William French Anderson

William French Anderson (born December 31, 1936) is an American physician, geneticist and molecular biologist. He is known as the Father of Gene Therapy. He graduated from Harvard College in 1958, Trinity College, Cambridge University (England) in 1960, and from Harvard Medical School in 1963. In 1990 he was the first person to succeed in carrying out gene therapy by treating a 4-year-old girl suffering from severe combined immunodeficiency (a disorder called "bubble boy disease").[1][2][3] In 2006, he was convicted of sexual abuse of a minor and in 2007 was sentenced to 14 years in prison. He was released May 17, 2018, for good behavior.

For other people of a similar name, see William Anderson.
William French Anderson
Dr. Anderson in 1990
Born (1936-12-31) December 31, 1936
Tulsa, Oklahoma
EducationHarvard College
Harvard Medical School
Trinity College, Cambridge University
Known forContributions to gene therapy
Scientific career
FieldsGenetics
molecular biology
Criminal statusReleased
Conviction(s)Lewd acts upon a child under the age of 14 (three counts)
Continuous sexual abuse (one count)
Criminal penalty14 years imprisonment

Early life and education

Anderson was born in Tulsa Oklahoma. His father was a civil engineer, his mother was a journalist and writer, and he had two older sisters. His was a very happy childhood.[1] He was recognized in high school for his scholarship, interest in science, and prowess on the track team. He won an Honorable Mention in the Westinghouse Science Talent Search for his pioneering work in demonstrating how Roman numerals could be used in arithmetical procedures. He was a 1954 graduate of Tulsa Central High School.

Anderson went to Harvard College where he published several papers as an undergraduate: his high school work on Roman numerals in Classical Philology in 1956,[4] arithmetical operations using Minoan linear B numerals in the American Journal of Archaeology in 1958,[5] a physical chemistry research paper in the Journal of the American Chemical Society in 1958,[6] and a research study on the effects of irradiation on DNA in the Journal of Cellular and Comparative Physiology in 1961.[7] In its March 19, 1956 issue, Time magazine called Anderson a "Harvard Prodigy" for his research work on ancient numerical systems.[8] He graduated from Harvard in 1958, and spent two years at Trinity College, Cambridge University (England) where he obtained an M.A., worked in the laboratory of Francis Crick, won a Full Blue on the track team, and met, and in 1961 married, his wife of now 58 years, Kathy, who was a fellow medical student at Cambridge.[1]

He returned to Harvard, to the Medical School, and was joined there by Kathy a year later. Anderson graduated in 1963 and spent a year internship in pediatric medicine at Children's Hospital in Boston. His wife graduated in 1964 and went on to have a very distinguished career in pediatric surgery. Anderson, after his intern year, spent a year conducting bacterial genetics research at Harvard Medical School and published his work in the Proceedings of the National Academy of Sciences USA in 1965.[9]

Career

Anderson then spent two years, 1965–1967, in the laboratory of Marshall Nirenberg at the National Institutes of Health where he helped finish the decipherment of the genetic code. Nirenberg rewarded his efforts by allowing him to make the first public presentation of the final genetic code before an audience of approximately 2,000 scientists at the April 1966, meeting of FASEB in Atlantic City.[1][10] After his successful post-doctoral fellowship with Nirenberg, Anderson was given his own laboratory in the NIH in July 1967. He made clear from the beginning that his goal was to develop a way to give a normal gene to children with a genetic defect in order to cure the genetic disease.[1] He, therefore, decided to begin by studying human disease on the molecular level. Over his career he has published more than 400 research papers, 39 editorials, and 5 books, and has received numerous awards and honors including 5 honorary doctorate degrees.

Discovery of eukaryotic protein synthesis initiation factors

As Anderson began his own career, protein synthesis in bacteria was at the forefront of molecular biology research. He set out to discover protein synthesis initiation factors in mammals. His first major accomplishment, in 1970, was the isolation from rabbit reticulocytes (immature red blood cells) of several factors that initiated hemoglobin synthesis on reticulocyte ribosomes.[11] It was later learned that these factors also initiated protein synthesis in essentially all eukaryotic systems.

Development of a cell-free protein synthesizing system

In order to isolate the predicted molecule "messenger RNA", a cell-free protein synthesizing system of mRNA-free ribosomes was needed. Initially, a cell-free tRNA-dependent protein synthesizing system was developed from rabbit reticulocytes ribosomes, using the endogenous mRNA on the ribosomes.[12] An analogous system was developed with human reticulocyte ribosomes.[13]

Isolation of human messenger RNA

A procedure was developed for stripping the putative mRNA from the ribosomes. This ribosomal wash from rabbit reticulocyte ribosomes was incubated in a cell-free system and rabbit hemoglobin was produced. The procedure for stripping endogenous mRNA from rabbit reticulocyte ribosomes was used on human reticulocyte ribosomes to obtain human globin mRNA.[14]

