Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 44

1.

Common Genetic Variants Found in HLA and KIR Immune Genes in Autism Spectrum Disorder.

Torres AR, Sweeten TL, Johnson RC, Odell D, Westover JB, Bray-Ward P, Ward DC, Davies CJ, Thomas AJ, Croen LA, Benson M.

Front Neurosci. 2016 Oct 20;10:463. eCollection 2016. Review.

2.

Generation of an inbred miniature pig model of retinitis pigmentosa.

Ross JW, Fernandez de Castro JP, Zhao J, Samuel M, Walters E, Rios C, Bray-Ward P, Jones BW, Marc RE, Wang W, Zhou L, Noel JM, McCall MA, DeMarco PJ, Prather RS, Kaplan HJ.

Invest Ophthalmol Vis Sci. 2012 Jan 31;53(1):501-7. doi: 10.1167/iovs.11-8784.

3.

Genome rearrangements detected by SNP microarrays in individuals with intellectual disability referred with possible Williams syndrome.

Pani AM, Hobart HH, Morris CA, Mervis CB, Bray-Ward P, Kimberley KW, Rios CM, Clark RC, Gulbronson MD, Gowans GC, Gregg RG.

PLoS One. 2010 Aug 31;5(8):e12349. doi: 10.1371/journal.pone.0012349.

4.

Inversion of the Williams syndrome region is a common polymorphism found more frequently in parents of children with Williams syndrome.

Hobart HH, Morris CA, Mervis CB, Pani AM, Kistler DJ, Rios CM, Kimberley KW, Gregg RG, Bray-Ward P.

Am J Med Genet C Semin Med Genet. 2010 May 15;154C(2):220-8. doi: 10.1002/ajmg.c.30258.

5.

Simultaneous detection of microsatellite repeats and SNPs in the macrophage migration inhibitory factor (MIF) gene by thin-film biosensor chips and application to rural field studies.

Zhong XB, Leng L, Beitin A, Chen R, McDonald C, Hsiao B, Jenison RD, Kang I, Park SH, Lee A, Gregersen P, Thuma P, Bray-Ward P, Ward DC, Bucala R.

Nucleic Acids Res. 2005 Aug 2;33(13):e121.

6.

Serum protein markers for early detection of ovarian cancer.

Mor G, Visintin I, Lai Y, Zhao H, Schwartz P, Rutherford T, Yue L, Bray-Ward P, Ward DC.

Proc Natl Acad Sci U S A. 2005 May 24;102(21):7677-82. Epub 2005 May 12.

7.

Sperm selection for ICSI: shape properties do not predict the absence or presence of numerical chromosomal aberrations.

Celik-Ozenci C, Jakab A, Kovacs T, Catalanotti J, Demir R, Bray-Ward P, Ward D, Huszar G.

Hum Reprod. 2004 Sep;19(9):2052-9. Epub 2004 Jun 17.

PMID:
15205404
8.

Efficacy of the swim-up method in eliminating sperm with diminished maturity and aneuploidy.

Jakab A, Kovacs T, Zavaczki Z, Borsos A, Bray-Ward P, Ward D, Huszar G.

Hum Reprod. 2003 Jul;18(7):1481-8.

PMID:
12832376
9.

Human sperm maintain their shape following decondensation and denaturation for fluorescent in situ hybridization: shape analysis and objective morphometry.

Celik-Ozenci C, Catalanotti J, Jakab A, Aksu C, Ward D, Bray-Ward P, Demir R, Huszar G.

Biol Reprod. 2003 Oct;69(4):1347-55. Epub 2003 Jun 25.

PMID:
12826571
10.

Comprehensive human genome amplification using multiple displacement amplification.

Dean FB, Hosono S, Fang L, Wu X, Faruqi AF, Bray-Ward P, Sun Z, Zong Q, Du Y, Du J, Driscoll M, Song W, Kingsmore SF, Egholm M, Lasken RS.

Proc Natl Acad Sci U S A. 2002 Apr 16;99(8):5261-6.

11.

Rapid DNA fiber technique for size measurements of linear and circular DNA probes.

Henegariu O, Grober L, Haskins W, Bowers PN, State MW, Ohmido N, Bray-Ward P, Ward DC.

Biotechniques. 2001 Aug;31(2):246-50. No abstract available.

12.

FISH assessment of aneuploidy frequencies in mature and immature human spermatozoa classified by the absence or presence of cytoplasmic retention.

Kovanci E, Kovacs T, Moretti E, Vigue L, Bray-Ward P, Ward DC, Huszar G.

Hum Reprod. 2001 Jun;16(6):1209-17.

PMID:
11387294
13.

Cryptic translocation identification in human and mouse using several telomeric multiplex fish (TM-FISH) strategies.

Henegariu O, Artan S, Greally JM, Chen XN, Korenberg JR, Vance GH, Stubbs L, Bray-Ward P, Ward DC.

