Sunday, November 25, 2007
HHMI Janelia Farm Graduate Program
The Howard Hughes Medical Institute offers two programs leading to the Ph.D. based at its Janelia Farm Research Campus, in partnership with the universities of Cambridge and Chicago. These accelerated programs are designed for a small number of well-prepared, highly committed, and gifted students. We offer opportunities for interdisciplinary research in an intense environment.
Most students spend one year at their chosen partner institution followed by three years of research work at Janelia Farm. If you join the program you will have two mentors: one at Janelia Farm and one at the partner university. You will fulfill all the academic requirements of your chosen partner university and your Ph.D. thesis will be examined there.
HOW TO APPLY:
Our application process is unconventional. We do ask for the usual academic and biographical information and reference letters. However, in addition we will ask you to nominate one (or more) Janelia Farm lab heads to be your mentor (and also one or more at the partner university, if you wish). We then ask you to write a short research proposal targeted to that person's lab. This proposal will be a very significant factor in our admission decisions. During the interview you will be asked to explain this proposal.
The seventeen Janelia Farm lab heads who are interested in recruiting a student are:
Albert Lee | ||
Anthony Leonardo | ||
All applicants must submit their materials via our web site. You will find more detailed application instructions at the application site.
DEADLINES:
We will review completed applications (including the reference letters) for the Fall 2008 class as they are received. The deadlines for submitting competed applications are:
University of Chicago: December 31, 2007
University of Cambridge: April 1, 200
Apply hereGRADUATE PROGRAM SUPPORT:
You will be fully supported financially while participating in the Janelia Farm graduate program, so long as you remain in good standing academically and are deemed by your committee to be making satisfactory progress.
While in the United States (Janelia or Chicago):
Currently $30,000 per year
Health insurance, plus other benefits
While at the University of Cambridge:
$30,000 per year (paid in UK pounds)
Health care provided by the National Health Service
INTERNATIONAL STUDENT VISAS:
If you are coming to Janelia from outside of the United States, you are responsible for determining if a visa is required and to apply through your local embassy or consulate. We will sponsor visas for participants to enter the United States, as appropriate and as permitted.
In recent years, this process has become quite slow in some countries, taking up to several months. Therefore, we suggest that you apply for your visa as soon as possible after admission.
Source: HHMIThursday, November 22, 2007
Stem Cell Studies Won't Sway Big Pharma
Stem cell breakthroughs too early-stage to shake-up venture capital investing from Big Pharma, analysts say.
NEW YORK (CNNMoney.com) -- The recent breakthroughs in stem cell research, where adult cells were "reprogrammed" to act like embryonic stem cells, are too early-stage to have much influence on Big Pharma's venture capital investments, experts say."[The new studies] are really early-stage so I don't think it's really changing the landscape," said Eun Yang, biotech analyst for Jefferies & Co. "I doubt that it's going to chase away a lot of the Big Pharma money. But I'm not sure that people are going to start pouring money into this venture."
Two separate teams of researchers, one from the University of Wisconsin in Madison and the other from Kyoto University in Japan, said on Tuesday that they discovered how to reprogram adult cells to mimic the activity of embryonic stem cells.
If this new technology continues to work in later-stage studies, it could theoretically sidestep the controversial use of human embryonic stem cells, which have attracted the ire of the pro-life lobby. In 2001, President Bush limited federal funding for human embryonic stem cell research to only those lines that existed at the time, and in June of 2007 he vetoed a Congressional effort to lift these restrictions.
Biotech stocks were volatile in Tuesday trading, after the researchers published their findings in Science and Cell. The stock for Geron Corp., (Charts) the only publicly-traded company that works with human embryonic stem cells, dropped 6 percent. But stock activity was mixed among those biotechs that use stem cells from adult human tissue: Cytori Therapeutics' (Charts) stock went up;Osiris Therapeutics (Charts) and Stemcells Inc. (Charts) went down.
But this stock reaction isn't going to mirror the activities of Big Pharma venture capital investors, analysts say. So far, Novocell Inc., a privately-held biotech specializing in human embryonic stem cells, is one of the biggest recipients of venture capital investment, to the tune of $25 million from Johnson & Johnson (Charts, Fortune 500) in July.
