Advances in Genetics | Buch | 978-0-12-821685-9 | sack.de

Buch, Englisch, 392 Seiten, Format (B × H): 152 mm x 229 mm, Gewicht: 770 g

Advances in Genetics

Buch, Englisch, 392 Seiten, Format (B × H): 152 mm x 229 mm, Gewicht: 770 g

ISBN: 978-0-12-821685-9
Verlag: William Andrew Publishing


Advances in Genetics, Volume 105, provides the latest information on the rapidly evolving field of genetics, presenting new medical breakthroughs that are occurring as a result of advances in our knowledge of the topic. The book continually publishes important reviews of the broadest interest to geneticists and their colleagues in affiliated disciplines, critically analyzing future directions.
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Zielgruppe


Molecular geneticists, clinical geneticists, neurologists, neuroscientists, molecular biologists, and biochemists

Weitere Infos & Material


- Pathogen and host genetics underpinning cryptococcal disease

Carolina Coelho and Rhys A. Farrer

- Role of RNA-interacting proteins in modulating plant-microbe interactions

Saurabh Pandey, Namisha Sharma and Manoj Prasad

- FMRP ribonucleoprotein complexes and RNA homeostasis

Gabriela Aparecida Marcondes Suardi and Luciana Amaral Haddad

- "Electrifying dysmorphology": Potassium channelopathies causing dysmorphic syndromes

Mark James Hamilton and Mohnish Suri

- Recent advances in oomycete genomics

Jamie McGowan and David A. Fitzpatrick

- Antibiotic drug discovery: Challenges and perspectives in the light of emerging antibiotic resistance

Keshab Bhattarai, Rina Bastola and Bikash Baral

- Application of yeast to studying amyloid and prion diseases

Yury O. Chernoff, Anastasia V. Grizel, Aleksandr A. Rubel, Andrew A. Zelinsky, Pavithra Chandramowlishwaran and Tatiana A. Chernova


Kumar, Dhavendra
Professor Kumar has considerable previous experience in writing and editing books and journals related to genetics and genomics. His books include Genomics and Clinical Medicine and Genomics and Health in the Developing World. He founded and leads the new open access journal Applied and Translational Genomics, published by Elsevier. He has published 40 articles in the journals literature.
Professor Dhavendra Kumar is a Visiting Professor, Genomic Policy Unit, Faculty of Life Sciences and Education, The University of South Wales and Consultant in Clinical Genetics at the University Hospital of Wales, Institute of Medical Genetics, Cardiff University, Cardiff, United Kingdom. He is one of the Consultants for the All Wales Medical Genetics Service and the lead Clinician for Clinical Cardiovascular Genetics. After qualifying in Medicine from the King George's Medical College, University of Lucknow, India, he completed postgraduate training in Pediatrics with an MD. Since 1980 he has pursued a career in Medical Genetics in the UK. In 1990 he became a Diplomate of the American Board of Medical Genetics. He is a Fellow of the American College of Medical Genetics (FACMG) and as well as Royal Colleges of Physicians (FRCP-London and FRCP-Ireland) and Pediatrics and Child Health (FRCPCH-UK).

In 2015, he was conferred with the higher degree of DSc by his Alma Mater, King George's Medical University, Lucknow (UP, India) based on his life-time contributions and achievements to genetic and genomic applications in medicine and health.


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