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Items: 1 to 50 of 90

1.

Structural insights into the 3'-end mRNA maturation machinery: Snapshot on polyadenylation signal recognition.

Thore S, Fribourg S.

Biochimie. 2019 Mar 28. pii: S0300-9084(19)30085-9. doi: 10.1016/j.biochi.2019.03.016. [Epub ahead of print]

PMID:
30930282
2.

Structural and interaction analysis of the Rrp5 C-terminal region.

Pérébaskine N, Thore S, Fribourg S.

FEBS Open Bio. 2018 Aug 30;8(10):1605-1614. doi: 10.1002/2211-5463.12495. eCollection 2018 Oct.

3.

Varicella-zoster virus CNS vasculitis and RNA polymerase III gene mutation in identical twins.

Carter-Timofte ME, Hansen AF, Mardahl M, Fribourg S, Rapaport F, Zhang SY, Casanova JL, Paludan SR, Christiansen M, Larsen CS, Mogensen TH.

Neurol Neuroimmunol Neuroinflamm. 2018 Sep 7;5(6):e500. doi: 10.1212/NXI.0000000000000500. eCollection 2018 Nov.

4.

Domain definition and interaction mapping for the endonuclease complex hNob1/hPno1.

Raoelijaona F, Thore S, Fribourg S.

RNA Biol. 2018;15(9):1174-1180. doi: 10.1080/15476286.2018.1517013. Epub 2018 Sep 18.

PMID:
30176151
5.

The Npa1p complex chaperones the assembly of the earliest eukaryotic large ribosomal subunit precursor.

Joret C, Capeyrou R, Belhabich-Baumas K, Plisson-Chastang C, Ghandour R, Humbert O, Fribourg S, Leulliot N, Lebaron S, Henras AK, Henry Y.

PLoS Genet. 2018 Aug 31;14(8):e1007597. doi: 10.1371/journal.pgen.1007597. eCollection 2018 Aug.

6.

Distinct roles of Pcf11 zinc-binding domains in pre-mRNA 3'-end processing.

Guéguéniat J, Dupin AF, Stojko J, Beaurepaire L, Cianférani S, Mackereth CD, Minvielle-Sébastia L, Fribourg S.

Nucleic Acids Res. 2017 Sep 29;45(17):10115-10131. doi: 10.1093/nar/gkx674.

7.

Inborn errors in RNA polymerase III underlie severe varicella zoster virus infections.

Ogunjimi B, Zhang SY, Sørensen KB, Skipper KA, Carter-Timofte M, Kerner G, Luecke S, Prabakaran T, Cai Y, Meester J, Bartholomeus E, Bolar NA, Vandeweyer G, Claes C, Sillis Y, Lorenzo L, Fiorenza RA, Boucherit S, Dielman C, Heynderickx S, Elias G, Kurotova A, Auwera AV, Verstraete L, Lagae L, Verhelst H, Jansen A, Ramet J, Suls A, Smits E, Ceulemans B, Van Laer L, Plat Wilson G, Kreth J, Picard C, Von Bernuth H, Fluss J, Chabrier S, Abel L, Mortier G, Fribourg S, Mikkelsen JG, Casanova JL, Paludan SR, Mogensen TH.

J Clin Invest. 2017 Sep 1;127(9):3543-3556. doi: 10.1172/JCI92280. Epub 2017 Aug 7.

8.

Pwp2 mediates UTP-B assembly via two structurally independent domains.

Boissier F, Schmidt CM, Linnemann J, Fribourg S, Perez-Fernandez J.

Sci Rep. 2017 Jun 9;7(1):3169. doi: 10.1038/s41598-017-03034-y.

9.

Sqt1p is an eight-bladed WD40 protein.

Frénois F, Legrand P, Fribourg S.

Acta Crystallogr F Struct Biol Commun. 2016 Jan;72(Pt 1):59-64. doi: 10.1107/S2053230X15024097. Epub 2016 Jan 1.

10.

Structural analysis of human RPC32β-RPC62 complex.

Boissier F, Dumay-Odelot H, Teichmann M, Fribourg S.

J Struct Biol. 2015 Dec;192(3):313-319. doi: 10.1016/j.jsb.2015.09.004. Epub 2015 Sep 21.

PMID:
26394183
11.

Recessive mutations in POLR1C cause a leukodystrophy by impairing biogenesis of RNA polymerase III.

