A. Merriam

发表

A chronic inflammatory response dominates the skeletal muscle molecular signature in dystrophin-deficient mdx mice.

J. D. Porter, J. S. Rao, S. Khanna, 2002, Human molecular genetics.

extraocular and hindlimb muscle signatures during myogenesis in novel cell lines from Distinctive morphological and gene/protein expression

J. D. Porter, B. Gong, S. Khanna, 2015 .

Distinctive morphological and gene/protein expression signatures during myogenesis in novel cell lines from extraocular and hindlimb muscle.

J. D. Porter, B. Gong, S. Khanna, 2006, Physiological genomics.

A Quadripotential Mesenchymal Progenitor Cell Isolated from the Marrow of an Adult Mouse

A. Caplan, B. Johnstone, Jung U. Yoo, 1999, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Characterization of the collagen phenotype of rabbit proximal tubule cells in culture.

R. Harris, A. Merriam, M. Haralson, 1999, Connective tissue research.

isometric function during repetitive activation Absence of myofibrillar creatine kinase and diaphragm

J. D. Porter, W. Guo, W. Labeikovsky, 2015 .

Persistent over-expression of specific CC class chemokines correlates with macrophage and T-cell recruitment in mdx skeletal muscle

J. D. Porter, Wei Guo, S. Khanna, 2003, Neuromuscular Disorders.

Extraocular muscle is spared despite the absence of an intact sarcoglycan complex in γ- or δ-sarcoglycan-deficient mice

J. D. Porter, E. McNally, A. Merriam, 2001, Neuromuscular Disorders.

Temporal and spatial mRNA expression patterns of TGF-β1, 2, 3 and TβRI, II, III in skeletal muscles of mdx mice

J. D. Porter, B. Gong, Lan-Fang Zhou, 2006, Neuromuscular Disorders.

Dissection of temporal gene expression signatures of affected and spared muscle groups in dystrophin-deficient (mdx) mice.

J. D. Porter, B. Gong, S. Khanna, 2003, Human molecular genetics.

Conserved and muscle-group-specific gene expression patterns shape postnatal development of the novel extraocular muscle phenotype.

J. D. Porter, B. Gong, S. Khanna, 2004, Physiological genomics.

Postnatal suppression of myomesin, muscle creatine kinase and the M-line in rat extraocular muscle

J. D. Porter, B. Gong, A. Merriam, 2003, Journal of Experimental Biology.

Paradoxical absence of M lines and downregulation of creatine kinase in mouse extraocular muscle.

J. D. Porter, W. Guo, K. Hayess, 2003, Journal of applied physiology.

Temporal gene expression profiling of dystrophin-deficient (mdx) mouse diaphragm identifies conserved and muscle group-specific mechanisms in the pathogenesis of muscular dystrophy.

J. D. Porter, B. Gong, S. Khanna, 2004, Human molecular genetics.

Analysis of gene expression differences between utrophin/dystrophin-deficient vs mdx skeletal muscles reveals a specific upregulation of slow muscle genes in limb muscles

J. D. Porter, B. Gong, J. Rafael-Fortney, 2006, Neurogenetics.

Constitutive properties, not molecular adaptations, mediate extraocular muscle sparing in dystrophic mdx mice

Francisco H Andrade, Michael Willem, J. D. Porter, 2003, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Extraocular muscle is defined by a fundamentally distinct gene expression profile

J. D. Porter, J. Li, J. S. Rao, 2001, Proceedings of the National Academy of Sciences of the United States of America.

Comprehensive expression profiling by muscle tissue class and identification of the molecular niche of extraocular muscle

J. D. Porter, B. Gong, S. Khanna, 2003, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Claudin-5 localizes to the lateral membranes of cardiomyocytes and is altered in utrophin/dystrophin-deficient cardiomyopathic mice.

B. Gong, J. Rafael-Fortney, A. Merriam, 2005, Journal of molecular and cellular cardiology.

Temporal and spatial mRNA expression patterns of TGF-beta1, 2, 3 and TbetaRI, II, III in skeletal muscles of mdx mice.

J. D. Porter, B. Gong, Lan-Fang Zhou, 2006, Neuromuscular disorders : NMD.

Conserved and muscle group-specific gene expression patterns shape postnatal development of the novel extraocular muscle phenotype

B. Gong, S. Khanna, A. Merriam, 2004 .