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The early dorsal signal in vertebrate embryos requires endolysosomal membrane trafficking. , Azbazdar Y., Bioessays. January 1, 2024; 46 (1): e2300179.
A maternal dorsoventral prepattern revealed by an asymmetric distribution of ventralizing molecules before fertilization in Xenopus laevis. , Castro Colabianchi AM., Front Cell Dev Biol. January 1, 2024; 12 1365705.
Solubility phase transition of maternal RNAs during vertebrate oocyte-to- embryo transition. , Hwang H., Dev Cell. December 4, 2023; 58 (23): 2776-2788.e5.
L-bodies are RNA-protein condensates driving RNA localization in Xenopus oocytes. , Neil CR., Mol Biol Cell. December 1, 2021; 32 (22): ar37.
Staufen1, Kinesin1 and microtubule function in cyclin B1 mRNA transport to the animal polar cytoplasm of zebrafish oocytes. , Takahashi K., Biochem Biophys Res Commun. September 18, 2018; 503 (4): 2778-2783.
Hermes (Rbpms) is a Critical Component of RNP Complexes that Sequester Germline RNAs during Oogenesis. , Aguero T ., J Dev Biol. March 1, 2016; 4 (1):
A novel role for Celf1 in vegetal RNA localization during Xenopus oogenesis. , Bauermeister D., Dev Biol. September 15, 2015; 405 (2): 214-24.
Possible involvement of insulin-like growth factor 2 mRNA-binding protein 3 in zebrafish oocyte maturation as a novel cyclin B1 mRNA-binding protein that represses the translation in immature oocytes. , Takahashi K., Biochem Biophys Res Commun. May 23, 2014; 448 (1): 22-7.
Directional transport is mediated by a Dynein-dependent step in an RNA localization pathway. , Gagnon JA., PLoS Biol. January 1, 2013; 11 (4): e1001551.
Expression of XNOA 36 in the mitochondrial cloud of Xenopus laevis oocytes. , Vaccaro MC., Zygote. August 1, 2012; 20 (3): 237-42.
Interactions of 40LoVe within the ribonucleoprotein complex that forms on the localization element of Xenopus Vg1 mRNA. , Kroll TT ., Mech Dev. July 1, 2009; 126 (7): 523-38.
Multiple kinesin motors coordinate cytoplasmic RNA transport on a subpopulation of microtubules in Xenopus oocytes. , Messitt TJ., Dev Cell. September 1, 2008; 15 (3): 426-436.
Motility screen identifies Drosophila IGF-II mRNA-binding protein--zipcode-binding protein acting in oogenesis and synaptogenesis. , Boylan KL., PLoS Genet. February 1, 2008; 4 (2): e36.
PTB/ hnRNP I is required for RNP remodeling during RNA localization in Xenopus oocytes. , Lewis RA., Mol Cell Biol. January 1, 2008; 28 (2): 678-86.
The mRNA coding for Xenopus glutamate receptor interacting protein 2 (XGRIP2) is maternally transcribed, transported through the late pathway and localized to the germ plasm. , Kaneshiro K., Biochem Biophys Res Commun. April 20, 2007; 355 (4): 902-6.
40LoVe interacts with Vg1RBP/ Vera and hnRNP I in binding the Vg1-localization element. , Czaplinski K., RNA. February 1, 2006; 12 (2): 213-22.
Identification of asymmetrically localized transcripts along the animal-vegetal axis of the Xenopus egg. , Kataoka K., Dev Growth Differ. October 1, 2005; 47 (8): 511-21.
Identification of 40LoVe, a Xenopus hnRNP D family protein involved in localizing a TGF-beta-related mRNA during oogenesis. , Czaplinski K., Dev Cell. April 1, 2005; 8 (4): 505-15.
The RNA ligands for mouse proline-rich RNA-binding protein (mouse Prrp) contain two consensus sequences in separate loop structure. , Hori T., Nucleic Acids Res. January 12, 2005; 33 (1): 190-200.
Two distinct Staufen isoforms in Xenopus are vegetally localized during oogenesis. , Allison R., RNA. November 1, 2004; 10 (11): 1751-63.
Dynamic changes in intranuclear and subcellular localizations of mouse Prrp/ DAZAP1 during spermatogenesis: the necessity of the C-terminal proline-rich region for nuclear import and localization. , Kurihara Y., Arch Histol Cytol. November 1, 2004; 67 (4): 325-33.
Localization of RNAs to the mitochondrial cloud in Xenopus oocytes through entrapment and association with endoplasmic reticulum. , Chang P., Mol Biol Cell. October 1, 2004; 15 (10): 4669-81.
Nuclear RNP complex assembly initiates cytoplasmic RNA localization. , Kress TL., J Cell Biol. April 26, 2004; 165 (2): 203-11.
