9781621825456 - my life, my science: pursuing a cure for huntington's disease de wexler, nancy sabin (16 resultados)
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Librería: GreatBookPrices, Columbia, MD, Estados Unidos de AmericaGreatBookPrices
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EUR 38,08
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Condición: New.
Idioma: Inglés
Editorial: Cold Spring Harbor Laboratory Press 3/10/2026, 2026
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Librería: BargainBookStores, Grand Rapids, MI, Estados Unidos de AmericaBargainBookStores
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EUR 40,43
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Hardback or Cased Book. Condición: New. My Life, My Science: Pursuing a Cure for Huntington's Disease. Book.
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Librería: GreatBookPrices, Columbia, MD, Estados Unidos de AmericaGreatBookPrices
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EUR 40,69
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Librería: Rarewaves USA, HEBRON, KY, Estados Unidos de AmericaRarewaves USA
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EUR 47,00
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Librería: GreatBookPricesUK, Woodford Green, Reino UnidoGreatBookPricesUK
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EUR 41,88
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Librería: GreatBookPricesUK, Woodford Green, Reino UnidoGreatBookPricesUK
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EUR 43,17
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Librería: Revaluation Books, Exeter, Reino UnidoRevaluation Books
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EUR 55,47
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Hardcover. Condición: Brand New. 190 pages. 9.00x6.00x9.00 inches. In Stock.
Idioma: Inglés
Editorial: Cold Spring Harbor Laboratory Press Mär 2026, 2026
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Librería: AHA-BUCH GmbH, Einbeck, AlemaniaAHA-BUCH GmbH
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EUR 57,68
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Buch. Condición: Neu. Neuware - 'An intimate and eloquent memoir of scientific discovery, social policy-making, and self-reflection that is as inspiring as it is harrowing. With verve, wit, and passion, Wexler tells her story of creating a new model for biomedical research while racing to find a cure for the lethal family diseas…e she herself will one day inherit.' -- Dr. Sanjay Gupta, neurosurgeon, CNN medical reporter, and author 'Nancy Wexler's story is a lesson in courage, fortitude, heroism, and above all . love. I read it in one gulp. My heart is full.' -- Carol Burnett, actor and writer When Nancy Wexler was 23, her father revealed that the mysterious illness inexorably diminishing her mother had a name. Huntington's disease, a fatal, hereditary, neurodegenerative disorder. Newly aware she had a fifty-fifty chance of developing the same condition, Wexler could have retreated. Instead, she immersed herself in what has become a lifetime's pursuit of the causes of the disease and a cure. She pioneered groundbreaking fieldwork that enabled the identification of the responsible gene. She took charge of what is now the Huntington's Disease Foundation and made it a force to be reckoned with. And when the human genome became a focus of scientific study, she was an eloquent voice for patients in disease gene research and insistent advocate for ethical use of genome sequence information. Now living with Huntington's disease, Nancy Wexler has drawn on decades of letters, research notes, and vivid memories to describe her remarkable life with warmth, wit, and unsparing honesty. She takes us from a privileged but shadowed California childhood to the shores of Venezuela's Lake Maracaibo, where she and colleagues earned the community trust that enabled them to collect blood samples and construct pedigrees, to the innovative consortium of research laboratories where those samples revealed the malevolent gene, to the halls of Congress where she pressed legislators for resources, and the boardrooms where philanthropists were persuaded into action. In this book, Wexler tells a unique story about the intertwining of personal stakes and professional passions, a testament to her courage, persistence, and belief that science can change destinies--one life, one family, one gene at a time.
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Librería: Rarewaves USA United, HEBRON, KY, Estados Unidos de AmericaRarewaves USA United
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EUR 48,90
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Hardback. Condición: New.
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Librería: Rarewaves.com UK, London, Reino UnidoRarewaves.com UK
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EUR 43,16
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Hardback. Condición: New.
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Librería: Grand Eagle Retail, Bensenville, IL, Estados Unidos de AmericaGrand Eagle Retail
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EUR 45,87
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Hardcover. Condición: new. Hardcover. "An intimate and eloquent memoir of scientific discovery, social policy-making, and self-reflection that is as inspiring as it is harrowing. With verve, wit, and passion, Nancy Wexler tells her own story of creating a new model for biomedical research while racing to find a cure for the leth…al family disease she herself will one day inherit. Searing and illuminating." -- Dr. Sanjay Gupta, neurosurgeon, CNN medical reporter, and author "Nancy Wexler's story is a lesson in courage, fortitude, heroism, and above all . love. I read it in one gulp. My heart is full." -- Carol Burnett, actor and writer When Nancy Wexler was 23, her father revealed that the mysterious illness inexorably diminishing her mother had a name. Huntington's disease, a fatal, hereditary, neurodegenerative disorder. Newly aware she had a fifty-fifty chance of developing the same condition, Wexler could have retreated. Instead, she immersed herself in what has become a lifetime's pursuit of the causes of the disease and a cure. She pioneered groundbreaking fieldwork that enabled the identification of the responsible gene. She took charge of what is now the Huntington's Disease Foundation and made it a force to be reckoned with. And when the human genome became a focus of scientific study, she was an eloquent voice for patients in disease gene research and insistent advocate for ethical use of genome sequence information. Now living with Huntington's disease, Nancy Wexler has drawn on decades of letters, research notes, and vivid memories to describe her remarkable life with warmth, wit, and unsparing honesty. She takes us from a privileged but shadowed California childhood to the shores of Venezuela's Lake Maracaibo, where she and colleagues earned the community trust that enabled them to collect blood samples and construct pedigrees, to the innovative consortium of research laboratories where those samples revealed the malevolent gene, to the halls of Congress where she pressed legislators for resources, and the boardrooms where philanthropists were persuaded into action. In this book, Wexler tells a unique story about the intertwining of personal stakes and professional passions, a testament to her courage, persistence, and belief that science can change destinies--one life, one family, one gene at a time. This item is printed on demand. Shipping may be from multiple locations in the US or from the UK, depending on stock availability.
