3TP Method for Detection of Breast and Prostate Cancer

English
Prof. Hadassa Degani
 
Prof. Hadassa Degani studied the mechanisms that supply cancerous tumors with oxygen and nutrients. Using magnetic resonance imaging, she developed a new technique, called 3TP, that produces an image of blood vessels feeding the tumor and makes it possible to distinguish between malignant and benign growths.
 
 

Application

 
In 2003, the non-invasive 3TP method received FDA clearance for use in the detection of breast and prostate cancer. It enables doctors to distinguish between malignant tumors and benign lumps by scanning instead of cutting.
Prof. Hadassa Degani
Life Sciences
English

How Does a Body Evolve from Two Cells?

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Lymphatic system of an adult zebrafish, from the lab of Dr. Karina Yaniv
 
 

 

 

It has been called a mystery and a miracle. It is truly a process so complex that we’re just beginning to tease apart the series of events that produces a complete organism in a matter of days, weeks or months. It begins with the genome: the set of genes often described as the blueprint for a body. But genes only carry instructions for making proteins. How much of each kind of protein, how many of each kind of cell, how those cells differentiate and develop, and how they form a heart or an artery – these are “written” in intricate layers of interaction between genes, proteins, cells, developing organs and even the embryo’s environment.

Just unraveling the progress of a single organ is an extremely ambitious undertaking. How does the heart, for example, grow into a piece of precision machinery with chambers, valves and perfectly synchronized pumping mechanisms? And how do the branching veins and arteries that transport the blood develop in concert with the growing limbs and organs?

In the Faculty of Biology, Dr. Eldad Tzahor is learning how heart cells develop. Contrary to the idea that such an organ can be generated from a single “heart” progenitor, he has found that heart cells originate in different parts of the embryo, and that the process is guided by dynamic signals, which he is now working to decipher. Dr. Karina Yaniv researches how blood and lymphatic vessels form during embryonic development. Her findings may, in the future, aid in designing methods of new blood vessel growth and renewal to treat atherosclerosis and other cardiovascular diseases, as well as in blocking the growth of blood vessels that feed tumors.
 
Drs. Eldad Tzahor and Karina Yaniv
 
 

 

Dr. Eldad Tzahor’s research is supported by the Kahn Family Research Center for Systems Biology of the Human Cell; the Helen and Martin Kimmel Institute for Stem Cell Research; the Kirk Center for Childhood Cancer and Immunological Disorders; the Jeanne and Joseph Nissim Foundation for Life Sciences Research; and the Yeda-Sela Center for Basic Research. Dr. Tzahor is the incumbent of the Gertrude and Philip Nollman Career Development Chair.

Dr. Karina Yaniv’s research is supported by the Abraham and Sonia Rochlin Foundation; Lois Rosen, Los Angeles, CA; the estate of David Arthur Barton; the estate of Paul Ourieff; and the estate of George Talis.

 
 
Lymphatic system of an adult zebrafish, from the lab of Dr. Karina Yaniv
Life Sciences
English

Life-Giving Research

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Hannah Esther Angel Kaman. Sucessful pregnancy

 
 
 

 

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Basic research often takes years to be translated into medical applications, but once in a while, a finding can change lives almost immediately.

In 2006, Prof. Nava Dekel of the Biological Regulation Department, together with doctors in the IVF unit of Kaplan Medical Center, made the surprising discovery that performing a uterine biopsy – causing a slight injury to the lining of the uterus – just before a woman undergoes in vitro fertilization (IVF) doubles the chances of a successful pregnancy. The injury apparently provokes a response that makes the uterus more receptive to the embryo's implantation.

The next year, Dekel was in Toronto, Canada, giving a lecture in the framework of the Weizmann Women and Science series, organized by Weizmann Canada. That lecture was reported in a local Jewish newspaper, where it caught the attention of Howard and Roslyn Kaman. After years of unsuccessful fertility treatments, failed IVF and miscarriages, the couple gained new hope. They contacted Dekel, and she referred them to Drs. Amichai Barash and Irit Granot, who had participated in the original research along with Drs. Yael Kalma and Yulia Gnainsky of the Weizmann Institute.

The Rehovot doctors provided a detailed description of the procedure, which was then performed in a fertility clinic in Toronto. The result: A healthy baby girl, Hannah Esther Angel Kaman, was born this past October.   

