Papers associated with optic chiasm

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	The re-establishment of retinotectal projections after uncrossing the optic chiasma in Xenopus laevis with one compound eye., Gaze RM., J Physiol. April 1, 1970; 207 (2): 51P-52P.
	The retinotectal projections after uncrossing the optic chiasma in Xenopus with one compound eye., Straznicky K., J Embryol Exp Morphol. December 1, 1971; 26 (3): 523-42.
	Factors determining decussation at the optic chiasma by developing retinotectal fibres in Xenopus., Beazley LD., Exp Brain Res. November 14, 1975; 23 (5): 491-504.
	Prenatal development of central optic pathways in albino rats., Lund RD., J Comp Neurol. January 15, 1976; 165 (2): 247-64.
	LHRH-like system in the brain of Xenopus laevis Daud: immunohistochemical idenfication., Doerr-Schott J., Cell Tissue Res. September 29, 1976; 172 (4): 477-86.
	Origin of the retina from both sides of the embryonic brain: a contribution to the problem of crossing at the optic chiasma., Jacobson M., Science. November 10, 1978; 202 (4368): 637-9.
	Factors involved in the development of ipsilateral retinothalamic projections in Xenopus laevis., Kennard C., J Embryol Exp Morphol. October 1, 1981; 65 199-217.
	Induction of the ipsilateral retinothalamic projection in Xenopus laevis by thyroxine., Hoskins SG., Nature. February 23, 1984; 307 (5953): 730-3.
	Stereotyped and variable growth of redirected Mauthner axons., Katz MJ., Dev Biol. July 1, 1984; 104 (1): 199-209.
	Control of the development of the ipsilateral retinothalamic projection in Xenopus laevis by thyroxine: results and speculation., Hoskins SG., J Neurobiol. May 1, 1986; 17 (3): 203-29.
	The pituitary adrenocorticotropes originate from neural ridge tissue in Xenopus laevis., Eagleson GW., J Embryol Exp Morphol. June 1, 1986; 95 1-14.
	Optic fibers follow aberrant pathways from rotated eyes in Xenopus laevis., Grant P., J Comp Neurol. August 15, 1986; 250 (3): 364-76.
	Fibre organization and reorganization in the retinotectal projection of Xenopus., Taylor JS., Development. March 1, 1987; 99 (3): 393-410.
	Specific cell surface labels in the visual centers of Xenopus laevis tadpole identified using monoclonal antibodies., Takagi S., Dev Biol. July 1, 1987; 122 (1): 90-100.
	The restrictive effect of early exposure to lithium upon body pattern in Xenopus development, studied by quantitative anatomy and immunofluorescence., Cooke J., Development. January 1, 1988; 102 (1): 85-99.
	A developmental and ultrastructural study of the optic chiasma in Xenopus., Wilson MA., Development. March 1, 1988; 102 (3): 537-53.
	The appearance of neural and glial cell markers during early development of the nervous system in the amphibian embryo., Messenger NJ., Development. September 1, 1989; 107 (1): 43-54.
	The course of regenerating retinal axons in the frog chiasma: the influence of axons from the other eye., Taylor JS., Anat Embryol (Berl). January 1, 1990; 181 (4): 405-12.
	The early development of the frog retinotectal projection., Taylor JS., Development. January 1, 1991; Suppl 2 95-104.
	The switch from larval to adult globin gene expression in Xenopus laevis is mediated by erythroid cells from distinct compartments., Weber R., Development. August 1, 1991; 112 (4): 1021-9.
	Xlcaax-1 is localized to the basolateral membrane of kidney tubule and other polarized epithelia during Xenopus development., Cornish JA., Dev Biol. March 1, 1992; 150 (1): 108-20.
	Identification and developmental expression of a novel low molecular weight neuronal intermediate filament protein expressed in Xenopus laevis., Charnas LR., J Neurosci. August 1, 1992; 12 (8): 3010-24.
	The return of phosphorylated and nonphosphorylated epitopes of neurofilament proteins to the regenerating optic nerve of Xenopus laevis., Zhao Y., J Comp Neurol. May 1, 1994; 343 (1): 158-72.
	The optic tract and tectal ablation influence the composition of neurofilaments in regenerating optic axons of Xenopus laevis., Zhao Y., J Neurosci. June 1, 1995; 15 (6): 4629-40.
	Xenopus laevis actin-depolymerizing factor/cofilin: a phosphorylation-regulated protein essential for development., Abe H., J Cell Biol. March 1, 1996; 132 (5): 871-85.
