David G. Allen mainly investigates Calcium, Internal medicine, Biophysics, Calcium metabolism and Endocrinology. The various areas that he examines in his Calcium study include Endoplasmic reticulum, Biochemistry, Myofibril and Muscle contraction, Anatomy. His biological study focuses on Skeletal muscle.
David G. Allen studied Skeletal muscle and Muscular dystrophy that intersect with Duchenne muscular dystrophy and Cell biology. His study in Biophysics is interdisciplinary in nature, drawing from both Isometric exercise, Calcium in biology, Intracellular, Aequorin and Contraction. His Calcium in biology research is multidisciplinary, incorporating perspectives in Cardiac muscle and Myogenesis.
His primary scientific interests are in Internal medicine, Endocrinology, Calcium, Biophysics and Skeletal muscle. His Internal medicine study frequently draws connections to other fields, such as Cardiology. In his research, Muscular dystrophy is intimately related to Duchenne muscular dystrophy, which falls under the overarching field of Endocrinology.
David G. Allen combines subjects such as Endoplasmic reticulum and Muscle contraction with his study of Calcium. His research on Biophysics also deals with topics like
David G. Allen mainly focuses on Internal medicine, Endocrinology, Cell biology, Skeletal muscle and Intracellular. His Endocrinology research is multidisciplinary, relying on both Endoplasmic reticulum, TRPC1, Duchenne muscular dystrophy and Calcium. David G. Allen studies Calcium in biology, a branch of Calcium.
In the field of Cell biology, his study on Function and Cell signaling overlaps with subjects such as Sinoatrial node and Scavenger receptor. His Skeletal muscle research incorporates themes from Biophysics and Biochemistry. He interconnects Extracellular, Ischemia, Rat heart and Amiloride in the investigation of issues within Intracellular.
His main research concerns Internal medicine, Endocrinology, Biochemistry, Cell biology and Dystrophin. When carried out as part of a general Internal medicine research project, his work on Mean age, Endometrium and Neuroendocrine carcinoma is frequently linked to work in Large cell, therefore connecting diverse disciplines of study. His Endocrinology study incorporates themes from TRPC1, Calcium and Anatomy.
He is interested in Calcium metabolism, which is a field of Calcium. His study looks at the intersection of Biochemistry and topics like Skeletal muscle with Membrane permeability. His Calcium in biology research extends to Dystrophin, which is thematically connected.
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Skeletal Muscle Fatigue: Cellular Mechanisms
D. G. Allen;G. D. Lamb;H. Westerblad.
Physiological Reviews (2008)
Muscle Fatigue: Lactic Acid or Inorganic Phosphate the Major Cause?
Håkan Westerblad;David G. Allen;Jan Lännergren.
Physiology (2002)
The effects of muscle length on intracellular calcium transients in mammalian cardiac muscle.
D G Allen;S Kurihara.
The Journal of Physiology (1982)
The cellular basis of the length-tension relation in cardiac muscle
D.G. Allen;J.C. Kentish.
Journal of Molecular and Cellular Cardiology (1985)
Myocardial contractile function during ischemia and hypoxia.
D G Allen;C H Orchard.
Circulation Research (1987)
Calcium transients in aequorin-injected frog cardiac muscle.
David G. Allen;David G. Allen;John R. Blinks.
Nature (1978)
Skeletal muscle hypertrophy is mediated by a Ca2+-dependent calcineurin signalling pathway.
Christopher Semsarian;Ming-Jie Wu;Yue-Kun Ju;Tadeusz Marciniec.
Nature (1999)
Cellular mechanisms of fatigue in skeletal muscle.
H. Westerblad;J. A. Lee;J. Lannergren;D. G. Allen.
American Journal of Physiology-cell Physiology (1991)
Effect of hydrogen peroxide and dithiothreitol on contractile function of single skeletal muscle fibres from the mouse.
Francisco H. Andrade;Francisco H. Andrade;Michael B. Reid;David G. Allen;Håkan Westerblad.
The Journal of Physiology (1998)
Early events in stretch-induced muscle damage.
David L Morgan;D G Allen.
Journal of Applied Physiology (1999)
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