Synthesis of normal and mutant globin proteins using human globin mRNA

Stripped rabbit reticulocyte ribosomes were programmed with mRNA isolated from thalassemia, sickle cell anemia, or normal human reticulocytes. The rabbit ribosome cell-free system was able to produce normal human globin from normal human mRNA, sickle cell globin from sickle cell mRNA, and the abnormal alpha/beta globin chain abnormality of thalassemia from thalassemia mRNA.[15][16]

Microinjection of globin DNA into mammalian cell nuclei

As a first approach for developing a human gene therapy procedure, standard microinjection techniques were modified to permit the injection of DNA plasmids into the nucleus of mammalian cells.[17] Human globin genes were microinjected into mouse fibroblasts and into mouse oocytes and shown to express human globin mRNA.[18][19]

Development of retroviral gene therapy vectors

Microinjecting a few non-stem cells was clearly not an efficient procedure for a clinical protocol. In 1984, Anderson published a major review in Science in which he analyzed the "Prospects for Human Gene Therapy"[20] and concluded that the most promising approach was to use retroviral vectors as a delivery vehicle. He immediately established a close, long-term collaboration  with one of the top retroviral vector  scientists: Eli Gilboa, then at  Princeton. Together they developed vectors that could efficiently carry a gene package into mouse or human cells in culture.[21][22]

The most efficient vector, N2, carrying a neomycin resistance gene, was used to transduce mouse bone marrow cells. The N2-transduced cells were injected into lethally irradiated mice where they repopulated the marrow. The presence and expression of the N2 vector could be detected in the repopulated mouse bone marrow cells by testing for the resistance of the marrow cells to the toxic antibiotic neomycin.[23]

Once the procedure was working successfully in mice, successful studies were done in non human primates.[24][25] In addition, extensive safety studies were done in the vector transduced animals.[26]

Successful gene therapy of a human patient

Attempting to perform gene therapy by inserting recombinant DNA into a human being was extremely controversial after an illegal attempt was made in 1980. Anderson, together with bioethicist John Fletcher, set the ethical standard for this type of clinical protocol in his 1980 article in New England Journal of Medicine entitled: "Gene Therapy In Human Beings: When Is It Ethical To Begin?"[27] An extensive regulatory process was established during the late 1980s, including the creation of the Human Gene Therapy Subcommittee as a first round of regulatory oversight. Only after approval by that formal public governmental review did the gene therapy clinical protocol move on for review by the Recombinant DNA Advisory Committee (RAC), the FDA, and other ethics/regulatory committees. The media followed every step closely.

Anderson teamed with Michael Blaese, a prominent immunologist in the National Cancer Institute (NCI), and Steven Rosenberg, a prominent cancer surgeon and immunotherapy advocate, also in the NCI. The initial protocol was a safety study where only the N2 vector, previously shown to be safe when used in non-human primates, was administered to cancer patients, on Rosenberg's NCI clinical cancer service, who volunteered for the study. A full "gene therapy" regulatory review was carried out. The clinical protocol began on May 22, 1989, and included 10 patients. The procedure was shown to be safe.[28] Rosenberg went on to develop gene therapy/immunotherapy clinical protocols for cancer.[29]

Anderson and Blaese carried out the first gene therapy protocol, on a 4-year-old girl, named Ashanthi DeSilva, who was critically ill with Adenosine Deaminase Deficiency Severe Combined Immunodeficiency Disease (ADA SCID). Preliminary studies included development of a retroviral vector containing the ADA gene together with additional safety features,[30] creation of ADA deficient human T cell lines used for testing ADA vectors,[31] and creation of a biotechnology company, Genetic Therapy Inc., to manufacture the ADA vector, called LASN, under strict GMP FDA requirements. Anderson also created, and became editor-in-chief of, a new journal, Human Gene Therapy, in 1990. This new journal published not only original scientific research papers but also articles on ethical and regulatory issues relating to gene therapy.

Ashanthi received her first infusion of cells on September 14, 1990, with no complications.[32][33] She received 10 more infusions over the next 2 years. Her immune evaluation studies became normal and she became healthy with no major infections.[34][35] A thorough immune status follow-up was done after 12 years: she remained healthy with 20% of her lymphocytes still carrying an active retroviral ADA gene - a sufficient percentage to ensure immunologic protection.[36] She is now 33 years old, married, and works as a journalist and writer.

Late career research projects

In 1992, Anderson followed his wife to Los Angeles where she accepted the position of Chief of Surgery at Los Angeles Children's Hospital. He became Professor of Biochemistry and Pediatrics at the University of Southern California (USC). Anderson maintained his intense interest in gene therapy and was able to develop a retroviral gene therapy vector that could target the collagen matrix surrounding cancer nodules.[37] He wrote a number of reviews of gene therapy in both the scientific literature[38][39][40] and in the popular literature.[41][42]

Anticipating the value of lab-on-a-chip technology for the molecular analysis of individual cells, Anderson joined forces with Stephen Quake, Professor  of Applied Physics at California Institute of Technology. Quake was developing lab-on-a-chip technology using soft polymers. Anderson became a Visiting Associate in Applied Physics at CalTech from 2001 to 2006, while maintaining his USC positions, and succeeded in developing an improved microfluidic valve that was patented and has become the core of soft polymer lab-on-a-chip   devices.[43][44]

His final project before he was arrested was the discovery and identification of a factor in the serum of irradiated animals that could rescue lethally irradiated animals even 24 hours after the  irradiation.[45] Purification from the serum demonstrated that the factor was Interleukin 12. During the 12 years that Anderson has been in prison, IL-12 has been shown to potentially be a very important adjuvant drug in cancer treatment.

