scholarly article | Q13442814 |
P356 | DOI | 10.1016/S0166-6851(97)00064-9 |
P698 | PubMed publication ID | 9247927 |
P50 | author | Agnès Germot | Q73214407 |
P2093 | author name string | H Philippe | |
H Le Guyader | |||
P2860 | cites work | Complete nucleotide sequences of the genes encoding translation elongation factors 1 alpha and 2 from a microsporidian parasite, Glugea plecoglossi: implications for the deepest branching of eukaryotes | Q47813974 |
Alpha-tubulin from early-diverging eukaryotic lineages and the evolution of the tubulin family | Q48057474 | ||
Phylogenetic analysis of beta-tubulin sequences from amitochondrial protozoa | Q48065215 | ||
Phylogenetic analysis of 70 kD heat shock protein sequences suggests a chimeric origin for the eukaryotic cell nucleus | Q48077742 | ||
Eukaryotes with no mitochondria | Q55933605 | ||
Eukaryotic ribosomes that lack a 5.8S RNA | Q59063762 | ||
Ribosomal RNA trees misleading? | Q59082972 | ||
Molecular data suggest an early acquisition of the mitochondrion endosymbiont | Q63647809 | ||
Evidence for the smallest nuclear genome (2.9 Mb) in the microsporidium Encephalitozoon cuniculi | Q71288478 | ||
Phylogenetic relationships of Bacteria based on comparative sequence analysis of elongation factor Tu and ATP-synthase beta-subunit genes | Q72188135 | ||
Towards a new perspective in protozoan evolution | Q104116283 | ||
Direct evidence for secondary loss of mitochondria in Entamoeba histolytica | Q24563714 | ||
A common evolutionary origin for mitochondria and hydrogenosomes | Q24633297 | ||
The RecA protein as a model molecule for molecular systematic studies of bacteria: comparison of trees of RecAs and 16S rRNAs from the same species | Q24635216 | ||
The winds of (evolutionary) change: breathing new life into microbiology | Q24669805 | ||
Molecular evolution of the HSP70 multigene family | Q27940113 | ||
Evaluation of the maximum likelihood estimate of the evolutionary tree topologies from DNA sequence data, and the branching order in hominoidea | Q28245344 | ||
Archaeal phylogeny: reexamination of the phylogenetic position of Archaeoglobus fulgidus in light of certain composition-induced artifacts | Q33954463 | ||
Root of the universal tree of life based on ancient aminoacyl-tRNA synthetase gene duplications | Q34308020 | ||
Presence of a mitochondrial-type 70-kDa heat shock protein in Trichomonas vaginalis suggests a very early mitochondrial endosymbiosis in eukaryotes | Q34410877 | ||
A plastid of probable green algal origin in Apicomplexan parasites. | Q34738267 | ||
Evidence that eukaryotic triosephosphate isomerase is of alpha-proteobacterial origin | Q35994610 | ||
Presence and cellular distribution of a 60-kDa protein related to mitochondrial hsp60 in Giardia lamblia. | Q36722073 | ||
Species sampling has a major impact on phylogenetic inference | Q36745492 | ||
A possible mitochondrial gene in the early-branching amitochondriate protist Trichomonas vaginalis | Q37046515 | ||
Small subunit ribosomal RNA+ of Hexamita inflata and the quest for the first branch in the eukaryotic tree | Q38565106 | ||
MUST, a computer package of Management Utilities for Sequences and Trees | Q38567793 | ||
Cloning of the hsp70 (dnaK) genes from Rhizobium meliloti and Pseudomonas cepacia: phylogenetic analyses of mitochondrial origin based on a highly conserved protein sequence | Q39899679 | ||
Molecular chaperones in protein folding: the art of avoiding sticky situations | Q40621904 | ||
Ribosomal DNA sequences of Encephalitozoon hellem and Encephalitozoon cuniculi: species identification and phylogenetic construction | Q41080773 | ||
Chromosomal localization of five genes in Encephalitozoon cuniculi (Microsporidia). | Q41171629 | ||
Protein phylogeny of translation elongation factor EF-1 alpha suggests microsporidians are extremely ancient eukaryotes | Q47181399 | ||
Ribosomal RNA sequence suggests microsporidia are extremely ancient eukaryotes | Q47399583 | ||
P433 | issue | 2 | |
P921 | main subject | Nosema Locustae pathogen | Q7061774 |
mitochondrion | Q39572 | ||
P304 | page(s) | 159-168 | |
P577 | publication date | 1997-08-01 | |
P1433 | published in | Molecular and Biochemical Parasitology | Q15752756 |
P1476 | title | Evidence for loss of mitochondria in Microsporidia from a mitochondrial-type HSP70 in Nosema locustae | |
P478 | volume | 87 |
Q28765971 | A briefly argued case that mitochondria and plastids are descendants of endosymbionts, but that the nuclear compartment is not |
