scholarly article | Q13442814 |
P50 | author | Travis E Hartman | Q56506533 |
Robert Sebra | Q63406368 | ||
William Jacobs | Q67270373 | ||
P2093 | author name string | Timothy Driscoll | |
Catherine Vilchèze | |||
Alice R Wattam | |||
Christopher A Kerantzas | |||
Shahina B Maqbool | |||
Eric K Nordberg | |||
JoAnn M Tufariello | |||
Laura E Cole | |||
R Brent Calder | |||
Eva Yang | |||
Jack A Fischer | |||
P2860 | cites work | The RAST Server: rapid annotations using subsystems technology | Q21263157 |
Massive gene decay in the leprosy bacillus | Q22122381 | ||
Unusual Diheme Conformation of the Heme-Degrading Protein from Mycobacterium tuberculosis | Q27658200 | ||
Discovery and characterization of a unique mycobacterial heme acquisition system | Q27667213 | ||
Discovery of a Siderophore Export System Essential for Virulence of Mycobacterium tuberculosis | Q27676547 | ||
A yeast manganese transporter related to the macrophage protein involved in conferring resistance to mycobacteria | Q27939911 | ||
Cloning and characterization of a mammalian proton-coupled metal-ion transporter | Q28245045 | ||
The salicylate-derived mycobactin siderophores of Mycobacterium tuberculosis are essential for growth in macrophages | Q28343891 | ||
Mechanistic insights into a novel exporter-importer system of Mycobacterium tuberculosis unravel its role in trafficking of iron | Q28472648 | ||
Identification of an ABC transporter required for iron acquisition and virulence in Mycobacterium tuberculosis | Q28486535 | ||
The structure of MbtI from Mycobacterium tuberculosis, the first enzyme in the biosynthesis of the siderophore mycobactin, reveals it to be a salicylate synthase | Q28486666 | ||
Identification of a Mycobacterium tuberculosis gene cluster encoding the biosynthetic enzymes for assembly of the virulence-conferring siderophore mycobactin | Q28486708 | ||
Global analysis of the Mycobacterium tuberculosis Zur (FurB) regulon | Q28486821 | ||
ideR, An essential gene in mycobacterium tuberculosis: role of IdeR in iron-dependent gene expression, iron metabolism, and oxidative stress response | Q28486874 | ||
Mycobacterium tuberculosis expresses a novel pH-dependent divalent cation transporter belonging to the Nramp family | Q28486934 | ||
A genetic locus required for iron acquisition in Mycobacterium tuberculosis | Q28487138 | ||
Mycobacterial Esx-3 is required for mycobactin-mediated iron acquisition | Q28487139 | ||
Characterization of a Mycobacterium tuberculosis ESX-3 conditional mutant: essentiality and rescue by iron and zinc | Q28487459 | ||
The Mycobacterium tuberculosis IdeR is a dual functional regulator that controls transcription of genes involved in iron acquisition, iron storage and survival in macrophages | Q28487578 | ||
Feo--transport of ferrous iron into bacteria. | Q30159790 | ||
Mycobacterium tuberculosis DeltaRD1 DeltapanCD: a safe and limited replicating mutant strain that protects immunocompetent and immunocompromised mice against experimental tuberculosis. | Q30355795 | ||
The Mycobacterium marinum G13 promoter is a strong sigma 70-like promoter that is expressed in Escherichia coli and mycobacteria species | Q30711097 | ||
Production of mycobacterial cell wall glycopeptidolipids requires a member of the MbtH-like protein family | Q31069254 | ||
Mycobacterium haemophilum osteomyelitis: case report and review of the literature | Q33239515 | ||
A new Mycobacterium species causing diffuse lepromatous leprosy | Q33385581 | ||
Comparative sequence analysis of Mycobacterium leprae and the new leprosy-causing Mycobacterium lepromatosis | Q33487071 | ||
Systematic genetic nomenclature for type VII secretion systems. | Q33513967 | ||
Analysis of the exochelin locus in Mycobacterium smegmatis: biosynthesis genes have homology with genes of the peptide synthetase family | Q33736702 | ||
