Watch the Special Story of this Surrogate mother

Tv Focus on Students Studying abroad

Watch the Bicycle that Costs Rs 2 lacs

Internet will die by 2010 ?...

Electronic Car XENO made by DVR College of Engineering , Hyderabad..

'స్వైన్‌ప్లూ' - కొత్త ఫ్లూ వ్యాధి

మెక్సికోలో బయటపడిన కొత్త ఫ్లూ వ్యాధి అంతకంతకూ తీవ్రమవడంతో ప్రపంచమంతా అప్రమత్తమైంది. కొద్దిరోజుల క్రితమే 'స్వైన్‌ప్లూ' వ్యాధి మెక్కికో, అమెరికా, ఫ్రాన్స్ దేశాల్లో ప్రబలింది. ఈ వ్యాధి కారణంగా మెక్సికోలో ఇప్పటివరకు వందమందికి పైగా మృత్యువాత పడ్డారని ప్రాథమిక సమాచారాన్ని బట్టి తెలుస్తోంది. జంతువులు, పశువుల వంటి క్షీరణాల ద్వారా ఇది మనుషులకు వ్యాపిస్తోంది. ఈ వ్యాధి చాలా ప్రమాదకరమని, మందులకు లొంగకుండా ఉండే స్థాయికి కూడా చేరగలదని ఐక్యరాజ్యసమితి ప్రకటించింది. ప్రపంచమంతా దీన్ని ఎదుర్కొనేందుకు సర్వ సన్నద్ధంగా ఉందని తెలిపింది. వ్యాధి నిరోధక మందులు అన్ని చోట్లకు పంపుతున్నామని కొన్ని విమానాశ్రయాల్లో కూడా వ్యాధి నిర్ధారణ పరీక్షలు జరుగుతున్నాయని సమితి తెలియజేసింది. ఈ 'స్వైన్‌ప్లూ' తొలిసారిగా థాయిలాండ్‌లో కనపించింది. ఇతర ప్లూ వ్యాధుల నివారణకు వాడే మందులు దీనిని అరికట్టలేవు. అంతర్జాతీయంగా ఈ ప్లూ పట్ల ప్రజారోగ్య వ్యవస్థ అప్రమత్తం కావాలని ప్రపంచ ఆరోగ్య సంస్థ పిలుపునిచ్చింది.

biotech jobs

Looking for science & biotech jobs/News? Access hundreds of thousands of jobs today in biotechnology,and general science fields.

Read the recent Research report about--
"Embryonic stem cells could help to overcome immune rejection problems"
http://www.bharatcareers.com/jobsearch/viewjob.asp?jobid=100016932

MITOCHONDRIAL DNA MUTATIONS CAN CAUSE DEGENERATIVE HEART AND MUSCLE DISEASE

Mitochondrial DNA mutations can cause degenerative heart and muscle disease :

IRVINE — A single change in the DNA of mitochondria – the cellular power plants that generate energy in all human cells – has been found to cause degenerative heart and muscle disease, according to University of California, Irvine researchers.

The study provides new insights into age-related disease and further proof that the mitochondria play a central role in human health. Study results appear in the Feb. 15 issue of Science. (For more about mitochondria, see below.)

Douglas Wallace, director of the Center for Molecular and Mitochondrial Medicine and Genetics at UC Irvine and study leader, says the findings also address a core dilemma facing efforts to cure and treat inherited degenerative diseases, including chronic heart and muscle disease.

“While these diseases traditionally have been assumed to result from mutations in the genes encoded by DNA in the cell’s nucleus,” he said, “most common degenerative diseases frequently do not exhibit inheritance patterns wholly consistent with our understanding of these nuclear DNA genetics. Our demonstration that mutations in the mitochondrial DNA can also cause the same diseases means that both nuclear and mitochondrial DNA genes that affect mitochondrial function can contribute to disease risk.”

A complete understanding of the importance of mitochondrial defects caused by either mitochondrial or nuclear DNA mutations could lead to treatments effective for age-related diseases that affect millions worldwide, Wallace added.