"[Novocell] would make an interesting acquisition target if J&J wanted to rapidly enter the sector," said Dr. Cathy Prescott, director of the biotech consulting company Biolatris, in an email to CNNMoney.com. "[If Novocell's experiments] make good progress in the clinic then I would predict that the company would be able to raise future capital."
Source: Aaron Smith, CNNMoney.comResearchers Turn Skin Cells Into Stem Cells
The work builds on a study published last year by Shinya Yamanaka of Kyoto University in Japan, which showed that mouse tail cells could be transformed into ES-like cells by inserting four genes (ScienceNOW, 3 July 2006). Those genes are normally switched off after embryonic cells differentiate into the various cell types. In June this year, Yamanaka and another group reported that the cells were truly pluripotent, meaning that they had the potential to grow into any tissue in the body (ScienceNOW, 6 June).
Now the race to repeat the feat in human cells has ended in a tie: Two groups report today that they have reprogrammed human skin cells into so-called induced pluripotent cells (iPSs). In a paper published online in Cell, Yamanaka and his colleagues show that their mouse technique works with human cells as well. And in a paper published online in Science, James Thomson of the University of Wisconsin, Madison, and his colleagues report success in reprogramming human cells, again by inserting just four genes, two of which are different from those Yamanaka uses.
In the new work, Yamanaka and his colleagues used a retrovirus to ferry into adult cells the same four genes they had previously used to reprogram mouse cells: OCT3/4, SOX2, KLF4, and c-MYC. They reprogrammed cells taken from the facial skin of a 36-year-old woman and from connective tissue from a 69-year-old man. Roughly one iPS cell line was produced for every 5000 cells the researchers treated using the technique, an efficiency that enabled them to produce several cell lines from each experiment.
Thomson's team started from scratch, identifying its own list of 14 candidate reprogramming genes. Like Yamanaka's group, the team used a systematic process of elimination to identify four factors: OCT3 and SOX2, as Yamanaka used, and two different genes, NANOG and LIN28. The group reprogrammed cells from fetal skin and from the foreskin of a newborn boy. The researchers were able to transform about one in 10,000 cells, less than Yamanaka's technique achieved, Thomson says, but still enough to create several cell lines from a single experiment.
Although promising, both techniques share a downside. The retroviruses used to insert the genes could cause tumors in tissues grown from the cells. The crucial next step, everyone agrees, is to find a way to reprogram cells by switching on the genes rather than inserting new copies. The field is moving quickly toward that goal, says stem cell researcher Douglas Melton of Harvard University. "It is not hard to imagine a time when you could add small molecules that would tickle the same networks as these genes" and produce reprogrammed cells without genetic alterations, he says.
Once the kinks are worked out, "the whole field is going to completely change," says stem cell researcher Jose Cibelli of Michigan State University in East Lansing. "People working on ethics will have to find something new to worry about."
Source: By Gretchen Vogel ScienceNOW Daily News 20 November 2007
Saturday, November 10, 2007
Why should we pursue an advanced degree?
I cited a report from wikipedia, which shows strong association between salary levels and education attainment. Overall, advanced degrees offer significant advantages for household incomes.
Household income as well as per capita income in the United States rise significantly as the educational attainment increases. In 2005 graduates with a Master's in Business Administration (MBA) who accepted job offers are expected to earn a base salary of $88,626. They are also expected to receive "…[a]n average signing bonus of $17,428." According to the US Census Bureau persons with doctorates in the United States had an average income of roughly $81,400. The average for an advanced degree was $72,824 with men averaging $90,761 and women averaging $50,756 annually. Year-round full-time workers with a professional degree had an average income of $109,600 while those with a Master's degree had an average income of $62,300. Overall "…[a]verage earnings ranged from $18,900 for high school dropouts to $25,900 for high school graduates, $45,400 for college graduates and $99,300 for workers with professional degrees (M.D., D.O., J.D., D.D.S., or D.V.M.).
For full text, click here.
