Laura Carrel
All publications ( 27 )
  • Carrel L. Park C. Tyekucheva S. Dunn J. Chiaromonte F. Makova KD. Genomic environment predicts expression patterns on the human inactive X chromosome. 2006 Sep 29. PLoS Genet. 2(9):e151.
    National Institute of General Medical Sciences
    National Human Genome Research Institute
  • Carrel L. Molecular biology. "X"-rated chromosomal rendezvous. 2006 Feb 24. Science. 311(5764):1107-9.
  • Carrel L. Willard HF. X-inactivation profile reveals extensive variability in X-linked gene expression in females. 2005 Mar 17. Nature. 434(7031):400-4.
  • Ross MT. Grafham DV. Coffey AJ. Scherer S. McLay K. Muzny D. Platzer M. Howell GR. Burrows C. Bird CP. Frankish A. Lovell FL. Howe KL. Ashurst JL. Fulton RS. Sudbrak R. Wen G. Jones MC. Hurles ME. Andrews TD. Scott CE. Searle S. Ramser J. Whittaker A. Deadman R. Carter NP. Hunt SE. Chen R. Cree A. Gunaratne P. Havlak P. Hodgson A. Metzker ML. Richards S. Scott G. Steffen D. Sodergren E. Wheeler DA. Worley KC. Ainscough R. Ambrose KD. Ansari-Lari MA. Aradhya S. Ashwell RI. Babbage AK. Bagguley CL. Ballabio A. Banerjee R. Barker GE. Barlow KF. Barrett IP. Bates KN. Beare DM. Beasley H. Beasley O. Beck A. Bethel G. Blechschmidt K. Brady N. Bray-Allen S. Bridgeman AM. Brown AJ. Brown MJ. Bonnin D. Bruford EA. Buhay C. Burch P. Burford D. Burgess J. Burrill W. Burton J. Bye JM. Carder C. Carrel L. Chako J. Chapman JC. Chavez D. Chen E. Chen G. Chen Y. Chen Z. Chinault C. Ciccodicola A. Clark SY. Clarke G. Clee CM. Clegg S. Clerc-Blankenburg K. Clifford K. Cobley V. Cole CG. Conquer JS. Corby N. Connor RE. David R. Davies J. Davis C. Davis J. Delgado O. Deshazo D. Dhami P. Ding Y. Dinh H. Dodsworth S. Draper H. Dugan-Rocha S. Dunham A. Dunn M. Durbin KJ. Dutta I. Eades T. Ellwood M. Emery-Cohen A. Errington H. Evans KL. Faulkner L. Francis F. Frankland J. Fraser AE. Galgoczy P. Gilbert J. Gill R. Glöckner G. Gregory SG. Gribble S. Griffiths C. Grocock R. Gu Y. Gwilliam R. Hamilton C. Hart EA. Hawes A. Heath PD. Heitmann K. Hennig S. Hernandez J. Hinzmann B. Ho S. Hoffs M. Howden PJ. Huckle EJ. Hume J. Hunt PJ. Hunt AR. Isherwood J. Jacob L. Johnson D. Jones S. de Jong PJ. Joseph SS. Keenan S. Kelly S. Kershaw JK. Khan Z. Kioschis P. Klages S. Knights AJ. Kosiura A. Kovar-Smith C. Laird GK. Langford C. Lawlor S. Leversha M. Lewis L. Liu W. Lloyd C. Lloyd DM. Loulseged H. Loveland JE. Lovell JD. Lozado R. Lu J. Lyne R. Ma J. Maheshwari M. Matthews LH. McDowall J. McLaren S. McMurray A. Meidl P. Meitinger T. Milne S. Miner G. Mistry SL. Morgan M. Morris S. Müller I. Mullikin JC. Nguyen N. Nordsiek G. Nyakatura G. O'Dell CN. Okwuonu G. Palmer S. Pandian R. Parker D. Parrish J. Pasternak S. Patel D. Pearce AV. Pearson DM. Pelan SE. Perez L. Porter KM. Ramsey Y. Reichwald K. Rhodes S. Ridler KA. Schlessinger D. Schueler MG. Sehra HK. Shaw-Smith C. Shen H. Sheridan EM. Shownkeen R. Skuce CD. Smith ML. Sotheran EC. Steingruber