about
Amplification and overexpression of TGIF2, a novel homeobox gene of the TALE superclass, in ovarian cancer cell linesJunctional Rab13-binding protein (JRAB) regulates cell spreading via filaminsOverexpression of PDZK1 within the 1q12-q22 amplicon is likely to be associated with drug-resistance phenotype in multiple myelomaSNO is a probable target for gene amplification at 3q26 in squamous-cell carcinomas of the esophagusGenome-wide array-based comparative genomic hybridization analysis of pancreatic adenocarcinoma: identification of genetic indicators that predict patient outcomeNF90 in posttranscriptional gene regulation and microRNA biogenesisKrüppel-like factor 12 plays a significant role in poorly differentiated gastric cancer progression.Promoter analysis and chromosomal mapping of human EBAG9 gene.Genetically distinct and clinically relevant classification of hepatocellular carcinoma: putative therapeutic targets.Current status of collaborative relationships between dialysis facilities and dental facilities in Japan: results of a nationwide survey.The association of elastin gene variants with two angiographic subtypes of polypoidal choroidal vasculopathy.Evaluation of an association between plasma total homocysteine and schizophrenia by a Mendelian randomization analysis.Sex differences of leukocytes DNA methylation adjusted for estimated cellular proportions.SASPase regulates stratum corneum hydration through profilaggrin-to-filaggrin processing.Blood diagnostic biomarkers for major depressive disorder using multiplex DNA methylation profiles: discovery and validationInitiation of recombination suppression and PAR formation during the early stages of neo-sex chromosome differentiation in the Okinawa spiny rat, Tokudaia muenninkiDeep intronic GPR143 mutation in a Japanese family with ocular albinismDGCR6 at the proximal part of the DiGeorge critical region is involved in conotruncal heart defects.A FRMD7 variant in a Japanese family causes congenital nystagmusThe Xq22 inversion breakpoint interrupted a novel Ras-like GTPase gene in a patient with Duchenne muscular dystrophy and profound mental retardation.Plasma total homocysteine is associated with DNA methylation in patients with schizophrenia.Specific molecular signatures of non-tumor liver tissue may predict a risk of hepatocarcinogenesis.Translocation (1;22)(p36;q11.2) with concurrent del(22)(q11.2) resulted in homozygous deletion of SNF5/INI1 in a newly established cell line derived from extrarenal rhabdoid tumor.A novel PTCH1 mutation in a patient with Gorlin syndrome.A novel COL11A1 mutation affecting splicing in a patient with Stickler syndrome.Dermokine as a novel biomarker for early-stage colorectal cancer.Overexpression of NF-κB inducing kinase underlies constitutive NF-κB activation in lung cancer cells.Identification of PAK4 as a putative target gene for amplification within 19q13.12-q13.2 in oral squamous-cell carcinoma.ITCH is a putative target for a novel 20q11.22 amplification detected in anaplastic thyroid carcinoma cells by array-based comparative genomic hybridization.Genome-wide DNA methylation profiles in liver tissue at the precancerous stage and in hepatocellular carcinoma.Frequent silencing of a putative tumor suppressor gene melatonin receptor 1 A (MTNR1A) in oral squamous-cell carcinoma.Identification of SMURF1 as a possible target for 7q21.3-22.1 amplification detected in a pancreatic cancer cell line by in-house array-based comparative genomic hybridization.Association of KLK5 overexpression with invasiveness of urinary bladder carcinoma cells.Establishment of a cell line from a malignant rhabdoid tumor of the liver lacking the function of two tumor suppressor genes, hSNF5/INI1 and p16.Involvement of overexpressed wild-type BRAF in the growth of malignant melanoma cell lines.A case with concurrent duplication, triplication, and uniparental isodisomy at 1q42.12-qter supporting microhomology-mediated break-induced replication model for replicative rearrangements.Aberrant DNA methylation of blood in schizophrenia by adjusting for estimated cellular proportions.Caffeine yields aneuploidy through asymmetrical cell division caused by misalignment of chromosomes.The cryptic Y-autosome translocation in the small Indian mongoose, Herpestes auropunctatus, revealed by molecular cytogenetic approaches.Molecular cloning of t(2;7)(p24.3;p14.2), a novel chromosomal translocation in myelodysplastic syndrome-derived acute myeloid leukemia.
P50
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P50
description
hulumtues
@sq
onderzoeker
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researcher
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հետազոտող
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name
Issei Imoto
@ast
Issei Imoto
@en
Issei Imoto
@es
Issei Imoto
@nl
Issei Imoto
@sl
type
label
Issei Imoto
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Issei Imoto
@en
Issei Imoto
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Issei Imoto
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Issei Imoto
@sl
prefLabel
Issei Imoto
@ast
Issei Imoto
@en
Issei Imoto
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Issei Imoto
@nl
Issei Imoto
@sl
P106
P21
P31
P496
0000-0002-4150-7938
P569
2000-01-01T00:00:00Z