R. Funayama

PROFILE

Homepage
No homepage is listed.
ORCID
No ORCID is listed.
Affiliations
No affiliations are listed.
Aliases
R. Funayama, Ryoichi Funayama, Ryo Funayama
Publication record
96 papers · 5,691 citations · H-index 35

PAPERS

Metabolic cell death of labile iron deficiency as a vulnerability of head and neck squamous cell carcinoma evaded by BACH1
20250 citationsauthor #11
Alternative Splicing of FBLN2 Generates a Prometastatic Extracellular Matrix in Gastrointestinal Cancers by Determining N‐Glycosylation of Fibulin 2
20251 citationsauthor #1
Downregulation of ABCC3 activates MAPK signaling through accumulation of deoxycholic acid in colorectal cancer cells
20249 citationsauthor #4
Updated Genetic Analysis of Japanese Familial ALS Patients Carrying SOD1 Variants Revealed Phenotypic Differences for Common Variants
20242 citationsauthor #7
Calreticulin exposure induced by anticancer drugs is associated with the p53 signaling pathway in colorectal cancer cells.
20241 citationsauthor #6
BACH1 inhibits senescence, obesity, and short lifespan by ferroptotic FGF21 secretion.
202411 citationsauthor #10
Accelerated plasma-cell differentiation in Bach2-deficient mouse B cells is caused by altered IRF4 functions
20249 citationsauthor #5
Abstract 1479: ABCC3 (MRP3)-mediated export of deoxycholic acid regulates MAPK signaling in colorectal adenoma and adenocarcinoma
20241 citationsauthor #4
Genomic adaptive potential to cold environments in the invasive red swamp crayfish
202317 citationsauthor #4
Collagen XVII regulates tumor growth in pancreatic cancer through interaction with the tumor microenvironment
202310 citationsauthor #2
Nuclear pore pathology underlying multisystem proteinopathy type 3‐related inclusion body myopathy
20231 citationsauthor #6
Neonatal developmental and epileptic encephalopathy with movement disorders and arthrogryposis: A case report with a novel missense variant of SCN1A.
20232 citationsauthor #11
A novel variant in the transmembrane 4 domain of ANO3 identified in a two-year-old girl with developmental delay and tremor
20222 citationsauthor #7
High levels of chromosomal instability facilitate the tumor growth and sphere formation
20227 citationsauthor #3
Phenotypic heterogeneity in individuals with MECOM variants in 2 families
202213 citationsauthor #7
Heterozygous calcyclin-binding protein/Siah1-interacting protein (CACYBP/SIP) gene pathogenic variant linked to a dominant family with paucity of interlobular bile duct
20220 citationsauthor #12
Novel POLE mutations identified in patients with IMAGE-I syndrome cause aberrant subcellular localisation and protein degradation in the nucleus
20224 citationsauthor #8
Sex-Specific Differences in the Transcriptome of the Human Dorsolateral Prefrontal Cortex in Schizophrenia
202211 citationsauthor #3
Wnt5a in cancer-associated fibroblasts promotes colorectal cancer progression.
202129 citationsauthor #9
Alternative microexon splicing by RBFOX2 and PTBP1 is associated with metastasis in colorectal cancer
202124 citationsauthor #2
Reduced PHOX2B stability causes axonal growth impairment in motor neurons with TARDBP mutations
20219 citationsauthor #7
A novel deletion in the C-terminal region of HSPB8 in a family with rimmed vacuolar myopathy
202111 citationsauthor #9
Inhibition of S-Adenosylmethionine Synthesis Promotes Erythropoiesis Via Epigenetic Modifications
20210 citationsauthor #7
Theme 05 - HUMAN CELL BIOLOGY AND PATHOLOGY (including iPSC studies)
20210 citationsauthor #7
The Autism-Related Protein SETD5 Controls Neural Cell Proliferation through Epigenetic Regulation of rDNA Expression
202026 citationsauthor #8
Variants That Affect Function of Calcium Channel TRPV6 Are Associated With Early-onset Chronic Pancreatitis: TRPV6 and pancreatitis.
202091 citationsauthor #11
Chromatin Protein PC4 Orchestrates B Cell Differentiation by Collaborating with IKAROS and IRF4.
202022 citationsauthor #9
Correction: Biallelic GALM pathogenic variants cause a novel type of galactosemia
20202 citationsauthor #16
BACH1 promotes pancreatic cancer metastasis by repressing epithelial genes and enhancing epithelial-mesenchymal transition.
202086 citationsauthor #10
Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice
202034 citationsauthor #12
Germline-Activating RRAS2 Mutations Cause Noonan Syndrome.
