83 related articles for article (PubMed ID: 21472247)
1. CpG islands around exon 1 in the succinyl-CoA:3-ketoacid CoA transferase (SCOT) gene are hypomethylated even in human and mouse hepatic tissues where SCOT gene expression is completely suppressed.
Fukao T; Zhang G; Matsuo N; Kondo N
Mol Med Rep; 2010; 3(2):355-9. PubMed ID: 21472247
[TBL] [Abstract][Full Text] [Related]
2. Liver-specific silencing of the human gene encoding succinyl-CoA: 3-ketoacid CoA transferase.
Orii KE; Fukao T; Song XQ; Mitchell GA; Kondo N
Tohoku J Exp Med; 2008 Jul; 215(3):227-36. PubMed ID: 18648183
[TBL] [Abstract][Full Text] [Related]
3. Aberrant methylation and silencing of ARHI, an imprinted tumor suppressor gene in which the function is lost in breast cancers.
Yuan J; Luo RZ; Fujii S; Wang L; Hu W; Andreeff M; Pan Y; Kadota M; Oshimura M; Sahin AA; Issa JP; Bast RC; Yu Y
Cancer Res; 2003 Jul; 63(14):4174-80. PubMed ID: 12874023
[TBL] [Abstract][Full Text] [Related]
4. Enzymes of ketone body utilization in human tissues: protein and messenger RNA levels of succinyl-coenzyme A (CoA):3-ketoacid CoA transferase and mitochondrial and cytosolic acetoacetyl-CoA thiolases.
Fukao T; Song XQ; Mitchell GA; Yamaguchi S; Sukegawa K; Orii T; Kondo N
Pediatr Res; 1997 Oct; 42(4):498-502. PubMed ID: 9380443
[TBL] [Abstract][Full Text] [Related]
5. Methylation patterns of the human beta-glucuronidase gene locus: boundaries of methylation and general implications for frequent point mutations at CpG dinucleotides.
Tomatsu S; Orii KO; Islam MR; Shah GN; Grubb JH; Sukegawa K; Suzuki Y; Orii T; Kondo N; Sly WS
Genomics; 2002 Mar; 79(3):363-75. PubMed ID: 11863366
[TBL] [Abstract][Full Text] [Related]
6. Succinyl-CoA:3-ketoacid CoA transferase (SCOT): cloning of the human SCOT gene, tertiary structural modeling of the human SCOT monomer, and characterization of three pathogenic mutations.
Fukao T; Mitchell GA; Song XQ; Nakamura H; Kassovska-Bratinova S; Orii KE; Wraith JE; Besley G; Wanders RJ; Niezen-Koning KE; Berry GT; Palmieri M; Kondo N
Genomics; 2000 Sep; 68(2):144-51. PubMed ID: 10964512
[TBL] [Abstract][Full Text] [Related]
7. Symmetric and asymmetric DNA methylation in the human IGF2-H19 imprinted region.
Vu TH; Li T; Nguyen D; Nguyen BT; Yao XM; Hu JF; Hoffman AR
Genomics; 2000 Mar; 64(2):132-43. PubMed ID: 10729220
[TBL] [Abstract][Full Text] [Related]
8. Single-base substitution at the last nucleotide of exon 6 (c.671G>A), resulting in the skipping of exon 6, and exons 6 and 7 in human succinyl-CoA:3-ketoacid CoA transferase (SCOT) gene.
Yamada K; Fukao T; Zhang G; Sakurai S; Ruiter JP; Wanders RJ; Kondo N
Mol Genet Metab; 2007 Mar; 90(3):291-7. PubMed ID: 17169596
[TBL] [Abstract][Full Text] [Related]
9. A new class of tissue-specifically methylated regions involving entire CpG islands in the mouse.
Suzuki M; Sato S; Arai Y; Shinohara T; Tanaka S; Greally JM; Hattori N; Shiota K
Genes Cells; 2007 Dec; 12(12):1305-14. PubMed ID: 18076568
[TBL] [Abstract][Full Text] [Related]
10. Cell type-specific methylation of an intronic CpG island controls expression of the MCJ gene.
Strathdee G; Davies BR; Vass JK; Siddiqui N; Brown R
Carcinogenesis; 2004 May; 25(5):693-701. PubMed ID: 14729589
[TBL] [Abstract][Full Text] [Related]
11. Regulation of tissue-specific expression of renal organic anion transporters by hepatocyte nuclear factor 1 α/β and DNA methylation.