Prof. Nava Dekel's research is supported by the Dwek Family Biomedical Research Fund; the Kirk Center for Childhood Cancer and Immunological Disorders; and the Dr. Pearl H. Levine Foundation for Research in the Neurosciences. Prof. Dekel is the incumbent of the Philip M. Klutznick Professorial Chair of Developmental Biology.
 
Hannah Esther Angel Kaman. Sucessful pregnancy
Life Sciences
English

Cells Move like Millipedes

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 A scanning electron microscope image of a white blood cell with “legs”

 

 

 
 
How do white blood cells – immune system “soldiers” – cross the blood vessel barrier to get to the site of infection or injury? Until recently, it was believed that these cells advanced like inchworms, sticking front and back, folding and extending to push themselves forward. Yet in research recently published in Immunity, Prof. Ronen Alon and his research student, Ziv Shulman, of the Immunology Department showed that the rapid movement of the white blood cells is more like that of millipedes.
 
The cell creates numerous tiny “legs” no more than a micron in length, rich in adhesion points that bind to partner adhesion molecules on the surface of the blood vessels. Tens of these legs attach and detach in sequence within seconds, enabling them to move rapidly while keeping a good grip on the vessels’ sides.
 
Images produced by scanning and transmission electron microscopes, taken by Drs. Eugenia Klein and Vera Shinder of the Institute’s Electron Microscopy Unit, showed that upon attaching to the blood vessel wall, the white blood cell legs “dig” themselves into the endothelium, pressing down on its surface. The scientists believe that the tiny legs are trifunctional: used for gripping, moving and sensing distress signals from the damaged tissue.
 
In future studies, the scientists plan to check whether aggressive immune reactions (such as in autoimmune diseases) can be regulated by interrupting the digging of immune cell legs into the endothelium. They also plan to investigate whether cancerous blood cells metastasize through the blood stream using similar mechanisms.
 
Prof. Ronen Alon’s research is supported by the De Benedetti Foundation-Cherasco 1547. Prof. Alon is the incumbent of the Linda Jacobs Chair in Immune and Stem Cell Research.
 
 
A scanning electron microscope image of a white blood cell with “legs”
Life Sciences
English

Checking the Dosage

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Yoram Groner. Finding the causes of Down syndrome

 
 
 
 
 

Three decades of work on Down syndrome is bringing its cause into focus

 
In 1866, British physician John Langdon Down described the disorder now known as Down syndrome. Despite wide-scale prenatal testing, about 1 in 800 babies in the Western world is born with this disorder. In addition to developmental disabilities, Down syndrome patients suffer from poor muscle function, diabetes and leukemia, and are at a higher risk of Alzheimer's disease.
 
About 50 years ago, it was discovered that people with Down syndrome have an extra copy of chromosome 21. How does an extra copy of an intact gene cause such problems? The case was far from clear-cut: Overexpression of a particular gene does not necessarily result in the overproduction of its encoded protein. In plants, for example, overexpression of genes is a widespread phenomenon that causes no harm.
 
Answers are beginning to emerge, thanks to the pioneering work of Prof. Yoram Groner of the Molecular Genetics Department.
 
In endeavoring to understand how a third copy of chromosome21 causes Down syndrome, scientists have considered two possible scenarios: One widely held "developmental instability" hypothesis suggests that the symptoms are the direct consequence of a disturbance in the chromosome balance, resulting in a disruption of homeostasis. The alternative – the gene dosage effect hypothesis – suggests that symptoms of the syndrome are caused by over-production of some or many of the proteins encoded by chromosome 21 genes, which then leads to a disturbance in the metabolic balance required for proper development and normal body function.
Groner favored the gene dosage effect hypothesis and made it his goal to prove it. The challenge he set himself was to isolate an individual gene from chromosome 21 and demonstrate that it causes known symptoms of Down syndrome. This undertaking was revolutionary in 1979: Information on chromosome 21 was marginal; no molecular tests were available to measure gene expression; and the technology for cloning genes was in its infancy.
 
Groner and his team found that Down syndrome patients have an abnormally high level of an enzyme called SOD1 in their blood. But was the SOD1 gene located on chromosome 21? And if so, what role did it play in the disorder? In the early 1980s, tackling these issues, which are today routine in the field of genetic research, was almost beyond the scope of conventional science.
 