HE. Steward CA. Storey R. Swann RM. Swarbreck D. Tabor PE. Taudien S. Taylor T. Teague B. Thomas K. Thorpe A. Timms K. Tracey A. Trevanion S. Tromans AC. d'Urso M. Verduzco D. Villasana D. Waldron L. Wall M. Wang Q. Warren J. Warry GL. Wei X. West A. Whitehead SL. Whiteley MN. Wilkinson JE. Willey DL. Williams G. Williams L. Williamson A. Williamson H. Wilming L. Woodmansey RL. Wray PW. Yen J. Zhang J. Zhou J. Zoghbi H. Zorilla S. Buck D. Reinhardt R. Poustka A. Rosenthal A. Lehrach H. Meindl A. Minx PJ. Hillier LW. Willard HF. Wilson RK. Waterston RH. Rice CM. Vaudin M. Coulson A. Nelson DL. Weinstock G. Sulston JE. Durbin R. Hubbard T. Gibbs RA. Beck S. Rogers J. Bentley DR. The DNA sequence of the human X chromosome. 2005 Mar 17. Nature. 434(7031):325-37.
  • Carrel L. Evolutionary biology: chromosome chain makes a link. 2004 Dec 16. Nature. 432(7019):817-8.
  • Hidaka K. Caffrey JJ. Hua L. Zhang T. Falck JR. Nickel GC. Carrel L. Barnes LD. Shears SB. An adjacent pair of human NUDT genes on chromosome X are preferentially expressed in testis and encode two new isoforms of diphosphoinositol polyphosphate phosphohydrolase. 2002 Sep 6. J Biol Chem. 277(36):32730-8.
  • Hall LL. Byron M. Sakai K. Carrel L. Willard HF. Lawrence JB. An ectopic human XIST gene can induce chromosome inactivation in postdifferentiation human HT-1080 cells. 2002 Jun 25. Proc Natl Acad Sci U S A. 99(13):8677-82.
    National Institute of General Medical Sciences
    National Institute of Child Health and Human Development
  • Tiller GE. Hannig VL. Dozier D. Carrel L. Trevarthen KC. Wilcox WR. Mundlos S. Haines JL. Gedeon AK. Gecz J. A recurrent RNA-splicing mutation in the SEDL gene causes X-linked spondyloepiphyseal dysplasia tarda. 2001 Jun. Am J Hum Genet. 68(6):1398-407.
  • Willard HF. Carrel L. Making sense (and antisense) of the X inactivation center. 2001 Aug 28. Proc Natl Acad Sci U S A. 98(18):10025-7.
  • Bailey JA. Carrel L. Chakravarti A. Eichler EE. Molecular evidence for a relationship between LINE-1 elements and X chromosome inactivation: the Lyon repeat hypothesis. 2000 Jun 6. Proc Natl Acad Sci U S A. 97(12):6634-9.
    National Institute of General Medical Sciences
    National Human Genome Research Institute
  • Mroz K. Carrel L. Hunt PA. Germ cell development in the XXY mouse: evidence that X chromosome reactivation is independent of sexual differentiation. 1999 Mar 1. Dev Biol. 207(1):229-38.
    National Institute of Child Health and Human Development
  • Carrel L. Willard HF. Heterogeneous gene expression from the inactive X chromosome: an X-linked gene that escapes X inactivation in some human cell lines but is inactivated in others. 1999 Jun 22. Proc Natl Acad Sci U S A. 96(13):7364-9.
    National Institute of General Medical Sciences
  • Carrel L. Cottle AA. Goglin KC. Willard HF. A first-generation X-inactivation profile of the human X chromosome. 1999 Dec 7. Proc Natl Acad Sci U S A. 96(25):14440-4.
