Koehler, Carla M.
![Sudoc [ABES], France](/viaf/images/flags/SUDOC.png "Sudoc [ABES], France")
Carla M. Koehler American biochemist
VIAF ID: 61798066 (Personal)
Permalink: http://viaf.org/viaf/61798066
Preferred Forms
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Carla M. Koehler
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American biochemist
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Koehler
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Carla M.
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Koehler, Carla M.
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100 1 _
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Koehler, Carla M.
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100 1 _
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Koehler, Carla M.
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100 1 _
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Koehler, Carla M.
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100 1 _ ‡a Koehler, Carla M.
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100 1 _ ‡a Koehler, Carla M.
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100 1 _ ‡a Koehler, Carla M.
4xx's: Alternate Name Forms (1)
5xx's: Related Names (1)
Works
| Title | Sources |
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| Adaptation of a Genetic Screen Reveals an Inhibitor for Mitochondrial Protein Import Component Tim44. |
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| Assembly of the three small Tim proteins precedes docking to the mitochondrial carrier translocase |
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| Atomic structure of a toxic, oligomeric segment of SOD1 linked to amyotrophic lateral sclerosis (ALS). |
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| Barth syndrome mutations that cause tafazzin complex lability |
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| The calcium-binding aspartate/glutamate carriers, citrin and aralar1, are new substrates for the DDP1/TIMM8a-TIMM13 complex |
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| The cardiolipin transacylase, tafazzin, associates with two distinct respiratory components providing insight into Barth syndrome |
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| A Chemical Biology Approach to Model Pontocerebellar Hypoplasia Type 1B (PCH1B). |
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| Correcting human mitochondrial mutations with targeted RNA import |
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| Defective mitochondrial protein translocation precludes normal Caenorhabditis elegans development |
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| Defining functional classes of Barth syndrome mutation in humans |
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| Defining the role of oxygen tension in human neural progenitor fate |
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| ER-mitochondria contacts: Actin dynamics at the ER control mitochondrial fission via calcium release. |
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| FAM210B is an erythropoietin target and regulates erythroid heme synthesis by controlling mitochondrial iron import and ferrochelatase activity |
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| Hereditary spastic paraplegia: respiratory choke or unactivated substrate? |
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| Human deafness dystonia syndrome is caused by a defect in assembly of the DDP1/TIMM8a-TIMM13 complex |
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| Importing mitochondrial proteins: machineries and mechanisms |
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| Loss of function of SLC25A46 causes lethal congenital pontocerebellar hypoplasia. |
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| Macrocytic anemia and mitochondriopathy resulting from a defect in sideroflexin 4. |
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| Mammalian polynucleotide phosphorylase is an intermembrane space RNase that maintains mitochondrial homeostasis |
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| Mia40 Protein Serves as an Electron Sink in the Mia40-Erv1 Import Pathway |
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| Mitochondrial function and biogenesis |
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| Mitochondrial mislocalization and altered assembly of a cluster of Barth syndrome mutant tafazzins |
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| Mitochondrial Transfer by Photothermal Nanoblade Restores Metabolite Profile in Mammalian Cells. |
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| Molecular machines involved in protein transport across cellular membranes |
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| Patterns that define the four domains conserved in known and novel isoforms of the protein import receptor Tom20 |
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| Pharmacologic rescue of an enzyme-trafficking defect in primary hyperoxaluria 1. |
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| PNPase knockout results in mtDNA loss and an altered metabolic gene expression program |
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| PNPASE regulates RNA import into mitochondria |
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| Rapid degradation of mutant SLC25A46 by the ubiquitin-proteasome system results in MFN1/2-mediated hyperfusion of mitochondria |
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| Reconstitution of the mia40-erv1 oxidative folding pathway for the small tim proteins |
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| Redox regulation of protein folding in the mitochondrial intermembrane space |
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| Repurposing Approach Identifies Auranofin with Broad Spectrum Antifungal Activity That Targets Mia40-Erv1 Pathway |
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| A role for cytochrome c and cytochrome c peroxidase in electron shuttling from Erv1. |
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| The role of Hot13p and redox chemistry in the mitochondrial TIM22 import pathway |
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| The role of Tim9p in the assembly of the TIM22 import complexes |
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| Role of twin Cys-Xaa9-Cys motif cysteines in mitochondrial import of the cytochrome C oxidase biogenesis factor Cmc1. |
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| Stendomycin selectively inhibits TIM23-dependent mitochondrial protein import. |
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| The Taz1p transacylase is imported and sorted into the outer mitochondrial membrane via a membrane anchor domain. |
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| The TCL1 oncoprotein binds the RNase PH domains of the PNPase exoribonuclease without affecting its RNA degrading activity |
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| Tim54p connects inner membrane assembly and proteolytic pathways in the mitochondrion |
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| The Tim8–Tim13 Complex Has Multiple Substrate Binding Sites and Binds Cooperatively to Tim23 |
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| The Tim9p-Tim10p complex binds to the transmembrane domains of the ADP/ATP carrier |
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| TMEM14C is required for erythroid mitochondrial heme metabolism |
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| UCP2 regulates energy metabolism and differentiation potential of human pluripotent stem cells |
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