Lab Invest. 2001 Apr;81(4):483-91.

PMID:
11304567
14.

Small marker chromosome identification in metaphase and interphase using centromeric multiplex fish (CM-FISH).

Henegariu O, Bray-Ward P, Artan S, Vance GH, Qumsyieh M, Ward DC.

Lab Invest. 2001 Apr;81(4):475-81.

PMID:
11304566
15.

Visualization of oligonucleotide probes and point mutations in interphase nuclei and DNA fibers using rolling circle DNA amplification.

Zhong XB, Lizardi PM, Huang XH, Bray-Ward PL, Ward DC.

Proc Natl Acad Sci U S A. 2001 Mar 27;98(7):3940-5.

16.

Improvements in cytogenetic slide preparation: controlled chromosome spreading, chemical aging and gradual denaturing.

Henegariu O, Heerema NA, Lowe Wright L, Bray-Ward P, Ward DC, Vance GH.

Cytometry. 2001 Feb 1;43(2):101-9.

PMID:
11169574
17.

Cloning, characterization, and chromosomal mapping of a human electroneutral Na(+)-driven Cl-HCO3 exchanger.

Grichtchenko II, Choi I, Zhong X, Bray-Ward P, Russell JM, Boron WF.

J Biol Chem. 2001 Mar 16;276(11):8358-63. Epub 2000 Dec 27.

18.

Assignment of SYNJ1 to human chromosome 21q22.2 and Synj12 to the murine homologous region on chromosome 16C3-4 by in situ hybridization.

Cremona O, Nimmakayalu M, Haffner C, Bray-Ward P, Ward DC, De Camilli P.

Cytogenet Cell Genet. 2000;88(1-2):89-90. No abstract available.

PMID:
10773674
19.

Simple method for preparation of fluor/hapten-labeled dUTP.

Nimmakayalu M, Henegariu O, Ward DC, Bray-Ward P.

Biotechniques. 2000 Mar;28(3):518-22.

20.

Custom fluorescent-nucleotide synthesis as an alternative method for nucleic acid labeling.

Henegariu O, Bray-Ward P, Ward DC.

Nat Biotechnol. 2000 Mar;18(3):345-8.

PMID:
10700155
21.

Multiplex fluorescence in situ hybridization and cross species color banding of a case of chronic myeloid leukemia in blastic crisis with a complex Philadelphia translocation.

Harrison CJ, Gibbons B, Yang F, Butler T, Cheung KL, Kearney L, Dirscherl L, Bray-Ward P, Gregson M, Ferguson-Smith M.

Cancer Genet Cytogenet. 2000 Jan 15;116(2):105-10.

PMID:
10640141
22.

Assignment of the 2P domain, acid-sensitive potassium channel OAT1 gene KCNK3 to human chromosome bands 2p24.1-->p23.3 and murine 5B by in situ hybridization.

Manjunath NA, Bray-Ward P, Goldstein SA, Gallagher PG.

Cytogenet Cell Genet. 1999;86(3-4):242-3. No abstract available.

PMID:
10575216
23.

Colour-changing karyotyping: an alternative to M-FISH/SKY.

Henegariu O, Heerema NA, Bray-Ward P, Ward DC.

Nat Genet. 1999 Nov;23(3):263-4. No abstract available.

PMID:
10545937
24.

Genomic structure, chromosomal mapping, and promoter region analysis of murine uridine phosphorylase gene.

Cao D, Nimmakayalu MA, Wang F, Zhang D, Handschumacher RE, Bray-Ward P, Pizzorno G.

Cancer Res. 1999 Oct 1;59(19):4997-5001.

25.

Genetics of childhood disorders: VI. FISH, FISH, and more FISH.

Ward D, Bray-Ward P, Lombroso PJ.

J Am Acad Child Adolesc Psychiatry. 1999 Sep;38(9):1200-2. Review. No abstract available.

PMID:
10504822
26.

Characteristics of three homologous 202 genes (Ifi202a, Ifi202b, and Ifi202c) from the murine interferon-activatable gene 200 cluster.

Wang H, Chatterjee G, Meyer JJ, Liu CJ, Manjunath NA, Bray-Ward P, Lengyel P.

Genomics. 1999 Sep 15;60(3):281-94.

PMID:
10493828
27.

Characterization of the human myeloid leukemia-derived cell line GF-D8 by multiplex fluorescence in situ hybridization, subtelomeric probes, and comparative genomic hybridization.

Tosi S, Giudici G, Rambaldi A, Scherer SW, Bray-Ward P, Dirscherl L, Biondi A, Kearney L.

Genes Chromosomes Cancer. 1999 Mar;24(3):213-21.

PMID:
10451701
28.
29.

Mutation detection and single-molecule counting using isothermal rolling-circle amplification.

Lizardi PM, Huang X, Zhu Z, Bray-Ward P, Thomas DC, Ward DC.

Nat Genet. 1998 Jul;19(3):225-32.

