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Items: 1 to 50 of 393

1.

The pericentromeric region of human chromosome 11: evidence for a chromosome-specific duplication.

Zhang J, Qin S, Sait SN, Haley LL, Henry WM, Higgins MJ, Nowak NJ, Shows TB, Gerhard DS.

Cytogenet Cell Genet. 2001;94(3-4):137-41.

PMID:
11856870
2.

Intrachromosomal genomic instability in human sporadic colorectal cancer measured by genome-wide allelotyping and inter-(simple sequence repeat) PCR.

Anderson GR, Brenner BM, Swede H, Chen N, Henry WM, Conroy JM, Karpenko MJ, Issa JP, Bartos JD, Brunelle JK, Jahreis GP, Kahlenberg MS, Basik M, Sait S, Rodriguez-Bigas MA, Nowak NJ, Petrelli NJ, Shows TB, Stoler DL.

Cancer Res. 2001 Nov 15;61(22):8274-83.

3.

Mapping of genes and transcribed sequences in a gene rich 400-kb region on human chromosome 11p15.1-->p14.

Caldwell GM, Eddy RL, Day CD, Haley LH, Cooper PR, Sait SS, Hejtmancik F, Smith RJ, Morton CC, Higgins MJ, Shows TB.

Cytogenet Cell Genet. 2001;92(1-2):103-7.

PMID:
11306805
4.

Comparative structure, proximal promoter elements, and chromosome location of the human eosinophil major basic protein genes.

Plager DA, Weiler DA, Loegering DA, Johnson WB, Haley L, Eddy RL, Shows TB, Gleich GJ.

Genomics. 2001 Feb 1;71(3):271-81.

PMID:
11170744
5.

p16 (cdkN2/MTS1/INK4A) expression in sporadic colorectal carcinomas.

Rodriguez LM, Penetrante RB, Nowak NJ, Rodriguez-Bigas M, Driscoll DL, Hoover E, Petrelli NJ, Shows TB.

Curr Surg. 2000 Nov;57(6):638. No abstract available.

PMID:
11120318
6.

Spermatid-specific expression of the novel X-linked gene product SPAN-X localized to the nucleus of human spermatozoa.

Westbrook VA, Diekman AB, Klotz KL, Khole VV, von Kap-Herr C, Golden WL, Eddy RL, Shows TB, Stoler MH, Lee CY, Flickinger CJ, Herr JC.

Biol Reprod. 2000 Aug;63(2):469-81.

PMID:
10906052
7.

Assignment of ubiquilin2 (UBQLN2) to human chromosome xp11. 23-->p11.1 by GeneBridge radiation hybrids.

Kaye FJ, Shows TB.

Cytogenet Cell Genet. 2000;89(1-2):116-7. No abstract available.

PMID:
10894951
8.

MAGOH interacts with a novel RNA-binding protein.

Zhao XF, Nowak NJ, Shows TB, Aplan PD.

Genomics. 2000 Jan 1;63(1):145-8.

PMID:
10662555
9.

Genome-wide allelotyping indicates increased loss of heterozygosity on 9p and 14q in early age of onset colorectal cancer.

Weber TK, Conroy J, Keitz B, Rodriguez-Bigas M, Petrelli NJ, Stoler DL, Anderson GR, Shows TB, Nowak NJ.

Cytogenet Cell Genet. 1999;86(2):142-7.

PMID:
10545706
10.

Assignment of TLL1 and TLL2, which encode human BMP-1/Tolloid-related metalloproteases, to chromosomes 4q32-->q33 and 10q23-->q24 and assignment of murine Tll2 to chromosome 19.

Scott IC, Clark TG, Takahara K, Hoffman GG, Eddy RL, Haley LL, Shows TB, Greenspan DS.

Cytogenet Cell Genet. 1999;86(1):64-5. No abstract available.

PMID:
10516436
11.

A maternally methylated CpG island in KvLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith-Wiedemann syndrome.

Smilinich NJ, Day CD, Fitzpatrick GV, Caldwell GM, Lossie AC, Cooper PR, Smallwood AC, Joyce JA, Schofield PN, Reik W, Nicholls RD, Weksberg R, Driscoll DJ, Maher ER, Shows TB, Higgins MJ.

Proc Natl Acad Sci U S A. 1999 Jul 6;96(14):8064-9.

12.

Bestrophin gene mutations in patients with Best vitelliform macular dystrophy.

Caldwell GM, Kakuk LE, Griesinger IB, Simpson SA, Nowak NJ, Small KW, Maumenee IH, Rosenfeld PJ, Sieving PA, Shows TB, Ayyagari R.

