David Baltimore

David Baltimore (born March 7, 1938) is an American biologist, university administrator, and 1975 Nobel laureate in Physiology or Medicine, he is a Professor of Biology at the California Institute of Technology, where he served as president from 1997 to 2006. He also serves as the director of the Joint Center for Translational Medicine, which joins Caltech and UCLA in a program to translate basic science discoveries into clinical realities. He served as president of the California Institute of Technology (Caltech) from 1997 to 2006, and is currently the President Emeritus and Robert Andrews Millikan Professor of Biology at Caltech. He also served as president of Rockefeller University from 1990 to 1991, and was president of the American Association for the Advancement of Science in 2007. Baltimore has profoundly influenced international science, including key contributions to immunology, virology, cancer research, biotechnology, and recombinant DNA research, through his accomplishments as a researcher, administrator, educator, and public advocate for science and engineering. He has trained many doctoral students and postdoctoral fellows, several of whom have gone on to notable and distinguished research careers. In addition to the Nobel Prize, he has received a number of awards, including the U.S. National Medal of Science in 1999. Baltimore currently sits on the Board of Sponsors[2] for the Bulletin of the Atomic Scientists and is a consultant to the Science Philanthropy Alliance.

David Baltimore
Baltimore in 2013
6th President of California Institute of Technology
In office
1997–2005
Preceded byThomas Eugene Everhart
Succeeded byJean-Lou Chameau
6th President of Rockefeller University
In office
1990–1991
Preceded byJoshua Lederberg
Succeeded byTorsten Wiesel
Personal details
Born (1938-03-07) March 7, 1938
New York City, New York, USA
NationalityUnited States
Spouse(s)
(
m. 1968)
Childrenone
Alma mater
Websitewww.bbe.caltech.edu/content/david-baltimore
Known for
Awards
Scientific career
FieldsCell biology, microbiology
Institutions
ThesisThe diversion of macromolecular synthesis in L-cells towards ends dictated by mengovirus (1964)
Doctoral advisorRichard Franklin
Doctoral studentsSara Cherry
External video
Nobel Prize Interview with Dr. David Baltimore, 26 April 2001, Nobel Prize.org
David Baltimore: Danger from the Wild: HIV, Can We Conquer It?, iBiology

Early life and education
Baltimore in the 1970s

Baltimore was born on March 7, 1938 in New York City to Gertrude (Lipschitz) and Richard Baltimore. Raised in the Queens neighborhoods of Forest Hills and Rego Park, Queens, he moved with his family to suburban Great Neck, New York while he was in second grade because his mother felt that the city schools were inadequate. His father had been raised as an Orthodox Jew and his mother was an atheist, and Baltimore observed Jewish holidays and would attend synagogue with his father through his Bar Mitzvah.[3] He graduated from Great Neck North High School in 1956, and credits his interest in biology to a high-school summer spent at the Jackson Laboratory's Summer Student Program in Bar Harbor, Maine.[4][5]

Baltimore earned his Bachelor's degree with high honors at Swarthmore College in 1960.[6] He credits his interest in molecular biology to George Streisinger under whose mentorship he worked for one summer at Cold Spring Harbor Laboratory.[6] Baltimore's future promise was evident in his work as a graduate student when he entered MIT's graduate program in biology in 1960 with a brash and brilliant approach to learning science.[7] His early interest in phage genetics quickly yielded to a passion for animal viruses. He took the Cold Spring Harbor course on animal virology in 1961 and he moved to Richard Franklin's lab at the Rockefeller Institute at New York City which was one of the few labs pioneering molecular research on animal virology. There he made fundamental discoveries on virus replication and its effect on cell metabolism, including the first description of an RNA replicase. He completed his PhD thesis work in 1964.[8]

Career and research

After his PhD, Baltimore returned to MIT for postdoctoral research with James Darnell in 1963. He continued his work on virus replication using poliovirus and pursued training in enzymology with Jerard Hurwitz at Albert Einstein College of Medicine in 1964/1965.