Thursday, November 8, 2007
Phoenix Lights was an alien spacecraft, former AZ Gov. says
Sunday, November 4, 2007
Journal Impact Factors 2006 Contiues: 201- 500
Journal Title | IF |
HUM REPROD UPDATE | 6.793 |
ADV FUNCT MATER | 6.779 |
MOL CELL BIOL | 6.773 |
MOL BIOL EVOL | 6.726 |
FASEB J | 6.721 |
AUTOPHAGY | 6.708 |
CHEM BIOL | 6.677 |
J BONE MINER RES | 6.635 |
TRAFFIC | 6.612 |
CRIT CARE MED | 6.599 |
ONCOGENE | 6.582 |
PLANT J | 6.565 |
AM J CLIN NUTR | 6.562 |
MOL BIOL CELL | 6.562 |
J CELL MOL MED | 6.555 |
HUM MUTAT | 6.473 |
J CELL SCI | 6.427 |
PROG NUCL MAG RES SP | 6.417 |
CEREB CORTEX | 6.368 |
REV MED VIROL | 6.347 |
NUCLEIC ACIDS RES | 6.317 |
J IMMUNOL | 6.293 |
AGING CELL | 6.276 |
PHYSIOLOGY | 6.268 |
ANNU REV NUCL PART S | 6.214 |
CLIN INFECT DIS | 6.186 |
CLIN CANCER RES | 6.177 |
J COSMOL ASTROPART P | 6.175 |
LEUKEMIA | 6.146 |
CRIT REV CL LAB SCI | 6.138 |
PLANT PHYSIOL | 6.125 |
ASTROPHYS J | 6.119 |
CANCER METAST REV | 6.115 |
INT J COMPUT VISION | 6.085 |
J HEPATOL | 6.073 |
THORAX | 6.064 |
PLOS PATHOG | 6.056 |
CEPHALALGIA | 6.049 |
INT REV PHYS CHEM | 6.036 |
GOLD BULL | 6.029 |
SMALL | 6.024 |
HYPERTENSION | 6.007 |
CRIT REV ORAL BIOL M | 6 |
INT REV CYTOL | 5.988 |
PROG SURF SCI | 5.968 |
BIOESSAYS | 5.965 |
Q REV BIOL | 5.944 |
AM J PATHOL | 5.917 |
NEUROPSYCHOPHARMACOL | 5.889 |
SEMIN RADIAT ONCOL | 5.889 |
ATHEROSCLEROSIS SUPP | 5.875 |
DNA REPAIR | 5.868 |
TRENDS MOL MED | 5.864 |
ENVIRON HEALTH PERSP | 5.861 |
MOL THER | 5.841 |
PHYS TODAY | 5.839 |
CARDIOVASC RES | 5.826 |
LAB CHIP | 5.821 |
J BIOL CHEM | 5.808 |
J CLIN ENDOCR METAB | 5.799 |
ANN RHEUM DIS | 5.767 |
CURR DRUG METAB | 5.762 |
J PATHOL | 5.759 |
BLOOD REV | 5.756 |
DRUG METAB REV | 5.754 |
STRUCTURE | 5.738 |
PROTEOMICS | 5.735 |
NEUROSCIENTIST | 5.71 |
NEUROLOGY | 5.69 |
CURR OPIN LIPIDOL | 5.689 |
ADV PROTEIN CHEM | 5.685 |
PROG BIOPHYS MOL BIO | 5.684 |
CURR CANCER DRUG TAR | 5.677 |
MRS BULL | 5.671 |
ANAL CHEM | 5.646 |
MOL MICROBIOL | 5.634 |
AIDS | 5.632 |
REV PHYSIOL BIOCH P | 5.625 |
AM J GASTROENTEROL | 5.608 |
NEUROBIOL AGING | 5.599 |
BRAIN RES REV | 5.595 |
MOL INTERV | 5.595 |
BIOL REV | 5.565 |
NEUROIMAGE | 5.559 |
J CLIN PSYCHIAT | 5.533 |
PROG NUCLEIC ACID RE | 5.529 |
CLIN CHEM | 5.454 |
FREE RADICAL BIO MED | 5.44 |
BRIT J PSYCHIAT | 5.436 |
BIOSCIENCE | 5.424 |
J HIGH ENERGY PHYS | 5.393 |
PHARMACOGENET GENOM | 5.391 |
STROKE | 5.391 |
INT MATER REV | 5.382 |
CARCINOGENESIS | 5.366 |
NAT CLIN PRACT ONCOL | 5.364 |
J INFECT DIS | 5.363 |
J VIROL | 5.341 |
ALLERGY | 5.334 |
SEMIN LIVER DIS | 5.302 |
HEALTH TECHNOL ASSES | 5.29 |
