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Not since the atomic bomb has a technology so alarmed its inventors that they warned the world about its use. Not, that is, until the spring of 2015, when biologist Jennifer Doudna called for a worldwide moratorium on the use of the new gene-editing tool CRISPR - a revolutionary new technology that she helped create - to make heritable changes in human embryos.

The body is magnificent but it doesn't come with a lifetime warranty or an operating manual. You're the result of millions of years of evolution, but many of the adaptations that helped your ancestors survive are now working overtime to accelerate the aging process. The assumption here is that we are our genes and therefore trapped by the past. The good news is that your genetic code - the DNA sequence that is the biochemical basis of heredity - can play a minor role in the way you age.

We’re constantly seeking answers to these fundamental human questions, and now, science has the answers. The foods we enjoy, the people we love, the emotions we feel, and the beliefs we hold can all be traced back to our DNA, germs, and environment. This witty, colloquial book is popular science at its best, describing in everyday language how genetics, epigenetics, microbiology, and psychology work together to influence our personality and actions.  

By identifying the structure of DNA, the molecule of life, Francis Crick and James Watson revolutionized biochemistry and won themselves a Nobel Prize. At the time, Watson was only 24, a young scientist hungry to make his mark. His uncompromisingly honest account of the heady days of their thrilling sprint against other world-class researchers to solve one of science's greatest mysteries gives a dazzlingly clear picture of a world of brilliant scientists with great gifts, very human ambitions, and bitter rivalries.

In the mid-1970s, scientists began using DNA sequences to reexamine the history of all life. Perhaps the most startling discovery to come out of this new field is horizontal gene transfer (HGT), or the movement of genes across species lines. For instance, we now know that roughly eight percent of the human genome arrived not through traditional inheritance from directly ancestral forms, but sideways by viral infection - a type of HGT. In The Tangled Tree David Quammen chronicles these discoveries through the lives of the researchers who made them.

Los genes no son los responsables de la desigualdad pero llevan impresas las marcas que ha dejado a lo largo de nuestra historia. La creciente desigualdad en el siglo XXI es un grave problema social y sus causas y consecuencias provocan debates y controversias que implican desde agentes sociales y políticos hasta economistas. En Desigualdad, Carles Lalueza-Fox ofrece una visión totalmente nueva de este tema al examinar las huellas genéticas dejadas por la desigualdad en los humanos a lo largo de su historia.

Over 500,000 years ago, a single gene mutated. It spread over time, becoming critical in the journey transforming our earliest ancestors into fully modern humans, capable of navigating the entire planet and beyond. Then just a few thousand years ago, humans gradually outsourced knowledge to writing, and we displaced art and music from the heart of learning. This is the extraordinary story of the discovery of a supergene that makes us uniquely human.

¿Qué tiene de malo manipular nuestra naturaleza? ¿Dónde están las líneas rojas, si las hay? El filósofo Michael Sandel trata de responder a esta pregunta a través de un ameno pero profundo repaso del campo de la bioética.

Научившись "читатa" ДНК не только современного Homo sapiens, но и наших далеких предков, мы получили возможность совершать путешествия во времени. В этой книге ведомый генетиком-антропологом Эвелин Эйер читатель пройдет теми же путями, какими передвигались наши исчезнувшие родственники — неандертальцы, денисовцы и загадочный степной народ, положивший начало всем индоевропейским языкам; проследует по следам бухарских евреев, войск Чингисхана и тысячи "королевских дочерей", отправленных Людовиком XIV заселять Новую Францию, взойдет на борт корабля, увозящего с родины африканских рабов.

Ingrassia lost his mother, two sisters, brother, and nephew to cancer—different cancers developing at different points throughout their lives. And while highly unusual, his family is not the only one to wonder whether their heartbreak is the result of unbelievable bad luck, or if there might be another explanation. Through meticulous research and riveting storytelling, Ingrassia takes us from the 1960s—when Dr. Frederick Pei Li and Dr. Joseph Fraumeni Jr. first met, not yet knowing that they would help make a groundbreaking discovery that would affect cancer patients for decades to come.

