N. Mokbel

发表

Grb10 Deletion Enhances Muscle Cell Proliferation, Differentiation and GLUT4 Plasma Membrane Translocation

Nolan J. Hoffman, N. Turner, G. Cooney, 2014, Journal of cellular physiology.

Grb10 regulates the development of fiber number in skeletal muscle

N. Turner, G. Cooney, R. Daly, 2012, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

The Vitamin D Receptor (VDR) Is Expressed in Skeletal Muscle of Male Mice and Modulates 25-Hydroxyvitamin D (25OHD) Uptake in Myofibers

R. Mason, N. Mokbel, C. Girgis, 2014, Endocrinology.

K7del is a common TPM2 gene mutation associated with nemaline myopathy and raised myofibre calcium sensitivity.

J. Trewhella, M. Kreissl, V. Lehtokari, 2013, Brain : a journal of neurology.

Vitamin D Receptor Ablation and Vitamin D Deficiency Result in Reduced Grip Strength, Altered Muscle Fibers, and Increased Myostatin in Mice

N. Mokbel, C. Girgis, R. Clifton-Bligh, 2015, Calcified Tissue International.

Ablation of Grb10 Specifically in Muscle Impacts Muscle Size and Glucose Metabolism in Mice

N. Turner, G. Cooney, R. Daly, 2018, Endocrinology.

Disease Severity and Thin Filament Regulation in M9R TPM3 Nemaline Myopathy

B. Ilkovski, N. Laing, V. Fowler, 2008, Journal of neuropathology and experimental neurology.

Therapies for Musculoskeletal Disease: Can we Treat Two Birds with One Stone?

N. Mokbel, C. Girgis, D. Digirolamo, 2014, Current Osteoporosis Reports.

PLIN5 deletion remodels intracellular lipid composition and causes insulin resistance in muscle

P. Meikle, N. Mokbel, M. Watt, 2014, Molecular metabolism.

In Vitro Analysis of Rod Composition and Actin Dynamics in Inherited Myopathies

B. Ilkovski, K. North, N. Mokbel, 2010, Journal of neuropathology and experimental neurology.

Muscle weakness in TPM3-myopathy is due to reduced Ca2+-sensitivity and impaired acto-myosin cross-bridge cycling in slow fibres.

G. Ravenscroft, B. Ilkovski, C. Ottenheijm, 2015, Human molecular genetics.

Muscle weakness in TPM 3-myopathy is due to reduced Ca 2 +-sensitivity and impaired acto-myosin cross-bridge cycling in slow fi bres

G. Ravenscroft, B. Ilkovski, C. Ottenheijm, 2015 .

Vitamin D signaling regulates proliferation, differentiation, and myotube size in C2C12 skeletal muscle cells.

N. Mokbel, C. Girgis, R. Clifton-Bligh, 2014, Endocrinology.

Vitamin D Receptor Ablation and Vitamin D Deficiency Result in Reduced Grip Strength, Altered Muscle Fibers, and Increased Myostatin in Mice

N. Mokbel, C. Girgis, R. Clifton-Bligh, 2015, Calcified Tissue International.

The Vitamin D Receptor (VDR) Is Expressed in Skeletal Muscle of Male Mice and Modulates 25-Hydroxyvitamin D (25OHD) Uptake in Myofibers

R. Mason, N. Mokbel, C. Girgis, 2014, Endocrinology.

K7del is a common TPM2 gene mutation associated with nemaline myopathy and raised myofibre calcium sensitivity.

J. Trewhella, M. Kreissl, V. Lehtokari, 2013, Brain : a journal of neurology.