Pages that link to "Q37736777"
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The following pages link to The human mitochondrial replication fork in health and disease (Q37736777):
Displaying 50 items.
- Antimutator Alleles of Yeast DNA Polymerase Gamma Modulate the Balance between DNA Synthesis and Excision (Q21134954) (← links)
- NDUFA12L mitochondrial complex-I assembly factor: Implications for taupathies (Q26764822) (← links)
- Primer removal during mammalian mitochondrial DNA replication (Q26797996) (← links)
- Genes and Pathways Involved in Adult Onset Disorders Featuring Muscle Mitochondrial DNA Instability (Q26801194) (← links)
- Human mitochondrial DNA replication (Q26828886) (← links)
- The human mitochondrial transcriptome and the RNA-binding proteins that regulate its expression (Q27016551) (← links)
- Accessorizing the human mitochondrial transcription machinery (Q27025764) (← links)
- Alkyladenine DNA glycosylase (AAG) localizes to mitochondria and interacts with mitochondrial single-stranded binding protein (mtSSB) (Q28282687) (← links)
- Unbiased Mitoproteome Analyses Confirm Non-canonical RNA, Expanded Codon Translations (Q28596502) (← links)
- Novel subcellular localization of the DNA helicase Twinkle at the kinetochore complex during mitosis in neuronal-like progenitor cells. (Q30382614) (← links)
- The N-terminal domain of the Drosophila mitochondrial replicative DNA helicase contains an iron-sulfur cluster and binds DNA (Q34107139) (← links)
- Genes and genetic testing in hereditary ataxias. (Q34347658) (← links)
- Modeling pathogenic mutations of human twinkle in Drosophila suggests an apoptosis role in response to mitochondrial defects (Q34405895) (← links)
- MGME1 processes flaps into ligatable nicks in concert with DNA polymerase γ during mtDNA replication (Q34528068) (← links)
- Tracking replication enzymology in vivo by genome-wide mapping of ribonucleotide incorporation. (Q35152167) (← links)
- Two novel mutations in PEO1 (twinkle) gene associated with chronic external ophthalmoplegia. (Q35171361) (← links)
- On the sequence-directed nature of human gene mutation: the role of genomic architecture and the local DNA sequence environment in mediating gene mutations underlying human inherited disease (Q35226155) (← links)
- The inversion of the Control Region in three mitogenomes provides further evidence for an asymmetric model of vertebrate mtDNA replication (Q35288143) (← links)
- Diabetic retinopathy, superoxide damage and antioxidants. (Q35545811) (← links)
- Simultaneous DNA and RNA Mapping of Somatic Mitochondrial Mutations across Diverse Human Cancers (Q35678495) (← links)
- Coding constraints modulate chemically spontaneous mutational replication gradients in mitochondrial genomes (Q35714496) (← links)
- Human mitochondrial DNA helicase TWINKLE is both an unwinding and annealing helicase (Q35922647) (← links)
- Damaged Mitochondrial DNA Replication System and the Development of Diabetic Retinopathy (Q36001839) (← links)
- Therapeutic Targeting of the Mitochondria Initiates Excessive Superoxide Production and Mitochondrial Depolarization Causing Decreased mtDNA Integrity (Q36234714) (← links)
- Next-generation sequencing reveals DGUOK mutations in adult patients with mitochondrial DNA multiple deletions (Q36411043) (← links)
- Mitochondrial biogenesis in epithelial cancer cells promotes breast cancer tumor growth and confers autophagy resistance (Q36472242) (← links)
- Mutations in DNA2 link progressive myopathy to mitochondrial DNA instability (Q36595107) (← links)
- Mitochondrial biogenesis: a therapeutic target for neurodevelopmental disorders and neurodegenerative diseases (Q36771650) (← links)
- TWINKLE is an essential mitochondrial helicase required for synthesis of nascent D-loop strands and complete mtDNA replication (Q36787217) (← links)
- Homologous DNA strand exchange activity of the human mitochondrial DNA helicase TWINKLE. (Q36914602) (← links)
- Oxidative DNA damage stalls the human mitochondrial replisome (Q37057236) (← links)
- Biochemical Characterization of the Human Mitochondrial Replicative Twinkle Helicase: SUBSTRATE SPECIFICITY, DNA BRANCH MIGRATION, AND ABILITY TO OVERCOME BLOCKADES TO DNA UNWINDING. (Q37065777) (← links)
- Of circles, forks and humanity: Topological organisation and replication of mammalian mitochondrial DNA (Q37835192) (← links)
- Mechanisms of mitochondrial diseases (Q37909459) (← links)
- Enzymes involved in organellar DNA replication in photosynthetic eukaryotes (Q38256375) (← links)
- Mitochondrial DNA maintenance: an appraisal (Q38569294) (← links)
- ER-mitochondria contacts couple mtDNA synthesis with mitochondrial division in human cells (Q38758060) (← links)
- DNA Damage Tolerance by Eukaryotic DNA Polymerase and Primase PrimPol (Q41183468) (← links)
- Mitochondrial SSBP1 protects cells from proteotoxic stresses by potentiating stress-induced HSF1 transcriptional activity. (Q41241698) (← links)
- Mitochondrial complex I inhibition as a possible mechanism of chlorpyrifos induced neurotoxicity (Q41786520) (← links)
- Regulation of DNA replication at the end of the mitochondrial D-loop involves the helicase TWINKLE and a conserved sequence element. (Q42117981) (← links)
- In vivo mutagenesis reveals that OriL is essential for mitochondrial DNA replication (Q42263413) (← links)
- Mitochondrial DNA repair: a novel therapeutic target for heart failure (Q46585553) (← links)
- The spectrum of epilepsy caused by POLG mutations (Q48113427) (← links)
- Novel mutations in typical and atypical genetic loci through exome sequencing in autosomal recessive cerebellar ataxia families (Q50356490) (← links)
- The presence of rNTPs decreases the speed of mitochondrial DNA replication. (Q55174541) (← links)
- Copy-choice recombination during mitochondrial L-strand synthesis causes DNA deletions (Q61795898) (← links)
- An overview of mammalian mitochondrial DNA replication mechanisms (Q89182617) (← links)
- History of DNA Helicases (Q89975997) (← links)
- Dominant mutations in mtDNA maintenance gene SSBP1 cause optic atrophy and foveopathy (Q90255272) (← links)