The efforts of Groner and his colleagues led to the first ever cloning of a gene from chromosome 21 and the decoding of its DNA sequence. Groner's group created genetically modified cells (so-called transgenic cells) that produce high levels of SOD1. These transgenic cells had physical defects and excess levels of hydrogen peroxide.
 
One such abnormality was the cells' inability to accumulate neurotransmitters (nervous system modulators). Groner and his team revealed the molecular mechanism that causes this abnormality, tracing the defect to a special protein pump that draws neurotransmitters into the cell. This discovery provided direct evidence that the gene dosage effect of chromosome 21 causes significant physical mal-function in the cell.
 
How does this malfunction tie in with Down syndrome? To answer this question, Groner and his team created, for the first time, a mouse model for gene dosage: a transgenic mouse containing an SOD1 gene. These transgenic mice had high levels of SOD1 and very low levels of the neurotransmitter serotonin in their blood – close to those found in Down syndrome infants, verifying that features of Down syndrome can be attributed to the gene dosage.
 
Further research revealed that overexpressed SOD1 produced significantly higher amounts of hydrogen peroxide in the mice, causing defects in the pumps that draw serotonin from the blood into certain blood cells, where it normally accumulates. When this pump fails, the serotonin remains in the bloodstream, where it is broken down, leading to reduced levels of serotonin in these cells and, later, in the brains of the transgenic mice – similar to what is observed in Down syndrome patients.
 
The intriguing finding that increased SOD1 impairs neuro-transmitter uptake enabled Groner's team to unravel one of the long-standing puzzles in Down syndrome clinical treatment: Attempts were made in the late 1960s to raise the low blood serotonin levels in these patients, but many experienced severe seizures, bringing the studies to a halt. Why does the administration of serotonin cause spasms in infants with Down syndrome? The team were able to resolve the underlying mechanism: When the defective pumps failed to transport serotonin into the infants' blood cells, the added serotonin collected instead in the synapses – the spaces between nerve cells – bringing on the seizures. 
 

Groundbreaking Studies

 
Prof. Yoram Groner established the Weizmann Institute of Science's Molecular Genetics Department (from the former Genetics and Virology Departments), and later served as the Institute's Deputy President. Groner was recently awarded the 2008 EMET Prize for Life Sciences for, among other achievements, "his groundbreaking studies in the molecular biology of Down Syndrome, which proved the gene dosage effect theory in the trisomy of chromosome 21."
 
Prof. Yoram Groner's research is supported by the J & R Center for Scientific Research; the David and Fela Shapell Family Center for Genetic Disorders Research; and the Dr. Miriam and Sheldon G. Adelson Medical Research Foundation. Prof. Groner is the incumbent of the Dr. Barnet Berris Professorial Chair of Cancer Research.
 
Prof. Yoram Groner.
Life Sciences
English

Supernannies

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 Vicki Plaks, Tal Birnberg, Prof. Nava Dekel, Dr. Steffen Jung and Prof. Michal Neeman. Critical pregnancy stage

 

 

 

 

 

 

 

 

 

 

 

 

 

 

By the time a fertilized egg completes the trip from ovaries to uterus, it has already been transformed into a tiny ball of cells called a blastocyst. Its next step is fraught with risks: Around half of all blastocysts will fail in their attempts to implant in the uterus. Some will be rejected due to abnormalities, but others won't make it because the uterus for some reason doesn't provide them with the conditions they need to thrive and grow.

From the moment a blastocyst settles on an inviting spot on the uterus lining, the surrounding cells begin to change and grow. Soon, a spongy, blood-rich mass called the decidua forms from the uterine tissue. Most of the decidua disappears once a proper placenta is formed, but the decidua tissue is crucial for nurturing the new embryo during the precarious first stage of pregnancy.

Changes in the uterine wall at this time include alterations in the population of immune cells that normally inhabit the uterus. For instance, cells called dendritic cells cluster near the newly implanted blastocyst. Dendritic cells of different types are found throughout the body, where they generally help to form one of its first lines of defense against invading microorganisms, scouting the tissues and alerting the immune system to potential threats.

