Diverse perspectives on Henrietta Lacks,

HeLa cells, and the ethical considerations raised by the use of human tissue in medical research.  

Whether you are interested in her personal story,

 the scientific impact of HeLa cells, or the ethical debates, these books provide valuable insights into a fascinating and complex subject.

Henrietta Lacks, whose immortal cell line known as HeLa has played a crucial role in scientific research, has been the subject of various authored works. These works explore the life of Henrietta Lacks, the impact of HeLa cells on medical science, and the ethical implications surrounding the use of her cells without her knowledge or consent. Here are some of the notable authored works on Henrietta Lacks and HeLa:

"The Henrietta Lacks Legacy Group" by Lacks Family: The Lacks family has actively advocated for their grandmother's legacy and control over her genetic material. While they have not authored a specific book, they have established the Henrietta Lacks Legacy Group to preserve her memory, support educational initiatives, and promote ethical discussions about tissue ownership.

"The Ghost of Henrietta Lacks" by Carl Djerassi (2013): This fictional work explores the ghost of Henrietta Lacks as she visits various characters involved in her story, reflecting on the ethical implications of her immortal cells and the impact on medical science.

"Henrietta Lacks: An Unsung Heroine" by S. O. Adeyemi (2016): This book focuses on Henrietta Lacks' life, emphasizing her personal struggles and the contributions of African-American women to medical science.

"The Radium Girls: The Dark Story of America's Shining Women" by Kate Moore (2017): While not directly about Henrietta Lacks, this book draws parallels with the exploitation of women's bodies in medical research and the industrial use of radium, highlighting broader ethical concerns.

"Taking the Medicine: A Short History of Medicine's Beautiful Idea, and Our Difficulty Swallowing It" by Druin Burch (2010): This book discusses the concept of consent in medical research and briefly touches on the case of Henrietta Lacks.

"The Immortal Life of Henrietta Lacks" by Rebecca Skloot (2010): This is perhaps the most well-known and widely read book about Henrietta Lacks. It delves into the life of Henrietta, her medical history, and the development of the HeLa cell line. The book also examines the impact of HeLa cells on medical research and raises ethical questions about tissue ownership and informed consent.

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