Other activities

Anderson and his wife have been married for 58 years and have a very strong bond between them. The 3 other activities that have played a major role in Anderson's life are sports, sports medicine, and forensic medicine.

Sports

Track - Anderson has been a competitive runner his entire life primarily at the 400- meter distance. He still competes in age-oriented local and regional track meets.[1]

Martial Arts - Anderson is a 5th degree black belt in Taekwondo and was certified a Master in 1988 by the Kukkiwon in Seoul Korea. In the mid-1990s, he missed competing and, since Taekwondo did not have a senior division, he acquired a black belt in karate. He then competed in the AAU national karate competition, and, in 1998, was national champion in sparring in the oldest age division. He also taught martial arts for 20 years.[1]

Sports Medicine

Anderson has been a ring doctor and tournament doctor in a large number of competitions. In 1981, he became the Team Physician for the National Taekwondo Team, and was also the Team Physician at the 1988 Olympics in Seoul Korea when Taekwondo became an Olympic sport.[1] He has written several sports medicine articles on prevention and treatment of taekwondo injuries.[46][47][48] In addition, he was Chairman of the Medical Committee of the World Taekwondo Federation from 1985 to 1988.

Forensic Medicine

Anderson is best known in forensic medicine for his forensic analysis of the famous April 11, 1986, FBI firefight which, at the time, was the deadliest firefight in the history of the FBI. His analysis, privately printed in 1996, was accepted by the FBI as the official version and every new FBI agent was given a copy of his report. After 10 years, the FBI allowed Anderson to make the report public and it was published with a new Foreword by Paladin Press in 2006.[49]

Anderson also published a forensic analysis of the Wyatt Earp killing,[50] as well as a study of the bruises beneath soft body armor when bullets of various calibers strike a person wearing the armor.[51]

Sexual abuse conviction

Anderson was arrested on July 30, 2004, on allegations of sexual abuse of a minor.[52] He was convicted and jailed on July 19, 2006, of three counts of lewd acts upon a child under the age of 14, and one count of continuous sexual abuse.[53] On February 2, 2007, he was sentenced to 14 years in prison and ordered to pay $68,000 in restitution, fines, and fees.[54] The girl was the daughter of his senior lab scientist and business partner. The jury was played a sting meeting recording between Anderson and the victim in which Anderson is heard to say a number of damaging statements.[55]

Anderson has asserted his innocence.[56] He has argued that the sting recording had been altered by the police to turn a recording that would have proven his innocence to one suggesting guilt.[57] He lost all his appeals through the court system, and served his entire sentence, which was shortened based on good behavior. He was released from prison on May 17, 2018, and is currently serving a 5-year parole.

Published books

Development of Iron Chelators for Clinical Use. Anderson, W.F. and Hiller, H.C., eds., DHEW Publ. No. (NIH) 76-994, 1976.

Fourth Cooley's Anemia Symposium. Anderson, W.F.; Bank, A.; Zaino, E.C., eds., Ann. NY Acad. Sci., Vol. 344, 1980.

Development of Iron Chelators for Clinical Use: Proceedings of the Second Symposium. Martell, A.E.; Anderson, W.F.; Badman, D., eds., Elsevier-North Holland, New York, 1981.

Fifth Cooley's Anemia Symposium. Bank, A.; Anderson, W.F.; Zaino, E.C., eds., Ann. NY Acad. Sci., Vol. 445, 1985.

Forensic Analysis of the April 11, 1986, FBI Firefight. Anderson, W.F., Paladin Press, 2006. ISBN 1581604904

Issued patents

"Gene Therapy".  USA #5399346, issued 3/21/1995.  Anderson, Blaese, Rosenberg.  [A]

"Retroviral Vectors". USA #5672510, issued 9/30/1997. Eglitis, Thompson, Anderson. [A]

"Vectors including foreign genes and negative selective markers". USA #5925345, issued 7/20/1999.  Blaese, Anderson, McLachlin, Chiang. Eglitis. [A]

"Targetable vector particles". USA #5985655, issued 11/16/99. Anderson, Baltrucki, Mason.  [A]

"Retroviral envelopes having modified hyper variable polyproline regions".  USA #6004798, issued 12/21/1999.  Anderson, Wu.  [A]

"TGF.beta. l responsive bone marrow derived cells to express a recombinant protein". USA #6063593, issued 5/16/2000.  Gordon, Hall, Anderson.  [B]

