Papers associated with anatomical region (and vim)

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	Regeneration from three cellular sources and ectopic mini-retina formation upon neurotoxic retinal degeneration in Xenopus., Parain K., Glia. April 1, 2024; 72 (4): 759-776.
	TBC1D32 variants disrupt retinal ciliogenesis and cause retinitis pigmentosa., Bocquet B., JCI Insight. November 8, 2023; 8 (21):
	Rapid changes in tissue mechanics regulate cell behaviour in the developing embryonic brain., Thompson AJ., Elife. January 15, 2019; 8
	The Xenopus animal cap transcriptome: building a mucociliary epithelium., Angerilli A., Nucleic Acids Res. September 28, 2018; 46 (17): 8772-8787.
	Serine Threonine Kinase Receptor-Associated Protein Deficiency Impairs Mouse Embryonic Stem Cells Lineage Commitment Through CYP26A1-Mediated Retinoic Acid Homeostasis., Jin L., Stem Cells. September 1, 2018; 36 (9): 1368-1379.
	Similarity in gene-regulatory networks suggests that cancer cells share characteristics of embryonic neural cells., Zhang Z., J Biol Chem. August 4, 2017; 292 (31): 12842-12859.
	In Vivo Analysis of the Neurovascular Niche in the Developing Xenopus Brain., Lau M., eNeuro. July 31, 2017; 4 (4):
	Id genes are essential for early heart formation., Cunningham TJ., Genes Dev. July 1, 2017; 31 (13): 1325-1338.
	JAK-STAT pathway activation in response to spinal cord injury in regenerative and non-regenerative stages of Xenopus laevis., Tapia VS., Regeneration (Oxf). February 1, 2017; 4 (1): 21-35.
	Identification and characterization of Xenopus tropicalis common progenitors of Sertoli and peritubular myoid cell lineages., Tlapakova T., Biol Open. September 15, 2016; 5 (9): 1275-82.
	A Retinoic Acid-Hedgehog Cascade Coordinates Mesoderm-Inducing Signals and Endoderm Competence during Lung Specification., Rankin SA, Rankin SA., Cell Rep. June 28, 2016; 16 (1): 66-78.
	A noncanonical Frizzled2 pathway regulates epithelial-mesenchymal transition and metastasis., Gujral TS., Cell. November 6, 2014; 159 (4): 844-56.
	Tcf21 regulates the specification and maturation of proepicardial cells., Tandon P., Development. June 1, 2013; 140 (11): 2409-21.
	Spinal cord regeneration in Xenopus tadpoles proceeds through activation of Sox2-positive cells., Gaete M., Neural Dev. April 26, 2012; 7 13.
	In vivo time-lapse imaging of cell proliferation and differentiation in the optic tectum of Xenopus laevis tadpoles., Bestman JE., J Comp Neurol. February 1, 2012; 520 (2): 401-33.
	pTransgenesis: a cross-species, modular transgenesis resource., Love NR., Development. December 1, 2011; 138 (24): 5451-8.
	Analyzing the function of a hox gene: an evolutionary approach., Michaut L., Dev Growth Differ. December 1, 2011; 53 (9): 982-93.
	Proliferation, migration and differentiation in juvenile and adult Xenopus laevis brains., D'Amico LA., Dev Biol. August 8, 2011; 1405 31-48.
	The nucleoporin Nup88 is interacting with nuclear lamin A., Lussi YC., Mol Biol Cell. April 1, 2011; 22 (7): 1080-90.
	Role of Tbx2 in defining the territory of the pronephric nephron., Cho GS., Development. February 1, 2011; 138 (3): 465-74.
	Retinal patterning by Pax6-dependent cell adhesion molecules., Rungger-Brändle E., Dev Neurobiol. September 15, 2010; 70 (11): 764-80.
	The dynamic properties of intermediate filaments during organelle transport., Chang L., J Cell Sci. August 15, 2009; 122 (Pt 16): 2914-23.
	Muscular dystrophy candidate gene FRG1 is critical for muscle development., Hanel ML., Dev Dyn. June 1, 2009; 238 (6): 1502-12.
	The POU homeobox protein Oct-1 regulates radial glia formation downstream of Notch signaling., Kiyota T., Dev Biol. March 15, 2008; 315 (2): 579-92.
	Ets-1 regulates radial glia formation during vertebrate embryogenesis., Kiyota T., Organogenesis. October 1, 2007; 3 (2): 93-101.