Independent investigator

In February 1965, Baltimore was recruited by Renato Dulbecco to the newly established Salk Institute for Biological Studies in La Jolla as an independent research associate. There he investigated poliovirus RNA replication and began a long and storied career of mentoring other scientists' early careers including Marc Girard, and Michael Jacobson. They discovered the mechanism of proteolytic cleavage of viral polyprotein precursors,[9] pointing to the importance of proteolytic processing in the synthesis of eukaryotic proteins.[10][11] He also met his future wife, Alice Huang, who began working with Baltimore at Salk in 1967.[11][12] He and Alice together carried out key experiments on defective interfering particles and viral pseudo types. During this work, he made a key discovery that polio produced its viral proteins as a single large polyprotein that was subsequently processed into individual functional peptides.[10][11]

Massachusetts Institute of Technology

Reverse transcriptase

In 1968, he was recruited by soon-to-be Nobel laureate Salvador Luria to the Department of Biology at MIT as an Associate Professor of Microbiology.[13] Alice S. Huang also moved to MIT to continue her research on vesicular stomatitis virus (VSV). They became a couple, and married in October 1968.[12] At MIT, Huang, Baltimore, and graduate student Martha Stampfer discovered that VSV involved an RNA-dependent RNA polymerase within the virus particle, and used a novel replication strategy to replicate its RNA genome. VSV entered a host cell as a single negative strand of RNA, but brought with it RNA polymerase to stimulate the processes of transcription and replication of more RNA.[11][12][14]

Baltimore extended this work and examined two RNA tumor viruses, Rauscher murine leukemia virus and Rous sarcoma virus.[11][15] He went on to discover reverse transcriptase (RTase or RT) – the enzyme that polymerizes DNA from an RNA template. In doing so, he discovered a distinct class of viruses, later name retroviruses, that use an RNA template to catalyze synthesis of viral DNA.[16] This overturned the simplified version of the central dogma of molecular biology that stated that genetic information flows unidirectionally from DNA to RNA to proteins.[15][17][18] Reverse transcriptase is essential for the reproduction of retroviruses, allowing such viruses to turn viral RNA strands into viral DNA strands. The viruses that fall into this category include HIV.[12][16]

The discovery of reverse transcriptase, made contemporaneously with Howard Temin, who had proposed the provirus hypothesis, showed that genetic information could traffic bidirectionally between DNA and RNA. They published these findings in back-to-back papers in the prestigious journal, Nature.[19][20] This discovery was heralded as evidence that molecular and virological approaches to understanding cancer would yield new cures for the dreaded disease. This may have influenced President Richard Nixon's War on Cancer which was launched in 1971 and substantially increased research funding for the disease. In 1972, at the age of 34, Baltimore was awarded tenure as a Professor of Biology at MIT, a post that he held until 1997. In 1975, at the age of 37, Baltimore shared the Nobel Prize for Physiology or Medicine with Howard Temin and Renato Dulbecco. The citation reads, "for their discoveries concerning the interaction between tumor viruses and the genetic material of the cell."[21] At the time, Baltimore's greatest contribution to virology was his discovery of reverse transcriptase.

Asilomar conference on recombinant DNA

Baltimore also helped Paul Berg and Maxine Singer to organize the Asilomar Conference on Recombinant DNA, held in February 1975. The conference discussed possible dangers of new biotechnology, drew up voluntary safety guidelines, and issued a call for an ongoing moratorium on certain types of experiments and review of possible experiments.[3] Baltimore was well aware of the importance of the changes occurring in the laboratory: "The whole Asilomar process opened up to the world that modern biology had new powers that you had never conceived of before."[7]:111

