Biomedical subjects

Ravi Jain

Publications and source records attributed to Ravi Jain.

7 recordsLinked to original sources

PubMed2007

10-W-level diode-pumped compact 2.78 microm ZBLAN fiber laser.

We report on >9W transverse-fundamental-mode CW output near 3 mum from a 4m heavily erbium-doped ZBLAN double-clad fiber laser pumped by a collimated 100 W 975 nm laser diode array. The pump threshold of the fiber laser was about 1W, and the slope efficiency was 21.3%. The peak wavelength of free running was about 2708 nm at low pump power and moved to around 2785 nm at high pump power. Output of 9W was obtained when the launched pump power was 42.8W. The output, however, fluctuated intensively like a pulsed laser, and the operation broke down with optical damage of the pumping end facet when the pump was increased beyond 42.8 W. Therefore, alleviation of the operation fluctuation, heat management, and strengthening the pumping fiber are crucial considerations for the stable operation of 10-W-level mid-IR ZBLAN fiber lasers.

Journal Article↗

PubMed2006

Numerical analysis and experimental results of high-power Er/Pr:ZBLAN 2.7 microm fiber lasers with different pumping designs.

Gain factor and output performance of erbium-praseodymium codoped ZBLAN double-clad fiber lasers at 2.7 microm with different pumping designs were calculated and analyzed. Single-end backward pumping with a highly reflective mirror butted against one fiber end and dual-end pumping with Fresnel reflections from both fiber ends were found to be the most efficient pumping designs. Ten-watt-level Er/Pr:ZBLAN fiber lasers proved to be achievable with recent diode laser and ZBLAN fiber technologies. Their corresponding optimum fiber lengths for different pumping configurations were determined. It was also found that fiber lasers with a flat evolution of gain factor can obtain the largest output power. Experimental results of 4 m and 12 m fiber lasers showed very good agreement with simulation results.

Journal Article↗

PubMed2005

Coagulation of nanoparticles in reverse micellar systems: a Monte Carlo model.

The process of formation of nanoparticles obtained by mixing two micellized, aqueous solutions has been simulated using the Monte Carlo technique. The model includes the phenomena of finite nucleation, growth via intermicellar exchange, and coagulation of nanoparticles after their formation. Using the model, an exploratory study has been conducted to analyze whether the coagulation of nanoparticles is the reason for the formation of nanoparticles whose sizes are comparable to the size of the reverse micelles. The model explains the possible mechanism of coagulation of semiconductor nanoparticles formed within reverse micelles and its effect on the evolution of their size with time. The model is predictive in nature, and the simulation results compare well with those observed experimentally.

Journal Article↗

PubMed2004

MicroRNA-143 regulates adipocyte differentiation.

MicroRNAs (miRNAs) are endogenously expressed 20-24 nucleotide RNAs thought to repress protein translation through binding to a target mRNA (1-3). Only a few of the more than 250 predicted human miRNAs have been assigned any biological function. In an effort to uncover miRNAs important during adipocyte differentiation, antisense oligonucleotides (ASOs) targeting 86 human miRNAs were transfected into cultured human pre-adipocytes, and their ability to modulate adipocyte differentiation was evaluated. Expression of 254 miRNAs in differentiating adipocytes was also examined on a miRNA microarray. Here we report that the combination of expression data and functional assay results identified a role for miR-143 in adipocyte differentiation. miR-143 levels increased in differentiating adipocytes, and inhibition of miR-143 effectively inhibited adipocyte differentiation. In addition, protein levels of the proposed miR-143 target ERK5 (4) were higher in ASO-treated adipocytes. These results demonstrate that miR-143 is involved in adipocyte differentiation and may act through target gene ERK5.

Adipocytes↗

PubMed2004

Monte Carlo models for nanoparticle formation in two microemulsion systems.

The process of formation of nanoparticles obtained by mixing two micellized, aqueous solutions has been simulated using the Monte Carlo technique. The model includes the phenomena of finite reaction, nucleation, and growth via intermicellar exchange. This exploratory study examines the characteristic particle size distributions (PSDs) that result from using combinations of different initial reactant distributions (Poissonian and geometric) and different types of intermicellar exchange protocols (random, cooperative, and binomial). It is observed that the PSDs obtained using an initial Poissonian distribution of reactants and random exchange rules are similar to reported experimental results for CdS nanoparticles. The effect of exchange efficiency and reaction rate has also been studied. It is seen that a high exchange efficiency leads to relatively larger particle sizes. Also, a slow reaction rate has been shown to lead to the formation of larger nanoparticles.

Journal Article↗

PubMed2003

Horizontal gene transfer accelerates genome innovation and evolution.

Horizontal gene transfer (HGT) spreads genetic diversity by moving genes across species boundaries. By rapidly introducing newly evolved genes into existing genomes, HGT circumvents the slow step of ab initio gene creation and accelerates genome innovation. However, HGT can only affect organisms that readily exchange genes (exchange communities). In order to define exchange communities and understand the internal and external environmental factors that regulate HGT, we analyzed approximately 20,000 genes contained in eight free-living prokaryotic genomes. These analyses indicate that HGT occurs among organisms that share similar factors. The most significant are genome size, genome G/C composition, carbon utilization, and oxygen tolerance.

Archaea↗

PubMed2002

Horizontal gene transfer in microbial genome evolution.

Horizontal gene transfer is the collective name for processes that permit the exchange of DNA among organisms of different species. Only recently has it been recognized as a significant contribution to inter-organismal gene exchange. Traditionally, it was thought that microorganisms evolved clonally, passing genes from mother to daughter cells with little or no exchange of DNA among diverse species. Studies of microbial genomes, however, have shown that genomes contain genes that are closely related to a number of different prokaryotes, sometimes to phylogenetically very distantly related ones. (Doolittle et al., 1990, J. Mol. Evol. 31, 383-388; Karlin et al., 1997, J. Bacteriol. 179, 3899-3913; Karlin et al., 1998, Annu. Rev. Genet. 32, 185-225; Lawrence and Ochman, 1998, Proc. Natl. Acad. Sci. USA 95, 9413-9417; Rivera et al., 1998, Proc. Natl. Acad. Sci. USA 95, 6239-6244; Campbell, 2000, Theor. Popul. Biol. 57 71-77; Doolittle, 2000, Sci. Am. 282, 90-95; Ochman and Jones, 2000, Embo. J. 19, 6637-6643; Boucher et al. 2001, Curr. Opin., Microbiol. 4, 285-289; Wang et al., 2001, Mol. Biol. Evol. 18, 792-800). Whereas prokaryotic and eukaryotic evolution was once reconstructed from a single 16S ribosomal RNA (rRNA) gene, the analysis of complete genomes is beginning to yield a different picture of microbial evolution, one that is wrought with the lateral movement of genes across vast phylogenetic distances. (Lane et al., 1988, Methods Enzymol. 167, 138-144; Lake and Rivera, 1996, Proc. Natl. Acad. Sci. USA 91, 2880-2881; Lake et al., 1999, Science 283, 2027-2028).

Archaea↗