Genomics. 1999 May 15;58(1):98-101.

PMID:
10331951
13.

Structure and chromosomal localization of the human and murine genes for the macrophage MARCO receptor.

Kangas M, Brännström A, Elomaa O, Matsuda Y, Eddy R, Shows TB, Tryggvason K.

Genomics. 1999 May 15;58(1):82-9.

PMID:
10331948
14.

The imprinted domain in mouse distal Chromosome 7: reagents for mutagenesis and sequencing.

Day CD, Smilinich NJ, Fitzpatrick GV, deJong PJ, Shows TB, Higgins MJ.

Mamm Genome. 1999 Feb;10(2):182-5. No abstract available.

PMID:
9922400
15.

A model system to study genomic imprinting of human genes.

Gabriel JM, Higgins MJ, Gebuhr TC, Shows TB, Saitoh S, Nicholls RD.

Proc Natl Acad Sci U S A. 1998 Dec 8;95(25):14857-62.

16.

Mapping, genomic organization and promoter analysis of the human prostate-specific membrane antigen gene.

O'Keefe DS, Su SL, Bacich DJ, Horiguchi Y, Luo Y, Powell CT, Zandvliet D, Russell PJ, Molloy PL, Nowak NJ, Shows TB, Mullins C, Vonder Haar RA, Fair WR, Heston WD.

Biochim Biophys Acta. 1998 Nov 26;1443(1-2):113-27.

PMID:
9838072
17.

Coding sequence and expression patterns of mouse chordin and mapping of the cognate mouse chrd and human CHRD genes.

Pappano WN, Scott IC, Clark TG, Eddy RL, Shows TB, Greenspan DS.

Genomics. 1998 Sep 1;52(2):236-9.

PMID:
9782094
18.

NUP98-HOXD13 gene fusion in therapy-related acute myelogenous leukemia.

Raza-Egilmez SZ, Jani-Sait SN, Grossi M, Higgins MJ, Shows TB, Aplan PD.

Cancer Res. 1998 Oct 1;58(19):4269-73.

19.

Transcript mapping of the human chromosome 11q12-q13.1 gene-rich region identifies several newly described conserved genes.

Cooper PR, Nowak NJ, Higgins MJ, Church DM, Shows TB.

Genomics. 1998 May 1;49(3):419-29.

PMID:
9615227
20.

Promoter sequence, expression, and fine chromosomal mapping of the human gene (MLP) encoding the MARCKS-like protein: identification of neighboring and linked polymorphic loci for MLP and MACS and use in the evaluation of human neural tube defects.

Stumpo DJ, Eddy RL Jr, Haley LL, Sait S, Shows TB, Lai WS, Young WS 3rd, Speer MC, Dehejia A, Polymeropoulos M, Blackshear PJ.

Genomics. 1998 Apr 15;49(2):253-64.

PMID:
9598313
21.

Divergently transcribed overlapping genes expressed in liver and kidney and located in the 11p15.5 imprinted domain.

Cooper PR, Smilinich NJ, Day CD, Nowak NJ, Reid LH, Pearsall RS, Reece M, Prawitt D, Landers J, Housman DE, Winterpacht A, Zabel BU, Pelletier J, Weissman BE, Shows TB, Higgins MJ.

Genomics. 1998 Apr 1;49(1):38-51.

PMID:
9570947
22.

Linkage-disequilibrium mapping without genotyping.

Cheung VG, Gregg JP, Gogolin-Ewens KJ, Bandong J, Stanley CA, Baker L, Higgins MJ, Nowak NJ, Shows TB, Ewens WJ, Nelson SF, Spielman RS.

Nat Genet. 1998 Mar;18(3):225-30.

PMID:
9500543
23.

The mammalian homologue of mago nashi encodes a serum-inducible protein.

Zhao XF, Colaizzo-Anas T, Nowak NJ, Shows TB, Elliott RW, Aplan PD.

Genomics. 1998 Jan 15;47(2):319-22.

PMID:
9479507
24.

Contig maps and genomic sequencing identify candidate genes in the usher 1C locus.

Higgins MJ, Day CD, Smilinich NJ, Ni L, Cooper PR, Nowak NJ, Davies C, de Jong PJ, Hejtmancik F, Evans GA, Smith RJ, Shows TB.

Genome Res. 1998 Jan;8(1):57-68.

25.

A gene map of the Best's vitelliform macular dystrophy region in chromosome 11q12-q13.1.