MIT Cancer Center

After winning the Nobel Prize, Baltimore reorganized his laboratory, refocusing on immunology and virology, with immunoglobulin gene expression as a major area of interest. In 1973, he was awarded a prestigious American Cancer Society Professor of Microbiology that provided substantial salary support. Also in 1973, he became one of the early faculty members in the newly organized MIT Center for Cancer capping a creative and industrious period of his career with nearly fifty research publications including the paradigm-shifting paper on reverse transcriptase. The MIT CRC was led by Salvador E. Luria and quickly achieved pre-eminence with a remarkable group of faculty including Baltimore, Phillips Robbins, Herman Eisen, Philip Sharp, and Robert Weinberg, who all went on to illustrious research careers.[13] Baltimore was honored as a Fellow of the American Academy of Arts and Sciences in 1974.[6] He returned to New York City in 1975, for a year-long sabbatical at Rockefeller University working with Jim Darnell. In 1975, at the age of 37, he shared the Nobel Prize for Physiology or Medicine with Howard Temin and Renato Dulbecco. The citation reads, "for their discoveries concerning the interaction between tumor viruses and the genetic material of the cell."[21] At the time, Baltimore's greatest contribution to virology was his discovery of reverse transcriptase (Rtase or RT) which is essential for the reproduction of retroviruses such as HIV and was discovered independently, and at about the same time, by Mizutani and Temin.[10] Following this, his lab and intellectual interests expanded tackling new problems such as the pathogenesis of Abelson murine leukemia virus (AMuLV), lymphocyte differentiation and related topic in immunology. In 1980, his group isolated the oncogene in AMuLV and showed it was a member of a new class of protein kinases that used the amino acid tyrosine as a phosphoacceptor.[22] This type of enzymatic activity was also discovered by Tony Hunter, who has done extensive work in the area. He also continued to pursue fundamental questions in RNA viruses and in 1981, Baltimore and Vincent Racaniello, a post-doctoral fellow in his laboratory, used recombinant DNA technology to generate a plasmid encoding the genome of poliovirus, an animal RNA virus.[9] The plasmid DNA was introduced into cultured mammalian cells and infectious poliovirus was produced. The infectious clone, DNA encoding the genome of a virus, is a standard tool used today in virology.

Whitehead Institute of Biomedical Research

In 1982, with a charitable donation by businessman and philanthropist Edwin C. "Jack" Whitehead, Baltimore was asked to help establish a self-governed research institute dedicated to basic biomedical research.[23] They devised a unique structure of an independent research institute composed of "members" with a close relationship with the Department of Biology of MIT. The Whitehead Institute for Biomedical Research (WIBR) was launched with $35 million to construct and equip a new building located across the street from the MIT cancer center in Cambridge Massachusetts. The institute also received $5 million per year in guaranteed income and a substantial endowment in his will (for a total gift of $135 million). Under Baltimore's leadership, a distinguished group of founding members including Gerald Fink, Rudolf Jaenisch, Harvey Lodish, and Robert Weinberg was assembled and eventually grew to 20 members in disciplines ranging from immunology, genetics, and oncology to fundamental developmental studies in mice and fruit flies.[24] Whitehead Institute's contributions to bioscience have long been second to none. Less than a decade after its founding with continued leadership by Baltimore, the Whitehead Institute was named the top research institution in the world in molecular biology and genetics, and over a recent 10-year period, papers published by Whitehead scientists were the most cited papers of any biological research institute.

After establishing the Institute in a beautiful newly constructed research building across the street from the MIT cancer center, he served as Director of the WIBR serving to expand the faculty and research areas into key areas of research including mouse and drosophila genetics. The Whitehead Institute has been rated as doing "World leading research in genetics and molecular biology",[25] and was an important partner in the Human Genome Project.[26]

During this time, Baltimore's own research program thrived in the new Institute. Important breakthroughs from Baltimore's lab include the discovery of the key transcription factor NF-κB by Dr. Ranjan Sen and David Baltimore in 1986.[27] Their intention was to identify nuclear factors required for lg gene expression in B lymphocytes. What they discovered, NF-κB, turned out to have much broader importance. NF-κB is involved in regulating cellular responses and belongs to the category of "rapid-acting" primary transcription factors. Their discovery led to an "information explosion" involving "one of the most intensely studied signaling paradigms of the last two decades."[28]

As early as 1984, Rudolf Grosschedl and David Weaver, postdoctoral fellows, in Baltimore's laboratory, were experimenting with the creation of transgenic mice as a model for the study of disease. They suggested that "control of lg gene rearrangement might be the only mechanism that determines the specificity of heavy chain gene expression within the lymphoid cell lineage."[29] in 1987, they created transgenic mice with the fused gene that developed fatal leukemia.