BRAIN PATHOL | 5.274 |
CURR PHARM DESIGN | 5.27 |
DRUG RESIST UPDATE | 5.268 |
RADIOLOGY | 5.251 |
DIABETOLOGIA | 5.247 |
AM J EPIDEMIOL | 5.241 |
NEWS PHYSIOL SCI | 5.241 |
ENDOCRINOLOGY | 5.236 |
CURR OPIN NEUROL | 5.229 |
GENET EPIDEMIOL | 5.226 |
CURR MED CHEM | 5.207 |
ONCOLOGIST | 5.206 |
ARCH NEUROL-CHICAGO | 5.204 |
CURR OPIN HEMATOL | 5.202 |
NUCL PHYS B | 5.199 |
J COGNITIVE NEUROSCI | 5.197 |
BIOMATERIALS | 5.196 |
INT J NEUROPSYCHOPH | 5.184 |
ANN ONCOL | 5.179 |
MEDICINE | 5.167 |
J MOL MED-JMM | 5.157 |
J PROTEOME RES | 5.151 |
J THROMB HAEMOST | 5.138 |
MOL CANCER THER | 5.137 |
SLEEP | 5.126 |
J MED CHEM | 5.115 |
RNA | 5.111 |
CHEM MATER | 5.104 |
LEARN MEMORY | 5.099 |
EMERG INFECT DIS | 5.094 |
J MED GENET | 5.087 |
SLEEP MED REV | 5.083 |
EUR RESPIR J | 5.076 |
CELL MICROBIOL | 5.07 |
TRAC-TREND ANAL CHEM | 5.068 |
ACM T INFORM SYST | 5.059 |
MON NOT R ASTRON SOC | 5.057 |
PHYS LETT B | 5.043 |
HAEMATOL-HEMATOL J | 5.032 |
B WORLD HEALTH ORGAN | 5.029 |
CHEM-EUR J | 5.015 |
GLIA | 5.013 |
PEDIATRICS | 5.012 |
ADV APPL MECH | 5 |
CRIT REV THER DRUG | 5 |
J NUCL MED | 4.986 |
ANTIVIR THER | 4.982 |
MOL ENDOCRINOL | 4.967 |
NEURO-ONCOLOGY | 4.939 |
ADV IMMUNOL | 4.935 |
PLOS COMPUT BIOL | 4.914 |
NEOPLASIA | 4.913 |
TRENDS PARASITOL | 4.907 |
PHYS REV D | 4.896 |
BIOINFORMATICS | 4.894 |
DEV BIOL | 4.893 |
J COMPUT CHEM | 4.893 |
J MOL BIOL | 4.89 |
HUM BRAIN MAPP | 4.888 |
CELL SIGNAL | 4.887 |
ESSAYS BIOCHEM | 4.885 |
J MOL CELL CARDIOL | 4.859 |
ASTRON J | 4.854 |
CURR MOL MED | 4.85 |
EUR UROL | 4.85 |
PSYCHONEUROENDOCRINO | 4.85 |
J CEREBR BLOOD F MET | 4.843 |
FRONT ECOL ENVIRON | 4.842 |
PAIN | 4.836 |
ADV PARASIT | 4.826 |
GASTROINTEST ENDOSC | 4.825 |
MOL ECOL | 4.825 |
PFLUG ARCH EUR J PHY | 4.807 |
CURR OPIN RHEUMATOL | 4.805 |
INT J BIOCHEM CELL B | 4.804 |
CURR OPIN INFECT DIS | 4.795 |
TOP CURR CHEM | 4.789 |
ECOLOGY | 4.782 |
GENE THER | 4.782 |
KIDNEY INT | 4.773 |
EUR J IMMUNOL | 4.772 |
MOL IMMUNOL | 4.768 |
J AM ACAD CHILD PSY | 4.767 |
ENDOCR-RELAT CANCER | 4.763 |
ADV SYNTH CATAL | 4.762 |
MOL CANCER RES | 4.759 |
BIOPHYS J | 4.757 |
SPRINGER SEMIN IMMUN | 4.754 |
ARCH DIS CHILD-FETAL | 4.734 |
FARADAY DISCUSS | 4.731 |
MIS QUART | 4.731 |
J INTERN MED | 4.73 |
TRENDS CARDIOVAS MED | 4.724 |
TOXICOL APPL PHARM | 4.722 |
INT J CANCER | 4.693 |
J GEN PHYSIOL | 4.685 |
J SEX MED | 4.676 |
BREAST CANCER RES TR | 4.671 |
AM NAT | 4.66 |
ORG LETT | 4.659 |
CELL MOL LIFE SCI | 4.655 |
J BIOL RHYTHM | 4.633 |
CURR OPIN COLLOID IN | 4.63 |
ENVIRON MICROBIOL | 4.63 |
LIVER TRANSPLANT | 4.629 |
MOL CELL NEUROSCI | 4.607 |
