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Items: 49

1.

Influence of Repressive Histone and DNA Methylation upon D4Z4 Transcription in Non-Myogenic Cells.

Das S, Chadwick BP.

PLoS One. 2016 Jul 28;11(7):e0160022. doi: 10.1371/journal.pone.0160022. eCollection 2016.

2.

Deletion of DXZ4 on the human inactive X chromosome alters higher-order genome architecture.

Darrow EM, Huntley MH, Dudchenko O, Stamenova EK, Durand NC, Sun Z, Huang SC, Sanborn AL, Machol I, Shamim M, Seberg AP, Lander ES, Chadwick BP, Aiden EL.

Proc Natl Acad Sci U S A. 2016 Aug 2;113(31):E4504-12. doi: 10.1073/pnas.1609643113. Epub 2016 Jul 18.

3.
4.

Quantitative dose-response curves from subcellular lipid multilayer microarrays.

Kusi-Appiah AE, Lowry TW, Darrow EM, Wilson KA, Chadwick BP, Davidson MW, Lenhert S.

Lab Chip. 2015 Aug 21;15(16):3397-404. doi: 10.1039/c5lc00478k.

5.

A region of euchromatin coincides with an extensive tandem repeat on the mouse (Mus musculus) inactive X chromosome.

Darrow EM, Seberg AP, Das S, Figueroa DM, Sun Z, Moseley SC, Chadwick BP.

Chromosome Res. 2014 Sep;22(3):335-50. doi: 10.1007/s10577-014-9424-x. Epub 2014 May 13.

PMID:
24821208
6.

A novel tRNA variable number tandem repeat at human chromosome 1q23.3 is implicated as a boundary element based on conservation of a CTCF motif in mouse.

Darrow EM, Chadwick BP.

Nucleic Acids Res. 2014 Jun;42(10):6421-35. doi: 10.1093/nar/gku280. Epub 2014 Apr 21.

7.

Molecular versatility: the many faces and functions of noncoding RNA.

Chadwick BP, Scott KC.

Chromosome Res. 2013 Dec;21(6-7):555-9. doi: 10.1007/s10577-013-9397-1. No abstract available.

8.

Boosting transcription by transcription: enhancer-associated transcripts.

Darrow EM, Chadwick BP.

Chromosome Res. 2013 Dec;21(6-7):713-24. doi: 10.1007/s10577-013-9384-6. Review.

9.
10.

The WSTF-ISWI chromatin remodeling complex transiently associates with the human inactive X chromosome during late S-phase prior to BRCA1 and γ-H2AX.

Culver-Cochran AE, Chadwick BP.

PLoS One. 2012;7(11):e50023. doi: 10.1371/journal.pone.0050023. Epub 2012 Nov 14.

11.

The mouse DXZ4 homolog retains Ctcf binding and proximity to Pls3 despite substantial organizational differences compared to the primate macrosatellite.

Horakova AH, Calabrese JM, McLaughlin CR, Tremblay DC, Magnuson T, Chadwick BP.

Genome Biol. 2012 Aug 20;13(8):R70. doi: 10.1186/gb-2012-13-8-r70.

12.

The macrosatellite DXZ4 mediates CTCF-dependent long-range intrachromosomal interactions on the human inactive X chromosome.

Horakova AH, Moseley SC, McLaughlin CR, Tremblay DC, Chadwick BP.

Hum Mol Genet. 2012 Oct 15;21(20):4367-77. Epub 2012 Jul 12.

13.

A unified phylogeny-based nomenclature for histone variants.

Talbert PB, Ahmad K, Almouzni G, Ausió J, Berger F, Bhalla PL, Bonner WM, Cande WZ, Chadwick BP, Chan SW, Cross GA, Cui L, Dimitrov SI, Doenecke D, Eirin-López JM, Gorovsky MA, Hake SB, Hamkalo BA, Holec S, Jacobsen SE, Kamieniarz K, Khochbin S, Ladurner AG, Landsman D, Latham JA, Loppin B, Malik HS, Marzluff WF, Pehrson JR, Postberg J, Schneider R, Singh MB, Smith MM, Thompson E, Torres-Padilla ME, Tremethick DJ, Turner BM, Waterborg JH, Wollmann H, Yelagandula R, Zhu B, Henikoff S.

Epigenetics Chromatin. 2012 Jun 21;5:7. doi: 10.1186/1756-8935-5-7.

14.

YY1 associates with the macrosatellite DXZ4 on the inactive X chromosome and binds with CTCF to a hypomethylated form in some male carcinomas.

