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1 al membrane proteins, which are required for peroxisome biogenesis.
2 pastoris is characterized by a deficiency in peroxisome biogenesis.
3 or, one of at least 15 peroxins required for peroxisome biogenesis.
4 t PpPas2p is involved in the early stages of peroxisome biogenesis.
5          Our data show that VPS13D regulates peroxisome biogenesis.
6 MARCH5 is central for mitochondria-dependent peroxisome biogenesis.
7 nd plasmalogens, the ER also plays a role in peroxisome biogenesis.
8  chloroplast biogenesis, SP1 plays a role in peroxisome biogenesis.
9  two AAA-ATPases that play a crucial role in peroxisome biogenesis.
10 of Pex1/Pex6 and dynamin-related proteins in peroxisome biogenesis.
11 n are induced in oleate and coordinated with peroxisome biogenesis.
12 f the phosphoprotein ScPex11p coincides with peroxisome biogenesis.
13 ction, YCL056c, and Pex proteins involved in peroxisome biogenesis.
14 at indicate a defect in lipid metabolism and peroxisome biogenesis.
15 eins in addition to their canonical roles in peroxisome biogenesis.
16 tion is independent of its role at the ER in peroxisome biogenesis.
17 n of genes required for lipid metabolism and peroxisome biogenesis.
18 the requirements of early and late events of peroxisome biogenesis.
19 r peroxisome-induction conditions, impairing peroxisome biogenesis.
20 enetically defined as proteins necessary for peroxisome biogenesis.
21 ional assays to identify genes with roles in peroxisome biogenesis.
22 g peroxisomal proteins and genes involved in peroxisome biogenesis.
23 61-related gene, SSH1, also has no effect on peroxisome biogenesis.
24 hat loss of Sec61p activity has no effect on peroxisome biogenesis.
25  respiratory deficiency dramatically induces peroxisome biogenesis.
26 more than 20 PEX genes that are required for peroxisome biogenesis.
27 roxisomes and does not inhibit PEX3-mediated peroxisome biogenesis.
28 PBD cell lines are shaping current models of peroxisome biogenesis.
29  a peroxisomal protein (peroxin) involved in peroxisome biogenesis.
30 l enzyme abnormalities as well as defects of peroxisome biogenesis.
31 hat Pex4p and Pex22p act at the same step in peroxisome biogenesis.
32 g that Pex19p functions at an early stage of peroxisome biogenesis.
33 vel and implies a role for these vesicles in peroxisome biogenesis.
34 f genes required for glycerol metabolism and peroxisome biogenesis.
35 ythms were aligned with 12-h oscillations in peroxisome biogenesis and activity, reactive oxygen spec
36 in growth on fatty acids, one is involved in peroxisome biogenesis and at least two are required for
37 drome, and with car1, a protein required for peroxisome biogenesis and caryogamy in the filamentous f
38     This review highlights the links between peroxisome biogenesis and degradation, incorporating an
39 ganelles has implications for all aspects of peroxisome biogenesis and function and may help address
40 ion of the PEX12 transcript exhibit impaired peroxisome biogenesis and function, inhibition of plant
41  Both are implicated in genetic disorders of peroxisome biogenesis and function.
42  glycerol metabolism, and genes required for peroxisome biogenesis and function.
43      This study reports a novel mechanism of peroxisome biogenesis and metabolic regulation via TGF-b
44   In this review we focus on the genetics of peroxisome biogenesis and on how defects in this process
45  disorder characterized by severe defects in peroxisome biogenesis and peroxisomal protein import.
46 anding of players and mechanisms involved in peroxisome biogenesis and peroxisome degradation, very f
47 e show that removal of VAPA and VAPB impairs peroxisome biogenesis and PKC regulation.