To prove the importance of mitochondrial DNA mutations for health, the UC Irvine researchers generated a relatively mild mitochondrial DNA mutation in mouse cells, which reduced a key enzyme of mitochondrial energy production by 50 percent.

They then used female mouse embryonic stem cells to create mice in which this mitochondrial DNA energy deficiency mutation was inherited through the female germ line, which is the reproductive cells and other genetic material passed to offspring. Mice harboring the mutant mitochondrial DNA appeared normal early in life, but by one year they developed marked muscle and heart disease, similar to disease that can develop in humans.

“Consequently, mitochondrial DNA mutations and their related energy defects are sufficient to cause age-related disease,” said Wallace, the Donald Bren Professor of Biological Sciences and Molecular Medicine and a National Academy of Sciences member. “Therefore, mitochondrial energy deficiency may be a common factor in these diseases.”

Weiwei Fan, Katrina Waymire, Navneet Narula, Peng Li, Christophe Rocher, Pinar Coskun, Mani Vannan, Jaget Narula and Grant MacGregor of UC Irvine also participated in this study, which is supported by the National Institutes of Health and the California Institute of Regenerative Medicine.

About mitochondria: Mitochondria exist in all human cells and have their own DNA. They generate energy by burning the calories that we eat with the oxygen that we breathe, much like a coal-burning power plant. In addition to energy, mitochondrial combustion generates “smoke” in the form of oxygen radicals. These oxygen radicals damage the mitochondrial DNA giving it a very high mutation rate, both in the tissues of our bodies and also in the cells of the female germ line.

Since the mitochondrial DNA is outside of the cell’s nucleus and not associated with its DNA, it is inherited exclusively from the mother and is present in thousands of copies per cell.

As the mitochondrial DNA of our cells accumulates damage with age, the blueprints required to sustain energy production are lost, the body’s equivalent of a brownout. The resulting age-related decline in cellular energy production ultimately leads to tissue and organ failure and the development of clinical disease or illness. Thus the accumulation of mtDNA damage may explain aging and the delayed-onset and progressive course of age-related diseases and aging.

SCIENCE VIDEOS

Signal transduction

http://bioisolutions.blogspot.com/2008/01/signal-transduction.html



Allergy

http://bioisolutions.blogspot.com/2008/01/allergy.html 29 Jan Julian
mRNA Splicing:

http://bioisolutions.blogspot.com/2008/01/mrna-splicing-splicing.html



Lac Operon:

http://bioisolutions.blogspot.com/2008/01/lac-operon.html

Intracellular Infection by Salmonella:

http://bioisolutions.blogspot.com/2008/01/intracellular-infection-by-salmonella.html

Apoptosis:

http://bioisolutions.blogspot.com/2008/01/apoptosis.html

GENETICS AND BREAST CANCER

WHAT IS GENETIC - IDEA ABOUT GENETICS:
http://www.geocities.com/dnafacts/

http://www.geocities.com/sciencejmc/

GLOBAL RISE IN BREAST CANCER IS DUE TO WESTERN LIFESTYLES:
Of all the exports from our modern world, breast cancer ranks as among the most dubious. Once thought to be a disease of the rich, it is now a global epidemic. The rise of the cancer in Europe and America -- cases have jumped 80 percent in the UK since the 1970s -- is being mirrored across the world. And scientists say increasing prosperity and the "Westernization" of traditional lifestyles is to blame. A richer diet, smaller families, delayed childbearing and reduced breastfeeding have driven the increase in the West, together with rising obesity and increased alcohol consumption, specialists say. Now these trends are being seen everywhere -- with a growing burden of malignant disease in their wake. An estimated 1.3 million new cases were diagnosed around the world last year. It is the commonest cancer in the UK and across Europe, even though it affects almost only one gender. In 2006, it outranked lung cancer, which affects both sexes, for the first time.