CURR TOP MICROBIOL | 4.606 |
ANN MED | 4.594 |
AM J RESP CELL MOL | 4.593 |
CANCER | 4.582 |
PHILOS T R SOC B | 4.579 |
J LEUKOCYTE BIOL | 4.572 |
J CLIN PSYCHOPHARM | 4.561 |
J INVEST DERMATOL | 4.535 |
GENES IMMUN | 4.533 |
J CATAL | 4.533 |
J APPL ECOL | 4.527 |
AGEING RES REV | 4.526 |
CHEM COMMUN | 4.521 |
AM J MED | 4.518 |
INT J EPIDEMIOL | 4.517 |
HUM GENE THER | 4.514 |
J IMMUNOTHER | 4.508 |
CRIT REV SOLID STATE | 4.5 |
PROG QUANT ELECTRON | 4.5 |
BRIT J HAEMATOL | 4.498 |
CELL PROLIFERAT | 4.492 |
ANTIOXID REDOX SIGN | 4.491 |
CRIT REV ONCOL HEMAT | 4.49 |
CURR ISSUES MOL BIOL | 4.481 |
SEMIN NUCL MED | 4.473 |
DRUGS | 4.472 |
MOL PHARMACOL | 4.469 |
AM J MED GENET B | 4.463 |
INT J RADIAT ONCOL | 4.463 |
BRIT J CANCER | 4.459 |
BMC EVOL BIOL | 4.455 |
LAB INVEST | 4.453 |
J PHYSIOL-LONDON | 4.407 |
INTENS CARE MED | 4.406 |
SOFT MATTER | 4.391 |
INT J NONLINEAR SCI | 4.386 |
GENES BRAIN BEHAV | 4.385 |
J NEUROPATH EXP NEUR | 4.371 |
CANCER TREAT REV | 4.37 |
ATMOS CHEM PHYS | 4.362 |
J LIPID RES | 4.357 |
SCHIZOPHRENIA BULL | 4.352 |
CRYST GROWTH DES | 4.339 |
EPIDEMIOLOGY | 4.339 |
GLOBAL CHANGE BIOL | 4.339 |
AM J PHYSIOL-CELL PH | 4.334 |
PROG ENERG COMBUST | 4.333 |
PSYCHOTHER PSYCHOSOM | 4.333 |
CURR OPIN DRUG DISC | 4.319 |
CANCER IMMUNOL IMMUN | 4.313 |
IEEE T PATTERN ANAL | 4.306 |
BIOL CELL | 4.303 |
EVOLUTION | 4.292 |
CANCER EPIDEM BIOMAR | 4.289 |
J MATER CHEM | 4.287 |
ADV POLYM SCI | 4.284 |
MACROMOLECULES | 4.277 |
CURR DRUG TARGETS | 4.274 |
CLADISTICS | 4.27 |
SCHIZOPHR RES | 4.264 |
J NEUROCHEM | 4.26 |
FISH FISH | 4.257 |
AM J PHYSIOL-LUNG C | 4.25 |
NEUROGENETICS | 4.25 |
NEW PHYTOL | 4.245 |
GENETICS | 4.242 |
J ECOL | 4.239 |
BBA-BIOENERGETICS | 4.237 |
HIPPOCAMPUS | 4.232 |
J PINEAL RES | 4.228 |
SEMIN HEMATOL | 4.213 |
CNS DRUGS | 4.21 |
J NEUROBIOL | 4.209 |
ANESTHESIOLOGY | 4.207 |
AM J PHYSIOL-RENAL | 4.199 |
GREEN CHEM | 4.192 |
CANCER GENE THER | 4.187 |
AM J MED GENET C | 4.169 |
CURR TOP MED CHEM | 4.167 |
EUR J CANCER | 4.167 |
BREAST CANCER RES | 4.157 |
EXP NEUROL | 4.156 |
ANTIMICROB AGENTS CH | 4.153 |
AM J SURG PATHOL | 4.144 |
CURR OPIN NEPHROL HY | 4.137 |
PLANT CELL ENVIRON | 4.135 |
BIOSENS BIOELECTRON | 4.132 |
ACM COMPUT SURV | 4.13 |
NEUROBIOL DIS | 4.128 |
AM J PHYSIOL-ENDOC M | 4.123 |
CELL CALCIUM | 4.118 |
CLIN PHARMACOKINET | 4.115 |
J PHYS CHEM B | 4.115 |
Thursday, November 1, 2007
NIH Research Funding: Realities