"Factor IX delivery method using bone marrow-derived cells". USA# 6277369, issued 8/21/2001.  Gordon, Anderson, Hall.  [B]

"Targeting pharmaceutical agents to injured tissues". USA #6387663, issued 5/14/2002. Hall, Gordon, Starnes, Anderson.  [B]

"Gene therapy methods using bone marrow-derived cells expressing blood clotting factors". USA #6410015, issued 6/5/2002.  Gordon, Hall, Anderson.  [B]

"Gene delivery system and methods of use". USA #6410313, issued 6/25/2002. Kasahara, Logg, Anderson.   [C]

"Targetable vector particles". USA# 6503501, issued 1/7/2003. Anderson, Baltrucki, Mason.  [A]

"Vectors including foreign genes and negative selective markers". USA #6761884, issued 7/13 2004. Anderson, Blaese, Chiang, Eglitis, McLachlin. [A]

"Osteogenic cell growth using a TGF.beta.1-vonWillebrand's factor fusion protein".  USA #6844191, issued 1/18/2005.  Hall, Gordon, Anderson, Starnes.  [B]

"Modified viral surface proteins for binding to extracellular matrix components". USA #6864082, issued 3/8/2005. Hall, Gordon, Anderson, Starnes.  [B]

"Gene therapy for proliferative vitreoretinopathy". USA #6869935, issued 3/22/2005. Anderson, Hinton, Ryan.   [D]

"Gene delivery system and methods of use". USA #6899871, issued 5/31/2005. Kasahara, Logg, Anderson.   [C]

"Targeting pharmaceutical agents to injured tissues". USA #6955898, issued 10/18/2005. Hall, Gordon, Starnes, Anderson.  [B]

"Retroviral vectors including modified envelope escort proteins". USA #7078483, issued 7/18/2006.  Anderson, Gordon, Hall.  [B]

"Expression of cyclin Gl in tumors". USA #7605142, issued 10/26/2006. Gordon, Hall, Anderson.   (B]

"Gene Therapy".  USA #RE39788, issued 8/21/2007.  Anderson, Blaese, Rosenberg.  [A]

PMDS microfluidic components and methods of operation of same". USA #7611673, issued 11/3/2009. Kartalov, Scherer, Anderson.  [E]

"Uses ofIL-12 in hematopoiesis". USA #7939058, issued 5/10/2011. Chen, Zhao, Anderson.  [F]

"Microfluidic autoregulator devices and arrays for operation with Newtonian fluids". USA #7992587, issued 8/9/2011. Kartalov, Scherer, Anderson, Walker. [E]

"Microfluidic large scale integration". USA #8220494, issued 7/17/2012. Studer, Quake, Anderson, Maerkel.  [E]

"Gene delivery system and method of use". USA #8652460, issued 2/18/2014. Kasahara, Logg, Anderson.  [C]

"Gene delivery system and methods of use". USA #8741279, issued 6/3/2014. Kasahara, Logg, Reid, Anderson.   [C]

"Microfluidic nucleic acid analysis". USA #8871446, issued 10/28/2014. Hong, Studer, Anderson, Quake, Leadbetter.  [E]

"Uses of  IL-12 in hematopoiesis". USA#8920990, issued 12/30/14. Chen, Zhao,  Anderson.[F]

"Method for treating deficiency in hematopoiesis". USA #9023337, issued 5/5/15. Chen, Zhao, Anderson.  [F]

"Uses  of IL-12 in  hematopoiesis". USA #9173922, issued 11/3/15. Chen, Zhao,  Anderson.[F]

"Method for bone marrow preservation or recovery''. USA #9402882, issued 8/2/16. Chen, Zhao, Anderson.  [F]

"Microfluidic nucleic acid analysis". USA #9579650, issued 2/28/17. Hong, Studer, Anderson, Quake, Leadbetter. [E]

"Uses of IL-12 in hematopoiesis". USA #10029000, issued 7/24/18. Chen, Zhao, Anderson.  [F]

SUMMARY:

Group [A]: 8 patents

Original gene therapy patents - owned by U.S. Government

Group [B]:  9 patents

Cancer targeted gene therapy patents-owned by University of Southern California

Group [C]:  4 patents

Replicating retroviral vectors for cancer gene therapy patents - owned by University of Southern California

Group [D]:   1 patent

Eye diseases gene therapy patent - owned by University of Southern California

Group [E]:  5 patents

Microfluidics (Lab-on-a-Chip) patents to allow personalized gene therapy by treating an individual patient's own stem cells - owned by Cal Tech and/or Stanford

Group [F]:  6 patents

IL-12 patents: Adjuvant therapy to support cancer gene therapy- owned by University of Southern California