In Japan, Singapore and Korea -- countries once renowned for their low rates -- cases have doubled or tripled in the past 40 years.

In China, urban cancer registries have recorded 20 to 30 percent increases in the past decade. India has seen similar rises and cases have doubled in parts of Africa. There are doubts, especially in Africa, about how far better recording has contributed to the apparent rise. But scientists agree that the disease is rampaging across the globe. However, they disagree about the best way to curb it. Some claim the best hope lies in developing a preventive drug -- a hormonal cocktail that would act like a vaccine and provide lifelong protection -- and criticize the world's failure to focus attention on it. Others demand political action, raising public awareness and galvanising governments to provide screening and early treatment that gives women the best chance of surviving. A third school of thought emphasises the need for a public health strategy to highlight the risks of alcohol, obesity and lack of exercise.

Peggy Porter, of the Fred Hutchinson Research Centre in Seattle, Wash., writing in the current New England Journal of Medicine, says the world must wake up to the growing threat."As more countries modernize, more women will enter an increasingly sedentary workforce, delay childbearing, exert control over their reproductive lives, live longer and eat a more Westernized diet. Their breast cancer rates will no doubt increase. It is crucial that women's awareness of their risk and their expectations of their government and the medical community regarding detection and treatment increase at a similar rate."

Professor Porter said the biggest barrier to improved care for women was ignorance. "In a lot of countries, women are still afraid to know. When Betty Ford [wife of US President Gerald Ford] admitted she had breast cancer in 1974, it changed the world. Women who had seen it as a death sentence became willing to talk about it, pushed for more care and more research. Other countries need to follow that lead."

Valerie Beral, head of the Cancer Research UK epidemiology unit at Oxford University, said that to blame Westernization was to miss the central cause -- changes in child-bearing.

"We don't need to seek subtle explanations when we know the main one. China has gone from the six-child family to the one-child family in a couple of generations. Most women in the past had six or seven children -- it was fairly standard across the world. Each child was breastfed for two to two-and-a-half years, which meant they stopped ovulating and didn't conceive. The hormonal changes that occur around child-bearing and during breastfeeding are protective for life."

We need to investigate the nature of this hormonal protection and synthesize it, she said. "If we could find out why child-bearing gives life-long protection against breast cancer we might develop a hormonal cocktail that could be given to women at age 18 for a year which would have the same effect. I am frustrated that this is not a research priority."

Peter Boyle, head of the International Agency for Cancer Research in Lyon, which will publish global cancer rates next month, said alcohol was the most worrying driver for younger women. "The rise is a huge problem and one which is growing enormously quickly. There are places which 30 years ago had very low rates where it is growing very rapidly. In every region it is the commonest or second most common cancer.

"My concern is over the rise in drinking, especially among young women. For each single unit of alcohol per day, the risk rises by 7 percent. It's the ladettes who hit the bars on a Friday night that I worry about."

Why Rates Have Risen

The rising breast cancer rates around the world are linked to increased exposure to the female hormone estrogen, because of changes in reproduction and diet.
Improved nutrition means girls reach puberty earlier and menopause later. A century ago, girls had their first periods at 16 and 17, but today it is more likely to be 12 to 13.
Each year that menopause is delayed increases the risk of contracting breast cancer by 3 percent.
Increased numbers of women going out to work has led to later births, smaller families and fewer women breastfeeding. Each year that childbirth is postponed beyond the mid-20s increases the breast cancer risk by 3 percent.
The more children a woman has, the lower her risk of breast cancer, so the trend towards smaller families has increased many women's exposure.
Breast cancer rates vary widely around the world. Japan has one fifth of the cases diagnosed in the U.S. However, Japanese women who move to the U.S. rapidly acquire the same risk as American women.
Breast cancer in the U.K. has risen by 84 percent since the 1970s. In 2005, 38,212 women were diagnosed with the disease.
Breast cancer is the commonest cancer in the UK even though it mostly affects one sex (there are a few hundred cases in men). Lung cancer, the next most common, which affects both sexes, was diagnosed in 30,997 men and women in 2005.