    National Institute of General Medical Sciences
  • Dal Zotto L. Quaderi NA. Elliott R. Lingerfelter PA. Carrel L. Valsecchi V. Montini E. Yen CH. Chapman V. Kalcheva I. Arrigo G. Zuffardi O. Thomas S. Willard HF. Ballabio A. Disteche CM. Rugarli EI. The mouse Mid1 gene: implications for the pathogenesis of Opitz syndrome and the evolution of the mammalian pseudoautosomal region. 1998 Mar. Hum Mol Genet. 7(3):489-99.
    National Institute of General Medical Sciences
  • Carrel L. Willard HF. Counting on Xist. 1998 Jul. Nat Genet. 19(3):211-2.
  • Greenfield A. Carrel L. Pennisi D. Philippe C. Quaderi N. Siggers P. Steiner K. Tam PP. Monaco AP. Willard HF. Koopman P. The UTX gene escapes X inactivation in mice and humans. 1998 Apr. Hum Mol Genet. 7(4):737-42.
  • Brown CJ. Carrel L. Willard HF. Expression of genes from the human active and inactive X chromosomes. 1997 Jun. Am J Hum Genet. 60(6):1333-43.
    National Institute of General Medical Sciences
  • Carrel L. Hunt PA. Willard HF. Tissue and lineage-specific variation in inactive X chromosome expression of the murine Smcx gene. 1996 Sep. Hum Mol Genet. 5(9):1361-6.
    National Institute of General Medical Sciences
    National Institute of Child Health and Human Development
  • Carrel L. Clemson CM. Dunn JM. Miller AP. Hunt PA. Lawrence JB. Willard HF. X inactivation analysis and DNA methylation studies of the ubiquitin activating enzyme E1 and PCTAIRE-1 genes in human and mouse. 1996 Mar. Hum Mol Genet. 5(3):391-401.
    National Institute of General Medical Sciences
  • Carrel L. Willard HF. An assay for X inactivation based on differential methylation at the fragile X locus, FMR1. 1996 Jul 12. Am J Med Genet. 64(1):27-30.
    National Institute of General Medical Sciences
  • Coleman MP. Ambrose HJ. Carrel L. Németh AH. Willard HF. Davies KE. A novel gene, DXS8237E, lies within 20 kb upstream of UBE1 in Xp11.23 and has a different X inactivation status. 1996 Jan 1. Genomics. 31(1):135-8.
  • Brown CJ. Miller AP. Carrel L. Rupert JL. Davies KE. Willard HF. The DXS423E gene in Xp11.21 escapes X chromosome inactivation. 1995 Feb. Hum Mol Genet. 4(2):251-5.
    National Institute of General Medical Sciences
  • Sultana R. Adler DA. Edelhoff S. Carrel L. Lee KH. Chapman VC. Willard HF. Disteche CM. The mouse Sb1.8 gene located at the distal end of the X chromosome is subject to X inactivation. 1995 Feb. Hum Mol Genet. 4(2):257-63.
    National Institute of General Medical Sciences
  • Lafrenière RG. Carrel L. Willard HF. A novel transmembrane transporter encoded by the XPCT gene in Xq13.2. 1994 Jul. Hum Mol Genet. 3(7):1133-9.
    National Institute of General Medical Sciences
    National Human Genome Research Institute
  • Greig GM. Sharp CB. Carrel L. Willard HF. Duplicated zinc finger protein genes on the proximal short arm of the human X chromosome: isolation, characterization and X-inactivation studies. 1993 Oct. Hum Mol Genet. 2(10):1611-8.
    National Institute of General Medical Sciences
  • Willard HF. Brown CJ. Carrel L. Hendrich B. Miller AP. Epigenetic and chromosomal control of gene expression: molecular and genetic analysis of X chromosome inactivation. 1993. Cold Spring Harb Symp Quant Biol. 58:315-22.
    National Institute of General Medical Sciences
  • Lafrenière RG. Brown CJ. Powers VE. Carrel L. Davies KE. Barker DF. Willard HF. Physical mapping of 60 DNA markers in the p21.1----q21.3 region of the human X chromosome. 1991 Oct. Genomics. 11(2):352-63.
    National Human Genome Research Institute