Moseley SC, Rizkallah R, Tremblay DC, Anderson BR, Hurt MM, Chadwick BP.

Nucleic Acids Res. 2012 Feb;40(4):1596-608. doi: 10.1093/nar/gkr964. Epub 2011 Nov 7.

15.

Variation in array size, monomer composition and expression of the macrosatellite DXZ4.

Tremblay DC, Moseley S, Chadwick BP.

PLoS One. 2011 Apr 22;6(4):e18969. doi: 10.1371/journal.pone.0018969.

16.
17.

Expression, tandem repeat copy number variation and stability of four macrosatellite arrays in the human genome.

Tremblay DC, Alexander G Jr, Moseley S, Chadwick BP.

BMC Genomics. 2010 Nov 15;11:632. doi: 10.1186/1471-2164-11-632.

18.

Macrosatellite epigenetics: the two faces of DXZ4 and D4Z4.

Chadwick BP.

Chromosoma. 2009 Dec;118(6):675-81. doi: 10.1007/s00412-009-0233-5. Epub 2009 Aug 19. Review.

PMID:
19690880
19.

The Mi-2/NuRD complex associates with pericentromeric heterochromatin during S phase in rapidly proliferating lymphoid cells.

Helbling Chadwick L, Chadwick BP, Jaye DL, Wade PA.

Chromosoma. 2009 Aug;118(4):445-57. doi: 10.1007/s00412-009-0207-7. Epub 2009 Mar 19.

21.

The insulator factor CTCF controls MHC class II gene expression and is required for the formation of long-distance chromatin interactions.

Majumder P, Gomez JA, Chadwick BP, Boss JM.

J Exp Med. 2008 Apr 14;205(4):785-98. doi: 10.1084/jem.20071843. Epub 2008 Mar 17.

22.

The XIST noncoding RNA functions independently of BRCA1 in X inactivation.

Xiao C, Sharp JA, Kawahara M, Davalos AR, Difilippantonio MJ, Hu Y, Li W, Cao L, Buetow K, Ried T, Chadwick BP, Deng CX, Panning B.

Cell. 2007 Mar 9;128(5):977-89.

24.

BRCA1 associates with the inactive X chromosome in late S-phase, coupled with transient H2AX phosphorylation.

Chadwick BP, Lane TF.

Chromosoma. 2005 Dec;114(6):432-9. Epub 2005 Nov 15.

PMID:
16240122
25.

Beyond the Xi: macroH2A chromatin distribution and post-translational modification in an avian system.

Abbott DW, Chadwick BP, Thambirajah AA, Ausió J.

J Biol Chem. 2005 Apr 22;280(16):16437-45. Epub 2005 Feb 17.

26.

Multiple spatially distinct types of facultative heterochromatin on the human inactive X chromosome.

Chadwick BP, Willard HF.

Proc Natl Acad Sci U S A. 2004 Dec 14;101(50):17450-5. Epub 2004 Dec 1.

27.

Barring gene expression after XIST: maintaining facultative heterochromatin on the inactive X.

Chadwick BP, Willard HF.

Semin Cell Dev Biol. 2003 Dec;14(6):359-67. Review.

PMID:
15015743
28.

Chromatin of the Barr body: histone and non-histone proteins associated with or excluded from the inactive X chromosome.

Chadwick BP, Willard HF.

Hum Mol Genet. 2003 Sep 1;12(17):2167-78. Epub 2003 Jul 15.

PMID:
12915472
29.

SETting the stage. Eed-Enx1 leaves an epigenetic signature on the inactive X chromosome.

Chadwick BP, Willard HF.

Dev Cell. 2003 Apr;4(4):445-7. Review.

30.

A 5.9-kb tandem repeat at the euchromatin-heterochromatin boundary of the X chromosome of Drosophila melanogaster.

O'Hare K, Chadwick BP, Constantinou A, Davis AJ, Mitchelson A, Tudor M.

Mol Genet Genomics. 2002 Jul;267(5):647-55. Epub 2002 Jun 18.

PMID:
12172804
31.

Cell cycle-dependent localization of macroH2A in chromatin of the inactive X chromosome.

Chadwick BP, Willard HF.

J Cell Biol. 2002 Jun 24;157(7):1113-23. Epub 2002 Jun 24.

32.
33.

Histone H2A variants and the inactive X chromosome: identification of a second macroH2A variant.

Chadwick BP, Willard HF.