Many scientists are dismayed that it is more difficult to get funded today than it was before the NIH budget doubled in 1990s. What can explain this apparent paradox? The core reason is the increase in the number of new applications and applicants for NIH grants (see above figure). In 1998, NIH received 24,151 applications for new and competing research project grants; NIH expects to receive over 46,000 in 2006 and over 49,000 in 2007. The doubling in the demand for grants is primarily due to a large increase in the number of new scientists applying for grants. In 1998, there were about 19,000 scientists applying for competing awards. In 2006, NIH expects to receive applications from approximately 34,000 scientists and forecasts that over 36,000 scientists will apply in 2007.
The principal cause of this remarkable growth in grant demand is the unprecedented expansion of research capacity across the country that began in 1999. Stimulated by successive administrations' and Congress's calling for more research on emerging health issues, academic institutions responded. Increased demand, inflation effects, and flat budgets are the main drivers of today's challenges.
Source: "NIH in the Post-Doubling Era: Realities and Strategies" Science. 2006 Nov 17; 314(5802):1088-90.
A Lost Generation
- Over the past generation, the age at which American biomedical researchers with PhD degrees succeed in obtaining their first R01 award from the National Institutes of Health (NIH) has increased from 34.2 to 41.7 years of age.
- As time goes on, ever-larger proportions of NIH funds are diverted to funding research collaboratives of various sizes to the detriment of small, investigator-initiated projects. However, the history of the last half-century demonstrates in a compelling fashion that much of the innovation in American biomedical research comes from young researchers working in relatively small, highly mobile, creative research groups.
- Only 10% of submitted grant applications are funded in NIH.
- These factors, when taken together, have made careers in biomedical research increasingly unattractive for many young people. Imagine the prospects of predoctoral students starting out in their early 20s, who confront a wait of two decades until they can procure their first R01 grant, become scientifically independent, and flex their scientific muscles for the first time.
Robert Allan Weinberg is a Daniel K. Ludwig Professor for Cancer Research at MIT and a founding member of the Whitehead Institute for Biomedical Research. He is best known for his first discoveries of the first human oncogene Ras and the first tumor supressor gene Rb.
Sources: Cell and Wikipedia
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