TOTAL: 33 gene therapy patents

8 owned by U.S. Government

20 owned by University of Southern California

5 owned by Cal Tech and/or Stanford

Awards and honors
1954-1964 Harvard National Scholarship
1955 Detur Prize (for straight "A" academic marks)
1957-1958 Francis H. Burr Scholar of Harvard University
1957 Phi Beta Kappa
1958 A.B. degree, magna cum laude, Harvard College
1958-1959 Charles Henry Fiske Ill Scholar at Trinity College, Cambridge University, England
1959-1960 Knox Fellow at Trinity College, Cambridge University, England
1963 M.D. degree, magna cum laude, Harvard Medical School
1977 The Thomas B. Cooley Award for Scientific Achievement, awarded by the Cooley's Anemia Blood and Research Foundation for Children
1982 Outstanding Performance Award, Department of Health and Human Services (HHS)
1984 Outstanding Performance Award, HHS
1985 Outstanding Performance Award, HHS
1986 Outstanding Performance Award, HHS
1986 Wall-Copeland Lecturer, Children's National Medical Center, Washington DC
1987 Outstanding Performance Award, HHS
1988 Outstanding Performance Award, HHS
1989 Outstanding Performance Award, HHS
1989 Abbott Lecture in Molecular Biology, University of Illinois at Chicago
1990 Outstanding Performance Award, HHS
1991 The 1991 Mary Ann Liebert Biotherapeutics Award
1991 The Maud L. Menten Lecture, University of Pittsburgh
1991 Ralph R. Braund Award in Cancer Research, University of Tennessee
1991 President's Award Lecture, American Thoracic Society
1991 Presidential Meritorious Executive Rank Award, HHS
1992 Mider Lecture, NIH
1992 Timely Topics Lecture, United States and Canadian Academy of Pathology
1992 Frontiers in Clinical Science Lecture, American Federation for Clinical Research
1992 Distinguished Service Award, HHS
1992 Honorary Doctorate of Humane Letters, University of Oklahoma
1992 1992 Award for Excellence in Technology Transfer, awarded by the Federal Laboratory Consortium, Executive Branch, U.S. Government
1992 Fellow, AAAS
1992 Myron Karon Memorial Lectureship, Children's Hospital Los Angeles, Los Angeles, CA
1993 Distinguished Scientist Lecture, International and American Associations for Dental Research
1993 Charles Shepard Science Award, National Center for Infectious Diseases, HHS
1993 Plenary Lecture, 17th International Congress of Genetics
1993 CIBA-Drew Award in Biomedical Research
1993 Martin Memorial Lecture, 79th Annual Clinical Congress of the American College of Surgeons
1993 Plenary Lecture, American Academy of Pediatrics
1993 The National Hemophilia Foundation - Dr. Murray Thelin Award
1994 The King Faisal International Prize in Medicine
1994 Gross Memorial Lecture, American Pediatric Surgical Association
1994 Alan Gregg Memorial Lecture, Association of American Medical Colleges
1994 TIGR/NIST Distinguished Speaker
1994 1994 BioPharm Person of the Year Award
1994 Runner up:  Time Magazine Man-of-the-Year
1995 Keynote Lecture, Gene Therapy and Molecular Medicine Conference, Keystone Symposia
1995 Finalist, 1995 Jefferson Award for "Greatest Public Service by a Private Citizen", American Institute for Public Service
1995 The National Biotechnology Award, Oxford Bioscience Partners
1995 Keynote Lecture, 3rd Annual European Gene Therapy Workshop, Barcelona, Spain
1995 Sheen Award, National Westminster Bank
1996 Genesis Award, Pacific Center for Health Policy and Ethics, USC
1996 Honorary Doctorate of Science, University of Tulsa
1996 1996 Humanitarian Award, National Organization of Rare Disorders (NORD)
1996 Tribute Symposium "ln Utero Stem Cell Transplantation and Gene Therapy, A Scientific Symposium in Honor of: W. French Anderson, M.D. and George Stamatoyannopoulos, M.D., Dr. Sci".
1996 Keynote Speaker, Inauguration Programme, San Raffaele Biomedical Science Park Congress Centre, Milan Italy
1997 Heroes of Medicine, Time Magazine
1997 Masters of Medicine, CBS TV News
1998 Outstanding Graduate Student Teacher of the Year, USC School of Medicine
1998 Frontiers in Biomedicine Lecturer, George Washington University School of Medicine
1998 Inductee, Oklahoma Hall of Fame
1999 President's Invited Lecture, Pacific Coast Surgical Association
2000 Special Lecture, American  Association  of Neurological Surgeons
2000 Awardee,  "Treasures of  Los Angeles"
2001 Invited Lecture: "Repairing Broken Genes", The Smithsonian Institution
2001 Plenary Lecture, American Association of Clinical Chemists
2002 Honorary Doctor of Science, Upstate Medical University, State University of New York
2002 Hamdan International Award for Medical Excellence
2003 Coudert Institute Award for Medical Sciences
2003 Pioneers of Molecular Biology, Time Magazine
2003 Honorary Professor, Sun Vat-sen University Cancer Center, Guangzhou, China
2003 Honorary Professor, Peking Union Medical Center, Beijing China
2004 Profiles in Science, National Library of Medicine, NIH