David G. Schatz and Marjorie Oettinger, as students in Baltimore's research group in 1988 and 1989, identified the protein pair that rearranges immunoglobulin genes, the recombination-activating gene RAG-1 and RAG-2.[30] this was a key discovery in determining how the immune system can have specificity for a given molecule out of many possibilities,[31] and was considered by Baltimore as of 2005 to be "our most significant discovery in immunology".[6]:Addendum, May 2005

In 1990, as a student in David Baltimore's laboratory at MIT, George Q. Daley demonstrated that a fusion protein called bcr-abl is sufficient to stimulate cell growth and cause chronic myelogenous leukemia (CML). This work helped to identify a class of proteins that become hyperactive in specific types of cancer cells. It helped to lay the groundwork for a new type of drug, attacking cancer at the genetic level: Brian Druker's development of the anti-cancer drug Imatinib (Gleevec), which deactivates bcr-abl proteins. Gleevec has shown impressive results in treating chronic myelogenous leukemia and also promise in treating gastrointestinal stromal tumor (GIST).[32][33][34]

Rockefeller University

Baltimore served as the Director of the Whitehead Institute until July 1, 1990 when he was appointed the sixth President of Rockefeller University in New York City. He moved his research group to New York and continued to make creative contributions to virology and cellular regulation. He also began important reforms in faculty management and promoted the status of junior faculty at the University. After resigning on December 3, 1991, Baltimore remained on the Rockefeller University faculty and continued research until spring of 1994. He then rejoined the MIT faculty as the Ivan R. Cottrell Professor of Molecular Biology and Immunology.

California Institute of Technology
From left: JPL Director Charles Elachi, La Canada-Flintridge Mayor Greg Brown, Baltimore and JPL Deputy Director Eugene Tattini (2006).

On May 13, 1997, Baltimore was appointed president of the California Institute of Technology (Caltech).[35][36][37][38][39] He began serving in the office October 15, 1997 and was inaugurated March 9, 1998.[40]

During Baltimore's tenure at Caltech, United States President Bill Clinton awarded Baltimore the National Medal of Science in 1999 for his numerous contributions to the scientific world. In 2004, Rockefeller University gave Baltimore its highest honor, Doctor of Science (honoris causa).[41]

In 2003, as a postdoctoral fellow in David Baltimore's lab at Caltech, Matthew Porteus (now professor of Pediatrics at Stanford University and cofounder of CRISPR Therapeutics) was the first to demonstrate precise gene editing in human cells using chimeric nucleases.[42]

In October 2005, Baltimore resigned the office of the president at Caltech[43] (see Luk van Parijs case). Former Georgia Tech Provost Jean-Lou Chameau succeeded Baltimore as president of Caltech.[44] Baltimore remains the Millikan Professor of Biology at Caltech and is an active member of the Institute's community.[45]

His laboratory at Caltech is focused on two major research areas: understanding the mammalian immune system and creating viral vectors to make the immune system more effective in resisting cancer. Understanding the diverse activity of the NF-κB transcription factor is one focus. NF-κB is now known to activate as many as 1000 genes in response to various stimuli. It is also known to play different roles in different cells.[45]

Another focus is understanding the functions of microRNA. MicroRNAs provide fine control over gene expression by regulating the amount of protein made by particular messenger RNAs.[45] In recent research led by Jimmy Zhao, Baltimore's team has discovered a small RNA molecule called microRNA-146a (miR-146a) and bred a strain of mice that lacks miR146a. They have used the miR146a(-) mice as a model to study the effects of chronic inflammation on the activity of hematopoietic stem cells (HSCs). Their results suggest that microRNA-146a protects HSCs during chronic inflammation, and that its lack may contribute to blood cancers and bone marrow failure.[46]

