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    Results: 1 to 20 of 81

    1.

    DNA replication origin interference increases the spacing between initiation events in human cells.

    Lebofsky R, Heilig R, Sonnleitner M, Weissenbach J, Bensimon A.

    Mol Biol Cell. 2006 Dec;17(12):5337-45. Epub 2006 Sep 27.PMID: 17005913 [PubMed - indexed for MEDLINE]Related articlesFree article

    2.

    [Bacteriological sampling of surfaces: importance of the step of enrichment and the choice of the culture media]

    Meunier O, Hernandez C, Piroird M, Heilig R, Steinbach D, Freyd A.

    Ann Biol Clin (Paris). 2005 Sep-Oct;63(5):481-6. French. PMID: 16230282 [PubMed - indexed for MEDLINE]Related articlesFree article

    3.

    Mutations in the transporter ABCA12 are associated with lamellar ichthyosis type 2.

    Lefévre C, Audebert S, Jobard F, Bouadjar B, Lakhdar H, Boughdene-Stambouli O, Blanchet-Bardon C, Heilig R, Foglio M, Weissenbach J, Lathrop M, Prud'homme JF, Fischer J.

    Hum Mol Genet. 2003 Sep 15;12(18):2369-78. Epub 2003 Jul 15.PMID: 12915478 [PubMed - indexed for MEDLINE]Related articlesFree article

    4.

    [Sequencing the human genome: chromosome 14, the 4th chromosome completed]

    Heilig R, Fonknechten N.

    Med Sci (Paris). 2003 May;19(5):522-5. French. No abstract available. PMID: 12836379 [PubMed - indexed for MEDLINE]Related articlesFree article

    5.

    An integrated analysis of the genome of the hyperthermophilic archaeon Pyrococcus abyssi.

    Cohen GN, Barbe V, Flament D, Galperin M, Heilig R, Lecompte O, Poch O, Prieur D, Quérellou J, Ripp R, Thierry JC, Van der Oost J, Weissenbach J, Zivanovic Y, Forterre P.

    Mol Microbiol. 2003 Mar;47(6):1495-512.PMID: 12622808 [PubMed - indexed for MEDLINE]Related articles

    6.

    The DNA sequence and analysis of human chromosome 14.

    Heilig R, Eckenberg R, Petit JL, Fonknechten N, Da Silva C, Cattolico L, Levy M, Barbe V, de Berardinis V, Ureta-Vidal A, Pelletier E, Vico V, Anthouard V, Rowen L, Madan A, Qin S, Sun H, Du H, Pepin K, Artiguenave F, Robert C, Cruaud C, Brüls T, Jaillon O, Friedlander L, Samson G, Brottier P, Cure S, Ségurens B, Anière F, Samain S, Crespeau H, Abbasi N, Aiach N, Boscus D, Dickhoff R, Dors M, Dubois I, Friedman C, Gouyvenoux M, James R, Madan A, Mairey-Estrada B, Mangenot S, Martins N, Ménard M, Oztas S, Ratcliffe A, Shaffer T, Trask B, Vacherie B, Bellemere C, Belser C, Besnard-Gonnet M, Bartol-Mavel D, Boutard M, Briez-Silla S, Combette S, Dufossé-Laurent V, Ferron C, Lechaplais C, Louesse C, Muselet D, Magdelenat G, Pateau E, Petit E, Sirvain-Trukniewicz P, Trybou A, Vega-Czarny N, Bataille E, Bluet E, Bordelais I, Dubois M, Dumont C, Guérin T, Haffray S, Hammadi R, Muanga J, Pellouin V, Robert D, Wunderle E, Gauguet G, Roy A, Sainte-Marthe L, Verdier J, Verdier-Discala C, Hillier L, Fulton L, McPherson J, Matsuda F, Wilson R, Scarpelli C, Gyapay G, Wincker P, Saurin W, Quétier F, Waterston R, Hood L, Weissenbach J.

    Nature. 2003 Feb 6;421(6923):601-7. Epub 2003 Jan 1.PMID: 12508121 [PubMed - indexed for MEDLINE]Related articles

    7.

