Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 98

1.

Genomic organization, physical mapping, and expression analysis of the human protein arginine methyltransferase 1 gene.

Scorilas A, Black MH, Talieri M, Diamandis EP.

Biochem Biophys Res Commun. 2000 Nov 19;278(2):349-59.

PMID:
11097842
[PubMed - indexed for MEDLINE]
2.

Cloning of a gene (SR-A1), encoding for a new member of the human Ser/Arg-rich family of pre-mRNA splicing factors: overexpression in aggressive ovarian cancer.

Scorilas A, Kyriakopoulou L, Katsaros D, Diamandis EP.

Br J Cancer. 2001 Jul 20;85(2):190-8.

PMID:
11461075
[PubMed - indexed for MEDLINE]
Free PMC Article
3.

Identification and characterization of a novel human testis-specific kinase substrate gene which is downregulated in testicular tumors.

Scorilas A, Yousef GM, Jung K, Rajpert-De Meyts E, Carsten S, Diamandis EP.

Biochem Biophys Res Commun. 2001 Jul 13;285(2):400-8.

PMID:
11444856
[PubMed - indexed for MEDLINE]
4.
5.

Molecular characterization of a new gene, CEAL1, encoding for a carcinoembryonic antigen-like protein with a highly conserved domain of eukaryotic translation initiation factors.

Scorilas A, Chiang PM, Katsaros D, Yousef GM, Diamandis EP.

Gene. 2003 May 22;310:79-89.

PMID:
12801635
[PubMed - indexed for MEDLINE]
6.

Alternative splicing yields protein arginine methyltransferase 1 isoforms with distinct activity, substrate specificity, and subcellular localization.

Goulet I, Gauvin G, Boisvenue S, Côté J.

J Biol Chem. 2007 Nov 9;282(45):33009-21. Epub 2007 Sep 11.

PMID:
17848568
[PubMed - indexed for MEDLINE]
Free Article
7.
8.

Identification and characterization of two putative human arginine methyltransferases (HRMT1L1 and HRMT1L2).

Scott HS, Antonarakis SE, Lalioti MD, Rossier C, Silver PA, Henry MF.

Genomics. 1998 Mar 15;48(3):330-40.

PMID:
9545638
[PubMed - indexed for MEDLINE]
9.

Molecular characterization, tissue expression, and mapping of a novel Siglec-like gene (SLG2) with three splice variants.

Yousef GM, Ordon MH, Foussias G, Diamandis EP.

Biochem Biophys Res Commun. 2001 Jun 22;284(4):900-10.

PMID:
11409878
[PubMed - indexed for MEDLINE]
10.

WWOX, a novel WW domain-containing protein mapping to human chromosome 16q23.3-24.1, a region frequently affected in breast cancer.

Bednarek AK, Laflin KJ, Daniel RL, Liao Q, Hawkins KA, Aldaz CM.

Cancer Res. 2000 Apr 15;60(8):2140-5.

PMID:
10786676
[PubMed - indexed for MEDLINE]
Free Article
11.
12.
13.

Molecular cloning, physical mapping, and expression analysis of a novel gene, BCL2L12, encoding a proline-rich protein with a highly conserved BH2 domain of the Bcl-2 family.

Scorilas A, Kyriakopoulou L, Yousef GM, Ashworth LK, Kwamie A, Diamandis EP.

Genomics. 2001 Mar 1;72(2):217-21.

PMID:
11401436
[PubMed - indexed for MEDLINE]
14.
15.

Identification and phylogenetic analyses of the protein arginine methyltransferase gene family in fish and ascidians.

Hung CM, Li C.

Gene. 2004 Oct 13;340(2):179-87.

PMID:
15475159
[PubMed - indexed for MEDLINE]
16.

Genomic structure and chromosomal mapping of the gene coding for ICBP90, a protein involved in the regulation of the topoisomerase IIalpha gene expression.

Hopfner R, Mousli M, Garnier JM, Redon R, du Manoir S, Chatton B, Ghyselinck N, Oudet P, Bronner C.

Gene. 2001 Mar 21;266(1-2):15-23.

PMID:
11290415
[PubMed - indexed for MEDLINE]
17.
19.

Molecular cloning of the human kallikrein 15 gene (KLK15). Up-regulation in prostate cancer.

Yousef GM, Scorilas A, Jung K, Ashworth LK, Diamandis EP.

J Biol Chem. 2001 Jan 5;276(1):53-61.

PMID:
11010966
[PubMed - indexed for MEDLINE]
Free Article
20.

Cloning and molecular characterization of two splice variants of a new putative member of the Siglec-3-like subgroup of Siglecs.

Foussias G, Taylor SM, Yousef GM, Tropak MB, Ordon MH, Diamandis EP.

Biochem Biophys Res Commun. 2001 Jun 22;284(4):887-99.

PMID:
11409877
[PubMed - indexed for MEDLINE]

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk