Yukio Fujiki

Q: What Schools Are Affiliated With Yukio Fujiki

Yukio Fujiki is affiliated with the following schools: Hokkaido University, Kyushu University, University of Tokyo, Rockefeller University, Nagoya University, Cornell University, University of Hyogo, Saitama University, Kyoto University

Yukio Fujiki's AcademicInfluence.com Rankings

Yukio Fujiki

Business

#710

World Rank

#781

Historical Rank

Management

#255

World Rank

#276

Historical Rank

business Degrees

Yukio Fujiki

Chemistry

#3302

World Rank

#4310

Historical Rank

Analytical Chemistry

#121

World Rank

#128

Historical Rank

Physical Chemistry

#434

World Rank

#484

Historical Rank

chemistry Degrees

Download Badge

Business
Chemistry

Yukio Fujiki's Degrees

PhD Agricultural Chemistry Hokkaido University
Masters Chemistry Kyoto University
Bachelors Chemistry Kyoto University

Why Is Yukio Fujiki Influential?

(Suggest an Edit or Addition)

(See a Problem?)

Yukio Fujiki's Published Works

Number of citations in a given year to any of this author's works

Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

Isolation of intracellular membranes by means of sodium carbonate treatment: application to endoplasmic reticulum (1982) (1625)
Biogenesis of peroxisomes. (1985) (1073)
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1 (2021) (811)
A unified nomenclature for peroxisome biogenesis factors (1996) (417)
Polypeptide and phospholipid composition of the membrane of rat liver peroxisomes: comparison with endoplasmic reticulum and mitochondrial membranes (1982) (344)
A human gene responsible for Zellweger syndrome that affects peroxisome assembly. (1992) (342)
Amino-terminal presequence of the precursor of peroxisomal 3-ketoacyl-CoA thiolase is a cleavable signal peptide for peroxisomal targeting. (1991) (286)
Restoration by a 35K membrane protein of peroxisome assembly in a peroxisome-deficient mammalian cell mutant (1991) (241)
Human PEX19: cDNA cloning by functional complementation, mutation analysis in a patient with Zellweger syndrome, and potential role in peroxisomal membrane assembly. (1999) (228)
The Mammalian Peroxin Pex5pL, the Longer Isoform of the Mobile Peroxisome Targeting Signal (PTS) Type 1 Transporter, Translocates the Pex7p·PTS2 Protein Complex into Peroxisomes via Its Initial Docking Site, Pex14p* (2000) (218)
Peroxisome Targeting Signal Type 1 (PTS1) Receptor Is Involved in Import of Both PTS1 and PTS2: Studies withPEX5-Defective CHO Cell Mutants (1998) (209)
Isolation and characterization of Chinese hamster ovary cell mutants defective in assembly of peroxisomes (1990) (208)
Peroxisomal Targeting Signal Receptor Pex5p Interacts with Cargoes and Import Machinery Components in a Spatiotemporally Differentiated Manner: Conserved Pex5p WXXXF/Y Motifs Are Critical for Matrix Protein Import (2002) (205)
Dark-inducible genes from Arabidopsis thaliana are associated with leaf senescence and repressed by sugars. (2001) (203)
Shuttling Mechanism of Peroxisome Targeting Signal Type 1 Receptor Pex5: ATP-Independent Import and ATP-Dependent Export (2005) (197)
Peroxisome targeting signal of rat liver acyl-coenzyme A oxidase resides at the carboxy terminus (1989) (193)
Synthesis of a major integral membrane polypeptide of rat liver peroxisomes on free polysomes. (1984) (184)
The pathogenic peroxin Pex26p recruits the Pex1p–Pex6p AAA ATPase complexes to peroxisomes (2003) (183)
Mutation in PEX16 is causal in the peroxisome-deficient Zellweger syndrome of complementation group D. (1998) (170)
The × Gene of Hepatitis B Virus Induced Growth Stimulation and Tumorigenic Transformation of Mouse NIH3T3 Cells (1989) (168)
An Arabidopsis Homolog of Yeast ATG6/VPS30 Is Essential for Pollen Germination1[W] (2007) (163)
Fis1, DLP1, and Pex11p coordinately regulate peroxisome morphogenesis. (2007) (148)
Multiple genes, including a member of the AAA family, are essential for degradation of unassembled subunit 2 of cytochrome c oxidase in yeast mitochondria (1995) (142)
Import of peroxisomal membrane proteins: the interplay of Pex3p- and Pex19p-mediated interactions. (2006) (141)
The peroxisomal membrane protein import receptor Pex3p is directly transported to peroxisomes by a novel Pex19p- and Pex16p-dependent pathway (2008) (136)
Disruption of the Interaction of the Longer Isoform of Pex5p, Pex5pL, with Pex7p Abolishes Peroxisome Targeting Signal Type 2 Protein Import in Mammals (2000) (120)
The peroxin pex3p initiates membrane assembly in peroxisome biogenesis. (2000) (118)
Carboxyl-terminal consensus Ser-Lys-Leu-related tripeptide of peroxisomal proteins functions in vitro as a minimal peroxisome-targeting signal. (1992) (117)
The Peroxin Pex14p (1999) (117)
Peroxisome biogenesis and peroxisome biogenesis disorders (2000) (113)
Partial disassembly of peroxisomes (1985) (113)
Characterization of the signal peptide at the amino terminus of the rat peroxisomal 3-ketoacyl-CoA thiolase precursor. (1994) (112)
Cysteine Ubiquitination of PTS1 Receptor Pex5p Regulates Pex5p Recycling (2011) (110)
Posttranslational Regulation of Fatty Acyl-CoA Reductase 1, Far1, Controls Ether Glycerophospholipid Synthesis*♦ (2010) (106)
Peroxisome biogenesis in mammalian cells (2014) (105)
Molecular Anatomy of the Peroxin Pex12p (2000) (104)
Peroxisome assembly factor–2, a putative ATPase cloned by functional complementation on a peroxisome–deficient mammalian cell mutant (1995) (103)
Mutations in PEX10 is the cause of Zellweger peroxisome deficiency syndrome of complementation group B. (1998) (103)
PEX12, the Pathogenic Gene of Group III Zellweger Syndrome: cDNA Cloning by Functional Complementation on a CHO Cell Mutant, Patient Analysis, and Characterization of Pex12p (1998) (103)
Multiple signaling pathways in gene expression during sugar starvation. Pharmacological analysis of din gene expression in suspension-cultured cells of Arabidopsis. (2000) (101)
Recruitment of the RNA Helicase RHAU to Stress Granules via a Unique RNA-binding Domain* (2008) (101)
A Novel Fluorescent Sensor Protein for Visualization of Redox States in the Cytoplasm and in Peroxisomes (2010) (100)
Human peroxisome assembly factor-2 (PAF-2): a gene responsible for group C peroxisome biogenesis disorder in humans. (1996) (98)
Human PEX1 cloned by functional complementation on a CHO cell mutant is responsible for peroxisome-deficient Zellweger syndrome of complementation group I. (1998) (96)
The membrane peroxin PEX3 induces peroxisome-ubiquitination-linked pexophagy (2014) (95)
The peroxin Pex14p is involved in LC3-dependent degradation of mammalian peroxisomes. (2008) (92)
Tail-anchored PEX26 targets peroxisomes via a PEX19-dependent and TRC40-independent class I pathway (2013) (91)
Nonsense and temperature-sensitive mutations in PEX13 are the cause of complementation group H of peroxisome biogenesis disorders. (1999) (87)
Sec16B is involved in the endoplasmic reticulum export of the peroxisomal membrane biogenesis factor peroxin 16 (Pex16) in mammalian cells (2011) (82)
Post-translational import of fatty acyl-CoA oxidase and catalase into peroxisomes of rat liver in vitro. (1985) (82)
Intracellular Localization, Function, and Dysfunction of the Peroxisome-targeting Signal Type 2 Receptor, Pex7p, in Mammalian Cells* (2002) (81)
Acyl-Coa oxidase and hydratase-dehydrogenase, two enzymes of the peroxisomal beta-oxidation system, are synthesized on free polysomes of clofibrate-treated rat liver (1984) (80)
Functional Domains and Dynamic Assembly of the Peroxin Pex14p, the Entry Site of Matrix Proteins* (2006) (79)
cDNA cloning and characterization of a constitutively expressed isoform of the human peroxin Pex11p. (1998) (78)
Identification of PEX3 as the gene mutated in a Zellweger syndrome patient lacking peroxisomal remnant structures. (2000) (77)
Animal cell mutants represent two complementation groups of peroxisome-defective Zellweger syndrome. (1992) (75)
Mutations in novel peroxin gene PEX26 that cause peroxisome-biogenesis disorders of complementation group 8 provide a genotype-phenotype correlation. (2003) (75)
PHOSPHATIDYLSERINE SYNTHASE1 is required for microspore development in Arabidopsis thaliana. (2011) (75)
BIOGENESIS OF PEROXISOMAL PROTEINS IN VIVO AND IN VITRO * (1982) (74)
In Vitro Transport of Membrane Proteins to Peroxisomes by Shuttling Receptor Pex19p* (2006) (72)
Zellwegar Syndrome: Biochemical and Morphological Studies on Two Patients Treated with Clofibrate (1985) (72)
Temperature-sensitive mutation in PEX1 moderates the phenotypes of peroxisome deficiency disorders. (1998) (71)
PEX3 is the causal gene responsible for peroxisome membrane assembly-defective Zellweger syndrome of complementation group G. (2000) (71)
A cytoplasmic AAA family peroxin, Pex1p, interacts with Pex6p. (1998) (70)
Clofibrate‐inducible, 28‐kDa peroxisomal integral membrane protein is encoded by PEX11 (1998) (70)
Ligand‐dependent nucleo‐cytoplasmic shuttling of peroxisome proliferator‐activated receptors, PPARα and PPARγ (2012) (70)
