(Ilmumisaeg: 07-Apr-2026, PDF+DRM, Kirjastus: Taylor & Francis Ltd, ISBN-13: 9781040525784)
This book comprehensively explores the latest advancements in multiomics strategies for diagnosing gallbladder cancer. The initial section delves into the genetic mutations and molecular pathways critical for the onset and progression of gallbladder...Loe edasi...
(Ilmumisaeg: 07-Apr-2026, EPUB+DRM, Kirjastus: Taylor & Francis Ltd, ISBN-13: 9781040676622)
This book comprehensively explores the latest advancements in multiomics strategies for diagnosing gallbladder cancer. The initial section delves into the genetic mutations and molecular pathways critical for the onset and progression of gallbladder...Loe edasi...
(Ilmumisaeg: 31-Mar-2026, PDF+DRM, Kirjastus: Oxford University Press Inc, ISBN-13: 9780197809044)
Atlas of X-Linked Intellectual Disability Syndromes, 3rd Edition is a comprehensive reference for clinicians, laboratory geneticists, and researchers working to diagnose and understand X-linked intellectual disability (XLID). This updated edition pre...Loe edasi...
(Ilmumisaeg: 31-Mar-2026, EPUB+DRM, Kirjastus: Oxford University Press Inc, ISBN-13: 9780197809037)
Atlas of X-Linked Intellectual Disability Syndromes, 3rd Edition is a comprehensive reference for clinicians, laboratory geneticists, and researchers working to diagnose and understand X-linked intellectual disability (XLID). This updated edition pre...Loe edasi...
This book provides updated findings and trends of hereditary breast and ovarian cancer (HBOC) research and clinical practice, offering a comprehensive overview of the latest advancement. It captures the dynamic changes in HBOC treatment, driven by in...Loe edasi...
This book provides updated findings and trends of hereditary breast and ovarian cancer (HBOC) research and clinical practice, offering a comprehensive overview of the latest advancement. It captures the dynamic changes in HBOC treatment, driven by in...Loe edasi...
Soziale Angste und Misstrauen gegenuber Fremden sind tiefe, evolutionar sinnvolle Schutzmechanismen. Was passiert, wenn diese Barrieren genetisch vollstandig geloscht werden? Das Williams-Beuren-Syndrom (WBS) ist eine extrem seltene genetische Storun...Loe edasi...
It is one of the most horrifying and heartbreaking conditions in modern genetics. Lesch-Nyhan Syndrome is an ultra-rare metabolic disorder caused by the deficiency of a single enzyme (HPRT1). While this defect leads to a massive overproduction of uri...Loe edasi...
The human body possesses a miraculous ability to heal itself. When skin is cut, it forms a scar; when a bone breaks, it fuses back together. But in extremely rare cases, this biological defense mechanism glitches, turning the bodys greatest asset in...Loe edasi...
(Ilmumisaeg: 13-Feb-2026, PDF+DRM, Kirjastus: Springer-Verlag New York Inc., ISBN-13: 9781071651506)
This third edition provides protocols on fluorescence in situ hybridization (FISH) and comparative genomic hybridization approaches. Chapters provide new and updated methods on probe, cell types, tissues, organisms, plants, microorganisms, multicolor...Loe edasi...
(Ilmumisaeg: 13-Feb-2026, EPUB+DRM, Kirjastus: Springer-Verlag New York Inc., ISBN-13: 9781071651506)
This third edition provides protocols on fluorescence in situ hybridization (FISH) and comparative genomic hybridization approaches. Chapters provide new and updated methods on probe, cell types, tissues, organisms, plants, microorganisms, multicolor...Loe edasi...
Engineers have played an important and often underrecognized role in advances in the treatment and management of sickle cell disease and in recent curative breakthroughs. This comprehensive and cutting-edge edited volume brings together renowned expe...Loe edasi...
Engineers have played an important and often underrecognized role in advances in the treatment and management of sickle cell disease and in recent curative breakthroughs. This comprehensive and cutting-edge edited volume brings together renowned expe...Loe edasi...
This book presents the latest research on combination cancer therapy and the transformative role of microRNA (miRNA) modulation in improving treatment precision and outcomes. It explores how miRNAs—key regulators of gene expression—can en...Loe edasi...
This book presents the latest research on combination cancer therapy and the transformative role of microRNA (miRNA) modulation in improving treatment precision and outcomes. It explores how miRNAs—key regulators of gene expression—can en...Loe edasi...
(Ilmumisaeg: 08-Jan-2026, EPUB+DRM, Kirjastus: Oxford University Press Inc, ISBN-13: 9780197796313)
The future of precision health care is being driven by the increasingly rapid evolution of technologies. Over the past century, health care has benefited tremendously from the steady introduction of new tools, such as imaging, vaccines, immunology, b...Loe edasi...
(Ilmumisaeg: 08-Jan-2026, PDF+DRM, Kirjastus: Oxford University Press Inc, ISBN-13: 9780197796306)
The future of precision health care is being driven by the increasingly rapid evolution of technologies. Over the past century, health care has benefited tremendously from the steady introduction of new tools, such as imaging, vaccines, immunology, b...Loe edasi...
The 6th Genomics, Neuroscience, Therapeutics, and Data Innovation Summit (GeNeDIS 2024) focuses on the latest major challenges in scientific research, new drug targets, the development of novel biomarkers, new imaging techniques, novel protocols for...Loe edasi...
The 6th Genomics, Neuroscience, Therapeutics, and Data Innovation Summit (GeNeDIS 2024) focuses on the latest major challenges in scientific research, new drug targets, the development of novel biomarkers, new imaging techniques, novel protocols for...Loe edasi...
This book explores the intricate world of epigenetics and its pivotal role in precision medicine and the identification of epigenetic biomarkers for patient stratification, highlighting the importance of non-coding RNAs (ncRNAs), DNA methylation and...Loe edasi...