Public policy

Baltimore recently joined with other scientists to call for a worldwide moratorium on use of a new genome-editing technique to alter inheritable human DNA.[47] A key step enabling researchers to slice up any DNA sequence they choose was developed by Emmanuelle Charpentier, then at Umea University in Sweden, and Jennifer A. Doudna of the University of California, Berkeley.[48] Reminiscent of the Asilomar conference on recombinant DNA in 1975, those involved want both scientists and the public to be more aware of the ethical issues and risks involved with new techniques for genome modification.[47]

In addition to his influence on public policy for recombinant DNA research, Baltimore has influenced national policy concerning the AIDS epidemic. In 1986, he and Sheldon M. Wolff were invited by the National Academy of Sciences and the Institute of Medicine to coauthor an independent report: Confronting AIDS (1986), in which they called for a $1 billion research program for HIV/AIDS.[3][49] As of 1996 he was appointed head of the National Institutes of Health (NIH) AIDS Vaccine Research Committee (AVRC).[50]

Baltimore is a member of the National Academy of Sciences USA (NAS), 1974;[51] the American Academy of Arts and Sciences, 1974; the NAS Institute of Medicine (IOM), 1974;[52] the American Association of Immunologists, 1984.[53] He was elected a Foreign Member of the Royal Society (ForMemRS) in 1987;[54][55] the French Academy of Sciences, 2000;[56] and the American Association for Cancer Research (AACR).[52] He is also a member of the Pontifical Academy of Sciences, 1978.[57] In 2006 Baltimore was elected to a three-year term as president of the American Association for the Advancement of Science (AAAS).[52]

Baltimore is a member of the USA Science and Engineering Festival's Advisory Board[58] and an Xconomist (an editorial advisor for the tech news and media company, Xconomy).[59] Baltimore also serves on The Jackson Laboratory's board of trustees,[60] the Bulletin of the Atomic Scientists' Board of Sponsors,[61] Amgen, Inc.'s board of directors,[62] and numerous other organizations and their boards.

Controversies

Imanishi-Kari case
Main article: Thereza Imanishi-Kari

During the late 1980s and early 1990s, Thereza Imanishi-Kari, a scientist who was not in Baltimore's laboratory but in a separate, independent laboratory at MIT, was implicated in a case of scientific fraud. The case received extensive news coverage and a Congressional investigation. The case was linked to Baltimore's name because of his scientific collaboration with and later his strong defense of Imanishi-Kari against accusations of fraud.

In 1986, while a Professor of Biology at MIT and Director at Whitehead, Baltimore co-authored a scientific paper on immunology with Thereza Imanishi-Kari (an Assistant Professor of Biology who had her own laboratory at MIT) as well as four others.[63] A postdoctoral fellow in Imanishi-Kari's laboratory, Margot O'Toole, who was not an author, reported concerns about the paper, ultimately accusing Imanishi-Kari of fabricating data in a cover-up. Baltimore, however, refused to retract the paper.

O'Toole soon dropped her challenge, but the NIH, which had funded the contested paper's research, began investigating, at the insistence of Walter W. Stewart, a self-appointed fraud buster, and Ned Feder, his lab head at the NIH.[64] Representative John Dingell (D-MI) also aggressively pursued it, eventually calling in U.S. Secret Service (USSS; U.S. Treasury) document examiners.[65]

Around October 1989, when Baltimore was appointed president of Rockefeller University, around a third of the faculty opposed his appointment because of concerns about his behaviour in the Imanishi-Kari case. He visited every laboratory, one by one, to hear those concerns directly from each group of researchers.[64]

In a draft report dated March 14, 1991 and based mainly on USSS forensics findings, NIH's fraud unit, then called the Office of Scientific Integrity (OSI), accused Imanishi-Kari of falsifying and fabricating data. It also criticized Baltimore for failing to embrace O'Toole's challenge. Less than a week later, the report was leaked to the press.[66] Baltimore and three co-authors then retracted the paper; Imanishi-Kari and Moema H. Reis did not sign the retraction.[67] In the report, Baltimore admitted that he was "too willing to accept" Imanishi-Kari's explanations, and felt he "did too little to seek an independent verification of her data and conclusions."[68] Baltimore publicly apologized for not taking a whistle-blower's charge seriously.[69]

