Identification of a novel single nucleotide polymorphism (SNP) in the human organic cation transporter-like 2-antisense (ORCTL2S) gene
スポンサーリンク
概要
- 論文の詳細を見る
- 2000-01-01
著者
-
SOEJIMA Hidenobu
Department of Pathology, University of Otago Medical School
-
HIGASHIMOTO Ken
Department of Biomolecular Sciences, Division of Molecular Biology and Genetics, Faculty of Medicine
-
MUKAI Tsunehiro
Department of Biomolecular Sciences, Division of Molecular Biology and Genetics, Faculty of Medicine
-
Mukai Tsunehiro
Saga University The Administration Office
-
Mukai T
Saga Medical School Saga
-
Mukai Tsunehiro
Department Of Biomolecular Sciences Saga Medical School
-
Higashimoto Ken
Division Of Molecular Genetics And Epigenetics Department Of Biomolecular Sciences Faculty Of Medici
-
Soejima H
Division Of Molecular Genetics And Epigenetics Department Of Biomolecular Sciences Faculty Of Medici
-
Soejima Hidenobu
Department Of Pathology University Of Otago Medical School
-
Katsuki T
Department Of Oral Surgery Saga Medical School
-
KATSUKI Takesi
Department of Oral Surgery, Saga Medical School
-
Soejima Hidenobu
Department Of Biomolecular Sciences Faculty Of Medicine Saga University
関連論文
- In situ detection of insulin-like growth factor II (IGF2) and H19 gene expression in hepatocellular carcinoma
- Expression profile of LIT1/KCNQ1OT1 and epigenetic status at the KvDMR1 in colorectal cancers
- Expression of MEF2 Genes during Human Cardiac Development
- Mouse Mef2b Gene: Unique Member of MEF2 Gene Family
- A SacII polymorphism in the human ASCL2 (HASH2) gene region
- MeCP2 knockdown reveals DNA methylation-independent gene repression of target genes in living cells and a bias in the cellular location of target gene products
- The Essential Role of Histone H3 Lys9 Di-Methylation and MeCP2 Binding in MGMT Silencing with Poor DNA Methylation of the Promoter CpG Island
- The First Exon of the Rat Aldolase C Gene Is Essential for Restoring the Chromatin Structure in Transgenic Mice
- Copy-Dependent and Position-Independent Expression of Rat Aldolase A Gene^1
- IS038 New mutations of FBN1 gene found in Japanese patients with Marfan syndrome
- Significant Reduction of WT1 Gene Expression, Possibly Due to Epigenetic Alteration in Wilms' Tumor
- A Novel Imprinted Gene, KCNQ1DN, within the WT2 Critical Region of Human Chromosome 11p15.5 and Its Reduced Expression in Wilm's Tumors^1
- Antisense Transcription Occurs at the Promoter of a Mouse Imprinted Gene, Commd1, on the Repressed Paternal Allele
- An NsiI RFLP in the human long QT intronic transcript 1 (LIT1)
- Identification of a novel single nucleotide polymorphism (SNP) in the human organic cation transporter-like 2-antisense (ORCTL2S) gene
- Identification of a novel isoform of Murr1 transcript, U2mu, which is transcribed from the portions of two closely located but oppositely oriented genes
- Organotypic culture of human bone marrow adipose tissue
- A Novel Imprinted Gene, KCNQ1DN, within the WT2 Critical Region of Human Chromosome 11p15.5 and Its Reduced Expression in Wilms' Tumors.
- Congenital hyperinsulinism in an infant with paternal uniparental disomy on chromosome 11p15 : Few clinical features suggestive of Beckwith-Wiedemann syndrome
- Epigenetic and genetic alterations of the imprinting disorder Beckwith-Wiedemann syndrome and related disorders