Wackerhage, Henning

Anabolic signaling deficits underlie amino acid resistance of wasting, aging muscle

Cuthbertson, D., Smith, K., Babraj, J., Leese, G., Waddell, T., Atherton, P., Wackerhage, H., Taylor, P. M., & Rennie, M. J. (2005) · The FASEB Journal

Muscle metabolism and nutritionNutrition and Health in Aging

Cited by 1,211

Disassociation between the effects of amino acids and insulin on signaling, ubiquitin ligases, and protein turnover in human muscle

Greenhaff, P. L., Karagounis, L. G., Peirce, N., Simpson, E. J., Hazell, M., Layfield, R., Wackerhage, H., Smith, K., Atherton, P., Selby, A., et al. (2008) · American Journal of Physiology-Endocrinology and Metabolism

Muscle metabolism and nutritionMuscle Physiology and Disorders

Cited by 495

Selective activation of AMPK‐PGC‐1α or PKB‐TSC2‐mTOR signaling can explain specific adaptive responses to endurance or resistance training‐like electrical muscle stimulation

Atherton, P. J., Babraj, J. A., Smith, K., Singh, J., Rennie, M. J., & Wackerhage, H. (2005) · The FASEB Journal

Muscle metabolism and nutritionMuscle Physiology and Disorders

Cited by 475

Control of the size of the human muscle mass

Rennie, M. J., Wackerhage, H., Spangenburg, E. E., & Booth, F. W. (2004) · Annual Review of Physiology

Muscle Physiology and DisordersMuscle metabolism and nutrition

Cited by 399

Stimuli and sensors that initiate skeletal muscle hypertrophy following resistance exercise

Wackerhage, H., Schoenfeld, B. J., Hamilton, D. L., Lehti, M., & Hulmi, J. J. (2019) · Journal of Applied Physiology

Muscle Physiology and DisordersMuscle metabolism and nutrition

Cited by 357

The Hippo pathway member Yap plays a key role in influencing fate decisions in muscle satellite cells

Judson, R. N., Tremblay, A. M., Knopp, P., White, R. B., Urcia, R., De Bari, C., Zammit, P. S., Camargo, F. D., & Wackerhage, H. (2012) · Journal of Cell Science

Hippo pathway signaling and YAP/TAZMuscle Physiology and Disorders

Cited by 190

Branched-Chain Amino Acids as Fuels and Anabolic Signals in HumanMuscle

Rennie, M. J., Bohé, J., Smith, K., Wackerhage, H., & Greenhaff, P. (2006) · The Journal of Nutrition

Muscle metabolism and nutritionMuscle Physiology and Disorders

Cited by 185

The Hippo Transducer YAP1 Transforms Activated Satellite Cells and Is a Potent Effector of Embryonal Rhabdomyosarcoma Formation

Tremblay, A. M., Missiaglia, E., Galli, G. G., Hettmer, S., Urcia, R., Carrara, M., Judson, R. N., Thway, K., Nadal, G., Selfe, J. L., et al. (2014) · Cancer Cell

Hippo pathway signaling and YAP/TAZSarcoma Diagnosis and Treatment

Cited by 178

Yap is a novel regulator of C2C12 myogenesis

Watt, K. I., Judson, R., Medlow, P., Reid, K., Kurth, T. B., Burniston, J. G., Ratkevicius, A., Bari, C. D., & Wackerhage, H. (2010) · Biochemical and Biophysical Research Communications

Hippo pathway signaling and YAP/TAZMuscle Physiology and Disorders

Cited by 144

The Hippo signal transduction network in skeletal and cardiac muscle

Wackerhage, H., Del Re, D. P., Judson, R. N., Sudol, M., & Sadoshima, J. (2014) · Science Signaling

Hippo pathway signaling and YAP/TAZCongenital heart defects research

Cited by 92

Genes Whose Gain or Loss-Of-Function Increases Skeletal Muscle Mass in Mice: A Systematic Literature Review

Verbrugge, S. A. J., Schönfelder, M., Becker, L., Yaghoob Nezhad, F., Hrabě de Angelis, M., & Wackerhage, H. (2018) · Frontiers in Physiology

Muscle Physiology and DisordersGenetics and Physical Performance

Cited by 56

The Hippo signal transduction network for exercise physiologists

Gabriel, B. M., Hamilton, D. L., Tremblay, A. M., & Wackerhage, H. (2016) · Journal of Applied Physiology

Hippo pathway signaling and YAP/TAZSignaling Pathways in Disease

Cited by 48

Serine synthesis pathway enzyme PHGDH is critical for muscle cell biomass, anabolic metabolism, and mTORC1 signaling

Mäntyselkä, S., Kolari, K., Baumert, P., Ylä-Outinen, L., Kuikka, L., Lahtonen, S., Permi, P., Wackerhage, H., Kalenius, E., Kivelä, R., et al. (2024) · American Journal of Physiology-Endocrinology and Metabolism

Muscle metabolism and nutritionMuscle Physiology and Disorders

Cited by 25

Genes controlling skeletal muscle glucose uptake and their regulation by endurance and resistance exercise

Verbrugge, S. A. J., Alhusen, J. A., Kempin, S., Pillon, N. J., Rozman, J., Wackerhage, H., & Kleinert, M. (2022) · Journal of Cellular Biochemistry

Metabolism, Diabetes, and CancerAdipose Tissue and Metabolism

Cited by 21

Inter-set stretch: A potential time-efficient strategy for enhancing skeletal muscle adaptations

Schoenfeld, B. J., Wackerhage, H., & De Souza, E. (2022) · Frontiers in Sports and Active Living

Sports Performance and TrainingMuscle metabolism and nutrition

Cited by 21

Effects of Skeletal Muscle Hypertrophy on Fat Mass and Glucose Homeostasis in Humans and Animals: A Narrative Review with Systematic Literature Search

Havers, T., Held, S., Schönfelder, M., Geisler, S., & Wackerhage, H. (2025) · Sports Medicine

Muscle Physiology and DisordersDiabetes, Cardiovascular Risks, and Lipoproteins

Cited by 19

Myotube growth is associated with cancer-like metabolic reprogramming and is limited by phosphoglycerate dehydrogenase

Stadhouders, L. E. M., Smith, J. A. B., Gabriel, B. M., Verbrugge, S. A. J., Hammersen, T. D., Kolijn, D., Vogel, I. S. P., Mohamed, A. D., de Wit, G. M. J., Offringa, C., et al. (2023) · Experimental Cell Research

Muscle Physiology and DisordersCancer, Hypoxia, and Metabolism

Cited by 19

Turning fat into muscle: can this be an alternative to anti‐obesity drugs such as semaglutide?

Wackerhage, H., Hinrichs, A., Wolf, E., & Hrabě de Angelis, M. (2024) · The Journal of Physiology

Adipose Tissue and MetabolismMuscle Physiology and Disorders

Cited by 8

Fusion of Normoxic- and Hypoxic-Preconditioned Myoblasts Leads to Increased Hypertrophy

Pircher, T., Wackerhage, H., Akova, E., Böcker, W., Aszodi, A., & Saller, M. M. (2022) · Cells

Muscle Physiology and DisordersCardiovascular and exercise physiology

Cited by 7