    Assignment of FUT8 to chicken chromosome band 5q1.4 and to human chromosome 14q23.2-->q24.1 by in situ hybridization. Conserved and compared synteny between human and chicken.

    Coullin P, Crooijmans RP, Groenen MA, Heilig R, Mollicone R, Oriol R, Candelier JJ.

    Cytogenet Genome Res. 2002;97(3-4):234-8.PMID: 12438718 [PubMed - indexed for MEDLINE]Related articles

    8.

    Comprehensive analysis of a large genomic sequence at the putative B-cell chronic lymphocytic leukaemia (B-CLL) tumour suppresser gene locus.

    Rondeau G, Moreau I, Bézieau S, Petit JL, Heilig R, Fernandez S, Pennarun E, Myers JS, Batzer MA, Moisan JP, Devilder MC.

    Mutat Res. 2001 Dec;458(3-4):55-70.PMID: 11691637 [PubMed - indexed for MEDLINE]Related articles

    9.

    Mutations in CGI-58, the gene encoding a new protein of the esterase/lipase/thioesterase subfamily, in Chanarin-Dorfman syndrome.

    Lefèvre C, Jobard F, Caux F, Bouadjar B, Karaduman A, Heilig R, Lakhdar H, Wollenberg A, Verret JL, Weissenbach J, Ozgüc M, Lathrop M, Prud'homme JF, Fischer J.

    Am J Hum Genet. 2001 Nov;69(5):1002-12. Epub 2001 Oct 2.PMID: 11590543 [PubMed - indexed for MEDLINE]Related articlesFree article

    10.

    A new recurrent and specific cryptic translocation, t(5;14)(q35;q32), is associated with expression of the Hox11L2 gene in T acute lymphoblastic leukemia.

    Bernard OA, Busson-LeConiat M, Ballerini P, Mauchauffé M, Della Valle V, Monni R, Nguyen Khac F, Mercher T, Penard-Lacronique V, Pasturaud P, Gressin L, Heilig R, Daniel MT, Lessard M, Berger R.

    Leukemia. 2001 Oct;15(10):1495-504.PMID: 11587205 [PubMed - indexed for MEDLINE]Related articles

    11.

    Genome evolution at the genus level: comparison of three complete genomes of hyperthermophilic archaea.

    Lecompte O, Ripp R, Puzos-Barbe V, Duprat S, Heilig R, Dietrich J, Thierry JC, Poch O.

    Genome Res. 2001 Jun;11(6):981-93.PMID: 11381026 [PubMed - indexed for MEDLINE]Related articlesFree article

    12.

    The complete genome sequence of the murine respiratory pathogen Mycoplasma pulmonis.

    Chambaud I, Heilig R, Ferris S, Barbe V, Samson D, Galisson F, Moszer I, Dybvig K, Wróblewski H, Viari A, Rocha EP, Blanchard A.

    Nucleic Acids Res. 2001 May 15;29(10):2145-53.PMID: 11353084 [PubMed - indexed for MEDLINE]Related articlesFree article

    13.

    Mutations in the gene encoding SLURP-1 in Mal de Meleda.

    Fischer J, Bouadjar B, Heilig R, Huber M, Lefèvre C, Jobard F, Macari F, Bakija-Konsuo A, Ait-Belkacem F, Weissenbach J, Lathrop M, Hohl D, Prud'homme JF.

    Hum Mol Genet. 2001 Apr 1;10(8):875-80.PMID: 11285253 [PubMed - indexed for MEDLINE]Related articlesFree article

    14.

    A physical map of human chromosome 14.

    Brüls T, Gyapay G, Petit JL, Artiguenave F, Vico V, Qin S, Tin-Wollam AM, Da Silva C, Muselet D, Mavel D, Pelletier E, Levy M, Fujiyama A, Matsuda F, Wilson R, Rowen L, Hood L, Weissenbach J, Saurin W, Heilig R.

    Nature. 2001 Feb 15;409(6822):947-8.PMID: 11237018 [PubMed - indexed for MEDLINE]Related articles

    15.

    A physical map of the human genome.

