| scholarly article | Q13442814 |
| P2093 | author name string | Luca Scorrano | |
| Luiza K Sanjuán Szklarz | |||
| P2860 | cites work | OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28 | Q24290356 |
| Control of mitochondrial morphology by a human mitofusin | Q24290831 | ||
| Dynamin-related protein Drp1 is required for mitochondrial division in mammalian cells | Q24291591 | ||
| The mitochondrial protein hFis1 regulates mitochondrial fission in mammalian cells through an interaction with the dynamin-like protein DLP1 | Q24308767 | ||
| Mff is an essential factor for mitochondrial recruitment of Drp1 during mitochondrial fission in mammalian cells | Q24315625 | ||
| Loss of OPA1 perturbates the mitochondrial inner membrane structure and integrity, leading to cytochrome c release and apoptosis | Q24338169 | ||
| OPA1 requires mitofusin 1 to promote mitochondrial fusion | Q24560014 | ||
| Roles of the mammalian mitochondrial fission and fusion mediators Fis1, Drp1, and Opa1 in apoptosis | Q24562044 | ||
| Fission and selective fusion govern mitochondrial segregation and elimination by autophagy | Q24652230 | ||
| Phosphorylation and cleavage of presenilin-associated rhomboid-like protein (PARL) promotes changes in mitochondrial morphology | Q24675079 | ||
| Mitochondrial membrane remodelling regulated by a conserved rhomboid protease | Q27935531 | ||
| Loss of Drp1 function alters OPA1 processing and changes mitochondrial membrane organization | Q47900211 | ||
| Organelle isolation: functional mitochondria from mouse liver, muscle and cultured filroblasts | Q60056610 | ||
| A mutation in the yeast heat-shock factor gene causes temperature-sensitive defects in both mitochondrial protein import and the cell cycle | Q27936788 | ||
| Nuclear gene OPA1, encoding a mitochondrial dynamin-related protein, is mutated in dominant optic atrophy | Q28140286 | ||
| Negative regulation of the Apaf-1 apoptosome by Hsp70 | Q28143100 | ||
| hFis1, a novel component of the mammalian mitochondrial fission machinery | Q28208369 | ||
| PAMP and PARL, two novel putative metalloproteases interacting with the COOH-terminus of Presenilin-1 and -2 | Q28221207 | ||
| OPA1 controls apoptotic cristae remodeling independently from mitochondrial fusion | Q28251846 | ||
| Mitochondrial rhomboid PARL regulates cytochrome c release during apoptosis via OPA1-dependent cristae remodeling | Q28506506 | ||
| Regulation of mitochondrial morphology through proteolytic cleavage of OPA1 | Q28571639 | ||
| Regulation of OPA1 processing and mitochondrial fusion by m-AAA protease isoenzymes and OMA1 | Q28594164 | ||
| SLP-2 is required for stress-induced mitochondrial hyperfusion | Q28594182 | ||
| Mitofusin-1 protein is a generally expressed mediator of mitochondrial fusion in mammalian cells | Q28854600 | ||
| Mitochondrial membrane potential regulates PINK1 import and proteolytic destabilization by PARL | Q29615624 | ||
| Disruption of fusion results in mitochondrial heterogeneity and dysfunction | Q29616566 | ||
| The role of dynamin-related protein 1, a mediator of mitochondrial fission, in apoptosis | Q29616568 | ||
| During autophagy mitochondria elongate, are spared from degradation and sustain cell viability. | Q29616569 | ||
| A distinct pathway remodels mitochondrial cristae and mobilizes cytochrome c during apoptosis | Q29620536 | ||
| Opa1-mediated cristae opening is Bax/Bak and BH3 dependent, required for apoptosis, and independent of Bak oligomerization | Q30485835 | ||
| Hsp27 negatively regulates cell death by interacting with cytochrome c. | Q33917298 | ||
| Regulation of skeletal muscle oxidative capacity and insulin signaling by the mitochondrial rhomboid protease PARL. | Q34113727 | ||
| Intramembrane proteolysis: theme and variations. | Q34342964 | ||
| Mitochondrial fission and cristae disruption increase the response of cell models of Huntington's disease to apoptotic stimuli | Q34605764 | ||
| A cut short to death: Parl and Opa1 in the regulation of mitochondrial morphology and apoptosis | Q34623508 | ||