48 psis thaliana) PEX12 protein is required for peroxisome biogenesis and plays an essential role throug
49 nd energy metabolism, while also influencing peroxisome biogenesis and proliferation, thereby exempli
50  epithelial cell differentiation upregulates peroxisome biogenesis and promotes robust type III inter
51 ta demonstrate an important role for PEX1 in peroxisome biogenesis and suggest that mutations in this
52 PEX6 form a complex of central importance to peroxisome biogenesis and that mutations affecting this
53             In the absence of both proteins, peroxisome biogenesis and the intra-ER sorting of Pex2 a
54                        In humans, defects in peroxisome biogenesis are the cause of lethal diseases t
55  TGF-beta1 signaling down-regulated not only peroxisome biogenesis but also the metabolism of these o
56 s a protein required for the early stages of peroxisome biogenesis, but its precise function and site
57                                 Compromising peroxisome biogenesis, by repressing PEX3 expression, po
58  (RCDP) is an autosomal recessive disease of peroxisome biogenesis characterized by deficiencies in s
59 sicle coat-assembly, centrosomes, autophagy, peroxisome biogenesis, cytoskeleton, ribosome maturation
60 pared to wild-type PEX6 c.2578C results in a peroxisome biogenesis defect and thus constitutes the ca
61                                           In peroxisome biogenesis-defective (pex) mutants of the yea
62 wo novel schemes for the direct selection of peroxisome-biogenesis-defective (pex) mutants of the met
63 eas some of these proteins are stabilized in peroxisome biogenesis deficiency models lacking MARCH5 e
64                     PEX7 mutations cause the peroxisome biogenesis disorder (PBD) rhizomelic chondrod
65 odysplasia punctata (RCDP), a severe, lethal peroxisome biogenesis disorder characterized by aberrant
66 3 or [1-14C]22:5n-3 to DHA as did cells from peroxisome biogenesis disorder patients comprising eight
67 l and diseased (Pex7 deficiency modeling the peroxisome biogenesis disorder, RCDP) mouse brain tissue
68 at comprises complementation group 11 of the peroxisome biogenesis disorders (PBD).
69 nset neurodegenerative conditions, including Peroxisome Biogenesis Disorders (PBD).
70                                          The peroxisome biogenesis disorders (PBDs) are a group of ge
71                                          The peroxisome biogenesis disorders (PBDs) are a group of le
72 defects in peroxisome assembly result in the peroxisome biogenesis disorders (PBDs), a group of genet
73 l matrix proteins and are referred to as the peroxisome biogenesis disorders (PBDs).
74 s in a group of neurological diseases termed peroxisome biogenesis disorders (PBDs).
75           Loss of peroxisome function causes peroxisome biogenesis disorders and severe childhood dis
76 sponsible for complementation group 8 of the peroxisome biogenesis disorders and showed that it encod
77  stabilization as a therapeutic strategy for peroxisome biogenesis disorders arising from the G843D m
78 for the majority of the most severe forms of peroxisome biogenesis disorders in humans.
79 utations in PEX5 or 12 other PEX genes cause peroxisome biogenesis disorders, collectively named the
80  the most commonly affected peroxin in human peroxisome biogenesis disorders.
81  protein import and are the leading cause of peroxisome biogenesis disorders.
82 e our understanding of the etiology of human peroxisome biogenesis disorders.
83                                          The peroxisome-biogenesis disorders (PBDs) are a genetically
84                                          The peroxisome-biogenesis disorders (PBDs) are a group of ge
85                                          The peroxisome-biogenesis disorders (PBDs) are a set of ofte
86  causes of a spectrum of autosomal-recessive peroxisome-biogenesis disorders (PBDs), including Zellwe
87 cking protein for other proteins that affect peroxisome biogenesis, division, and segregation.
88 sive disorders that are caused by defects in peroxisome biogenesis due to bi-allelic mutations in any
89 ons, including membrane fusion, proteolysis, peroxisome biogenesis, endosome sorting and meiotic spin
90 on between PpPex1p and PpPex6p in regulating peroxisome biogenesis events.
91                      Similarly, depletion of peroxisome biogenesis factor Pex14 leads to the accumula
92  Seed 1 (SSE1) gene encodes a homolog of the peroxisome biogenesis factor Pex16p, and a loss-of-funct
93 d sustained neuroinflammatory responses with peroxisome biogenesis factor suppression despite limited
94                                              Peroxisome biogenesis factor transcripts (PEX3, PEX5L, P
95  investigated host neuroimmune responses and peroxisome biogenesis factors during severe acute respir
96 ontology categories: fatty acid degradation, peroxisome biogenesis, fatty acid synthesis, and retinol
97                          Inactivation of the peroxisome biogenesis gene PEX10 was crucial in obtainin
98  mutants, we isolated a viable allele of the peroxisome biogenesis gene PEX13 with striking peroxisom
99  this report we demonstrate the induction of peroxisome biogenesis genes in both plant and animal cel
100 tor, Mxr1 activates methanol utilization and peroxisome biogenesis genes in the methylotrophic yeast,
101                  The molecular mechanisms of peroxisome biogenesis have begun to emerge; in contrast,
102 s involved in peroxisomal protein import and peroxisome biogenesis) have become clearer.