BT COMPANY AND BT NEWS

BT COMPANY AND DAILY NEWS ABOUT BT:
http://www.fiercebiotech.com/

RECOMBINANT DNA TECHNOLOGY

Recombinant DNA technology :

Here is how recombinant technology works:

Recombinant technology begins with the isolation of a gene of interest. The gene is then inserted into a vector and cloned. A vector is a piece of DNA that is capable of independent growth; commonly used vectors are bacterial plasmids and viral phages. The gene of interest (foreign DNA) is integrated into the plasmid or phage, and this is referred to as recombinant DNA.


Before introducing the vector containing the foreign DNA into host cells to express the protein, it must be cloned. Cloning is necessary to produce numerous copies of the DNA since the initial supply is inadequate to insert into host cells.


Once the vector is isolated in large quantities, it can be introduced into the desired host cells such as mammalian, yeast, or special bacterial cells. The host cells will then synthesize the foreign protein from the recombinant DNA. When the cells are grown in vast quantities, the foreign or recombinant protein can be isolated and purified in large amounts.

Other uses for recombinant DNA

Recombinant DNA technology is not only an important tool in scientific research, but it has also impacted the diagnosis and treatment of diseases and genetic disorders in many areas of medicine. It has enabled many advances, including:

Isolation of large quantities of pure protein
In addition to the follicle-stimulating hormone (FSH) used in Follistim® AQ Cartridge and Follistim® AQ Vial, insulin, growth hormone and other proteins are now available as recombinant products. Physicians no longer have to rely on biological products (e.g. urine-derived FSH), that don't possess the same level of purity and consistency of recombinant products to treat their patients.


Identification of mutations
People may be tested for the presence of mutated proteins that may be associated with breast cancer, retino-blastoma, and neurofibromatosis.


Diagnosis of affected and carrier states for hereditary diseases
Tests exist to determine if people are carriers of the cystic fibrosis gene, the Huntington’s disease gene, the Tay-Sachs disease gene, or the Duchenne muscular dystrophy gene.


Transferring of genes from one organism to another
People suffering from cystic fibrosis, rheumatoid arthritis, vascular disease, and certain cancers may now benefit from the progress made in gene therapy.


Mapping of human genes on chromosomes
Scientists are able to link mutations and disease states to specific sites on chromosomes.

GOOD SITE FOR TOTAL MOLECULAR BIOLOGY:

1.http://www.molecular-plant-biotechnology.info/recombinant-DNA-technology/recombinant-DNA-technology.htm
2.http://www.biology.arizona.edu/molecular_bio/problem_sets/Recombinant_DNA_Technology/recombinant_dna.html



RECOMBINANT DNA TECHNOLOGY:

Recombinant DNA Technology - In nature, gene transfers are rather imprecise, and their range, in tenns of species involved, is remarkably limited. The above problems are circumvented by the recombinant DNA technology. A recombinant DNA molecule is produced by joining together two or more DNA segments usually originating from different organisms.

More specifically, a recombinant DNA molecule is a vector into which the desired DNA fragment has been inserted to enable its cloning in an appropriate host. This is achieved by using specific enzymes for cutting the DNA (restriction enzymes) into suitable fragments and then for joining together the appropriate fragments (ligation).


In this manner, a gene may be produced, which contains the. coding region from one organism joined to regulatory sequences from another organism; such a gene is called chimaeric gene. Clearly, the capability to produce recombinant DNA molecules has given man the power and opportunity to create novel gene functions to suit specific needs.

Recombinant DNA molecules are produced with one of the following three objectives:

(1) to obtain a large number of copies of specific DNA fragments,

(2) to recover large quantities of the protein produced by the concerned gene, or

(3) to integrate the gene in question into the chromosome of a target organism where it expresses itself. Even for the latter two objectives, it is essential to first obtain a large number of copies of the concerned genes.

