Kremmidiotis G - Search Results

1

Common chromosomal fragile site FRA16D sequence: identification of the FOR gene spanning FRA16D and homozygous deletions and translocation breakpoints in cancer cells.

Ried K, Finnis M, Hobson L, Mangelsdorf M, Dayan S, Nancarrow JK, Woollatt E, Kremmidiotis G, Gardner A, Venter D, Baker E, Richards RI. Ried K, et al. Among authors: kremmidiotis g. Hum Mol Genet. 2000 Jul 1;9(11):1651-63. doi: 10.1093/hmg/9.11.1651. Hum Mol Genet. 2000. PMID: 10861292

2

The de novo chromosome 16 translocations of two patients with abnormal phenotypes (mental retardation and epilepsy) disrupt the A2BP1 gene.

Bhalla K, Phillips HA, Crawford J, McKenzie OLD, Mulley JC, Eyre H, Gardner AE, Kremmidiotis G, Callen DF. Bhalla K, et al. Among authors: kremmidiotis g. J Hum Genet. 2004;49(6):308-311. doi: 10.1007/s10038-004-0145-4. Epub 2004 May 18. J Hum Genet. 2004. PMID: 15148587

3

The Batten disease gene product (CLN3p) is a Golgi integral membrane protein.

Kremmidiotis G, Lensink IL, Bilton RL, Woollatt E, Chataway TK, Sutherland GR, Callen DF. Kremmidiotis G, et al. Hum Mol Genet. 1999 Mar;8(3):523-31. doi: 10.1093/hmg/8.3.523. Hum Mol Genet. 1999. PMID: 9949212

4

Sequencing, transcript identification, and quantitative gene expression profiling in the breast cancer loss of heterozygosity region 16q24.3 reveal three potential tumor-suppressor genes.

Powell JA, Gardner AE, Bais AJ, Hinze SJ, Baker E, Whitmore S, Crawford J, Kochetkova M, Spendlove HE, Doggett NA, Sutherland GR, Callen DF, Kremmidiotis G. Powell JA, et al. Among authors: kremmidiotis g. Genomics. 2002 Sep;80(3):303-10. doi: 10.1006/geno.2002.6828. Genomics. 2002. PMID: 12213200

5

Localization of human cadherin genes to chromosome regions exhibiting cancer-related loss of heterozygosity.

Kremmidiotis G, Baker E, Crawford J, Eyre HJ, Nahmias J, Callen DF. Kremmidiotis G, et al. Genomics. 1998 May 1;49(3):467-71. doi: 10.1006/geno.1998.5281. Genomics. 1998. PMID: 9615235

6

Aberrant CBFA2T3B gene promoter methylation in breast tumors.

Bais AJ, Gardner AE, McKenzie OL, Callen DF, Sutherland GR, Kremmidiotis G. Bais AJ, et al. Among authors: kremmidiotis g. Mol Cancer. 2004 Aug 10;3:22. doi: 10.1186/1476-4598-3-22. Mol Cancer. 2004. PMID: 15301688 Free PMC article.

7

Neuronal sodium-channel alpha1-subunit mutations in generalized epilepsy with febrile seizures plus.

Wallace RH, Scheffer IE, Barnett S, Richards M, Dibbens L, Desai RR, Lerman-Sagie T, Lev D, Mazarib A, Brand N, Ben-Zeev B, Goikhman I, Singh R, Kremmidiotis G, Gardner A, Sutherland GR, George AL Jr, Mulley JC, Berkovic SF. Wallace RH, et al. Among authors: kremmidiotis g. Am J Hum Genet. 2001 Apr;68(4):859-65. doi: 10.1086/319516. Epub 2001 Mar 13. Am J Hum Genet. 2001. PMID: 11254444 Free PMC article.

8

CBFA2T3 (MTG16) is a putative breast tumor suppressor gene from the breast cancer loss of heterozygosity region at 16q24.3.

Kochetkova M, McKenzie OL, Bais AJ, Martin JM, Secker GA, Seshadri R, Powell JA, Hinze SJ, Gardner AE, Spendlove HE, O'Callaghan NJ, Cleton-Jansen AM, Cornelisse C, Whitmore SA, Crawford J, Kremmidiotis G, Sutherland GR, Callen DF. Kochetkova M, et al. Among authors: kremmidiotis g. Cancer Res. 2002 Aug 15;62(16):4599-604. Cancer Res. 2002. PMID: 12183414

9

Molecular and functional analyses of the human and mouse genes encoding AFG3L1, a mitochondrial metalloprotease homologous to the human spastic paraplegia protein.

Kremmidiotis G, Gardner AE, Settasatian C, Savoia A, Sutherland GR, Callen DF. Kremmidiotis G, et al. Genomics. 2001 Aug;76(1-3):58-65. doi: 10.1006/geno.2001.6560. Genomics. 2001. PMID: 11549317

10

Expression profiling reveals functionally important genes and coordinately regulated signaling pathway genes during in vitro angiogenesis.

Hahn CN, Su ZJ, Drogemuller CJ, Tsykin A, Waterman SR, Brautigan PJ, Yu S, Kremmidiotis G, Gardner A, Solomon PJ, Goodall GJ, Vadas MA, Gamble JR. Hahn CN, et al. Among authors: kremmidiotis g. Physiol Genomics. 2005 Jun 16;22(1):57-69. doi: 10.1152/physiolgenomics.00278.2004. Epub 2005 Apr 19. Physiol Genomics. 2005. PMID: 15840639

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