Plasmalogen homeostasis – regulation of plasmalogen biosynthesis and its physiological consequence in mammals (2017) (69)
The Membrane Biogenesis Peroxin Pex16p (2002) (68)
Isolation and characterization of mutant animal cell line defective in alkyl-dihydroxyacetonephosphate synthase: localization and transport of plasmalogens to post-Golgi compartments. (2008) (67)
Functional domain mapping of peroxin Pex19p: interaction with Pex3p is essential for function and translocation (2006) (67)
Molecular cloning and sequence of the complementary DNA encoding human mitochondrial acetoacetyl-coenzyme A thiolase and study of the variant enzymes in cultured fibroblasts from patients with 3-ketothiolase deficiency. (1990) (66)
PEX12 encodes an integral membrane protein of peroxisomes (1997) (66)
Molecular defects in genetic diseases of peroxisomes. (1997) (64)
Topogenesis of Peroxisomal Membrane Protein Requires a Short, Positively Charged Intervening-loop Sequence and Flanking Hydrophobic Segments (2001) (64)
Deficiency of a Retinal Dystrophy Protein, Acyl-CoA Binding Domain-containing 5 (ACBD5), Impairs Peroxisomal β-Oxidation of Very-long-chain Fatty Acids* (2016) (63)
Peroxisome homeostasis: Mechanisms of division and selective degradation of peroxisomes in mammals. (2016) (63)
Synthesis of 3-ketoacyl-CoA thiolase of rat liver peroxisomes on free polyribosomes as a larger precursor. Induction of thiolase mRNA activity by clofibrate. (1985) (62)
Molecular Mechanisms of Import of Peroxisome-targeting Signal Type 2 (PTS2) Proteins by PTS2 Receptor Pex7p and PTS1 Receptor Pex5pL* (2006) (61)
Dynamic and Functional Assembly of the AAA Peroxins, Pex1p and Pex6p, and Their Membrane Receptor Pex26p* (2006) (60)
Two Proteases, Trypsin Domain-containing 1 (Tysnd1) and Peroxisomal Lon Protease (PsLon), Cooperatively Regulate Fatty Acid β-Oxidation in Peroxisomal Matrix* (2011) (59)
Peroxisome division is impaired in a CHO cell mutant with an inactivating point-mutation in dynamin-like protein 1 gene. (2006) (59)
Genetic basis of peroxisome-assembly mutants of humans, Chinese hamster ovary cells, and yeast: identification of a new complementation group of peroxisome-biogenesis disorders apparently lacking peroxisomal-membrane ghosts. (1998) (59)
Hsp70 regulates the interaction between the peroxisome targeting signal type 1 (PTS1)-receptor Pex5p and PTS1. (2001) (57)
Newly Identified Chinese Hamster Ovary Cell Mutants Are Defective in Biogenesis of Peroxisomal Membrane Vesicles (Peroxisomal Ghosts), Representing a Novel Complementation Group in Mammals* (1998) (57)
Mff functions with Pex11pβ and DLP1 in peroxisomal fission (2013) (56)
Isolation and Characterization of cDNA Clones for the E1β and E2 Subunits of the Branched-chain α-Ketoacid Dehydrogenase Complex in Arabidopsis * (2000) (55)
Novel families of vacuolar amino acid transporters (2008) (55)
AWP1/ZFAND6 Functions in Pex5 Export by Interacting with Cys‐Monoubiquitinated Pex5 and Pex6 AAA ATPase (2012) (55)
The VDAC2–BAK axis regulates peroxisomal membrane permeability (2017) (54)
Topogenesis and Homeostasis of Fatty Acyl-CoA Reductase 1* (2013) (54)
Temperature-sensitive phenotypes of peroxisome-assembly processes represent the milder forms of human peroxisome-biogenesis disorders. (1998) (52)
Lessons from peroxisome-deficient Chinese hamster ovary (CHO) cell mutants. (2006) (51)
Peroxisome assembly factor 1: nonsense mutation in a peroxisome-deficient Chinese hamster ovary cell mutant and deletion analysis (1994) (48)
New splicing variants of mitochondrial Rho GTPase-1 (Miro1) transport peroxisomes (2018) (48)
Very-long-chain polyunsaturated fatty acids accumulate in phosphatidylcholine of fibroblasts from patients with Zellweger syndrome and acyl-CoA oxidase1 deficiency. (2014) (47)
Purification and Characterization, of Rice Bran Lipase II (1976) (47)
Functional heterogeneity of C-terminal peroxisome targeting signal 1 in PEX5-defective patients. (1999) (46)
Presence of the peroxisomal 22-kDa integral membrane protein in the liver of a person lacking recognizable peroxisomes (Zellweger syndrome). (1986) (46)
Molecular cloning and nucleotide sequence of cDNA encoding the entire precursor of rat mitochondrial acetoacetyl-CoA thiolase. (1989) (44)
Docosahexaenoic acid mediates peroxisomal elongation, a prerequisite for peroxisome division (2012) (43)
Distinct Modes of Ubiquitination of Peroxisome-targeting Signal Type 1 (PTS1) Receptor Pex5p Regulate PTS1 Protein Import* (2014) (42)
New insights into dynamic and functional assembly of the AAA peroxins, Pex1p and Pex6p, and their membrane receptor Pex26p in shuttling of PTS1-receptor Pex5p during peroxisome biogenesis. (2012) (42)
Peroxin Pex14p is the key component for coordinated autophagic degradation of mammalian peroxisomes by direct binding to LC3‐II (2015) (42)
cDNA cloning and characterization of the third isoform of human peroxin Pex11p. (2003) (42)
Peroxisome biogenesis disorders: molecular basis for impaired peroxisomal membrane assembly: in metabolic functions and biogenesis of peroxisomes in health and disease. (2012) (42)
Dysregulation of Plasmalogen Homeostasis Impairs Cholesterol Biosynthesis* (2015) (42)
Isolation and characterization of peroxisome-deficient Chinese hamster ovary cell mutants representing human complementation group III. (1997) (41)
Plasmalogen biosynthesis is spatiotemporally regulated by sensing plasmalogens in the inner leaflet of plasma membranes (2017) (40)
Mutations in the Peroxin Pex26p Responsible for Peroxisome Biogenesis Disorders of Complementation Group 8 Impair Its Stability, Peroxisomal Localization, and Interaction with the Pex1p·Pex6p Complex* (2006) (39)
AAA Peroxins and Their Recruiter Pex26p Modulate the Interactions of Peroxins Involved in Peroxisomal Protein Import* (2014) (39)
Peroxisome biogenesis and human peroxisome-deficiency disorders (2016) (38)
Phenotype-genotype relationships in peroxisome biogenesis disorders of PEX1-defective complementation group 1 are defined by Pex1p-Pex6p interaction. (2001) (38)
Pex11mediates peroxisomal proliferation by promoting deformation of the lipid membrane (2015) (38)
Isolation and characterization of novel peroxisome biogenesis-defective Chinese hamster ovary cell mutants using green fluorescent protein. (1999) (38)
Enzymatic Properties of Rice Bran Lipase (1973) (38)
Systematic Identification of Regulators of Oxidative Stress Reveals Non-canonical Roles for Peroxisomal Import and the Pentose Phosphate Pathway. (2020) (37)
Isolation of a new peroxisome-deficient CHO cell mutant defective in peroxisome targeting signal-1 receptor. (1997) (37)
Isolation, characterization and mutation analysis of PEX13-defective Chinese hamster ovary cell mutants. (1999) (37)
Pex5p Imports Folded Tetrameric Catalase by Interaction with Pex13p (2012) (36)
Newly identified Chinese hamster ovary cell mutants defective in peroxisome biogenesis represent two novel complementation groups in mammals. (1997) (36)
Reduction of Ether-Type Glycerophospholipids, Plasmalogens, by NF-κB Signal Leading to Microglial Activation (2017) (35)
Crystal structure of the conserved N-terminal domain of the peroxisomal matrix protein import receptor, Pex14p (2008) (34)
Genomic structure and identification of 11 novel mutations of the PEX6 (peroxisome assembly factor‐2) gene in patients with peroxisome biogenesis disorders (1999) (33)
In vitro import of peroxisome-targeting signal type 2 (PTS2) receptor Pex7p into peroxisomes. (2009) (33)
Activation of the promoters of Arabidopsis genes for the branched-chain alpha-keto acid dehydrogenase complex in transgenic tobacco BY-2 cells under sugar starvation. (2002) (32)
Topogenesis of peroxisomal proteins (1990) (32)
Response to darkness of late-responsive dark-inducible genes is positively regulated by leaf age and negatively regulated by calmodulin-antagonist-sensitive signalling in Arabidopsis thaliana. (2005) (32)
Recent insights into peroxisome biogenesis and associated diseases (2020) (32)
Defective PEX gene products correlate with the protein import, biochemical abnormalities, and phenotypic heterogeneity in peroxisome biogenesis disorders (1999) (32)
Peroxisomes control mitochondrial dynamics and the mitochondrion-dependent apoptosis pathway (2019) (31)
The peroxin Pex6p gene is impaired in peroxisomal biogenesis disorders of complementation group 6 (2001) (30)
Recruiting Mechanism of the AAA Peroxins, Pex1p and Pex6p, to Pex26p on the Peroxisomal Membrane (2011) (29)
Molecular cloning of the aminopeptidase Y gene of Saccharomyces cerevisiae. Sequence analysis and gene disruption of a new aminopeptidase. (1994) (29)
Temperature-Sensitive Mutation of PEX6 in Peroxisome Biogenesis Disorders in Complementation Group C (CG-C): Comparative Study of PEX6 and PEX1 (2000) (29)
Complementation study of peroxisome-deficient disorders by immunofluorescence staining and characterization of fused cells (1992) (28)
Post-translational import of 3-ketoacyl-CoA thiolase into rat liver peroxisomes in vitro. (1994) (27)
Induction, identification, and cell-free translation of mRNAs coding for peroxisomal proteins in Candida tropicalis. (1986) (27)
Newly identified Chinese hamster ovary cell mutants defective in peroxisome assembly represent complementation group A of human peroxisome biogenesis disorders and one novel group in mammals. (1999) (27)
Dynamic and functional assembly of the AAA peroxins, Pex1p and Pex6p, and their membrane receptor Pex26p involved in shuttling of the PTS1 receptor Pex5p in peroxisome biogenesis. (2008) (27)
A novel aberrant splicing mutation of the PEX16 gene in two patients with Zellweger syndrome. (2002) (26)
Studies on the disulfide bonds in human pituitary follicle-stimulating hormone. (1980) (26)
Onsite GTP fuelling via DYNAMO1 drives division of mitochondria and peroxisomes (2018) (24)
Assembly of Peroxisomal Membrane Proteins via the Direct Pex19p‐Pex3p Pathway (2016) (24)
Molecular mechanism of detectable catalase-containing particles, peroxisomes, in fibroblasts from a PEX2-defective patient. (2000) (24)
Photoassimilation, Assimilate Translocation and Plasmodesmal Biogenesis in the Source Leaves of Arabidopsis thaliana Grown Under an Increased Atmospheric CO2 Concentration (2014) (23)
Peroxisome biogenesis disorders: identification of a new complementation group distinct from peroxisome-deficient CHO mutants and not complemented by human PEX 13. (1998) (23)
Amino acid sequence of the beta-subunit of the follicle-stimulating hormone from equine pituitary glands. (1978) (23)
Parkin‐mediated ubiquitylation redistributes MITOL/March5 from mitochondria to peroxisomes (2019) (23)
Transmembrane topology of the peroxin, Pex2p, an essential component for the peroxisome assembly. (1999) (22)
Defective lipid remodeling of GPI anchors in peroxisomal disorders, Zellweger syndrome, and rhizomelic chondrodysplasia punctata (2012) (22)
Overexpression of human acyl-CoA thioesterase upregulates peroxisome biogenesis. (2004) (22)
Functional identification of AtAVT3, a family of vacuolar amino acid transporters, in Arabidopsis (2017) (20)
Cloning of cDNA coding for peroxisomal acyl-CoA oxidase from the yeast Candida tropicalis pK233. (1985) (20)
Mitochondrial phosphatidylethanolamine level modulates Cyt c oxidase activity to maintain respiration capacity in Arabidopsis thaliana rosette leaves. (2013) (20)
Restoration of biochemical function of the peroxisome in the temperature-sensitive mild forms of peroxisome biogenesis disorder in humans (2000) (20)
Isolation and amino acid sequence of the alpha-subunit of follicle-stimulating hormone from equine pituitary glands. (1978) (20)
Effect of spermidine on N-formylmethionyl-tRNA binding to 30S ribosomal subunits and on N-formylmethionyl-tRNA dependent polypeptide synthesis. (1978) (18)
Characterization of the Interaction between Recombinant Human Peroxin Pex3p and Pex19p (2008) (18)
Identification of beta-oxidation enzymes among peroxisomal polypeptides. Increase in Coomassie blue-stainable protein after clofibrate treatment. (1982) (18)
Pex5p stabilizes Pex14p: a study using a newly isolated pex5 CHO cell mutant, ZPEG101. (2013) (16)
The peroxisome counteracts oxidative stresses by suppressing catalase import via Pex14 phosphorylation (2020) (15)
Biogenesis of Nonspecific Lipid Transfer Protein and Sterol Carrier Protein x (2001) (15)
Peroxisome biogenesis deficiency attenuates the BDNF-TrkB pathway-mediated development of the cerebellum (2018) (15)
Assignment of the human peroxisome assembly factor-1 gene (PXMP3) responsible for Zellweger syndrome to chromosome 8q21.1 by fluorescence in situ hybridization. (1994) (15)
A novel mutation, R125X in peroxisome assembly factor‐1 responsible for zellweger syndrome (1998) (14)
Genetic and molecular bases of peroxisome biogenesis disorders (2001) (14)
Characterization of Minor Subunit of Rice Bran Lipase (1978) (14)
Chemical Properties of Major Subunit of Rice Bran Lipase (1978) (14)
Mitotic phosphorylation of Pex14p regulates peroxisomal import machinery (2020) (13)
Nuclear transport of peroxisome-proliferator activated receptor α. (2011) (13)
Peroxisome: Metabolic Functions and Biogenesis. (2020) (13)
BAK regulates catalase release from peroxisomes (2017) (13)
Accumulation of glycolipids in mutant Chinese hamster ovary cells (Z65) with defective peroxisomal assembly and comparison of the metabolic rate of glycosphingolipids between Z65 cells and wild-type CHO-K1 cells. (1999) (13)
