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Differential nuclear import sets the timing of protein access to the embryonic genome. , Nguyen T., Nat Commun. October 6, 2022; 13 (1): 5887.
In vitro chromatin templates to study nucleotide excision repair. , Liu X., DNA Repair (Amst). December 1, 2015; 36 68-76.
Small ubiquitin-like modifier (SUMO)-mediated repression of the Xenopus Oocyte 5 S rRNA genes. , Malik MQ., J Biol Chem. December 19, 2014; 289 (51): 35468-81.
Zn-, Cd-, and Pb-transcription factor IIIA: properties, DNA binding, and comparison with TFIIIA-finger 3 metal complexes. , Huang M., J Inorg Biochem. May 1, 2004; 98 (5): 775-85.
Restricted specificity of Xenopus TFIIIA for transcription of somatic 5S rRNA genes. , Ghose R., Mol Cell Biol. March 1, 2004; 24 (6): 2467-77.
Binding of zinc finger protein transcription factor IIIA to its cognate DNA sequence with single UV photoproducts at specific sites and its effect on DNA repair. , Kwon Y., J Biol Chem. November 14, 2003; 278 (46): 45451-9.
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.
The Xenopus B2 factor involved in TFIIIA gene regulation is closely related to Sp1 and interacts in a complex with USF. , Penberthy WT., Gene. February 27, 2003; 305 (2): 205-15.
A homolog of FBP2/ KSRP binds to localized mRNAs in Xenopus oocytes. , Kroll TT ., Development. December 1, 2002; 129 (24): 5609-19.
Phosphorylation of Xenopus transcription factor IIIA by an oocyte protein kinase CK2. , Westmark CJ., Biochem J. March 1, 2002; 362 (Pt 2): 375-82.
DNA methylation at promoter regions regulates the timing of gene activation in Xenopus laevis embryos. , Stancheva I ., Dev Biol. March 1, 2002; 243 (1): 155-65.
cDNA cloning, DNA binding, and evolution of mammalian transcription factor IIIA. , Hanas JS., Gene. January 9, 2002; 282 (1-2): 43-52.
Assembly of the nuclear transcription and processing machinery: Cajal bodies (coiled bodies) and transcriptosomes. , Gall JG ., Mol Biol Cell. December 1, 1999; 10 (12): 4385-402.
How do linker histones mediate differential gene expression? , Crane-Robinson C., Bioessays. May 1, 1999; 21 (5): 367-71.
Regulation of DNA binding activity and nuclear transport of B- Myb in Xenopus oocytes. , Humbert-Lan G., J Biol Chem. April 9, 1999; 274 (15): 10293-300.
Tight correlation between inhibition of DNA repair in vitro and transcription factor IIIA binding in a 5S ribosomal RNA gene. , Conconi A., EMBO J. March 1, 1999; 18 (5): 1387-96.
Inhibition of RNA polymerase III transcription by a ribosome-associated kinase activity. , Westmark CJ., Nucleic Acids Res. October 15, 1998; 26 (20): 4758-64.
Differential nucleosome positioning on Xenopus oocyte and somatic 5 S RNA genes determines both TFIIIA and H1 binding: a mechanism for selective H1 repression. , Panetta G., J Mol Biol. September 25, 1998; 282 (3): 683-97.
Role of histone H1 as an architectural determinant of chromatin structure and as a specific repressor of transcription on Xenopus oocyte 5S rRNA genes. , Sera T., Mol Cell Biol. July 1, 1998; 18 (7): 3668-80.
Nucleosome translational position, not histone acetylation, determines TFIIIA binding to nucleosomal Xenopus laevis 5S rRNA genes. , Howe L., Mol Cell Biol. March 1, 1998; 18 (3): 1156-62.
Molecular biology of vertebrate transcription factor IIIA: cloning and characterization of TFIIIA from channel catfish oocytes. , Ogilvie MK., Gene. December 12, 1997; 203 (2): 103-12.
Nucleoskeleton and nucleo-cytoplasmic transport in oocytes and early development of Xenopus laevis. , Rudt F., Int J Dev Biol. February 1, 1996; 40 (1): 273-8.
Analysis of the binding of Xenopus transcription factor IIIA to oocyte 5 S rRNA and to the 5 S rRNA gene. , Rawlings SL., J Biol Chem. January 12, 1996; 271 (2): 868-77.
Differential binding of oocyte-type and somatic-type 5S rRNA to TFIIIA and ribosomal protein L5 in Xenopus oocytes: specialization for storage versus mobilization. , Allison LA., Dev Biol. April 1, 1995; 168 (2): 284-95.
Characterization of the 5 S RNA binding activity of Xenopus zinc finger protein p43. , Zang WQ., J Mol Biol. February 3, 1995; 245 (5): 549-58.
Overlapping transcription by RNA polymerases II and III of the Xenopus TFIIIA gene in somatic cells. , Martinez E., J Biol Chem. October 14, 1994; 269 (41): 25692-8.