	Xefiltin, a Xenopus laevis neuronal intermediate filament protein, is expressed in actively growing optic axons during development and regeneration., Zhao Y., J Neurobiol. November 20, 1997; 33 (6): 811-24.
	Melanopsin: An opsin in melanophores, brain, and eye., Provencio I., Proc Natl Acad Sci U S A. January 6, 1998; 95 (1): 340-5.
	Overexpression of a novel Xenopus rel mRNA gene induces tumors in early embryos., Yang S., J Biol Chem. May 29, 1998; 273 (22): 13746-52.
	Vax1 is a novel homeobox-containing gene expressed in the developing anterior ventral forebrain., Hallonet M., Development. July 1, 1998; 125 (14): 2599-610.
	Identification of suprachiasmatic melanotrope-inhibiting neurons in Xenopus laevis: a confocal laser-scanning microscopy study., Ubink R., J Comp Neurol. July 20, 1998; 397 (1): 60-8.
	Expression pattern of insulin receptor mRNA during Xenopus laevis embryogenesis., Groigno L., Mech Dev. August 1, 1999; 86 (1-2): 151-4.
	A novel fork head gene mediates early steps during Xenopus lens formation., Kenyon KL., Development. November 1, 1999; 126 (22): 5107-16.
	A role for voltage-gated potassium channels in the outgrowth of retinal axons in the developing visual system., McFarlane S., J Neurosci. February 1, 2000; 20 (3): 1020-9.
	Ephrin-B regulates the Ipsilateral routing of retinal axons at the optic chiasm., Nakagawa S., Neuron. March 1, 2000; 25 (3): 599-610.
	Patterns of calretinin, calbindin, and tyrosine-hydroxylase expression are consistent with the prosomeric map of the frog diencephalon., Milán FJ., J Comp Neurol. March 27, 2000; 419 (1): 96-121.
	Regulation of sgk by aldosterone and its effects on the epithelial Na(+) channel., Shigaev A., Am J Physiol Renal Physiol. April 1, 2000; 278 (4): F613-9.
	An essential role of the neuronal cell adhesion molecule contactin in development of the Xenopus primary sensory system., Fujita N., Dev Biol. May 15, 2000; 221 (2): 308-20.
	Pax genes in development and maturation of the vertebrate visual system: implications for optic nerve regeneration., Ziman MR., Histol Histopathol. January 1, 2001; 16 (1): 239-49.
	Expression of the Xvax2 gene demarcates presumptive ventral telencephalon and specific visual structures in Xenopus laevis., Liu Y., Mech Dev. January 1, 2001; 100 (1): 115-8.
	Distinct roles of maf genes during Xenopus lens development., Ishibashi S., Mech Dev. March 1, 2001; 101 (1-2): 155-66.
	Functional organization of the suprachiasmatic nucleus of Xenopus laevis in relation to background adaptation., Kramer BM., J Comp Neurol. April 9, 2001; 432 (3): 346-55.
	Vax2 inactivation in mouse determines alteration of the eye dorsal-ventral axis, misrouting of the optic fibres and eye coloboma., Barbieri AM., Development. February 1, 2002; 129 (3): 805-13.
	Metalloproteases and guidance of retinal axons in the developing visual system., Webber CA., J Neurosci. September 15, 2002; 22 (18): 8091-100.
	Activin A induces craniofacial cartilage from undifferentiated Xenopus ectoderm in vitro., Furue M., Proc Natl Acad Sci U S A. November 26, 2002; 99 (24): 15474-9.
	Alpha-melanophore-stimulating hormone in the brain, cranial placode derivatives, and retina of Xenopus laevis during development in relation to background adaptation., Kramer BM., J Comp Neurol. January 27, 2003; 456 (1): 73-83.
	Normal chiasmatic routing of uncrossed projections from the ventrotemporal retina in albino Xenopus frogs., Grant S., J Comp Neurol. April 14, 2003; 458 (4): 425-39.
	Increased expression of multiple neurofilament mRNAs during regeneration of vertebrate central nervous system axons., Gervasi C., J Comp Neurol. June 23, 2003; 461 (2): 262-75.
	Ephrin-B2 and EphB1 mediate retinal axon divergence at the optic chiasm., Williams SE., Neuron. September 11, 2003; 39 (6): 919-35.
	Xenopus laevis CB1 cannabinoid receptor: molecular cloning and mRNA distribution in the central nervous system., Cottone E., J Comp Neurol. September 29, 2003; 464 (4): 487-96.
	New views on retinal axon development: a navigation guide., Mann F., Int J Dev Biol. January 1, 2004; 48 (8-9): 957-64.

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