Verlag: Bulletin of the Geological Society of China, 1933
Anbieter: Masalai Press, Oakland, CA, USA
Soft cover. Zustand: Good. 5 pp. text + 1 plate. Extracted from volume 12 of Bulletin of the Geological Society of China. The described fish are Mesoclupea showchangensis and Mesoclupea globicephala. 0.0.
4°.(4),74 S. Orig.-Kartonage. Taiping Reihe Nr. 1. - Einband etwas berieben und fleckig; Ecken und Kanten stärker bestoßen; Besitzervermerk unter dem Titel.
Anbieter: Ria Christie Collections, Uxbridge, Vereinigtes Königreich
EUR 167,95
Anzahl: Mehr als 20 verfügbar
In den WarenkorbZustand: New. In.
EUR 180,32
Anzahl: Mehr als 20 verfügbar
In den WarenkorbGebunden. Zustand: New. Provides comprehensive, up-to-date reviews by leading investigators on diverse topics of SMA, including clinical features and patient care, SMN genetics and protein functions, animal models, disease pathology and mechanisms, biomarkers, current the.
Anbieter: AHA-BUCH GmbH, Einbeck, Deutschland
Buch. Zustand: Neu. Neuware - Spinal Muscular Atrophy: Disease Mechanisms and Therapy provides the latest information on a condition that is characterized by motoneuron loss and muscle atrophy, and is the leading genetic cause of infant mortality. Since the identification of the gene responsible for SMA in 1995, there have been important advances in the basic understanding of disease mechanisms, and in therapeutic development. This book provides a comprehensive accounting of recent advances in basic and clinical research that covers SMA clinical features and standards of care, multifaceted aspects of SMN protein functions and SMA disease pathology, various animal models, and biomarkers, as well as current therapeutic development. This title is ideal for graduate students/postdocs and principal investigators who are already in the SMA field and need to keep updated on recent findings and approaches, and for those who are new to, or would like to join, the field. Likewise, users will find an excellent source of reading for biotech/pharma scientists, clinical researchers, and practitioners, regulators, and patients and their advocacy organizations. Furthermore, this book is a handy reference for researchers and clinicians who may want to apply the research strategies and therapeutic approaches in SMA to other rare diseases.