References
  1. Burke, Bob and Barry Epperson (2003). W. French Anderson: Father of Gene Therapy. Oklahoma City: Oklahoma Heritage Association. ISBN 1885596251. OCLC 52290918.
  2. Lyon, Jeff and Peter Gomer (1995), Altered Fates: Gene Therapy and the Retooling of Human Life, W.W. Norton & Company, ISBN 0393315282
  3. Thompson, Larry (1994), Correcting The Code: Inventing the Genetic Cure for the Human Body, Simon & Schuster, ISBN 0-671-77082-9
  4. Anderson, W.F.: Arithmetical computations in Roman numerals. Classical Philology, LI: 145-150, 1956.
  5. Anderson, W.F.: Arithmetical procedure in Minoan linear A and in Minoan-Greek linear B. Amer. J. Archaeology, 62: 363-368, 1958.
  6. Anderson, W.F.; Bell, J.A.; Diamond, J.M., Wilson, K.R.: Rate of thermal isomerization of cis-butene-2. J. Amer. Chem. Soc., 80: 2384-2386, 1958.
  7. Marmur, J.; Anderson, W.F.; Matthews, L.; Berns, K.; Gajewska, E.; Lane, D.; Doty, P.: The effects of ultraviolet light on the biological and physical chemical properties of deoxyribonucleic acids. J. Cell. and Comp. Physiol., Suppl. 1, 58: 33-55, 1961.
  8. "The Prodigies", Time Magazine, March 19, 1956, page 83
  9. Anderson, W.F.; Gorini, L.; Breckenridge, l.: Role of ribosomes in streptomycin activated suppression. Proc. Natl. Acad. Sci. USA, 54: 1076-1083, 1965.
  10. Nirenberg, M.; Caskey, T.; Marshall, R.; Brimacombe, R.; Kellogg, D.; Doctor, B.; Hatfield, D.; Levin, J.; Rottman, F.; Pestka, S.; Wilcox, M.; Anderson, W.F.: The RNA code and protein synthesis. Cold Spring Harb. Symp. Quant. Biol., 31: 11-24, 1966.
  11. Prichard, P.M.; Gilbert, J.M.; Shafritz, D.A.; Anderson, W.F.: Factors for the initiation of haemoglobin synthesis by rabbit reticulocyte ribosomes.  Nature, 226: 511-514, 1970.
  12. Gilbert, J.M. and Anderson, W.F.: Cell-free hemoglobin synthesis, II. Characteristics of the transfer ribonucleic acid-dependent assay system. J. Biol. Chem., 245: 2342-2349, 1970.
  13. Gilbert, J.M.; Thornton, A.G.; Nienhuis, A.W.; Anderson, W.F.: Cell-free hemoglobin synthesis in beta-thalassemia. Proc. Natl. Acad. Sci. USA, 67: 1854-1861, 1970.
  14. Nienhuis, A.W.; Laycock, D.G.; Anderson, W.F.: Translation of rabbit haemoglobin messenger RNA by thalassemic and non-thalassemic ribosomes. Nature New Biology, 231: 205-208, 1971.
  15. Nienhuis, A.W. and Anderson, W.F.: Isolation and translation of hemoglobin messenger RNA from thalassemia, sickle cell anemia, and normal human reticulocytes. J. Clin. Invest., 50: 2458-2460, 1971.
  16. Nienhuis, A.W.; Canfield, P.H.; Anderson, W.F.: Hemoglobin messenger RNA from human bone marrow: Isolation and translation in homozygous and heterozygous thalassemia.  J. Clin. Invest., 52: 1735-1745, 1973.
  17. Anderson, W.F. and Diacumakos, E.G.: Genetic engineering in mammalian cells. Scientific American. 245: 106-121, 1981.
  18. Anderson, W.F.; Killos, l.; Sanders-Haigh, L.; Kretschmer, P.J.; Diacumakos, E.G.: Replication and expression of thymidine kinase and human globin genes microinjected into mouse fibroblasts.   Proc. Natl.  Acad. Sci.  USA,  77: 5399-5403, 1980.
  19. Humphries, R.K.; Berg, P.; DiPietro, J.; Bernstein, S.; Baur, A.; Nienhuis, A.W.; Anderson, W.F.: Transfer of human and murine globin-gene sequences into transgenic mice. Am. J. Hum. Genet.• 37: 295-310, 1985.
  20. Anderson, W.F., Prospects for human gene therapy.  Science, 226: 401-409, 1984.
  21. Yu, S.-F; von Ruden, T.; Kantoff, P.; Garber, C.; Seiberg, M.; Ruther, U.; Anderson, W.F.; Wagner, E.F.; Gilboa, E.: Self-inactivating retroviral vectors designed for transfer of whole genes into mammalian cells. Proc. Natl. Acad. Sci. USA, 83: 3194-3198, 1986.
  22. Gilboa, E.; Eglitis, M.A.; Kantoff, P.W.; Anderson, W.F.: Transfer and expression of cloned genes using retroviral vectors.  Bio Techniques, 4: 504-512. 1986.