To achieve this, the DNA segments are integrated into a self-replicating DNA molecule called vector; most commonly used vectors are either bacterial plasmids or DNA viruses. All these steps concerned with piecing together DNA segments of diverse origin and placing them into a suitable vector together constitute recombinant DNA technology.

The DNA segment to be cloned is called DNA insert

Recombinant DNAs are introduced into a suitable organism, usually a bacterium; this organism is called host, while the process is called transformation. The transformed host cells are selected and cloned.

The recombinant DNA present in such clones would replicate either in synchrony with or independent of the host cell; the gene present in 'the vector mayor may not express itself, i.e., direct the synthesis of concerned polypeptide. The step concerned with transformation of a suitable host with recombinant DNA, and cloning of the transformed cells is called DNA cloning or gene cloning.

However, often DNA or gene cloning is taken to include both the development of recombinant DNAs as well as their cloning in a suitable host. Similarly, often the term recombinant DNA technology is used as a synonym for DNA or gene cloning used in the broader sense. A rather popular term for these activities is genetic engineering.

A clone consists of asexual progeny of a single individual or cell, while the process/technique of producing a clone is called cloning. As a result, all the individuals of a clone have the same genotype, which is also identical with that of the individual from which the clone was derived.

Therefore, the genomes present in members of a single clone are also identical; this applies to the recombinant DNA as well. Therefore, gene or DNA cloning produces large numbers of copies of the gene/DNA being cloned.

Recombinant DNA Technology in the Synthesis of Human Insulin :

http://www.littletree.com.au/dna.htm

http://present.smith.udel.edu/biotech/rDNA.html.

SOME IMPORTANT QUESTIONS AND ANSWERS:

http://biog-101-104.bio.cornell.edu/BIOG101_104/tutorials/recomb_DNA.html

r DNA TECHNOLOGY BASIC TOOLS :

http://www.sci-ed-ga.org/modules/dna/index.html

Recombinant DNA Technology for the 21st Century:


http://www.biochemsoctrans.org/bst/034/0313/0340313.pdf

YOUTUBE BEST VIDEO ON rDNA TECHNOLOGY:

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GOOD INFORMATION IN ALL FIELD

SOME GOOD INFORMATION IN THIS SITE:

http://bioisolutions.blogspot.com/

BIOLOGY VIDEOS

Biology videos
Angioplasty animation


http://bioisolutions.blogspot.com/2008/01/angioplasty.html


Electron Transport Chain

http://bioisolutions.blogspot.com/2008/01/electron-transport-chain.html



mRNA Splicing

http://bioisolutions.blogspot.com/2008/01/mrna-splicing-splicing.html


Lac Operon

http://bioisolutions.blogspot.com/2008/01/lac-operon.htm



Signal transduction

http://bioisolutions.blogspot.com/2008/01/signal-transduction.html




Computational Analysis of Biological Sequence

http://bioisolutions.blogspot.com/2008/01/computational-analysis-of-biological.html



Allergy

http://bioisolutions.blogspot.com/2008/01/allergy.html



Intracellular Infection by Salmonella

http://bioisolutions.blogspot.com/2008/01/intracellular-infection-by-salmonella.html



