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Items: 1 to 20 of 86

1.

Cloning and characterization of 13 novel transcripts and the human RGS8 gene from the 1q25 region encompassing the hereditary prostate cancer (HPC1) locus.

Sood R, Bonner TI, Makalowska I, Stephan DA, Robbins CM, Connors TD, Morgenbesser SD, Su K, Faruque MU, Pinkett H, Graham C, Baxevanis AD, Klinger KW, Landes GM, Trent JM, Carpten JD.

Genomics. 2001 Apr 15;73(2):211-22.

PMID:
11318611
2.

A 6-Mb high-resolution physical and transcription map encompassing the hereditary prostate cancer 1 (HPC1) region.

Carpten JD, Makalowska I, Robbins CM, Scott N, Sood R, Connors TD, Bonner TI, Smith JR, Faruque MU, Stephan DA, Pinkett H, Morgenbesser SD, Su K, Graham C, Gregory SG, Williams H, McDonald L, Baxevanis AD, Klingler KW, Landes GM, Trent JM.

Genomics. 2000 Feb 15;64(1):1-14.

PMID:
10708513
3.

Identification of 9 novel transcripts and two RGSL genes within the hereditary prostate cancer region (HPC1) at 1q25.

Silva AP, Salim AC, Bulgarelli A, de Souza JE, Osório E, Caballero OL, Iseli C, Stevenson BJ, Jongeneel CV, de Souza SJ, Simpson AJ, Camargo AA.

Gene. 2003 May 22;310:49-57.

PMID:
12801632
5.

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
6.

Transcription mapping of the 5q- syndrome critical region: cloning of two novel genes and sequencing, expression, and mapping of a further six novel cDNAs.

Boultwood J, Fidler C, Strickson AJ, Watkins F, Kostrzewa M, Jaju RJ, Müller U, Wainscoat JS.

Genomics. 2000 May 15;66(1):26-34.

PMID:
10843801
7.

cDNA sequencing and analysis of POV1 (PB39): a novel gene up-regulated in prostate cancer.

Cole KA, Chuaqui RF, Katz K, Pack S, Zhuang Z, Cole CE, Lyne JC, Linehan WM, Liotta LA, Emmert-Buck MR.

Genomics. 1998 Jul 15;51(2):282-7.

PMID:
9722952
9.

A novel human RasGAP-like gene that maps within the prostate cancer susceptibility locus at chromosome 1q25.

Noto S, Maeda T, Hattori S, Inazawa J, Imamura M, Asaka M, Hatakeyama M.

FEBS Lett. 1998 Dec 11;441(1):127-31.

10.

Low frequency of allelic imbalance at the prostate cancer susceptibility loci HPC1 and 1p36 in Swedish men with hereditary prostate cancer.

Ahman AK, Jonsson BA, Damber JE, Bergh A, Emanuelsson M, Grönberg H.

Genes Chromosomes Cancer. 2000 Dec;29(4):292-6.

PMID:
11066072
11.

The region on 9p associated with 46,XY sex reversal contains several transcripts expressed in the urogenital system and a novel doublesex-related domain.

Ottolenghi C, Veitia R, Quintana-Murci L, Torchard D, Scapoli L, Souleyreau-Therville N, Beckmann J, Fellous M, McElreavey K.

Genomics. 2000 Mar 1;64(2):170-8.

PMID:
10729223
12.
13.

Characterization of 954 bovine full-CDS cDNA sequences.

Harhay GP, Sonstegard TS, Keele JW, Heaton MP, Clawson ML, Snelling WM, Wiedmann RT, Van Tassell CP, Smith TP.

BMC Genomics. 2005 Nov 23;6:166.

14.

Analysis of the prostate cancer cell line LNCaP transcriptome using a sequencing-by-synthesis approach.

Bainbridge MN, Warren RL, Hirst M, Romanuik T, Zeng T, Go A, Delaney A, Griffith M, Hickenbotham M, Magrini V, Mardis ER, Sadar MD, Siddiqui AS, Marra MA, Jones SJ.

BMC Genomics. 2006 Sep 29;7:246.

15.
16.

Construction of a 350-kb sequence-ready 11q13 cosmid contig encompassing the markers D11S4933 and D11S546: mapping of 11 genes and 3 tumor-associated translocation breakpoints.

van Asseldonk M, Schepens M, de Bruijn D, Janssen B, Merkx G, Geurts van Kessel A.

Genomics. 2000 May 15;66(1):35-42.

PMID:
10843802
17.

Identification, characterization and mapping of the human ZIS (zinc-finger, splicing) gene.

Nakano M, Yoshiura K, Oikawa M, Miyoshi O, Yamada K, Kondo S, Miwa N, Soeda E, Jinno Y, Fujii T, Niikawa N.

Gene. 1998 Dec 28;225(1-2):59-65.

PMID:
9931435
18.

Novel genes mapping to the critical region of the 5q- syndrome.

Boultwood J, Fidler C, Soularue P, Strickson AJ, Kostrzewa M, Jaju RJ, Cotter FE, Fairweather N, Monaco AP, Müller U, Lovett M, Jabs EW, Auffray C, Wainscoat JS.

Genomics. 1997 Oct 1;45(1):88-96.

PMID:
9339364
19.

Defining a common region of deletion at 13q21 in human cancers.

Chen C, Brabham WW, Stultz BG, Frierson HF Jr, Barrett JC, Sawyers CL, Isaacs JT, Dong JT.

Genes Chromosomes Cancer. 2001 Aug;31(4):333-44.

PMID:
11433524
20.

A common deletion at chromosomal region 17q21 in sporadic prostate tumors distal to BRCA1.

Dai Q, Deubler DA, Maxwell TM, Zhu XL, Cui J, Rohr LR, Stephenson RA, Brothman AR.

Genomics. 2001 Feb 1;71(3):324-9.

PMID:
11170749

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