Hum Mol Genet. 2001 May 1;10(10):1101-13.

PMID:
11331621
34.
35.

Expression and characterization of soluble and membrane-bound human nucleoside triphosphate diphosphohydrolase 6 (CD39L2).

Hicks-Berger CA, Chadwick BP, Frischauf AM, Kirley TL.

J Biol Chem. 2000 Nov 3;275(44):34041-5.

36.

Report and abstracts of the Sixth International Workshop on chromosome 9.

Chadwick BP, Campbell LJ, Jackson CL, Ozelius L, Slaugenhaupt SA, Stephenson DA, Edwards JH, Wiest J, Povey S.

Ann Hum Genet. 1999 Mar;63(Pt 2):101-24.

PMID:
10738523
37.

Cloning, mapping, and expression of a novel brain-specific transcript in the familial dysautonomia candidate region on chromosome 9q31.

Chadwick BP, Leyne M, Gill S, Liebert CB, Mull J, Mezey E, Robbins CM, Pinkett HW, Makalowska I, Maayan C, Blumenfeld A, Axelrod FB, Brownstein M, Gusella JF, Slaugenhaupt SA.

Mamm Genome. 2000 Jan;11(1):81-3. No abstract available.

PMID:
10603000
38.

Cloning, genomic organization and expression of a putative human transmembrane protein related to the Caenorhabditis elegans M01F1.4 gene.

Chadwick BP, Gill S, Leyne M, Mull J, Liebert CB, Robbins CM, Pinkett HW, Makalowska I, Maayan C, Blumenfeld A, Axelrod FB, Brownstein M, Slaugenhaupt SA.

Gene. 1999 Nov 15;240(1):67-73.

PMID:
10564813
39.

Cloning, mapping and expression of UBL3, a novel ubiquitin-like gene.

Chadwick BP, Kidd T, Sgouros J, Ish-Horowicz D, Frischauf AM.

Gene. 1999 Jun 11;233(1-2):189-95.

PMID:
10375635
40.

Cloning, mapping, and expression of two novel actin genes, actin-like-7A (ACTL7A) and actin-like-7B (ACTL7B), from the familial dysautonomia candidate region on 9q31.

Chadwick BP, Mull J, Helbling LA, Gill S, Leyne M, Robbins CM, Pinkett HW, Makalowska I, Maayan C, Blumenfeld A, Axelrod FB, Brownstein M, Gusella JF, Slaugenhaupt SA.

Genomics. 1999 Jun 15;58(3):302-9.

PMID:
10373328
41.

Assignment of persephin (PSPN), a human neurotrophic factor, to chromosome 19p13.3 by radiation hybrid mapping and somatic cell hybrid PCR.

Chadwick BP, Helbling LA, Angrist M, Chakravarti A, Gusella JF, Slaugenhaupt SA.

Cytogenet Cell Genet. 1998;83(3-4):236-7. No abstract available.

PMID:
10072588
42.

PHF2, a novel PHD finger gene located on human chromosome 9q22.

Hasenpusch-Theil K, Chadwick BP, Theil T, Heath SK, Wilkinson DG, Frischauf AM.

Mamm Genome. 1999 Mar;10(3):294-8.

PMID:
10051327
44.

The human homologue of the ninjurin gene maps to the candidate region of hereditary sensory neuropathy type I (HSNI).

Chadwick BP, Heath SK, Williamson J, Obermayr F, Patel L, Sheer D, Frischauf AM.

Genomics. 1998 Jan 1;47(1):58-63.

PMID:
9465296
45.

cDNA cloning and chromosomal mapping of a mouse gene with homology to NTPases.

Chadwick BP, Williamson J, Sheer D, Frischauf AM.

Mamm Genome. 1998 Feb;9(2):162-4. No abstract available.

PMID:
9457681
46.

Cloning and mapping of a human and mouse gene with homology to ecto-ATPase genes.

Chadwick BP, Frischauf AM.

Mamm Genome. 1997 Sep;8(9):668-72.

PMID:
9271669
47.

FKHL15, a new human member of the forkhead gene family located on chromosome 9q22.

Chadwick BP, Obermayr F, Frischauf AM.

Genomics. 1997 May 1;41(3):390-6.

PMID:
9169137
48.

Nuclear cap binding protein maps close to the xeroderma pigmentosum complementation group A (XPA) locus in human and mouse.

Chadwick BP, Obermayr F, Frischauf AM.

Genomics. 1996 Aug 1;35(3):632-3. No abstract available.

PMID:
8812508
49.

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