Mycobacterium haemophilum as a novel etiology of cervical lymphadenitis in an otherwise healthy adult patient | Q33963612 | ||
Disruption of the gene homologous to mammalian Nramp1 in Mycobacterium tuberculosis does not affect virulence in mice | Q34128847 | ||
MbtH-Like Proteins as Integral Components of Bacterial Nonribosomal Peptide Synthetases | Q34138341 | ||
ABC transporter-mediated uptake of iron, siderophores, heme and vitamin B12. | Q34290799 | ||
The membrane protein FeoB contains an intramolecular G protein essential for Fe(II) uptake in bacteria | Q34415897 | ||
Mycobacterium haemophilum infections in heart transplant recipients: case report and review of the literature | Q34746830 | ||
Real-time PCR assay using fine-needle aspirates and tissue biopsy specimens for rapid diagnosis of mycobacterial lymphadenitis in children. | Q34782239 | ||
The ESX-3 secretion system is necessary for iron and zinc homeostasis in Mycobacterium tuberculosis | Q35025557 | ||
Clinical manifestations, diagnosis, and treatment of Mycobacterium haemophilum infections | Q35361550 | ||
Mycobacterium haemophilum: microbiology and expanding clinical and geographic spectra of disease in humans | Q35371930 | ||
MmpS4 promotes glycopeptidolipids biosynthesis and export in Mycobacterium smegmatis | Q61755426 | ||
Unusual mycobacteria in 5 Cases of opportunistic infections | Q66982266 | ||
The skin and immunosuppression | Q67502543 | ||
Structural elucidation and antigenicity of a novel phenolic glycolipid antigen from Mycobacterium haemophilum | Q67939188 | ||
Gaschromatography of Constitutive Fatty Acids inMycobacterium leprae | Q70284469 | ||
Mycobacterium haemophilum causing lymphadenitis in an otherwise healthy child | Q70981706 | ||
Genetic Manipulation of Mycobacterium tuberculosis | Q81928443 | ||
Recurrent Mycobacterium haemophilum in a renal transplant recipient | Q87159427 | ||
Report of disseminated Mycobacterium haemophilum infection after double cord blood allo-SCT | Q87402801 | ||
Insight into the evolution and origin of leprosy bacilli from the genome sequence of Mycobacterium lepromatosis | Q35378227 | ||
Direct identification of Mycobacterium haemophilum in skin lesions of immunocompromised patients by PCR-restriction endonuclease analysis | Q35718053 | ||
Further studies of a new pathogenic mycobacterium (M. haemophilum sp. nov.) | Q36513086 | ||
Mycobacteria with a growth requirement for ferric ammonium citrate, identified as Mycobacterium haemophilum. | Q36663547 | ||
Identification of genes involved in the sequestration of iron in mycobacteria: the ferric exochelin biosynthetic and uptake pathways. | Q36719012 | ||
Restriction fragment length polymorphism analysis of clinical isolates of Mycobacterium haemophilum | Q36723884 | ||
An official ATS/IDSA statement: diagnosis, treatment, and prevention of nontuberculous mycobacterial diseases | Q36727850 | ||
DNA polymorphisms detected in Mycobacterium haemophilum by pulsed-field gel electrophoresis | Q37165998 | ||
Evaluation of a simple method for growing Mycobacterium haemophilum | Q37200704 | ||
The SEED and the Rapid Annotation of microbial genomes using Subsystems Technology (RAST). | Q37661996 | ||
Recent insights into iron import by bacteria | Q37833350 | ||
Disseminated Mycobacterium haemophilum infection | Q37893778 | ||
Tubercle bacilli rely on a type VII army for pathogenicity | Q38031704 | ||
Take five - Type VII secretion systems of Mycobacteria | Q38165002 | ||
Identification of the Escherichia coli K-12 Nramp orthologue (MntH) as a selective divalent metal ion transporter | Q38314576 | ||
Intraventricular granulomatous mass associated with Mycobacterium haemophilum: A rare central nervous system manifestation in a patient with human immunodeficiency virus infection | Q38394554 | ||