Q36893145 | A mitochondrial Hsp70 orthologue in Vairimorpha necatrix: molecular evidence that microsporidia once contained mitochondria |
Q28218819 | A mitochondrial remnant in the microsporidian Trachipleistophora hominis |
Q24682058 | A mitochondrial-like chaperonin 60 gene in Giardia lamblia: evidence that diplomonads once harbored an endosymbiont related to the progenitor of mitochondria |
Q35823322 | A new vesicular compartment in Encephalitozoon cuniculi |
Q22065662 | A revised six-kingdom system of life |
Q48020763 | A small spliceosomal-type intron occurs in a ribosomal protein gene of the microsporidian Encephalitozoon cuniculi |
Q43770186 | Alpha and beta subunits of pyruvate dehydrogenase E1 from the microsporidian Nosema locustae: mitochondrion-derived carbon metabolism in microsporidia |
Q28776510 | Amitochondriate amoebae and the evolution of DNA-dependent RNA polymerase II |
Q52994145 | An empirical assessment of long-branch attraction artefacts in deep eukaryotic phylogenomics. |
Q34107198 | An overview of endosymbiotic models for the origins of eukaryotes, their ATP-producing organelles (mitochondria and hydrogenosomes), and their heterotrophic lifestyle |
Q40466813 | Analyses of the ribosomal DNA region in Nosema bombycis NIS 001. |
Q35029741 | Analysis of the beta-tubulin genes from Enterocytozoon bieneusi isolates from a human and rhesus macaque |
Q33193875 | Bacterial catalase in the microsporidian Nosema locustae: implications for microsporidian metabolism and genome evolution. |
Q83214151 | Changing perspectives on the origin of eukaryotes |
Q54499181 | Comparative analysis of the ribosomal components of the hydrogenosome-containing protist, Trichomonas vaginalis. |
Q47957626 | Critical analysis of eukaryotic phylogeny: a case study based on the HSP70 family. |
Q30847643 | Developmental expression of a tandemly repeated, glycine- and serine-rich spore wall protein in the microsporidian pathogen Encephalitozoon cuniculi |
Q39516352 | Distribution of substitution rates and location of insertion sites in the tertiary structure of ribosomal RNA. |
Q31921017 | Early branching eukaryotes? |
Q30860046 | Encephalitozoon cuniculi (Microspora) genome: physical map and evidence for telomere-associated rDNA units on all chromosomes. |
Q28144396 | Evidence from beta-tubulin phylogeny that microsporidia evolved from within the fungi |
Q34422234 | Evidence from small-subunit ribosomal RNA sequences for a fungal origin of Microsporidia. |
Q37051180 | Evidence of a reduced and modified mitochondrial protein import apparatus in microsporidian mitosomes |
Q28770149 | Evolution of eukaryotic transcription: insights from the genome of Giardia lamblia |
Q54706275 | Evolutionary diversification of mitochondrial proteomes: implications for human disease. |
Q33479336 | Evolutionary flexibility of protein complexes |
Q34514313 | Evolutionary relationships among "jakobid" flagellates as indicated by alpha- and beta-tubulin phylogenies. |
Q39841682 | Expression and Localization of an Hsp70 Protein in the Microsporidian Encephalitozoon cuniculi |
Q29013820 | Fish microsporidia: fine structural diversity and phylogeny |
Q22122366 | Genome sequence and gene compaction of the eukaryote parasite Encephalitozoon cuniculi |
Q42645673 | Giardia lamblia expresses a proteobacterial-like DnaK homolog |
Q41703476 | History assignment: when was the mitochondrion founded? |
Q77892032 | How good are deep phylogenetic trees? |
Q33518043 | Identification of transcriptional signals in Encephalitozoon cuniculi widespread among Microsporidia phylum: support for accurate structural genome annotation |
Q47738744 | Implications of protein import on the origin of hydrogenosomes |
Q45342090 | Long branch attraction effects and the status of "basal eukaryotes": phylogeny and structural analysis of the ribosomal RNA gene cluster of the free-living diplomonad Trepomonas agilis |
Q21093601 | Loss of the flagellum happened only once in the fungal lineage: phylogenetic structure of kingdom Fungi inferred from RNA polymerase II subunit genes |
Q54495720 | Malawimonas jakobiformis n. gen., n. sp. (Malawimonadidae n. fam.): A Jakoba-like Heterotrophic Nanoflagellate with Discoidal Mitochondrial Cristae |
Q85569317 | Meeting Report: XIIth Meeting of the International Society for Evolutionary Protistology Flagstaff, USA, August 2-4, 1998 |
Q31932082 | Microsporidia are related to Fungi: evidence from the largest subunit of RNA polymerase II and other proteins |
Q41653461 | Microsporidia: Obligate Intracellular Pathogens Within the Fungal Kingdom |