Purification and characterization of human transcription factor IIIA. , Moorefield B., J Biol Chem. August 19, 1994; 269 (33): 20857-65.
Specific regulation of Xenopus chromosomal 5S rRNA gene transcription in vivo by histone H1. , Bouvet P., Genes Dev. May 15, 1994; 8 (10): 1147-59.
A position-dependent transcription-activating domain in TFIIIA. , Mao X., Mol Cell Biol. December 1, 1993; 13 (12): 7496-506.
Selective recruitment of masked maternal mRNA from messenger ribonucleoprotein particles containing FRGY2 (mRNP4). , Tafuri SR., J Biol Chem. November 15, 1993; 268 (32): 24255-61.
Masking mRNA from translation in somatic cells. , Ranjan M., Genes Dev. September 1, 1993; 7 (9): 1725-36.
Proteolytic footprinting of transcription factor TFIIIA reveals different tightly binding sites for 5S RNA and 5S DNA. , Bogenhagen DF ., Mol Cell Biol. September 1, 1993; 13 (9): 5149-58.
Role of TFIIIA zinc fingers in vivo: analysis of single-finger function in developing Xenopus embryos. , Rollins MB., Mol Cell Biol. August 1, 1993; 13 (8): 4776-83.
Identification of nuclear factors which interact with the 5' flanking region of the EF-1 alpha O gene in Xenopus laevis. , Olesen OF., FEBS Lett. November 30, 1992; 313 (3): 205-9.
Comparison of the sequence and structure of transcription factor IIIA from Bufo americanus and Rana pipiens. , Gaskins CJ., Gene. October 21, 1992; 120 (2): 197-206.
Interaction of Xenopus TFIIIC with the TFIIIA.5 S RNA gene complex. , Keller HJ., J Biol Chem. September 5, 1992; 267 (25): 18190-8.
Differential binding of zinc fingers from Xenopus TFIIIA and p43 to 5S RNA and the 5S RNA gene. , Darby MK., Mol Cell Biol. July 1, 1992; 12 (7): 3155-64.
Characterization of a Xenopus oocyte factor that binds to a developmentally regulated cis-element in the TFIIIA gene. , Pfaff SL., Dev Biol. May 1, 1992; 151 (1): 306-16.
Isolation and characterization of the gene encoding EF-1 alpha O, an elongation factor 1-alpha expressed during early development of Xenopus laevis. , Frydenberg J., Gene. December 30, 1991; 109 (2): 185-92.
The genes encoding the major 42S storage particle proteins are expressed in male and female germ cells of Xenopus laevis. , Abdallah B., Development. November 1, 1991; 113 (3): 851-6.
Regulation of the Xenopus laevis transcription factor IIIA gene during oogenesis and early embryogenesis: negative elements repress the O- TFIIIA promoter in embryonic cells. , Pfaff SL., Dev Biol. June 1, 1991; 145 (2): 241-54.
An analysis of transcription factor TFIIIA-mediated DNA supercoiling. , Sekiguchi JM., DNA Cell Biol. April 1, 1991; 10 (3): 223-32.
Involvement of "hinge" nucleotides of Xenopus laevis 5 S rRNA in the RNA structural organization and in the binding of transcription factor TFIIIA. , Baudin F., J Mol Biol. March 5, 1991; 218 (1): 69-81.
Mutations in 5S DNA and 5S RNA have different effects on the binding of Xenopus transcription factor IIIA. , You QM., Biochemistry. March 5, 1991; 30 (9): 2495-500.
TFIIIA induced DNA bending: effect of low ionic strength electrophoresis buffer conditions. , Schroth GP., Nucleic Acids Res. February 11, 1991; 19 (3): 511-6.
The Xenopus B1 factor is closely related to the mammalian activator USF and is implicated in the developmental regulation of TFIIIA gene expression. , Kaulen H., Mol Cell Biol. January 1, 1991; 11 (1): 412-24.
Chromosomal footprinting of transcriptionally active and inactive oocyte-type 5S RNA genes of Xenopus laevis. , Engelke DR., Nucleic Acids Res. October 25, 1990; 18 (20): 6031-7.
Characterization of the equilibrium binding of Xenopus transcription factor IIIA to the 5 S RNA gene. , Romaniuk PJ., J Biol Chem. October 15, 1990; 265 (29): 17593-600.
Additional intragenic promoter elements of the Xenopus 5S RNA genes upstream from the TFIIIA-binding site. , Keller HJ., Mol Cell Biol. October 1, 1990; 10 (10): 5166-76.
Elongation factor 1 alpha ( EF-1 alpha) is concentrated in the Balbiani body and accumulates coordinately with the ribosomes during oogenesis of Xenopus laevis. , Viel A., Dev Biol. October 1, 1990; 141 (2): 270-8.