable microtubules on cleavage furrow positioning., Odell GM, Foe VE., J Cell Biol. November 3, 2008; 183 (3): 471-83.
	Stretch-activated calcium channels relay fast calcium waves propagated by calcium-induced calcium influx., Jaffe LF., Biol Cell. March 1, 2007; 99 (3): 175-84.
	Molecular architecture of axonemal microtubule doublets revealed by cryo-electron tomography., Sui H, Downing KH., Nature. July 27, 2006; 442 (7101): 475-8.
	Ciliary protein turnover continues in the presence of inhibitors of golgi function: evidence for membrane protein pools and unconventional intracellular membrane dynamics., Stephens RE., J Exp Zool. May 1, 2001; 289 (6): 335-49.
	A kinesin-related protein, KRP(180), positions prometaphase spindle poles during early sea urchin embryonic cell division., Rogers GC, Chui KK, Lee EW, Wedaman KP, Sharp DJ, Holland G, Morris RL, Scholey JM., J Cell Biol. August 7, 2000; 150 (3): 499-512.
	Composition and organization of tubulin isoforms reveals a variety of axonemal models., Péchart I, Kann ML, Levilliers N, Bré MH, Fouquet JP., Biol Cell. December 1, 1999; 91 (9): 685-97.
	The carboxy-terminal sequence Asp427-Glu432 of beta-tubulin plays an important function in axonemal motility., Audebert S, White D, Cosson J, Huitorel P, Eddé B, Gagnon C., Eur J Biochem. April 1, 1999; 261 (1): 48-56.
	Two proteins isolated from sea urchin sperm flagella: structural components common to the stable microtubules of axonemes and centrioles., Hinchcliffe EH, Linck RW., J Cell Sci. March 1, 1998; 111 ( Pt 5) 585-95.
	Synthesis and turnover of embryonic sea urchin ciliary proteins during selective inhibition of tubulin synthesis and assembly., Stephens RE., Mol Biol Cell. November 1, 1997; 8 (11): 2187-98.
	Posttranslational modifications of axonemal tubulin., Mary J, Redeker V, Le Caer JP, Rossier J, Schmitter JM., J Protein Chem. July 1, 1997; 16 (5): 403-7.
	The A and B tubules of the outer doublets of sea urchin sperm axonemes are composed of different tubulin variants., Multigner L, Pignot-Paintrand I, Saoudi Y, Job D, Plessmann U, Rüdiger M, Weber K., Biochemistry. August 20, 1996; 35 (33): 10862-71.
	The polyglutamylated lateral chain of alpha-tubulin plays a key role in flagellar motility., Gagnon C, White D, Cosson J, Huitorel P, Eddé B, Desbruyères E, Paturle-Lafanechère L, Multigner L, Job D, Cibert C., J Cell Sci. June 1, 1996; 109 ( Pt 6) 1545-53.
	Posttranslational modifications in the C-terminal tail of axonemal tubulin from sea urchin sperm., Mary J, Redeker V, Le Caer JP, Rossier J, Schmitter JM., J Biol Chem. April 26, 1996; 271 (17): 9928-33.
	Selective incorporation of architectural proteins into terminally differentiated molluscan gill cilia., Stephens RE., J Exp Zool. April 1, 1996; 274 (5): 300-9.
	Axonemal tubulin polyglycylation probed with two monoclonal antibodies: widespread evolutionary distribution, appearance during spermatozoan maturation and possible function in motility., Bré MH, Redeker V, Quibell M, Darmanaden-Delorme J, Bressac C, Cosson J, Huitorel P, Schmitter JM, Rossler J, Johnson T, Adoutte A, Levilliers N., J Cell Sci. April 1, 1996; 109 ( Pt 4) 727-38.
	Structural comparison of tektins and evidence for their determination of complex spacings in flagellar microtubules., Norrander JM, Perrone CA, Amos LA, Linck RW., J Mol Biol. March 29, 1996; 257 (2): 385-97.
	Excision and disassembly of sperm tail microtubules during sea urchin fertilization: requirements for microtubule dynamics., Fechter J, Schöneberg A, Schatten G., Cell Motil Cytoskeleton. January 1, 1996; 35 (4): 281-8.
	Monoclonal and polyclonal antibodies detect a new type of post-translational modification of axonemal tubulin., Levilliers N, Fleury A, Hill AM., J Cell Sci. September 1, 1995; 108 ( Pt 9) 3013-28.
	Ciliogenesis in sea urchin embryos--a subroutine in the program of development., Stephens RE., Bioessays. April 1, 1995; 17 (4): 331-40.
	At least one of the protofilaments in flagellar microtubules is not composed of tubulin., Nojima D, Linck RW, Egelman EH., Curr Biol. February 1, 1995; 5 (2): 158-67.