  23. Eglitis, M.A.; Kantoff, P.; Gilboa, E.; Anderson, W.F.: Gene expression in mice after high efficiency retroviral-mediated gene transfer. Science, 230: 1395-1398, 1985.
  24. Anderson,  W.F.; Kantoff, P.; Eglitis, M.;  Mclachlin, J.;   Karson, E.; Zwiebel, J.; Nienhuis,  A.; Karlsson, S.; Blaese, R.M.; Kohn, D.; Gilboa, E.; Armentano, D.; Zanjani, E.D.; Flake, A.; Harrison, M.R.; Gillio, A.; Bordignon, C.; O'Reilly, R.: Gene transfer and expression in nonhuman primates using retroviral vectors. Cold Spring Harb. Symp. Quant. Biol., 51: 1073-1081, 1986.
  25. Kantoff, P. W.; Gillio, A.P.; Mclachlin, J. R.; Bordignon, C.; Eglitis, M.A.; Kernan,  N. A.;  Moen, R. C.; Kohn, D. B.; Yu, S.-F.; Karson, E.; Karlsson, S.; Zwiebel, J. A.; Gilboa, E.; Blaese, R. M.;  Nienhuis, A.; O'Reilly, R. J.; Anderson, W. F.:  Expression of human adenosine deaminase in nonhuman primates after retrovirus-mediated gene transfer.  :!.:. Exp.  Med., 166: 219-234, 1987.
  26. Cornetta, K.; Morgan, R.A.; Gillio, A.; Sturm, S.; Baltrucki, L.; O'Reilly, R.; Anderson, W.F.: No retroviremia in long-term follow-up of monkeys exposed to a murine amphotropic retrovirus.  Hum. Gene Ther., 2: 215-219, 1991.
  27. Anderson, W.F. and Fletcher, J.C.: Gene therapy in human beings: When is it ethical to begin? N. Engl. J. Med., 303: 1293-1297, 1980.
  28. Rosenberg, S.A.; Aebersold, P.; Cornetta, K.; Kasid, A.; Morgan, R.A.; Moen, R.; Karson, E.M.; Lotze, M.T.; Yang, J.C.; Topalian, S.L.; Merino, M.J.; Culver, K.; Miller, A.O.; Blaese, M.D.; Anderson, W.F.: Gene transfer into humans--immunotherapy of patients with advanced melanoma, using tumor-infiltrating lymphocytes modified by retroviral gene transduction. N. Engl. J. Med., 323: 570-578,1990.
  29. Rosenberg, S.A., Anderson, W.F., Blaese, M., Hwu, P., Vannelli, J.R., Yang, J.C., Topalian, S.L., Schwartzentruber, O.J., Weber, J.S., Ettinghausen, S.E., Parkinson, D.N., White, D.E.: The development of gene therapy for the treatment of cancer. Ann. of Surg. 218: 455- 464, 1993.
  30. Kantoff, P.; Kohn, O.B.; Mitsuya, H.; Armentano, D.; Sieberg, M.; Zwiebel, J.A.; Eglitis, M.A.; Mclachlin, J.R.; Wiginton, D.A.; Hutton, J.J.; Horowitz, S.O.; Gilboa, E.; Blaese, R.M.; Anderson, W.F.: Correction of adenosine deaminase deficiency in human T and B cells using retroviral-mediated gene transfer. Proc. Natl. Acad. Sci. USA, 83: 6563-6567, 1986.
  31. Kohn, D.B.; Mitsuya, H.; Ballow, M.; Selegue, J.E.; Barankiewicz, J.; Cohen, A.; Gelfand, E.; Anderson, W.F.; Blaese, R.M.: Establishment and characterization of adenosine deaminase-deficient human T cell lines. J. lmmunol., 142: 3971-3977, 1989.
  32. Anderson, W.F.: Human Gene Therapy. Science, 256: 808-813, 1992.
  33. Anderson, W.F., McGarrity, G.J., Moen, R.C.: Report to the NIH Recombinant DNA Advisory Committee on murine replication-competent retrovirus (RCR) assays. Hum. Gene Ther., 4: 311-321, 1993
  34. Blaese, R.M., Culver, K.W., Miller, A.O., Carter, C.S., Fleisher, T., Clerici, M., Shearer, G., Chang, L., Chiang, Y., Tolstoshev, P., Greenblatt, J.J., Rosenberg, S.A., Klien, H., Berger, M., Muller, C.A., Ramsey, J.W., Muul, L., Morgan, R.A., and Anderson, W.F.: T lymphocyte-directed gene therapy for ADA deficiency SCID: Initial trial results after 4 years. Science. 270: 475-480, 1995.
  35. Mullen, C.A., Snitzer, K., Culver, K.W., Morgan, R.A., Anderson, W.F., Blaese, R. M.: Molecular analysis of T lymphocyte-directed gene therapy for adenosine deaminase deficiency: long-term expression in vivo of genes introduced with a retroviral vector. Hum. Gene Ther. 7:1123-1129, 1996.
