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64 results for “Bombyx mori”
Fig. 4 in Standard method for detecting Bombyx mori nucleopolyhedrovirus disease-resistant silkworm varieties
Fig. 4. IIM for placing silkworms on mulberry leaves. (A) One larva was placed on each leaf. (B) The larva eating the leaf. (C) The leaf after being eaten by the silkworm.
Fig. 3 in Standard method for detecting Bombyx mori nucleopolyhedrovirus disease-resistant silkworm varieties
Fig. 3. GIM for placing silkworms on mulberry leaves. (A) The leaves were arranged in the box after smearing them with BmNPV, and then they were air dried. (B) Five larvae were placed on each leaf. (C) The leaves after being eaten by the silkworms.
Figure 5 in Evaluation of chitosan and silver nanoparticles Against isolated pathogens from Mulberry Silkworm, Bombyx mori L. (Lepidoptera: Bombycidae) under laboratory conditions
Figure 5. TEM micrograph of chitosan nanoparticles prepared by ionic gelation method. Table 3. Antimicrobial activity of silver nanoparticles (µl) with different concentrations against fungal and bacterial isolates.
Figure 1 in Evaluation of chitosan and silver nanoparticles Against isolated pathogens from Mulberry Silkworm, Bombyx mori L. (Lepidoptera: Bombycidae) under laboratory conditions
Figure 1. Mean weight of healthy and infected fourth and fifth instar larvae of B. mori. Isolation and identification of bacterial isolates: Total of 7 bacterial were successfully isolated from the outer surface and the inner bоdy of silkworm larvae.
Figure 4 in Evaluation of chitosan and silver nanoparticles Against isolated pathogens from Mulberry Silkworm, Bombyx mori L. (Lepidoptera: Bombycidae) under laboratory conditions
Figure 4. Transmissiоn electron microscоpy micrоgraph of silver nanoparticles.
Figure 3 in Evaluation of chitosan and silver nanoparticles Against isolated pathogens from Mulberry Silkworm, Bombyx mori L. (Lepidoptera: Bombycidae) under laboratory conditions
Figure 3. Final dispersion formed after reduction (A) silver and (B) chitosan.
Mechanism of Ca2+ in regulating pupation defects of Bombyx mori after exposure to chlorantraniliprole
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Knockdown of BmorCPR67 gene disrupts prepupal–pupal transition of silkworm Bombyx mori by thinning the endocuticle
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Data from: Role of Atg3, Atg5, and Atg12 in the crosstalk between apoptosis and autophagy in the posterior silk gland of Bombyx mori
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X-ray diffraction images of juvenile hormone diol kinase from the silk worm Bombyx mori
<p>X-ray diffraction images of juvenile hormone diol kinase (JHDK) from the silk worm Bombyx mori</p>
Effect of Silkworms (Bombyx Mori L.) Pupae Extracts on Musculoskeletal Biomarkers in Adults
ClinicalTrials.gov study NCT04994054. IPD Sharing: NO. Countries: 1. Publications: 1.
Data from: Getting a full dose? Reconsidering sex chromosome dosage compensation in the silkworm, Bombyx mori
Dosage compensation – equalizing gene expression levels in response to differences in gene dose or copy number – is classically considered to play a critical role in the evolution of heteromorphic sex chromosomes. As the X and Y diverge through degradation and gene loss on the Y (or the W in female-heterogametic ZW taxa), it is expected that dosage compensation will evolve to correct for sex-specific differences in gene dose. While this is observed in some organisms, recent genome-wide expression studies in other taxa have revealed striking exceptions. In particular, reports that both birds and the silkworm moth (Bombyx mori) lack dosage compensation have spurred speculation that this is the rule for all female-heterogametic taxa. Here we revisit the issue of dosage compensation in silkworm by replicating and extending the previous analysis. Contrary to previous reports, our efforts reveal that the global male:female expression ratio does not differ between the Z and autosomes, a pattern typically associated with dosage compensated taxa. We believe the previous report of unequal male:female ratios on the Z reflects artifacts of microarray normalization in conjunction with not testing a major assumption that the male:female global expression ratio was unbiased for autosomal loci. However, we also find that the global Z chromosome expression is significantly reduced relative to autosomes, a pattern not expected in dosage compensated taxa. This combination of male:female parity with an overall reduction in expression for sex-linked loci is not consistent with the prevailing evolutionary theory of sex chromosome evolution and dosage compensation.
Fig. 2 in Standard method for detecting Bombyx mori nucleopolyhedrovirus disease-resistant silkworm varieties
Fig. 2. Mulberry leaf size standards of different larval stages for the IIM. (A) Leaf size for second-instar larvae. (B) Leaf size for third-instar larvae. (C) Leaf size for fourth-instar larvae. (D) Leaf size for fifth-instar larvae.
Data from: Getting a full dose? Reconsidering sex chromosome dosage compensation in the silkworm, Bombyx mori
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Expression of 50-500nt ncRNAs in silkworm Bombyx mori: developmental time courses
GEO Series GSE22913. Bombyx mori. 5 samples. Type: Non-coding RNA profiling by array.
Differentially expressed genes (DEGs) in oviducts of Yun7 and its giant egg mutant Yun7Ge of silkworm, Bombyx mori
GEO Series GSE173672. Bombyx mori. 4 samples. Type: Expression profiling by high throughput sequencing.
Expression of 50-500nt ncRNAs in silkworm Bombyx mori during two developmental transitions
GEO Series GSE22912. Bombyx mori. 2 samples. Type: Non-coding RNA profiling by array.
Identification of genome wide targets of the hox protein Ultrabithorax (Ubx) in larval wing buds of Bombyx mori (Daizo)
GEO Series GSE71990. Bombyx mori. 12 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
RNA associating with PIWI proteins in Bombyx mori BmN4 cells
GEO Series GSE150444. Bombyx mori. 9 samples. Type: Non-coding RNA profiling by high throughput sequencing.
Gene expression of ultra violet irradiation of silk worm Bombyx mori larvae
GEO Series GSE55816. Bombyx mori. 4 samples. Type: Expression profiling by array.
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