Amid concerns raised by negative publicity in connection with the scandal, Baltimore resigned as president of Rockefeller University[70] and rejoined the MIT Biology faculty.[71]

In July 1992, the US Attorney for the District of Maryland, who had been investigating the case, announced he would bring neither criminal nor civil charges against Imanishi-Kari.[72][73] In October 1994, however, OSI's successor, the Office of Research Integrity (ORI; HHS) found Imanishi-Kari guilty on 19 counts of research misconduct, basing its conclusions largely on Secret Service analysis of laboratory notebooks.

An HHS appeals panel began meeting in June 1995 to review all charges in detail. In June 1996, the panel ruled that the ORI had failed to prove even one of its 19 charges. After throwing out much of the documentary evidence gathered by the ORI, the panel dismissed all charges against Imanishi-Kari. As their final report stated, the HHS panel "found that much of what ORI presented was irrelevant, had limited probative value, was internally inconsistent, lacked reliability or foundation, was not credible or not corroborated, or was based on unwarranted assumptions." It did conclude that "The Cell paper as a whole is rife with errors of all sorts ... [including] some which, despite all these years and layers of review, have never previously been pointed out or corrected. Responsibility ... must be shared by all participants." Neither OSI nor ORI ever accused Baltimore of research misconduct.[74][75] The reputations of Stewart and Feder, who had pushed for the investigation, were very damaged.[75]

Baltimore has been both defended and criticized for his actions in this matter.[76][77][78][79][80][81][82] In 1993, Yale University mathematician Serge Lang strongly criticized Baltimore's behavior.[83] Historian of science Daniel Kevles, writing after the exoneration of Imanishi-Kari, recounted the affair in his 1998 book, The Baltimore Case.[84][85] Horace Freeland Judson also gives a critical assessment of Baltimore's actions in The Great Betrayal: Fraud In Science.[86] Baltimore has also written his own analysis.[87]

Luk van Parijs case

In October 2005, Baltimore resigned the office of the president of Caltech,[43] saying, "This is not a decision that I have made easily, but I am convinced that the interests of the Institute will be best served by a presidential transition at this particular time in its history..."[88] Soon after, at Baltimore's request, Caltech began investigating the work Luk van Parijs had conducted while a postdoc in Baltimore's laboratory.[89] Van Parijs first came under suspicion at MIT, for work done after he had left Baltimore's lab. After van Parijs had been fired by MIT, his doctoral supervisor also noted problems with work van Parijs did at the Brigham and Women's Hospital, before leaving Harvard to go to Baltimore's lab.[90] Concluding in March 2007, the Caltech investigation found van Parijs alone committed research misconduct and that four papers co-authored by Baltimore, van Parijs, and others required correction.[91]

Awards and honors

Personal life

Baltimore was married in 1968 to Dr. Alice S. Huang. They have one daughter.[94]

gollark: I mean, doing that *is* increasingly possible.
gollark: And/or randomly lucky.
gollark: Or any plan, because it's not an actual thinking agent and it doesn't have goals.
gollark: "Nature" does not have a coherent plan.
gollark: Developed countries have lower birthrates and stuff, having people *die* is not a very good thing.