Stöhr H, Marquardt A, Rivera A, Cooper PR, Nowak NJ, Shows TB, Gerhard DS, Weber BH.

Genome Res. 1998 Jan;8(1):48-56.

26.

Novel transcribed sequences within the BWS/WT2 region in 11p15.5: tissue-specific expression correlates with cancer type.

Crider-Miller SJ, Reid LH, Higgins MJ, Nowak NJ, Shows TB, Futreal PA, Weissman BE.

Genomics. 1997 Dec 15;46(3):355-63.

PMID:
9441738
27.

The human angiotensinase C gene (HUMPCP) maps to 11q14 within 700 kb of D11S901: a candidate gene for essential hypertension.

Watson B Jr, Nowak NJ, Myracle AD, Shows TB, Warnock DG.

Genomics. 1997 Sep 15;44(3):365-7. No abstract available.

PMID:
9325062
28.

The human transaldolase gene (TALDO1) is located on chromosome 11 at p15.4-p15.5.

Banki K, Eddy RL, Shows TB, Halladay DL, Bullrich F, Croce CM, Jurecic V, Baldini A, Perl A.

Genomics. 1997 Oct 1;45(1):233-8.

PMID:
9339383
29.

A 1-Mb physical map and PAC contig of the imprinted domain in 11p15.5 that contains TAPA1 and the BWSCR1/WT2 region.

Reid LH, Davies C, Cooper PR, Crider-Miller SJ, Sait SN, Nowak NJ, Evans G, Stanbridge EJ, deJong P, Shows TB, Weissman BE, Higgins MJ.

Genomics. 1997 Aug 1;43(3):366-75.

PMID:
9268640
30.

A 3-Mb contig from D11S987 to MLK3, a gene-rich region in 11q13.

Smith CM, Ma NS, Nowak NJ, Shows TB, Gerhard DS.

Genome Res. 1997 Aug;7(8):835-42.

31.

The human HNP36 gene is localized to chromosome 11q13 and produces alternative transcripts that are not mutated in multiple endocrine neoplasia, type 1 (MEN I) syndrome.

Williams JB, Rexer B, Sirripurapu S, John S, Goldstein R, Phillips JA 3rd, Haley LL, Sait SN, Shows TB, Smith CM, Gerhard DS.

Genomics. 1997 Jun 1;42(2):325-30.

PMID:
9192854
32.

A sequence-ready high-resolution physical map of the best macular dystrophy gene region in 11q12-q13.

Cooper PR, Nowak NJ, Higgins MJ, Simpson SA, Marquardt A, Stoehr H, Weber BH, Gerhard DS, de Jong PJ, Shows TB.

Genomics. 1997 Apr 15;41(2):185-92.

PMID:
9143493
33.

Chromosomal localization of a human mucin gene (MUC8) and cloning of the cDNA corresponding to the carboxy terminus.

Shankar V, Pichan P, Eddy RL Jr, Tonk V, Nowak N, Sait SN, Shows TB, Schultz RE, Gotway G, Elkins RC, Gilmore MS, Sachdev GP.

Am J Respir Cell Mol Biol. 1997 Mar;16(3):232-41.

PMID:
9070607
34.

Human fertilin beta: identification, characterization, and chromosomal mapping of an ADAM gene family member.

Vidaeus CM, von Kapp-Herr C, Golden WL, Eddy RL, Shows TB, Herr JC.

Mol Reprod Dev. 1997 Mar;46(3):363-9.

PMID:
9041139
35.

Framework YAC contig anchored into a 3.2-Mb high-resolution physical map in proximal 11q13.

Courseaux A, Szepetowski P, Fernandes M, Serizet C, Kawaguchi Y, Grosgeorge J, Perucca-Lostanlen D, Shows TB, Todd JA, Nowak NJ, Gaudray P.

Genomics. 1997 Feb 15;40(1):13-23.

PMID:
9070914
36.

A 5.5-Mb high-resolution integrated map of distal 11q13.

Merscher S, Bekri S, de Leeuw B, Pedeutour F, Grosgeorge J, Shows TB, Müllenbach R, Le Paslier D, Nowak NJ, Gaudray P.

Genomics. 1997 Feb 1;39(3):340-7.

PMID:
9119371
37.

Structure and chromosomal location of the human CD6 gene: detection of five human CD6 isoforms.

Bowen MA, Whitney GS, Neubauer M, Starling GC, Palmer D, Zhang J, Nowak NJ, Shows TB, Aruffo A.