	Monoclonal anti-dipeptide antibodies cross-react with detyrosinated and glutamylated forms of tubulins., Kuriyama R, Levin A, Nelson D, Madl J, Frankfurter A, Kimble M., Cell Motil Cytoskeleton. January 1, 1995; 30 (3): 171-82.
	The anatomy of flagellar microtubules: polarity, seam, junctions, and lattice., Song YH, Mandelkow E., J Cell Biol. January 1, 1995; 128 (1-2): 81-94.
	Mechanics of motility: distinct dynein binding domains on alpha- and beta-tubulin., Goldsmith M, Yarbrough L, van der Kooy D., Biochem Cell Biol. January 1, 1995; 73 (9-10): 665-71.
	Centrosomal components immunologically related to tektins from ciliary and flagellar microtubules., Steffen W, Fajer EA, Linck RW., J Cell Sci. August 1, 1994; 107 ( Pt 8) 2095-105.
	C/A dynein isolated from sea urchin sperm flagellar axonemes. Enzymatic properties and interaction with microtubules., Yokota E, Mabuchi I., J Cell Sci. February 1, 1994; 107 ( Pt 2) 353-61.
	Tubulin and tektin in sea urchin embryonic cilia: pathways of protein incorporation during turnover and regeneration., Stephens RE., J Cell Sci. February 1, 1994; 107 ( Pt 2) 683-92.
	Stabilization of sea urchin flagellar microtubules by histone H1., Multigner L, Gagnon J, Van Dorsselaer A, Job D., Nature. November 5, 1992; 360 (6399): 33-9.
	Evidence for a non-tubulin spindle matrix and for spindle components immunologically related to tektin filaments., Steffen W, Linck RW., J Cell Sci. April 1, 1992; 101 ( Pt 4) 809-22.
	Tubulin in sea urchin embryonic cilia: post-translational modifications during regeneration., Stephens RE., J Cell Sci. April 1, 1992; 101 ( Pt 4) 837-45.
	High-frequency vibration in flagellar axonemes with amplitudes reflecting the size of tubulin., Kamimura S, Kamiya R., J Cell Biol. March 1, 1992; 116 (6): 1443-54.
	A cytoplasmic dynein heavy chain in sea urchin embryos., Gibbons IR, Asai DJ, Tang WJ, Gibbons BH., Biol Cell. January 1, 1992; 76 (3): 303-9.
	End-stabilized microtubules observed in vitro: stability, subunit, interchange, and breakage., Dye RB, Flicker PF, Lien DY, Williams RC., Cell Motil Cytoskeleton. January 1, 1992; 21 (3): 171-86.
	Tubulin in sea urchin embryonic cilia: characterization of the membrane-periaxonemal matrix., Stephens RE., J Cell Sci. November 1, 1991; 100 ( Pt 3) 521-31.
	Molecular cloning and expression of sea urchin embryonic ciliary dynein beta heavy chain., Foltz KR, Asai DJ., Cell Motil Cytoskeleton. January 1, 1990; 16 (1): 33-46.
	Application of stains-all staining to the analysis of axonemal tubulins: identification of beta-tubulin and beta-isotubulins., Nakamura K, Masuyama E, Wada S, Okuno M., J Biochem Biophys Methods. January 1, 1990; 21 (3): 237-45.
	Assembly of a protein sharing epitopes with sperm dynein heavy chains into meiotic spindle in the prometaphase starfish oocyte., Ogawa K, Yokota E, Shirai H., Biol Cell. January 1, 1988; 64 (1): 57-66.
	A microtubule-activated ATPase from sea urchin eggs, distinct from cytoplasmic dynein and kinesin., Collins CA, Vallee RB., Proc Natl Acad Sci U S A. July 1, 1986; 83 (13): 4799-803.
	Characterization of the sea-urchin egg microtubule-activated ATPase., Collins CA, Vallee RB., J Cell Sci Suppl. January 1, 1986; 5 197-204.
	Monoclonal antibodies specific for an acetylated form of alpha-tubulin recognize the antigen in cilia and flagella from a variety of organisms., Piperno G, Fuller MT., J Cell Biol. December 1, 1985; 101 (6): 2085-94.
	Cytoskeletal architecture of isolated mitotic spindle with special reference to microtubule-associated proteins and cytoplasmic dynein., Hirokawa N, Takemura R, Hisanaga S., J Cell Biol. November 1, 1985; 101 (5 Pt 1): 1858-70.
	Translocation of vesicles from squid axoplasm on flagellar microtubules., Gilbert SP, Allen RD, Sloboda RD., Nature. May 1, 1985; 315 (6016): 245-8.
	ATP hydrolysis coupled to microtubule sliding in sea-urchin sperm flagella., Kamimura S, Yano M, Shimizu H., J Biochem. May 1, 1985; 97 (5): 1509-15.

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