Angiogenesis

http://bioisolutions.blogspot.com/2008/01/angiogenesis.html

SAS,TRAINING AND PROJECTS

BIOMEDVACCINE :
SAS ,TRAININGS AND PROJECTS @DNA RESEARCH CENTRE :
DNA Research Centre and Axis group announces new batches for different Modules in Bioinformatics, Biotechnology, Molecular Biology, and Recombinant DNA Technology. DRC proudly announces its involvement in DNA Forensics and Biotechnology Research. We have updated all the projects available with us and providing more challenging, live and industrial projects with different module of training programmes. DRC are privileged members of ABLE, BCIL, FQS, USP Brazil, Bode Tech Lorton, U.S.A etc and dealing with the companies like Beta Genetics and Face key for a wide range of services.
DRC has been contacted by A.P govt. for a fingerprinting and data mining cum data basing project for stopping fraud of Ration cards and work is in progress. DRC has developed different range of Bioinformatics and Biotechnology projects, some of them include EST data basing for Fruit fly, Human genome project (Cell markers data basing) etc .
BASIC MODULE(30 Days)
CORE MODULE (45 days)
ELECTIVE MODULE (60 days)
ADVANCE MODULE (90 days)
FOUNDATION MODULE (180 days)
IMMUNOINFORMATICS
METABOLOMICS
PATTERN RECOGNITION IN BIOLOGY
PHARMACOINFORMATICS
MEDICAL AND CLINICAL INFORMATICS
CHEMIOINFORMATICS/CHEMICAL INFORMATICS
SAS Clinical Trials/Proteomics/ Genomics etc
WET LABS @ DNA RESEARCH CENTRE
Microbial Biotechnology
Recombinat DNA Technology
Enzymology
Immunotechnology
Plant Tissue Culture
culture media:
Industrial Microbiology
Clinical Microbiology
Microbial Biotechnology

All the listed trainings except the wetlab Practicals are available via Online Mode via our web based facilities.
*Courses for one week and 20days are available, for details email or call us.
Note: Registration open till June 2008 batches.

Administrative office:

DNA Research Centre
12-13-1249, 1st floor
Besdies Andhra Bank
Tarnaka -500017
Hyderabad (India)

LAB Address:

DNA Research Centre
12-8-259/1
Near Aaiyappa Temple
Mettuguda Hyderabad-500017
dnaresearchcentre@gmail.com
www.dnares.in
Phone: +91-40-40180502/9247438983

NATURE REVIEWS OF MOLECULAR CELL BIOLOGY FROM 2000 TO 2006

Nature reviewhttp://rapidshare.com/files/34156458/NatRevMCB2000to2006.part1.rar

links of the Nature Reviews Molecular Cell Biology from 2000 (1st issue) to Dec. 2006.

http://rapidshare.com/files/34156483/NatRevMCB2000to2006.part2.rarhttp://rapidshare.com/files/34156406/NatRevMCB2000to2006.part3.rarhttp://rapidshare.com/files/34156398/NatRevMCB2000to2006.part4.rarhttp://rapidshare.com/files/34156424/NatRevMCB2000to2006.part5.rarhttp://rapidshare.com/files/34156496/NatRevMCB2000to2006.part6.rar
http://rapidshare.com/files/34156450/NatRevMCB2000to2006.part7.rar You have to download all parts 1 to 5 then type the password to extract the files fromthe link(Click here to get password) since all links are more than 100 MB (6 year collection) so it will take longgggg time to download all links, so beeeee patient while downloading.

CLONING WRONG OR RIGHT- THE PRESENT ISSUE

WHAT IS CLONING:http://learn.genetics.utah.edu/units/cloning/whatiscloning/

SMALL FOCUS ON CLONING:http://learn.genetics.utah.edu/units/cloning/

CLONING SHEET HUMAN GENOME PROJECT INFORMATION:http://www.ornl.gov/sci/techresources/Human_Genome/elsi/cloning.shtml

SCIENCE DAILY NEWS ON CLONING:http://www.sciencedaily.com/news/plants_animals/cloning/

CLONING AND STEM CELLS:http://www.liebertpub.com/publication.aspx?pub_id=9

CLONING RIGHT OR WRONG:http://www.vuhs.org/apbio/clone/

COMPANIES INVOLVED IN CLONING:

1. Advanced Cell Technologies (ACT).One Innovation Drive, Biotech Three, Worcester, MA

2. L'Alliance Boviteq (LAB) 1425, grand rang Saint-Fran ois,

3.Genetic Savings and Clone 3312 Longmire Dr., College Station, TX

4.Geron Corporation Menlo Park, CA5.Infigen 182

5 Infinity Drive, DeForest, WI

6.Lazaron BioTechnologies LLC. Louisiana Business & Technology Center, South Stadium Drive, Baton Rouge LA

7.Nexia Biotechnologies 21,025 Trans-Canada Highway Ste. Anne de Bellevue, QC H9X 3R2, Canada

8.PPL Therapeutics Scotland,U.K.