| Hax1 lacks BH modules and is peripherally associated to heavy membranes: implications for Omi/HtrA2 and PARL activity in the regulation of mitochondrial stress and apoptosis | Q34991732 | ||
| OPA1 processing reconstituted in yeast depends on the subunit composition of the m-AAA protease in mitochondria | Q35949122 | ||
| OPA1 processing controls mitochondrial fusion and is regulated by mRNA splicing, membrane potential, and Yme1L. | Q36119045 | ||
| Regulation of the mitochondrial dynamin-like protein Opa1 by proteolytic cleavage | Q36119051 | ||
| Death versus survival: functional interaction between the apoptotic and stress-inducible heat shock protein pathways | Q36274956 | ||
| Quality control of mitochondria: protection against neurodegeneration and ageing | Q36446844 | ||
| Coassembly of Mgm1 isoforms requires cardiolipin and mediates mitochondrial inner membrane fusion | Q37365417 | ||
| The changing shape of mitochondrial apoptosis | Q37568897 | ||
| The heat shock response: life on the verge of death | Q37802041 | ||
| Proteolytic processing of OPA1 links mitochondrial dysfunction to alterations in mitochondrial morphology | Q40227379 | ||
| Dynamics of mitochondria in living cells: shape changes, dislocations, fusion, and fission of mitochondria | Q40763148 | ||
| Hax1-mediated processing of HtrA2 by Parl allows survival of lymphocytes and neurons | Q41791615 | ||
| The release of cytochrome c from mitochondria during apoptosis of NGF-deprived sympathetic neurons is a reversible event | Q41837258 | ||
| Traveling Bax and forth from mitochondria to control apoptosis. | Q41869309 | ||
| Processing of the dynamin Msp1p in S. pombe reveals an evolutionary switch between its orthologs Mgm1p in S. cerevisiae and OPA1 in mammals. | Q42973575 | ||
| Characterization of OPA1 isoforms isolated from mouse tissues | Q44071219 | ||
| Cytosolic heat shock protein 60, hypoxia, and apoptosis | Q44220806 | ||
| Normal mitochondrial dynamics requires rhomboid-7 and affects Drosophila lifespan and neuronal function | Q47070303 | ||
| P433 | issue | 10 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 1886-1893 | |
| P577 | publication date | 2012-05-08 | |
| P1433 | published in | Biochimica et Biophysica Acta | Q864239 |
| P1476 | title | The antiapoptotic OPA1/Parl couple participates in mitochondrial adaptation to heat shock | |
| P478 | volume | 1817 |
| Q46471274 | Altered Mitochondrial Anatomy of Trigeminal Ganglia Neurons in Diabetes. |
| Q37431102 | Common variants in the PARL and PINK1 genes increase the risk to leprosy in Han Chinese from South China. |
| Q41100689 | Entamoeba histolytica rhomboid protease 1 has a role in migration and motility as validated by two independent genetic approaches |
| Q38611106 | Fusion or Fission: The Destiny of Mitochondria In Traumatic Brain Injury of Different Severities. |
| Q38122700 | Keeping mitochondria in shape: a matter of life and death |
| Q42381310 | Mitochondrial dysfunction in an Opa1(Q285STOP) mouse model of dominant optic atrophy results from Opa1 haploinsufficiency. |
| Q37686255 | Mitochondrial fusion and fission proteins: novel therapeutic targets for combating cardiovascular disease. |
| Q36096020 | Novel Roles of Epoxyeicosanoids in Regulating Cardiac Mitochondria |
| Q42704462 | Quercetin glycosides induced neuroprotection by changes in the gene expression in a cellular model of Parkinson's disease |
| Q46648250 | Rhomboid family gene expression profiling in breast normal tissue and tumor samples |
| Q46479013 | Role of dynamin-related protein 1-mediated mitochondrial fission in resistance of mouse C2C12 myoblasts to heat injury |
| Q38798007 | Stress-induced OMA1 activation and autocatalytic turnover regulate OPA1-dependent mitochondrial dynamics |
| Q52317009 | The Endoplasmic Reticulum Stress Response in Neuroprogressive Diseases: Emerging Pathophysiological Role and Translational Implications. |
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