Alejandra Ponce, experta en nutrigenómica, nos advierte que, contrario a lo que la medicina tradicional ha dictado, no es correcto seguir recomendaciones generales: hay que buscarun plan de alimentación adecuado para tus genes, de manera que goces hoy de una vida sana y que llegues a la vejez sin enfermedades. Aunque estamos programados genéticamente para presentar ciertos padecimientos, la combinación de una nutrición personalizada y un estilo de vida saludable hace posible retrasarlos o incluso silenciarlos para siempre.

A tiny mutation on the X chromosome can shape a family’s history. Passed down from a “carrier” parent to a child, fragile X syndrome is the most common inherited cause of intellectual disability and autism. Beyond that—and a rarity among genetic disorders—some fragile X carriers not only transmit the mutation, but also experience related conditions themselves.

Die CRISPR-Methode und die Zukunft der Medizin. Was macht die Natur, wenn ein neuer Feind auftaucht? Sie findet eine neue Strategie. Wenn eine Bakterie von einem Virus attackiert wird, verteidigt sie sich beispielsweise, indem sie ihre genetische Struktur ändert. Doch wie können diese Mechanismen nachgewiesen werden? Und welchen Nutzen hat dieses Wissen für die Medizin? Der Amerikanerin Jennifer Doudna und der Französin Emmanuelle Charpentier sind bahnbrechende Erkenntnisse im Bereich der Biochemie gelungen.

An almost limitless archive of our history lies hidden inside our bodies, and this book traces the ancient story of Scotland from that scientific viewpoint. The mushrooming of genetic studies, of DNA analysis, is rewriting history in spectacular fashion. In Scotland: A Genetic Journey, Alistair Moffat explores the history that is printed on our genes, and in a remarkable new approach, uncovers the detail of where Scots are from, where they have journeyed, and who they are - and in so doing, vividly colors in a DNA map of Scotland.

The field of biotechnology has evolved over the past four decades, developing medicines which are curing diseases. But this journey of success has been tough and arduous, built upon the shoulders of major failures.

Une extraordinaire histoire collective dont nous sommes tous les héritiers ! Les gènes sont une fascinante machine à remonter le temps depuis que nous savons faire "parler" non seulement l'ADN des Sapiens actuels, mais aussi celui de nos lointains ancêtres. Évelyne Heyer, biologiste française, professeure en génétique des populations, dévoile un récit de l'aventure humaine dans un style clair et accessible.

In 2018, the first genetically modified babies were reportedly born in China, made possible by the invention of CRISPR technology in 2012. This controversial advancement overturned the preexisting moral consensus, which had held for over 50 years before: While gene editing an adult person was morally acceptable, modifying babies, and thus subsequent generations, crossed a significant moral line. John H. Evans here provides a meta-level guide to how these debates move forward and their significance to society.

Resistance to malaria. Blue eyes. Lactose tolerance. What do all of these traits have in common? Every one of them has emerged in the last 10,000 years.

Since 2010, it has been possible to determine a person's genetic makeup in a matter of days at an accessible cost for many millions of people. Along with this technological breakthrough there has emerged a movement to use this information to help prospective parents "eliminate preventable genetic disease". As the prospect of systematically excluding the appearance of unwanted mutations in our children comes within reach, David B. Goldstein examines the possible consequences from these types of choices.

Una piccola sigla, un mondo di significati: il DNA è una risorsa contro le malattie, uno strumento per identificare gli assassini e una chiave per comprendere il comportamento umano. La sua storia è talmente antica da intrecciarsi con quella della comparsa della vita sulla Terra. E in futuro? Proviamo a parlarne direttamente con lui. Dalla genetica di Neandertal alla clonazione di esseri umani, metteremo a fuoco speranze (e timori) che grazie al DNA si aprono per la scienza e per le nostre esistenze.