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Her name was Henrietta Lacks, but scientists know her as HeLa. She was a poor black tobacco farmer whose cells--taken without her knowledge in 1951--became one of the most important tools in medicine, vital for developing the polio vaccine, cloning, gene mapping, and more. Henrietta's cells have been bought and sold by the billions, yes she remains virtually unknown, and her family can't afford health insurance. This phenomenal New York Times bestseller tells a riveting story of the collision between ethics, race, and medicine; of scientific discovery and faith healing; and of a daughter consumed with questions about the mother she never knew.
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Cancer, Cell culture, Research, Patients, Health, HeLa cells, African American women, Medical ethics, Human experimentation in medicine, Biography, History, Lacks, Henrietta, -- 1920-1951 -- Health, Cancer -- Patients -- Virginia -- Biography, African American women -- History, Human experimentation in medicine -- United States -- History, Cancer -- Research, Health and hygiene, Tissue Donors, Patienter, Forskning, Cancerpatienter, Zellkultur, History, 20th Century, Historia, Medicinska experiment på människor, Ethics, Cellodling, African Americans, Afro-amerikanskor, Medicinsk teknik, Cells, Medicinhistoria, Prejudice, Hälsa, HeLa-Zelle, Human Experimentation, Confidentiality, Etik, MEDICAL / Ethics, Tissue and Organ Procurement, Medizinische Ethik, Cytologie, Afro-amerikanska kvinnor, medicine, science, cervical cancer, radiation, effects of radiation, polio, vaccination, Biography & Autobiography, Nonfiction, Sociology, New York Times bestseller, nyt:combined_print_nonfiction=2012-03-03, Hela Cells, MEDICAL, HeLa Cells, University of South Alabama, Reading Level-Grade 11, Reading Level-Grade 12, Cancer, patients, biography, African american women, Cancer, research, Human experimentation in medicine, history, African americans, biography, Large type books, New York Times reviewed, BIOGRAPHY & AUTOBIOGRAPHY, Medical (incl. Patients), Cultural, Ethnic & Regional, General, HEALTH & FITNESS, Diseases, 44.01 history of medicine, 44.02 philosophy and ethics of medicine, Hela cells, Bioethics, Blacks, Human genetics, Neoplasms, Translational Medical Research, Informed Consent, Research Ethics, Medical Ethics, Cell Line, SOCIAL SCIENCE, HeLa-cellen, Bio-ethiek, Zwarten, Antropogenetica, Lacks, henrietta, -- 1920-1951 -- health, Cancer -- patients -- virginia -- biography, African american women -- history, Human experimentation in medicine -- united states -- history, Cancer -- research, Tissue donors, History, 20th century, African americans, Hela-zelle, Human experimentation, Medical / ethics, Tissue and organ procurement, Medizinische ethik, Medicine, Science, Cervical cancer, Radiation, Effects of radiation, Polio, Vaccination, Biography & autobiography, New york times bestseller, Nyt:combined_print_nonfiction=2012-03-03, Medical, University of south alabama, Reading level-grade 11, Reading level-grade 12Places
United States, Förenta staterna, USA, VirginiaShowing 6 featured editions. View all 24 editions?
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1
The Immortal Life of Henrietta Lacks
2011, Broadway Paperbacks
Paperback
in English
1400052181 9781400052189
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2
The immortal life of Henriette Lacks
2010, Thorndike Press
in English
- Large print ed.
1410427927 9781410427922
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6
The Immortal Life of Henrietta Lacks [Paperback] [Jan 07, 2011] Rebecca Skloot
Publish date unknown, PAN MACMILLAN U.K
paperback
1509854428 9781509854424
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Book Details
Edition Notes
Includes bibliographical references and index.
US/Canada edition
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Work Description
Her name was Henrietta Lacks, but scientists know her as HeLa. She was a poor black tobacco farmer whose cells—taken without her knowledge in 1951—became one of the most important tools in medicine, vital for developing the polio vaccine, cloning, gene mapping, in vitro fertilization, and more. Henrietta’s cells have been bought and sold by the billions, yet she remains virtually unknown, and her family can’t afford health insurance.
This New York Times bestseller takes readers on an extraordinary journey, from the “colored” ward of Johns Hopkins Hospital in the 1950s to stark white laboratories with freezers filled with HeLa cells, from Henrietta’s small, dying hometown of Clover, Virginia, to East Baltimore today, where her children and grandchildren live and struggle with the legacy of her cells. The Immortal Life of Henrietta Lacks tells a riveting story of the collision between ethics, race, and medicine; of scientific discovery and faith healing; and of a daughter consumed with questions about the mother she never knew. It’s a story inextricably connected to the dark history of experimentation on African Americans, the birth of bioethics, and the legal battles over whether we control the stuff we’re made of.
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