CUL4A-DDB1-Rbx1 E3 ligase controls the quality of the PTS2 receptor Pex7p. (2014) (12)
Impaired plasmalogen synthesis dysregulates liver X receptor-dependent transcription in cerebellum. (2019) (12)
Localization of Protein Kinase NDR2 to Peroxisomes and Its Role in Ciliogenesis* (2017) (12)
Correction by Gene Expression of Biochemical Abnormalities in Fibroblasts from Zellweger Patients (1996) (12)
A New Paradigm in Catalase Research. (2021) (12)
Isolation and characterization of novel phenotype CHO cell mutants defective in peroxisome assembly, using ICR191 as a potent mutagenic agent (2008) (11)
Isolation of cDNA clones coding for peroxisomal proteins of Candida tropicalis: identification and sequence of a clone for catalase. (1987) (11)
A novel pex2 mutant: catalase-deficient but temperature-sensitive PTS1 and PTS2 import. (2002) (11)
Defining the dynamin-based ring organizing center on the peroxisome-dividing machinery isolated from Cyanidioschyzon merolae (2017) (11)
Peroxisome counteracts oxidative stresses by suppressing catalase import via Pex14 phosphorylation (2020) (11)
Isolation and characterization of cDNA clones for the e1beta and E2 subunits of the branched-chain alpha-ketoacid dehydrogenase complex in Arabidopsis. (2000) (10)
A newly identified mutation in the PEX26 gene is associated with a milder form of Zellweger spectrum disorder (2018) (10)
A glucan having reticuloendothelial system-potentiating and anti-complementary activities from the tuber of Pinellia ternata. (1994) (9)
Distinct Functions of Acyl/Alkyl Dihydroxyacetonephosphate Reductase in Peroxisomes and Endoplasmic Reticulum (2020) (9)
Heating RNA before cell-free translation is essential for the efficient and reproducible synthesis of several peroxisomal proteins. (1984) (9)
Isolation of Chinese hamster ovary cell pex mutants: two PEX7-defective mutants. (2002) (9)
Molecular Basis of Mitochondrial and Peroxisomal Division Machineries (2020) (9)
Mild reduction of plasmalogens causes rhizomelic chondrodysplasia punctata: functional characterization of a novel mutation (2014) (8)
- 1-Dynamic and Functional Assembly of the AAA Peroxins , Pex 1 p and Pex 6 p , and Their Membrane Receptor Pex 26 p (2006) (8)
Studies on the unique presence of an N-acetylgalactosamine residue in the carbohydrate moieties of human follicle-stimulating hormone. (1982) (8)
Interaction defect of the medium isoform of PTS1-receptor Pex5p with PTS2-receptor Pex7p abrogates the PTS2 protein import into peroxisomes in mammals. (2011) (7)
Peroxisome biogenesis and molecular defects in peroxisome assembly disorders (2007) (7)
Approaches to Studies on Peroxisome Biogenesis and Human Peroxisome‐deficient Disorders (1996) (7)
Import of a 22-kDa Peroxisomal Integral Membrane Protein into Peroxisomes in Vitro (1989) (7)
Biogenesis of Peroxisomes in Rat Liver and Candida Tropicalis (1987) (6)
System to quantify the import of peroxisomal matrix proteins by fluorescence intensity (2013) (6)
A peroxisome deficiency–induced reductive cytosol state up-regulates the brain-derived neurotrophic factor pathway (2020) (6)
Mislocalization and inhibition of acetyl-CoA carboxylase 1 by a synthetic small molecule. (2012) (6)
Molecular cloning of cDNA for human mitochondrial acetoacetyl-CoA thiolase and molecular analysis of 3-ketothiolase deficiency (1990) (6)
Alterations in the molecular species of plasmalogen phospholipids and glycolipids due to peroxisomal dysfunction in Chinese hamster ovary-mutant Z65 cells by FABMS method. (2007) (6)
Monomer-dimer transition of the conserved N-terminal domain of the mammalian peroxisomal matrix protein import receptor, Pex14p. (2010) (6)
Dynamics of the nucleoside diphosphate kinase protein DYNAMO2 correlates with the changes in the global GTP level during the cell cycle of Cyanidioschyzon merolae (2019) (5)
Epigenetic floral homeotic mutation in pD991-AP3-derived T-DNA-tagged lines for CTP:Phosphorylcholine cytidylyltransferase (CCT) Genes: The homeotic mutation of the cct1-1 allele is enhanced by the cct2 allele and alleviated by CCT1 overexpression (2015) (5)
Mammalian Homologue NME3 of DYNAMO1 Regulates Peroxisome Division (2020) (5)
3-Ketothiolase deficiency: molecular heterogeneity of the enzyme defect and cloning of the cDNA. (1990) (4)
The cytosolic peroxisome-targeting signal (PTS)-receptors, Pex7p and Pex5pL, are sufficient to transport PTS2 proteins to peroxisomes. (2019) (4)