201949 citationsauthor #10
Biallelic variants/mutations of IL1RAP in patients with steroid-sensitive nephrotic syndrome.
20194 citationsauthor #12
Detection of NRAS mutation in cell-free DNA biological fluids from patients with kaposiform lymphangiomatosis
201957 citationsauthor #9
Aberrant axon branching via Fos-B dysregulation in FUS-ALS motor neurons
201955 citationsauthor #7
Recurrent de novo MAPK8IP3 variants cause neurological phenotypes
201938 citationsauthor #14
Cancer‐associated fibroblasts secrete Wnt2 to promote cancer progression in colorectal cancer
201972 citationsauthor #3
This information is current as Inhibitors Represses Cyclin-Dependent Kinase Proliferation of B Lymphocytes and Induced − Bach 2 Promotes B Cell Receptor Matsumoto
20180 citationsauthor #7
Bach2 Promotes B Cell Receptor–Induced Proliferation of B Lymphocytes and Represses Cyclin-Dependent Kinase Inhibitors
201829 citationsauthor #7
Zinc finger-IRF composite elements bound by Ikaros/IRF4 complexes function as gene repression in plasma cell.
201844 citationsauthor #7
Mutations in six nephrosis genes delineate a pathogenic pathway amenable to treatment
2018113 citationsauthor #38
Novel IARS2 mutations in Japanese siblings with CAGSSS, Leigh, and West syndrome.
201820 citationsauthor #5
Biallelic GALM pathogenic variants cause a novel type of galactosemia
201847 citationsauthor #16
Genomic analysis identifies masqueraders of full‐term cerebral palsy
201890 citationsauthor #16
Rett-like features and cortical visual impairment in a Japanese patient with HECW2 mutation.
201811 citationsauthor #8
Bone marrow PDGFR&agr;+Sca-1+-enriched mesenchymal stem cells support survival of and antibody production by plasma cells in vitro through IL-6
201814 citationsauthor #5
Inferring evolutionary responses of Anolis carolinensis introduced into the Ogasawara archipelago using whole genome sequence data
20170 citationsauthor #6
Dramatic response after functional hemispherectomy in a patient with epileptic encephalopathy carrying a de novo COL4A1 mutation.
201711 citationsauthor #14
A Bach2-Cebp Gene Regulatory Network for the Commitment of Multipotent Hematopoietic Progenitors.
201753 citationsauthor #9
Transforming Growth Factor β-Induced Proliferative Arrest Mediated by TRIM26-Dependent TAF7 Degradation and Its Antagonism by MYC
201713 citationsauthor #5
Inflammatory responses induce an identity crisis of alveolar macrophages, leading to pulmonary alveolar proteinosis
201714 citationsauthor #7
Inferring evolutionary responses of Anolis carolinensis introduced into the Ogasawara archipelago using whole genome sequence data
201710 citationsauthor #6
Protein‐arginine deiminase 2 suppresses proliferation of colon cancer cells through protein citrullination
201735 citationsauthor #1
Regulatory signatures of liver regeneration distilled by integrative analysis of mRNA, histone methylation, and proteomics
201718 citationsauthor #7
The double knockout of Bach1 and Bach2 in mice reveals shared compensatory mechanisms in regulating alveolar macrophage function and lung surfactant homeostasis.
201622 citationsauthor #5
Mutations in MECOM, encoding oncoprotein EVI1, cause amegakaryocytic thrombocytopenia with radioulnar synostosis, an inherited bone marrow failure syndrome
20161 citationsauthor #10
Genomewide approaches for BACH1 target genes in mouse embryonic fibroblasts showed BACH1‐Pparg pathway in adipogenesis
201628 citationsauthor #5
The aryl hydrocarbon receptor AhR links atopic dermatitis and air pollution via induction of the neurotrophic factor artemin
2016249 citationsauthor #5
Lack of Transcription Triggers H3K27me3 Accumulation in the Gene Body.
201671 citationsauthor #2
A large-scale targeted proteomics assay resource based on an in vitro human proteome
201681 citationsauthor #14
Nrf2 suppresses macrophage inflammatory response by blocking proinflammatory cytokine transcription
20161,585 citationsauthor #3
Wnt‐β‐catenin signaling regulates ABCC3 (MRP3) transporter expression in colorectal cancer
201637 citationsauthor #2
Human genetic variation database, a reference database of genetic variations in the Japanese population
2016283 citationsauthor #20
A Homeostatic Shift Facilitates Endoplasmic Reticulum Proteostasis through Transcriptional Integration of Proteostatic Stress Response Pathways