So what are these immune system fighters doing in the vicinity of the newly implanted blastocyst? The prevailing hypothesis is that these cells somehow play an opposite, protective role in implantation. Uterine dendritic cells, so the theory goes, help to prevent other immune cells from attacking the tiny blastocyst, which shares only half of its genes with its mother and might therefore be regarded by her immune system as a foreign menace.

To test this theory, two research students, Tal Birnberg and Vicki Plaks from the laboratories of Dr. Steffen Jung at the Institute's Immunology Department, and Profs. Nava Dekel and Michal Neeman of the Biological Regulation Department, in collaboration with Dr. Gil Mor of the Yale University School of Medicine, cross-bred mice so that the embryos were genetically identical to the mothers. They then removed the dendritic cells from the uterus using an in vivo cell depletion model developed by Jung during his postdoctoral studies at New York University. Because the immune system could not identify the embryo as foreign, there was no cause for rejection of the blastocysts – but implantation failed anyway.

If they don't defend the blastocysts, what role do the dendritic cells play? To investigate, the scientists again depleted the uterus of dendritic cells, this time in mice that had been induced to develop a decidua without a blastocyst (a technique perfected by Dekel's team). In every case, in vivo MRI studies showed the decidua-forming cells multiplied more slowly and didn't differentiate properly, and new blood vessels were slow to grow.

These findings led the researchers to the somewhat startling conclusion that these particular dendritic cells had taken on a completely new function. Rather than acting as front-line warriors of the immune system, or even protectors of the new embryo, they seemed to be involved in remodeling the nursery, helping to reshape the tissue surrounding the implantation site to provide for the needs of the new embryo. The scientists hope to continue this line of research and to identify exactly what factors are involved in creating a viable decidua. As well as shedding light on this vital but little understood stage of pregnancy, future studies based on this research may help to advance treatments for infertility.   

Prof. Nava Dekel's research is support-ed by the Dwek Family Biomedical Research Fund; the Kirk Center for Childhood Cancer and Immunological Disorders; and the Dr. Pearl H. Levine Foundation for Research in the Neuro-sciences. Prof. Dekel is the incumbent of the Philip M. Klutznick Professorial Chair of Developmental Biology.
 

Dr. Steffen Jung's research is supported by the Kekst Family Center for Medical Genetics; the Kirk Center for Childhood Cancer and Immunological Disorders; the Swiss Society of Friends of the Weizmann Institute of Science; the Fritz Thyssen Stiftung; the estate of Edith Goldensohn; the Women's Health Research Center funded by: the Bennett-Pritzker Endowment Fund, the Marvelle Koffler Program for Breast Cancer Research, the Harry and Jeanette Weinberg Women's Health Research Endowment and the Oprah Winfrey Biomedical Research Fund; and the Center for Health Sciences funded by the Dwek Family Biomedical Research Fund and the Maria and Bernhard Zondek Hormone Research Fund. Dr. Jung is the incumbent of the Pauline Recanati Career Development Chair of Immunology.
 

Prof. Michal Neeman's research is supported by the Clore Center for Biological Physics; the Abisch Frenkel Foundation for the Promotion of Life Sciences; the Phyllis and Joseph Gurwin Fund for Scientific Advancement; the Ridgefield Foundation; the Women's Health Research Center funded by: the Bennett-Pritzker Endowment Fund, the Marvelle Koffler Program for Breast Cancer Research, the Harry and Jeanette Weinberg Women's Health Research Endowment and the Oprah Winfrey Biomedical Research Fund. Prof. Neeman is the incumbent of the Helen and Morris Mauerberger Chair in Biological Sciences.

 
Composite image. Decidua and dendritic cells
 

 

 
Image of an embryo overlaid withan immunofluorescent image of the decidua (purple). Dendritic cells are in green and blood vessels in red
Life Sciences
English

Staying Alive

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Prof. Idit Shachar. Returning the self-destruct program
 
 
 
 
One of the characteristics of cancer cells is their refusal to die. In chronic lymphocytic leukemia (CLL), a blood cancer, white blood cells called B lymphocytes, or B cells, lose the internal self-destruct program for limiting their lifespan. Instead of maintaining a steady turnover in the blood, their numbers continue to grow, building up to dangerous levels in the blood, bone marrow and lymph nodes.
 