103                               During de novo peroxisome biogenesis, importomer complex proteins sort
104 plications, we recast mechanisms controlling peroxisome biogenesis in a framework that integrates inf
105               Their expression also restores peroxisome biogenesis in cells that are deficient in the
106                                              Peroxisome biogenesis in humans is not governed by PPARa
107  lipids, the trafficking of cholesterol, and peroxisome biogenesis in mammalian cells.
108 induced peroxisomal biogenesis, and abnormal peroxisome biogenesis in MARCH5/Pex14 and MARCH5/Pex3 dk
109 s occurs via a process that is homologous to peroxisome biogenesis in other eukaryotes.
110 cytosolic location, PEX26- delta ex5 rescues peroxisome biogenesis in PEX26-deficient cells as effici
111 EX26-Mito retains the full ability to rescue peroxisome biogenesis in PEX26-deficient cells.
112   We have cloned PEX15 which is required for peroxisome biogenesis in Saccharomyces cerevisiae.
113 es the progress made in our understanding of peroxisome biogenesis in the last few years, during whic
114 rt the cloning of PER6, a gene essential for peroxisome biogenesis in the methylotrophic yeast Pichia
115 amily, PpPex1p and PpPex6p, are required for peroxisome biogenesis in the yeast Pichia pastoris.
116 ral membrane peroxins (proteins required for peroxisome biogenesis) in Saccharomyces cerevisiae, Pex2
117 Refsum disease, and five of the disorders of peroxisome biogenesis, including rhizomelic chondrodyspl
118 d growth on oleic acid, but had no effect on peroxisome biogenesis, indicating a role for YLR284C in
119 which the model can be used to conclude that peroxisome biogenesis is dominated by de novo production
120                                              Peroxisome biogenesis is essential for cellular recovery
121        This may sound familiar, but in fact, peroxisome biogenesis is proving to be surprisingly uniq
122 udy of phosphatases and kinases required for peroxisome biogenesis is the first genome-wide analysis
123  of peroxisomal matrix proteins, crucial for peroxisome biogenesis, is mediated by the cytosolic rece
124  our studies reveal a novel role for Lrp1 in peroxisome biogenesis, lipid homeostasis, and OPC differ
125 , none are known, leading us to propose that peroxisome biogenesis may not require protein import int
126                  Pharmacologically enhancing peroxisome biogenesis mitigated both acute symptoms and
127                                    Peb1 is a peroxisome biogenesis mutant isolated in Saccharomyces c
128 nce increases considerably in the Deltapex14 peroxisome biogenesis mutant.
129 f the approximately 20 proteins required for peroxisome biogenesis, only four have been implicated in
130                   Among peroxins involved in peroxisome biogenesis, only Pex8p is predominantly intra
131                                      Several peroxisome biogenesis PEROXIN (PEX) genes encode protein
132 nol pathway enzymes and proteins involved in peroxisome biogenesis (PEX proteins) are induced in resp
133                           A recent model for peroxisome biogenesis postulates that peroxisomes form d
134                                          The peroxisome biogenesis protein peroxisomal membrane prote
135                                 Mutations in peroxisome biogenesis proteins (peroxins) can lead to de
136 e anomalies associated with the disorders of peroxisome biogenesis remains unknown.
137       In yeast and mammals, various steps in peroxisome biogenesis require the function of peroxin (P
138                                              Peroxisome biogenesis requires that proteins be transpor
139             We discovered that Mtb-triggered peroxisome biogenesis requires the ESX-1 type 7 secretio
140 ic reticulum (ER) plays an important role in peroxisome biogenesis; some peroxisomal membrane protein
141 me fission factors, leading us to infer that peroxisome biogenesis switches from de novo synthesis to
142 elated yeast peroxins (proteins required for peroxisome biogenesis) that are partially redundant in f
143  proteins (mostly peroxins) are required for peroxisome biogenesis, the role of only a few of these h
144 sing on transcriptional networks that induce peroxisomes biogenesis, the model-guided experiments all
145 s of evidence support a function for SSE1 in peroxisome biogenesis: the peroxisomal localization of a
146 has permitted categorization of disorders of peroxisome biogenesis, their molecular basis and mutatio
147         Here, we review our understanding of peroxisome biogenesis to propose and reframe models for

 
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