Thiffault I, Wolf NI, Forget D, Guerrero K, Tran LT, Choquet K, Lavallée-Adam M, Poitras C, Brais B, Yoon G, Sztriha L, Webster RI, Timmann D, van de Warrenburg BP, Seeger J, Zimmermann A, Máté A, Goizet C, Fung E, van der Knaap MS, Fribourg S, Vanderver A, Simons C, Taft RJ, Yates JR 3rd, Coulombe B, Bernard G.

Nat Commun. 2015 Jul 7;6:7623. doi: 10.1038/ncomms8623.

12.

Chemical shift assignments of a new folded domain from yeast Pcf11.

Xu X, Pérébaskine N, Minvielle-Sébastia L, Fribourg S, Mackereth CD.

Biomol NMR Assign. 2015 Oct;9(2):421-5. doi: 10.1007/s12104-015-9622-2. Epub 2015 Jul 2.

PMID:
26133941
13.

Clinical spectrum of 4H leukodystrophy caused by POLR3A and POLR3B mutations.

Wolf NI, Vanderver A, van Spaendonk RM, Schiffmann R, Brais B, Bugiani M, Sistermans E, Catsman-Berrevoets C, Kros JM, Pinto PS, Pohl D, Tirupathi S, Strømme P, de Grauw T, Fribourg S, Demos M, Pizzino A, Naidu S, Guerrero K, van der Knaap MS, Bernard G; 4H Research Group.

Neurology. 2014 Nov 18;83(21):1898-905. doi: 10.1212/WNL.0000000000001002. Epub 2014 Oct 22.

14.

Crucial role of the Rcl1p-Bms1p interaction for yeast pre-ribosomal RNA processing.

Delprato A, Al Kadri Y, Pérébaskine N, Monfoulet C, Henry Y, Henras AK, Fribourg S.

Nucleic Acids Res. 2014 Sep;42(15):10161-72. doi: 10.1093/nar/gku682. Epub 2014 Jul 26.

15.

Structural basis for ATP loss by Clp1p in a G135R mutant protein.

Dupin AF, Fribourg S.

Biochimie. 2014 Jun;101:203-7. doi: 10.1016/j.biochi.2014.01.017. Epub 2014 Feb 5.

PMID:
24508575
16.

Structural and functional aspects of winged-helix domains at the core of transcription initiation complexes.

Teichmann M, Dumay-Odelot H, Fribourg S.

Transcription. 2012 Jan-Feb;3(1):2-7. doi: 10.4161/trns.3.1.18917.

PMID:
22456313
17.

Recessive mutations in POLR3B, encoding the second largest subunit of Pol III, cause a rare hypomyelinating leukodystrophy.

Tétreault M, Choquet K, Orcesi S, Tonduti D, Balottin U, Teichmann M, Fribourg S, Schiffmann R, Brais B, Vanderver A, Bernard G.

Am J Hum Genet. 2011 Nov 11;89(5):652-5. doi: 10.1016/j.ajhg.2011.10.006. Epub 2011 Oct 27.

18.

An essential role for Clp1 in assembly of polyadenylation complex CF IA and Pol II transcription termination.

Haddad R, Maurice F, Viphakone N, Voisinet-Hakil F, Fribourg S, Minvielle-Sébastia L.

Nucleic Acids Res. 2012 Feb;40(3):1226-39. doi: 10.1093/nar/gkr800. Epub 2011 Oct 12.

19.

Mutations of POLR3A encoding a catalytic subunit of RNA polymerase Pol III cause a recessive hypomyelinating leukodystrophy.

Bernard G, Chouery E, Putorti ML, Tétreault M, Takanohashi A, Carosso G, Clément I, Boespflug-Tanguy O, Rodriguez D, Delague V, Abou Ghoch J, Jalkh N, Dorboz I, Fribourg S, Teichmann M, Megarbane A, Schiffmann R, Vanderver A, Brais B.

Am J Hum Genet. 2011 Sep 9;89(3):415-23. doi: 10.1016/j.ajhg.2011.07.014. Erratum in: Am J Hum Genet. 2012 Nov 2;91(5):972.

20.

Peptides derived from the bifunctional kinase/RNase enzyme IRE1α modulate IRE1α activity and protect cells from endoplasmic reticulum stress.

Bouchecareilh M, Higa A, Fribourg S, Moenner M, Chevet E.

