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Summary Anatomy Item Literature (3261) Expression Attributions Wiki
XB-ANAT-512

Papers associated with egg (and frzb2)

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The early dorsal signal in vertebrate embryos requires endolysosomal membrane trafficking., Azbazdar Y., Bioessays. January 1, 2024; 46 (1): e2300179.                            

Linker histone H1.8 inhibits chromatin binding of condensins and DNA topoisomerase II to tune chromosome length and individualization., Choppakatla P., Elife. August 18, 2021; 10                           

APE2 Zf-GRF facilitates 3'-5' resection of DNA damage following oxidative stress., Wallace BD., Proc Natl Acad Sci U S A. January 10, 2017; 114 (2): 304-309.

Spindle-to-Cortex Communication in Cleaving Frog Eggs., Mitchison TJ., Cold Spring Harb Symp Quant Biol. January 1, 2017; 82 165-171.          

A repeated IMP-binding motif controls oskar mRNA translation and anchoring independently of Drosophila melanogaster IMP., Munro TP., J Cell Biol. February 13, 2006; 172 (4): 577-88.              

The expression and alternative splicing of alpha-neurexins during Xenopus development., Zeng Z., Int J Dev Biol. January 1, 2006; 50 (1): 39-46.                  

[Presumed role of the gravity in the establishment of the symmetrization in amphibian embryos. Response provided by the biological experimentation in space]., Bautz A., Bull Acad Soc Lorraines Sci. January 1, 2002; 41 (1-2): 58-66.

Comparative aspects of animal oogenesis., Matova N., Dev Biol. March 15, 2001; 231 (2): 291-320.  

Different activities of the frizzled-related proteins frzb2 and sizzled2 during Xenopus anteroposterior patterning., Bradley L., Dev Biol. November 1, 2000; 227 (1): 118-32.                    

Characterization of the zebrafish Orb/CPEB-related RNA binding protein and localization of maternal components in the zebrafish oocyte., Bally-Cuif L., Mech Dev. September 1, 1998; 77 (1): 31-47.

Translocation of a localized maternal mRNA to the vegetal pole of Xenopus oocytes., Melton DA., Nature. July 2, 1987; 328 (6125): 80-2.

High-frequency twinning of Xenopus laevis embryos from eggs centrifuged before first cleavage., Black SD., Dev Biol. July 1, 1986; 116 (1): 228-40.

Kinematics of gray crescent formation in Xenopus eggs: the displacement of subcortical cytoplasm relative to the egg surface., Vincent JP., Dev Biol. February 1, 1986; 113 (2): 484-500.

All components required for the eventual activation of muscle-specific actin genes are localized in the subequatorial region of an uncleaved amphibian egg., Gurdon JB., Proc Natl Acad Sci U S A. January 1, 1985; 82 (1): 139-43.

Ion currents and membrane domains in the cleaving Xenopus egg., Kline D., J Cell Biol. December 1, 1983; 97 (6): 1753-61.

Cytoplasmic phases in the first cell cycle of the activated frog egg., Elinson RP., Dev Biol. December 1, 1983; 100 (2): 440-51.

Evidence for a functional role of the cytoskeleton in determination of the dorsoventral axis in Xenopus laevis eggs., Ubbels GA., J Embryol Exp Morphol. October 1, 1983; 77 15-37.

Axis determination in eggs of Xenopus laevis: a critical period before first cleavage, identified by the common effects of cold, pressure and ultraviolet irradiation., Scharf SR., Dev Biol. September 1, 1983; 99 (1): 75-87.            

A reinvestigation of the role of the grey crescent in axis formation in xenopus laevis., Gerhart J., Nature. August 6, 1981; 292 (5823): 511-6.

Changes of the external and internal pigment pattern upon fertilization in the egg of Xenopus laevis., Palecek J., J Embryol Exp Morphol. June 1, 1978; 45 203-14.

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