J Immunol. 1997 Feb 1;158(3):1149-56.

PMID:
9013954
38.

A 1.5-megabase physical map encompassing the multiple endocrine neoplasia type-1 (MEN1) locus on chromosome 11q13.

Wood TF, Srivatsan ES, Chakrabarti R, Ma GC, Kuan N, Samara GJ, Higgins MJ, Shows TB, Johnson CL, Wan YJ, Passaro EP Jr, Sawicki MP.

Genomics. 1996 Dec 1;38(2):166-73. Erratum in: Genomics 1997 May 15;42(1):183.

PMID:
8954798
39.

Positional cloning of a gene involved in hereditary multiple exostoses.

Wuyts W, Van Hul W, Wauters J, Nemtsova M, Reyniers E, Van Hul EV, De Boulle K, de Vries BB, Hendrickx J, Herrygers I, Bossuyt P, Balemans W, Fransen E, Vits L, Coucke P, Nowak NJ, Shows TB, Mallet L, van den Ouweland AM, McGaughran J, Halley DJ, Willems PJ.

Hum Mol Genet. 1996 Oct;5(10):1547-57.

PMID:
8894688
40.

Cloning, sequence and characterization of the human AMPD2 gene: evidence for transcriptional regulation by two closely spaced promoters.

Mahnke-Zizelman DK, van den Bergh F, Bausch-Jurken MT, Eddy R, Sait S, Shows TB, Sabina RL.

Biochim Biophys Acta. 1996 Aug 14;1308(2):122-32.

PMID:
8764830
41.

ML-1 cell line lacks a germline MLL locus.

Strout MP, Mrózek K, Heinonen K, Sait SN, Shows TB, Aplan PD.

Genes Chromosomes Cancer. 1996 Jul;16(3):204-10.

PMID:
8814454
42.

A human gene (DDX10) encoding a putative DEAD-box RNA helicase at 11q22-q23.

Savitsky K, Ziv Y, Bar-Shira A, Gilad S, Tagle DA, Smith S, Uziel T, Sfez S, Nahmias J, Sartiel A, Eddy RL, Shows TB, Collins FS, Shiloh Y, Rotman G.

Genomics. 1996 Apr 15;33(2):199-206.

PMID:
8660968
43.
44.

A high-resolution physical map of human chromosome 11.

Qin S, Nowak NJ, Zhang J, Sait SN, Mayers PG, Higgins MJ, Cheng Y, Li L, Munroe DJ, Gerhard DS, Weber BH, Bric E, Housman DE, Evans GA, Shows TB.

Proc Natl Acad Sci U S A. 1996 Apr 2;93(7):3149-54.

45.

Structure and chromosomal localization of the human salivary mucin gene, MUC7.

Bobek LA, Liu J, Sait SN, Shows TB, Bobek YA, Levine MJ.

Genomics. 1996 Feb 1;31(3):277-82.

PMID:
8838308
46.

Assignment of the human integral transmembrane protein 1 gene (ITM1) to human chromosome band 11q23.3 by in situ hybridization and YAC mapping.

Van Hul W, Hong G, Wauters J, Van Hul E, Nowak N, Shows TB, Willems PJ, Merregaert J.

Cytogenet Cell Genet. 1996;74(3):218-9. No abstract available.

PMID:
8941377
47.

Report of the Fifth International Workshop on Human Chromosome 11 Mapping 1996.

Shows TB, Alders M, Bennett S, Burbee D, Cartwright P, Chandrasekharappa S, Cooper P, Courseaux A, Davies C, Devignes MD, Devilee P, Elliott R, Evans G, Fantes J, Garner H, Gaudray P, Gerhard DS, Gessler M, Higgins M, Hummerich H, James M, Lagercrantz J, Litt M, Little P, Zabel B, et al.

Cytogenet Cell Genet. 1996;74(1-2):1-56. No abstract available.

PMID:
8893803
48.

Mouse and human homologues of the yeast origin of replication recognition complex subunit ORC2 and chromosomal localization of the cognate human gene ORC2L.

Takahara K, Bong M, Brevard R, Eddy RL, Haley LL, Sait SJ, Shows TB, Hoffman GG, Greenspan DS.

Genomics. 1996 Jan 1;31(1):119-22.

PMID:
8808289
49.

New members of the chemokine receptor gene family.

Raport CJ, Schweickart VL, Chantry D, Eddy RL Jr, Shows TB, Godiska R, Gray PW.

J Leukoc Biol. 1996 Jan;59(1):18-23. Review.

PMID:
8558062
50.

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