Kalikin LM - Search Results

1

Mutant deoxynucleotide carrier is associated with congenital microcephaly.

Rosenberg MJ, Agarwala R, Bouffard G, Davis J, Fiermonte G, Hilliard MS, Koch T, Kalikin LM, Makalowska I, Morton DH, Petty EM, Weber JL, Palmieri F, Kelley RI, Schäffer AA, Biesecker LG. Rosenberg MJ, et al. Among authors: kalikin lm. Nat Genet. 2002 Sep;32(1):175-9. doi: 10.1038/ng948. Epub 2002 Aug 19. Nat Genet. 2002. PMID: 12185364

2

Genomic and expression analyses of alternatively spliced transcripts of the MLL septin-like fusion gene (MSF) that map to a 17q25 region of loss in breast and ovarian tumors.

Kalikin LM, Sims HL, Petty EM. Kalikin LM, et al. Genomics. 2000 Jan 15;63(2):165-72. doi: 10.1006/geno.1999.6077. Genomics. 2000. PMID: 10673329

3

Genomic characterization of human SEC14L1 splice variants within a 17q25 candidate tumor suppressor gene region and identification of an unrelated embedded expressed sequence tag.

Kalikin LM, Bugeaud EM, Palmbos PL, Lyons RH Jr, Petty EM. Kalikin LM, et al. Mamm Genome. 2001 Dec;12(12):925-9. doi: 10.1007/s00335-001-2073-3. Mamm Genome. 2001. PMID: 11707779 Free article.

4

Characterization of a SEPT9 interacting protein, SEPT14, a novel testis-specific septin.

Peterson EA, Kalikin LM, Steels JD, Estey MP, Trimble WS, Petty EM. Peterson EA, et al. Among authors: kalikin lm. Mamm Genome. 2007 Nov;18(11):796-807. doi: 10.1007/s00335-007-9065-x. Epub 2007 Oct 6. Mamm Genome. 2007. PMID: 17922164

5

An integrated physical and gene map of human distal chromosome 17q24-proximal 17q25 encompassing multiple disease loci.

Kalikin LM, George RA, Keller MP, Bort S, Bowler NS, Law DJ, Chance PF, Petty EM. Kalikin LM, et al. Genomics. 1999 Apr 1;57(1):36-42. doi: 10.1006/geno.1998.5740. Genomics. 1999. PMID: 10191081

6

A region of interstitial 17q25 allelic loss in ovarian tumors coincides with a defined region of loss in breast tumors.

Kalikin LM, Frank TS, Svoboda-Newman SM, Wetzel JC, Cooney KA, Petty EM. Kalikin LM, et al. Oncogene. 1997 Apr 24;14(16):1991-4. doi: 10.1038/sj.onc.1201013. Oncogene. 1997. PMID: 9150366

7

Distal chromosome 17q loss in Barrett's esophageal and gastric cardia adenocarcinomas: implications for tumorigenesis.

Petty EM, Kalikin LM, Orringer MB, Beer DG. Petty EM, et al. Among authors: kalikin lm. Mol Carcinog. 1998 Aug;22(4):222-8. doi: 10.1002/(sici)1098-2744(199808)22:4<222::aid-mc3>3.0.co;2-l. Mol Carcinog. 1998. PMID: 9726814 Free article.

8

Detailed deletion analysis of sporadic breast tumors defines an interstitial region of allelic loss on 17q25.

Kalikin LM, Qu X, Frank TS, Caduff RF, Svoboda SM, Law DJ, Petty EM. Kalikin LM, et al. Genes Chromosomes Cancer. 1996 Sep;17(1):64-8. doi: 10.1002/(SICI)1098-2264(199609)17:1<64::AID-GCC10>3.0.CO;2-H. Genes Chromosomes Cancer. 1996. PMID: 8889509

9

High SEPT9_v1 expression in human breast cancer cells is associated with oncogenic phenotypes.

Gonzalez ME, Peterson EA, Privette LM, Loffreda-Wren JL, Kalikin LM, Petty EM. Gonzalez ME, et al. Among authors: kalikin lm. Cancer Res. 2007 Sep 15;67(18):8554-64. doi: 10.1158/0008-5472.CAN-07-1474. Cancer Res. 2007. PMID: 17875694

10

Isolation and mapping of a human septin gene to a region on chromosome 17q, commonly deleted in sporadic epithelial ovarian tumors.

Russell SE, McIlhatton MA, Burrows JF, Donaghy PG, Chanduloy S, Petty EM, Kalikin LM, Church SW, McIlroy S, Harkin DP, Keilty GW, Cranston AN, Weissenbach J, Hickey I, Johnston PG. Russell SE, et al. Among authors: kalikin lm. Cancer Res. 2000 Sep 1;60(17):4729-34. Cancer Res. 2000. PMID: 10987277

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