    McPherson JD, Marra M, Hillier L, Waterston RH, Chinwalla A, Wallis J, Sekhon M, Wylie K, Mardis ER, Wilson RK, Fulton R, Kucaba TA, Wagner-McPherson C, Barbazuk WB, Gregory SG, Humphray SJ, French L, Evans RS, Bethel G, Whittaker A, Holden JL, McCann OT, Dunham A, Soderlund C, Scott CE, Bentley DR, Schuler G, Chen HC, Jang W, Green ED, Idol JR, Maduro VV, Montgomery KT, Lee E, Miller A, Emerling S, Kucherlapati, Gibbs R, Scherer S, Gorrell JH, Sodergren E, Clerc-Blankenburg K, Tabor P, Naylor S, Garcia D, de Jong PJ, Catanese JJ, Nowak N, Osoegawa K, Qin S, Rowen L, Madan A, Dors M, Hood L, Trask B, Friedman C, Massa H, Cheung VG, Kirsch IR, Reid T, Yonescu R, Weissenbach J, Bruls T, Heilig R, Branscomb E, Olsen A, Doggett N, Cheng JF, Hawkins T, Myers RM, Shang J, Ramirez L, Schmutz J, Velasquez O, Dixon K, Stone NE, Cox DR, Haussler D, Kent WJ, Furey T, Rogic S, Kennedy S, Jones S, Rosenthal A, Wen G, Schilhabel M, Gloeckner G, Nyakatura G, Siebert R, Schlegelberger B, Korenberg J, Chen XN, Fujiyama A, Hattori M, Toyoda A, Yada T, Park HS, Sakaki Y, Shimizu N, Asakawa S, Kawasaki K, Sasaki T, Shintani A, Shimizu A, Shibuya K, Kudoh J, Minoshima S, Ramser J, Seranski P, Hoff C, Poustka A, Reinhardt R, Lehrach H; International Human Genome Mapping Consortium.

    Nature. 2001 Feb 15;409(6822):934-41.PMID: 11237014 [PubMed - indexed for MEDLINE]Related articles

    16.

    Initial sequencing and analysis of the human genome.

    Lander ES, Linton LM, Birren B, Nusbaum C, Zody MC, Baldwin J, Devon K, Dewar K, Doyle M, FitzHugh W, Funke R, Gage D, Harris K, Heaford A, Howland J, Kann L, Lehoczky J, LeVine R, McEwan P, McKernan K, Meldrim J, Mesirov JP, Miranda C, Morris W, Naylor J, Raymond C, Rosetti M, Santos R, Sheridan A, Sougnez C, Stange-Thomann N, Stojanovic N, Subramanian A, Wyman D, Rogers J, Sulston J, Ainscough R, Beck S, Bentley D, Burton J, Clee C, Carter N, Coulson A, Deadman R, Deloukas P, Dunham A, Dunham I, Durbin R, French L, Grafham D, Gregory S, Hubbard T, Humphray S, Hunt A, Jones M, Lloyd C, McMurray A, Matthews L, Mercer S, Milne S, Mullikin JC, Mungall A, Plumb R, Ross M, Shownkeen R, Sims S, Waterston RH, Wilson RK, Hillier LW, McPherson JD, Marra MA, Mardis ER, Fulton LA, Chinwalla AT, Pepin KH, Gish WR, Chissoe SL, Wendl MC, Delehaunty KD, Miner TL, Delehaunty A, Kramer JB, Cook LL, Fulton RS, Johnson DL, Minx PJ, Clifton SW, Hawkins T, Branscomb E, Predki P, Richardson P, Wenning S, Slezak T, Doggett N, Cheng JF, Olsen A, Lucas S, Elkin C, Uberbacher E, Frazier M, Gibbs RA, Muzny DM, Scherer SE, Bouck JB, Sodergren EJ, Worley KC, Rives CM, Gorrell JH, Metzker ML, Naylor SL, Kucherlapati RS, Nelson DL, Weinstock GM, Sakaki Y, Fujiyama A, Hattori M, Yada T, Toyoda A, Itoh T, Kawagoe C, Watanabe H, Totoki Y, Taylor T, Weissenbach J, Heilig R, Saurin W, Artiguenave F, Brottier P, Bruls T, Pelletier E, Robert C, Wincker P, Smith DR, Doucette-Stamm L, Rubenfield M, Weinstock K, Lee HM, Dubois J, Rosenthal A, Platzer M, Nyakatura G, Taudien S, Rump A, Yang H, Yu J, Wang J, Huang G, Gu J, Hood L, Rowen L, Madan A, Qin S, Davis RW, Federspiel NA, Abola AP, Proctor MJ, Myers RM, Schmutz J, Dickson M, Grimwood J, Cox DR, Olson MV, Kaul R, Raymond C, Shimizu N, Kawasaki K, Minoshima S, Evans GA, Athanasiou M, Schultz R, Roe BA, Chen F, Pan H, Ramser J, Lehrach H, Reinhardt R, McCombie WR, de la Bastide M, Dedhia N, Blöcker H, Hornischer K, Nordsiek G, Agarwala R, Aravind L, Bailey JA, Bateman A, Batzoglou S, Birney E, Bork P, Brown DG, Burge CB, Cerutti L, Chen HC, Church D, Clamp M, Copley RR, Doerks T, Eddy SR, Eichler EE, Furey TS, Galagan J, Gilbert JG, Harmon C, Hayashizaki Y, Haussler D, Hermjakob H, Hokamp K, Jang W, Johnson LS, Jones TA, Kasif S, Kaspryzk A, Kennedy S, Kent WJ, Kitts P, Koonin EV, Korf I, Kulp D, Lancet D, Lowe TM, McLysaght A, Mikkelsen T, Moran JV, Mulder N, Pollara VJ, Ponting CP, Schuler G, Schultz J, Slater G, Smit AF, Stupka E, Szustakowski J, Thierry-Mieg D, Thierry-Mieg J, Wagner L, Wallis J, Wheeler R, Williams A, Wolf YI, Wolfe KH, Yang SP, Yeh RF, Collins F, Guyer MS, Peterson J, Felsenfeld A, Wetterstrand KA, Patrinos A, Morgan MJ, de Jong P, Catanese JJ, Osoegawa K, Shizuya H, Choi S, Chen YJ; International Human Genome Sequencing Consortium.