  36. Muul, L.M., Tuschong, L.M., Soenen, S.l., Jagadeesh, G.J., Ramsey, W.J., Long, L., Carter, C.S., Garabedian, E.K., Alleyne, M., Brown, M., Bernstein, W., Schurman, S.H., Fleisher, T.A., Leitman, S.F., Dunbar, C.E., Blaese, R.M., Candotti, F.: Persistence and expression of the adenosine deaminase gene for 12 years and immune reaction to gene transfer components: long-term results of the first clinical gene therapy trial. Blood, 101:2563- 2569, 2003
  37. Gordon, E.M., Chen, Z.H., Liu, L., Whitley, M., Liu, l., Wei, D., Groshen, S., Hinton, D.R., Anderson, W.F., Beart, R.W., Hall, F.L.: Systemic administration of a matrix-targeted retroviral vector is efficacious for cancer gene therapy in mice. Hum. Gene. Ther.,12: 193-204, 2001.
  38. Anderson, W.F.: Human Gene Therapy. Nature, 392 [SUPP]: 25-30, 1998.
  39. Anderson, W. F.: The best of times, the worst of times. Science, 288: 627-629, 2000.
  40. Anderson, W.F.: Gene therapy scores against cancer. Nature Medicine 6: 862-863, 2000.
  41. Anderson, W.F.: Gene therapy.  Sci. Amer., 273:124-128, 1995.
  42. Anderson, W.F.: A cure that may cost us ourselves. Newsweek. New York. pp. 74-76, January 1, 2000
  43. Studer, V., Hang, G., Pandolfi, A., Ortiz, M., Anderson, W. F., Quake, S. R.: Scaling properties of a low-actuation pressure microfluidic valve. J. Applied Physics, 95: 393- 398, 2004.
  44. Marcus, J.S., Anderson, W.F., Quake, S.R.: Single cell mRNA isolation and analysis. Anal. Chem, , 2006 May 1; 78(9) 3084-9
  45. Zhao, Y., Zhan, Y., Burke, K.A., Anderson, W. F.: Soluble factor(s) from bone marrow cells can rescue lethally irradiated mice by protecting endogenous hematopoietic stem cells. Exp. Hemat., 33: 428-434, 2005.
  46. Anderson, W. French: Preventable Injuries in Taekwondo", Tae Kwon Do Journal, 1(4):13, 1982
  47. Anderson, W. French: "Prevention and Treatment of Taekwondo Injuries: General Principles", Tae Kwon Do Journal, Vol. 2(1): 8-9, 1983
  48. Anderson, W. French: "Prevention of Head Injuries in Taekwondo", Tae Kwon Do Journal, Vol. 4(1): 5-7, 1985.
  49. W. French Anderson, M.D., Forensic Analysis of the April 11, 1986, FBI Firefight, Paladin Press, 2006, ISBN 978-1-58160-490-0
  50. Anderson, W. French, "A Forensic Analysis of the Warren Earp Killing", in The Death of Warren Baxter Earp: A Closer Look, by Michael M. Hickey, Talei Publishers, Inc., Honolulu, Hawaii, pages 313-320, 2000.
  51. Lee, I., Kosko, B., Anderson, W.F.: Modeling gunshot bruises in soft body armor with an adaptive fuzzy system. IEEE Transactions on Systems, Man, and Cybernetics - Part B: Cybernetics, 35: 1374-1390, 2005.
  52. "Respected Mentor Now Abuse Suspect". LA Times. September 20, 2004.
  53. "W. French Anderson convicted". The Scientist Magazine®. Retrieved 2019-04-29.
  54. "Prominent USC Geneticist Sentenced to 14 Years for Molesting Girl_AP". AHRP. 2007-02-03. Retrieved 2019-04-29.
  55. ""Father of gene therapy" faces harsh reality: a tarnished legacy and an ankle monitor". STAT. 2018-07-23. Retrieved 2019-04-29.
  56. "Anderson Asserts Innocence".
  57. "Gene Therapy Pioneer William French Anderson To Be Freed From Prison This Spring". Beverly Hills Courier. 2018-03-16. Retrieved 2019-04-29.

Further reading
  • Burke, Bob and Barry Epperson (2003), W French Anderson: Father of Gene Therapy, Oklahoma Heritage Association, ISBN 1-885596-25-1
  • Lewis, Ricki (2012), The Forever Fix: Gene Therapy and the Boy Who Saved It, St. Martin's Press, ISBN 978-0-312-68190-6
  • Lyon, Jeff and Peter Gomer (1995), Altered Fates: Gene Therapy and the Retooling of Human Life, W.W. Norton & Company, ISBN 0-393-03596-4
  • Thompson, Larry (1994), Correcting The Code: Inventing the Genetic Cure for the Human Body, Simon & Schuster, ISBN 0-671-77082-9
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