A team of scientists headed by Prof. Idit Shachar of the Weizmann Institute’s Immunology Department and Dr. Michal Haran of the Kaplan Medical Center’s Hematology Institute recently discovered what keeps CLL cells alive. This survival mechanism, they found, is vulnerable to attack by antibodies that target it, causing the cancer cells to die. Their findings, which appeared recently in Proceedings of the National Academy of Sciences (PNAS), USA, may lead to future treatments for this disease, as well as for other diseases in which B lymphocytes accumulate in the blood.
 
The short life of a B cell involves an intricate give and take between the self-destruct mechanism and other factors that keep the cell alive. In previous research, Shachar had found that a specific receptor – a protein on the outer surface of healthy B cells – plays a vital role in helping the cells survive. She wondered if the same protein might also be a central player in the abnormally high survival rates of cancerous B cells. 
 
Members of Shachar’s research team, including Inbal Binsky, Diana Starlets, Yael Gore and Frida Lantner, together with Kaplan Medical Center doctors Haran, Lev Shvidel, Prof. Alan Berrebi and Nurit Harpaz; as well as scientists from Yale University and David Goldenberg of the Garden State Cancer Center in New Jersey, examined B cells taken from CLL patients. They discovered that even in the earliest stages of the disease, these cells have an unusually high level of this survival receptor. The scientists found that the act of protein binding to the receptor initiates a series of events within the cell that results in enhanced cell survival. One of the substances produced in this chain of events helps to regulate the cell’s lifespan, resulting in the maintenance of cell survival.
 
The team treated the CLL cells with an antibody that recognizes the survival receptor, blocking its activity and causing the cancer cell death rate to soar.
 
The antibodies they used are produced by the firm Immunomedics, in New Jersey, and are currently entering clinical trials for the treatment of several different types of cancer. Following this research, which has revealed the mechanism of the antibody’s actions, the company is planning trials for CLL as well.
 
Shachar: “The abnormally elevated levels of this receptor seem to be important factors in the development of this disease, right from the beginning, and they are responsible for the longevity of these cancerous B cells. Blocking the receptor or other stages in the pathway they activate might be a winning tactic, in the future, in the war against cancers involving B cells.”  
 
Prof. Idit Shachar’s research is supported by the Kirk Center for Childhood Cancer and Immunological Disorders; the Weizmann Institute of Science-Yale Exchange Program; the Abisch Frenkel Foundation for the Promotion of Life Sciences; and the Phyllis and Joseph Gurwin Fund for Scientific Advancement. Prof. Shachar is the incumbent of the Dr. Morton and Anne Kleiman Professorial Chair.
 
Prof. Idit Shachar
Life Sciences
English

One Hundred Times Stronger

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Natural interferon is widely used to treat a number of different cancers, but its effectiveness is rather modest. Weizmann Institute scientists have now succeeded in engineering a new version of interferon whose activity is 100 times stronger than that of the natural molecule.
 
Prof. Gideon Schreiber of the Institute’s Biological Chemistry Department was originally interested in a basic research question concerning interferons: How do these proteins produce two different kinds of effects inside the cell – either serving as the body’s first line of defense against viral infection or inducing programmed cell death, called apoptosis? Schreiber revealed that the different types of activity stem from the way interferon binds to its receptor. Moreover, his team identified the precise amino acids and structural features that affect the binding.
 
The scientists then created versions of interferon with different degrees of binding ability and different types of activity: They manipulated the interferon-receptor bond by replacing various amino acids in the interferon’s binding site and then testing the resulting interferon versions. Using this approach, they managed to create an interferon molecule, called YNS, that binds to cellular receptors much more strongly and, in a laboratory dish, is 100 times more effective than natural interferon at triggering the death of cancer cells. The scientists then found that the YNS molecule effectively eliminated human breast cancer cells in laboratory mice, while the natural interferon did not.
 
 
Yeda Research and Development Company, the Institute’s technology transfer arm, has patented the YNS molecule. If the new interferon proves sucessful ateliminating cancer cells in humans, it could be developed into an effective anti-cancer drug.  
 