201656 citationsauthor #4
Lack of genetic variation prevents adaptation at the geographic range margin in a damselfly
201648 citationsauthor #4
Next generation sequencing might become the new strategy to identify the candidate genes for pancreatitis
20160 citationsauthor #6
Role of a protein-citrullinating enzyme PADI2 in colon cancer
20160 citationsauthor #1
Reactivation of cell proliferation by continuous TGF-β treatment
20160 citationsauthor #3
Genomic analysis identifies candidate pathogenic variants in 9 of 18 patients with unexplained West syndrome
201566 citationsauthor #13
Isolated inclusion body myopathy caused by a multisystem proteinopathy–linked hnRNPA1 mutation
201535 citationsauthor #9
Genomic analysis identifies candidate pathogenic variants in 9 of 18 patients with unexplained West syndrome
20150 citationsauthor #13
Mutations in MECOM, Encoding Oncoprotein EVI1, Cause Radioulnar Synostosis with Amegakaryocytic Thrombocytopenia.
2015114 citationsauthor #9
Mutations in PIGL in a patient with Mabry syndrome
201533 citationsauthor #8
The artificial loss of Runx1 reduces the expression of quiescence-associated transcription factors in CD4(+) T lymphocytes.
201511 citationsauthor #4
GNE myopathy associated with congenital thrombocytopenia: a report of two siblings.
201462 citationsauthor #15
TBX1 Mutation Identified by Exome Sequencing in a Japanese Family with 22q11.2 Deletion Syndrome-Like Craniofacial Features and Hypocalcemia
201453 citationsauthor #6
Identification of acquired mutations by whole-genome sequencing in GATA-2 deficiency evolving into myelodysplasia and acute leukemia
201421 citationsauthor #3
HCV Infection Enhances Th17 Commitment, Which Could Affect the Pathogenesis of Autoimmune Diseases
201422 citationsauthor #5
RNA sequencing-based identification of aberrant imprinting in cloned mice.
201460 citationsauthor #8
Gain-of-function mutations in RIT1 cause Noonan syndrome, a RAS/MAPK pathway syndrome.
2013302 citationsauthor #19
Exome sequencing identifies a novel TTN mutation in a family with hereditary myopathy with early respiratory failure
201340 citationsauthor #10
Bach1 is critical for the transformation of mouse embryonic fibroblasts by RasV12 and maintains ERK signaling
201321 citationsauthor #5
Y Chromosome–Linked B and NK Cell Deficiency in Mice
201321 citationsauthor #8
Distinct MicroRNAs Expression Profile in Primary Biliary Cirrhosis and Evaluation of miR 505-3p and miR197-3p as Novel Biomarkers
201389 citationsauthor #3
Ras-Induced Changes in H3K27me3 Occur after Those in Transcriptional Activity
201345 citationsauthor #2
Runx1 Deficiency in CD4+ T Cells Causes Fatal Autoimmune Inflammatory Lung Disease Due to Spontaneous Hyperactivation of Cells
201257 citationsauthor #13
Nrf2–MafG heterodimers contribute globally to antioxidant and metabolic networks
2012399 citationsauthor #3
Re-investigation and RNA sequencing-based identification of genes with placenta-specific imprinted expression.
2012118 citationsauthor #4
Use of Illumina Deep Sequencing Technology To Differentiate Hepatitis C Virus Variants
201149 citationsauthor #3
A Canadian diplomat and arguments on the constitution of Japan
20090 citationsauthor #3
[Tumor-suppressing role of cellular senescence and chromatin structure].
20073 citationsauthor #1
Cellular senescence and chromatin structure
2007150 citationsauthor #1
Expression of Cell Cycle Molecules in Primate Corneal Endothelial Cells and Primate Cultivated Corneal Endothelial Cells
20070 citationsauthor #5
Loss of linker histone H1 in cellular senescence
2006233 citationsauthor #1
A History of Criticism of For Whom the Bell Tolls by E. Hemingway (1)
19971 citationsauthor #1
A Criticism of Terry Eagleton's Critique on Jude the Obscure
19950 citationsauthor #1
On S. T. Coleridge's Theory of Imagination : in relation to Kant
19840 citationsauthor #1

TIMELINE

1984 0 citations

1995 0 citations

1997 1 citations

2006 233 citations

2007 153 citations

2009 0 citations

2011 49 citations

2012 574 citations

2013 518 citations

2014 218 citations

2015 259 citations

2016 2,461 citations

2017 154 citations

2018 368 citations

2019 275 citations

2020 261 citations

2021 73 citations

2022 37 citations

2023 30 citations

2024 33 citations

2025 1 citations

COAUTHOR MAP

CONCEPT FOOTPRINT