Q33892754 | Microsporidia: accumulating molecular evidence that a group of amitochondriate and suspectedly primitive eukaryotes are just curious fungi |
Q30326996 | Microsporidia: emerging advances in understanding the basic biology of these unique organisms. |
Q32076603 | Microsporidia: emerging pathogenic protists |
Q39724620 | Microsporidian Encephalitozoon cuniculi, a unicellular eukaryote with an unusual chromosomal dispersion of ribosomal genes and a LSU rRNA reduced to the universal core. |
Q35127548 | Microsporidian mitosomes retain elements of the general mitochondrial targeting system |
Q33960415 | Microsporidiosis in mammals |
Q34190448 | Mitochondrial connection to the origin of the eukaryotic cell |
Q33989995 | Mitochondrion-derived organelles in protists and fungi |
Q37763217 | Mitochondrion-related organelles in eukaryotic protists |
Q34258655 | Molecular characteristics and physiology of microsporidia |
Q38343736 | Molecular evolution and structure of alpha-actinin |
Q33588906 | Molecular techniques for detection, species differentiation, and phylogenetic analysis of microsporidia. |
Q39006263 | Morphological characterization and HSP70-, IGS-based phylogenetic analysis of two microsporidian parasites isolated from Antheraea pernyi |
Q36497717 | Multiple secondary origins of the anaerobic lifestyle in eukaryotes |
Q46850751 | New evidence on the relationship between Microsporidia and Fungi: a genome-wide analysis by DarkHorse software. |
Q32030012 | On proteins of the microsporidian invasive apparatus: complete sequence of a polar tube protein of Encephalitozoon cuniculi |
Q37614307 | On the origin of chloroplasts, import mechanisms of chloroplast-targeted proteins, and loss of photosynthetic ability - review |
Q24675868 | On the origin of mitochondria: a genomics perspective |
Q47658456 | Origin and evolution of eukaryotic chaperonins: phylogenetic evidence for ancient duplications in CCT genes |
Q30975353 | Origin and evolution of the mitochondrial proteome |
Q28763672 | Origin of phagotrophic eukaryotes as social cheaters in microbial biofilms |
Q33916511 | Origins of hydrogenosomes and mitochondria: evolution and organelle biogenesis |
Q41712097 | Origins of microsporidia |
Q33745251 | Origins of mitochondria and hydrogenosomes |
Q53781044 | Parasites go the full monty. |
Q51982383 | Phylogenetic analysis of the complete genome sequence of Encephalitozoon cuniculi supports the fungal origin of microsporidia and reveals a high frequency of fast-evolving genes. |
Q48031040 | Phylogenetic placement of Trichonympha |
Q47812259 | Prokaryotic and eukaryotic features observed on the secondary structures of Giardia SSU rRNAs and its phylogenetic implications |
Q33251431 | Reciprocal illumination in the gene content tree of life |
Q34446386 | Reconstructing/deconstructing the earliest eukaryotes: how comparative genomics can help |
Q36493121 | Secondary absence of mitochondria in Giardia lamblia and Trichomonas vaginalis revealed by valyl-tRNA synthetase phylogeny |
Q48374406 | Sequence analysis of genes encoding ribosomal proteins of amitochondriate protists: L1 of Trichomonas vaginalis and L29 of Giardia lamblia |
Q40414783 | Sequence and analysis of chromosome I of the amitochondriate intracellular parasite Encephalitozoon cuniculi (Microspora) |
Q24558676 | Simplicity and complexity of microsporidian genomes |
Q54495798 | Some free-living flagellates (protista) from anoxic habitats |
Q61912445 | Structure and function of the Golgi organelle in parasitic protists |
Q34474970 | Sure facts and open questions about the origin and evolution of photosynthetic plastids |
Q29300435 | Testate amoebae in the Neoproterozoic Era: evidence from vase-shaped microfossils in the Chuar Group, Grand Canyon |
Q44143291 | The effects of elevated temperatures and various time-temperature combinations on the development of Brachiola (Nosema) algerae N. Comb. in mammalian cell culture |
Q31084322 | The microsporidian polar tube: evidence for a third polar tube protein (PTP3) in Encephalitozoon cuniculi |
Q24671773 | The origin of eukaryotes: the difference between prokaryotic and eukaryotic cells |
Q30432527 | The recent origins of spliceosomal introns revisited |
Q30929623 | Transfer of Nosema locustae (Microsporidia) to Antonospora locustae n. comb. based on molecular and ultrastructural data. |
Q39724427 | U2 and U6 snRNA genes in the microsporidian Nosema locustae: evidence for a functional spliceosome |
Q80381248 | What are the microsporidia? |
Q33738556 | Where is the root of the universal tree of life? |
Search more.