FASEB J. 2011 Sep;25(9):3115-29. doi: 10.1096/fj.11-182931. Epub 2011 Jun 16.

PMID:
21680894
21.

Locked tether formation by cooperative folding of Rna14p monkeytail and Rna15p hinge domains in the yeast CF IA complex.

Moreno-Morcillo M, Minvielle-Sébastia L, Fribourg S, Mackereth CD.

Structure. 2011 Apr 13;19(4):534-45. doi: 10.1016/j.str.2011.02.003.

22.

Structure-function analysis of hRPC62 provides insights into RNA polymerase III transcription initiation.

Lefèvre S, Dumay-Odelot H, El-Ayoubi L, Budd A, Legrand P, Pinaud N, Teichmann M, Fribourg S.

Nat Struct Mol Biol. 2011 Mar;18(3):352-8. doi: 10.1038/nsmb.1996. Epub 2011 Feb 27. Erratum in: Nat Struct Mol Biol. 2011 Apr;18(4):516.

PMID:
21358628
23.

Deciphering correct strategies for multiprotein complex assembly by co-expression: application to complexes as large as the histone octamer.

Diebold ML, Fribourg S, Koch M, Metzger T, Romier C.

J Struct Biol. 2011 Aug;175(2):178-88. doi: 10.1016/j.jsb.2011.02.001. Epub 2011 Feb 12.

PMID:
21320604
24.

Hexameric architecture of CstF supported by CstF-50 homodimerization domain structure.

Moreno-Morcillo M, Minvielle-Sébastia L, Mackereth C, Fribourg S.

RNA. 2011 Mar;17(3):412-8. doi: 10.1261/rna.2481011. Epub 2011 Jan 13.

25.

[Diamond-Blackfan anemia reveals the dark side of ribosome biogenesis].

Aguissa-Touré AH, Da Costa L, Leblanc T, Tchernia G, Fribourg S, Gleizes PE.

Med Sci (Paris). 2009 Jan;25(1):69-76. doi: 10.1051/medsci/200925169. Review. French.

26.

Exploring TAR-RNA aptamer loop-loop interaction by X-ray crystallography, UV spectroscopy and surface plasmon resonance.

Lebars I, Legrand P, Aimé A, Pinaud N, Fribourg S, Di Primo C.

Nucleic Acids Res. 2008 Dec;36(22):7146-56. doi: 10.1093/nar/gkn831. Epub 2008 Nov 7.

27.

RPS19 mutations in patients with Diamond-Blackfan anemia.

Campagnoli MF, Ramenghi U, Armiraglio M, Quarello P, Garelli E, Carando A, Avondo F, Pavesi E, Fribourg S, Gleizes PE, Loreni F, Dianzani I.

Hum Mutat. 2008 Jul;29(7):911-20. doi: 10.1002/humu.20752. Review.

PMID:
18412286
28.

Mutation of ribosomal protein RPS24 in Diamond-Blackfan anemia results in a ribosome biogenesis disorder.

Choesmel V, Fribourg S, Aguissa-Touré AH, Pinaud N, Legrand P, Gazda HT, Gleizes PE.

Hum Mol Genet. 2008 May 1;17(9):1253-63. doi: 10.1093/hmg/ddn015. Epub 2008 Jan 29.

PMID:
18230666
29.

Molecular basis of Diamond-Blackfan anemia: structure and function analysis of RPS19.

Gregory LA, Aguissa-Touré AH, Pinaud N, Legrand P, Gleizes PE, Fribourg S.

Nucleic Acids Res. 2007;35(17):5913-21. Epub 2007 Aug 28.

30.

The structure of the CstF-77 homodimer provides insights into CstF assembly.

Legrand P, Pinaud N, Minvielle-Sébastia L, Fribourg S.

Nucleic Acids Res. 2007;35(13):4515-22. Epub 2007 Jun 21.

31.

Impaired ribosome biogenesis in Diamond-Blackfan anemia.

Choesmel V, Bacqueville D, Rouquette J, Noaillac-Depeyre J, Fribourg S, Crétien A, Leblanc T, Tchernia G, Da Costa L, Gleizes PE.

Blood. 2007 Feb 1;109(3):1275-83. Epub 2006 Oct 19.

32.

The archaeal exosome core is a hexameric ring structure with three catalytic subunits.