Xvelo1 uses a novel 75-nucleotide signal sequence that drives vegetal localization along the late pathway in Xenopus oocytes. , Claussen M., Dev Biol. February 15, 2004; 266 (2): 270-84.
VgRBP71 stimulates cleavage at a polyadenylation signal in Vg1 mRNA, resulting in the removal of a cis-acting element that represses translation. , Kolev NG., Mol Cell. March 1, 2003; 11 (3): 745-55.
A homolog of FBP2/ KSRP binds to localized mRNAs in Xenopus oocytes. , Kroll TT ., Development. December 1, 2002; 129 (24): 5609-19.
A ubiquitous and conserved signal for RNA localization in chordates. , Betley JN., Curr Biol. October 15, 2002; 12 (20): 1756-61.
foxD5a, a Xenopus winged helix gene, maintains an immature neural ectoderm via transcriptional repression that is dependent on the C-terminal domain. , Sullivan SA., Dev Biol. April 15, 2001; 232 (2): 439-57.
The vegetally localized mRNA fatvg is associated with the germ plasm in the early embryo and is later expressed in the fat body. , Chan AP., Mech Dev. January 1, 2001; 100 (1): 137-40.
The Xenopus homologue of Bicaudal-C is a localized maternal mRNA that can induce endoderm formation. , Wessely O ., Development. May 1, 2000; 127 (10): 2053-62.
fatvg encodes a new localized RNA that uses a 25-nucleotide element (FVLE1) to localize to the vegetal cortex of Xenopus oocytes. , Chan AP., Development. November 1, 1999; 126 (22): 4943-53.
A Xenopus protein related to hnRNP I has a role in cytoplasmic RNA localization. , Cote CA., Mol Cell. September 1, 1999; 4 (3): 431-7.
From cortical rotation to organizer gene expression: toward a molecular explanation of axis specification in Xenopus. , Moon RT ., Bioessays. July 1, 1998; 20 (7): 536-45.
Expeditions to the pole: RNA localization in Xenopus and Drosophila. , Gavis ER., Trends Cell Biol. December 1, 1997; 7 (12): 485-92.
Dorsal determinants in the Xenopus egg are firmly associated with the vegetal cortex and behave like activators of the Wnt pathway. , Marikawa Y., Dev Biol. November 1, 1997; 191 (1): 69-79.
A vegetally localized T-box transcription factor in Xenopus eggs specifies mesoderm and endoderm and is essential for embryonic mesoderm formation. , Horb ME ., Development. May 1, 1997; 124 (9): 1689-98.
Establishment of the dorso- ventral axis in Xenopus embryos is presaged by early asymmetries in beta-catenin that are modulated by the Wnt signaling pathway. , Larabell CA ., J Cell Biol. March 10, 1997; 136 (5): 1123-36.
Elaboration of the messenger transport organizer pathway for localization of RNA to the vegetal cortex of Xenopus oocytes. , Kloc M ., Dev Biol. November 25, 1996; 180 (1): 119-30.
RNA transport to the vegetal cortex of Xenopus oocytes. , Zhou Y., Dev Biol. October 10, 1996; 179 (1): 173-83.
Xenopus Mad proteins transduce distinct subsets of signals for the TGF beta superfamily. , Graff JM ., Cell. May 17, 1996; 85 (4): 479-87.
Regulation of dorsal- ventral axis formation in Xenopus by intercellular and intracellular signalling. , Kimelman D ., Biochem Soc Symp. January 1, 1996; 62 13-23.
Xenopus poly (A) binding protein maternal RNA is localized during oogenesis and associated with large complexes in blastula. , Schroeder KE., Dev Genet. January 1, 1996; 19 (3): 268-76.
mRNA localisation during development. , Micklem DR., Dev Biol. December 1, 1995; 172 (2): 377-95.
Two distinct pathways for the localization of RNAs at the vegetal cortex in Xenopus oocytes. , Kloc M ., Development. February 1, 1995; 121 (2): 287-97.
Xwnt-11: a maternally expressed Xenopus wnt gene. , Ku M., Development. December 1, 1993; 119 (4): 1161-73.
A two-step model for the localization of maternal mRNA in Xenopus oocytes: involvement of microtubules and microfilaments in the translocation and anchoring of Vg1 mRNA. , Yisraeli JK ., Development. February 1, 1990; 108 (2): 289-98.
The material mRNA Vg1 is correctly localized following injection into Xenopus oocytes. , Yisraeli JK ., Nature. December 8, 1988; 336 (6199): 592-5.
Translocation of a localized maternal mRNA to the vegetal pole of Xenopus oocytes. , Melton DA ., Nature. July 2, 1987; 328 (6125): 80-2.