Akira Horii
0000-0002-3967-3291
Tohoku University
233 papers found
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Genomic analysis of 1p36-p35: a region harboring genes closely associated with various human diseases
Human BAC Contig Covering the Deleted Region in Pancreatic Cancer at 12q21
Frequent nuclear accumulation of β-catenin in pituitary adenoma
Homozygous deletion in a neuroblastoma cell line defined by a high-density STS map spanning human chromosome band 1p36
Characterization of the mutations of the K-ras, p53, p16, and SMAD4 genes in 15 human pancreatic cancer cell lines.
Exclusion ofSMAD4 mutation as an early genetic change in human pancreatic ductal tumorigenesis
Degree of apoptosis induced by adenovirus-mediated transduction of p53 or p73α depends on the p53 status of glioma cells
Structure, expression and mutational analysis of the hBRAG gene on 10q in the frequently deleted region in human endometrial cancer.
Not hMSH2 but hMLH1 is frequently silenced by hypermethylation in endometrial cancer but rarely silenced in pancreatic cancer with microsatellite instability.
Molecular Cloning and Expression of cDNA Encoding Chicken UDP-N-acetyl-d-glucosamine (GlcNAc): GlcNAcβ1–6(GlcNAcβ1–2)- Manα1-R[GlcNAc to Man]β1,4N-acetylglucosaminyltransferase VI
Frequent loss of copy number on the long arm of chromosome 21 in human esophageal squamous cell carcinoma.
Association of poor prognosis with loss of 12q, 17p, and 18q, and concordant loss of 6q/17p and 12q/18q in human pancreatic ductal adenocarcinoma
Identification and characterization of a 500-kb homozygously deleted region at 1p36.2-p36.3 in a neuroblastoma cell line
Anticorresponding mutations of the KRAS and PTEN genes in human endometrial cancer.
Identification of a 7-cM region of frequent allelic loss on chromosome band 16p13.3 that is specifically associated with anaplastic thyroid carcinoma.
Analysis of the candidate target genes for mutation in microsatellite instability-positive cancers of the colorectum, stomach, and endometrium.
p24/ING1-ALT1 and p47/ING1-ALT2, distinct alternative transcripts of p33/ING1
Genetic alterations in human pancreatic cancer
Mutational analysis of the CTNNB1 (β-catenin) gene in human endometrial cancer: Frequent mutations at codon 34 that cause nuclear accumulation
Erratum: Identification of three commonly deleted regions on chromosome arm 6q in human pancreatic cancer (genes chromosomes cancer (1999) 25:(60-64))
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