Prof. Gideon Schreiber’s research is supported by the Clore Center for Biological Physics; the Helen and Milton A. Kimmelman Center for Biomolecular Structure and Assembly; and Mr. and Mrs. Yossie Hollander, Israel.
Life Sciences
English

Time-Tested Transplants

English
 
 
In hemophilia, a mutated gene prevents the production of a critical blood-clotting protein. What if the body could be induced – by a transplant of healthy tissue – to begin producing this protein?
 
In research recently published in the Proceedings of the National Academy of Sciences (PNAS), Prof. Yair Reisner and Ph.D. student Anna Aronovich of the Weizmann Institute’s Immunology Department, together with colleagues, showed how such a transplant might in the future be made feasible.
 
By taking spleen tissue from embryonic pigs, the scientists found that harmful T cells, which are responsible for severe immune responses against the recipient, are not present prior to day 42 of gestation. They also found that tissue of this age exhibits optimal growth potential and secretes factor VIII, the blood-clotting protein missing in hemophilic patients. Hemophilic mice with spleen tissue transplanted from pig embryos at 42 days of gestation experienced completely normal blood clotting within a month or two of implantation.
 
Although a number of problems would need to be surmounted before researchers could begin to think of applying the technique to humans, the Institute team has provided evidence that transplanted embryonic tissue, whether human or pig, could one day help the body overcome hemophilia and other such genetic diseases.

Prof. Yair Reisner’s research receives major funding from Tissera Inc. His work is also supported by the J & R Center for Scientific Research; the Belle S. and Irving E. Meller Center for the Biology of Aging; the Gabrielle Rich Center for Transplantation Biology Research; the Abisch Frenkel Foundation for the Promotion of Life Sciences; the Loreen Arbus Foundation; the Crown Endowment Fund for Immunological Research; the Mario Negri Institute for Pharmacological Research – Weizmann Institute of Science Exchange Program; the Charles and David Wolfson Charitable Trust; Dr. and Mrs. Leslie Bernstein, Sacramento, CA; Mr. and Mrs. Irwin Goldberg, Las Vegas, NV; and Mr. and Mrs. Barry Reznik, Brooklyn, NY. Prof. Reisner is the incumbent of the Henry H. Drake Professorial Chair in Immunology.
Life Sciences
English

A Lucky Brake

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400 genes respond to growth signals

 

 

 

 

 

 

When a normal cell complies with a signal telling it to divide, it also begins to activate a “braking system” that eventually stops cell division. If that system is faulty, cancerous growth can result. As reported in Nature Genetics, Weizmann scientists sifted through a huge quantity of data on genes and their activities to identify some of the genes involved in this system of braking.

 

To tackle this monumental task, a team of Weizmann Institute researchers from diverse fields – Prof. Yosef Yarden of the Biological Regulation Department, Prof. Eytan Domany of the Physics of Complex Systems Department, Prof. Uri Alon of the Molecular Cell Biology Department and Dr. Eran Segal of the Computer Science and Applied Mathematics Department – pooled their knowledge and experience. Working with them were Prof. Gideon Rechavi of the Sheba Medical Center and researchers from the M. D. Anderson Cancer Center in Houston, Texas, headed by Prof. Gordon B. Mills.

 

In tests conducted on tissue from ovarian cancer patients, the scientists found a correlation between levels of activity in the “braking” genes, rates of survival and the aggressiveness of the disease. These findings point the way toward the development of a personal genetic profile that might pinpoint the genetic defects responsible for each individual cancer and help doctors tailor a treatment best suited to that particular patient. Such a genetic profile can also help predict the progression of the disease in each case.

 

Also participating in the study were research students Ido Amit, Ami Citri, Gabi Tarcic and Menachem Katz of the Biological Regulation Department and Tal Shay of the Physics of Complex Systems Department.   

 

Prof. Yosef Yarden’s research is supported by the M. D. Moross Institute for Cancer Research; the Goldhirsh Foundation; the Batsheva de Rothschild Foundation; Mr. Daniel Falkner, UK; the estate of Dr. Marvin Klein, Farmington Hills, MI; and Mrs. Bram Laub, Belgium. Prof. Yarden is the incumbent of the Harold and Zelda Goldenberg Professorial Chair in Molecular Cell Biology.

Activity of 400 genes following exposure to a growth signal over time. Red indicates hightened gene activity
Life Sciences
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