Lorentzen E, Walter P, Fribourg S, Evguenieva-Hackenberg E, Klug G, Conti E.

Nat Struct Mol Biol. 2005 Jul;12(7):575-81. Epub 2005 Jun 12.

PMID:
15951817
33.

Solution structure of the C-terminal domain of TFIIH P44 subunit reveals a novel type of C4C4 ring domain involved in protein-protein interactions.

Kellenberger E, Dominguez C, Fribourg S, Wasielewski E, Moras D, Poterszman A, Boelens R, Kieffer B.

J Biol Chem. 2005 May 27;280(21):20785-92. Epub 2005 Mar 24.

35.

A novel mode of RBD-protein recognition in the Y14-Mago complex.

Fribourg S, Gatfield D, Izaurralde E, Conti E.

Nat Struct Biol. 2003 Jun;10(6):433-9.

PMID:
12730685
36.

Expression of FLAG fusion proteins in insect cells: application to the multi-subunit transcription/DNA repair factor TFIIH.

Jawhari A, Uhring M, Crucifix C, Fribourg S, Schultz P, Poterszman A, Egly JM, Moras D.

Protein Expr Purif. 2002 Apr;24(3):513-23.

PMID:
11922769
37.
38.

Dissecting the interaction network of multiprotein complexes by pairwise coexpression of subunits in E. coli.

Fribourg S, Romier C, Werten S, Gangloff YG, Poterszman A, Moras D.

J Mol Biol. 2001 Feb 16;306(2):363-73.

PMID:
11237605
39.

Molecular structure of human TFIIH.

Schultz P, Fribourg S, Poterszman A, Mallouh V, Moras D, Egly JM.

Cell. 2000 Sep 1;102(5):599-607.

40.

Structural characterization of the cysteine-rich domain of TFIIH p44 subunit.

Fribourg S, Kellenberger E, Rogniaux H, Poterszman A, Van Dorsselaer A, Thierry JC, Egly JM, Moras D, Kieffer B.

J Biol Chem. 2000 Oct 13;275(41):31963-71.

41.

Obstetric maneuvers in cases of shoulder dystocia.

Fribourg S.

Am J Obstet Gynecol. 2000 May;182(5):1272. No abstract available.

PMID:
10819872
42.

Mutations in the XPD helicase gene result in XP and TTD phenotypes, preventing interaction between XPD and the p44 subunit of TFIIH.

Coin F, Marinoni JC, Rodolfo C, Fribourg S, Pedrini AM, Egly JM.

Nat Genet. 1998 Oct;20(2):184-8.

PMID:
9771713
43.

Mutations in the amino-terminal domain of the human poly(ADP-ribose) polymerase that affect its catalytic activity but not its DNA binding capacity.

Trucco C, Flatter E, Fribourg S, de Murcia G, Ménissier-de Murcia J.

FEBS Lett. 1996 Dec 16;399(3):313-6.

44.

Poly(ADP-ribose) polymerase: structure-function relationship.

Masson M, Rolli V, Dantzer F, Trucco C, Schreiber V, Fribourg S, Molinete M, Ruf A, Miranda EA, Niedergang C, et al.

Biochimie. 1995;77(6):456-61.

PMID:
7578429
45.

Definition of pelvic abscess--complex or not?

Fribourg S.

Am J Obstet Gynecol. 1994 Oct;171(4):1162-3. No abstract available.

PMID:
7943095
46.

Should women with familial ovarian cancer undergo prophylactic oophorectomy?

Fribourg S.

Obstet Gynecol. 1993 Feb;81(2):315-6. No abstract available.

PMID:
8423972
47.

Cesareans are more than skin deep.

Fribourg S.

Am J Obstet Gynecol. 1991 Dec;165(6 Pt 1):1899. No abstract available.

PMID:
1805835
48.

Cervical effacement: variation in belief among clinicians.

Fribourg S.

Obstet Gynecol. 1991 Nov;78(5 Pt 1):886-7. No abstract available.

PMID:
1796953
49.

Leuprolide depot before myomectomy.

Fribourg S.

Fertil Steril. 1990 Apr;53(4):754. No abstract available.

PMID:
2108064
50.

Perinatal death as a result of social factors.

Fribourg S.

Am J Obstet Gynecol. 1989 Dec;161(6 Pt 1):1748. No abstract available.

PMID:
2603939

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