Molecular cloning of Chinese hamster ceramide glucosyltransferase and its enhanced expression in peroxisome-defective mutant Z65 cells. (2002) (4)
A peroxisome deficiency-induced reductive cytosol state up-regulates the brain-derived neurotrophic factor pathway. (2020) (4)
DARK-INDUCED EXPRESSION OF GENES FOR BRANCHED-CHAIN α-KETO ACID DEHYDROGENASE IN Arabidopsis LEAVES. (1996) (4)
Peroxisome Biogenesis Disorders. (2006) (4)
Experimental Systems to Study Yeast Pexophagy. (2017) (4)
ATP8B2-Mediated Asymmetric Distribution of Plasmalogens Regulates Plasmalogen Homeostasis and Plays a Role in Intracellular Signaling (2022) (4)
[Biogenesis of peroxisome--targeting signal and peroxisome assembly factor]. (1992) (3)
Pex 5 p stabilizes Pex 14 p : a study using a newly isolated pex 5 CHO cell mutant , ZPEG 101 (2012) (3)
- 1In Vitro Transport of Membrane Proteins to Peroxisomes by Shuttling Receptor Pex 19 p (2005) (3)
Simplified determination of volatile organic compounds in water samples using active carbon. (1995) (2)
Identification of a Homozygous PEX26 Mutation in a Heimler Syndrome Patient (2021) (2)
Peroxisome Deficiency Impairs BDNF Signaling and Memory (2020) (2)
A newly isolated Pex7‐binding, atypical PTS2 protein P7BP2 is a novel dynein‐type AAA+ protein (2018) (2)
Molecular Complex Coordinating Peroxisome Morphogenesis in Mammalian Cells (2014) (2)
Peroxisomal Membrane and Matrix Protein Import Using a Semi-Intact Mammalian Cell System. (2017) (2)
[Peroxisome biogenesis and human disorders]. (2003) (2)
A Mouse Model System to Study Peroxisomal Roles in Neurodegeneration of Peroxisome Biogenesis Disorders. (2020) (2)
A temperature-sensitive CHO pex1 mutant with a novel mutation in the AAA Walker A1 motif. (2006) (2)
Plasmalogen mediates integration of adherens junction. (2019) (2)
Cell Death or Survival Against Oxidative Stress. (2018) (2)
Molecular Basis for Peroxisome Biogenesis Disorders (2014) (2)
Assessing Pexophagy in Mammalian Cells. (2017) (2)
Mild reduction of plasmalogens causes rhizomelic chondrodysplasia punctata: functional characterization of a novel mutation (2014) (1)
Erratum to Pex5p Imports Folded Tetrameric Catalase by Interaction with Pex13p. [Traffic 13, (2012), 1364-1377], DOI:10.1111/tra.12010 (2012) (1)
Peroxisome biogenesis: a novel inducible PEX19 splicing variant is involved in early stages of peroxisome proliferation (2017) (1)
Identification of Peroxisomal Protein Complexes with PTS Receptors, Pex5 and Pex7, in Mammalian Cells. (2018) (1)
Genetic defects in peroxisome morphogenesis (Pex11β, DLP1 , and NME3 ) affect DHA ‐phospholipid metabolism (2022) (1)
[Peroxisome biogenesis and human disorders]. (2003) (1)
De novo formation and maintenance of mammalian peroxisomes in the absence of PEX16. (2022) (1)
Origin and spatiotemporal dynamics of the peroxisomal endomembrane system (2014) (1)
Analysis of Plasmalogen Synthesis in Cultured Cells. (2017) (1)
Genetic defects in peroxisome morphogenesis (Pex11β, dynamin‐like protein 1, and nucleoside diphosphate kinase 3) affect docosahexaenoic acid‐phospholipid metabolism (2022) (1)
Blue Native PAGE: Applications to Study Peroxisome Biogenesis. (2017) (1)
[Human peroxisome-deficient disorders and pathogenic gene]. (1994) (1)
AAA+ proteins. Editorial. (2012) (1)
Genetic disruption of CRC 12S globulin increases seed oil content and seed yield in Arabidopsis thaliana (2013) (1)
Plasmalogen synthesis is spatiotemporally regulated by sensing plasmalogens in the inner leaflet of plasma membrane (2016) (0)
[Molecular biology of peroxisome biogenesis]. (1993) (0)
Peroxisomes control mitochondrial dynamics and the mitochondrion-dependent pathway of apoptosis (2018) (0)
Novel regulation systems maintaining peroxisomal functions and transport (2017) (0)
Peroxisomal topogenic signals and the etiology of peroxisome-deficient disease (1996) (0)
Cloning of cDNA coding for peroxisomal acyl-CoA oxidase from the yeast Candida tropicalis pK 233 ( transcriptional regulation / expression of «-oxidation enzyme activity / organelle biogenesis / mRNA size ) (2003) (0)
Homeostasis of Plasmalogens in Mammals (2019) (0)
SENESCENCE-ASSOCIATED EXPRESSION OF DIN GENES IS REGULATED BY SUGAR LEVELS IN Arabidopsis (1998) (0)
Regulation of dark-inducible genes in Arabidopsis (2001) (0)
2SA2-03 Peroxisome Biogenesis : Mechanistic insights into the import of matrix and membrane proteins(2SA2 Research frontiers of protein transport across the membrane,The 47th Annual Meeting of the Biophysical Society of Japan) (2009) (0)
Erratum (2012) (0)