9.ProBio Level 50 120 Collins Street Melbourne Victoria 3000, Australia.

10.The Roslin Institute Scotland, U.K

SOME LINKS RELATED TO CLONING:

EMBRYO CLONING:http://www.religioustolerance.org/cloning.htm

HUMAN CLONING:http://www.arhp.org/patienteducation/onlinebrochures/cloning/index.cfm?ID=282

CLONING OVERVIEW ;http://library.thinkquest.org/24355/

CVM AND ANIMAL CLONING:http://www.fda.gov/cvm/cloning.htm

WHEN CLONE WAS WRONG SEE WHAT WILL HAPPENED:http://www.dnaco.net/~vogelke/pictures/when-cloning-goes-wrong/

ANIMAL CLONING AND HOW DOLLY WAS CLONED:http://www.rds-online.org.uk/pages/page.asp?i_ToolbarID=5&i_PageID=162

cloning of dolly full detail:http://www.synapses.co.uk/science/clone.html

DOLLY THE SHEEP:http://www.nms.ac.uk/dollythesheep_1.aspx

CLONING AFTER DOLLY:http://www.cis.org.uk/resources/articles/article_archive/burke_cloning.htm

GOOD BYE, DOLLY FIRST CLONED SHEEP DIED:http://www.avma.org/onlnews/javma/apr03/030415f.asp

DOLLY IN EDINBURGH:http://www.24hourmuseum.org.uk/nwh_gfx_en/ART15679.html

PLS UR VOTE 4 HUMAN CLONING IS CORRECT OR NOT SEND COMMENTS

BIOTECH REVOLUTION COMING SOON

BIOTECH- A GENOMIC GATE WAY:http://www.brad.ac.uk/acad/sbtwc/gateway/OVERVIEW/Overview.htm

biotech revolution from 1970 to now:http://www.abc.net.au/science/features/biotech/

the myth of bt revolution:http://www.esrc.ac.uk/ESRCInfoCentre/about/CI/CP/Social_Sciences/issue59/myth_biotech.aspx?ComponentId=7540&SourcePageId=7573

bt in ireland revolution:http://www.esrc.ac.uk/ESRCInfoCentre/about/CI/CP/Social_Sciences/issue59/myth_biotech.aspx?ComponentId=7540&SourcePageId=7573

THE MYTH OF BT REVOLUTION:http://www.york.ac.uk/res/iht/projects/l218252087/mythofbiotechrevolution.pdf

DESIGN A GENE:http://freespace.virgin.net/diri.gini/designer.htm

BIOTECH COMPANY IN PUNE

BIOTECH COMPANY SINGAPORE BASED;
http://www.scigenltd.com/about_manufacturing.htm

BIOTECH COMPANIES

TOP TEN COMPANIES AND THEIR PROFILE - http://btmanagement.blogspot.com/
BIOTECH COMPANIES IN PUNE:http://sawratepssk-manohar.blogspot.com/2008/01/biotech-companies-in-pune-india.htmlhttp://decresume.blogspot.com/
BIOTECH COMPANIES: http://decresume.blogspot.com/
BIOTECH POSITION AND COMPANIES:http://biotechindustriesindia.blogspot.com/
BIOTECH COMPANIES IN INDIA:http://fiona-individuality.blogspot.com/
What is the scope of MSc in medical microbiology in India? :
http://medicalmsc.blogspot.com/
WHAT IS THE BT AND ITS POSITION IN INDIA;http://india-biotech.blogspot.com/
SOME BT COMPANIES AND MISTAKES OF JOB SEEKERS:http://biotechnology2020.blogspot.com/
LIST OF INDUSTRIES IN THE FIELD OF BT AND PHARMA:http://b4biojobs.blogspot.com/2007/08/biotech-companies.html