PMID:
9662393
30.

Human metalloprotease-disintegrin Kuzbanian regulates sympathoadrenal cell fate in development and neoplasia.

Yavari R, Adida C, Bray-Ward P, Brines M, Xu T.

Hum Mol Genet. 1998 Jul;7(7):1161-7.

PMID:
9618175
31.

The human HNRPD locus maps to 4q21 and encodes a highly conserved protein.

Dempsey LA, Li MJ, DePace A, Bray-Ward P, Maizels N.

Genomics. 1998 May 1;49(3):378-84.

PMID:
9615222
32.

A novel nucleic acid-binding protein that interacts with human rad51 recombinase.

Kovalenko OV, Golub EI, Bray-Ward P, Ward DC, Radding CM.

Nucleic Acids Res. 1997 Dec 15;25(24):4946-53.

33.

Genomic localization of the human gene for KCNA10, a cGMP-activated K channel.

Orias M, Bray-Ward P, Curran ME, Keating MT, Desir GV.

Genomics. 1997 May 15;42(1):33-7.

PMID:
9177773
34.

Pulsed-field gel electrophoresis and FISH mapping of chromosome 9q22: placement of a novel zinc finger gene within the NBCCS and ESS1 region.

Levanat S, Chidambaram A, Wicking C, Bray-Ward P, Pressman C, Toftgard R, Gailani MR, Myers JC, Wainwright B, Dean M, Bale AE.

Cytogenet Cell Genet. 1997;76(3-4):208-13.

PMID:
9186526
35.

FISH-Mapped CEPH YACs spanning 0 to 46 cM on human chromosome 6.

Bray-Ward P, Bowlus C, Choi J, Paslier DL, Weissenbach J, Gruen JR.

Genomics. 1996 Aug 15;36(1):104-11.

PMID:
8812421
36.

A transcription map of the major histocompatibility complex (MHC) class I region.

Gruen JR, Nalabolu SR, Chu TW, Bowlus C, Fan WF, Goei VL, Wei H, Sivakamasundari R, Liu Y, Xu HX, Parimoo S, Nallur G, Ajioka R, Shukla H, Bray-Ward P, Pan J, Weissman SM.

Genomics. 1996 Aug 15;36(1):70-85.

PMID:
8812418
38.

Integration of the cytogenetic, genetic, and physical maps of the human genome by FISH mapping of CEPH YAC clones.

Bray-Ward P, Menninger J, Lieman J, Desai T, Mokady N, Banks A, Ward DC.

Genomics. 1996 Feb 15;32(1):1-14.

PMID:
8786094
39.

Molecular characterization of breakpoints in patients with holoprosencephaly and definition of the HPE2 critical region 2p21.

Schell U, Wienberg J, Köhler A, Bray-Ward P, Ward DE, Wilson WG, Allen WP, Lebel RR, Sawyer JR, Campbell PL, Aughton DJ, Punnett HH, Lammer EJ, Kao FT, Ward DC, Muenke M.

Hum Mol Genet. 1996 Feb;5(2):223-9.

PMID:
8824878
40.

Emergence of the ZNF91 Krüppel-associated box-containing zinc finger gene family in the last common ancestor of anthropoidea.

Bellefroid EJ, Marine JC, Matera AG, Bourguignon C, Desai T, Healy KC, Bray-Ward P, Martial JA, Ihle JN, Ward DC.

Proc Natl Acad Sci U S A. 1995 Nov 7;92(23):10757-61.

41.

Internet-based support for bioscience research: a collaborative genome center for human chromosome 12.

Miller PL, Nadkarni PM, Kidd KK, Cheung K, Ward DC, Banks A, Bray-Ward P, Cupelli L, Herdman V, Marondel I, Montgomery K, Renault B, Yoon SJ, Krauter KS, Kucherlapati R.

J Am Med Inform Assoc. 1995 Nov-Dec;2(6):351-64.

42.

Frequent loss of heterozygosity at the TEL gene locus in acute lymphoblastic leukemia of childhood.

Stegmaier K, Pendse S, Barker GF, Bray-Ward P, Ward DC, Montgomery KT, Krauter KS, Reynolds C, Sklar J, Donnelly M, et al.

Blood. 1995 Jul 1;86(1):38-44.

43.

Fusion of the TEL gene on 12p13 to the AML1 gene on 21q22 in acute lymphoblastic leukemia.

Golub TR, Barker GF, Bohlander SK, Hiebert SW, Ward DC, Bray-Ward P, Morgan E, Raimondi SC, Rowley JD, Gilliland DG.

Proc Natl Acad Sci U S A. 1995 May 23;92(11):4917-21.

44.

CEPH viewer: a client-server database to browse and manipulate CEPH physical mapping and linkage data.

Nadkarni PM, Bray-Ward P.

Genomics. 1995 Jan 1;25(1):318-20. No abstract available.

PMID:
7774941

Supplemental Content

Loading ...
Support Center