Jin L; Kikuchi R; Saji T; Kusuhara H; Sugiyama Y
J Pharmacol Exp Ther; 2012 Mar; 340(3):648-55. PubMed ID: 22160269
[TBL] [Abstract][Full Text] [Related]
12. DNA methylation of the human oxytocin receptor gene promoter regulates tissue-specific gene suppression.
Kusui C; Kimura T; Ogita K; Nakamura H; Matsumura Y; Koyama M; Azuma C; Murata Y
Biochem Biophys Res Commun; 2001 Dec; 289(3):681-6. PubMed ID: 11726201
[TBL] [Abstract][Full Text] [Related]
13. Hypomethylation of the synuclein gamma gene CpG island promotes its aberrant expression in breast carcinoma and ovarian carcinoma.
Gupta A; Godwin AK; Vanderveer L; Lu A; Liu J
Cancer Res; 2003 Feb; 63(3):664-73. PubMed ID: 12566312
[TBL] [Abstract][Full Text] [Related]
14. CpG methylation at the USF-binding site is important for the liver-specific transcription of the chipmunk HP-27 gene.
Fujii G; Nakamura Y; Tsukamoto D; Ito M; Shiba T; Takamatsu N
Biochem J; 2006 Apr; 395(1):203-9. PubMed ID: 16396632
[TBL] [Abstract][Full Text] [Related]
15. DNA methylation paradigm shift: 15-lipoxygenase-1 upregulation in prostatic intraepithelial neoplasia and prostate cancer by atypical promoter hypermethylation.
Kelavkar UP; Harya NS; Hutzley J; Bacich DJ; Monzon FA; Chandran U; Dhir R; O'Keefe DS
Prostaglandins Other Lipid Mediat; 2007 Jan; 82(1-4):185-97. PubMed ID: 17164146
[TBL] [Abstract][Full Text] [Related]
16. Patients homozygous for the T435N mutation of succinyl-CoA:3-ketoacid CoA Transferase (SCOT) do not show permanent ketosis.
Fukao T; Shintaku H; Kusubae R; Zhang GX; Nakamura K; Kondo M; Kondo N
Pediatr Res; 2004 Dec; 56(6):858-63. PubMed ID: 15496607
[TBL] [Abstract][Full Text] [Related]
17. Mapping the methylation pattern by bisulfite genomic sequencing of the E-cadherin promoter CpG island in nasopharyngeal carcinoma.
Kao RH; Huang LC; Hsu YH
Anticancer Res; 2002; 22(6C):4109-13. PubMed ID: 12553040
[TBL] [Abstract][Full Text] [Related]
18. Succinyl-CoA:3-ketoacid CoA transferase (SCOT) deficiency: two pathogenic mutations, V133E and C456F, in Japanese siblings.
Song XQ; Fukao T; Watanabe H; Shintaku H; Hirayama K; Kassovska-Bratinova S; Kondo N; Mitchell GA
Hum Mutat; 1998; 12(2):83-8. PubMed ID: 9671268
[TBL] [Abstract][Full Text] [Related]
19. A 6-bp deletion at the splice donor site of the first intron resulted in aberrant splicing using a cryptic splice site within exon 1 in a patient with succinyl-CoA: 3-Ketoacid CoA transferase (SCOT) deficiency.
Fukao T; Sakurai S; Rolland MO; Zabot MT; Schulze A; Yamada K; Kondo N
Mol Genet Metab; 2006 Nov; 89(3):280-2. PubMed ID: 16765626
[TBL] [Abstract][Full Text] [Related]
20. Hepatitis B viral DNA is methylated in liver tissues.
Vivekanandan P; Thomas D; Torbenson M
J Viral Hepat; 2008 Feb; 15(2):103-7. PubMed ID: 18184192
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]