Solution structure of the Mycobacterium tuberculosis EsxG·EsxH complex: functional implications and comparisons with other M. tuberculosis Esx family complexes. | Q38676500 | ||
Mutational and phylogenetic analyses of the mycobacterial mbt gene cluster | Q38725050 | ||
Biochemical properties and fatty acid composition of Mycobacterium haemophilum: study of 16 isolates from Australian patients | Q39364517 | ||
Disseminated Mycobacterium haemophilum infection in a 72-year-old patient with rheumatoid arthritis on infliximab | Q39653185 | ||
Characterization of the ferrous iron uptake system of Escherichia coli | Q39937148 | ||
Mycobacterium haemophilum infections in bone marrow transplant recipients. | Q40377566 | ||
Mycobacterium haemophilum: An emerging pathogen | Q40494926 | ||
Human immunodeficiency virus-associated atypical mycobacterial skeletal infections | Q41089137 | ||
Mycobacterium haemophilum infection with prominent facial manifestation mimicking leprosy | Q41199621 | ||
Function of metal-ion homeostasis in the cell division cycle, mitochondrial protein processing, sensitivity to mycobacterial infection and brain function. | Q41363633 | ||
φ(2)GFP10, a high-intensity fluorophage, enables detection and rapid drug susceptibility testing of Mycobacterium tuberculosis directly from sputum samples. | Q41984560 | ||
Mycobacterium haemophilum Masquerading as Leprosy in a Renal Transplant Patient | Q42122265 | ||
Mycobacterium haemophilum: emerging or underdiagnosed in Brazil? | Q42547107 | ||
Mycobacterium haemophilum infection after alemtuzumab treatment. | Q43194264 | ||
A seven-gene, multilocus, genus-wide approach to the phylogeny of mycobacteria using supertrees | Q44957916 | ||
Skin lesions caused by Mycobacterium haemophilum | Q45204840 | ||
Is the bacterial ferrous iron transporter FeoB a living fossil? | Q47392023 | ||
ESX/type VII secretion systems of mycobacteria: Insights into evolution, pathogenicity and protection | Q47433141 | ||
The NRAMP proteins of Salmonella typhimurium and Escherichia coli are selective manganese transporters involved in the response to reactive oxygen | Q47854702 | ||
Exochelin genes in Mycobacterium smegmatis: identification of an ABC transporter and two non-ribosomal peptide synthetase genes | Q48027677 | ||
Chiasmitis caused by Mycobacterium haemophilum in an immunocompromised adult | Q48727009 | ||
The FeoA protein is necessary for the FeoB transporter to import ferrous iron | Q50026110 | ||
Cutaneous Mycobacterium haemophilum infection in a patient receiving infliximab for psoriasis. | Q50493304 | ||
Inactivation of the Mycobacterium tuberculosis Nramp orthologue (mntH) does not affect virulence in a mouse model of tuberculosis. | Q53977031 | ||
Mycobacterium haemophilum in immunocompromised patients. | Q54002956 | ||
Amplified fragment length polymorphism analysis of human clinical isolates of Mycobacterium haemophilum from different continents. | Q54470473 | ||
P433 | issue | 6 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | genomics | Q222046 |
whole genome sequencing | Q2068526 | ||
Mycobacterium haemophilum | Q6947030 | ||
emerging pathogen | Q108429945 | ||
P304 | page(s) | e01313-15 | |
P577 | publication date | 2015-11-17 | |
P1433 | published in | mBio | Q15817061 |
P1476 | title | The Complete Genome Sequence of the Emerging Pathogen Mycobacterium haemophilum Explains Its Unique Culture Requirements | |
P478 | volume | 6 |
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Q38609726 | Feline leprosy due to Candidatus 'Mycobacterium lepraefelis': Further clinical and molecular characterisation of eight previously reported cases and an additional 30 cases. |
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