    Nature. 2001 Feb 15;409(6822):860-921. Erratum in: Nature 2001 Aug 2;412(6846):565. Nature 2001 Jun 7;411(6838):720. Szustakowki, J [corrected to Szustakowski, J]. PMID: 11237011 [PubMed - indexed for MEDLINE]Related articles

    17.

    Bacterial mode of replication with eukaryotic-like machinery in a hyperthermophilic archaeon.

    Myllykallio H, Lopez P, López-García P, Heilig R, Saurin W, Zivanovic Y, Philippe H, Forterre P.

    Science. 2000 Jun 23;288(5474):2212-5.PMID: 10864870 [PubMed - indexed for MEDLINE]Related articlesFree article

    18.

    Characterization of the NPHP1 locus: mutational mechanism involved in deletions in familial juvenile nephronophthisis.

    Saunier S, Calado J, Benessy F, Silbermann F, Heilig R, Weissenbach J, Antignac C.

    Am J Hum Genet. 2000 Mar;66(3):778-89.PMID: 10712196 [PubMed - indexed for MEDLINE]Related articlesFree article

    19.

    A fine integrated map of the SPG4 locus excludes an expanded CAG repeat in chromosome 2p-linked autosomal dominant spastic paraplegia.

    Hazan J, Davoine CS, Mavel D, Fonknechten N, Paternotte C, Fizames C, Cruaud C, Samson D, Muselet D, Vega-Czarny N, Brice A, Gyapay G, Heilig R, Fontaine B, Weissenbach J.

    Genomics. 1999 Sep 15;60(3):309-19.PMID: 10493830 [PubMed - indexed for MEDLINE]Related articles

    20.

    Construction of a highly annotated cosmid contig spanning 550Kb within the X-linked nonspecific mental retardation candidate region at Xp21.3-22.1.

    Carrié A, Nepotes V, Billuart P, Beldjord C, Bienvenu T, Chelly J, Bruls T, Heilig R, Weissenbach J, Jun L, Marynen P.

    Am J Med Genet. 1999 Jul 30;85(3):252-4. No abstract available. PMID: 10398238 [PubMed - indexed for MEDLINE]Related articles

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