See also

References
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  2. "Board of Sponsors". Bulletin of the Atomic Scientists. Rachel Bronson.
  3. David Baltimore – Interviewed by Sara Lippincott; October – November 2009, California Institute of Technology. Accessed February 21, 2013. "But she was also committed to her family and to my father's right to have his religion, and we celebrated the major holidays, we fasted on Yom Kippur, and I walked with my father to the shul, which was a long walk from where we lived."
  4. Nobel Prize autobiography. Nobelprize.org (March 7, 1938). Retrieved on 2012-02-17.
  5. Kerr, Kathleen. "They Began Here" Archived June 9, 2008, at the Wayback Machine, Newsday. Accessed October 23, 2007. "David Baltimore, 1975 Nobel laureate and one of the nation's best-known scientists, is a good case in point. The 60-year-old Baltimore, who graduated from Great Neck High School in 1956..."
  6. "David Baltimore – Biographical". Nobel Prize.org. Retrieved May 23, 2015.
  7. Crotty, Shane (2003). Ahead of the Curve : David Baltimore's Life in Science. Berkeley, California: University of California Press. ISBN 9780520239043.
  8. Baltimore, David (1964). The diversion of macromolecular synthesis in L-cells towards ends dictated by mengovirus (Ph.D.). The Rockefeller University. OCLC 38131761 – via ProQuest.
  9. Baltimore, David. "Viruses, Polymerases and Cancer:Nobel Lecture, December 12, 1975" (PDF). Nobel Prize.org.
  10. Schlesinger, Sondra (April 29, 1995). David Baltimore, Transcript of Three Interviews Conducted by Sondra Schlesinger at New York City, New York; Cambridge, Massachusetts; and Boston, Massachusetts on 7 February 1994, 13 April 1995, 29 April 1995 (PDF). Philadelphia, PA: Chemical Heritage Foundation.
  11. Bhaskaran, Hillary (1999). "Alice Huang: Keeping Science and Life in Focus". Caltech news. 33 (1). Retrieved May 23, 2015.
  12. "Dr. Alice S. Huang, Ph.D." Baltimore Associates, California Institute of Technology.
  13. Luria, Salvador (1984). A slot machine, a broken test tube: an autobiography. Harper & Row.
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  23. "Whitehead Institute Introduction".
  24. "Whitehead Institute Founding Faculty".
  25. Cooke, Philip (2002). Knowledge economies : clusters, learning and co-operative advantage. London: Routledge. p. 144. ISBN 978-0415164092.
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  38. "A Luminary of Science for Caltech's Presidency; Nobelist Baltimore has the needed background and clout." LA Times, May 15, 1997, p. B8
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  48. Pollack, Andrew (March 3, 2014). "A Powerful New Way to Edit DNA". The New York Times. Retrieved May 25, 2015.
  49. Baltimore, David; Wolff, Sheldon M.; Institute of Medicine; National Academy of Sciences (1986). Confronting AIDS: Directions for Public Health, Health Care, and Research. Washington, D.C.: National Academy Press. doi:10.17226/938. ISBN 978-0-309-03699-3. PMID 25032467. Retrieved May 25, 2015.
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Library resources about
David Baltimore
By David Baltimore
  1. Baltimore D (June 1970). "RNA-dependent DNA polymerase in virions of RNA tumour viruses". Nature. 226 (5252): 1209–11. Bibcode:1970Natur.226.1209B. doi:10.1038/2261209a0. PMID 4316300.
  2. Temin HM, Mizutani S (June 1970). "RNA-dependent DNA polymerase in virions of Rous sarcoma virus". Nature. 226 (5252): 1211–3. Bibcode:1970Natur.226.1211T. doi:10.1038/2261211a0. PMID 4316301.
  • Department of Health & Human Services, Departmental Appeals Board, Research Integrity Adjudications Panel Thereza Imanishi-Kari, Ph.D. appeal ruling (Docket No. A-95-33, Decision No. 1582, June 21, 1996; Presentation missing footnotes 169–235 & footnote reference nos. 170–235).
  • Nobel Prize video interview
  • "The Discover Magazine Interview with David Baltimore" upon his retirement from the presidency of Caltech in 2006 * PBS interview with Baltimore on AIDS, hepatitis, vaccines and science politics
Academic offices
Preceded by
Joshua Lederberg		 President of Rockefeller University
1990–1991		 Succeeded by
Torsten Wiesel
Preceded by
Thomas Eugene Everhart		 President of the California Institute of Technology
1997–2005		 Succeeded by
Jean-Lou Chameau
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