Loeb LA - Search Results

1

Destabilization of tetraplex structures of the fragile X repeat sequence (CGG)n is mediated by homolog-conserved domains in three members of the hnRNP family.

Khateb S, Weisman-Shomer P, Hershco I, Loeb LA, Fry M. Khateb S, et al. Among authors: loeb la. Nucleic Acids Res. 2004 Aug 9;32(14):4145-54. doi: 10.1093/nar/gkh745. Print 2004. Nucleic Acids Res. 2004. PMID: 15302914 Free PMC article.

2

The fragile X syndrome d(CGG)n nucleotide repeats form a stable tetrahelical structure.

Fry M, Loeb LA. Fry M, et al. Among authors: loeb la. Proc Natl Acad Sci U S A. 1994 May 24;91(11):4950-4. doi: 10.1073/pnas.91.11.4950. Proc Natl Acad Sci U S A. 1994. PMID: 8197163 Free PMC article.

3

Human werner syndrome DNA helicase unwinds tetrahelical structures of the fragile X syndrome repeat sequence d(CGG)n.

Fry M, Loeb LA. Fry M, et al. Among authors: loeb la. J Biol Chem. 1999 Apr 30;274(18):12797-802. doi: 10.1074/jbc.274.18.12797. J Biol Chem. 1999. PMID: 10212265 Free article.

4

Human Ku antigen tightly binds and stabilizes a tetrahelical form of the Fragile X syndrome d(CGG)n expanded sequence.

Uliel L, Weisman-Shomer P, Oren-Jazan H, Newcomb T, Loeb LA, Fry M. Uliel L, et al. Among authors: loeb la. J Biol Chem. 2000 Oct 20;275(42):33134-41. doi: 10.1074/jbc.M005542200. J Biol Chem. 2000. PMID: 10924524 Free article.

5

Factor D is a selective single-stranded oligodeoxythymidine binding protein.

Fry M, Perrino FW, Levy A, Loeb LA. Fry M, et al. Among authors: loeb la. Nucleic Acids Res. 1988 Jan 11;16(1):199-211. doi: 10.1093/nar/16.1.199. Nucleic Acids Res. 1988. PMID: 3340524 Free PMC article.

6

Interactions between the Werner syndrome helicase and DNA polymerase delta specifically facilitate copying of tetraplex and hairpin structures of the d(CGG)n trinucleotide repeat sequence.

Kamath-Loeb AS, Loeb LA, Johansson E, Burgers PM, Fry M. Kamath-Loeb AS, et al. Among authors: loeb la. J Biol Chem. 2001 May 11;276(19):16439-46. doi: 10.1074/jbc.M100253200. Epub 2001 Feb 8. J Biol Chem. 2001. PMID: 11279038 Free article.

7

A DNA polymerase alpha pause site is a hot spot for nucleotide misinsertion.

Fry M, Loeb LA. Fry M, et al. Among authors: loeb la. Proc Natl Acad Sci U S A. 1992 Jan 15;89(2):763-7. doi: 10.1073/pnas.89.2.763. Proc Natl Acad Sci U S A. 1992. PMID: 1731352 Free PMC article.

8

Sequence specificity of pausing by DNA polymerases.

Weisman-Shomer P, Dube DK, Perrino FW, Stokes K, Loeb LA, Fry M. Weisman-Shomer P, et al. Among authors: loeb la. Biochem Biophys Res Commun. 1989 Nov 15;164(3):1149-56. doi: 10.1016/0006-291x(89)91789-0. Biochem Biophys Res Commun. 1989. PMID: 2686635

9

The Werner syndrome protein is distinguished from the Bloom syndrome protein by its capacity to tightly bind diverse DNA structures.

Kamath-Loeb A, Loeb LA, Fry M. Kamath-Loeb A, et al. Among authors: loeb la. PLoS One. 2012;7(1):e30189. doi: 10.1371/journal.pone.0030189. Epub 2012 Jan 17. PLoS One. 2012. PMID: 22272300 Free PMC article.

10

DNA polymerase-alpha: enzymology, function, fidelity, and mutagenesis.

Loeb LA, Liu PK, Fry M. Loeb LA, et al. Prog Nucleic Acid Res Mol Biol. 1986;33:57-110. doi: 10.1016/s0079-6603(08)60020-3. Prog Nucleic Acid Res Mol Biol. 1986. PMID: 3797680 No abstract available.

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