[Import of newly synthesized proteins to peroxisomes]. (1992) (0)
Mis-localization and inhibition of ACC1 by a synthetic small molecule. (2012) (0)
Protein Import into Peroxisomes: The Principles and Methods of Studying (2015) (0)
Dataset for: Plasmalogen homeostasis: regulation of plasmalogen biosynthesis and its physiological consequence in mammals (2017) (0)
Molecular basis of local energy generation during mitochondrial and peroxisomal division (2020) (0)
Peroxisome assembly and peroxisome biogenesis disorders (2002) (0)
A newly identified mutation in the PEX26 gene is associated with a distinctly milder form of Zellweger spectrum disorder (2019) (0)
ISOLATION AND CHARACTERIZATION OF A PHOSPHOMANNOSE ISOMERASE cDNA CLONE FROM Arabidopsis (2000) (0)
Generation of Peroxisome-Deficient Somatic Animal Cell Mutants. (2017) (0)
Peroxisomal matrix protein import: Identification of core components of membrane translocator (2017) (0)
Fukumoto and Yukio Fujiki Masanori Honsho , Shunsuke Asaoku , Keiko Acyl-CoA Reductase 1 Topogenesis and Homeostasis of Fatty Lipids (2013) (0)
Peroxisome homeostasis, dysfunctions and disorders (2017) (0)
[Biogenesis of peroxisomes and human peroxisomal disorders]. (1995) (0)
Peroxisome enzyme group and its biosynthetic mechanism. (1986) (0)
PEX 5 , and the affinity of LC 3-II for PEX 14 increases upon cell starvation (2014) (0)
Purification and characterization of protease M, a yeast mitochondrial nucleotide-stimulated metal protease: Its identification as CYM1 gene product, a mitochondrial presequence peptidase. (2022) (0)
Analysis of ultrastructure and molecular mechanism of the mitochondrion and peroxisome dividing machineries (2015) (0)
Onsite GTP fuelling via DYNAMO1 drives division of mitochondria and peroxisomes (2018) (0)
DARK-INDUCED EXPRESSION OF GENES FOR BRANCHED-CHAIN α-KETO ACID DEHYDROGENASE IS REGULATED BY SUGAR LEVEL IN Arabidopsis LEAVES (1997) (0)
Molecular Structure of a Peroxisomal Matrix Protein Transport Factor, Pex14p (2009) (0)
Regulation of plasmalogen biosynthesis in mammalian cells and tissues (2023) (0)
Peroxisome biogenesis deficiency in astrocytes causes aberrant axonal morphology (2016) (0)
Malformation of cerebellum in PEX14 -defecitve mouse (2017) (0)
In Vitro PMP Import Analysis Using Cell-Free Synthesized PMP and Isolated Peroxisomes. (2017) (0)
Analysis of Peroxisome Biogenesis by Phos-Tag SDS-PAGE. (2023) (0)
Peroxisome Biogenesis and Its Dysfunction (2008) (0)
ROLES OF ARABIDOPSIS ATG6/VPS30 IN AUTOPHAGY AND POLLEN GERMINATION (2006) (0)
PROMOTERS OF din GENES OF Arabidopsis ARE REGULATED BY SUGAR LEVEL (1999) (0)
Yukio Fujiki Masanori Honsho , Shunsuke Asaoku and Ether Glycerophospholipid Synthesis Acyl-CoA Reductase 1 , Far 1 , Controls Posttranslational Regulation of Fatty Lipids (2010) (0)
Alterations in ether lipid metabolism and the consequences for the mouse lipidome. (2023) (0)
[Peroxisome biogenesis and human peroxisomal disorders]. (2000) (0)
ペキソファジー：ペルオキシソームの機能・形成と分解 (2017) (0)
Molecular insights into peroxisome homeostasis and peroxisome biogenesis disorders. (2022) (0)
REPAIRED PEROXISOME ASSEMBLY: THE FUTURE BEGINS NOW (1993) (0)
[Biogenesis of peroxisomes: analyses at molecular and cellular levels]. (1990) (0)
Genetic basis of peroxisomes-assembly mutants of humans, Chinese hamster ovary cells, and yeast: identification of a new complementation group of peroxisome-biogenesis disorders apparently lacking peroxisomal-membrane ghosts (letter) (1998) (0)
Indentification of β‐oxidation enzymes among peroxisomal polypeptides (2001) (0)
Medicament anti-vih (1992) (0)
SUGAR REGULATION OF PROMOTER ACTIVITY OF THE GENES FOR TWO SUBUNITS OF BRANCHED-CHAIN α-KETO ACID DEHYDROGENASE (2000) (0)
Peroxisomal matrix protein transport requires a series of constitutional changes of Pex14p homo-oligomers. (2016) (0)
Author response: The peroxisome counteracts oxidative stresses by suppressing catalase import via Pex14 phosphorylation (2020) (0)
Fujiki Masanori Honsho , Yuichi Abe and Yukio impairs cholesterol biosynthesis Dysregulation of plasmalogen homeostasis (2015) (0)

This paper list is powered by the following services:

What Schools Are Affiliated With Yukio Fujiki?

Yukio Fujiki is affiliated with the following schools:

Yukio Fujiki's Academic­Influence.com Rankings

Yukio Fujiki's Degrees

Why Is Yukio Fujiki Influential?

Yukio Fujiki's Published Works

Published Works

What Schools Are Affiliated With Yukio Fujiki?

Yukio Fujiki's AcademicInfluence.com Rankings