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Librería: Majestic Books, Hounslow, Reino UnidoMajestic Books
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EUR 43,60
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Librería: Books Puddle, New York, NY, Estados Unidos de AmericaBooks Puddle
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EUR 49,88
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Librería: Biblios, frankfurt am main, HESSE, AlemaniaBiblios
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EUR 44,81
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Librería: CitiRetail, Stevenage, Reino UnidoCitiRetail
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EUR 43,19
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Hardcover. Condición: new. Hardcover. "An intimate and eloquent memoir of scientific discovery, social policy-making, and self-reflection that is as inspiring as it is harrowing. With verve, wit, and passion, Wexler tells her story of creating a new model for biomedical research while racing to find a cure for the lethal family…disease she herself will one day inherit." -- Dr. Sanjay Gupta, neurosurgeon, CNN medical reporter, and author "Nancy Wexler's story is a lesson in courage, fortitude, heroism, and above all . love. I read it in one gulp. My heart is full." -- Carol Burnett, actor and writer When Nancy Wexler was 23, her father revealed that the mysterious illness inexorably diminishing her mother had a name. Huntington's disease, a fatal, hereditary, neurodegenerative disorder. Newly aware she had a fifty-fifty chance of developing the same condition, Wexler could have retreated. Instead, she immersed herself in what has become a lifetime's pursuit of the causes of the disease and a cure. She pioneered groundbreaking fieldwork that enabled the identification of the responsible gene. She took charge of what is now the Huntington's Disease Foundation and made it a force to be reckoned with. And when the human genome became a focus of scientific study, she was an eloquent voice for patients in disease gene research and insistent advocate for ethical use of genome sequence information. Now living with Huntington's disease, Nancy Wexler has drawn on decades of letters, research notes, and vivid memories to describe her remarkable life with warmth, wit, and unsparing honesty. She takes us from a privileged but shadowed California childhood to the shores of Venezuela's Lake Maracaibo, where she and colleagues earned the community trust that enabled them to collect blood samples and construct pedigrees, to the innovative consortium of research laboratories where those samples revealed the malevolent gene, to the halls of Congress where she pressed legislators for resources, and the boardrooms where philanthropists were persuaded into action. In this book, Wexler tells a unique story about the intertwining of personal stakes and professional passions, a testament to her courage, persistence, and belief that science can change destinies--one life, one family, one gene at a time. This item is printed on demand. Shipping may be from our UK warehouse or from our Australian or US warehouses, depending on stock availability.
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Librería: AussieBookSeller, Truganina, VIC, AustraliaAussieBookSeller
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EUR 66,31
Envío por EUR 31,82Se envía de Australia a Estados Unidos de AmericaCantidad disponible: 1 disponibles
Hardcover. Condición: new. Hardcover. "An intimate and eloquent memoir of scientific discovery, social policy-making, and self-reflection that is as inspiring as it is harrowing. With verve, wit, and passion, Nancy Wexler tells her own story of creating a new model for biomedical research while racing to find a cure for the leth…al family disease she herself will one day inherit. Searing and illuminating." -- Dr. Sanjay Gupta, neurosurgeon, CNN medical reporter, and author "Nancy Wexler's story is a lesson in courage, fortitude, heroism, and above all . love. I read it in one gulp. My heart is full." -- Carol Burnett, actor and writer When Nancy Wexler was 23, her father revealed that the mysterious illness inexorably diminishing her mother had a name. Huntington's disease, a fatal, hereditary, neurodegenerative disorder. Newly aware she had a fifty-fifty chance of developing the same condition, Wexler could have retreated. Instead, she immersed herself in what has become a lifetime's pursuit of the causes of the disease and a cure. She pioneered groundbreaking fieldwork that enabled the identification of the responsible gene. She took charge of what is now the Huntington's Disease Foundation and made it a force to be reckoned with. And when the human genome became a focus of scientific study, she was an eloquent voice for patients in disease gene research and insistent advocate for ethical use of genome sequence information. Now living with Huntington's disease, Nancy Wexler has drawn on decades of letters, research notes, and vivid memories to describe her remarkable life with warmth, wit, and unsparing honesty. She takes us from a privileged but shadowed California childhood to the shores of Venezuela's Lake Maracaibo, where she and colleagues earned the community trust that enabled them to collect blood samples and construct pedigrees, to the innovative consortium of research laboratories where those samples revealed the malevolent gene, to the halls of Congress where she pressed legislators for resources, and the boardrooms where philanthropists were persuaded into action. In this book, Wexler tells a unique story about the intertwining of personal stakes and professional passions, a testament to her courage, persistence, and belief that science can change destinies--one life, one family, one gene at a time. This item is printed on demand. Shipping may be from our Sydney, NSW warehouse or from our UK or US warehouse, depending on stock availability.