	Expression patterns of chick Musashi-1 in the developing nervous system., Wilson JM., Gene Expr Patterns. August 1, 2007; 7 (7): 817-25.
	Investigation of nuclear architecture with a domain-presenting expression system., Dreger CK., J Struct Biol. January 1, 2002; 140 (1-3): 100-15.
	Glial-defined rhombomere boundaries in developing Xenopus hindbrain., Yoshida M., J Comp Neurol. August 14, 2000; 424 (1): 47-57.
	Post-transcriptional regulation of Xwnt-8 expression is required for normal myogenesis during vertebrate embryonic development., Tian Q., Development. August 1, 1999; 126 (15): 3371-80.
	Neural development in the marsupial frog Gastrotheca riobambae., Del Pino EM., Int J Dev Biol. July 1, 1998; 42 (5): 723-31.
	A Xenopus DAZ-like gene encodes an RNA component of germ plasm and is a functional homologue of Drosophila boule., Houston DW., Development. January 1, 1998; 125 (2): 171-80.
	Structure and assembly properties of the intermediate filament protein vimentin: the role of its head, rod and tail domains., Herrmann H., J Mol Biol. December 20, 1996; 264 (5): 933-53.
	A kinesin-like protein is required for germ plasm aggregation in Xenopus., Robb DL., Cell. November 29, 1996; 87 (5): 823-31.
	Effects of intermediate filament disruption on the early development of the peripheral nervous system of Xenopus laevis., Lin W., Dev Biol. October 10, 1996; 179 (1): 197-211.
	Disruption of intermediate filament organization leads to structural defects at the intersomite junction in Xenopus myotomal muscle., Cary RB., Development. April 1, 1995; 121 (4): 1041-52.
	Truncation mutagenesis of the non-alpha-helical carboxyterminal tail domain of vimentin reveals contributions to cellular localization but not to filament assembly., Rogers KR., Eur J Cell Biol. February 1, 1995; 66 (2): 136-50.
	Morphogenesis and the cytoskeleton: studies of the Xenopus embryo., Klymkowsky MW., Dev Biol. October 1, 1994; 165 (2): 372-84.
	Differential organization of desmin and vimentin in muscle is due to differences in their head domains., Cary RB., J Cell Biol. July 1, 1994; 126 (2): 445-56.
	Vimentin's tail interacts with actin-containing structures in vivo., Cary RB., J Cell Sci. June 1, 1994; 107 ( Pt 6) 1609-22.
	Desmin organization during the differentiation of the dorsal myotome in Xenopus laevis., Cary RB., Differentiation. April 1, 1994; 56 (1-2): 31-8.
	Host cell factors controlling vimentin organization in the Xenopus oocyte., Dent JA., J Cell Biol. November 1, 1992; 119 (4): 855-66.
	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.
	Assembly of a tail-less mutant of the intermediate filament protein, vimentin, in vitro and in vivo., Eckelt A., Eur J Cell Biol. August 1, 1992; 58 (2): 319-30.
	Identification of a nonapeptide motif in the vimentin head domain involved in intermediate filament assembly., Herrmann H., J Mol Biol. February 5, 1992; 223 (3): 637-50.
	Distinct distribution of vimentin and cytokeratin in Xenopus oocytes and early embryos., Torpey NP., J Cell Sci. January 1, 1992; 101 ( Pt 1) 151-60.
	Identification of vimentin and novel vimentin-related proteins in Xenopus oocytes and early embryos., Torpey NP., Development. December 1, 1990; 110 (4): 1185-95.
	Overexpression of wild-type and dominant negative mutant vimentin subunits in developing Xenopus embryos., Christian JL., New Biol. August 1, 1990; 2 (8): 700-11.
	An epithelium-type cytoskeleton in a glial cell: astrocytes of amphibian optic nerves contain cytokeratin filaments and are connected by desmosomes., Rungger-Brändle E., J Cell Biol. August 1, 1989; 109 (2): 705-16.
	Expression of intermediate filament proteins during development of Xenopus laevis. II. Identification and molecular characterization of desmin., Herrmann H., Development. February 1, 1989; 105 (2): 299-307.
	Expression of intermediate filament proteins during development of Xenopus laevis. I. cDNA clones encoding different forms of vimentin., Herrmann H., Development. February 1, 1989; 105 (2): 279-98.

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